Feingold E - Search Results

1

An excess of deleterious variants in VEGF-A pathway genes in Down-syndrome-associated atrioventricular septal defects.

Ackerman C, Locke AE, Feingold E, Reshey B, Espana K, Thusberg J, Mooney S, Bean LJ, Dooley KJ, Cua CL, Reeves RH, Sherman SL, Maslen CL. Ackerman C, et al. Among authors: feingold e. Am J Hum Genet. 2012 Oct 5;91(4):646-59. doi: 10.1016/j.ajhg.2012.08.017. Am J Hum Genet. 2012. PMID: 23040494 Free PMC article.

2

Allelic Interaction between CRELD1 and VEGFA in the Pathogenesis of Cardiac Atrioventricular Septal Defects.

Redig JK, Fouad GT, Babcock D, Reshey B, Feingold E, Reeves RH, Maslen CL. Redig JK, et al. Among authors: feingold e. AIMS Genet. 2014;1(1):1-19. doi: 10.3934/genet.2014.1.1#sthash.jksuJTeC.dpuf. AIMS Genet. 2014. PMID: 25328912 Free PMC article.

3

Genome-Wide Association Study of Down Syndrome-Associated Atrioventricular Septal Defects.

Ramachandran D, Zeng Z, Locke AE, Mulle JG, Bean LJ, Rosser TC, Dooley KJ, Cua CL, Capone GT, Reeves RH, Maslen CL, Cutler DJ, Feingold E, Sherman SL, Zwick ME. Ramachandran D, et al. Among authors: feingold e. G3 (Bethesda). 2015 Jul 20;5(10):1961-71. doi: 10.1534/g3.115.019943. G3 (Bethesda). 2015. PMID: 26194203 Free PMC article.

4

Variation in folate pathway genes contributes to risk of congenital heart defects among individuals with Down syndrome.

Locke AE, Dooley KJ, Tinker SW, Cheong SY, Feingold E, Allen EG, Freeman SB, Torfs CP, Cua CL, Epstein MP, Wu MC, Lin X, Capone G, Sherman SL, Bean LJ. Locke AE, et al. Among authors: feingold e. Genet Epidemiol. 2010 Sep;34(6):613-23. doi: 10.1002/gepi.20518. Genet Epidemiol. 2010. PMID: 20718043 Free PMC article.

5

Associations Between Medical History, Cognition, and Behavior in Youth With Down Syndrome: A Report From the Down Syndrome Cognition Project.

Rosser TC, Edgin JO, Capone GT, Hamilton DR, Allen EG, Dooley KJ, Anand P, Strang JF, Armour AC, Frank-Crawford MA, Channell MM, Pierpont EI, Feingold E, Maslen CL, Reeves RH, Sherman SL. Rosser TC, et al. Among authors: feingold e. Am J Intellect Dev Disabil. 2018 Nov;123(6):514-528. doi: 10.1352/1944-7558-123.6.514. Am J Intellect Dev Disabil. 2018. PMID: 30421968 Free PMC article.

6

Altered patterns of multiple recombinant events are associated with nondisjunction of chromosome 21.

Oliver TR, Tinker SW, Allen EG, Hollis N, Locke AE, Bean LJ, Chowdhury R, Begum F, Marazita M, Cheung V, Feingold E, Sherman SL. Oliver TR, et al. Among authors: feingold e. Hum Genet. 2012 Jul;131(7):1039-46. doi: 10.1007/s00439-011-1121-7. Epub 2011 Dec 9. Hum Genet. 2012. PMID: 22160426 Free PMC article.

7

Polymorphic haplotypes of CRELD1 differentially predispose Down syndrome and euploids individuals to atrioventricular septal defect.

Ghosh P, Bhaumik P, Ghosh S, Ozbek U, Feingold E, Maslen C, Sarkar B, Pramanik V, Biswas P, Bandyopadhyay B, Dey SK. Ghosh P, et al. Among authors: feingold e. Am J Med Genet A. 2012 Nov;158A(11):2843-8. doi: 10.1002/ajmg.a.35626. Epub 2012 Sep 14. Am J Med Genet A. 2012. PMID: 22987595

8

Association between maternal age and meiotic recombination for trisomy 21.

Lamb NE, Yu K, Shaffer J, Feingold E, Sherman SL. Lamb NE, et al. Among authors: feingold e. Am J Hum Genet. 2005 Jan;76(1):91-9. doi: 10.1086/427266. Epub 2004 Nov 18. Am J Hum Genet. 2005. PMID: 15551222 Free PMC article.

9

Linkage disequilibrium mapping in trisomic populations: analytical approaches and an application to congenital heart defects in Down syndrome.

Kerstann KF, Feingold E, Freeman SB, Bean LJ, Pyatt R, Tinker S, Jewel AH, Capone G, Sherman SL. Kerstann KF, et al. Among authors: feingold e. Genet Epidemiol. 2004 Nov;27(3):240-51. doi: 10.1002/gepi.20019. Genet Epidemiol. 2004. PMID: 15389927

10

Methods for genetic linkage analysis using trisomies.

Feingold E, Lamb NE, Sherman SL. Feingold E, et al. Am J Hum Genet. 1995 Feb;56(2):475-83. Am J Hum Genet. 1995. PMID: 7847384 Free PMC article.

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