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Page 1
Molecular genetics of congenital diaphragmatic defects.
Bielinska M, Jay PY, Erlich JM, Mannisto S, Urban Z, Heikinheimo M, Wilson DB. Bielinska M, et al. Among authors: erlich jm. Ann Med. 2007;39(4):261-74. doi: 10.1080/07853890701326883. Ann Med. 2007. PMID: 17558598 Free PMC article. Review.
Heterogeneity of genetic modifiers ensures normal cardiac development.
Winston JB, Erlich JM, Green CA, Aluko A, Kaiser KA, Takematsu M, Barlow RS, Sureka AO, LaPage MJ, Janss LL, Jay PY. Winston JB, et al. Among authors: erlich jm. Circulation. 2010 Mar 23;121(11):1313-21. doi: 10.1161/CIRCULATIONAHA.109.887687. Epub 2010 Mar 8. Circulation. 2010. PMID: 20212279 Free PMC article.
Complex trait analysis of ventricular septal defects caused by Nkx2-5 mutation.
Winston JB, Schulkey CE, Chen IB, Regmi SD, Efimova M, Erlich JM, Green CA, Aluko A, Jay PY. Winston JB, et al. Among authors: erlich jm. Circ Cardiovasc Genet. 2012 Jun;5(3):293-300. doi: 10.1161/CIRCGENETICS.111.961136. Epub 2012 Apr 24. Circ Cardiovasc Genet. 2012. PMID: 22534315 Free PMC article.
Insights into the treatment of inflammatory bowel disease in pregnancy.
Shannahan SE, Erlich JM, Peppercorn MA. Shannahan SE, et al. Among authors: erlich jm. Therap Adv Gastroenterol. 2019 May 27;12:1756284819852231. doi: 10.1177/1756284819852231. eCollection 2019. Therap Adv Gastroenterol. 2019. PMID: 31191713 Free PMC article. Review.