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Signals of recent positive selection in a worldwide sample of human populations.
Pickrell JK, Coop G, Novembre J, Kudaravalli S, Li JZ, Absher D, Srinivasan BS, Barsh GS, Myers RM, Feldman MW, Pritchard JK. Pickrell JK, et al. Among authors: barsh gs. Genome Res. 2009 May;19(5):826-37. doi: 10.1101/gr.087577.108. Epub 2009 Mar 23. Genome Res. 2009. PMID: 19307593 Free PMC article.
Digital gene expression for non-model organisms.
Hong LZ, Li J, Schmidt-Küntzel A, Warren WC, Barsh GS. Hong LZ, et al. Among authors: barsh gs. Genome Res. 2011 Nov;21(11):1905-15. doi: 10.1101/gr.122135.111. Epub 2011 Aug 15. Genome Res. 2011. PMID: 21844123 Free PMC article.
David R. Cox 1946-2013.
Barsh GS, Myers RM. Barsh GS, et al. Nat Genet. 2013 Jul;45(7):716. doi: 10.1038/ng.2679. Nat Genet. 2013. PMID: 23800862 No abstract available.
Ribosomal mutations cause p53-mediated dark skin and pleiotropic effects.
McGowan KA, Li JZ, Park CY, Beaudry V, Tabor HK, Sabnis AJ, Zhang W, Fuchs H, de Angelis MH, Myers RM, Attardi LD, Barsh GS. McGowan KA, et al. Among authors: barsh gs. Nat Genet. 2008 Aug;40(8):963-70. doi: 10.1038/ng.188. Epub 2008 Jul 20. Nat Genet. 2008. PMID: 18641651 Free PMC article.
Aberrant Inclusion of a Poison Exon Causes Dravet Syndrome and Related SCN1A-Associated Genetic Epilepsies.
Carvill GL, Engel KL, Ramamurthy A, Cochran JN, Roovers J, Stamberger H, Lim N, Schneider AL, Hollingsworth G, Holder DH, Regan BM, Lawlor J, Lagae L, Ceulemans B, Bebin EM, Nguyen J; EuroEPINOMICS Rare Epilepsy Syndrome, Myoclonic-Astatic Epilepsy, and Dravet Working Group; Barsh GS, Weckhuysen S, Meisler M, Berkovic SF, De Jonghe P, Scheffer IE, Myers RM, Cooper GM, Mefford HC. Carvill GL, et al. Among authors: barsh gs. Am J Hum Genet. 2018 Dec 6;103(6):1022-1029. doi: 10.1016/j.ajhg.2018.10.023. Am J Hum Genet. 2018. PMID: 30526861 Free PMC article.
Genetic architecture of skin and eye color in an African-European admixed population.
Beleza S, Johnson NA, Candille SI, Absher DM, Coram MA, Lopes J, Campos J, Araújo II, Anderson TM, Vilhjálmsson BJ, Nordborg M, Correia E Silva A, Shriver MD, Rocha J, Barsh GS, Tang H. Beleza S, et al. Among authors: barsh gs. PLoS Genet. 2013 Mar;9(3):e1003372. doi: 10.1371/journal.pgen.1003372. Epub 2013 Mar 21. PLoS Genet. 2013. PMID: 23555287 Free PMC article.
Genomic diagnosis for children with intellectual disability and/or developmental delay.
Bowling KM, Thompson ML, Amaral MD, Finnila CR, Hiatt SM, Engel KL, Cochran JN, Brothers KB, East KM, Gray DE, Kelley WV, Lamb NE, Lose EJ, Rich CA, Simmons S, Whittle JS, Weaver BT, Nesmith AS, Myers RM, Barsh GS, Bebin EM, Cooper GM. Bowling KM, et al. Among authors: barsh gs. Genome Med. 2017 May 30;9(1):43. doi: 10.1186/s13073-017-0433-1. Genome Med. 2017. PMID: 28554332 Free PMC article.
Modeling 3D facial shape from DNA.
Claes P, Liberton DK, Daniels K, Rosana KM, Quillen EE, Pearson LN, McEvoy B, Bauchet M, Zaidi AA, Yao W, Tang H, Barsh GS, Absher DM, Puts DA, Rocha J, Beleza S, Pereira RW, Baynam G, Suetens P, Vandermeulen D, Wagner JK, Boster JS, Shriver MD. Claes P, et al. Among authors: barsh gs. PLoS Genet. 2014 Mar 20;10(3):e1004224. doi: 10.1371/journal.pgen.1004224. eCollection 2014 Mar. PLoS Genet. 2014. PMID: 24651127 Free PMC article.
281 results