BPG is committed to discovery and dissemination of knowledge
Cited by in F6Publishing
For: Bult CJ, Blake JA, Smith CL, Kadin JA, Richardson JE; Mouse Genome Database Group. Mouse Genome Database (MGD) 2019. Nucleic Acids Res 2019;47:D801-6. [PMID: 30407599 DOI: 10.1093/nar/gky1056] [Cited by in Crossref: 440] [Cited by in F6Publishing: 455] [Article Influence: 220.0] [Reference Citation Analysis]
Number Citing Articles
1 Panfilio KA, Chuva de Sousa Lopes SM. The extended analogy of extraembryonic development in insects and amniotes. Philos Trans R Soc Lond B Biol Sci 2022;377:20210268. [PMID: 36252225 DOI: 10.1098/rstb.2021.0268] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
2 Sales Conniff A, Tur J, Kohena K, Zhang M, Gibbons J, Heller LC. Transcriptomic Analysis of the Acute Skeletal Muscle Effects after Intramuscular DNA Electroporation Reveals Inflammatory Signaling. Vaccines 2022;10:2037. [DOI: 10.3390/vaccines10122037] [Reference Citation Analysis]
3 Shang L, Zhou X. Spatially aware dimension reduction for spatial transcriptomics. Nat Commun 2022;13:7203. [PMID: 36418351 DOI: 10.1038/s41467-022-34879-1] [Reference Citation Analysis]
4 Liu L, Khan A, Sanchez-rodriguez E, Zanoni F, Li Y, Steers N, Balderes O, Zhang J, Krithivasan P, Ledesma RA, Fischman C, Hebbring SJ, Harley JB, Moncrieffe H, Kottyan LC, Namjou-khales B, Walunas TL, Knevel R, Raychaudhuri S, Karlson EW, Denny JC, Stanaway IB, Crosslin D, Rauen T, Floege J, Eitner F, Moldoveanu Z, Reily C, Knoppova B, Hall S, Sheff JT, Julian BA, Wyatt RJ, Suzuki H, Xie J, Chen N, Zhou X, Zhang H, Hammarström L, Viktorin A, Magnusson PKE, Shang N, Hripcsak G, Weng C, Rundek T, Elkind MSV, Oelsner EC, Barr RG, Ionita-laza I, Novak J, Gharavi AG, Kiryluk K. Genetic regulation of serum IgA levels and susceptibility to common immune, infectious, kidney, and cardio-metabolic traits. Nat Commun 2022;13:6859. [DOI: 10.1038/s41467-022-34456-6] [Reference Citation Analysis]
5 Mingardo E, Beaman G, Grote P, Nordenskjöld A, Newman W, Woolf AS, Eckstein M, Hilger AC, Dworschak GC, Rösch W, Ebert A, Stein R, Brusco A, Di Grazia M, Tamer A, Torres FM, Hernandez JL, Erben P, Maj C, Olmos JM, Riancho JA, Valero C, Hostettler IC, Houlden H, Werring DJ, Schumacher J, Gehlen J, Giel A, Buerfent BC, Arkani S, Åkesson E, Rotstein E, Ludwig M, Holmdahl G, Giorgio E, Berettini A, Keene D, Cervellione RM, Younsi N, Ortlieb M, Oswald J, Haid B, Promm M, Neissner C, Hirsch K, Stehr M, Schäfer F, Schmiedeke E, Boemers TM, van Rooij IALM, Feitz WFJ, Marcelis CLM, Lacher M, Nelson J, Ure B, Fortmann C, Gale DP, Chan MMY, Ludwig KU, Nöthen MM, Heilmann S, Zwink N, Jenetzky E, Odermatt B, Knapp M, Reutter H. A genome-wide association study with tissue transcriptomics identifies genetic drivers for classic bladder exstrophy. Commun Biol 2022;5:1203. [DOI: 10.1038/s42003-022-04092-3] [Reference Citation Analysis]
6 Deak P, Studnitzer B, Ung T, Steinhardt R, Swartz M, Esser-kahn A. Isolating and targeting a highly active, stochastic dendritic cell subpopulation for improved immune responses. Cell Reports 2022;41:111563. [DOI: 10.1016/j.celrep.2022.111563] [Reference Citation Analysis]
7 Mitra D, Mitra D, Sabri Bensaad M, Sinha S, Pant K, Pant M, Priyadarshini A, Singh P, Dassamiour S, Hambaba L, Panneerselvam P, Das Mohapatra PK. Evolution of bioinformatics and its impact on modern bio-science in the twenty-first century: Special attention to pharmacology, plant science and drug discovery. Computational Toxicology 2022;24:100248. [DOI: 10.1016/j.comtox.2022.100248] [Reference Citation Analysis]
8 Hekselman I, Vital A, Ziv-agam M, Kerber L, Yeger-lotem E. Affected cell types for hundreds of Mendelian diseases revealed by analysis of human and mouse single-cell data.. [DOI: 10.1101/2022.10.29.513906] [Reference Citation Analysis]
9 Groza T, Gomez FL, Mashhadi HH, Muñoz-fuentes V, Gunes O, Wilson R, Cacheiro P, Frost A, Keskivali-bond P, Vardal B, Mccoy A, Cheng TK, Santos L, Wells S, Smedley D, Mallon A, Parkinson H. The International Mouse Phenotyping Consortium: comprehensive knockout phenotyping underpinning the study of human disease. Nucleic Acids Research 2022. [DOI: 10.1093/nar/gkac972] [Reference Citation Analysis]
10 Ni P, Wilson D, Su Z. A map of cis-regulatory modules and constituent transcription factor binding sites in 80% of the mouse genome. BMC Genomics 2022;23:714. [PMID: 36261804 DOI: 10.1186/s12864-022-08933-7] [Reference Citation Analysis]
11 Cacheiro P, Westerberg CH, Mager J, Dickinson ME, Nutter LMJ, Muñoz-Fuentes V, Hsu CW, Van den Veyver IB, Flenniken AM, McKerlie C, Murray SA, Teboul L, Heaney JD, Lloyd KCK, Lanoue L, Braun RE, White JK, Creighton AK, Laurin V, Guo R, Qu D, Wells S, Cleak J, Bunton-Stasyshyn R, Stewart M, Harrisson J, Mason J, Haseli Mashhadi H, Parkinson H, Mallon AM, Smedley D; International Mouse Phenotyping Consortium., Genomics England Research Consortium. Mendelian gene identification through mouse embryo viability screening. Genome Med 2022;14:119. [PMID: 36229886 DOI: 10.1186/s13073-022-01118-7] [Reference Citation Analysis]
12 de la Fuente L, Del Pozo-valero M, Perea-romero I, Blanco-kelly F, Fernández-caballero L, Cortón M, Ayuso C, Mínguez P. Prioritization of new candidate genes for rare genetic diseases by a disease-aware evaluation of heterogeneous molecular networks.. [DOI: 10.1101/2022.10.07.22280759] [Reference Citation Analysis]
13 Gaddis N, Mathur R, Marks J, Zhou L, Quach B, Waldrop A, Levran O, Agrawal A, Randesi M, Adelson M, Jeffries PW, Martin NG, Degenhardt L, Montgomery GW, Wetherill L, Lai D, Bucholz K, Foroud T, Porjesz B, Runarsdottir V, Tyrfingsson T, Einarsson G, Gudbjartsson DF, Webb BT, Crist RC, Kranzler HR, Sherva R, Zhou H, Hulse G, Wildenauer D, Kelty E, Attia J, Holliday EG, McEvoy M, Scott RJ, Schwab SG, Maher BS, Gruza R, Kreek MJ, Nelson EC, Thorgeirsson T, Stefansson K, Berrettini WH, Gelernter J, Edenberg HJ, Bierut L, Hancock DB, Johnson EO. Multi-trait genome-wide association study of opioid addiction: OPRM1 and beyond. Sci Rep 2022;12:16873. [PMID: 36207451 DOI: 10.1038/s41598-022-21003-y] [Reference Citation Analysis]
14 Li ML, Wang S, Xu P, Tian HY, Bai M, Zhang YP, Shao Y, Xiong ZJ, Qi XG, Cooper DN, Zhang G, Zhu HH, Wu DD. Functional genomics analysis reveals the evolutionary adaptation and demographic history of pygmy lorises. Proc Natl Acad Sci U S A 2022;119:e2123030119. [PMID: 36161902 DOI: 10.1073/pnas.2123030119] [Reference Citation Analysis]
15 Corda PO, Santiago J, Fardilha M. G-Protein Coupled Receptors in Human Sperm: An In Silico Approach to Identify Potential Modulatory Targets. Molecules 2022;27:6503. [PMID: 36235040 DOI: 10.3390/molecules27196503] [Reference Citation Analysis]
16 Seal RL, Denny P, Bruford EA, Gribkova AK, Landsman D, Marzluff WF, McAndrews M, Panchenko AR, Shaytan AK, Talbert PB. A standardized nomenclature for mammalian histone genes. Epigenetics Chromatin 2022;15:34. [PMID: 36180920 DOI: 10.1186/s13072-022-00467-2] [Reference Citation Analysis]
17 Iyer NR, Shin J, Cuskey S, Tian Y, Nicol NR, Doersch TE, Seipel F, McCalla SG, Roy S, Ashton RS. Modular derivation of diverse, regionally discrete human posterior CNS neurons enables discovery of transcriptomic patterns. Sci Adv 2022;8:eabn7430. [PMID: 36179024 DOI: 10.1126/sciadv.abn7430] [Reference Citation Analysis]
18 Bhandary M, Sales Conniff A, Miranda K, Heller LC. Acute Effects of Intratumor DNA Electrotransfer. Pharmaceutics 2022;14:2097. [PMID: 36297532 DOI: 10.3390/pharmaceutics14102097] [Reference Citation Analysis]
19 Zhao F, Grimm SA, Jia S, Yao HH. Contribution of the Wolffian duct mesenchyme to the formation of the female reproductive tract. PNAS Nexus 2022;1. [DOI: 10.1093/pnasnexus/pgac182] [Reference Citation Analysis]
20 Bou Sleiman M, Roy S, Gao AW, Sadler MC, von Alvensleben GVG, Li H, Sen S, Harrison DE, Nelson JF, Strong R, Miller RA, Kutalik Z, Williams RW, Auwerx J. Sex- and age-dependent genetics of longevity in a heterogeneous mouse population. Science 2022;377:eabo3191. [PMID: 36173858 DOI: 10.1126/science.abo3191] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
21 Wang YJ, Zhang X, Lam CK, Guo H, Wang C, Zhang S, Wu JC, Snyder M, Li J. Systems analysis of de novo mutations in congenital heart diseases identified a protein network in the hypoplastic left heart syndrome. Cell Syst 2022:S2405-4712(22)00353-2. [PMID: 36167075 DOI: 10.1016/j.cels.2022.09.001] [Reference Citation Analysis]
22 Zou Z, Zhang C, Wang Q, Hou Z, Xiong Z, Kong F, Wang Q, Song J, Liu B, Liu B, Wang L, Lai F, Fan Q, Tao W, Zhao S, Ma X, Li M, Wu K, Zhao H, Chen ZJ, Xie W. Translatome and transcriptome co-profiling reveals a role of TPRXs in human zygotic genome activation. Science 2022;:eabo7923. [PMID: 36074823 DOI: 10.1126/science.abo7923] [Reference Citation Analysis]
23 Doostparast Torshizi A, Wang K. Tissue-wide cell-specific proteogenomic modeling reveals novel candidate risk genes in autism spectrum disorders. NPJ Syst Biol Appl 2022;8:31. [PMID: 36068227 DOI: 10.1038/s41540-022-00243-8] [Reference Citation Analysis]
24 Seong H, Kim Y, Sa S, Jeong Y, Hong J, Cho E. Genetic Parameter Estimation and Genome-Wide Association Analysis of Social Genetic Effects on Average Daily Gain in Purebreds and Crossbreds. Animals 2022;12:2300. [DOI: 10.3390/ani12172300] [Reference Citation Analysis]
25 Lagisetty Y, Bourquard T, Al-ramahi I, Mangleburg CG, Mota S, Soleimani S, Shulman JM, Botas J, Lee K, Lichtarge O. Identification of risk genes for Alzheimer’s disease by gene embedding. Cell Genomics 2022;2:100162. [DOI: 10.1016/j.xgen.2022.100162] [Reference Citation Analysis]
26 Zhu X, Ma S, Wong WH. Genetic effects of sequence-conserved enhancer-like elements on human complex traits.. [DOI: 10.1101/2022.08.19.504589] [Reference Citation Analysis]
27 Abbasi‐moshaii B, Moradi MH, Yin T, Rahimi‐mianji G, Nejati‐javaremi A, König S. Genome‐wide scan for selective sweeps identifies novel loci associated with resistance to mastitis in German Holstein cattle. J Animal Breeding Genetics. [DOI: 10.1111/jbg.12737] [Reference Citation Analysis]
28 Young M, Richard D, Grabowski M, Auerbach BM, de Bakker BS, Hagoort J, Muthuirulan P, Kharkar V, Kurki HK, Betti L, Birkenstock L, Lewton KL, Capellini TD. The developmental impacts of natural selection on human pelvic morphology. Sci Adv 2022;8:eabq4884. [PMID: 35977020 DOI: 10.1126/sciadv.abq4884] [Reference Citation Analysis]
29 Matsuura K, Mohamed HMA, Youssef MMM, Yoshida Y, Yamamoto T. Synaptotagmin 2 is ectopically overexpressed in excitatory presynapses of a widely used CaMKΙΙα-Cre mouse line. iScience 2022;25:104692. [PMID: 35856033 DOI: 10.1016/j.isci.2022.104692] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
30 Barros CP, Derks MF, Mohr J, Wood B, Crooijmans RP, Megens H, Bink MC, Groenen MA. A new haplotype-resolved turkey genome to enable turkey genetics and genomics research.. [DOI: 10.1101/2022.08.18.504375] [Reference Citation Analysis]
31 Meng X, Pan B, Zhang Z, Guo P, Wang C, Huang X, Si N, Jiang H. Functional Pathway and Process Enrichment Analysis of Genes Associated With Morphological Abnormalities of the Outer Ear. J Craniofac Surg 2022. [PMID: 35973123 DOI: 10.1097/SCS.0000000000008904] [Reference Citation Analysis]
32 Liska O, Boross G, Rocabert C, Szappanos B, Tengölics R, Papp B. Principles of metabolome conservation in animals.. [DOI: 10.1101/2022.08.15.503737] [Reference Citation Analysis]
33 Manes NP, Calzola JM, Kaplan PR, Fraser IDC, Germain RN, Meier-Schellersheim M, Nita-Lazar A. Absolute protein quantitation of the mouse macrophage Toll-like receptor and chemotaxis pathways. Sci Data 2022;9:491. [PMID: 35961990 DOI: 10.1038/s41597-022-01612-y] [Reference Citation Analysis]
34 Jones TE, Yates B, Braschi B, Gray K, Tweedie S, Seal RL, Bruford EA. The VGNC: Expanding Standardized Vertebrate Gene Nomenclature.. [DOI: 10.1101/2022.08.10.503477] [Reference Citation Analysis]
35 Zhou WZ, Li W, Shen H, Wang RW, Chen W, Zhang Y, Zeng Q, Wang H, Yuan M, Zeng Z, Cui J, Li CY, Ye FY, Zhou Z. CHDbase: A comprehensive knowledgebase for congenital heart disease-related genes and clinical manifestations. Genomics Proteomics Bioinformatics 2022:S1672-0229(22)00093-6. [PMID: 35961607 DOI: 10.1016/j.gpb.2022.08.001] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
36 Ma WF, Turner AW, Gancayco C, Wong D, Song Y, Mosquera JV, Auguste G, Hodonsky CJ, Prabhakar A, Ekiz HA, van der Laan SW, Miller CL. PlaqView 2.0: A comprehensive web portal for cardiovascular single-cell genomics. Front Cardiovasc Med 2022;9. [DOI: 10.3389/fcvm.2022.969421] [Reference Citation Analysis]
37 Nair NU, Cheng K, Naddaf L, Sharon E, Pal LR, Rajagopal PS, Unterman I, Aldape K, Hannenhalli S, Day CP, Tabach Y, Ruppin E. Cross-species identification of cancer resistance-associated genes that may mediate human cancer risk. Sci Adv 2022;8:eabj7176. [PMID: 35921407 DOI: 10.1126/sciadv.abj7176] [Reference Citation Analysis]
38 Li H, Chen H, Zhang X, Qi Y, Wang B, Cui Y, Ren J, Zhao Y, Chen Y, Zhu T, Wang Y, Yao L, Guo Y, Zhu H, Li Y, Situ C, Guo X. Global phosphoproteomic analysis identified key kinases regulating male meiosis in mouse. Cell Mol Life Sci 2022;79:467. [PMID: 35930080 DOI: 10.1007/s00018-022-04507-8] [Reference Citation Analysis]
39 Pozmanter C, Kelly SE, Curnutte H, Van Doren M. Tudor domain containing protein 5-like (Tdrd5l) identifies a novel germline granule that regulates maternal RNAs.. [DOI: 10.1101/2022.08.02.502436] [Reference Citation Analysis]
40 Swierkowska J, Karolak JA, Vishweswaraiah S, Mrugacz M, Radhakrishna U, Gajecka M. Decreased Levels of DNA Methylation in the PCDHA Gene Cluster as a Risk Factor for Early-Onset High Myopia in Young Children. Invest Ophthalmol Vis Sci 2022;63:31. [PMID: 36036911 DOI: 10.1167/iovs.63.9.31] [Reference Citation Analysis]
41 Hu S, Molina L, Tao J, Liu S, Hassan M, Singh S, Poddar M, Bell A, Sia D, Oertel M, Raeman R, Nejak-Bowen K, Singhi A, Luo J, Monga SP, Ko S. NOTCH-YAP1/TEAD-DNMT1 Axis Drives Hepatocyte Reprogramming Into Intrahepatic Cholangiocarcinoma. Gastroenterology 2022;163:449-65. [PMID: 35550144 DOI: 10.1053/j.gastro.2022.05.007] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
42 Liu G, Yang G, Zhao G, Guo C, Zeng Y, Xue Y, Zeng F. Spatial transcriptomic profiling to identify mesoderm progenitors with precision genomic screening and functional confirmation. Cell Prolif 2022;:e13298. [PMID: 35906841 DOI: 10.1111/cpr.13298] [Reference Citation Analysis]
43 Hao R, Guo Y, Wang C, Chen F, Di C, Dong S, Cao Q, Guo J, Rong Y, Yao S, Zhu D, Chen Y, Chen H, Yang T. Lineage-specific rearrangement of chromatin loops and epigenomic features during adipocytes and osteoblasts commitment. Cell Death Differ 2022. [DOI: 10.1038/s41418-022-01035-7] [Reference Citation Analysis]
44 Seal RL, Tweedie S, Bruford EA. A standardised nomenclature for long non-coding RNAs. IUBMB Life 2022. [PMID: 35880706 DOI: 10.1002/iub.2663] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
45 Cornes B, Paisie C, Swanzey E, Schile A, Brackett K, Reinholdt L, Srivastava A. PROTEIN CODING VARIATION IN OUTBRED LABORATORY MOUSE STOCKS PROVIDES A MOLECULAR BASIS FOR DISTINCT RESEARCH APPLICATIONS.. [DOI: 10.1101/2022.07.26.501579] [Reference Citation Analysis]
46 Gowri R, Rathipriya R. Drug Target Module Mining Using Biological Multifunctional Score‐Based Coclustering. Tele‐Healthcare 2022. [DOI: 10.1002/9781119841937.ch11] [Reference Citation Analysis]
47 Awotoye W, Mossey PA, Hetmanski JB, Gowans LJJ, Eshete MA, Adeyemo WL, Alade A, Zeng E, Adamson O, Naicker T, Anand D, Adeleke C, Busch T, Li M, Petrin A, Aregbesola BS, Braimah RO, Oginni FO, Oladele AO, Oladayo A, Kayali S, Olotu J, Hassan M, Pape J, Donkor P, Arthur FKN, Obiri-Yeboah S, Sabbah DK, Agbenorku P, Plange-Rhule G, Oti AA, Gogal RA, Beaty TH, Taub M, Marazita ML, Schnieders MJ, Lachke SA, Adeyemo AA, Murray JC, Butali A. Whole-genome sequencing reveals de-novo mutations associated with nonsyndromic cleft lip/palate. Sci Rep 2022;12:11743. [PMID: 35817949 DOI: 10.1038/s41598-022-15885-1] [Reference Citation Analysis]
48 Christen M, Rupp S, Van Soens I, Bhatti SFM, Matiasek K, von Klopmann T, Jagannathan V, Madden I, Batcher K, Bannasch D, Leeb T. SLC25A12 Missense Variant in Nova Scotia Duck Tolling Retrievers Affected by Cerebellar Degeneration-Myositis Complex (CDMC). Genes (Basel) 2022;13:1223. [PMID: 35886006 DOI: 10.3390/genes13071223] [Reference Citation Analysis]
49 Brasher MS, Mize TJ, Thomas AL, Hoeffer CA, Ehringer MA, Evans LM. Testing Human Anxiety Associations of Genes Previously Implicated by Mouse Anxiety Models.. [DOI: 10.1101/2022.07.08.499186] [Reference Citation Analysis]
50 Guo Y, Cai L, Liu X, Ma L, Zhang H, Wang B, Qi Y, Liu J, Diao F, Sha J, Guo X. Single-cell quantitative proteomic analysis of human oocyte maturation revealed high heterogeneity in in vitro matured oocytes. Mol Cell Proteomics 2022;:100267. [PMID: 35809850 DOI: 10.1016/j.mcpro.2022.100267] [Reference Citation Analysis]
51 Adlam D, Berrandou T, Georges A, Nelson CP, Giannoulatou E, Henry J, Ma L, Blencowe M, Turley TN, Yang M, Braund PS, Sadeg-sayoud I, Iismaa SE, Kosel ML, Zhou X, Hamby SE, Cheng J, Liu L, Tarr I, Muller DW, d’Escamard V, King A, Brunham LR, Baranowska-clarke AA, Debette S, Amouyel P, Olin JW, Patil S, Hesselson SE, Junday K, Kanoni S, Aragam K, Butterworth AS, Tweet MS, Gulati R, Combaret N, Kadian-dodov D, Kalman J, Fatkin D, Saw J, Webb TR, Hayes SN, Yang X, Ganesh SK, Olson TM, Kovacic JC, Graham RM, Samani NJ, Bouatia-naji N, CARDIoGRAMPlusC4D, MEGASTROKE, International stroke genetics consortium (ISGC) intracranial aneurysm working group, DISCO register investigators. Genome-wide association meta-analysis of spontaneous coronary artery dissection reveals common variants and genes related to artery integrity and tissue-mediated coagulation.. [DOI: 10.1101/2022.07.05.22277238] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
52 Luskin AT, Li L, Fu X, Barcomb K, Blackburn T, Li EM, Rana A, Simon RC, Sun L, Murry AD, Golden SA, Stuber GD, Ford CP, Gu L, Bruchas MR. A diverse network of pericoerulear neurons control arousal states.. [DOI: 10.1101/2022.06.30.498327] [Reference Citation Analysis]
53 Yun D, Zhou L, Shi J, Li X, Wu X, Sun F. G3BP2, a stress granule assembly factor, is dispensable for spermatogenesis in mice. PeerJ 2022;10:e13532. [DOI: 10.7717/peerj.13532] [Reference Citation Analysis]
54 Putnam HM, Trigg SA, White SJ, Spencer LH, Vadopalas B, Natarajan A, Hetzel J, Jaeger E, Soohoo J, Gallardo-escárate C, Goetz FW, Roberts SB. Dynamic DNA methylation contributes to carryover effects and beneficial acclimatization in geoduck clams.. [DOI: 10.1101/2022.06.24.497506] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
55 Wang YJ, Zhang X, Lam CK, Guo H, Wang C, Zhang S, Wu JC, Snyder M, Li J. Systems Analysis of de novo Mutations in Congenital Heart Diseases Identified a Molecular Network in Hypoplastic Left Heart Syndrome.. [DOI: 10.1101/2022.06.23.496464] [Reference Citation Analysis]
56 Nakano T, Takenaka M, Sugiyama M, Ishikawa A. QTL Mapping for Age-Related Eye Pigmentation in the Pink-Eyed Dilution Castaneus Mutant Mouse. Genes 2022;13:1138. [DOI: 10.3390/genes13071138] [Reference Citation Analysis]
57 Chen J, Goudey B, Zobel J, Geard N, Verspoor K. Exploring automatic inconsistency detection for literature-based gene ontology annotation. Bioinformatics 2022;38:i273-81. [PMID: 35758780 DOI: 10.1093/bioinformatics/btac230] [Reference Citation Analysis]
58 Pujol-Gualdo N, Läll K, Lepamets M, Rossi HR, Arffman RK, Piltonen TT, Mägi R, Laisk T; Estonian Biobank Research Team. Advancing our understanding of genetic risk factors and potential personalized strategies for pelvic organ prolapse. Nat Commun 2022;13:3584. [PMID: 35739095 DOI: 10.1038/s41467-022-31188-5] [Reference Citation Analysis]
59 Sánchez-gaya V, Rada-iglesias Á. POSTRE: a tool to predict the pathological effects of human structural variants.. [DOI: 10.1101/2022.06.20.496902] [Reference Citation Analysis]
60 Taznin T, Perera K, Gibert Y, Ward AC, Liongue C. Cytokine Receptor-Like Factor 3 (CRLF3) Contributes to Early Zebrafish Hematopoiesis. Front Immunol 2022;13:910428. [DOI: 10.3389/fimmu.2022.910428] [Reference Citation Analysis]
61 Ahangari M, Everest E, Nguyen TH, Verrelli BC, Webb BT, Bacanu SA, Tahir Turanli E, Riley BP. Genome-wide analysis of schizophrenia and multiple sclerosis identifies shared genomic loci with mixed direction of effects. Brain Behav Immun 2022;104:183-90. [PMID: 35714915 DOI: 10.1016/j.bbi.2022.06.007] [Reference Citation Analysis]
62 Rajendran A, Soory A, Khandelwal N, Ratnaparkhi G, Kamat SS. A multi-omics analysis reveals that the lysine deacetylase ABHD14B influences glucose metabolism in mammals. J Biol Chem 2022;:102128. [PMID: 35700823 DOI: 10.1016/j.jbc.2022.102128] [Reference Citation Analysis]
63 Aschner Y, Correll KA, Beke K, Foster DG, Roybal HM, Nelson MR, Meador CL, Strand M, Anderson KC, Moore CM, Reynolds PR, Kopf KW, Burnham EL, Downey GP. PTPα Promotes Fibroproliferative Responses After Acute Lung Injury. Am J Physiol Lung Cell Mol Physiol 2022. [PMID: 35670474 DOI: 10.1152/ajplung.00436.2021] [Reference Citation Analysis]
64 Farrell C, Mumford P, Wiseman FK. Rodent Modeling of Alzheimer's Disease in Down Syndrome: In vivo and ex vivo Approaches. Front Neurosci 2022;16:909669. [DOI: 10.3389/fnins.2022.909669] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
65 Han JS, Jeon YG, Oh M, Lee G, Nahmgoong H, Han SM, Choi J, Kim YY, Shin KC, Kim J, Jo K, Choe SS, Park EJ, Kim S, Kim JB. Adipocyte HIF2α functions as a thermostat via PKA Cα regulation in beige adipocytes. Nat Commun 2022;13:3268. [PMID: 35672324 DOI: 10.1038/s41467-022-30925-0] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
66 Aftab W, Lahiri S, Imhof A. ImShot: An Open-Source Software for Probabilistic Identification of Proteins In Situ and Visualization of Proteomics Data. Mol Cell Proteomics 2022;21:100242. [PMID: 35569805 DOI: 10.1016/j.mcpro.2022.100242] [Reference Citation Analysis]
67 Wotton JM, Peterson E, Flenniken AM, Bains RS, Veeraragavan S, Bower LR, Bubier JA, Parisien M, Bezginov A, Haselimashhadi H, Mason J, Moore MA, Stewart ME, Clary DA, Delbarre DJ, Anderson LC, D'Souza A, Goodwin LO, Harrison ME, Huang Z, Mckay M, Qu D, Santos L, Srinivasan S, Urban R, Vukobradovic I, Ward CS, Willett AM, Braun RE, Brown SDM, Dickinson ME, Heaney JD, Kumar V, Lloyd KCK, Mallon AM, McKerlie C, Murray SA, Nutter LMJ, Parkinson H, Seavitt JR, Wells S, Samaco RC, Chesler EJ, Smedley D, Diatchenko L, Baumbauer KM, Young EE, Bonin RP, Mandillo S, White JK; International Mouse Phenotyping Consortium. Identifying genetic determinants of inflammatory pain in mice using a large-scale gene-targeted screen. Pain 2022;163:1139-57. [PMID: 35552317 DOI: 10.1097/j.pain.0000000000002481] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
68 Scavuzzi BM, van Drongelen V, Kaur B, Fox JC, Liu J, Mesquita-ferrari RA, Kahlenberg JM, Farkash EA, Benavides F, Miller FW, Sawalha AH, Holoshitz J. The lupus susceptibility allele DRB1*03:01 encodes a disease-driving epitope.. [DOI: 10.1101/2022.05.31.494172] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
69 Ni P, Wilson D, Su Z. A map of cis-regulatory modules and constituent transcription factor binding sites in 80% of the mouse genome.. [DOI: 10.1101/2022.05.30.494043] [Reference Citation Analysis]
70 Green CR, Wessendorf-rodriguez KA, Turner R, Hover JD, Murphy AN, Wallace M, Metallo CM. Adipocytes reprogram carbon and nitrogen metabolism to maintain lipogenic flux in the absence of Bckdha.. [DOI: 10.1101/2022.05.27.493780] [Reference Citation Analysis]
71 Matentzoglu N, Balhoff JP, Bello SM, Bizon C, Brush M, Callahan TJ, Chute CG, Duncan WD, Evelo CT, Gabriel D, Graybeal J, Gray A, Gyori BM, Haendel M, Harmse H, Harris NL, Harrow I, Hegde HB, Hoyt AL, Hoyt CT, Jiao D, Jiménez-ruiz E, Jupp S, Kim H, Koehler S, Liener T, Long Q, Malone J, Mclaughlin JA, Mcmurry JA, Moxon S, Munoz-torres MC, Osumi-sutherland D, Overton JA, Peters B, Putman T, Queralt-rosinach N, Shefchek K, Solbrig H, Thessen A, Tudorache T, Vasilevsky N, Wagner AH, Mungall CJ. A Simple Standard for Sharing Ontological Mappings (SSSOM). Database 2022;2022. [DOI: 10.1093/database/baac035] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
72 Shiau CK, Huang JH, Liu YT, Tsai HK. Genome-wide identification of associations between enhancer and alternative splicing in human and mouse. BMC Genomics 2022;22:919. [PMID: 35534820 DOI: 10.1186/s12864-022-08537-1] [Reference Citation Analysis]
73 Seaby EG, Smedley D, Taylor Tavares AL, Brittain H, van Jaarsveld RH, Baralle D, Rehm HL, O'Donnell-Luria A, Ennis S; Genomics England Research Consortium. A gene-to-patient approach uplifts novel disease gene discovery and identifies 18 putative novel disease genes. Genet Med 2022:S1098-3600(22)00748-1. [PMID: 35532742 DOI: 10.1016/j.gim.2022.04.019] [Cited by in Crossref: 4] [Article Influence: 4.0] [Reference Citation Analysis]
74 Brown RE. Genetically modified mice for research on human diseases: A triumph for Biotechnology or a work in progress? The EuroBiotech Journal 2022;6:61-88. [DOI: 10.2478/ebtj-2022-0008] [Reference Citation Analysis]
75 Anderson SR, Roberts JM, Ghena N, Irvin EA, Schwakopf J, Cooperstein IB, Bosco A, Vetter ML. Neuronal apoptosis drives remodeling states of microglia and shifts in survival pathway dependence. Elife 2022;11:e76564. [PMID: 35481836 DOI: 10.7554/eLife.76564] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 3.0] [Reference Citation Analysis]
76 Ma L, Xu J, Tang Q, Cao Y, Kong R, Li K, Liu J, Jiang L. SLC2A3 variants in familial and sporadic congenital heart diseases in a Chinese Yunnan population. Clinical Laboratory Analysis. [DOI: 10.1002/jcla.24456] [Reference Citation Analysis]
77 Zhang H, Ding X, Jin J, Guo W, Yang Q, Chen P, Yao H, Ruan L, Tao Y, Chen X. Predicted mouse interactome and network-based interpretation of differentially expressed genes. PLoS ONE 2022;17:e0264174. [DOI: 10.1371/journal.pone.0264174] [Reference Citation Analysis]
78 Fisher E, Feng J. RNA splicing regulators play critical roles in neurogenesis. WIREs RNA 2022. [DOI: 10.1002/wrna.1728] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
79 Davis KW, Bilancia CG, Martin M, Vanzo R, Rimmasch M, Hom Y, Uddin M, Serrano MA. NeuroSCORE is a genome-wide omics-based model that identifies candidate disease genes of the central nervous system. Sci Rep 2022;12:5427. [PMID: 35361823 DOI: 10.1038/s41598-022-08938-y] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
80 Williams JA, Burgess S, Suckling J, Lalousis PA, Batool F, Griffiths SL, Palmer E, Karwath A, Barsky A, Gkoutos GV, Wood S, Barnes NM, David AS, Donohoe G, Neill JC, Deakin B, Khandaker GM, Upthegrove R; PIMS Collaboration. Inflammation and Brain Structure in Schizophrenia and Other Neuropsychiatric Disorders: A Mendelian Randomization Study. JAMA Psychiatry 2022. [PMID: 35353173 DOI: 10.1001/jamapsychiatry.2022.0407] [Cited by in Crossref: 10] [Cited by in F6Publishing: 15] [Article Influence: 10.0] [Reference Citation Analysis]
81 Choy KHK, Chan SY, Lam W, Jin J, Zheng T, Law TYS, Yu SS, Wang W, Li L, Xie G, Yim HCH, Chen H, Fok EKL. The repertoire of testicular extracellular vesicle cargoes and their involvement in inter-compartmental communication associated with spermatogenesis. BMC Biol 2022;20:78. [PMID: 35351114 DOI: 10.1186/s12915-022-01268-5] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
82 Gardner EJ, Neville MDC, Samocha KE, Barclay K, Kolk M, Niemi MEK, Kirov G, Martin HC, Hurles ME. Reduced reproductive success is associated with selective constraint on human genes. Nature 2022. [PMID: 35322230 DOI: 10.1038/s41586-022-04549-9] [Cited by in Crossref: 10] [Cited by in F6Publishing: 10] [Article Influence: 10.0] [Reference Citation Analysis]
83 Polat M, Şahin Fİ, Terzi YK. Model Organisms and Systems in Life Sciences. Cumhuriyet Medical Journal 2022. [DOI: 10.7197/cmj.991430] [Reference Citation Analysis]
84 Pfleiderer MM, Galej WP. Emerging insights into the function and structure of the Integrator complex. Transcription 2022;:1-15. [PMID: 35311473 DOI: 10.1080/21541264.2022.2047583] [Reference Citation Analysis]
85 Garcia-moreno A, López-domínguez R, Villatoro-garcía JA, Ramirez-mena A, Aparicio-puerta E, Hackenberg M, Pascual-montano A, Carmona-saez P. Functional Enrichment Analysis of Regulatory Elements. Biomedicines 2022;10:590. [DOI: 10.3390/biomedicines10030590] [Cited by in Crossref: 7] [Cited by in F6Publishing: 8] [Article Influence: 7.0] [Reference Citation Analysis]
86 Qian W, Zhang M, Wan K, Xie Y, Du S, Li J, Mu X, Qiu J, Xue X, Zhuang X, Wu Y, Liu F, Wang S. Genetic evidence for facial variation being a composite phenotype of cranial variation and facial soft tissue thickness. Journal of Genetics and Genomics 2022. [DOI: 10.1016/j.jgg.2022.02.020] [Reference Citation Analysis]
87 Liu S, He L, Bannister OB, Schnegelberger RD, Tao J, Althouse AD, Schopfer FJ, Wahlang B, Cave MC, Monga SP, Zhang X, Arteel GE, Beier JI. Western diet unmasks transient low-level vinyl chloride exposure-induced tumorigenesis; potential role of the (epi-)transcriptome.. [DOI: 10.1101/2022.02.24.481808] [Reference Citation Analysis]
88 Karsten L, Janson N, Le Joncour V, Alam S, Müller B, Tanjore Ramanathan J, Laakkonen P, Sewald N, Müller KM. Bivalent EGFR-Targeting DARPin-MMAE Conjugates. Int J Mol Sci 2022;23:2468. [PMID: 35269611 DOI: 10.3390/ijms23052468] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 3.0] [Reference Citation Analysis]
89 Krayem I, Sohrabi Y, Javorková E, Volkova V, Strnad H, Havelková H, Vojtíšková J, Aidarova A, Holáň V, Demant P, Lipoldová M. Genetic Influence on Frequencies of Myeloid-Derived Cell Subpopulations in Mouse. Front Immunol 2021;12:760881. [PMID: 35154069 DOI: 10.3389/fimmu.2021.760881] [Reference Citation Analysis]
90 Palma-Vera SE, Reyer H, Langhammer M, Reinsch N, Derezanin L, Fickel J, Qanbari S, Weitzel JM, Franzenburg S, Hemmrich-Stanisak G, Schoen J. Genomic characterization of the world's longest selection experiment in mouse reveals the complexity of polygenic traits. BMC Biol 2022;20:52. [PMID: 35189878 DOI: 10.1186/s12915-022-01248-9] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
91 Lv B, Zhang X, Pazour GJ. Regulation of Hedgehog Signaling Through Arih2-Mediated Smoothened Ubiquitination and Endoplasmic Reticulum-Associated Degradation.. [DOI: 10.1101/2022.02.20.481183] [Reference Citation Analysis]
92 Zhao F, Grimm SA, Jia S, Yao HH. Contribution of the Wolffian duct mesenchyme to the formation of the female reproductive tract.. [DOI: 10.1101/2022.02.16.480738] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
93 Mansour H, Banaganapalli B, Nasser KK, Al-aama JY, Shaik NA, Saadah OI, Elango R. Genome-Wide Association Study-Guided Exome Rare Variant Burden Analysis Identifies IL1R1 and CD3E as Potential Autoimmunity Risk Genes for Celiac Disease. Front Pediatr 2022;10:837957. [DOI: 10.3389/fped.2022.837957] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
94 Tansley S, Uttam S, Ureña Guzmán A, Yaqubi M, Pacis A, Parisien M, Deamond H, Wong C, Rabau O, Brown N, Haglund L, Ouellet J, Santaguida C, Ribeiro-da-Silva A, Tahmasebi S, Prager-Khoutorsky M, Ragoussis J, Zhang J, Salter MW, Diatchenko L, Healy LM, Mogil JS, Khoutorsky A. Single-cell RNA sequencing reveals time- and sex-specific responses of mouse spinal cord microglia to peripheral nerve injury and links ApoE to chronic pain. Nat Commun 2022;13:843. [PMID: 35149686 DOI: 10.1038/s41467-022-28473-8] [Cited by in Crossref: 14] [Cited by in F6Publishing: 15] [Article Influence: 14.0] [Reference Citation Analysis]
95 Theis JL, Niaz T, Sundsbak RS, Fogarty ZC, Bamlet WR, Hagler DJ, Olson TM. CELSR1 Risk Alleles in Familial Bicuspid Aortic Valve and Hypoplastic Left Heart Syndrome. Circ Genom Precis Med 2022;15:e003523. [PMID: 35133174 DOI: 10.1161/CIRCGEN.121.003523] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 3.0] [Reference Citation Analysis]
96 Deshpande A, Chu LF, Stewart R, Gitter A. Network inference with Granger causality ensembles on single-cell transcriptomics. Cell Rep 2022;38:110333. [PMID: 35139376 DOI: 10.1016/j.celrep.2022.110333] [Cited by in Crossref: 10] [Cited by in F6Publishing: 8] [Article Influence: 10.0] [Reference Citation Analysis]
97 Long H, Reeves R, Simon MM. Mouse genomic and cellular annotations. Mamm Genome. [DOI: 10.1007/s00335-021-09936-7] [Reference Citation Analysis]
98 Wilson JJ, Wei J, Daamen AR, Sears JD, Bechtel E, Mayberry CL, Stafford GA, Bechtold L, Grammer AC, Lipsky PE, Roopenian DC, Chang C. Augmented glucose dependency of autoreactive B cells provides a treatment target for lupus.. [DOI: 10.1101/2022.02.01.475510] [Reference Citation Analysis]
99 Paul B, Weeratunga S, Tillu VA, Hariri H, Henne WM, Collins BM. Structural Predictions of the SNX-RGS Proteins Suggest They Belong to a New Class of Lipid Transfer Proteins. Front Cell Dev Biol 2022;10:826688. [DOI: 10.3389/fcell.2022.826688] [Cited by in Crossref: 8] [Cited by in F6Publishing: 9] [Article Influence: 8.0] [Reference Citation Analysis]
100 Rosenthal SB, Wang H, Shi D, Liu C, Abagyan R, McEvoy LK, Chen CH. Mapping the gene network landscape of Alzheimer's disease through integrating genomics and transcriptomics. PLoS Comput Biol 2022;18:e1009903. [PMID: 35213535 DOI: 10.1371/journal.pcbi.1009903] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
101 Shang L, Zhou X. Spatially Aware Dimension Reduction for Spatial Transcriptomics.. [DOI: 10.1101/2022.01.19.476966] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 4.0] [Reference Citation Analysis]
102 Vike NL, Bari S, Stetsiv K, Walter A, Newman S, Kawata K, Bazarian JJ, Martinovich Z, Nauman EA, Talavage TM, Papa L, Slobounov SM, Breiter HC. A preliminary model of football-related neural stress that integrates metabolomics with transcriptomics and virtual reality. iScience 2022;25:103483. [PMID: 35106455 DOI: 10.1016/j.isci.2021.103483] [Reference Citation Analysis]
103 Novak G, Kyriakis D, Grzyb K, Bernini M, Rodius S, Dittmar G, Finkbeiner S, Skupin A. Single-cell transcriptomics of human iPSC differentiation dynamics reveal a core molecular network of Parkinson's disease. Commun Biol 2022;5:49. [PMID: 35027645 DOI: 10.1038/s42003-021-02973-7] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
104 Khan AA, Kim N, Korstanje R, Choi S. Loss-of-function mutation in Pcsk1 increases serum APOA1 level and LCAT activity in mice. Lab Anim Res 2022;38:1. [PMID: 34996527 DOI: 10.1186/s42826-021-00111-2] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
105 Schulten HJ, Al-Adwani F, Saddeq HAB, Alkhatabi H, Alganmi N, Karim S, Hussein D, Al-Ghamdi KB, Jamal A, Al-Maghrabi J, Al-Qahtani MH. Meta-analysis of whole-genome gene expression datasets assessing the effects of IDH1 and IDH2 mutations in isogenic disease models. Sci Rep 2022;12:57. [PMID: 34997121 DOI: 10.1038/s41598-021-04214-7] [Reference Citation Analysis]
106 Zhou W, Li W, Shen H, Wang RW, Chen W, Zhang Y, Zeng Q, Wang H, Yuan M, Zeng Z, Cui J, Li C, Ye FY, Zhou Z. CHDbase: A Comprehensive Knowledgebase for Congenital Heart Disease-related Genes and Clinical Manifestations.. [DOI: 10.1101/2022.01.06.475217] [Reference Citation Analysis]
107 Cooper TK, Meyerholz DK, Beck AP, Delaney MA, Piersigilli A, Southard TL, Brayton CF. Research-Relevant Conditions and Pathology of Laboratory Mice, Rats, Gerbils, Guinea Pigs, Hamsters, Naked Mole Rats, and Rabbits. ILAR J 2022:ilab022. [PMID: 34979559 DOI: 10.1093/ilar/ilab022] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
108 Piao M, Li P, Zeng X, Wang X, Kang L, Zhang J, Wei Y, Zhang S, Tang L, Zhu J, Kwok CK, Hu X, Zhang QC. An ultra low-input method for global RNA structure probing uncovers Regnase-1-mediated regulation in macrophages. Fundamental Research 2022;2:2-13. [DOI: 10.1016/j.fmre.2021.12.007] [Reference Citation Analysis]
109 Qian Y, Xiong Z, Li Y, Kayser M, Liu L, Liu F. The effects of Tbx15 and Pax1 on facial and other physical morphology in mice. FASEB Bioadv 2021;3:1011-9. [PMID: 34938962 DOI: 10.1096/fba.2021-00094] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
110 Lapolice TM, Huang Y. A deep learning framework for predicting human essential genes from population and functional genomic data.. [DOI: 10.1101/2021.12.21.473690] [Reference Citation Analysis]
111 Begley DA, Schofield PN, Sundberg JP. The Mouse Online. Pathology of Genetically Engineered and Other Mutant Mice 2021. [DOI: 10.1002/9781119624608.ch2] [Reference Citation Analysis]
112 Sheppard HW, Janke LJ, Rehg JE, Vogel P. Eye and Ear. Pathology of Genetically Engineered and Other Mutant Mice 2021. [DOI: 10.1002/9781119624608.ch22] [Reference Citation Analysis]
113 Nim HT, Dang L, Thiyagarajah H, Bakopoulos D, See M, Charitakis N, Sibbritt T, Eichenlaub MP, Archer SK, Fossat N, Burke RE, Tam PPL, Warr CG, Johnson TK, Ramialison M. A cis-regulatory-directed pipeline for the identification of genes involved in cardiac development and disease. Genome Biol 2021;22:335. [PMID: 34906219 DOI: 10.1186/s13059-021-02539-0] [Reference Citation Analysis]
114 Crespo-Piazuelo D, Ramayo-Caldas Y, González-Rodríguez O, Pascual M, Quintanilla R, Ballester M. A Co-Association Network Analysis Reveals Putative Regulators for Health-Related Traits in Pigs. Front Immunol 2021;12:784978. [PMID: 34899750 DOI: 10.3389/fimmu.2021.784978] [Reference Citation Analysis]
115 Beckman EJ, Martins F, Suzuki TA, Bi K, Keeble S, Good JM, Chavez A, Ballinger MA, Agwamba K, Nachman MW. The genomic basis of high-elevation adaptation in wild house mice (Mus musculus domesticus) from South America. Genetics 2021:iyab226. [PMID: 34897431 DOI: 10.1093/genetics/iyab226] [Reference Citation Analysis]
116 Hitomi Y, Aiba Y, Ueno K, Nishida N, Kawai Y, Kawashima M, Yasunami M, Gervais O, Ito M, Cordell HJ, Mells GF, Nagasaki M, Tokunaga K, Tsuiji M, Nakamura M. rs9459874 and rs1012656 in CCR6/FGFR1OP confer susceptibility to primary biliary cholangitis. J Autoimmun 2022;126:102775. [PMID: 34864633 DOI: 10.1016/j.jaut.2021.102775] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
117 Beder T, Aromolaran O, Dönitz J, Tapanelli S, Adedeji EO, Adebiyi E, Bucher G, Koenig R. Identifying essential genes across eukaryotes by machine learning. NAR Genom Bioinform 2021;3:lqab110. [PMID: 34859210 DOI: 10.1093/nargab/lqab110] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
118 Shichkova P, Coggan JS, Markram H, Keller D. A Standardized Brain Molecular Atlas: A Resource for Systems Modeling and Simulation. Front Mol Neurosci 2021;14:604559. [PMID: 34858137 DOI: 10.3389/fnmol.2021.604559] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
119 Paul B, Weeratunga S, Tillu VA, Hariri H, Henne WM, Collins BM. Structural predictions of the SNX-RGS proteins suggest they belong to a new class of lipid transfer proteins.. [DOI: 10.1101/2021.11.30.470681] [Reference Citation Analysis]
120 LeBlanc S, Allain EP, Girouard G, Mallet M, Amor MB. Expanded phenotype of primary ciliary dyskinesia related to DRC1 pathogenic variant with dysmorphisms and vascular anomalies. Am J Med Genet A 2021. [PMID: 34851034 DOI: 10.1002/ajmg.a.62586] [Reference Citation Analysis]
121 Farrar JS, Lownik JC, Way GW, Rodriguez MC, Celi FS, Martin RK. Identification of the transgene insertion site for an adipocyte-specific adiponectin-cre model and characterization of the functional consequences. Adipocyte 2021;10:91-100. [PMID: 33565916 DOI: 10.1080/21623945.2021.1880083] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
122 Nasseri G, Matin N, Tosefsky K, Stacey G, Flibotte S, Hollman R, Wild AR, Foster LJ, Bamji SX. Synaptic Activity-Dependent Changes in the Hippocampal Palmitoylome.. [DOI: 10.1101/2021.11.26.470153] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
123 Liu L, Khan A, Sanchez-rodriguez E, Zanoni F, Li Y, Steers N, Balderes O, Zhang J, Krithivasan P, Ledesma RA, Fischman C, Hebbring SJ, Harley JB, Moncrieffe H, Kottyan LC, Namjou-khales B, Walunas TL, Knevel R, Raychaudhuri S, Karlson EW, Denny JC, Stanaway IB, Crosslin D, Rauen T, Floege J, Eitner F, Moldoveanu Z, Reily C, Knoppova B, Hall S, Sheff JT, Julian BA, Wyatt RJ, Suzuki H, Xie J, Chen N, Zhou X, Zhang H, Hammarström L, Viktorin A, Magnusson PKE, Shang N, Hripcsak G, Weng C, Rundek T, Elkind MSV, Oelsner EC, Barr RG, Ionita-laza I, Novak J, Gharavi AG, Kiryluk K. Genetic regulation of serum IgA levels and susceptibility to common immune, infectious, kidney, and cardio-metabolic traits.. [DOI: 10.1101/2021.11.19.21265524] [Reference Citation Analysis]
124 Lee EH, Park JY, Kwon HJ, Han PL. Repeated exposure with short-term behavioral stress resolves pre-existing stress-induced depressive-like behavior in mice. Nat Commun 2021;12:6682. [PMID: 34795225 DOI: 10.1038/s41467-021-26968-4] [Cited by in Crossref: 5] [Cited by in F6Publishing: 6] [Article Influence: 5.0] [Reference Citation Analysis]
125 Aponte JD, Katz DC, Roth DM, Vidal-García M, Liu W, Andrade F, Roseman CC, Murray SA, Cheverud J, Graf D, Marcucio RS, Hallgrímsson B. Relating multivariate shapes to genescapes using phenotype-biological process associations for craniofacial shape. Elife 2021;10:e68623. [PMID: 34779766 DOI: 10.7554/eLife.68623] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
126 Martin PJ, Storer BE, Levine DM, Hansen JA. Genetic variants associated with inflammatory bowel disease and gut graft-versus-host disease. Blood Adv 2021;5:4456-64. [PMID: 34535014 DOI: 10.1182/bloodadvances.2021004959] [Reference Citation Analysis]
127 Kaldunski ML, Smith JR, Hayman GT, Brodie K, De Pons JL, Demos WM, Gibson AC, Hill ML, Hoffman MJ, Lamers L, Laulederkind SJF, Nalabolu HS, Thorat K, Thota J, Tutaj M, Tutaj MA, Vedi M, Wang SJ, Zacher S, Dwinell MR, Kwitek AE. The Rat Genome Database (RGD) facilitates genomic and phenotypic data integration across multiple species for biomedical research. Mamm Genome 2021. [PMID: 34741192 DOI: 10.1007/s00335-021-09932-x] [Cited by in Crossref: 2] [Cited by in F6Publishing: 3] [Article Influence: 2.0] [Reference Citation Analysis]
128 Holzer G, De Magistris P, Gramminger C, Sachdev R, Magalska A, Schooley A, Scheufen A, Lennartz B, Tatarek-Nossol M, Lue H, Linder MI, Kutay U, Preisinger C, Moreno-Andres D, Antonin W. The nucleoporin Nup50 activates the Ran guanine nucleotide exchange factor RCC1 to promote NPC assembly at the end of mitosis. EMBO J 2021;:e108788. [PMID: 34725842 DOI: 10.15252/embj.2021108788] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 4.0] [Reference Citation Analysis]
129 Medina-gomez C, Mullin BH, Chesi A, Prijatelj V, Kemp JP, Shochat-carvalho C, Trajanoska K, Wang C, Joro R, Evans TE, Schraut KE, Li-gao R, Ahluwalia TS, Zillikens MC, Zhu K, Mook-kanamori DO, Evans DS, Nethander M, Knol MJ, Thorleifsson G, Prokic I, Zemel B, Broer L, van Schoor N, Reppe S, Pawlak MA, Ralston SH, van der Velde N, Lorentzon M, Stefansson K, Adams HH, Wilson SG, Ikram MA, Walsh JP, Lakka TA, Gautvik KM, Wilson JF, Orwoll ES, van Duijn CM, Bønnelykke K, Uitterlinden AG, Stykársdóttir U, Spector TD, Tobias JH, Ohlsson C, Felix JF, Bisgaard H, Grant SF, Richards JB, Evans DM, van der Eerden B, van de Peppel J, Ackert-bicknell C, Karasik D, Kague E, Rivadeneira F. Genome Wide Association Metanalysis Of Skull Bone Mineral Density Identifies Loci Relevant For Osteoporosis And Craniosynostosis.. [DOI: 10.1101/2021.11.01.21265592] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 4.0] [Reference Citation Analysis]
130 Vysotskiy M, Zhong X, Miller-Fleming TW, Zhou D, Cox NJ, Weiss LA; Autism Working Group of the Psychiatric Genomics Consortium^., Bipolar Disorder Working Group of the Psychiatric Genomics Consortium^., Schizophrenia Working Group of the Psychiatric Genomics Consortium^. Integration of genetic, transcriptomic, and clinical data provides insight into 16p11.2 and 22q11.2 CNV genes. Genome Med 2021;13:172. [PMID: 34715901 DOI: 10.1186/s13073-021-00972-1] [Cited by in Crossref: 5] [Cited by in F6Publishing: 6] [Article Influence: 5.0] [Reference Citation Analysis]
131 Pir MS, Bilgin HI, Sayici A, Coşkun F, Torun FM, Zhao P, Kang Y, Cevik S, Kaplan OI. ConVarT: a search engine for matching human genetic variants with variants from non-human species. Nucleic Acids Res 2021:gkab939. [PMID: 34718716 DOI: 10.1093/nar/gkab939] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 3.0] [Reference Citation Analysis]
132 Jakob L, Müller TA, Rassner M, Kleinfelder H, Veratti P, Mitschke J, Miething C, Oostendorp RAJ, Pfeifer D, Waterhouse M, Duyster J. Murine Oncostatin M Has Opposing Effects on the Proliferation of OP9 Bone Marrow Stromal Cells and NIH/3T3 Fibroblasts Signaling through the OSMR. Int J Mol Sci 2021;22:11649. [PMID: 34769079 DOI: 10.3390/ijms222111649] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
133 Pais LS, Snow H, Weisburd B, Zhang S, Baxter S, Ditroia S, O’heir E, England E, Chao K, Lemire G, Osei-owusu I, Vannoy GE, Wilson M, Nguyen K, Arachchi H, Phu W, Solomonson M, Mano S, O’leary M, Lovgren A, Babb L, Austin-tse C, Rehm HL, Macarthur DG, O’donnell-luria A. seqr : a web-based analysis and collaboration tool for rare disease genomics.. [DOI: 10.1101/2021.10.27.21265326] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
134 Bang J, Han M, Yoo TJ, Qiao L, Jung J, Na J, Carlson BA, Gladyshev VN, Hatfield DL, Kim JH, Kim LK, Lee BJ. Identification of Signaling Pathways for Early Embryonic Lethality and Developmental Retardation in Sephs1-/- Mice. Int J Mol Sci 2021;22:11647. [PMID: 34769078 DOI: 10.3390/ijms222111647] [Cited by in Crossref: 4] [Cited by in F6Publishing: 6] [Article Influence: 4.0] [Reference Citation Analysis]
135 Zheng X, Li Z, Wang G, Wang H, Zhou Y, Zhao X, Cheng CY, Qiao Y, Sun F. Sperm epigenetic alterations contribute to inter- and transgenerational effects of paternal exposure to long-term psychological stress via evading offspring embryonic reprogramming. Cell Discov 2021;7:101. [PMID: 34711814 DOI: 10.1038/s41421-021-00343-5] [Cited by in Crossref: 6] [Cited by in F6Publishing: 6] [Article Influence: 6.0] [Reference Citation Analysis]
136 Bakker OB, Claringbould A, Westra H, Wiersma H, Boulogne F, Võsa U, Symmons SM, Jonkers IH, Franke L, Deelen P. Linking common and rare disease genetics through gene regulatory networks.. [DOI: 10.1101/2021.10.21.21265342] [Cited by in Crossref: 1] [Cited by in F6Publishing: 3] [Article Influence: 1.0] [Reference Citation Analysis]
137 Cooley LS, Rudewicz J, Souleyreau W, Emanuelli A, Alvarez-Arenas A, Clarke K, Falciani F, Dufies M, Lambrechts D, Modave E, Chalopin-Fillot D, Pineau R, Ambrosetti D, Bernhard JC, Ravaud A, Négrier S, Ferrero JM, Pagès G, Benzekry S, Nikolski M, Bikfalvi A. Experimental and computational modeling for signature and biomarker discovery of renal cell carcinoma progression. Mol Cancer 2021;20:136. [PMID: 34670568 DOI: 10.1186/s12943-021-01416-5] [Cited by in Crossref: 2] [Cited by in F6Publishing: 3] [Article Influence: 2.0] [Reference Citation Analysis]
138 Wang Q, Davis PB, Qi X, Chen SG, Gurney ME, Perry G, Doraiswamy PM, Xu R. Gut-microbiota-microglia-brain interactions in Alzheimer's disease: knowledge-based, multi-dimensional characterization. Alzheimers Res Ther 2021;13:177. [PMID: 34670619 DOI: 10.1186/s13195-021-00917-1] [Cited by in Crossref: 4] [Cited by in F6Publishing: 6] [Article Influence: 4.0] [Reference Citation Analysis]
139 Iyer NR, Shin J, Cuskey S, Tian Y, Nicol NR, Doersch TE, Mccalla SG, Roy S, Ashton RS. Modular Derivation and Unbiased Single-cell Analysis of Regional Human Hindbrain And Spinal Neurons Enables Discovery of Nuanced Transcriptomic Patterns along Developmental Axes.. [DOI: 10.1101/2021.10.14.464440] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
140 Petry B, Moreira GCM, Copola AGL, de Souza MM, da Veiga FC, Jorge EC, de Oliveira Peixoto J, Ledur MC, Koltes JE, Coutinho LL. SAP30 Gene Is a Probable Regulator of Muscle Hypertrophy in Chickens. Front Genet 2021;12:709937. [PMID: 34646299 DOI: 10.3389/fgene.2021.709937] [Reference Citation Analysis]
141 Wang H, Huang B, Wang J. Predict long-range enhancer regulation based on protein-protein interactions between transcription factors. Nucleic Acids Res 2021;49:10347-68. [PMID: 34570239 DOI: 10.1093/nar/gkab841] [Cited by in Crossref: 2] [Cited by in F6Publishing: 3] [Article Influence: 2.0] [Reference Citation Analysis]
142 Brosens E, Brouwer RWW, Douben H, van Bever Y, Brooks AS, Wijnen RMH, van IJcken WFJ, Tibboel D, Rottier RJ, de Klein A. Heritability and De Novo Mutations in Oesophageal Atresia and Tracheoesophageal Fistula Aetiology. Genes (Basel) 2021;12:1595. [PMID: 34680991 DOI: 10.3390/genes12101595] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
143 Mohenska M, Tan NM, Tokolyi A, Furtado MB, Costa MW, Perry AJ, Hatwell-Humble J, van Duijvenboden K, Nim HT, Ji YMM, Charitakis N, Bienroth D, Bolk F, Vivien C, Knaupp AS, Powell DR, Elliott DA, Porrello ER, Nilsson SK, Del Monte-Nieto G, Rosenthal NA, Rossello FJ, Polo JM, Ramialison M. 3D-cardiomics: A spatial transcriptional atlas of the mammalian heart. J Mol Cell Cardiol 2021;163:20-32. [PMID: 34624332 DOI: 10.1016/j.yjmcc.2021.09.011] [Cited by in Crossref: 4] [Cited by in F6Publishing: 6] [Article Influence: 4.0] [Reference Citation Analysis]
144 Gordon-Larsen P, French JE, Moustaid-Moussa N, Voruganti VS, Mayer-Davis EJ, Bizon CA, Cheng Z, Stewart DA, Easterbrook JW, Shaikh SR. Synergizing Mouse and Human Studies to Understand the Heterogeneity of Obesity. Adv Nutr 2021;12:2023-34. [PMID: 33885739 DOI: 10.1093/advances/nmab040] [Cited by in Crossref: 6] [Cited by in F6Publishing: 6] [Article Influence: 6.0] [Reference Citation Analysis]
145 Wang M, Fang Z, Yoo B, Bejerano G, Peltz G. The Effect of Population Structure on Murine Genome-Wide Association Studies. Front Genet 2021;12:745361. [PMID: 34589118 DOI: 10.3389/fgene.2021.745361] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
146 Kunej T. Integrative Map of HIF1A Regulatory Elements and Variations. Genes (Basel) 2021;12:1526. [PMID: 34680921 DOI: 10.3390/genes12101526] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 4.0] [Reference Citation Analysis]
147 Ammous Z, Rawlins LE, Jones H, Leslie JS, Wenger O, Scott E, Deline J, Herr T, Evans R, Scheid A, Kennedy J, Chioza BA, Ames RM, Cross HE, Puffenberger EG, Harries L, Baple EL, Crosby AH. A biallelic SNIP1 Amish founder variant causes a recognizable neurodevelopmental disorder. PLoS Genet 2021;17:e1009803. [PMID: 34570759 DOI: 10.1371/journal.pgen.1009803] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 3.0] [Reference Citation Analysis]
148 Schierbaum LM, Schneider S, Herms S, Sivalingam S, Fabian J, Reutter H, Weber S, Merz WM, Tkaczyk M, Miklaszewska M, Sikora P, Szmigielska A, Krzemien G, Zachwieja K, Szczepanska M, Taranta-Janusz K, Kroll P, Polok M, Zaniew M, Hilger AC. Genome-Wide Survey for Microdeletions or -Duplications in 155 Patients with Lower Urinary Tract Obstructions (LUTO). Genes (Basel) 2021;12:1449. [PMID: 34573432 DOI: 10.3390/genes12091449] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
149 Milchevskaya V, Bugnon P, ten Buren EB, Brand F, Tresch A, Buch T. Group size planning of breedings of gene-modified animals.. [DOI: 10.1101/2021.09.17.460764] [Reference Citation Analysis]
150 Engel SR, Wong ED, Nash RS, Aleksander S, Alexander M, Douglass E, Karra K, Miyasato SR, Simison M, Skrzypek MS, Weng S, Cherry JM. New Data and Collaborations at the Saccharomyces Genome Database: Updated reference genome, alleles, and the Alliance of Genome Resources.. [DOI: 10.1101/2021.09.16.460706] [Reference Citation Analysis]
151 Gaddis N, Mathur R, Marks J, Zhou L, Quach B, Waldrop A, Levran O, Agrawal A, Randesi M, Adelson M, Jeffries PW, Johnson EC, Martin NG, Degenhardt L, Montgomery GW, Wetherill L, Lai D, Bucholz K, Foroud T, Porjesz B, Webb BT, Crist RC, Kranzler HR, Zhou H, Hulse G, Wildenauer D, Kelty E, Attia J, Holliday EG, Mcevoy M, Scott RJ, Schwab SG, Maher BS, Gruza R, Kreek M, Nelson EC, Berrettini WH, Gelernter J, Edenberg H, Bierut L, Hancock DB, Johnson EO. Multi-trait genome-wide association study of opioid addiction: OPRM1 and Beyond.. [DOI: 10.1101/2021.09.13.21263503] [Cited by in Crossref: 5] [Cited by in F6Publishing: 6] [Article Influence: 5.0] [Reference Citation Analysis]
152 Leyrolle Q, Decoeur F, Dejean C, Brière G, Leon S, Bakoyiannis I, Baroux E, Sterley TL, Bosch-Bouju C, Morel L, Amadieu C, Lecours C, St-Pierre MK, Bordeleau M, De Smedt-Peyrusse V, Séré A, Schwendimann L, Grégoire S, Bretillon L, Acar N, Joffre C, Ferreira G, Uricaru R, Thebault P, Gressens P, Tremblay ME, Layé S, Nadjar A. N-3 PUFA deficiency disrupts oligodendrocyte maturation and myelin integrity during brain development. Glia 2021. [PMID: 34519378 DOI: 10.1002/glia.24088] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
153 Boer EF, Van Hollebeke HF, Maclary ET, Holt C, Yandell M, Shapiro MD. A ROR2 coding variant is associated with craniofacial variation in domestic pigeons. Curr Biol 2021:S0960-9822(21)01204-5. [PMID: 34551284 DOI: 10.1016/j.cub.2021.08.068] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
154 Below CR, Kelly J, Brown A, Humphries JD, Hutton C, Xu J, Lee BY, Cintas C, Zhang X, Hernandez-Gordillo V, Stockdale L, Goldsworthy MA, Geraghty J, Foster L, O'Reilly DA, Schedding B, Askari J, Burns J, Hodson N, Smith DL, Lally C, Ashton G, Knight D, Mironov A, Banyard A, Eble JA, Morton JP, Humphries MJ, Griffith LG, Jørgensen C. A microenvironment-inspired synthetic three-dimensional model for pancreatic ductal adenocarcinoma organoids. Nat Mater 2021. [PMID: 34518665 DOI: 10.1038/s41563-021-01085-1] [Cited by in Crossref: 27] [Cited by in F6Publishing: 27] [Article Influence: 27.0] [Reference Citation Analysis]
155 Nomura Y, Nomura J, Nishikawa T, Takumi T. Reciprocal differentiation via GABAergic components and ASD-related phenotypes in hES with 1q21.1 CNV.. [DOI: 10.1101/2021.09.13.460033] [Reference Citation Analysis]
156 Umlai UI, Bangarusamy DK, Estivill X, Jithesh PV. Genome sequencing data analysis for rare disease gene discovery. Brief Bioinform 2021:bbab363. [PMID: 34498682 DOI: 10.1093/bib/bbab363] [Cited by in Crossref: 3] [Cited by in F6Publishing: 4] [Article Influence: 3.0] [Reference Citation Analysis]
157 Lines MA, Cuillerier A, Chakraborty P, Naas T, Duque Lasio ML, Michaud J, Pileggi C, Harper ME, Burelle Y, Toler TL, Sondheimer N, Crawford HP, Millan F, Geraghty MT. A recurrent de novo ATP5F1A substitution associated with neonatal complex V deficiency. Eur J Hum Genet 2021;29:1719-24. [PMID: 34483339 DOI: 10.1038/s41431-021-00956-0] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
158 Clarke M, Lemma R, Walton D, Volpe G, Noyvert B, Gabrielsen O, Frampton J. MYB insufficiency disrupts proteostasis in hematopoietic stem cells leading to age-related neoplasia.. [DOI: 10.1101/2021.09.04.458970] [Reference Citation Analysis]
159 Zhu T, Qi X, Chen Y, Wang L, Lv X, Yang W, Zhang J, Li K, Ning Z, Jiang Z, Qu L. Positive selection of skeleton-related genes during duck domestication revealed by whole genome sequencing. BMC Ecol Evol 2021;21:165. [PMID: 34488647 DOI: 10.1186/s12862-021-01894-7] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
160 Choi J, Jang YJ, Dabrowska C, Iich E, Evans KV, Hall H, Janes SM, Simons BD, Koo BK, Kim J, Lee JH. Release of Notch activity coordinated by IL-1β signalling confers differentiation plasticity of airway progenitors via Fosl2 during alveolar regeneration. Nat Cell Biol 2021;23:953-66. [PMID: 34475534 DOI: 10.1038/s41556-021-00742-6] [Cited by in Crossref: 13] [Cited by in F6Publishing: 13] [Article Influence: 13.0] [Reference Citation Analysis]
161 Boer CG, Hatzikotoulas K, Southam L, Stefánsdóttir L, Zhang Y, Coutinho de Almeida R, Wu TT, Zheng J, Hartley A, Teder-Laving M, Skogholt AH, Terao C, Zengini E, Alexiadis G, Barysenka A, Bjornsdottir G, Gabrielsen ME, Gilly A, Ingvarsson T, Johnsen MB, Jonsson H, Kloppenburg M, Luetge A, Lund SH, Mägi R, Mangino M, Nelissen RRGHH, Shivakumar M, Steinberg J, Takuwa H, Thomas LF, Tuerlings M, Babis GC, Cheung JPY, Kang JH, Kraft P, Lietman SA, Samartzis D, Slagboom PE, Stefansson K, Thorsteinsdottir U, Tobias JH, Uitterlinden AG, Winsvold B, Zwart JA, Davey Smith G, Sham PC, Thorleifsson G, Gaunt TR, Morris AP, Valdes AM, Tsezou A, Cheah KSE, Ikegawa S, Hveem K, Esko T, Wilkinson JM, Meulenbelt I, Lee MTM, van Meurs JBJ, Styrkársdóttir U, Zeggini E; arcOGEN Consortium., HUNT All-In Pain., ARGO Consortium., Regeneron Genetics Center. Deciphering osteoarthritis genetics across 826,690 individuals from 9 populations. Cell 2021;184:4784-4818.e17. [PMID: 34450027 DOI: 10.1016/j.cell.2021.07.038] [Cited by in Crossref: 52] [Cited by in F6Publishing: 57] [Article Influence: 52.0] [Reference Citation Analysis]
162 Starcher AE, Peissig K, Stanton JB, Churchill GA, Cai D, Maxwell JT, Grider A, Love K, Chen SY, Coleman AE, Strauss E, Pazdro R. A systems approach using Diversity Outbred mice distinguishes the cardiovascular effects and genetics of circulating GDF11 from those of its homolog, myostatin. G3 (Bethesda) 2021:jkab293. [PMID: 34510201 DOI: 10.1093/g3journal/jkab293] [Reference Citation Analysis]
163 Hunter WB, Wintermantel WM. Optimizing Efficient RNAi-Mediated Control of Hemipteran Pests (Psyllids, Leafhoppers, Whitefly): Modified Pyrimidines in dsRNA Triggers. Plants (Basel) 2021;10:1782. [PMID: 34579315 DOI: 10.3390/plants10091782] [Cited by in Crossref: 5] [Cited by in F6Publishing: 6] [Article Influence: 5.0] [Reference Citation Analysis]
164 Hanspers K, Kutmon M, Coort SL, Digles D, Dupuis LJ, Ehrhart F, Hu F, Lopes EN, Martens M, Pham N, Shin W, Slenter DN, Waagmeester A, Willighagen EL, Winckers LA, Evelo CT, Pico AR. Ten simple rules for creating reusable pathway models for computational analysis and visualization. PLoS Comput Biol 2021;17:e1009226. [PMID: 34411100 DOI: 10.1371/journal.pcbi.1009226] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 3.0] [Reference Citation Analysis]
165 Demetci P, Cheng W, Darnell G, Zhou X, Ramachandran S, Crawford L. Multi-scale inference of genetic trait architecture using biologically annotated neural networks. PLoS Genet 2021;17:e1009754. [PMID: 34411094 DOI: 10.1371/journal.pgen.1009754] [Cited by in Crossref: 5] [Cited by in F6Publishing: 6] [Article Influence: 5.0] [Reference Citation Analysis]
166 Raza A, Diehl SA, Case LK, Krementsov DN, Li D, Kost J, Ball RL, Chesler EJ, Philip VM, Huang R, Chen Y, Ma R, Tyler AL, Mahoney JM, Blankenhorn EP, Teuscher C. Genetic Analysis of Bphse: a Novel Gene Complementing Resistance to Bordetella pertussis-Induced Histamine Sensitization.. [DOI: 10.1101/2021.08.18.456822] [Reference Citation Analysis]
167 Wohler E, Martin R, Griffith S, Rodrigues EDS, Antonescu C, Posey JE, Coban-Akdemir Z, Jhangiani SN, Doheny KF, Lupski JR, Valle D, Hamosh A, Sobreira N. PhenoDB, GeneMatcher and VariantMatcher, tools for analysis and sharing of sequence data. Orphanet J Rare Dis 2021;16:365. [PMID: 34407837 DOI: 10.1186/s13023-021-01916-z] [Cited by in Crossref: 12] [Cited by in F6Publishing: 12] [Article Influence: 12.0] [Reference Citation Analysis]
168 Lagger C, Ursu E, Equey A, Avelar RA, Pisco AO, Tacutu R, de Magalhães JP. scAgeCom: a murine atlas of age-related changes in intercellular communication inferred with the package scDiffCom.. [DOI: 10.1101/2021.08.13.456238] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 4.0] [Reference Citation Analysis]
169 Kim J, Kim MG, Jeong SH, Kim HJ, Son SW. STAT3 maintains skin barrier integrity by modulating SPINK5 and KLK5 expression in keratinocytes. Exp Dermatol 2021. [PMID: 34378233 DOI: 10.1111/exd.14445] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
170 Konopka T, Ng S, Smedley D. Diffusion enables integration of heterogeneous data and user-driven learning in a desktop knowledge-base. PLoS Comput Biol 2021;17:e1009283. [PMID: 34379637 DOI: 10.1371/journal.pcbi.1009283] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
171 Li Q, Chen W, Wang C, Liu Z, Gu Y, Xu X, Xu J, Jiang T, Xu M, Wang Y, Chen C, Zhong Y, Zhang Y, Yao L, Jin G, Hu Z, Zhou P. Whole-exome sequencing reveals common and rare variants in immunologic and neurological genes implicated in achalasia. Am J Hum Genet 2021;108:1478-87. [PMID: 34197731 DOI: 10.1016/j.ajhg.2021.06.004] [Reference Citation Analysis]
172 Bozkurt T, Alanay Y, Isik U, Sezerman U. Re-analysis of whole-exome sequencing data reveals a novel splicing variant in the SLC2A1 in a patient with GLUT1 Deficiency Syndrome 1 accompanied by hemangioma: a case report. BMC Med Genomics 2021;14:197. [PMID: 34332575 DOI: 10.1186/s12920-021-01045-3] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
173 Duek P, Mary C, Zahn-Zabal M, Bairoch A, Lane L. Functionathon: a manual data mining workflow to generate functional hypotheses for uncharacterized human proteins and its application by undergraduate students. Database (Oxford) 2021;2021:baab046. [PMID: 34318869 DOI: 10.1093/database/baab046] [Cited by in Crossref: 4] [Cited by in F6Publishing: 5] [Article Influence: 4.0] [Reference Citation Analysis]
174 Wang S, Chai X, Yan Z, Zhao S, Yang Y, Li X, Niu Y, Lin G, Su Z, Wu Z, Zhang TJ, Wu N. Novel FGFR1 Variants Are Associated with Congenital Scoliosis. Genes (Basel) 2021;12:1126. [PMID: 34440300 DOI: 10.3390/genes12081126] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
175 Requena F, Abdallah HH, García A, Nitschké P, Romana S, Malan V, Rausell A. CNVxplorer: a web tool to assist clinical interpretation of CNVs in rare disease patients. Nucleic Acids Res 2021;49:W93-W103. [PMID: 34019647 DOI: 10.1093/nar/gkab347] [Cited by in Crossref: 6] [Cited by in F6Publishing: 7] [Article Influence: 6.0] [Reference Citation Analysis]
176 Wang H, Robinson JL, Kocabas P, Gustafsson J, Anton M, Cholley PE, Huang S, Gobom J, Svensson T, Uhlen M, Zetterberg H, Nielsen J. Genome-scale metabolic network reconstruction of model animals as a platform for translational research. Proc Natl Acad Sci U S A 2021;118:e2102344118. [PMID: 34282017 DOI: 10.1073/pnas.2102344118] [Cited by in Crossref: 15] [Cited by in F6Publishing: 16] [Article Influence: 15.0] [Reference Citation Analysis]
177 de Souza ID, Reis CF, Morais DAA, Fernandes VGS, Cavalcante JVF, Dalmolin RJS. Ancestry analysis indicates two different sets of essential genes in eukaryotic model species. Funct Integr Genomics 2021;21:523-31. [PMID: 34279742 DOI: 10.1007/s10142-021-00794-9] [Reference Citation Analysis]
178 Somepalli G, Sahoo S, Singh A, Hannenhalli S. Prioritizing and characterizing functionally relevant genes across human tissues. PLoS Comput Biol 2021;17:e1009194. [PMID: 34270548 DOI: 10.1371/journal.pcbi.1009194] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
179 Stanzick KJ, Li Y, Schlosser P, Gorski M, Wuttke M, Thomas LF, Rasheed H, Rowan BX, Graham SE, Vanderweff BR, Patil SB, Robinson-Cohen C, Gaziano JM, O'Donnell CJ, Willer CJ, Hallan S, Åsvold BO, Gessner A, Hung AM, Pattaro C, Köttgen A, Stark KJ, Heid IM, Winkler TW; VA Million Veteran Program. Discovery and prioritization of variants and genes for kidney function in >1.2 million individuals. Nat Commun 2021;12:4350. [PMID: 34272381 DOI: 10.1038/s41467-021-24491-0] [Cited by in Crossref: 29] [Cited by in F6Publishing: 34] [Article Influence: 29.0] [Reference Citation Analysis]
180 Payseur BA, Jing P. Genomic Targets of Positive Selection in Giant Mice from Gough Island. Mol Biol Evol 2021;38:911-26. [PMID: 33022034 DOI: 10.1093/molbev/msaa255] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
181 Topham L, Gregoire S, Kang H, Salmon-Divon M, Lax E, Millecamps M, Szyf M, Stone L. The methyl donor S-adenosyl methionine reverses the DNA methylation signature of chronic neuropathic pain in mouse frontal cortex. Pain Rep 2021;6:e944. [PMID: 34278163 DOI: 10.1097/PR9.0000000000000944] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
182 Saleh AJ, Nothwang HG. Differential expression of microRNAs in the developing avian auditory hindbrain. J Comp Neurol 2021;529:3477-96. [PMID: 34180540 DOI: 10.1002/cne.25205] [Reference Citation Analysis]
183 Lin GW, Liang YC, Wu P, Chen CK, Lai YC, Jiang TX, Haung YH, Chuong CM. Regional specific differentiation of integumentary organs: SATB2 is involved in α- and β-keratin gene cluster switching in the chicken. Dev Dyn 2021. [PMID: 34240503 DOI: 10.1002/dvdy.396] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 3.0] [Reference Citation Analysis]
184 Ray D, Venkataraghavan S, Zhang W, Leslie EJ, Hetmanski JB, Weinberg SM, Murray JC, Marazita ML, Ruczinski I, Taub MA, Beaty TH. Pleiotropy method reveals genetic overlap between orofacial clefts at multiple novel loci from GWAS of multi-ethnic trios. PLoS Genet 2021;17:e1009584. [PMID: 34242216 DOI: 10.1371/journal.pgen.1009584] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 4.0] [Reference Citation Analysis]
185 Aviña-Padilla K, Ramírez-Rafael JA, Herrera-Oropeza GE, Muley VY, Valdivia DI, Díaz-Valenzuela E, García-García A, Varela-Echavarría A, Hernández-Rosales M. Evolutionary Perspective and Expression Analysis of Intronless Genes Highlight the Conservation of Their Regulatory Role. Front Genet 2021;12:654256. [PMID: 34306008 DOI: 10.3389/fgene.2021.654256] [Cited by in Crossref: 10] [Cited by in F6Publishing: 10] [Article Influence: 10.0] [Reference Citation Analysis]
186 Kishore R, Arnaboldi V, Van Slyke CE, Chan J, Nash RS, Urbano JM, Dolan ME, Engel SR, Shimoyama M, Sternberg PW, Genome Resources TAO. Automated generation of gene summaries at the Alliance of Genome Resources. Database (Oxford) 2020;2020:baaa037. [PMID: 32559296 DOI: 10.1093/database/baaa037] [Cited by in Crossref: 11] [Cited by in F6Publishing: 12] [Article Influence: 11.0] [Reference Citation Analysis]
187 Mills MC, Tropf FC, Brazel DM, van Zuydam N, Vaez A, Pers TH, Snieder H, Perry JRB, Ong KK, den Hoed M, Barban N, Day FR; eQTLGen Consortium., BIOS Consortium., Human Reproductive Behaviour Consortium. Identification of 371 genetic variants for age at first sex and birth linked to externalising behaviour. Nat Hum Behav 2021. [PMID: 34211149 DOI: 10.1038/s41562-021-01135-3] [Cited by in Crossref: 8] [Cited by in F6Publishing: 8] [Article Influence: 8.0] [Reference Citation Analysis]
188 Pinson MR, Holloway KN, Douglas JC, Kane CJM, Miranda RC, Drew PD. Divergent and overlapping hippocampal and cerebellar transcriptome responses following developmental ethanol exposure during the secondary neurogenic period. Alcohol Clin Exp Res 2021;45:1408-23. [PMID: 34060105 DOI: 10.1111/acer.14633] [Cited by in Crossref: 2] [Cited by in F6Publishing: 3] [Article Influence: 2.0] [Reference Citation Analysis]
189 Cisterna A, González-vidal A, Ruiz D, Ortiz J, Gómez-pascual A, Chen Z, Nalls M, Faghri F, Hardy J, Díez I, Maietta P, Álvarez S, Ryten M, Botía JA. PhenoExam: an R package and Web application for the examination of phenotypes linked to genes and gene sets.. [DOI: 10.1101/2021.06.29.450324] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
190 Matsuura K, Mohamed HMA, Youssef MMM, Yamamoto T. Synaptotagmin 2 is ectopically overexpressed in excitatory presynapses of a widely used CaMKIIα-Cre mouse line.. [DOI: 10.1101/2021.06.30.450492] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
191 Sambaturu N, Pusadkar V, Hannenhalli S, Chandra N. PathExt: a general framework for path-based mining of omics-integrated biological networks. Bioinformatics 2021;37:1254-62. [PMID: 33305329 DOI: 10.1093/bioinformatics/btaa941] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 4.0] [Reference Citation Analysis]
192 Nalamalapu RR, Yue M, Stone AR, Murphy S, Saha MS. The tweety Gene Family: From Embryo to Disease. Front Mol Neurosci 2021;14:672511. [PMID: 34262434 DOI: 10.3389/fnmol.2021.672511] [Cited by in Crossref: 8] [Cited by in F6Publishing: 9] [Article Influence: 8.0] [Reference Citation Analysis]
193 Lv B, Stuck MW, Desai PB, Cabrera OA, Pazour GJ. E3 ubiquitin ligase Wwp1 regulates ciliary dynamics of the Hedgehog receptor Smoothened. J Cell Biol 2021;220:e202010177. [PMID: 34161574 DOI: 10.1083/jcb.202010177] [Cited by in Crossref: 8] [Cited by in F6Publishing: 8] [Article Influence: 8.0] [Reference Citation Analysis]
194 Santana González L, Artibani M, Ahmed AA. Studying Müllerian duct anomalies - from cataloguing phenotypes to discovering causation. Dis Model Mech 2021;14:dmm047977. [PMID: 34160006 DOI: 10.1242/dmm.047977] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
195 Rupert JE, Jengelley DHA, Zimmers TA. In Vitro, In Vivo, and In Silico Methods for Assessment of Muscle Size and Muscle Growth Regulation. Shock 2020;53:605-15. [PMID: 31939770 DOI: 10.1097/SHK.0000000000001498] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 4.0] [Reference Citation Analysis]
196 Chambers I, Kumar P, Lichtenberg J, Wang P, Yu J, Phillips J, Kane M, Bodine D, Hamza I. MRP5 and MRP9 Play a Concerted Role in Male Reproduction and Mitochondrial Function.. [DOI: 10.1101/2021.06.19.449033] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
197 Choi J, Jang YJ, Dabrowska C, Iich E, Evans KV, Hall H, Janes SM, Simons BD, Koo B, Kim J, Lee J. Release of Notch activity coordinated by IL-1β signalling confers differentiation plasticity of airway progenitors via Fosl2 during alveolar regeneration.. [DOI: 10.1101/2021.06.19.449004] [Reference Citation Analysis]
198 Almeida MP, Kambakam S, Liu F, Ming Z, Welker JM, Wierson WA, Schultz-rogers LE, Ekker SC, Clark KJ, Essner JJ, Mcgrail M. Zebrafish Cre/lox regulated UFlip alleles generated by CRISPR/Cas targeted integration provide cell-type specific conditional gene inactivation.. [DOI: 10.1101/2021.06.18.448732] [Reference Citation Analysis]
199 Laisk T, Lepamets M, Koel M, Abner E, Mägi R; Estonian Biobank Research Team. Genome-wide association study identifies five risk loci for pernicious anemia. Nat Commun 2021;12:3761. [PMID: 34145262 DOI: 10.1038/s41467-021-24051-6] [Cited by in Crossref: 10] [Cited by in F6Publishing: 10] [Article Influence: 10.0] [Reference Citation Analysis]
200 Seaby EG, Rehm HL, O'Donnell-Luria A. Strategies to Uplift Novel Mendelian Gene Discovery for Improved Clinical Outcomes. Front Genet 2021;12:674295. [PMID: 34220947 DOI: 10.3389/fgene.2021.674295] [Cited by in Crossref: 8] [Cited by in F6Publishing: 9] [Article Influence: 8.0] [Reference Citation Analysis]
201 Verma P, Parte P. Revisiting the Characteristics of Testicular Germ Cell Lines GC-1(spg) and GC-2(spd)ts. Mol Biotechnol 2021. [PMID: 34125394 DOI: 10.1007/s12033-021-00352-5] [Cited by in Crossref: 2] [Cited by in F6Publishing: 3] [Article Influence: 2.0] [Reference Citation Analysis]
202 Reynolds ND, Aceves NM, Liu JL, Compton JR, Leary DH, Freitas BT, Pegan SD, Doctor KZ, Wu FY, Hu X, Legler PM. The SARS-CoV-2 SSHHPS Recognized by the Papain-like Protease. ACS Infect Dis 2021;7:1483-502. [PMID: 34019767 DOI: 10.1021/acsinfecdis.0c00866] [Cited by in Crossref: 6] [Cited by in F6Publishing: 7] [Article Influence: 6.0] [Reference Citation Analysis]
203 Bader AS, Bushell M. Damage-Net: A program for DNA repair meta-analysis identifies a network of novel repair genes that facilitate cancer evolution. DNA Repair (Amst) 2021;105:103158. [PMID: 34147942 DOI: 10.1016/j.dnarep.2021.103158] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
204 Regua AT, Arrigo A, Doheny D, Wong GL, Lo HW. Transgenic mouse models of breast cancer. Cancer Lett 2021;516:73-83. [PMID: 34090924 DOI: 10.1016/j.canlet.2021.05.027] [Cited by in Crossref: 3] [Cited by in F6Publishing: 4] [Article Influence: 3.0] [Reference Citation Analysis]
205 Marquardt S, Pavlopoulou A, Takan I, Dhar P, Pützer BM, Logotheti S. A Systems-Based Key Innovation-Driven Approach Infers Co-option of Jaw Developmental Programs During Cancer Progression. Front Cell Dev Biol 2021;9:682619. [PMID: 34150777 DOI: 10.3389/fcell.2021.682619] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
206 Li M, Olotu J, Buxo-Martinez CJ, Mossey PA, Anand D, Busch T, Alade A, Gowans LJJ, Eshete M, Adeyemo WL, Naicker T, Awotoye WO, Gupta S, Adeleke C, Bravo V, Huang S, Adamson OO, Toraño AM, Bello CA, Soto M, Soto M, Ledesma R, Marquez M, Cordero JF, Lopez-Del Valle LM, Salcedo MI, Debs N, Petrin A, Malloy H, Elhadi K, James O, Ogunlewe MO, Abate F, Hailu A, Mohammed I, Gravem P, Deribew M, Gesses M, Hassan M, Pape J, Obiri-Yeboah S, Arthur FKN, Oti AA, Donkor P, Marazita ML, Lachke SA, Adeyemo AA, Murray JC, Butali A. Variant analyses of candidate genes in orofacial clefts in multi-ethnic populations. Oral Dis 2021. [PMID: 34061439 DOI: 10.1111/odi.13932] [Reference Citation Analysis]
207 Buchanan J, Elabbady L, Collman F, Jorstad NL, Bakken TE, Ott C, Glatzer J, Bleckert AA, Bodor AL, Brittan D, Bumbarger DJ, Mahalingam G, Seshamani S, Schneider-mizell C, Takeno MM, Torres R, Yin W, Hodge RD, Castro M, Dorkenwald S, Ih D, Jordan CS, Kemnitz N, Lee K, Lu R, Macrina T, Mu S, Popovych S, Silversmith WM, Tartavull I, Turner NL, Wilson AM, Wong W, Wu J, Zlateski A, Zung J, Lippincott-schwartz J, Lein ES, Seung HS, Bergles DE, Reid RC, da Costa NM. Oligodendrocyte precursor cells prune axons in the mouse neocortex.. [DOI: 10.1101/2021.05.29.446047] [Cited by in Crossref: 12] [Cited by in F6Publishing: 12] [Article Influence: 12.0] [Reference Citation Analysis]
208 Palma-vera SE, Reyer H, Langhammer M, Reinsch N, Derežanin L, Fickel J, Qanbari S, Weitzel J, Franzenburg S, Hemmrich-stanisak G, Schön J. Genomic characterization of world’s longest selection experiment in mouse reveals the complexity of polygenic traits.. [DOI: 10.1101/2021.05.28.446207] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
209 Durán Alonso MB, Vendrell V, López-Hernández I, Alonso MT, Martin DM, Giráldez F, Carramolino L, Giovinazzo G, Vázquez E, Torres M, Schimmang T. Meis2 Is Required for Inner Ear Formation and Proper Morphogenesis of the Cochlea. Front Cell Dev Biol 2021;9:679325. [PMID: 34124068 DOI: 10.3389/fcell.2021.679325] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
210 Colella JP, Tigano A, Dudchenko O, Omer AD, Khan R, Bochkov ID, Aiden EL, MacManes MD. Limited Evidence for Parallel Evolution Among Desert-Adapted Peromyscus Deer Mice. J Hered 2021;112:286-302. [PMID: 33686424 DOI: 10.1093/jhered/esab009] [Cited by in Crossref: 6] [Cited by in F6Publishing: 5] [Article Influence: 6.0] [Reference Citation Analysis]
211 Nair NU, Cheng K, Naddaf L, Sharon E, Pal LR, Rajagopal PS, Unterman I, Aldape K, Hannenhalli S, Day C, Tabach Y, Ruppin E. Cross-species identification of cancer-resistance associated genes uncovers their relevance to human cancer risk.. [DOI: 10.1101/2021.05.19.444895] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
212 Edwards NA, Shacham-Silverberg V, Weitz L, Kingma PS, Shen Y, Wells JM, Chung WK, Zorn AM. Developmental basis of trachea-esophageal birth defects. Dev Biol 2021;477:85-97. [PMID: 34023332 DOI: 10.1016/j.ydbio.2021.05.015] [Cited by in Crossref: 8] [Cited by in F6Publishing: 8] [Article Influence: 8.0] [Reference Citation Analysis]
213 Dan H, Ruan T, Sampogna RV. Circadian Clock Regulation of Developmental Time in the Kidney. Cell Rep 2020;31:107661. [PMID: 32433970 DOI: 10.1016/j.celrep.2020.107661] [Cited by in Crossref: 5] [Cited by in F6Publishing: 8] [Article Influence: 5.0] [Reference Citation Analysis]
214 Zhu X, Duren Z, Wong WH. Modeling regulatory network topology improves genome-wide analyses of complex human traits. Nat Commun 2021;12:2851. [PMID: 33990562 DOI: 10.1038/s41467-021-22588-0] [Cited by in Crossref: 7] [Cited by in F6Publishing: 7] [Article Influence: 7.0] [Reference Citation Analysis]
215 Teruya K, Oguma A, Arai K, Nishizawa K, Iwabuchi S, Watanabe-Matsui M, Sakasegawa Y, Schätzl H, Gilch S, Doh-Ura K. Polymorphisms in glia maturation factor β gene are markers of cellulose ether effectiveness in prion-infected mice. Biochem Biophys Res Commun 2021;560:105-11. [PMID: 33984767 DOI: 10.1016/j.bbrc.2021.04.116] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
216 Yates B, Gray KA, Jones TEM, Bruford EA. Updates to HCOP: the HGNC comparison of orthology predictions tool. Brief Bioinform 2021:bbab155. [PMID: 33959747 DOI: 10.1093/bib/bbab155] [Cited by in Crossref: 6] [Cited by in F6Publishing: 7] [Article Influence: 6.0] [Reference Citation Analysis]
217 Sun Y, Zuo Z, Kuang Y. Prolactin-Releasing Peptide Differentially Regulates Gene Transcriptomic Profiles in Mouse Bone Marrow-Derived Macrophages. Int J Mol Sci 2021;22:4456. [PMID: 33923285 DOI: 10.3390/ijms22094456] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
218 Wu Z, Gong H, Zhang M, Tong X, Ai H, Xiao S, Perez-Enciso M, Yang B, Huang L. A worldwide map of swine short tandem repeats and their associations with evolutionary and environmental adaptations. Genet Sel Evol 2021;53:39. [PMID: 33892623 DOI: 10.1186/s12711-021-00631-4] [Cited by in Crossref: 2] [Cited by in F6Publishing: 3] [Article Influence: 2.0] [Reference Citation Analysis]
219 Birling MC, Yoshiki A, Adams DJ, Ayabe S, Beaudet AL, Bottomley J, Bradley A, Brown SDM, Bürger A, Bushell W, Chiani F, Chin HG, Christou S, Codner GF, DeMayo FJ, Dickinson ME, Doe B, Donahue LR, Fray MD, Gambadoro A, Gao X, Gertsenstein M, Gomez-Segura A, Goodwin LO, Heaney JD, Hérault Y, de Angelis MH, Jiang ST, Justice MJ, Kasparek P, King RE, Kühn R, Lee H, Lee YJ, Liu Z, Lloyd KCK, Lorenzo I, Mallon AM, McKerlie C, Meehan TF, Fuentes VM, Newman S, Nutter LMJ, Oh GT, Pavlovic G, Ramirez-Solis R, Rosen B, Ryder EJ, Santos LA, Schick J, Seavitt JR, Sedlacek R, Seisenberger C, Seong JK, Skarnes WC, Sorg T, Steel KP, Tamura M, Tocchini-Valentini GP, Wang CL, Wardle-Jones H, Wattenhofer-Donzé M, Wells S, Wiles MV, Willis BJ, Wood JA, Wurst W, Xu Y, Teboul L, Murray SA; International Mouse Phenotyping Consortium (IMPC). A resource of targeted mutant mouse lines for 5,061 genes. Nat Genet 2021;53:416-9. [PMID: 33833456 DOI: 10.1038/s41588-021-00825-y] [Cited by in Crossref: 31] [Cited by in F6Publishing: 37] [Article Influence: 31.0] [Reference Citation Analysis]
220 Beder T, Aromolaran O, Dönitz J, Tapanelli S, Adedeji EO, Adebiyi E, Bucher G, Koenig R. Identifying essential genes across eukaryotes by machine learning.. [DOI: 10.1101/2021.04.15.439934] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
221 García-moreno A, López-domínguez R, Ramirez-mena A, Pascual-montano A, Aparicio-puerta E, Hackenberg M, Carmona-saez P. GeneCodis 4: Expanding the modular enrichment analysis to regulatory elements.. [DOI: 10.1101/2021.04.15.439962] [Cited by in Crossref: 10] [Cited by in F6Publishing: 11] [Article Influence: 10.0] [Reference Citation Analysis]
222 Gangoso E, Southgate B, Bradley L, Rus S, Galvez-Cancino F, McGivern N, Güç E, Kapourani CA, Byron A, Ferguson KM, Alfazema N, Morrison G, Grant V, Blin C, Sou I, Marques-Torrejon MA, Conde L, Parrinello S, Herrero J, Beck S, Brandner S, Brennan PM, Bertone P, Pollard JW, Quezada SA, Sproul D, Frame MC, Serrels A, Pollard SM. Glioblastomas acquire myeloid-affiliated transcriptional programs via epigenetic immunoediting to elicit immune evasion. Cell 2021;184:2454-2470.e26. [PMID: 33857425 DOI: 10.1016/j.cell.2021.03.023] [Cited by in Crossref: 71] [Cited by in F6Publishing: 76] [Article Influence: 71.0] [Reference Citation Analysis]
223 Zhao Y, Hou Y, Xu Y, Luan Y, Zhou H, Qi X, Hu M, Wang D, Wang Z, Fu Y, Li J, Zhang S, Chen J, Han J, Li X, Zhao S. A compendium and comparative epigenomics analysis of cis-regulatory elements in the pig genome. Nat Commun 2021;12:2217. [PMID: 33850120 DOI: 10.1038/s41467-021-22448-x] [Cited by in Crossref: 21] [Cited by in F6Publishing: 23] [Article Influence: 21.0] [Reference Citation Analysis]
224 Shemesh N, Jubran J, Dror S, Simonovsky E, Basha O, Argov C, Hekselman I, Abu-Qarn M, Vinogradov E, Mauer O, Tiago T, Carra S, Ben-Zvi A, Yeger-Lotem E. The landscape of molecular chaperones across human tissues reveals a layered architecture of core and variable chaperones. Nat Commun 2021;12:2180. [PMID: 33846299 DOI: 10.1038/s41467-021-22369-9] [Cited by in Crossref: 25] [Cited by in F6Publishing: 25] [Article Influence: 25.0] [Reference Citation Analysis]
225 Aromolaran O, Aromolaran D, Isewon I, Oyelade J. Machine learning approach to gene essentiality prediction: a review. Brief Bioinform 2021:bbab128. [PMID: 33842944 DOI: 10.1093/bib/bbab128] [Cited by in Crossref: 13] [Cited by in F6Publishing: 16] [Article Influence: 13.0] [Reference Citation Analysis]
226 Deal KK, Chandrashekar AS, Beaman MM, Branch MC, Buehler DP, Conway SJ, Southard-Smith EM. Altered sacral neural crest development in Pax3 spina bifida mutants underlies deficits of bladder innervation and function. Dev Biol 2021;476:173-88. [PMID: 33839113 DOI: 10.1016/j.ydbio.2021.03.024] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 3.0] [Reference Citation Analysis]
227 Hunker AC, Soden ME, Krayushkina D, Heymann G, Awatramani R, Zweifel LS. Conditional Single Vector CRISPR/SaCas9 Viruses for Efficient Mutagenesis in the Adult Mouse Nervous System. Cell Rep 2020;30:4303-4316.e6. [PMID: 32209486 DOI: 10.1016/j.celrep.2020.02.092] [Cited by in Crossref: 27] [Cited by in F6Publishing: 14] [Article Influence: 27.0] [Reference Citation Analysis]
228 Holzer G, de Magistris P, Gramminger C, Sachdev R, Magalska A, Schooley A, Anja S, Lennartz B, Tatarek-nossol M, Lue H, Linder MI, Kutay U, Preisinger C, Moreno-andres D, Antonin W. The nucleoporin Nup50 activates the Ran guanyl-nucleotide exchange factor RCC1 to promote mitotic NPC assembly.. [DOI: 10.1101/2021.03.31.437874] [Reference Citation Analysis]
229 Gurumurthy CB, Saunders TL, Ohtsuka M. Designing and generating a mouse model: frequently asked questions. J Biomed Res 2021;35:76-90. [PMID: 33797414 DOI: 10.7555/JBR.35.20200197] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
230 Walz C, Brenmoehl J, Trakooljul N, Noce A, Caffier C, Ohde D, Langhammer M, Wimmers K, Ponsuksili S, Hoeflich A. Control of Protein and Energy Metabolism in the Pituitary Gland in Response to Three-Week Running Training in Adult Male Mice. Cells 2021;10:736. [PMID: 33810540 DOI: 10.3390/cells10040736] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
231 Abdik E, Çakır T. Systematic investigation of mouse models of Parkinson's disease by transcriptome mapping on a brain-specific genome-scale metabolic network. Mol Omics 2021;17:492-502. [PMID: 34370801 DOI: 10.1039/d0mo00135j] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
232 Horner NR, Venkataraman S, Armit C, Casero R, Brown JM, Wong MD, van Eede MC, Henkelman RM, Johnson S, Teboul L, Wells S, Brown SD, Westerberg H, Mallon AM. LAMA: automated image analysis for the developmental phenotyping of mouse embryos. Development 2021;148:dev192955. [PMID: 33574040 DOI: 10.1242/dev.192955] [Cited by in Crossref: 4] [Cited by in F6Publishing: 5] [Article Influence: 4.0] [Reference Citation Analysis]
233 Liu L, Wang H, Xu GL, Liu L. Tet1 Deficiency Leads to Premature Ovarian Failure. Front Cell Dev Biol 2021;9:644135. [PMID: 33834024 DOI: 10.3389/fcell.2021.644135] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 4.0] [Reference Citation Analysis]
234 Requena F, Abdallah HH, García A, Nitschké P, Romana S, Malan V, Rausell A. CNVxplorer: a web tool to assist clinical interpretation of CNVs in rare disease patients.. [DOI: 10.1101/2021.03.19.21253806] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
235 Topham L, Gregoire S, Kang H, Salmon-Divon M, Lax E, Millecamps M, Szyf M, Stone LS. The transition from acute to chronic pain: dynamic epigenetic reprogramming of the mouse prefrontal cortex up to 1 year after nerve injury. Pain 2020;161:2394-409. [PMID: 32427748 DOI: 10.1097/j.pain.0000000000001917] [Cited by in Crossref: 12] [Cited by in F6Publishing: 14] [Article Influence: 12.0] [Reference Citation Analysis]
236 Liu YQ, Liu Y, Zhang Q, Xiao T, Deng HW. Identification of Novel Pleiotropic SNPs Associated with Osteoporosis and Rheumatoid Arthritis. Calcif Tissue Int 2021;109:17-31. [PMID: 33740106 DOI: 10.1007/s00223-021-00817-4] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
237 Boer EF, Van Hollebeke HF, Holt C, Yandell M, Shapiro MD. A ROR2 coding variant is associated with craniofacial variation in domestic pigeons.. [DOI: 10.1101/2021.03.15.435542] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
238 Fleck JS, Sanchís-Calleja F, He Z, Santel M, Boyle MJ, Camp JG, Treutlein B. Resolving organoid brain region identities by mapping single-cell genomic data to reference atlases. Cell Stem Cell 2021;28:1148-1159.e8. [PMID: 33711282 DOI: 10.1016/j.stem.2021.02.015] [Cited by in Crossref: 25] [Cited by in F6Publishing: 29] [Article Influence: 25.0] [Reference Citation Analysis]
239 Oh KP, Shiels AB, Shiels L, Blondel DV, Campbell KJ, Saah JR, Lloyd AL, Thomas PQ, Gould F, Abdo Z, Godwin JR, Piaggio AJ. Population genomics of invasive rodents on islands: Genetic consequences of colonization and prospects for localized synthetic gene drive. Evol Appl 2021;14:1421-35. [PMID: 34025776 DOI: 10.1111/eva.13210] [Cited by in Crossref: 9] [Cited by in F6Publishing: 10] [Article Influence: 9.0] [Reference Citation Analysis]
240 Doncheva NT, Palasca O, Yarani R, Litman T, Anthon C, Groenen MAM, Stadler PF, Pociot F, Jensen LJ, Gorodkin J. Human pathways in animal models: possibilities and limitations. Nucleic Acids Res 2021;49:1859-71. [PMID: 33524155 DOI: 10.1093/nar/gkab012] [Cited by in Crossref: 9] [Cited by in F6Publishing: 12] [Article Influence: 9.0] [Reference Citation Analysis]
241 Zhao F, Grimm SA, Yao HH. Molecular Actions Underlying Wolffian Duct Regression in Sexual Differentiation of Murine Reproductive Tracts. Sex Dev 2020;14:51-9. [PMID: 33684916 DOI: 10.1159/000513878] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
242 Barcellona MN, Speer JE, Jing L, Gupta MC, Buchowski JM, Kelly MP, Setton LA. Engineered Peptide-Functionalized Hydrogels Modulate the RNA Transcriptome of Human Nucleus Pulposus Cells In Vitro.. [DOI: 10.1101/2021.03.05.434094] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
243 Urzúa-Traslaviña CG, Leeuwenburgh VC, Bhattacharya A, Loipfinger S, van Vugt MATM, de Vries EGE, Fehrmann RSN. Improving gene function predictions using independent transcriptional components. Nat Commun 2021;12:1464. [PMID: 33674610 DOI: 10.1038/s41467-021-21671-w] [Cited by in Crossref: 11] [Cited by in F6Publishing: 13] [Article Influence: 11.0] [Reference Citation Analysis]
244 Zlobin AS, Nikulin PS, Volkova NA, Zinovieva NA, Iolchiev BS, Bagirov VA, Borodin PM, Aksenovich TI, Tsepilov YA. Multivariate Analysis Identifies Eight Novel Loci Associated with Meat Productivity Traits in Sheep. Genes (Basel) 2021;12:367. [PMID: 33806625 DOI: 10.3390/genes12030367] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
245 Ongaro-Carcy R, Scott-Boyer MP, Dessemond A, Belleau F, Leclercq M, Périn O, Droit A. KibioR & Kibio: a new architecture for next-generation data querying and sharing in big biology. Bioinformatics 2021:btab157. [PMID: 33751043 DOI: 10.1093/bioinformatics/btab157] [Reference Citation Analysis]
246 Srivastava P, Kane A, Harrison C, Levin M. A Meta-Analysis of Bioelectric Data in Cancer, Embryogenesis, and Regeneration. Bioelectricity 2021;3:42-67. [PMID: 34476377 DOI: 10.1089/bioe.2019.0034] [Cited by in Crossref: 12] [Cited by in F6Publishing: 14] [Article Influence: 12.0] [Reference Citation Analysis]
247 Colgan TJ, Moran PA, Archer LC, Wynne R, Hutton SA, McGinnity P, Reed TE. Evolution and Expression of the Immune System of a Facultatively Anadromous Salmonid. Front Immunol 2021;12:568729. [PMID: 33717060 DOI: 10.3389/fimmu.2021.568729] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 3.0] [Reference Citation Analysis]
248 Hitomi Y, Aiba Y, Kawai Y, Kojima K, Ueno K, Nishida N, Kawashima M, Gervais O, Khor SS, Nagasaki M, Tokunaga K, Nakamura M, Tsuiji M. rs1944919 on chromosome 11q23.1 and its effector genes COLCA1/COLCA2 confer susceptibility to primary biliary cholangitis. Sci Rep 2021;11:4557. [PMID: 33633225 DOI: 10.1038/s41598-021-84042-x] [Cited by in Crossref: 2] [Cited by in F6Publishing: 4] [Article Influence: 2.0] [Reference Citation Analysis]
249 Zaghlool SB, Sharma S, Molnar M, Matías-García PR, Elhadad MA, Waldenberger M, Peters A, Rathmann W, Graumann J, Gieger C, Grallert H, Suhre K. Revealing the role of the human blood plasma proteome in obesity using genetic drivers. Nat Commun 2021;12:1279. [PMID: 33627659 DOI: 10.1038/s41467-021-21542-4] [Cited by in Crossref: 16] [Cited by in F6Publishing: 18] [Article Influence: 16.0] [Reference Citation Analysis]
250 Restrepo CM, Llanes A, Herrera L, Ellis E, Lleonart R, Fernández PL. Gene expression patterns associated with Leishmania panamensis infection in macrophages from BALB/c and C57BL/6 mice. PLoS Negl Trop Dis 2021;15:e0009225. [PMID: 33617537 DOI: 10.1371/journal.pntd.0009225] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
251 Niskanen JE, Reunanen V, Salonen M, Bannasch D, Lappalainen AK, Lohi H, Hytönen MK. Canine DVL2 variant contributes to brachycephalic phenotype and caudal vertebral anomalies. Hum Genet 2021. [PMID: 33599851 DOI: 10.1007/s00439-021-02261-8] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 3.0] [Reference Citation Analysis]
252 Studstill CJ, Pritzl CJ, Seo YJ, Kim DY, Xia C, Wolf JJ, Nistala R, Vijayan M, Cho YB, Kang KW, Lee SM, Hahm B. Sphingosine kinase 2 restricts T cell immunopathology but permits viral persistence. J Clin Invest 2020;130:6523-38. [PMID: 32897877 DOI: 10.1172/JCI125297] [Cited by in Crossref: 13] [Cited by in F6Publishing: 13] [Article Influence: 13.0] [Reference Citation Analysis]
253 Davis KW, Bilancia CG, Martin M, Vanzo R, Rimmasch M, Hom Y, Uddin M, Serrano M. NeuroSCORE: A Genome-wide Omics-Based Model to Identify Candidate Disease Genes of the Central Nervous System.. [DOI: 10.1101/2021.02.04.429640] [Reference Citation Analysis]
254 Rincic M, Rados M, Kopic J, Krsnik Z, Liehr T. 7p21.3 Together With a 12p13.32 Deletion in a Patient With Microcephaly-Does 12p13.32 Locus Possibly Comprises a Candidate Gene Region for Microcephaly? Front Mol Neurosci 2021;14:613091. [PMID: 33613193 DOI: 10.3389/fnmol.2021.613091] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
255 Shparberg R, Dewi CU, Gnanasambandapillai V, Liyanage L, O'Connor MD. Single cell RNA-sequencing data generated from human pluripotent stem cell-derived lens epithelial cells. Data Brief 2021;34:106657. [PMID: 33521174 DOI: 10.1016/j.dib.2020.106657] [Cited by in Crossref: 2] [Article Influence: 2.0] [Reference Citation Analysis]
256 Abels ER, Nieland L, Hickman S, Broekman MLD, El Khoury J, Maas SLN. Comparative Analysis Identifies Similarities between the Human and Murine Microglial Sensomes. Int J Mol Sci 2021;22:1495. [PMID: 33540859 DOI: 10.3390/ijms22031495] [Cited by in Crossref: 9] [Cited by in F6Publishing: 11] [Article Influence: 9.0] [Reference Citation Analysis]
257 Ietswaart R, Gyori BM, Bachman JA, Sorger PK, Churchman LS. GeneWalk identifies relevant gene functions for a biological context using network representation learning. Genome Biol 2021;22:55. [PMID: 33526072 DOI: 10.1186/s13059-021-02264-8] [Cited by in Crossref: 12] [Cited by in F6Publishing: 16] [Article Influence: 12.0] [Reference Citation Analysis]
258 Tweedie S, Braschi B, Gray K, Jones TEM, Seal RL, Yates B, Bruford EA. Genenames.org: the HGNC and VGNC resources in 2021. Nucleic Acids Res 2021;49:D939-46. [PMID: 33152070 DOI: 10.1093/nar/gkaa980] [Cited by in Crossref: 141] [Cited by in F6Publishing: 154] [Article Influence: 141.0] [Reference Citation Analysis]
259 Baldarelli RM, Smith CM, Finger JH, Hayamizu TF, McCright IJ, Xu J, Shaw DR, Beal JS, Blodgett O, Campbell J, Corbani LE, Frost PJ, Giannatto SC, Miers DB, Kadin JA, Richardson JE, Ringwald M. The mouse Gene Expression Database (GXD): 2021 update. Nucleic Acids Res 2021;49:D924-31. [PMID: 33104772 DOI: 10.1093/nar/gkaa914] [Cited by in Crossref: 17] [Cited by in F6Publishing: 18] [Article Influence: 17.0] [Reference Citation Analysis]
260 Gurumayum S, Jiang P, Hao X, Campos TL, Young ND, Korhonen PK, Gasser RB, Bork P, Zhao XM, He LJ, Chen WH. OGEE v3: Online GEne Essentiality database with increased coverage of organisms and human cell lines. Nucleic Acids Res 2021;49:D998-D1003. [PMID: 33084874 DOI: 10.1093/nar/gkaa884] [Cited by in Crossref: 17] [Cited by in F6Publishing: 18] [Article Influence: 17.0] [Reference Citation Analysis]
261 Hu Y, Comjean A, Rodiger J, Liu Y, Gao Y, Chung V, Zirin J, Perrimon N, Mohr SE. FlyRNAi.org-the database of the Drosophila RNAi screening center and transgenic RNAi project: 2021 update. Nucleic Acids Res 2021;49:D908-15. [PMID: 33104800 DOI: 10.1093/nar/gkaa936] [Cited by in Crossref: 10] [Cited by in F6Publishing: 10] [Article Influence: 10.0] [Reference Citation Analysis]
262 Rogg M, Maier JI, Dotzauer R, Artelt N, Kretz O, Helmstädter M, Abed A, Sammarco A, Sigle A, Sellung D, Dinse P, Reiche K, Yasuda-Yamahara M, Biniossek ML, Walz G, Werner M, Endlich N, Schilling O, Huber TB, Schell C. SRGAP1 Controls Small Rho GTPases To Regulate Podocyte Foot Process Maintenance. J Am Soc Nephrol 2021;32:563-79. [PMID: 33514561 DOI: 10.1681/ASN.2020081126] [Cited by in Crossref: 9] [Cited by in F6Publishing: 9] [Article Influence: 9.0] [Reference Citation Analysis]
263 Burger LL, Wagenmaker ER, Phumsatitpong C, Olson DP, Moenter SM. Prenatal Androgenization Alters the Development of GnRH Neuron and Preoptic Area RNA Transcripts in Female Mice. Endocrinology 2020;161:bqaa166. [PMID: 33095238 DOI: 10.1210/endocr/bqaa166] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 3.0] [Reference Citation Analysis]
264 Althagafi A, Alsubaie L, Kathiresan N, Mineta K, Aloraini T, Almutairi F, Alfadhel M, Gojobori T, Alfares A, Hoehndorf R. DeepSVP: Integration of genotype and phenotype for structural variant prioritization using deep learning.. [DOI: 10.1101/2021.01.28.428557] [Reference Citation Analysis]
265 Yu X, Pan X, Zhang S, Zhang YH, Chen L, Wan S, Huang T, Cai YD. Identification of Gene Signatures and Expression Patterns During Epithelial-to-Mesenchymal Transition From Single-Cell Expression Atlas. Front Genet 2020;11:605012. [PMID: 33584803 DOI: 10.3389/fgene.2020.605012] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 3.0] [Reference Citation Analysis]
266 Kanev GK, de Graaf C, Westerman BA, de Esch IJP, Kooistra AJ. KLIFS: an overhaul after the first 5 years of supporting kinase research. Nucleic Acids Res 2021;49:D562-9. [PMID: 33084889 DOI: 10.1093/nar/gkaa895] [Cited by in Crossref: 32] [Cited by in F6Publishing: 34] [Article Influence: 32.0] [Reference Citation Analysis]
267 Xu C, Lopez R, Mehlman E, Regier J, Jordan MI, Yosef N. Probabilistic harmonization and annotation of single-cell transcriptomics data with deep generative models. Mol Syst Biol 2021;17:e9620. [PMID: 33491336 DOI: 10.15252/msb.20209620] [Cited by in Crossref: 64] [Cited by in F6Publishing: 72] [Article Influence: 64.0] [Reference Citation Analysis]
268 Blake JA, Baldarelli R, Kadin JA, Richardson JE, Smith CL, Bult CJ; Mouse Genome Database Group. Mouse Genome Database (MGD): Knowledgebase for mouse-human comparative biology. Nucleic Acids Res 2021;49:D981-7. [PMID: 33231642 DOI: 10.1093/nar/gkaa1083] [Cited by in Crossref: 19] [Cited by in F6Publishing: 23] [Article Influence: 19.0] [Reference Citation Analysis]
269 Somepalli G, Sahoo S, Singh A, Hannenhalli S. Prioritizing and characterizing functionally relevant genes across human tissues.. [DOI: 10.1101/2021.01.22.427774] [Reference Citation Analysis]
270 Yao X, Glessner JT, Li J, Qi X, Hou X, Zhu C, Li X, March ME, Yang L, Mentch FD, Hain HS, Meng X, Xia Q, Hakonarson H, Li J. Integrative analysis of genome-wide association studies identifies novel loci associated with neuropsychiatric disorders. Transl Psychiatry 2021;11:69. [PMID: 33479212 DOI: 10.1038/s41398-020-01195-5] [Cited by in Crossref: 13] [Cited by in F6Publishing: 13] [Article Influence: 13.0] [Reference Citation Analysis]
271 Fang L, Li Y, Ma L, Xu Q, Tan F, Chen G. GRNdb: decoding the gene regulatory networks in diverse human and mouse conditions. Nucleic Acids Res 2021;49:D97-D103. [PMID: 33151298 DOI: 10.1093/nar/gkaa995] [Cited by in Crossref: 20] [Cited by in F6Publishing: 22] [Article Influence: 20.0] [Reference Citation Analysis]
272 Li N, Shan N, Lu L, Wang Z. tRFtarget: a database for transfer RNA-derived fragment targets. Nucleic Acids Res 2021;49:D254-60. [PMID: 33035346 DOI: 10.1093/nar/gkaa831] [Cited by in Crossref: 21] [Cited by in F6Publishing: 23] [Article Influence: 21.0] [Reference Citation Analysis]
273 Gene Ontology Consortium. The Gene Ontology resource: enriching a GOld mine. Nucleic Acids Res 2021;49:D325-34. [PMID: 33290552 DOI: 10.1093/nar/gkaa1113] [Cited by in Crossref: 1024] [Cited by in F6Publishing: 1106] [Article Influence: 1024.0] [Reference Citation Analysis]
274 Sezerman U, Bozkurt T, Sadife Isleyen F. Integrating Evolutionary Genetics to Medical Genomics: Evolutionary Approaches to Investigate Disease-Causing Variants. Methods in Molecular Medicine 2021. [DOI: 10.5772/intechopen.92738] [Reference Citation Analysis]
275 Stacy A, Andrade-Oliveira V, McCulloch JA, Hild B, Oh JH, Perez-Chaparro PJ, Sim CK, Lim AI, Link VM, Enamorado M, Trinchieri G, Segre JA, Rehermann B, Belkaid Y. Infection trains the host for microbiota-enhanced resistance to pathogens. Cell 2021;184:615-627.e17. [PMID: 33453153 DOI: 10.1016/j.cell.2020.12.011] [Cited by in Crossref: 68] [Cited by in F6Publishing: 74] [Article Influence: 68.0] [Reference Citation Analysis]
276 Fuentealba M, Fabian DK, Dönertaş HM, Thornton JM, Partridge L. Transcriptomic profiling of long- and short-lived mutant mice implicates mitochondrial metabolism in ageing and shows signatures of normal ageing in progeroid mice. Mech Ageing Dev 2021;194:111437. [PMID: 33454277 DOI: 10.1016/j.mad.2021.111437] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 4.0] [Reference Citation Analysis]
277 Aviña-padilla K, Ramírez-rafael JA, Herrera-oropeza GE, Muley V, Valdivia DI, Díaz-valenzuela E, García-garcía A, Varela-echavarría A, Hernández-rosales M. Evolutionary Perspective and Expression Analysis of Intronless Genes Highlight the Conservation on Their Regulatory Role.. [DOI: 10.1101/2021.01.13.426573] [Reference Citation Analysis]
278 Friedel CC, Whisnant AW, Djakovic L, Rutkowski AJ, Friedl MS, Kluge M, Williamson JC, Sai S, Vidal RO, Sauer S, Hennig T, Grothey A, Milić A, Prusty BK, Lehner PJ, Matheson NJ, Erhard F, Dölken L. Dissecting Herpes Simplex Virus 1-Induced Host Shutoff at the RNA Level. J Virol 2021;95:e01399-20. [PMID: 33148793 DOI: 10.1128/JVI.01399-20] [Cited by in Crossref: 12] [Cited by in F6Publishing: 14] [Article Influence: 12.0] [Reference Citation Analysis]
279 Pir MS, Bilgin HI, Sayici A, Coşkun F, Torun FM, Zhao P, Kang Y, Cevik S, Kaplan OI. ConVarT: a search engine for matching human genetic variants with variants from non-human species.. [DOI: 10.1101/2021.01.07.424951] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 3.0] [Reference Citation Analysis]
280 Del Gobbo GF, Yin Y, Choufani S, Butcher EA, Wei J, Rajcan-Separovic E, Bos H, von Dadelszen P, Weksberg R, Robinson WP, Yuen RKC. Genomic imbalances in the placenta are associated with poor fetal growth. Mol Med 2021;27:3. [PMID: 33413077 DOI: 10.1186/s10020-020-00253-4] [Cited by in Crossref: 6] [Cited by in F6Publishing: 7] [Article Influence: 6.0] [Reference Citation Analysis]
281 Kaur S, Roberts DD. Differential intolerance to loss of function and missense mutations in genes that encode human matricellular proteins. J Cell Commun Signal 2021;15:93-105. [PMID: 33415696 DOI: 10.1007/s12079-020-00598-9] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
282 Gonzaga-jauregui C, Zepeda Mendoza CJ. Genomic sequencing of rare diseases. Genomics of Rare Diseases 2021. [DOI: 10.1016/b978-0-12-820140-4.00001-6] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
283 Lisacek F, Aoki-kinoshita KF, Vora JK, Mazumder R, Tiemeyer M. Glycoinformatics Resources Integrated Through the GlySpace Alliance. Comprehensive Glycoscience 2021. [DOI: 10.1016/b978-0-12-819475-1.00107-3] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
284 Gonzaga-jauregui C. Challenges and opportunities in rare diseases research. Genomics of Rare Diseases 2021. [DOI: 10.1016/b978-0-12-820140-4.00013-2] [Reference Citation Analysis]
285 Boer EF, Van Hollebeke HF, Holt C, Yandell M, Shapiro MD. A <i>ROR2</i> Coding Variant is Associated with Craniofacial Variation in Domestic Pigeons. SSRN Journal. [DOI: 10.2139/ssrn.3808295] [Reference Citation Analysis]
286 Dimitrakopoulos GN, Klapa MI, Moschonas NK. PICKLE 3.0: Enriching the human Meta-database with the mouse protein interactome extended via mouse-human orthology. Bioinformatics 2020:btaa1070. [PMID: 33367505 DOI: 10.1093/bioinformatics/btaa1070] [Cited by in Crossref: 6] [Cited by in F6Publishing: 7] [Article Influence: 3.0] [Reference Citation Analysis]
287 Kahsay R, Vora J, Navelkar R, Mousavi R, Fochtman BC, Holmes X, Pattabiraman N, Ranzinger R, Mahadik R, Williamson T, Kulkarni S, Agarwal G, Martin M, Vasudev P, Garcia L, Edwards N, Zhang W, Natale DA, Ross K, Aoki-Kinoshita KF, Campbell MP, York WS, Mazumder R. GlyGen data model and processing workflow. Bioinformatics 2020;36:3941-3. [PMID: 32324859 DOI: 10.1093/bioinformatics/btaa238] [Cited by in Crossref: 16] [Cited by in F6Publishing: 16] [Article Influence: 8.0] [Reference Citation Analysis]
288 Russkikh N, Antonets D, Shtokalo D, Makarov A, Vyatkin Y, Zakharov A, Terentyev E. Style transfer with variational autoencoders is a promising approach to RNA-Seq data harmonization and analysis. Bioinformatics 2020;36:5076-85. [PMID: 33026062 DOI: 10.1093/bioinformatics/btaa624] [Cited by in Crossref: 5] [Cited by in F6Publishing: 5] [Article Influence: 2.5] [Reference Citation Analysis]
289 Oh S, Abdelnabi J, Al-Dulaimi R, Aggarwal A, Ramos M, Davis S, Riester M, Waldron L. HGNChelper: identification and correction of invalid gene symbols for human and mouse. F1000Res 2020;9:1493. [PMID: 33564398 DOI: 10.12688/f1000research.28033.1] [Cited by in Crossref: 7] [Cited by in F6Publishing: 8] [Article Influence: 3.5] [Reference Citation Analysis]
290 Oh S, Abdelnabi J, Al-Dulaimi R, Aggarwal A, Ramos M, Davis S, Riester M, Waldron L. HGNChelper: identification and correction of invalid gene symbols for human and mouse. F1000Res 2020;9:1493. [PMID: 33564398 DOI: 10.12688/f1000research.28033.2] [Reference Citation Analysis]
291 Xu F, Gao J, Munkhsaikhan U, Li N, Gu Q, Pierre JF, Starlard-Davenport A, Towbin JA, Cui Y, Purevjav E, Lu L. The Genetic Dissection of Ace2 Expression Variation in the Heart of Murine Genetic Reference Population. Front Cardiovasc Med 2020;7:582949. [PMID: 33330645 DOI: 10.3389/fcvm.2020.582949] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 2.0] [Reference Citation Analysis]
292 Chambers BE, Clark EG, Gatz AE, Wingert RA. Kctd15 regulates nephron segment development by repressing Tfap2a activity. Development 2020;147:dev191973. [PMID: 33028614 DOI: 10.1242/dev.191973] [Cited by in Crossref: 4] [Cited by in F6Publishing: 6] [Article Influence: 2.0] [Reference Citation Analysis]
293 Gilly A, Park YC, Png G, Barysenka A, Fischer I, Bjørnland T, Southam L, Suveges D, Neumeyer S, Rayner NW, Tsafantakis E, Karaleftheri M, Dedoussis G, Zeggini E. Whole-genome sequencing analysis of the cardiometabolic proteome. Nat Commun 2020;11:6336. [PMID: 33303764 DOI: 10.1038/s41467-020-20079-2] [Cited by in Crossref: 8] [Cited by in F6Publishing: 9] [Article Influence: 4.0] [Reference Citation Analysis]
294 Mizuno S, Hirota JN, Ishii C, Iwasaki H, Sano Y, Furuichi T. Comprehensive Profiling of Gene Expression in the Cerebral Cortex and Striatum of BTBRTF/ArtRbrc Mice Compared to C57BL/6J Mice. Front Cell Neurosci 2020;14:595607. [PMID: 33362469 DOI: 10.3389/fncel.2020.595607] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 2.0] [Reference Citation Analysis]
295 Di Matteo A, Belloni E, Pradella D, Cappelletto A, Volf N, Zacchigna S, Ghigna C. Alternative splicing in endothelial cells: novel therapeutic opportunities in cancer angiogenesis. J Exp Clin Cancer Res 2020;39:275. [PMID: 33287867 DOI: 10.1186/s13046-020-01753-1] [Cited by in Crossref: 10] [Cited by in F6Publishing: 11] [Article Influence: 5.0] [Reference Citation Analysis]
296 Hu S, Molina L, Tao J, Liu S, Hassan M, Singh S, Poddar M, Bell A, Sia D, Oertel M, Raeman R, Nejak-bowen K, Singhi A, Luo J, Monga SP, Ko S. NOTCH-YAP1/TEAD-DNMT1 axis regulates hepatocyte reprogramming into intrahepatic cholangiocarcinoma.. [DOI: 10.1101/2020.12.03.410993] [Reference Citation Analysis]
297 Krull F, Hirschfeld M, Wemheuer WE, Brenig B. Frameshift Variant in Novel Adenosine-A1-Receptor Homolog Associated With Bovine Spastic Syndrome/Late-Onset Bovine Spastic Paresis in Holstein Sires. Front Genet 2020;11:591794. [PMID: 33329738 DOI: 10.3389/fgene.2020.591794] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
298 Ng AHM, Khoshakhlagh P, Rojo Arias JE, Pasquini G, Wang K, Swiersy A, Shipman SL, Appleton E, Kiaee K, Kohman RE, Vernet A, Dysart M, Leeper K, Saylor W, Huang JY, Graveline A, Taipale J, Hill DE, Vidal M, Melero-Martin JM, Busskamp V, Church GM. A comprehensive library of human transcription factors for cell fate engineering. Nat Biotechnol 2021;39:510-9. [PMID: 33257861 DOI: 10.1038/s41587-020-0742-6] [Cited by in Crossref: 46] [Cited by in F6Publishing: 54] [Article Influence: 23.0] [Reference Citation Analysis]
299 Dolan ME, Hill DP, Mukherjee G, McAndrews MS, Chesler EJ, Blake JA. Investigation of COVID-19 comorbidities reveals genes and pathways coincident with the SARS-CoV-2 viral disease. Sci Rep 2020;10:20848. [PMID: 33257774 DOI: 10.1038/s41598-020-77632-8] [Cited by in Crossref: 22] [Cited by in F6Publishing: 24] [Article Influence: 11.0] [Reference Citation Analysis]
300 Yoo H, La H, Lee EJ, Choi HJ, Oh J, Thang NX, Hong K. ATP-Dependent Chromatin Remodeler CHD9 Controls the Proliferation of Embryonic Stem Cells in a Cell Culture Condition-Dependent Manner. Biology (Basel) 2020;9:E428. [PMID: 33261017 DOI: 10.3390/biology9120428] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
301 Doshida Y, Sano H, Iwabuchi S, Aigaki T, Yoshida M, Hashimoto S, Ishigami A. Age-associated changes in the transcriptomes of non-cultured adipose-derived stem cells from young and old mice assessed via single-cell transcriptome analysis. PLoS One 2020;15:e0242171. [PMID: 33237970 DOI: 10.1371/journal.pone.0242171] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 2.0] [Reference Citation Analysis]
302 Brennan JA, Chen Q, Gams A, Dyavanapalli J, Mendelowitz D, Peng W, Efimov IR. Evidence of Superior and Inferior Sinoatrial Nodes in the Mammalian Heart. JACC Clin Electrophysiol 2020;6:1827-40. [PMID: 33357580 DOI: 10.1016/j.jacep.2020.09.012] [Cited by in Crossref: 24] [Cited by in F6Publishing: 28] [Article Influence: 12.0] [Reference Citation Analysis]
303 Laisk T, Soares ALG, Ferreira T, Painter JN, Censin JC, Laber S, Bacelis J, Chen CY, Lepamets M, Lin K, Liu S, Millwood IY, Ramu A, Southcombe J, Andersen MS, Yang L, Becker CM, Børglum AD, Gordon SD, Bybjerg-Grauholm J, Helgeland Ø, Hougaard DM, Jin X, Johansson S, Juodakis J, Kartsonaki C, Kukushkina V, Lind PA, Metspalu A, Montgomery GW, Morris AP, Mors O, Mortensen PB, Njølstad PR, Nordentoft M, Nyholt DR, Lippincott M, Seminara S, Salumets A, Snieder H, Zondervan K, Werge T, Chen Z, Conrad DF, Jacobsson B, Li L, Martin NG, Neale BM, Nielsen R, Walters RG, Granne I, Medland SE, Mägi R, Lawlor DA, Lindgren CM. The genetic architecture of sporadic and multiple consecutive miscarriage. Nat Commun 2020;11:5980. [PMID: 33239672 DOI: 10.1038/s41467-020-19742-5] [Cited by in Crossref: 19] [Cited by in F6Publishing: 20] [Article Influence: 9.5] [Reference Citation Analysis]
304 Thessen AE, Walls RL, Vogt L, Singer J, Warren R, Buttigieg PL, Balhoff JP, Mungall CJ, McGuinness DL, Stucky BJ, Yoder MJ, Haendel MA. Transforming the study of organisms: Phenomic data models and knowledge bases. PLoS Comput Biol 2020;16:e1008376. [PMID: 33232313 DOI: 10.1371/journal.pcbi.1008376] [Cited by in Crossref: 3] [Cited by in F6Publishing: 4] [Article Influence: 1.5] [Reference Citation Analysis]
305 Zaro BW, Noh JJ, Mascetti VL, Demeter J, George B, Zukowska M, Gulati GS, Sinha R, Flynn RA, Banuelos A, Zhang A, Wilkinson AC, Jackson P, Weissman IL. Proteomic analysis of young and old mouse hematopoietic stem cells and their progenitors reveals post-transcriptional regulation in stem cells. Elife 2020;9:e62210. [PMID: 33236985 DOI: 10.7554/eLife.62210] [Cited by in Crossref: 11] [Cited by in F6Publishing: 11] [Article Influence: 5.5] [Reference Citation Analysis]
306 Kulmanov M, Hoehndorf R. DeepPheno: Predicting single gene loss-of-function phenotypes using an ontology-aware hierarchical classifier. PLoS Comput Biol 2020;16:e1008453. [PMID: 33206638 DOI: 10.1371/journal.pcbi.1008453] [Cited by in Crossref: 10] [Cited by in F6Publishing: 12] [Article Influence: 5.0] [Reference Citation Analysis]
307 Huang J, Zhong Y, Makohon-moore AP, White T, Jasin M, Norell MA, Wheeler WC, Iacobuzio-donahue CA. Selection for Decreased BRCA2 Functional Activity in Homo sapiens After Divergence from the Chimpanzee-Human Last Common Ancestor.. [DOI: 10.1101/2020.11.16.384677] [Reference Citation Analysis]
308 Ray D, Venkataraghavan S, Zhang W, Leslie EJ, Hetmanski JB, Marazita ML, Ruczinski I, Taub MA, Beaty TH. Pleiotropy method identifies genetic overlap between orofacial clefts at multiple loci from GWAS of multi-ethnictrios.. [DOI: 10.1101/2020.11.13.20231654] [Reference Citation Analysis]
309 Lu T, Mar JC. Investigating transcriptome-wide sex dimorphism by multi-level analysis of single-cell RNA sequencing data in ten mouse cell types. Biol Sex Differ 2020;11:61. [PMID: 33153500 DOI: 10.1186/s13293-020-00335-2] [Cited by in Crossref: 10] [Cited by in F6Publishing: 10] [Article Influence: 5.0] [Reference Citation Analysis]
310 Li S, Shao H, Chang L. The Important Role of Perituberal Tissue in Epileptic Patients with Tuberous Sclerosis Complex by the Transcriptome Analysis. Biomed Res Int 2020;2020:4980609. [PMID: 33123575 DOI: 10.1155/2020/4980609] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
311 Gorski M, Jung B, Li Y, Matias-Garcia PR, Wuttke M, Coassin S, Thio CHL, Kleber ME, Winkler TW, Wanner V, Chai JF, Chu AY, Cocca M, Feitosa MF, Ghasemi S, Hoppmann A, Horn K, Li M, Nutile T, Scholz M, Sieber KB, Teumer A, Tin A, Wang J, Tayo BO, Ahluwalia TS, Almgren P, Bakker SJL, Banas B, Bansal N, Biggs ML, Boerwinkle E, Bottinger EP, Brenner H, Carroll RJ, Chalmers J, Chee ML, Chee ML, Cheng CY, Coresh J, de Borst MH, Degenhardt F, Eckardt KU, Endlich K, Franke A, Freitag-Wolf S, Gampawar P, Gansevoort RT, Ghanbari M, Gieger C, Hamet P, Ho K, Hofer E, Holleczek B, Xian Foo VH, Hutri-Kähönen N, Hwang SJ, Ikram MA, Josyula NS, Kähönen M, Khor CC, Koenig W, Kramer H, Krämer BK, Kühnel B, Lange LA, Lehtimäki T, Lieb W, Loos RJF, Lukas MA, Lyytikäinen LP, Meisinger C, Meitinger T, Melander O, Milaneschi Y, Mishra PP, Mononen N, Mychaleckyj JC, Nadkarni GN, Nauck M, Nikus K, Ning B, Nolte IM, O'Donoghue ML, Orho-Melander M, Pendergrass SA, Penninx BWJH, Preuss MH, Psaty BM, Raffield LM, Raitakari OT, Rettig R, Rheinberger M, Rice KM, Rosenkranz AR, Rossing P, Rotter JI, Sabanayagam C, Schmidt H, Schmidt R, Schöttker B, Schulz CA, Sedaghat S, Shaffer CM, Strauch K, Szymczak S, Taylor KD, Tremblay J, Chaker L, van der Harst P, van der Most PJ, Verweij N, Völker U, Waldenberger M, Wallentin L, Waterworth DM, White HD, Wilson JG, Wong TY, Woodward M, Yang Q, Yasuda M, Yerges-Armstrong LM, Zhang Y, Snieder H, Wanner C, Böger CA, Köttgen A, Kronenberg F, Pattaro C, Heid IM; Lifelines Cohort Study., Regeneron Genetics Center. Meta-analysis uncovers genome-wide significant variants for rapid kidney function decline. Kidney Int 2021;99:926-39. [PMID: 33137338 DOI: 10.1016/j.kint.2020.09.030] [Cited by in Crossref: 14] [Cited by in F6Publishing: 11] [Article Influence: 7.0] [Reference Citation Analysis]
312 Adadey SM, Wonkam-Tingang E, Twumasi Aboagye E, Nayo-Gyan DW, Boatemaa Ansong M, Quaye O, Awandare GA, Wonkam A. Connexin Genes Variants Associated with Non-Syndromic Hearing Impairment: A Systematic Review of the Global Burden. Life (Basel) 2020;10:E258. [PMID: 33126609 DOI: 10.3390/life10110258] [Cited by in Crossref: 6] [Cited by in F6Publishing: 7] [Article Influence: 3.0] [Reference Citation Analysis]
313 Crouse WL, Kelada SNP, Valdar W. Inferring the Allelic Series at QTL in Multiparental Populations. Genetics 2020;216:957-83. [PMID: 33082282 DOI: 10.1534/genetics.120.303393] [Cited by in Crossref: 10] [Cited by in F6Publishing: 10] [Article Influence: 5.0] [Reference Citation Analysis]
314 Fuentealba M, Fabian DK, Dönertaş HM, Thornton JM, Partridge L. Transcriptomic profiling of long- and short-lived mutant mice implicates mitochondrial metabolism in ageing and shows signatures of normal ageing in progeroid mice.. [DOI: 10.1101/2020.10.20.347013] [Reference Citation Analysis]
315 Jin SC, Dong W, Kundishora AJ, Panchagnula S, Moreno-De-Luca A, Furey CG, Allocco AA, Walker RL, Nelson-Williams C, Smith H, Dunbar A, Conine S, Lu Q, Zeng X, Sierant MC, Knight JR, Sullivan W, Duy PQ, DeSpenza T, Reeves BC, Karimy JK, Marlier A, Castaldi C, Tikhonova IR, Li B, Peña HP, Broach JR, Kabachelor EM, Ssenyonga P, Hehnly C, Ge L, Keren B, Timberlake AT, Goto J, Mangano FT, Johnston JM, Butler WE, Warf BC, Smith ER, Schiff SJ, Limbrick DD Jr, Heuer G, Jackson EM, Iskandar BJ, Mane S, Haider S, Guclu B, Bayri Y, Sahin Y, Duncan CC, Apuzzo MLJ, DiLuna ML, Hoffman EJ, Sestan N, Ment LR, Alper SL, Bilguvar K, Geschwind DH, Günel M, Lifton RP, Kahle KT. Exome sequencing implicates genetic disruption of prenatal neuro-gliogenesis in sporadic congenital hydrocephalus. Nat Med 2020;26:1754-65. [PMID: 33077954 DOI: 10.1038/s41591-020-1090-2] [Cited by in Crossref: 34] [Cited by in F6Publishing: 36] [Article Influence: 17.0] [Reference Citation Analysis]
316 Laisk T, Lepamets M, Mägi R. Genome-wide association study identifies five risk loci for pernicious anemia and implicates the role of HLA-DR15 haplotype.. [DOI: 10.1101/2020.10.13.20211912] [Reference Citation Analysis]
317 Ke L, Yang DC, Wang Y, Ding Y, Gao G. AnnoLnc2: the one-stop portal to systematically annotate novel lncRNAs for human and mouse. Nucleic Acids Res 2020;48:W230-8. [PMID: 32406920 DOI: 10.1093/nar/gkaa368] [Cited by in Crossref: 20] [Cited by in F6Publishing: 22] [Article Influence: 10.0] [Reference Citation Analysis]
318 Niazi Y, Thomsen H, Smolkova B, Vodickova L, Vodenkova S, Kroupa M, Vymetalkova V, Kazimirova A, Barancokova M, Volkovova K, Staruchova M, Hoffmann P, Nöthen MM, Dusinska M, Musak L, Vodicka P, Hemminki K, Försti A. Impact of genetic polymorphisms in kinetochore and spindle assembly genes on chromosomal aberration frequency in healthy humans. Mutat Res Genet Toxicol Environ Mutagen 2020;858-860:503253. [PMID: 33198934 DOI: 10.1016/j.mrgentox.2020.503253] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
319 Salunkhe S, Vaidya T. CD40-miRNA axis controls prospective cell fate determinants during B cell differentiation. Molecular Immunology 2020;126:46-55. [DOI: 10.1016/j.molimm.2020.07.007] [Cited by in Crossref: 10] [Cited by in F6Publishing: 10] [Article Influence: 5.0] [Reference Citation Analysis]
320 Hillman P, Baker C, Hebert L, Brown M, Hixson J, Ashley-Koch A, Morrison AC, Northrup H, Au KS. Identification of novel candidate risk genes for myelomeningocele within the glucose homeostasis/oxidative stress and folate/one-carbon metabolism networks. Mol Genet Genomic Med 2020;8:e1495. [PMID: 32960507 DOI: 10.1002/mgg3.1495] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 1.5] [Reference Citation Analysis]
321 Dolan ME, Hill DP, Mukherjee G, McAndrews MS, Chesler EJ, Blake JA. Investigation of COVID-19 comorbidities reveals genes and pathways coincident with the SARS-CoV-2 viral disease. bioRxiv 2020:2020. [PMID: 32995795 DOI: 10.1101/2020.09.21.306720] [Cited by in Crossref: 1] [Cited by in F6Publishing: 3] [Article Influence: 0.5] [Reference Citation Analysis]
322 Hunker AC, Zweifel LS. Protocol to Design, Clone, and Validate sgRNAs for In Vivo Reverse Genetic Studies. STAR Protoc 2020;1:100070. [PMID: 33043306 DOI: 10.1016/j.xpro.2020.100070] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 1.5] [Reference Citation Analysis]
323 Woolley SA, Hayes SE, Shariflou MR, Nicholas FW, Willet CE, O'Rourke BA, Tammen I. Molecular basis of a new ovine model for human 3M syndrome-2. BMC Genet 2020;21:106. [PMID: 32933480 DOI: 10.1186/s12863-020-00913-8] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
324 Manshaei R, Merico D, Reuter MS, Engchuan W, Mojarad BA, Chaturvedi R, Heung T, Pellecchia G, Zarrei M, Nalpathamkalam T, Khan R, Okello JBA, Liston E, Curtis M, Yuen RKC, Marshall CR, Jobling RK, Oechslin E, Wald RM, Silversides CK, Scherer SW, Kim RH, Bassett AS. Genes and Pathways Implicated in Tetralogy of Fallot Revealed by Ultra-Rare Variant Burden Analysis in 231 Genome Sequences. Front Genet 2020;11:957. [PMID: 33110418 DOI: 10.3389/fgene.2020.00957] [Cited by in Crossref: 8] [Cited by in F6Publishing: 10] [Article Influence: 4.0] [Reference Citation Analysis]
325 Bubier JA, He H, Philip VM, Roy T, Hernandez CM, Bernat R, Donohue KD, O'Hara BF, Chesler EJ. Genetic variation regulates opioid-induced respiratory depression in mice. Sci Rep 2020;10:14970. [PMID: 32917924 DOI: 10.1038/s41598-020-71804-2] [Cited by in Crossref: 15] [Cited by in F6Publishing: 15] [Article Influence: 7.5] [Reference Citation Analysis]
326 Thoene S, Mandal T, Vegi NM, Quintanilla-Martinez L, Rösler R, Wiese S, Metzeler KH, Herold T, Haferlach T, Döhner K, Döhner H, Schwarzmüller L, Klingmüller U, Buske C, Rawat VPS, Feuring-Buske M. The ParaHox gene Cdx4 induces acute erythroid leukemia in mice. Blood Adv 2019;3:3729-39. [PMID: 31770439 DOI: 10.1182/bloodadvances.2019000761] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 1.5] [Reference Citation Analysis]
327 Stanzick KJ, Li Y, Gorski M, Wuttke M, Pattaro C, Köttgen A, Stark KJ, Heid IM, Winkler TW. Discovery and prioritization of variants and genes for kidney function in >1.2 million individuals.. [DOI: 10.1101/2020.09.04.283713] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
328 Best SA, Hess JB, Souza-fonseca-guimaraes F, Cursons J, Kersbergen A, Dong X, Rautela J, Hyslop SR, Ritchie ME, Davis MJ, Leong TL, Irving L, Steinfort D, Huntington ND, Sutherland KD. Harnessing Natural Killer Immunity in Metastatic SCLC. Journal of Thoracic Oncology 2020;15:1507-21. [DOI: 10.1016/j.jtho.2020.05.008] [Cited by in Crossref: 26] [Cited by in F6Publishing: 31] [Article Influence: 13.0] [Reference Citation Analysis]
329 Garcia-Moreno A, Carmona-Saez P. Computational Methods and Software Tools for Functional Analysis of miRNA Data. Biomolecules 2020;10:E1252. [PMID: 32872205 DOI: 10.3390/biom10091252] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 2.0] [Reference Citation Analysis]
330 Han L, Chaturvedi P, Kishimoto K, Koike H, Nasr T, Iwasawa K, Giesbrecht K, Witcher PC, Eicher A, Haines L, Lee Y, Shannon JM, Morimoto M, Wells JM, Takebe T, Zorn AM. Single cell transcriptomics identifies a signaling network coordinating endoderm and mesoderm diversification during foregut organogenesis. Nat Commun 2020;11:4158. [PMID: 32855417 DOI: 10.1038/s41467-020-17968-x] [Cited by in Crossref: 69] [Cited by in F6Publishing: 76] [Article Influence: 34.5] [Reference Citation Analysis]
331 Winkler TW, Grassmann F, Brandl C, Kiel C, Günther F, Strunz T, Weidner L, Zimmermann ME, Korb CA, Poplawski A, Schuster AK, Müller-Nurasyid M, Peters A, Rauscher FG, Elze T, Horn K, Scholz M, Cañadas-Garre M, McKnight AJ, Quinn N, Hogg RE, Küchenhoff H, Heid IM, Stark KJ, Weber BHF. Genome-wide association meta-analysis for early age-related macular degeneration highlights novel loci and insights for advanced disease. BMC Med Genomics 2020;13:120. [PMID: 32843070 DOI: 10.1186/s12920-020-00760-7] [Cited by in Crossref: 23] [Cited by in F6Publishing: 24] [Article Influence: 11.5] [Reference Citation Analysis]
332 Polymenis M. Ribosomal proteins: mutant phenotypes by the numbers and associated gene expression changes. Open Biol 2020;10:200114. [PMID: 32810425 DOI: 10.1098/rsob.200114] [Cited by in Crossref: 7] [Cited by in F6Publishing: 7] [Article Influence: 3.5] [Reference Citation Analysis]
333 Widmayer SJ, Handel MA, Aylor DL. Age and Genetic Background Modify Hybrid Male Sterility in House Mice. Genetics 2020;216:585-97. [PMID: 32817010 DOI: 10.1534/genetics.120.303474] [Cited by in Crossref: 12] [Cited by in F6Publishing: 12] [Article Influence: 6.0] [Reference Citation Analysis]
334 Hannigan MM, Hoffman AM, Thompson JW, Zheng T, Nicchitta CV. Quantitative Proteomics Links the LRRC59 Interactome to mRNA Translation on the ER Membrane. Mol Cell Proteomics 2020;19:1826-49. [PMID: 32788342 DOI: 10.1074/mcp.RA120.002228] [Cited by in Crossref: 8] [Cited by in F6Publishing: 8] [Article Influence: 4.0] [Reference Citation Analysis]
335 Ichino N, Serres MR, Urban RM, Urban MD, Treichel AJ, Schaefbauer KJ, Greif LE, Varshney GK, Skuster KJ, McNulty MS, Daby CL, Wang Y, Liao HK, El-Rass S, Ding Y, Liu W, Anderson JL, Wishman MD, Sabharwal A, Schimmenti LA, Sivasubbu S, Balciunas D, Hammerschmidt M, Farber SA, Wen XY, Xu X, McGrail M, Essner JJ, Burgess SM, Clark KJ, Ekker SC. Building the vertebrate codex using the gene breaking protein trap library. Elife 2020;9:e54572. [PMID: 32779569 DOI: 10.7554/eLife.54572] [Cited by in Crossref: 6] [Cited by in F6Publishing: 6] [Article Influence: 3.0] [Reference Citation Analysis]
336 Shah SG, Mandloi T, Kunte P, Natu A, Rashid M, Reddy D, Gadewal N, Gupta S. HISTome2: a database of histone proteins, modifiers for multiple organisms and epidrugs. Epigenetics Chromatin 2020;13:31. [PMID: 32746900 DOI: 10.1186/s13072-020-00354-8] [Cited by in Crossref: 11] [Cited by in F6Publishing: 12] [Article Influence: 5.5] [Reference Citation Analysis]
337 Icick R, Forget B, Cloëz-Tayarani I, Pons S, Maskos U, Besson M. Genetic susceptibility to nicotine addiction: Advances and shortcomings in our understanding of the CHRNA5/A3/B4 gene cluster contribution. Neuropharmacology 2020;177:108234. [PMID: 32738310 DOI: 10.1016/j.neuropharm.2020.108234] [Cited by in Crossref: 5] [Cited by in F6Publishing: 6] [Article Influence: 2.5] [Reference Citation Analysis]
338 Holcomb AJ, Brown L, Tawfik O, Madan R, Shnayder Y, Thomas SM, Wallace NA. DNA repair gene expression is increased in HPV positive head and neck squamous cell carcinomas. Virology 2020;548:174-81. [PMID: 32838940 DOI: 10.1016/j.virol.2020.07.004] [Cited by in Crossref: 4] [Cited by in F6Publishing: 3] [Article Influence: 2.0] [Reference Citation Analysis]
339 Gupta M, Concepcion CP, Fahey CG, Keshishian H, Bhutkar A, Brainson CF, Sanchez-Rivera FJ, Pessina P, Kim JY, Simoneau A, Paschini M, Beytagh MC, Stanclift CR, Schenone M, Mani DR, Li C, Oh A, Li F, Hu H, Karatza A, Bronson RT, Shaw AT, Hata AN, Wong KK, Zou L, Carr SA, Jacks T, Kim CF. BRG1 Loss Predisposes Lung Cancers to Replicative Stress and ATR Dependency. Cancer Res 2020;80:3841-54. [PMID: 32690724 DOI: 10.1158/0008-5472.CAN-20-1744] [Cited by in Crossref: 16] [Cited by in F6Publishing: 17] [Article Influence: 8.0] [Reference Citation Analysis]
340 Demetci P, Cheng W, Darnell G, Zhou X, Ramachandran S, Crawford L. Multi-scale Inference of Genetic Trait Architecture using Biologically Annotated Neural Networks.. [DOI: 10.1101/2020.07.02.184465] [Cited by in Crossref: 6] [Cited by in F6Publishing: 6] [Article Influence: 3.0] [Reference Citation Analysis]
341 Siemsen BM, Landin JD, McFaddin JA, Hooker KN, Chandler LJ, Scofield MD. Chronic intermittent ethanol and lipopolysaccharide exposure differentially alter Iba1-derived microglia morphology in the prelimbic cortex and nucleus accumbens core of male Long-Evans rats. J Neurosci Res 2021;99:1922-39. [PMID: 32621337 DOI: 10.1002/jnr.24683] [Cited by in Crossref: 5] [Cited by in F6Publishing: 6] [Article Influence: 2.5] [Reference Citation Analysis]
342 Colella JP, Tigano A, Dudchenko O, Omer AD, Khan R, Bochkov ID, Aiden EL, Macmanes MD. Limited evidence for parallel evolution among desert adapted Peromyscus deer mice.. [DOI: 10.1101/2020.06.29.178392] [Reference Citation Analysis]
343 Boros É, Prontvai B, Kellermayer Z, Balogh P, Sarlós P, Vincze Á, Varga C, Maróti Z, Bálint B, Nagy I. Transcriptome Based Profiling of the Immune Cell Gene Signature in Rat Experimental Colitis and Human IBD Tissue Samples. Biomolecules 2020;10:E974. [PMID: 32610492 DOI: 10.3390/biom10070974] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 1.5] [Reference Citation Analysis]
344 Widmayer SJ, Handel MA, Aylor DL. Age and genetic background modify hybrid male sterility in house mice.. [DOI: 10.1101/2020.06.26.173047] [Reference Citation Analysis]
345 Xiong L, Schoenberg WA, Swartz JD. Macroscale network feedback structure of transcriptome during cell fate transition.. [DOI: 10.1101/2020.06.24.169490] [Reference Citation Analysis]
346 Li H, Liu S, Du Y, Tan J, Luo J, Sun Y. Hub Proteins Involved in RAW 264.7 Macrophages Exposed to Direct Current Electric Field. Int J Mol Sci 2020;21:E4505. [PMID: 32599940 DOI: 10.3390/ijms21124505] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
347 Vysotskiy M, Zhong X, Miller-fleming TW, Zhou D, Cox NJ, Weiss LA, Autism Working Group of the Psychiatric Genomics Consortium, Bipolar Disorder Working Group of the Psychiatric Genomics Consortium, Schizophrenia Working Group of the Psychiatric Genomics Consortium. Integration of genetic, transcriptomic, and clinical data provides insight into 16p11.2 and 22q11.2 CNV genes.. [DOI: 10.1101/2020.06.23.166181] [Reference Citation Analysis]
348 Yusuff T, Jensen M, Yennawar S, Pizzo L, Karthikeyan S, Gould DJ, Sarker A, Gedvilaite E, Matsui Y, Iyer J, Lai ZC, Girirajan S. Drosophila models of pathogenic copy-number variant genes show global and non-neuronal defects during development. PLoS Genet 2020;16:e1008792. [PMID: 32579612 DOI: 10.1371/journal.pgen.1008792] [Cited by in Crossref: 7] [Cited by in F6Publishing: 8] [Article Influence: 3.5] [Reference Citation Analysis]
349 Cheleuitte-nieves C, Lipman NS. Improving Replicability, Reproducibility, And Reliability In Preclinical Research: A Shared Responsibility. ILAR Journal 2019;60:113-9. [DOI: 10.1093/ilar/ilaa009] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
350 Rosikiewicz W, Chen X, Dominguez PM, Ghamlouch H, Aoufouchi S, Bernard OA, Melnick A, Li S. TET2 deficiency reprograms the germinal center B cell epigenome and silences genes linked to lymphomagenesis. Sci Adv 2020;6:eaay5872. [PMID: 32596441 DOI: 10.1126/sciadv.aay5872] [Cited by in Crossref: 19] [Cited by in F6Publishing: 18] [Article Influence: 9.5] [Reference Citation Analysis]
351 Bubier JA, He H, Philip VM, Roy T, Hernandez CM, Donohue KD, O’hara BF, Chesler EJ. Genetic Variation Regulates Opioid-Induced Respiratory Depression in Mice.. [DOI: 10.1101/2020.06.15.152249] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
352 Nowoshilow S, Tanaka EM. Introducing www.axolotl-omics.org - an integrated -omics data portal for the axolotl research community. Exp Cell Res 2020;394:112143. [PMID: 32540400 DOI: 10.1016/j.yexcr.2020.112143] [Cited by in Crossref: 11] [Cited by in F6Publishing: 6] [Article Influence: 5.5] [Reference Citation Analysis]
353 Adadey SM, Esoh KK, Quaye O, Amedofu GK, Awandare GA, Wonkam A. GJB4 and GJC3 variants in non-syndromic hearing impairment in Ghana. Exp Biol Med (Maywood) 2020;245:1355-67. [PMID: 32524838 DOI: 10.1177/1535370220931035] [Cited by in Crossref: 2] [Cited by in F6Publishing: 3] [Article Influence: 1.0] [Reference Citation Analysis]
354 Panov J, Simchi L, Feuermann Y, Kaphzan H. Bioinformatics Analyses of the Transcriptome Reveal Ube3a-Dependent Effects on Mitochondrial-Related Pathways. Int J Mol Sci 2020;21:E4156. [PMID: 32532103 DOI: 10.3390/ijms21114156] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 2.0] [Reference Citation Analysis]
355 Zhuang QK, Galvez JH, Xiao Q, AlOgayil N, Hyacinthe J, Taketo T, Bourque G, Naumova AK. Sex Chromosomes and Sex Phenotype Contribute to Biased DNA Methylation in Mouse Liver. Cells 2020;9:E1436. [PMID: 32527045 DOI: 10.3390/cells9061436] [Cited by in Crossref: 9] [Cited by in F6Publishing: 9] [Article Influence: 4.5] [Reference Citation Analysis]
356 Huang SSY, Makhlouf M, AbouMoussa EH, Ruiz Tejada Segura ML, Mathew LS, Wang K, Leung MC, Chaussabel D, Logan DW, Scialdone A, Garand M, Saraiva LR. Differential regulation of the immune system in a brain-liver-fats organ network during short-term fasting. Mol Metab 2020;40:101038. [PMID: 32526449 DOI: 10.1016/j.molmet.2020.101038] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 2.0] [Reference Citation Analysis]
357 van der Weyden L, Swiatkowska A, Iyer V, Speak AO, Adams DJ. A Genome-Wide Screen in Mice To Identify Cell-Extrinsic Regulators of Pulmonary Metastatic Colonisation. G3 (Bethesda) 2020;10:1869-77. [PMID: 32245826 DOI: 10.1534/g3.120.401128] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 0.5] [Reference Citation Analysis]
358 Sun YH, Wang A, Song C, Srivastava RK, Au KF, Li XZ. Single-molecule long-read sequencing reveals a conserved selection mechanism determining intact long RNA and miRNA profiles in sperm.. [DOI: 10.1101/2020.05.28.122382] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
359 Kafer GR, Cesare AJ. A Survey of Essential Genome Stability Genes Reveals That Replication Stress Mitigation Is Critical for Peri-Implantation Embryogenesis. Front Cell Dev Biol 2020;8:416. [PMID: 32548123 DOI: 10.3389/fcell.2020.00416] [Cited by in Crossref: 7] [Cited by in F6Publishing: 7] [Article Influence: 3.5] [Reference Citation Analysis]
360 Gardner EJ, Neville MDC, Samocha KE, Barclay K, Kolk M, Niemi MEK, Kirov G, Martin HC, Hurles ME. Reduced reproductive success is associated with selective constraint on human genes.. [DOI: 10.1101/2020.05.26.116111] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 1.5] [Reference Citation Analysis]
361 Alliance of Genome Resources Consortium. Alliance of Genome Resources Portal: unified model organism research platform. Nucleic Acids Res 2020;48:D650-8. [PMID: 31552413 DOI: 10.1093/nar/gkz813] [Cited by in Crossref: 98] [Cited by in F6Publishing: 110] [Article Influence: 49.0] [Reference Citation Analysis]
362 Smith JR, Hayman GT, Wang SJ, Laulederkind SJF, Hoffman MJ, Kaldunski ML, Tutaj M, Thota J, Nalabolu HS, Ellanki SLR, Tutaj MA, De Pons JL, Kwitek AE, Dwinell MR, Shimoyama ME. The Year of the Rat: The Rat Genome Database at 20: a multi-species knowledgebase and analysis platform. Nucleic Acids Res 2020;48:D731-42. [PMID: 31713623 DOI: 10.1093/nar/gkz1041] [Cited by in Crossref: 32] [Cited by in F6Publishing: 42] [Article Influence: 16.0] [Reference Citation Analysis]
363 Bogue MA, Philip VM, Walton DO, Grubb SC, Dunn MH, Kolishovski G, Emerson J, Mukherjee G, Stearns T, He H, Sinha V, Kadakkuzha B, Kunde-Ramamoorthy G, Chesler EJ. Mouse Phenome Database: a data repository and analysis suite for curated primary mouse phenotype data. Nucleic Acids Res 2020;48:D716-23. [PMID: 31696236 DOI: 10.1093/nar/gkz1032] [Cited by in Crossref: 20] [Cited by in F6Publishing: 27] [Article Influence: 10.0] [Reference Citation Analysis]
364 Shefchek KA, Harris NL, Gargano M, Matentzoglu N, Unni D, Brush M, Keith D, Conlin T, Vasilevsky N, Zhang XA, Balhoff JP, Babb L, Bello SM, Blau H, Bradford Y, Carbon S, Carmody L, Chan LE, Cipriani V, Cuzick A, Della Rocca M, Dunn N, Essaid S, Fey P, Grove C, Gourdine JP, Hamosh A, Harris M, Helbig I, Hoatlin M, Joachimiak M, Jupp S, Lett KB, Lewis SE, McNamara C, Pendlington ZM, Pilgrim C, Putman T, Ravanmehr V, Reese J, Riggs E, Robb S, Roncaglia P, Seager J, Segerdell E, Similuk M, Storm AL, Thaxon C, Thessen A, Jacobsen JOB, McMurry JA, Groza T, Köhler S, Smedley D, Robinson PN, Mungall CJ, Haendel MA, Munoz-Torres MC, Osumi-Sutherland D. The Monarch Initiative in 2019: an integrative data and analytic platform connecting phenotypes to genotypes across species. Nucleic Acids Res 2020;48:D704-15. [PMID: 31701156 DOI: 10.1093/nar/gkz997] [Cited by in Crossref: 105] [Cited by in F6Publishing: 109] [Article Influence: 52.5] [Reference Citation Analysis]
365 Hao R, Guo Y, Guo J, Rong Y, Yao S, Chen Y, Dong S, Zhu D, Chen H, Yang T. 3D chromatin organization changes modulate adipogenesis and osteogenesis.. [DOI: 10.1101/2020.05.25.114272] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
366 Gorelick AN, Sánchez-Rivera FJ, Cai Y, Bielski CM, Biederstedt E, Jonsson P, Richards AL, Vasan N, Penson AV, Friedman ND, Ho YJ, Baslan T, Bandlamudi C, Scaltriti M, Schultz N, Lowe SW, Reznik E, Taylor BS. Phase and context shape the function of composite oncogenic mutations. Nature 2020;582:100-3. [PMID: 32461694 DOI: 10.1038/s41586-020-2315-8] [Cited by in Crossref: 20] [Cited by in F6Publishing: 22] [Article Influence: 10.0] [Reference Citation Analysis]
367 Luo Y, Hitz BC, Gabdank I, Hilton JA, Kagda MS, Lam B, Myers Z, Sud P, Jou J, Lin K, Baymuradov UK, Graham K, Litton C, Miyasato SR, Strattan JS, Jolanki O, Lee JW, Tanaka FY, Adenekan P, O'Neill E, Cherry JM. New developments on the Encyclopedia of DNA Elements (ENCODE) data portal. Nucleic Acids Res 2020;48:D882-9. [PMID: 31713622 DOI: 10.1093/nar/gkz1062] [Cited by in Crossref: 38] [Cited by in F6Publishing: 51] [Article Influence: 19.0] [Reference Citation Analysis]
368 Cheong A, Archambault D, Degani R, Iverson E, Tremblay KD, Mager J. Nuclear-encoded mitochondrial ribosomal proteins are required to initiate gastrulation. Development 2020;147:dev188714. [PMID: 32376682 DOI: 10.1242/dev.188714] [Cited by in Crossref: 11] [Cited by in F6Publishing: 12] [Article Influence: 5.5] [Reference Citation Analysis]
369 Piñero J, Ramírez-Anguita JM, Saüch-Pitarch J, Ronzano F, Centeno E, Sanz F, Furlong LI. The DisGeNET knowledge platform for disease genomics: 2019 update. Nucleic Acids Res 2020;48:D845-55. [PMID: 31680165 DOI: 10.1093/nar/gkz1021] [Cited by in Crossref: 328] [Cited by in F6Publishing: 508] [Article Influence: 164.0] [Reference Citation Analysis]
370 Crouse WL, Kelada SN, Valdar W. Inferring the Allelic Series at QTL in Multiparental Populations.. [DOI: 10.1101/2020.05.23.112326] [Reference Citation Analysis]
371 Friedel CC, Whisnant AW, Djakovic L, Rutkowski AJ, Friedl M, Kluge M, Williamson JC, Sai S, Vidal RO, Sauer S, Hennig T, Prusty B, Lehner PJ, Matheson NJ, Erhard F, Dölken L. Dissecting HSV-1-induced host shut-off at RNA level.. [DOI: 10.1101/2020.05.20.106039] [Reference Citation Analysis]
372 Zhu Z, Guan Z, Liu G, Wang Y, Zhang Z. SGID: a comprehensive and interactive database of the silkworm. Database (Oxford) 2019;2019:baz134. [PMID: 31836898 DOI: 10.1093/database/baz134] [Cited by in Crossref: 9] [Cited by in F6Publishing: 11] [Article Influence: 4.5] [Reference Citation Analysis]
373 Lee S, Gleeson JG. Closing in on Mechanisms of Open Neural Tube Defects. Trends Neurosci 2020;43:519-32. [PMID: 32423763 DOI: 10.1016/j.tins.2020.04.009] [Cited by in Crossref: 17] [Cited by in F6Publishing: 17] [Article Influence: 8.5] [Reference Citation Analysis]
374 Mills MC, Tropf FC, Brazel DM, van Zuydam N, Vaez A, Pers TH, Snieder H, Perry JR, Ong KK, den Hoed M, Barban N, Day FR, eQTLGen Consortium, BIOS Consortium. Identification of 370 genetic loci for age at first sex and birth linked to externalising behaviour.. [DOI: 10.1101/2020.05.06.081273] [Cited by in Crossref: 7] [Cited by in F6Publishing: 6] [Article Influence: 3.5] [Reference Citation Analysis]
375 Wall E, Scoles J, Joo A, Klein O, Quinonez C, Bush JO, Martin GR, Laird DJ. The UCSF Mouse Inventory Database Application, an Open Source Web App for Sharing Mutant Mice Within a Research Community. G3 (Bethesda) 2020;10:1503-10. [PMID: 32152007 DOI: 10.1534/g3.120.401086] [Reference Citation Analysis]
376 Gottmann P, Ouni M, Zellner L, Jähnert M, Rittig K, Walther D, Schürmann A. Polymorphisms in miRNA binding sites involved in metabolic diseases in mice and humans. Sci Rep 2020;10:7202. [PMID: 32350386 DOI: 10.1038/s41598-020-64326-4] [Cited by in Crossref: 5] [Cited by in F6Publishing: 5] [Article Influence: 2.5] [Reference Citation Analysis]
377 Murcia Pienkowski V, Kucharczyk M, Rydzanicz M, Poszewiecka B, Pachota K, Młynek M, Stawiński P, Pollak A, Kosińska J, Wojciechowska K, Lejman M, Cieślikowska A, Wicher D, Stembalska A, Matuszewska K, Materna-Kiryluk A, Gambin A, Chrzanowska K, Krajewska-Walasek M, Płoski R. Breakpoint Mapping of Symptomatic Balanced Translocations Links the EPHA6, KLF13 and UBR3 Genes to Novel Disease Phenotype. J Clin Med 2020;9:E1245. [PMID: 32344861 DOI: 10.3390/jcm9051245] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 1.5] [Reference Citation Analysis]
378 Masuda N, Murakami K, Kita Y, Hamada A, Kamada M, Teramoto Y, Sakatani T, Matsumoto K, Sano T, Saito R, Okuno Y, Ogawa O, Kobayashi T. Trp53 Mutation in Keratin 5 (Krt5)-Expressing Basal Cells Facilitates the Development of Basal Squamous-Like Invasive Bladder Cancer in the Chemical Carcinogenesis of Mouse Bladder. Am J Pathol 2020;190:1752-62. [PMID: 32339497 DOI: 10.1016/j.ajpath.2020.04.005] [Cited by in Crossref: 4] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
379 Alliance of Genome Resources Consortium. The Alliance of Genome Resources: Building a Modern Data Ecosystem for Model Organism Databases. Genetics 2019;213:1189-96. [PMID: 31796553 DOI: 10.1534/genetics.119.302523] [Cited by in Crossref: 29] [Cited by in F6Publishing: 30] [Article Influence: 14.5] [Reference Citation Analysis]
380 Avilla MN, Malecki KMC, Hahn ME, Wilson RH, Bradfield CA. The Ah Receptor: Adaptive Metabolism, Ligand Diversity, and the Xenokine Model. Chem Res Toxicol 2020;33:860-79. [PMID: 32259433 DOI: 10.1021/acs.chemrestox.9b00476] [Cited by in Crossref: 42] [Cited by in F6Publishing: 45] [Article Influence: 21.0] [Reference Citation Analysis]
381 Huang SS, Makhlouf M, Aboumoussa EH, Ruiz Tejada Segura ML, Mathew LS, Wang K, Leung MC, Chaussabel D, Logan DW, Scialdone A, Garand M, Saraiva LR. Differential regulation of the immune system in a brain-liver-fats organ network during short term fasting.. [DOI: 10.1101/2020.04.05.026351] [Reference Citation Analysis]
382 Kiu R, Treveil A, Harnisch LC, Caim S, Leclaire C, van Sinderen D, Korcsmaros T, Hall LJ. Bifidobacterium breve UCC2003 induces a distinct global transcriptomic programme in neonatal murine intestinal epithelial cells.. [DOI: 10.1101/2020.03.27.011692] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
383 Breitfeld J, Kehr S, Müller L, Stadler PF, Böttcher Y, Blüher M, Stumvoll M, Kovacs P. Developmentally Driven Changes in Adipogenesis in Different Fat Depots Are Related to Obesity. Front Endocrinol (Lausanne) 2020;11:138. [PMID: 32273869 DOI: 10.3389/fendo.2020.00138] [Cited by in Crossref: 7] [Cited by in F6Publishing: 7] [Article Influence: 3.5] [Reference Citation Analysis]
384 Zhu X, Duren Z, Wong WH. Modeling Regulatory Network Topology Improves Genome-Wide Analyses of Complex Human Traits.. [DOI: 10.1101/2020.03.13.990010] [Cited by in Crossref: 1] [Article Influence: 0.5] [Reference Citation Analysis]
385 Omelchenko A, Menon H, Donofrio SG, Kumar G, Chapman HM, Roshal J, Martinez-Montes ER, Wang TL, Spaller MR, Firestein BL. Interaction Between CRIPT and PSD-95 Is Required for Proper Dendritic Arborization in Hippocampal Neurons. Mol Neurobiol 2020;57:2479-93. [PMID: 32157575 DOI: 10.1007/s12035-020-01895-5] [Cited by in Crossref: 4] [Cited by in F6Publishing: 3] [Article Influence: 2.0] [Reference Citation Analysis]
386 Shemesh N, Jubran J, Abu-qarn M, Simonovky E, Basha O, Hekselman I, Dror S, Vinogradov E, Carra S, Ben-zvi A, Yeger-lotem E. The landscape of molecular chaperones across human tissues reveals a layered architecture of core and variable chaperones.. [DOI: 10.1101/2020.03.04.976720] [Reference Citation Analysis]
387 Hannigan MM, Hoffman AM, Thompson JW, Zheng T, Nicchitta CV. Quantitative proteomics links the LRRC59 interactome to mRNA translation on the ER membrane.. [DOI: 10.1101/2020.03.04.975474] [Reference Citation Analysis]
388 Manshaei R, Merico D, Reuter MS, Engchuan W, Mojarad BA, Chaturvedi R, Heung T, Pellecchia G, Zarrei M, Nalpathamkalam T, Khan R, Okello JBA, Liston E, Curtis M, Yuen RK, Marshall CR, Jobling RK, Scherer SW, Kim RH, Bassett AS. Genes and pathways implicated in tetralogy of Fallot revealed by ultra-rare variant burden analysis in 231 genome sequences.. [DOI: 10.1101/2020.03.02.972653] [Reference Citation Analysis]
389 Wolf MM, Kimryn Rathmell W, Beckermann KE. Modeling clear cell renal cell carcinoma and therapeutic implications. Oncogene 2020;39:3413-26. [PMID: 32123314 DOI: 10.1038/s41388-020-1234-3] [Cited by in Crossref: 40] [Cited by in F6Publishing: 45] [Article Influence: 20.0] [Reference Citation Analysis]
390 Ambeskovic M, Ilnytskyy Y, Kiss D, Currie C, Montina T, Kovalchuk I, Metz GAS. Ancestral stress programs sex-specific biological aging trajectories and non-communicable disease risk. Aging (Albany NY) 2020;12:3828-47. [PMID: 32087063 DOI: 10.18632/aging.102848] [Cited by in Crossref: 9] [Cited by in F6Publishing: 9] [Article Influence: 4.5] [Reference Citation Analysis]
391 Singh MD, Jensen M, Lasser M, Huber E, Yusuff T, Pizzo L, Lifschutz B, Desai I, Kubina A, Yennawar S, Kim S, Iyer J, Rincon-Limas DE, Lowery LA, Girirajan S. NCBP2 modulates neurodevelopmental defects of the 3q29 deletion in Drosophila and Xenopus laevis models. PLoS Genet 2020;16:e1008590. [PMID: 32053595 DOI: 10.1371/journal.pgen.1008590] [Cited by in Crossref: 19] [Cited by in F6Publishing: 19] [Article Influence: 9.5] [Reference Citation Analysis]
392 van der Weyden L, Swiatkowska A, Iyer V, Speak AO, Adams DJ. A genome-wide screen in mice to identify cell-extrinsic regulators of pulmonary metastatic colonisation.. [DOI: 10.1101/2020.02.10.941401] [Reference Citation Analysis]
393 Harris RM, Kao H, Alarcón JM, Fenton AA, Hofmann HA. Transcriptome analysis of hippocampal subfields identifies gene expression profiles associated with long-term active place avoidance memory.. [DOI: 10.1101/2020.02.05.935759] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
394 Luo L, Ambrozkiewicz MC, Benseler F, Chen C, Dumontier E, Falkner S, Furlanis E, Gomez AM, Hoshina N, Huang WH, Hutchison MA, Itoh-Maruoka Y, Lavery LA, Li W, Maruo T, Motohashi J, Pai EL, Pelkey KA, Pereira A, Philips T, Sinclair JL, Stogsdill JA, Traunmüller L, Wang J, Wortel J, You W, Abumaria N, Beier KT, Brose N, Burgess HA, Cepko CL, Cloutier JF, Eroglu C, Goebbels S, Kaeser PS, Kay JN, Lu W, Luo L, Mandai K, McBain CJ, Nave KA, Prado MAM, Prado VF, Rothstein J, Rubenstein JLR, Saher G, Sakimura K, Sanes JR, Scheiffele P, Takai Y, Umemori H, Verhage M, Yuzaki M, Zoghbi HY, Kawabe H, Craig AM. Optimizing Nervous System-Specific Gene Targeting with Cre Driver Lines: Prevalence of Germline Recombination and Influencing Factors. Neuron 2020;106:37-65.e5. [PMID: 32027825 DOI: 10.1016/j.neuron.2020.01.008] [Cited by in Crossref: 63] [Cited by in F6Publishing: 70] [Article Influence: 31.5] [Reference Citation Analysis]
395 Wang S, Zheng Y, Li J, Yu Y, Zhang W, Song M, Liu Z, Min Z, Hu H, Jing Y, He X, Sun L, Ma L, Esteban CR, Chan P, Qiao J, Zhou Q, Izpisua Belmonte JC, Qu J, Tang F, Liu GH. Single-Cell Transcriptomic Atlas of Primate Ovarian Aging. Cell 2020;180:585-600.e19. [PMID: 32004457 DOI: 10.1016/j.cell.2020.01.009] [Cited by in Crossref: 140] [Cited by in F6Publishing: 161] [Article Influence: 70.0] [Reference Citation Analysis]
396 Konopka T, Smedley D. Incremental data integration for tracking genotype-disease associations. PLoS Comput Biol 2020;16:e1007586. [PMID: 31986132 DOI: 10.1371/journal.pcbi.1007586] [Cited by in Crossref: 6] [Cited by in F6Publishing: 7] [Article Influence: 3.0] [Reference Citation Analysis]
397 Kasak L, Laan M. Monogenic causes of non-obstructive azoospermia: challenges, established knowledge, limitations and perspectives. Hum Genet 2021;140:135-54. [DOI: 10.1007/s00439-020-02112-y] [Cited by in Crossref: 35] [Cited by in F6Publishing: 37] [Article Influence: 17.5] [Reference Citation Analysis]
398 Cooley LS, Rudewicz J, Souleyreau W, Clarke K, Falciani F, Dufies M, Verbeke S, Emanuelli A, Benzekry S, Taing C, Ribot EJ, Miraux S, Lambrechts D, Modave E, Pineau R, Derieppe M, Ambrosetti D, Bernhard J, Ravaud A, Négrier S, Ferrero J, Pagès G, Nikolski M, Bikfalvi A. A multi-layered systems approach for renal cell carcinoma.. [DOI: 10.1101/2020.01.13.904235] [Reference Citation Analysis]
399 Spoor S, Cheng CH, Sanderson LA, Condon B, Almsaeed A, Chen M, Bretaudeau A, Rasche H, Jung S, Main D, Bett K, Staton M, Wegrzyn JL, Feltus FA, Ficklin SP. Tripal v3: an ontology-based toolkit for construction of FAIR biological community databases. Database (Oxford) 2019;2019:baz077. [PMID: 31328773 DOI: 10.1093/database/baz077] [Cited by in Crossref: 16] [Cited by in F6Publishing: 18] [Article Influence: 8.0] [Reference Citation Analysis]
400 Winkler TW, Grassmann F, Brandl C, Kiel C, Günther F, Strunz T, Weidner L, Zimmermann ME, Korb CA, Poplawski A, Schuster AK, Müller-nurasyid M, Peters A, Rauscher FG, Elze T, Horn K, Scholz M, Cañadas-garre M, Mcknight AJ, Quinn N, Hogg RE, Küchenhoff H, Heid IM, Stark KJ, Weber BH. Genome-wide association meta-analysis for early age-related macular degeneration highlights novel loci and insights for advanced disease.. [DOI: 10.1101/2019.12.20.883801] [Reference Citation Analysis]
401 Dvořáková E, Kumar S, Kléma J, Železný F, Drbal K, Song M. Evaluating Model-free Directional Dependency Methods on Single-cell RNA Sequencing Data with Severe Dropout. Proceedings of the 2019 6th International Conference on Bioinformatics Research and Applications 2019. [DOI: 10.1145/3383783.3383793] [Reference Citation Analysis]
402 Gilly A, Park Y, Png G, Barysenka A, Fischer I, Bjornland T, Southam L, Suveges D, Neumeyer S, Rayner NW, Tsafantakis E, Karaleftheri M, Dedoussis G, Zeggini E. Whole genome sequencing analysis of the cardiometabolic proteome.. [DOI: 10.1101/854752] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 1.0] [Reference Citation Analysis]
403 Kolishovski G, Lamoureux A, Hale P, Richardson JE, Recla JM, Adesanya O, Simons A, Kunde-Ramamoorthy G, Bult CJ. The JAX Synteny Browser for mouse-human comparative genomics. Mamm Genome 2019;30:353-61. [PMID: 31776723 DOI: 10.1007/s00335-019-09821-4] [Cited by in Crossref: 9] [Cited by in F6Publishing: 6] [Article Influence: 3.0] [Reference Citation Analysis]
404 Yusuff T, Jensen M, Yennawar S, Pizzo L, Karthikeyan S, Gould DJ, Sarker A, Gedvilaite E, Matsui Y, Iyer J, Lai Z, Girirajan S. Drosophila models of pathogenic copy-number variant genes show global and non-neuronal defects during development.. [DOI: 10.1101/855338] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 0.7] [Reference Citation Analysis]
405 Birling M, Yoshiki A, Adams DJ, Ayabe S, Beaudet AL, Bottomley J, Bradley A, Brown SD, Bürger A, Bushell W, Chiani F, Chin HG, Christou S, Codner GF, Demayo FJ, Dickinson ME, Doe B, Donahue LR, Fray MD, Gambadoro A, Gao X, Gertsenstein M, Gomez-segura A, Goodwin LO, Heaney JD, Hérault Y, de Angelis MH, Jiang S, Justice MJ, Kasparek P, King RE, Kühn R, Lee H, Lee YJ, Liu Z, Kent Lloyd KC, Lorenzo I, Mallon A, Mckerlie C, Meehan TF, Newman S, Nutter LM, Oh GT, Pavlovic G, Ramirez-solis R, Rosen B, Ryder EJ, Santos LA, Schick J, Seavitt JR, Sedlacek R, Seisenberger C, Seong JK, Skarnes WC, Sorg T, Steel KP, Tamura M, Tocchini-valentini GP, Leo Wang C, Wardle-jones H, Wattenhofer-donzé M, Wells S, Willis BJ, Wood JA, Wurst W, Xu Y, Teboul L, Murray SA, IMPC Consortium. A resource of targeted mutant mouse lines for 5,061 genes.. [DOI: 10.1101/844092] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 1.0] [Reference Citation Analysis]
406 Yang Q, Chen H, Ye J, Liu C, Wei R, Chen C, Huang L. Genetic Diversity and Signatures of Selection in 15 Chinese Indigenous Dog Breeds Revealed by Genome-Wide SNPs. Front Genet 2019;10:1174. [PMID: 31803243 DOI: 10.3389/fgene.2019.01174] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 1.3] [Reference Citation Analysis]
407 Shohat S, Shifman S. Genes essential for embryonic stem cells are associated with neurodevelopmental disorders. Genome Res 2019;29:1910-8. [PMID: 31649057 DOI: 10.1101/gr.250019.119] [Cited by in Crossref: 8] [Cited by in F6Publishing: 9] [Article Influence: 2.7] [Reference Citation Analysis]
408 Netherton J, Ogle R, Hetherington L, Velkov T, Rose R, Baker M. DNA variants are an unlikely explanation for the changing quality of spermatozoa within the same individual. Hum Fertil (Camb) 2019;:1-13. [PMID: 31642381 DOI: 10.1080/14647273.2019.1679397] [Reference Citation Analysis]
409 Baloghova N, Lidak T, Cermak L. Ubiquitin Ligases Involved in the Regulation of Wnt, TGF-β, and Notch Signaling Pathways and Their Roles in Mouse Development and Homeostasis. Genes (Basel) 2019;10:E815. [PMID: 31623112 DOI: 10.3390/genes10100815] [Cited by in Crossref: 12] [Cited by in F6Publishing: 13] [Article Influence: 4.0] [Reference Citation Analysis]
410 Zhang P, Itan Y. Biological Network Approaches and Applications in Rare Disease Studies. Genes (Basel) 2019;10:E797. [PMID: 31614842 DOI: 10.3390/genes10100797] [Cited by in Crossref: 14] [Cited by in F6Publishing: 16] [Article Influence: 4.7] [Reference Citation Analysis]
411 Russkikh N, Antonets D, Shtokalo D, Makarov A, Vyatkin Y, Zakharov A, Terentyev E. Style transfer with variational autoencoders is a promising approach to RNA-Seq data harmonization and analysis.. [DOI: 10.1101/791962] [Reference Citation Analysis]
412 Chen JJ, Nathaniel DL, Raghavan P, Nelson M, Tian R, Tse E, Hong JY, See SK, Mok SA, Hein MY, Southworth DR, Grinberg LT, Gestwicki JE, Leonetti MD, Kampmann M. Compromised function of the ESCRT pathway promotes endolysosomal escape of tau seeds and propagation of tau aggregation. J Biol Chem 2019;294:18952-66. [PMID: 31578281 DOI: 10.1074/jbc.RA119.009432] [Cited by in Crossref: 66] [Cited by in F6Publishing: 70] [Article Influence: 22.0] [Reference Citation Analysis]
413 Angelopoulos N, Wielemaker J. Advances in Big Data Bio Analytics. Electron Proc Theor Comput Sci 2019;306:309-322. [DOI: 10.4204/eptcs.306.36] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.3] [Reference Citation Analysis]
414 Bamshad MJ, Nickerson DA, Chong JX. Mendelian Gene Discovery: Fast and Furious with No End in Sight. Am J Hum Genet 2019;105:448-55. [PMID: 31491408 DOI: 10.1016/j.ajhg.2019.07.011] [Cited by in Crossref: 95] [Cited by in F6Publishing: 67] [Article Influence: 31.7] [Reference Citation Analysis]
415 Ietswaart R, Gyori BM, Bachman JA, Sorger PK, Churchman LS. GeneWalk identifies relevant gene functions for a biological context using network representation learning.. [DOI: 10.1101/755579] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 1.3] [Reference Citation Analysis]
416 Zhu Z, Guan Z, Liu G, Wang Y, Zhang Z. SGID: a comprehensive and interactive database of the silkworm.. [DOI: 10.1101/739961] [Reference Citation Analysis]
417 Gustafson JA, Park SS, Cunningham ML. Calvarial osteoblast gene expression in patients with craniosynostosis leads to novel polygenic mouse model. PLoS One 2019;14:e0221402. [PMID: 31442251 DOI: 10.1371/journal.pone.0221402] [Cited by in Crossref: 6] [Cited by in F6Publishing: 6] [Article Influence: 2.0] [Reference Citation Analysis]
418 Guimaraes-Young A, Feddersen CR, Dupuy AJ. Sleeping Beauty Mouse Models of Cancer: Microenvironmental Influences on Cancer Genetics. Front Oncol 2019;9:611. [PMID: 31338332 DOI: 10.3389/fonc.2019.00611] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 0.7] [Reference Citation Analysis]
419 Robbins SM, Thimm MA, Valle D, Jelin AC. Genetic diagnosis in first or second trimester pregnancy loss using exome sequencing: a systematic review of human essential genes. J Assist Reprod Genet 2019;36:1539-48. [PMID: 31273585 DOI: 10.1007/s10815-019-01499-6] [Cited by in Crossref: 18] [Cited by in F6Publishing: 18] [Article Influence: 6.0] [Reference Citation Analysis]
420 Tonino P, Kiss B, Gohlke J, Smith JE 3rd, Granzier H. Fine mapping titin's C-zone: Matching cardiac myosin-binding protein C stripes with titin's super-repeats. J Mol Cell Cardiol 2019;133:47-56. [PMID: 31158359 DOI: 10.1016/j.yjmcc.2019.05.026] [Cited by in Crossref: 21] [Cited by in F6Publishing: 22] [Article Influence: 7.0] [Reference Citation Analysis]
421 Yüksel Z, Yazol M, Gümüş E. Pathogenic homozygous variations in ACTL6B cause DECAM syndrome: Developmental delay, Epileptic encephalopathy, Cerebral Atrophy, and abnormal Myelination. Am J Med Genet A 2019;179:1603-8. [PMID: 31134736 DOI: 10.1002/ajmg.a.61210] [Cited by in Crossref: 2] [Cited by in F6Publishing: 5] [Article Influence: 0.7] [Reference Citation Analysis]
422 Chen JJ, Nathaniel DL, Raghavan P, Nelson M, Tian R, Tse E, Hong JY, See SK, Mok S, Hein MY, Southworth DR, Grinberg LT, Gestwicki JE, Leonetti MD, Kampmann M. Compromised function of the ESCRT pathway promotes endolysosomal escape of tau seeds and propagation of tau aggregation.. [DOI: 10.1101/637785] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 0.7] [Reference Citation Analysis]
423 Singh MD, Jensen M, Lasser M, Huber E, Yusuff T, Pizzo L, Lifschutz B, Desai I, Kubina A, Yennawar S, Kim S, Iyer J, Rincon-limas DE, Lowery LA, Girirajan S. NCBP2modulates neurodevelopmental defects of the 3q29 deletion inDrosophilaandX. laevismodels.. [DOI: 10.1101/614750] [Cited by in Crossref: 1] [Article Influence: 0.3] [Reference Citation Analysis]
424 Gagnier L, Belancio VP, Mager DL. Mouse germ line mutations due to retrotransposon insertions. Mob DNA 2019;10:15. [PMID: 31011371 DOI: 10.1186/s13100-019-0157-4] [Cited by in Crossref: 59] [Cited by in F6Publishing: 58] [Article Influence: 19.7] [Reference Citation Analysis]
425 Shohat S, Shifman S. Genes essential for embryonic stem cells are associated with neurodevelopmental disorders.. [DOI: 10.1101/567073] [Reference Citation Analysis]
426 Smith JR, Bolton ER, Dwinell MR. The Rat: A Model Used in Biomedical Research. Methods Mol Biol 2019;2018:1-41. [PMID: 31228150 DOI: 10.1007/978-1-4939-9581-3_1] [Cited by in Crossref: 10] [Cited by in F6Publishing: 11] [Article Influence: 3.3] [Reference Citation Analysis]
427 [DOI: 10.1101/2020.09.16.300632] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
428 [DOI: 10.1101/756825] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Reference Citation Analysis]
429 [DOI: 10.1101/534834] [Cited by in Crossref: 13] [Cited by in F6Publishing: 11] [Reference Citation Analysis]