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For: Wanke KA, Devanna P, Vernes SC. Understanding Neurodevelopmental Disorders: The Promise of Regulatory Variation in the 3'UTRome. Biol Psychiatry 2018;83:548-57. [PMID: 29289333 DOI: 10.1016/j.biopsych.2017.11.006] [Cited by in Crossref: 29] [Cited by in F6Publishing: 30] [Article Influence: 4.8] [Reference Citation Analysis]
Number Citing Articles
1 Melo ARV, Raposo M, Ventura M, Martins S, Pavão S, Alonso I, Bettencourt C, Lima M. Genetic Variation in ATXN3 (Ataxin-3) 3'UTR: Insights into the Downstream Regulatory Elements of the Causative Gene of Machado-Joseph Disease/Spinocerebellar Ataxia Type 3. Cerebellum 2023;22:37-45. [PMID: 35034258 DOI: 10.1007/s12311-021-01358-0] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
2 Boudhiba N, Sfar S, Helaoui A, Bouanene I, Hołysz M, Skalska E, Bouchahda H, Jagodziński PP, Kenani A. Association between the ELAVL1 gene single nucleotide polymorphisms and the Genetic Susceptibility to cervical cancer by high resolution melting in a Tunisian population. Mol Biol Rep 2023. [PMID: 36626067 DOI: 10.1007/s11033-022-07868-2] [Reference Citation Analysis]
3 McAfee JC, Bell JL, Krupa O, Matoba N, Stein JL, Won H. Focus on your locus with a massively parallel reporter assay. J Neurodev Disord 2022;14:50. [PMID: 36085003 DOI: 10.1186/s11689-022-09461-x] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
4 López I, Förster J. Trastornos del neurodesarrollo: dónde estamos hoy y hacia dónde nos dirigimos. Revista Médica Clínica Las Condes 2022;33:367-378. [DOI: 10.1016/j.rmclc.2022.06.004] [Reference Citation Analysis]
5 Yolles M, Frieden R. Viruses as Living Systems—A Metacybernetic View. Systems 2022;10:70. [DOI: 10.3390/systems10030070] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 2.0] [Reference Citation Analysis]
6 Bai Y, Qin Y, Fan Z, Morrison RM, Nam K, Zarour HM, Koldamova R, Padiath QS, Kim S, Park HJ. scMAPA: Identification of cell-type-specific alternative polyadenylation in complex tissues. Gigascience 2022;11:giac033. [PMID: 35488860 DOI: 10.1093/gigascience/giac033] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
7 Navarro E, Mallén A, Hueso M. Dynamic Variations of 3'UTR Length Reprogram the mRNA Regulatory Landscape. Biomedicines 2021;9:1560. [PMID: 34829789 DOI: 10.3390/biomedicines9111560] [Cited by in Crossref: 4] [Cited by in F6Publishing: 5] [Article Influence: 2.0] [Reference Citation Analysis]
8 Park Y, Page N, Salamon I, Li D, Rasin MR. Making sense of mRNA landscapes: Translation control in neurodevelopment. Wiley Interdiscip Rev RNA 2021;:e1674. [PMID: 34137510 DOI: 10.1002/wrna.1674] [Cited by in Crossref: 2] [Cited by in F6Publishing: 3] [Article Influence: 1.0] [Reference Citation Analysis]
9 Wright CF, Quaife NM, Ramos-Hernández L, Danecek P, Ferla MP, Samocha KE, Kaplanis J, Gardner EJ, Eberhardt RY, Chao KR, Karczewski KJ, Morales J, Gallone G, Balasubramanian M, Banka S, Gompertz L, Kerr B, Kirby A, Lynch SA, Morton JEV, Pinz H, Sansbury FH, Stewart H, Zuccarelli BD, Cook SA, Taylor JC, Juusola J, Retterer K, Firth HV, Hurles ME, Lara-Pezzi E, Barton PJR, Whiffin N; Genomics England Research Consortium. Non-coding region variants upstream of MEF2C cause severe developmental disorder through three distinct loss-of-function mechanisms. Am J Hum Genet 2021;108:1083-94. [PMID: 34022131 DOI: 10.1016/j.ajhg.2021.04.025] [Cited by in Crossref: 18] [Cited by in F6Publishing: 11] [Article Influence: 9.0] [Reference Citation Analysis]
10 Ross JP, Dion PA, Rouleau GA. Genetic Basis of ALS. Spectrums of Amyotrophic Lateral Sclerosis 2021. [DOI: 10.1002/9781119745532.ch2] [Reference Citation Analysis]
11 Moriano J, Martínez-gil N, Andirkó A, Balcells S, Grinberg D, Boeckx C. Human-derived alleles in SOST and RUNX2 3′UTRs cause differential regulation in a bone cell-line model.. [DOI: 10.1101/2021.04.21.440797] [Reference Citation Analysis]
12 Alvarez-Mora MI, Corominas J, Gilissen C, Sanchez A, Madrigal I, Rodriguez-Revenga L. Novel Compound Heterozygous Mutation in TRAPPC9 Gene: The Relevance of Whole Genome Sequencing. Genes (Basel) 2021;12:557. [PMID: 33921338 DOI: 10.3390/genes12040557] [Cited by in Crossref: 4] [Cited by in F6Publishing: 6] [Article Influence: 2.0] [Reference Citation Analysis]
13 Yan L, Shen R, Cao Z, Han C, Zhang Y, Liu Y, Yang X, Xie M, Li H. A Novel Missense Variant in the Gene PPP2R5D Causes a Rare Neurodevelopmental Disorder with Increased Phenotype. Biomed Res Int 2021;2021:6661860. [PMID: 33628804 DOI: 10.1155/2021/6661860] [Cited by in Crossref: 1] [Cited by in F6Publishing: 3] [Article Influence: 0.5] [Reference Citation Analysis]
14 Zhang HQ, Wang JY, Li ZF, Cui L, Huang SS, Zhu LB, Sun Y, Yang R, Fan HH, Zhang X, Zhu JH. DNA Methyltransferase 1 Is Dysregulated in Parkinson's Disease via Mediation of miR-17. Mol Neurobiol 2021;58:2620-33. [PMID: 33483902 DOI: 10.1007/s12035-021-02298-w] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 1.5] [Reference Citation Analysis]
15 Wright CF, Quaife NM, Ramos-hernández L, Danecek P, Ferla MP, Samocha KE, Kaplanis J, Gardner EJ, Eberhardt RY, Chao KR, Karczewski KJ, Morales J, Balasubramanian M, Banka S, Gompertz L, Kerr B, Kirby A, Lynch SA, Morton JE, Pinz H, Sansbury FH, Stewart H, Zuccarelli BD, Cook SA, Taylor JC, Juusola J, Retterer K, Firth HV, Hurles ME, Lara-pezzi E, Barton PJ, Whiffin N, Genomics England Research Consortium. Non-coding variants upstream of MEF2C cause severe developmental disorder through three distinct loss-of-function mechanisms.. [DOI: 10.1101/2020.11.15.20229807] [Reference Citation Analysis]
16 Grozdanov PN, Masoumzadeh E, Kalscheuer VM, Bienvenu T, Billuart P, Delrue MA, Latham MP, MacDonald CC. A missense mutation in the CSTF2 gene that impairs the function of the RNA recognition motif and causes defects in 3' end processing is associated with intellectual disability in humans. Nucleic Acids Res 2020;48:9804-21. [PMID: 32816001 DOI: 10.1093/nar/gkaa689] [Cited by in Crossref: 6] [Cited by in F6Publishing: 7] [Article Influence: 2.0] [Reference Citation Analysis]
17 Su D. Up-regulation of MiR-145-5p promotes the growth and migration in LPS-treated HUVECs through inducing macrophage polarization to M2. J Recept Signal Transduct Res 2021;41:434-41. [PMID: 32998623 DOI: 10.1080/10799893.2020.1818095] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 0.7] [Reference Citation Analysis]
18 Liu YP, Luo ZR, Wang C, Cai H, Zhao TT, Li H, Shao SJ, Guo HD. Electroacupuncture Promoted Nerve Repair After Peripheral Nerve Injury by Regulating miR-1b and Its Target Brain-Derived Neurotrophic Factor. Front Neurosci 2020;14:525144. [PMID: 33132818 DOI: 10.3389/fnins.2020.525144] [Cited by in Crossref: 6] [Cited by in F6Publishing: 8] [Article Influence: 2.0] [Reference Citation Analysis]
19 Yang J, Liu A, He I, Bai Y. Bioinformatics Analysis Revealed Novel 3'UTR Variants Associated with Intellectual Disability. Genes (Basel) 2020;11:E998. [PMID: 32858868 DOI: 10.3390/genes11090998] [Cited by in Crossref: 5] [Cited by in F6Publishing: 5] [Article Influence: 1.7] [Reference Citation Analysis]
20 Liu Y, Fischer AD, St. Pierre CL, Macias-velasco JF, Lawson HA, Dougherty JD. TRAP-based allelic translation efficiency imbalance analysis to identify genetic regulation of ribosome occupancy in specific cell typesin vivo.. [DOI: 10.1101/2020.08.24.265389] [Reference Citation Analysis]
21 Göpferich M, George NO, Muelas AD, Bizyn A, Pascual R, Fijalkowska D, Kalamakis G, Müller U, Krijgsveld J, Mendez R, Fariñas I, Huber W, Anders S, Martin-villalba A. Single cell 3’UTR analysis identifies changes in alternative polyadenylation throughout neuronal differentiation and in autism.. [DOI: 10.1101/2020.08.12.247627] [Cited by in Crossref: 6] [Cited by in F6Publishing: 6] [Article Influence: 2.0] [Reference Citation Analysis]
22 Dong T, Guan Q, Hu W, Zhang M, Zhang Y, Chen M, Wang X, Xia Y. Prenatal exposure to glufosinate ammonium disturbs gut microbiome and induces behavioral abnormalities in mice. Journal of Hazardous Materials 2020;389:122152. [DOI: 10.1016/j.jhazmat.2020.122152] [Cited by in Crossref: 15] [Cited by in F6Publishing: 9] [Article Influence: 5.0] [Reference Citation Analysis]
23 Navarro E, Mallén A, Cruzado JM, Torras J, Hueso M. Unveiling ncRNA regulatory axes in atherosclerosis progression. Clin Transl Med 2020;9:5. [PMID: 32009226 DOI: 10.1186/s40169-020-0256-3] [Cited by in Crossref: 17] [Cited by in F6Publishing: 18] [Article Influence: 5.7] [Reference Citation Analysis]
24 Grozdanov PN, Masoumzadeh E, Kalscheuer VM, Bienvenu T, Billuart P, Delrue M, Latham MP, Macdonald CC. A Point Mutation in the RNA Recognition Motif of CSTF2 Associated with Intellectual Disability in Humans Causes Defects in 3′ End Processing.. [DOI: 10.1101/2020.01.02.893107] [Reference Citation Analysis]
25 Wang W, Corominas R, Lin GN. De novo Mutations From Whole Exome Sequencing in Neurodevelopmental and Psychiatric Disorders: From Discovery to Application. Front Genet 2019;10:258. [PMID: 31001316 DOI: 10.3389/fgene.2019.00258] [Cited by in Crossref: 35] [Cited by in F6Publishing: 36] [Article Influence: 8.8] [Reference Citation Analysis]
26 Peng S, Huang GL, Xu N, Lu Y, Zeng L, Li X, Luo S, Lyu X, Jiang Q, Li T, He Z. The human ATF1 rs11169571 polymorphism associated with risk of nasopharyngeal carcinoma in Southern Chinese populations. Cancer Med 2019;8:1893-8. [PMID: 30905073 DOI: 10.1002/cam4.2022] [Cited by in Crossref: 2] [Cited by in F6Publishing: 3] [Article Influence: 0.5] [Reference Citation Analysis]
27 Laffleur B, Basu U. Biology of RNA Surveillance in Development and Disease. Trends Cell Biol 2019;29:428-45. [PMID: 30755352 DOI: 10.1016/j.tcb.2019.01.004] [Cited by in Crossref: 11] [Cited by in F6Publishing: 8] [Article Influence: 2.8] [Reference Citation Analysis]
28 Grassi E, Santoro R, Umbach A, Grosso A, Oliviero S, Neri F, Conti L, Ala U, Provero P, DiCunto F, Merlo GR. Choice of Alternative Polyadenylation Sites, Mediated by the RNA-Binding Protein Elavl3, Plays a Role in Differentiation of Inhibitory Neuronal Progenitors. Front Cell Neurosci 2018;12:518. [PMID: 30687010 DOI: 10.3389/fncel.2018.00518] [Cited by in Crossref: 20] [Cited by in F6Publishing: 22] [Article Influence: 5.0] [Reference Citation Analysis]
29 Yang L, Li Y, Gong R, Gao M, Feng C, Liu T, Sun Y, Jin M, Wang D, Yuan Y, Yan G, He M, Idiiatullina E, Ma W, Han Z, Zhang L, Huang Q, Ding F, Cai B, Yang F. The Long Non-coding RNA-ORLNC1 Regulates Bone Mass by Directing Mesenchymal Stem Cell Fate. Mol Ther 2019;27:394-410. [PMID: 30638773 DOI: 10.1016/j.ymthe.2018.11.019] [Cited by in Crossref: 55] [Cited by in F6Publishing: 55] [Article Influence: 11.0] [Reference Citation Analysis]
30 Zhang Y, Carrion SA, Zhang Y, Zhang X, Zinski AL, Michal JJ, Jiang Z. Alternative polyadenylation analysis in animals and plants: newly developed strategies for profiling, processing and validation. Int J Biol Sci 2018;14:1709-14. [PMID: 30416385 DOI: 10.7150/ijbs.27168] [Cited by in Crossref: 5] [Cited by in F6Publishing: 5] [Article Influence: 1.0] [Reference Citation Analysis]
31 Devanna P, van de Vorst M, Pfundt R, Gilissen C, Vernes SC. Genome-wide investigation of an ID cohort reveals de novo 3'UTR variants affecting gene expression. Hum Genet 2018;137:717-21. [PMID: 30097719 DOI: 10.1007/s00439-018-1925-9] [Cited by in Crossref: 13] [Cited by in F6Publishing: 10] [Article Influence: 2.6] [Reference Citation Analysis]