Sherman SL - Search Results

1

Smarter clustering methods for SNP genotype calling.

Lin Y, Tseng GC, Cheong SY, Bean LJ, Sherman SL, Feingold E. Lin Y, et al. Among authors: sherman sl. Bioinformatics. 2008 Dec 1;24(23):2665-71. doi: 10.1093/bioinformatics/btn509. Epub 2008 Sep 29. Bioinformatics. 2008. PMID: 18826959 Free PMC article.

2

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: sherman sl. Genet Epidemiol. 2010 Sep;34(6):613-23. doi: 10.1002/gepi.20518. Genet Epidemiol. 2010. PMID: 20718043 Free PMC article.

3

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: sherman sl. 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.

4

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: sherman sl. G3 (Bethesda). 2015 Jul 20;5(10):1961-71. doi: 10.1534/g3.115.019943. G3 (Bethesda). 2015. PMID: 26194203 Free PMC article.

5

Regionally Smoothed Meta-Analysis Methods for GWAS Datasets.

Begum F, Sharker MH, Sherman SL, Tseng GC, Feingold E. Begum F, et al. Among authors: sherman sl. Genet Epidemiol. 2016 Feb;40(2):154-60. doi: 10.1002/gepi.21949. Epub 2015 Dec 28. Genet Epidemiol. 2016. PMID: 26707090 Free PMC article.

6

A trisomic transmission disequilibrium test.

Xu Z, Kerstann KF, Sherman SL, Chakravarti A, Feingold E. Xu Z, et al. Among authors: sherman sl. Genet Epidemiol. 2004 Feb;26(2):125-31. doi: 10.1002/gepi.10302. Genet Epidemiol. 2004. PMID: 14748012

7

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: sherman sl. Genet Epidemiol. 2004 Nov;27(3):240-51. doi: 10.1002/gepi.20019. Genet Epidemiol. 2004. PMID: 15389927

8

Multipoint estimation of genetic maps for human trisomies with one parent or other partial data.

Feingold E, Brown AS, Sherman SL. Feingold E, et al. Among authors: sherman sl. Am J Hum Genet. 2000 Mar;66(3):958-68. doi: 10.1086/302799. Am J Hum Genet. 2000. PMID: 10712210 Free PMC article.

9

An examination of the relationship between hotspots and recombination associated with chromosome 21 nondisjunction.

Oliver TR, Middlebrooks CD, Tinker SW, Allen EG, Bean LJ, Begum F, Feingold E, Chowdhury R, Cheung V, Sherman SL. Oliver TR, et al. Among authors: sherman sl. PLoS One. 2014 Jun 13;9(6):e99560. doi: 10.1371/journal.pone.0099560. eCollection 2014. PLoS One. 2014. PMID: 24926858 Free PMC article.

10

Genome-Wide Association Study of Meiotic Recombination Phenotypes.

Begum F, Chowdhury R, Cheung VG, Sherman SL, Feingold E. Begum F, et al. Among authors: sherman sl. G3 (Bethesda). 2016 Dec 7;6(12):3995-4007. doi: 10.1534/g3.116.035766. G3 (Bethesda). 2016. PMID: 27733454 Free PMC article.

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