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Identification of PSMB5 as a genetic modifier of fragile X-associated tremor/ataxia syndrome.
Kong HE, Lim J, Linsalata A, Kang Y, Malik I, Allen EG, Cao Y, Shubeck L, Johnston R, Huang Y, Gu Y, Guo X, Zwick ME, Qin Z, Wingo TS, Juncos J, Nelson DL, Epstein MP, Cutler DJ, Todd PK, Sherman SL, Warren ST, Jin P. Kong HE, et al. Among authors: epstein mp. Proc Natl Acad Sci U S A. 2022 May 31;119(22):e2118124119. doi: 10.1073/pnas.2118124119. Epub 2022 May 26. Proc Natl Acad Sci U S A. 2022. PMID: 35617426 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.
154 results