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In search for genetic determinants of clinically meaningful differential cardiovascular event reduction by pravastatin in the PHArmacogenetic study of Statins in the Elderly at risk (PHASE)/PROSPER study.
Postmus I, Johnson PC, Trompet S, de Craen AJ, Slagboom PE, Devlin JJ, Shiffman D, Sacks FM, Kearney PM, Stott DJ, Buckley BM, Sattar N, Ford I, Westendorp RG, Jukema JW. Postmus I, et al. Among authors: devlin jj. Atherosclerosis. 2014 Jul;235(1):58-64. doi: 10.1016/j.atherosclerosis.2014.04.009. Epub 2014 Apr 26. Atherosclerosis. 2014. PMID: 24816038 Clinical Trial.
Genome-wide study of gene variants associated with differential cardiovascular event reduction by pravastatin therapy.
Shiffman D, Trompet S, Louie JZ, Rowland CM, Catanese JJ, Iakoubova OA, Kirchgessner TG, Westendorp RG, de Craen AJ, Slagboom PE, Buckley BM, Stott DJ, Sattar N, Devlin JJ, Packard CJ, Ford I, Sacks FM, Jukema JW. Shiffman D, et al. Among authors: devlin jj. PLoS One. 2012;7(5):e38240. doi: 10.1371/journal.pone.0038240. Epub 2012 May 30. PLoS One. 2012. PMID: 22666496 Free PMC article. Clinical Trial.
Genetic variants in the KIF6 region and coronary event reduction from statin therapy.
Li Y, Sabatine MS, Tong CH, Ford I, Kirchgessner TG, Packard CJ, Robertson M, Rowland CM, Bare LA, Shepherd J, Devlin JJ, Iakoubova OA. Li Y, et al. Among authors: devlin jj. Hum Genet. 2011 Jan;129(1):17-23. doi: 10.1007/s00439-010-0892-6. Epub 2010 Oct 1. Hum Genet. 2011. PMID: 20886236 Free PMC article.
Evaluation of the paraoxonases as candidate genes for stroke: Gln192Arg polymorphism in the paraoxonase 1 gene is associated with increased risk of stroke.
Ranade K, Kirchgessner TG, Iakoubova OA, Devlin JJ, DelMonte T, Vishnupad P, Hui L, Tsuchihashi Z, Sacks FM, Sabatine MS, Braunwald E, White TJ, Shaw PM, Dracopoli NC. Ranade K, et al. Among authors: devlin jj. Stroke. 2005 Nov;36(11):2346-50. doi: 10.1161/01.STR.0000185703.88944.7d. Epub 2005 Oct 20. Stroke. 2005. PMID: 16239632
Genetic variations associated with recurrent venous thrombosis.
van Hylckama Vlieg A, Flinterman LE, Bare LA, Cannegieter SC, Reitsma PH, Arellano AR, Tong CH, Devlin JJ, Rosendaal FR. van Hylckama Vlieg A, et al. Among authors: devlin jj. Circ Cardiovasc Genet. 2014 Dec;7(6):806-13. doi: 10.1161/CIRCGENETICS.114.000682. Epub 2014 Sep 10. Circ Cardiovasc Genet. 2014. PMID: 25210051
Genetic risk, coronary heart disease events, and the clinical benefit of statin therapy: an analysis of primary and secondary prevention trials.
Mega JL, Stitziel NO, Smith JG, Chasman DI, Caulfield M, Devlin JJ, Nordio F, Hyde C, Cannon CP, Sacks F, Poulter N, Sever P, Ridker PM, Braunwald E, Melander O, Kathiresan S, Sabatine MS. Mega JL, et al. Among authors: devlin jj. Lancet. 2015 Jun 6;385(9984):2264-2271. doi: 10.1016/S0140-6736(14)61730-X. Epub 2015 Mar 4. Lancet. 2015. PMID: 25748612 Free PMC article.
Association of the Trp719Arg polymorphism in kinesin-like protein 6 with myocardial infarction and coronary heart disease in 2 prospective trials: the CARE and WOSCOPS trials.
Iakoubova OA, Tong CH, Rowland CM, Kirchgessner TG, Young BA, Arellano AR, Shiffman D, Sabatine MS, Campos H, Packard CJ, Pfeffer MA, White TJ, Braunwald E, Shepherd J, Devlin JJ, Sacks FM. Iakoubova OA, et al. Among authors: devlin jj. J Am Coll Cardiol. 2008 Jan 29;51(4):435-43. doi: 10.1016/j.jacc.2007.05.057. J Am Coll Cardiol. 2008. PMID: 18222353 Free article.
118 results