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For: Sirugo G, Williams SM, Tishkoff SA. The Missing Diversity in Human Genetic Studies. Cell 2019;177:1080. [PMID: 31051100 DOI: 10.1016/j.cell.2019.04.032] [Cited by in Crossref: 51] [Cited by in F6Publishing: 63] [Article Influence: 17.0] [Reference Citation Analysis]
Number Citing Articles
1 Ma Y, Patil S, Zhou X, Mukherjee B, Fritsche LG. ExPRSweb: An online repository with polygenic risk scores for common health-related exposures. Am J Hum Genet 2022:S0002-9297(22)00404-9. [PMID: 36152628 DOI: 10.1016/j.ajhg.2022.09.001] [Reference Citation Analysis]
2 Jacobs BM, Peter M, Giovannoni G, Noyce AJ, Morris HR, Dobson R. Towards a global view of multiple sclerosis genetics. Nat Rev Neurol 2022. [PMID: 36075979 DOI: 10.1038/s41582-022-00704-y] [Reference Citation Analysis]
3 Atkinson EG, Dalvie S, Pichkar Y, Kalungi A, Majara L, Stevenson A, Abebe T, Akena D, Alemayehu M, Ashaba FK, Atwoli L, Baker M, Chibnik LB, Creanza N, Daly MJ, Fekadu A, Gelaye B, Gichuru S, Injera WE, James R, Kariuki SM, Kigen G, Koen N, Koenen KC, Koenig Z, Kwobah E, Kyebuzibwa J, Musinguzi H, Mwema RM, Neale BM, Newman CP, Newton CRJC, Ongeri L, Ramachandran S, Ramesar R, Shiferaw W, Stein DJ, Stroud RE, Teferra S, Yohannes MT, Zingela Z, Martin AR; NeuroGAP-Psychosis Study Team. Genetic structure correlates with ethnolinguistic diversity in eastern and southern Africa. Am J Hum Genet 2022;109:1667-79. [PMID: 36055213 DOI: 10.1016/j.ajhg.2022.07.013] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
4 Agyemang K, Johansen AM, Barker GW, Pennison MJ, Sheffield K, Jimenez H, Blackman C, Sharma S, Fordjour PA, Singh R, Cook KL, Lin HK, Zhang W, Lo HW, Watabe K, Sun P, Langefeld CD, Pasche B. TGFBR1*6A as a modifier of breast cancer risk and progression: advances and future prospects. NPJ Breast Cancer 2022;8:84. [PMID: 35853889 DOI: 10.1038/s41523-022-00446-6] [Reference Citation Analysis]
5 Caliebe A, Tekola-Ayele F, Darst BF, Wang X, Song YE, Gui J, Sebro RA, Balding DJ, Saad M, Dubé MP; IGES ELSI Committee. Including diverse and admixed populations in genetic epidemiology research. Genet Epidemiol 2022. [PMID: 35842778 DOI: 10.1002/gepi.22492] [Reference Citation Analysis]
6 Funayama M, Nishioka K, Li Y, Hattori N. Molecular genetics of Parkinson's disease: Contributions and global trends. J Hum Genet 2022. [PMID: 35821405 DOI: 10.1038/s10038-022-01058-5] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
7 Kerner G, Quintana-Murci L. The genetic and evolutionary determinants of COVID-19 susceptibility. Eur J Hum Genet 2022. [PMID: 35760904 DOI: 10.1038/s41431-022-01141-7] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
8 Bastard P, Hsiao KC, Zhang Q, Choin J, Best E, Chen J, Gervais A, Bizien L, Materna M, Harmant C, Roux M, Hawley NL, Weeks DE, McGarvey ST, Sandoval K, Barberena-Jonas C, Quinto-Cortés CD, Hagelberg E, Mentzer AJ, Robson K, Coulibaly B, Seeleuthner Y, Bigio B, Li Z, Uzé G, Pellegrini S, Lorenzo L, Sbihi Z, Latour S, Besnard M, Adam de Beaumais T, Jacqz Aigrain E, Béziat V, Deka R, Esera Tulifau L, Viali S, Reupena MS, Naseri T, McNaughton P, Sarkozy V, Peake J, Blincoe A, Primhak S, Stables S, Gibson K, Woon ST, Drake KM, Hill AVS, Chan CY, King R, Ameratunga R, Teiti I, Aubry M, Cao-Lormeau VM, Tangye SG, Zhang SY, Jouanguy E, Gray P, Abel L, Moreno-Estrada A, Minster RL, Quintana-Murci L, Wood AC, Casanova JL. A loss-of-function IFNAR1 allele in Polynesia underlies severe viral diseases in homozygotes. J Exp Med 2022;219:e20220028. [PMID: 35442418 DOI: 10.1084/jem.20220028] [Cited by in Crossref: 5] [Cited by in F6Publishing: 4] [Article Influence: 5.0] [Reference Citation Analysis]
9 Cong PK, Bai WY, Li JC, Yang MY, Khederzadeh S, Gai SR, Li N, Liu YH, Yu SH, Zhao WW, Liu JQ, Sun Y, Zhu XW, Zhao PP, Xia JW, Guan PL, Qian Y, Tao JG, Xu L, Tian G, Wang PY, Xie SY, Qiu MC, Liu KQ, Tang BS, Zheng HF. Genomic analyses of 10,376 individuals in the Westlake BioBank for Chinese (WBBC) pilot project. Nat Commun 2022;13:2939. [PMID: 35618720 DOI: 10.1038/s41467-022-30526-x] [Cited by in Crossref: 5] [Article Influence: 5.0] [Reference Citation Analysis]
10 Quiat D, Kim SW, Zhang Q, Morton SU, Pereira AC, DePalma SR, Willcox JAL, McDonough B, DeLaughter DM, Gorham JM, Curran JJ, Tumblin M, Nicolau Y, Artunduaga MA, Quintanilla-Dieck L, Osorno G, Serrano L, Hamdan U, Eavey RD, Seidman CE, Seidman JG. An ancient founder mutation located between ROBO1 and ROBO2 is responsible for increased microtia risk in Amerindigenous populations. Proc Natl Acad Sci U S A 2022;119:e2203928119. [PMID: 35584116 DOI: 10.1073/pnas.2203928119] [Reference Citation Analysis]
11 Qin Z, Huang T, Guo M, Wang SM. Distinct landscapes of deleterious variants in DNA damage repair system in ethnic human populations. Life Sci Alliance 2022;5:e202101319. [PMID: 35595529 DOI: 10.26508/lsa.202101319] [Reference Citation Analysis]
12 Brown JEH, Zamora AN, Outram S, Sparks TN, Lianoglou BR, Norstad M, Sahin Hodoglugil NN, Norton ME, Ackerman SL. “Let’s Just Wait Until She’s Born”: Temporal Factors That Shape Decision-Making for Prenatal Genomic Sequencing Amongst Families Underrepresented in Genomic Research. Front Genet 2022;13:882703. [DOI: 10.3389/fgene.2022.882703] [Reference Citation Analysis]
13 Wojcik GL, Murphy J, Edelson JL, Gignoux CR, Ioannidis AG, Manning A, Rivas MA, Buyske S, Hendricks AE. Opportunities and challenges for the use of common controls in sequencing studies. Nat Rev Genet 2022. [PMID: 35581355 DOI: 10.1038/s41576-022-00487-4] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 2.0] [Reference Citation Analysis]
14 Choudhury A, Brandenburg JT, Chikowore T, Sengupta D, Boua PR, Crowther NJ, Agongo G, Asiki G, Gómez-Olivé FX, Kisiangani I, Maimela E, Masemola-Maphutha M, Micklesfield LK, Nonterah EA, Norris SA, Sorgho H, Tinto H, Tollman S, Graham SE, Willer CJ, Hazelhurst S, Ramsay M; AWI-Gen study., H3Africa Consortium. Meta-analysis of sub-Saharan African studies provides insights into genetic architecture of lipid traits. Nat Commun 2022;13:2578. [PMID: 35546142 DOI: 10.1038/s41467-022-30098-w] [Cited by in Crossref: 2] [Article Influence: 2.0] [Reference Citation Analysis]
15 Mars N, Kerminen S, Feng YA, Kanai M, Läll K, Thomas LF, Skogholt AH, Della Briotta Parolo P, Neale BM, Smoller JW, Gabrielsen ME, Hveem K, Mägi R, Matsuda K, Okada Y, Pirinen M, Palotie A, Ganna A, Martin AR, Ripatti S; Biobank Japan Project., FinnGen. Genome-wide risk prediction of common diseases across ancestries in one million people. Cell Genom 2022;2:None. [PMID: 35591975 DOI: 10.1016/j.xgen.2022.100118] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
16 Mendoza-Revilla J, Chacón-Duque JC, Fuentes-Guajardo M, Ormond L, Wang K, Hurtado M, Villegas V, Granja V, Acuña-Alonzo V, Jaramillo C, Arias W, Barquera R, Gómez-Valdés J, Villamil-Ramírez H, Silva de Cerqueira CC, Badillo Rivera KM, Nieves-Colón MA, Gignoux CR, Wojcik GL, Moreno-Estrada A, Hünemeier T, Ramallo V, Schuler-Faccini L, Gonzalez-José R, Bortolini MC, Canizales-Quinteros S, Gallo C, Poletti G, Bedoya G, Rothhammer F, Balding D, Fumagalli M, Adhikari K, Ruiz-Linares A, Hellenthal G. Disentangling Signatures of Selection Before and After European Colonization in Latin Americans. Mol Biol Evol 2022;39:msac076. [PMID: 35460423 DOI: 10.1093/molbev/msac076] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
17 Krainc T, Fuentes A. Genetic ancestry in precision medicine is reshaping the race debate. Proc Natl Acad Sci U S A 2022;119:e2203033119. [PMID: 35294278 DOI: 10.1073/pnas.2203033119] [Reference Citation Analysis]
18 Elmentaite R, Domínguez Conde C, Yang L, Teichmann SA. Single-cell atlases: shared and tissue-specific cell types across human organs. Nat Rev Genet 2022. [PMID: 35217821 DOI: 10.1038/s41576-022-00449-w] [Cited by in Crossref: 5] [Cited by in F6Publishing: 2] [Article Influence: 5.0] [Reference Citation Analysis]
19 Lubin E, Bryant L, Aicher J, Li D, Bhoj E. Analysis of histone variant constraint and tissue expression suggests five potential novel human disease genes: H2AFY2, H2AFZ, H2AFY, H2AFV, H1F0. Hum Genet. [DOI: 10.1007/s00439-022-02432-1] [Reference Citation Analysis]
20 Jiménez-Kaufmann A, Chong AY, Cortés A, Quinto-Cortés CD, Fernandez-Valverde SL, Ferreyra-Reyes L, Cruz-Hervert LP, Medina-Muñoz SG, Sohail M, Palma-Martinez MJ, Delgado-Sánchez G, Mongua-Rodríguez N, Mentzer AJ, Hill AVS, Moreno-Macías H, Huerta-Chagoya A, Aguilar-Salinas CA, Torres M, Kim HL, Kalsi N, Schuster SC, Tusié-Luna T, Del-Vecchyo DO, García-García L, Moreno-Estrada A. Imputation Performance in Latin American Populations: Improving Rare Variants Representation With the Inclusion of Native American Genomes. Front Genet 2021;12:719791. [PMID: 35046991 DOI: 10.3389/fgene.2021.719791] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
21 Null M, Yilmaz F, Astling D, Yu HC, Cole JB, Hallgrímsson B, Santorico SA, Spritz RA, Shaikh TH, Hendricks AE. Genome-wide analysis of copy number variants and normal facial variation in a large cohort of Bantu Africans. HGG Adv 2022;3:100082. [PMID: 35047866 DOI: 10.1016/j.xhgg.2021.100082] [Reference Citation Analysis]
22 Kim W, Patsopoulos NA. Genetics and functional genomics of multiple sclerosis. Semin Immunopathol 2022. [PMID: 35022889 DOI: 10.1007/s00281-021-00907-3] [Cited by in Crossref: 4] [Cited by in F6Publishing: 3] [Article Influence: 4.0] [Reference Citation Analysis]
23 Natri HM, Hudjashov G, Jacobs G, Kusuma P, Saag L, Darusallam CC, Metspalu M, Sudoyo H, Cox MP, Gallego Romero I, Banovich NE. Genetic architecture of gene regulation in Indonesian populations identifies QTLs associated with global and local ancestries. Am J Hum Genet 2022;109:50-65. [PMID: 34919805 DOI: 10.1016/j.ajhg.2021.11.017] [Cited by in Crossref: 3] [Cited by in F6Publishing: 1] [Article Influence: 3.0] [Reference Citation Analysis]
24 Gao Y, Felsky D, Reyes-Dumeyer D, Sariya S, Rentería MA, Ma Y, Klein HU, Cosentino S, De Jager PL, Bennett DA, Brickman AM, Schellenberg GD, Mayeux R, Barral S; CHAP, UKBB, ADNI, ROSMAP, LLFS, NIA-LOAD and ADGC consortia. Integration of GWAS and brain transcriptomic analyses in a multiethnic sample of 35,245 older adults identifies DCDC2 gene as predictor of episodic memory maintenance. Alzheimers Dement 2021. [PMID: 34873813 DOI: 10.1002/alz.12524] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
25 Atkinson EG, Bloemendal A, Maihofer AX, Nievergelt CM, Daly MJ, Neale BM. Reply to: On powerful GWAS in admixed populations. Nat Genet 2021;53:1634-5. [PMID: 34824479 DOI: 10.1038/s41588-021-00975-z] [Reference Citation Analysis]
26 Pal T. Diversity in cancer genomics research is a matter of equity and scientific discovery. Genet Med 2021:S1098-3600(21)05396-X. [PMID: 34906472 DOI: 10.1016/j.gim.2021.11.016] [Reference Citation Analysis]
27 Zhang C, Hansen MEB, Tishkoff SA. Advances in integrative African genomics. Trends Genet 2021:S0168-9525(21)00284-5. [PMID: 34740451 DOI: 10.1016/j.tig.2021.09.013] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 2.0] [Reference Citation Analysis]
28 Wu YY, Thompson MD, Youkhana F, Pirkle CM. Interaction Between Physical Activity and Polygenic Score on Type 2 Diabetes Mellitus in Older Black and White Participants From the Health and Retirement Study. J Gerontol A Biol Sci Med Sci 2021;76:1214-21. [PMID: 33515027 DOI: 10.1093/gerona/glab025] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
29 Akinyemi RO, Yaria J, Ojagbemi A, Guerchet M, Okubadejo N, Njamnshi AK, Sarfo FS, Akpalu A, Ogbole G, Ayantayo T, Adokonou T, Paddick SM, Ndetei D, Bosche J, Ayele B, Damas A, Coker M, Mbakile-Mahlanza L, Ranchod K, Bobrow K, Anazodo U, Damasceno A, Seshadri S, Pericak-Vance M, Lawlor B, Miller BL, Owolabi M, Baiyewu O, Walker R, Gureje O, Kalaria RN, Ogunniyi A; African Dementia Consortium (AfDC). Dementia in Africa: Current evidence, knowledge gaps, and future directions. Alzheimers Dement 2021. [PMID: 34569714 DOI: 10.1002/alz.12432] [Cited by in F6Publishing: 2] [Reference Citation Analysis]
30 Whitlock EL, Gross ER, King CR, Avidan MS. Anaesthetic depth and delirium: a challenging balancing act. Br J Anaesth 2021;127:667-71. [PMID: 34503835 DOI: 10.1016/j.bja.2021.08.003] [Cited by in Crossref: 1] [Cited by in F6Publishing: 7] [Article Influence: 1.0] [Reference Citation Analysis]
31 Lin M, Caberto C, Wan P, Li Y, Lum-Jones A, Tiirikainen M, Pooler L, Nakamura B, Sheng X, Porcel J, Lim U, Setiawan VW, Le Marchand L, Wilkens LR, Haiman CA, Cheng I, Chiang CWK. Population-specific reference panels are crucial for genetic analyses: an example of the CREBRF locus in Native Hawaiians. Hum Mol Genet 2020;29:2275-84. [PMID: 32491157 DOI: 10.1093/hmg/ddaa083] [Cited by in Crossref: 11] [Cited by in F6Publishing: 10] [Article Influence: 11.0] [Reference Citation Analysis]
32 Guan F, Ni T, Zhu W, Williams LK, Cui LB, Li M, Tubbs J, Sham PC, Gui H. Integrative omics of schizophrenia: from genetic determinants to clinical classification and risk prediction. Mol Psychiatry 2021. [PMID: 34193973 DOI: 10.1038/s41380-021-01201-2] [Cited by in Crossref: 7] [Cited by in F6Publishing: 6] [Article Influence: 7.0] [Reference Citation Analysis]
33 Ramos PS. Unravelling the complex genetic regulation of immune cells. Nat Rev Rheumatol 2021;17:131-2. [PMID: 33328616 DOI: 10.1038/s41584-020-00563-1] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
34 Palmer RHC, Johnson EC, Won H, Polimanti R, Kapoor M, Chitre A, Bogue MA, Benca-Bachman CE, Parker CC, Verma A, Reynolds T, Ernst J, Bray M, Kwon SB, Lai D, Quach BC, Gaddis NC, Saba L, Chen H, Hawrylycz M, Zhang S, Zhou Y, Mahaffey S, Fischer C, Sanchez-Roige S, Bandrowski A, Lu Q, Shen L, Philip V, Gelernter J, Bierut LJ, Hancock DB, Edenberg HJ, Johnson EO, Nestler EJ, Barr PB, Prins P, Smith DJ, Akbarian S, Thorgeirsson T, Walton D, Baker E, Jacobson D, Palmer AA, Miles M, Chesler EJ, Emerson J, Agrawal A, Martone M, Williams RW. Integration of evidence across human and model organism studies: A meeting report. Genes Brain Behav 2021;:e12738. [PMID: 33893716 DOI: 10.1111/gbb.12738] [Cited by in F6Publishing: 2] [Reference Citation Analysis]
35 De Lillo A, D'Antona S, Pathak GA, Wendt FR, De Angelis F, Fuciarelli M, Polimanti R. Cross-ancestry genome-wide association studies identified heterogeneous loci associated with differences of allele frequency and regulome tagging between participants of European descent and other ancestry groups from the UK Biobank. Hum Mol Genet 2021;30:1457-67. [PMID: 33890984 DOI: 10.1093/hmg/ddab114] [Reference Citation Analysis]
36 O'Connell KS, Coombes BJ. Genetic contributions to bipolar disorder: current status and future directions. Psychol Med 2021;:1-12. [PMID: 33879273 DOI: 10.1017/S0033291721001252] [Cited by in Crossref: 5] [Cited by in F6Publishing: 6] [Article Influence: 5.0] [Reference Citation Analysis]
37 Dannemann M, Gallego Romero I. Harnessing pluripotent stem cells as models to decipher human evolution. FEBS J 2021. [PMID: 33876573 DOI: 10.1111/febs.15885] [Cited by in Crossref: 3] [Cited by in F6Publishing: 4] [Article Influence: 3.0] [Reference Citation Analysis]
38 Boahen CK, Joosten LAB, Netea MG, Kumar V. Conceptualization of population-specific human functional immune-genomics projects to identify factors that contribute to variability in immune and infectious diseases. Heliyon 2021;7:e06755. [PMID: 33912719 DOI: 10.1016/j.heliyon.2021.e06755] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
39 Non AL. Social epigenomics: are we at an impasse? Epigenomics 2021. [PMID: 33749316 DOI: 10.2217/epi-2020-0136] [Cited by in Crossref: 1] [Cited by in F6Publishing: 6] [Article Influence: 1.0] [Reference Citation Analysis]
40 Romero-Gutiérrez E, Vázquez-Cárdenas P, Moreno-Macías H, Salas-Pacheco J, Tusié-Luna T, Arias-Carrión O. Differences in MTHFR and LRRK2 variant's association with sporadic Parkinson's disease in Mexican Mestizos correlated to Native American ancestry. NPJ Parkinsons Dis 2021;7:13. [PMID: 33574311 DOI: 10.1038/s41531-021-00157-y] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
41 Yelmen B, Decelle A, Ongaro L, Marnetto D, Tallec C, Montinaro F, Furtlehner C, Pagani L, Jay F. Creating artificial human genomes using generative neural networks. PLoS Genet 2021;17:e1009303. [PMID: 33539374 DOI: 10.1371/journal.pgen.1009303] [Cited by in Crossref: 6] [Cited by in F6Publishing: 14] [Article Influence: 6.0] [Reference Citation Analysis]
42 Dannemann M. The Population-Specific Impact of Neandertal Introgression on Human Disease. Genome Biol Evol 2021;13:evaa250. [PMID: 33247712 DOI: 10.1093/gbe/evaa250] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 2.0] [Reference Citation Analysis]
43 Samadder NJ, Riegert-Johnson D, Boardman L, Rhodes D, Wick M, Okuno S, Kunze KL, Golafshar M, Uson PLS Jr, Mountjoy L, Ertz-Archambault N, Patel N, Rodriguez EA, Lizaola-Mayo B, Lehrer M, Thorpe CS, Yu NY, Esplin ED, Nussbaum RL, Sharp RR, Azevedo C, Klint M, Hager M, Macklin-Mantia S, Bryce AH, Bekaii-Saab TS, Sekulic A, Stewart AK. Comparison of Universal Genetic Testing vs Guideline-Directed Targeted Testing for Patients With Hereditary Cancer Syndrome. JAMA Oncol 2021;7:230-7. [PMID: 33126242 DOI: 10.1001/jamaoncol.2020.6252] [Cited by in Crossref: 24] [Cited by in F6Publishing: 58] [Article Influence: 24.0] [Reference Citation Analysis]
44 Wiley AS. Pearl lecture: Biological normalcy: A new framework for biocultural analysis of human population variation. Am J Hum Biol 2021;33:e23563. [PMID: 33458923 DOI: 10.1002/ajhb.23563] [Cited by in F6Publishing: 2] [Reference Citation Analysis]
45 Kikut A, Sanyal M, Vaughn M, Ridley-Merriweather KE, Head K, Salowe R, Lomax-Reese S, Lewis M, Ross AG, Cui QN, Addis V, Sankar PS, Miller-Ellis E, O'Brien JM. Learning from Black/African American Participants: Applying the Integrated Behavioral Model to Assess Recruitment Strategies for a Glaucoma Genetic Study. Health Commun 2020;:1-10. [PMID: 33345602 DOI: 10.1080/10410236.2020.1853897] [Cited by in F6Publishing: 3] [Reference Citation Analysis]
46 Sharif SM, Blyth M, Ahmed M, Sheridan E, Saltus R, Yu J, Tonkin E, Kirk M. Enhancing inclusion of diverse populations in genomics: A competence framework. J Genet Couns 2020;29:282-92. [PMID: 32250032 DOI: 10.1002/jgc4.1263] [Cited by in F6Publishing: 4] [Reference Citation Analysis]
47 Fortes-Lima C, Schlebusch C. Closing the Gaps in Genomic Research. Trends Genet 2021;37:104-6. [PMID: 33246657 DOI: 10.1016/j.tig.2020.11.005] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
48 Lanata CM, Blazer A, Criswell LA. The Contribution of Genetics and Epigenetics to Our Understanding of Health Disparities in Rheumatic Diseases. Rheum Dis Clin North Am 2021;47:65-81. [PMID: 34042055 DOI: 10.1016/j.rdc.2020.09.005] [Cited by in F6Publishing: 2] [Reference Citation Analysis]
49 Wohlers I, Künstner A, Munz M, Olbrich M, Fähnrich A, Calonga-Solís V, Ma C, Hirose M, El-Mosallamy S, Salama M, Busch H, Ibrahim S. An integrated personal and population-based Egyptian genome reference. Nat Commun 2020;11:4719. [PMID: 32948767 DOI: 10.1038/s41467-020-17964-1] [Cited by in Crossref: 5] [Cited by in F6Publishing: 6] [Article Influence: 2.5] [Reference Citation Analysis]
50 McGuire AL, Gabriel S, Tishkoff SA, Wonkam A, Chakravarti A, Furlong EEM, Treutlein B, Meissner A, Chang HY, López-Bigas N, Segal E, Kim JS. The road ahead in genetics and genomics. Nat Rev Genet 2020;21:581-96. [PMID: 32839576 DOI: 10.1038/s41576-020-0272-6] [Cited by in Crossref: 22] [Cited by in F6Publishing: 42] [Article Influence: 11.0] [Reference Citation Analysis]
51 Matoba N, Liang D, Sun H, Aygün N, McAfee JC, Davis JE, Raffield LM, Qian H, Piven J, Li Y, Kosuri S, Won H, Stein JL. Common genetic risk variants identified in the SPARK cohort support DDHD2 as a candidate risk gene for autism. Transl Psychiatry 2020;10:265. [PMID: 32747698 DOI: 10.1038/s41398-020-00953-9] [Cited by in Crossref: 27] [Cited by in F6Publishing: 18] [Article Influence: 13.5] [Reference Citation Analysis]
52 Botton MR, Whirl-Carrillo M, Del Tredici AL, Sangkuhl K, Cavallari LH, Agúndez JAG, Duconge J, Lee MTM, Woodahl EL, Claudio-Campos K, Daly AK, Klein TE, Pratt VM, Scott SA, Gaedigk A. PharmVar GeneFocus: CYP2C19. Clin Pharmacol Ther 2021;109:352-66. [PMID: 32602114 DOI: 10.1002/cpt.1973] [Cited by in Crossref: 8] [Cited by in F6Publishing: 22] [Article Influence: 4.0] [Reference Citation Analysis]
53 Nuñez-Rios DL, Chaskel R, Lopez A, Galeano L, Lattig MC. The role of 5-HTTLPR in autism spectrum disorder: New evidence and a meta-analysis of this polymorphism in Latin American population with psychiatric disorders. PLoS One 2020;15:e0235512. [PMID: 32614901 DOI: 10.1371/journal.pone.0235512] [Cited by in Crossref: 1] [Cited by in F6Publishing: 3] [Article Influence: 0.5] [Reference Citation Analysis]
54 Park Y, Kim H, Seo H, Choi JY, Ma Y, Yun S, Min BJ, Seo ME, Yoo KH, Kang HJ, Im HJ, Kim JH. Homozygote CRIM1 variant is associated with thiopurine-induced neutropenia in leukemic patients with both wildtype NUDT15 and TPMT. J Transl Med 2020;18:265. [PMID: 32611418 DOI: 10.1186/s12967-020-02416-7] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 0.5] [Reference Citation Analysis]
55 Griswold AJ, Sivasankaran SK, Van Booven D, Gardner OK, Rajabli F, Whitehead PL, Hamilton-Nelson KL, Adams LD, Scott AM, Hofmann NK, Vance JM, Cuccaro ML, Bush WS, Martin ER, Byrd GS, Haines JL, Pericak-Vance MA, Beecham GW. Immune and Inflammatory Pathways Implicated by Whole Blood Transcriptomic Analysis in a Diverse Ancestry Alzheimer's Disease Cohort. J Alzheimers Dis 2020;76:1047-60. [PMID: 32597797 DOI: 10.3233/JAD-190855] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 0.5] [Reference Citation Analysis]
56 Dannemann M, He Z, Heide C, Vernot B, Sidow L, Kanton S, Weigert A, Treutlein B, Pääbo S, Kelso J, Camp JG. Human Stem Cell Resources Are an Inroad to Neandertal DNA Functions. Stem Cell Reports 2020;15:214-25. [PMID: 32559457 DOI: 10.1016/j.stemcr.2020.05.018] [Cited by in Crossref: 7] [Cited by in F6Publishing: 5] [Article Influence: 3.5] [Reference Citation Analysis]
57 Wells JCK, Stock JT. Life History Transitions at the Origins of Agriculture: A Model for Understanding How Niche Construction Impacts Human Growth, Demography and Health. Front Endocrinol (Lausanne) 2020;11:325. [PMID: 32508752 DOI: 10.3389/fendo.2020.00325] [Cited by in Crossref: 8] [Cited by in F6Publishing: 16] [Article Influence: 4.0] [Reference Citation Analysis]
58 Harlemon M, Ajayi O, Kachambwa P, Kim MS, Simonti CN, Quiver MH, Petersen DC, Mittal A, Fernandez PW, Hsing AW, Baichoo S, Agalliu I, Jalloh M, Gueye SM, Snyper NYF, Adusei B, Mensah JE, Abrahams AOD, Adebiyi AO, Orunmuyi AT, Aisuodionoe-Shadrach OI, Nwegbu MM, Joffe M, Chen WC, Irusen H, Neugut AI, Quintana Y, Seutloali M, Fadipe MB, Warren C, Woehrmann MH, Zhang P, Ongaco CM, Mawhinney M, McBride J, Andrews CV, Adams M, Pugh E, Rebbeck TR, Petersen LN, Lachance J. A Custom Genotyping Array Reveals Population-Level Heterogeneity for the Genetic Risks of Prostate Cancer and Other Cancers in Africa. Cancer Res 2020;80:2956-66. [PMID: 32393663 DOI: 10.1158/0008-5472.CAN-19-2165] [Cited by in Crossref: 5] [Cited by in F6Publishing: 11] [Article Influence: 2.5] [Reference Citation Analysis]
59 Levin MG, Rader DJ. Polygenic Risk Scores and Coronary Artery Disease: Ready for Prime Time? Circulation 2020;141:637-40. [DOI: 10.1161/circulationaha.119.044770] [Cited by in Crossref: 16] [Cited by in F6Publishing: 18] [Article Influence: 8.0] [Reference Citation Analysis]
60 van Reisen M, Stokmans M, Mawere M, Basajja M, Ong'ayo AO, Nakazibwe P, Kirkpatrick C, Chindoza K. FAIR Practices in Africa. Data Intellegence 2020;2:246-56. [DOI: 10.1162/dint_a_00047] [Cited by in Crossref: 4] [Cited by in F6Publishing: 3] [Article Influence: 2.0] [Reference Citation Analysis]
61 van Reisen M, Stokmans M, Basajja M, Ong'ayo AO, Kirkpatrick C, Mons B. Towards the Tipping Point for FAIR Implementation. Data Intellegence 2020;2:264-75. [DOI: 10.1162/dint_a_00049] [Cited by in Crossref: 9] [Cited by in F6Publishing: 7] [Article Influence: 4.5] [Reference Citation Analysis]
62 Nofziger C, Turner AJ, Sangkuhl K, Whirl-Carrillo M, Agúndez JAG, Black JL, Dunnenberger HM, Ruano G, Kennedy MA, Phillips MS, Hachad H, Klein TE, Gaedigk A. PharmVar GeneFocus: CYP2D6. Clin Pharmacol Ther 2020;107:154-70. [PMID: 31544239 DOI: 10.1002/cpt.1643] [Cited by in Crossref: 53] [Cited by in F6Publishing: 76] [Article Influence: 17.7] [Reference Citation Analysis]
63 Dias R, Torkamani A. Artificial intelligence in clinical and genomic diagnostics. Genome Med. 2019;11:70. [PMID: 31744524 DOI: 10.1186/s13073-019-0689-8] [Cited by in Crossref: 45] [Cited by in F6Publishing: 70] [Article Influence: 15.0] [Reference Citation Analysis]
64 Nuytemans K, Manrique CP, Uhlenberg A, Scott WK, Cuccaro ML, Luca CC, Singer C, Vance JM. Motivations for Participation in Parkinson Disease Genetic Research Among Hispanics versus Non-Hispanics. Front Genet 2019;10:658. [PMID: 31379924 DOI: 10.3389/fgene.2019.00658] [Cited by in Crossref: 4] [Cited by in F6Publishing: 8] [Article Influence: 1.3] [Reference Citation Analysis]