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Rare variants in MYH15 modify amyotrophic lateral sclerosis risk.
Kim H, Lim J, Bao H, Jiao B, Canon SM, Epstein MP, Xu K, Jiang J, Parameswaran J, Li Y, Moberg KH, Landers JE, Fournier C, Allen EG, Glass JD, Wingo TS, Jin P. Kim H, et al. Among authors: epstein mp. Hum Mol Genet. 2019 Jul 15;28(14):2309-2318. doi: 10.1093/hmg/ddz063. Hum Mol Genet. 2019. PMID: 30985904 Free PMC article.
Association of FMR1 repeat size with ovarian dysfunction.
Sullivan AK, Marcus M, Epstein MP, Allen EG, Anido AE, Paquin JJ, Yadav-Shah M, Sherman SL. Sullivan AK, et al. Among authors: epstein mp. Hum Reprod. 2005 Feb;20(2):402-12. doi: 10.1093/humrep/deh635. Epub 2004 Dec 17. Hum Reprod. 2005. PMID: 15608041
A Statistical Approach for Testing Cross-Phenotype Effects of Rare Variants.
Broadaway KA, Cutler DJ, Duncan R, Moore JL, Ware EB, Jhun MA, Bielak LF, Zhao W, Smith JA, Peyser PA, Kardia SLR, Ghosh D, Epstein MP. Broadaway KA, et al. Among authors: epstein mp. Am J Hum Genet. 2016 Mar 3;98(3):525-540. doi: 10.1016/j.ajhg.2016.01.017. Am J Hum Genet. 2016. PMID: 26942286 Free PMC article.
PEMapper and PECaller provide a simplified approach to whole-genome sequencing.
Johnston HR, Chopra P, Wingo TS, Patel V; International Consortium on Brain and Behavior in 22q11.2 Deletion Syndrome; Epstein MP, Mulle JG, Warren ST, Zwick ME, Cutler DJ. Johnston HR, et al. Among authors: epstein mp. Proc Natl Acad Sci U S A. 2017 Mar 7;114(10):E1923-E1932. doi: 10.1073/pnas.1618065114. Epub 2017 Feb 21. Proc Natl Acad Sci U S A. 2017. PMID: 28223510 Free PMC article.
147 results