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21 results

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Page 1
Adaptive evolution of pelvic reduction in sticklebacks by recurrent deletion of a Pitx1 enhancer.
Chan YF, Marks ME, Jones FC, Villarreal G Jr, Shapiro MD, Brady SD, Southwick AM, Absher DM, Grimwood J, Schmutz J, Myers RM, Petrov D, Jónsson B, Schluter D, Bell MA, Kingsley DM. Chan YF, et al. Among authors: southwick am. Science. 2010 Jan 15;327(5963):302-5. doi: 10.1126/science.1182213. Epub 2009 Dec 10. Science. 2010. PMID: 20007865 Free PMC article.
Susceptibility locus for clinical and subclinical coronary artery disease at chromosome 9p21 in the multi-ethnic ADVANCE study.
Assimes TL, Knowles JW, Basu A, Iribarren C, Southwick A, Tang H, Absher D, Li J, Fair JM, Rubin GD, Sidney S, Fortmann SP, Go AS, Hlatky MA, Myers RM, Risch N, Quertermous T. Assimes TL, et al. Hum Mol Genet. 2008 Aug 1;17(15):2320-8. doi: 10.1093/hmg/ddn132. Epub 2008 Apr 28. Hum Mol Genet. 2008. PMID: 18443000 Free PMC article.
Characterizing the admixed African ancestry of African Americans.
Zakharia F, Basu A, Absher D, Assimes TL, Go AS, Hlatky MA, Iribarren C, Knowles JW, Li J, Narasimhan B, Sidney S, Southwick A, Myers RM, Quertermous T, Risch N, Tang H. Zakharia F, et al. Genome Biol. 2009;10(12):R141. doi: 10.1186/gb-2009-10-12-r141. Epub 2009 Dec 22. Genome Biol. 2009. PMID: 20025784 Free PMC article.
Genome-wide association and meta-analysis of bipolar disorder in individuals of European ancestry.
Scott LJ, Muglia P, Kong XQ, Guan W, Flickinger M, Upmanyu R, Tozzi F, Li JZ, Burmeister M, Absher D, Thompson RC, Francks C, Meng F, Antoniades A, Southwick AM, Schatzberg AF, Bunney WE, Barchas JD, Jones EG, Day R, Matthews K, McGuffin P, Strauss JS, Kennedy JL, Middleton L, Roses AD, Watson SJ, Vincent JB, Myers RM, Farmer AE, Akil H, Burns DK, Boehnke M. Scott LJ, et al. Among authors: southwick am. Proc Natl Acad Sci U S A. 2009 May 5;106(18):7501-6. doi: 10.1073/pnas.0813386106. Epub 2009 Apr 28. Proc Natl Acad Sci U S A. 2009. PMID: 19416921 Free PMC article.
A near null variant of 12/15-LOX encoded by a novel SNP in ALOX15 and the risk of coronary artery disease.
Assimes TL, Knowles JW, Priest JR, Basu A, Borchert A, Volcik KA, Grove ML, Tabor HK, Southwick A, Tabibiazar R, Sidney S, Boerwinkle E, Go AS, Iribarren C, Hlatky MA, Fortmann SP, Myers RM, Kuhn H, Risch N, Quertermous T. Assimes TL, et al. Atherosclerosis. 2008 May;198(1):136-44. doi: 10.1016/j.atherosclerosis.2007.09.003. Epub 2007 Oct 23. Atherosclerosis. 2008. PMID: 17959182 Free PMC article.
Matrix metalloproteinase circulating levels, genetic polymorphisms, and susceptibility to acute myocardial infarction among patients with coronary artery disease.
Hlatky MA, Ashley E, Quertermous T, Boothroyd DB, Ridker P, Southwick A, Myers RM, Iribarren C, Fortmann SP, Go AS; Atherosclerotic Disease, Vascular Function and Genetic Epidemiology (ADVANCE) Study. Hlatky MA, et al. Am Heart J. 2007 Dec;154(6):1043-51. doi: 10.1016/j.ahj.2007.06.042. Am Heart J. 2007. PMID: 18035073
21 results