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Identifying genetic factors that contribute to the increased risk of congenital heart defects in infants with Down syndrome.
Trevino CE, Holleman AM, Corbitt H, Maslen CL, Rosser TC, Cutler DJ, Johnston HR, Rambo-Martin BL, Oberoi J, Dooley KJ, Capone GT, Reeves RH, Cordell HJ, Keavney BD, Agopian AJ, Goldmuntz E, Gruber PJ, O'Brien JE Jr, Bittel DC, Wadhwa L, Cua CL, Moskowitz IP, Mulle JG, Epstein MP, Sherman SL, Zwick ME. Trevino CE, et al. Among authors: epstein mp. Sci Rep. 2020 Oct 22;10(1):18051. doi: 10.1038/s41598-020-74650-4. Sci Rep. 2020. PMID: 33093519 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
Depression and anxiety symptoms among women who carry the FMR1 premutation: impact of raising a child with fragile X syndrome is moderated by CRHR1 polymorphisms.
Hunter JE, Leslie M, Novak G, Hamilton D, Shubeck L, Charen K, Abramowitz A, Epstein MP, Lori A, Binder E, Cubells JF, Sherman SL. Hunter JE, et al. Among authors: epstein mp. Am J Med Genet B Neuropsychiatr Genet. 2012 Jul;159B(5):549-59. doi: 10.1002/ajmg.b.32061. Epub 2012 May 9. Am J Med Genet B Neuropsychiatr Genet. 2012. PMID: 22573456 Free PMC article.
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.
147 results