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GEneSTATION 1.0: a synthetic resource of diverse evolutionary and functional genomic data for studying the evolution of pregnancy-associated tissues and phenotypes.
Kim M, Cooper BA, Venkat R, Phillips JB, Eidem HR, Hirbo J, Nutakki S, Williams SM, Muglia LJ, Capra JA, Petren K, Abbot P, Rokas A, McGary KL. Kim M, et al. Among authors: williams sm. Nucleic Acids Res. 2016 Jan 4;44(D1):D908-16. doi: 10.1093/nar/gkv1137. Epub 2015 Nov 14. Nucleic Acids Res. 2016. PMID: 26567549 Free PMC article.
Putting pleiotropy and selection into context defines a new paradigm for interpreting genetic data.
Predazzi IM, Rokas A, Deinard A, Schnetz-Boutaud N, Williams ND, Bush WS, Tacconelli A, Friedrich K, Fazio S, Novelli G, Haines JL, Sirugo G, Williams SM. Predazzi IM, et al. Among authors: williams nd, williams sm. Circ Cardiovasc Genet. 2013 Jun;6(3):299-307. doi: 10.1161/CIRCGENETICS.113.000126. Epub 2013 Apr 24. Circ Cardiovasc Genet. 2013. PMID: 23616601 Free PMC article.
Recurrent tissue-specific mtDNA mutations are common in humans.
Samuels DC, Li C, Li B, Song Z, Torstenson E, Boyd Clay H, Rokas A, Thornton-Wells TA, Moore JH, Hughes TM, Hoffman RD, Haines JL, Murdock DG, Mortlock DP, Williams SM. Samuels DC, et al. Among authors: williams sm. PLoS Genet. 2013 Nov;9(11):e1003929. doi: 10.1371/journal.pgen.1003929. Epub 2013 Nov 7. PLoS Genet. 2013. PMID: 24244193 Free PMC article.
Evolutionarily derived networks to inform disease pathways.
Graham BE, Darabos C, Huang M, Muglia LJ, Moore JH, Williams SM. Graham BE, et al. Among authors: williams sm. Genet Epidemiol. 2017 Dec;41(8):866-875. doi: 10.1002/gepi.22078. Epub 2017 Sep 25. Genet Epidemiol. 2017. PMID: 28944497 Free PMC article.
Whole exome sequencing reveals HSPA1L as a genetic risk factor for spontaneous preterm birth.
Huusko JM, Karjalainen MK, Graham BE, Zhang G, Farrow EG, Miller NA, Jacobsson B, Eidem HR, Murray JC, Bedell B, Breheny P, Brown NW, Bødker FL, Litterman NK, Jiang PP, Russell L, Hinds DA, Hu Y; 23andMe Research Team; Rokas A, Teramo K, Christensen K, Williams SM, Rämet M, Kingsmore SF, Ryckman KK, Hallman M, Muglia LJ. Huusko JM, et al. Among authors: williams sm. PLoS Genet. 2018 Jul 12;14(7):e1007394. doi: 10.1371/journal.pgen.1007394. eCollection 2018 Jul. PLoS Genet. 2018. PMID: 30001343 Free PMC article.
Correction: Whole exome sequencing reveals HSPA1L as a genetic risk factor for spontaneous preterm birth.
Huusko JM, Karjalainen MK, Graham BE, Zhang G, Farrow EG, Miller NA, Jacobsson B, Eidem HR, Murray JC, Bedell B, Breheny P, Brown NW, Bødker FL, Litterman NK, Jiang PP, Russell L, Hinds DA, Hu Y; 23andMe Research Team; Rokas A, Teramo K, Christensen K, Williams SM, Rämet M, Kingsmore SF, Ryckman KK, Hallman M, Muglia LJ. Huusko JM, et al. Among authors: williams sm. PLoS Genet. 2018 Sep 13;14(9):e1007673. doi: 10.1371/journal.pgen.1007673. eCollection 2018 Sep. PLoS Genet. 2018. PMID: 30212495 Free PMC article.
Dissecting maternal and fetal genetic effects underlying the associations between maternal phenotypes, birth outcomes, and adult phenotypes: A mendelian-randomization and haplotype-based genetic score analysis in 10,734 mother-infant pairs.
Chen J, Bacelis J, Sole-Navais P, Srivastava A, Juodakis J, Rouse A, Hallman M, Teramo K, Melbye M, Feenstra B, Freathy RM, Smith GD, Lawlor DA, Murray JC, Williams SM, Jacobsson B, Muglia LJ, Zhang G. Chen J, et al. Among authors: williams sm. PLoS Med. 2020 Aug 25;17(8):e1003305. doi: 10.1371/journal.pmed.1003305. eCollection 2020 Aug. PLoS Med. 2020. PMID: 32841251 Free PMC article.
910 results