Center-Authored Papers

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Howson JMM, Zhao W, Barnes DR, Ho W-K, Young R, Paul DS, Waite LL, Freitag DF, Fauman EB, Salfati EL et al..  2017.  Fifteen new risk loci for coronary artery disease highlight arterial-wall-specific mechanisms.. Nature genetics. Abstract
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Marouli E, Graff M, Medina-Gomez C, Lo KS, Wood AR, Kjaer TR, Fine RS, Lu Y, Schurmann C, Highland HM et al..  2017.  Rare and low-frequency coding variants alter human adult height.. Nature. 542(7640):186-190. Abstract
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Schmidt AF, Swerdlow DI, Holmes MV, Patel RS, Fairhurst-Hunter Z, Lyall DM, Hartwig FP, Horta BL, Hyppönen E, Power C et al..  2016.  PCSK9 genetic variants and risk of type 2 diabetes: a mendelian randomisation study.. The lancet. Diabetes & endocrinology. Abstract
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Webb TR, Erdmann J, Stirrups KE, Stitziel NO, Masca NGD, Jansen H, Kanoni S, Nelson CP, Ferrario PG, König IR et al..  2017.  Systematic Evaluation of Pleiotropy Identifies 6 Further Loci Associated With Coronary Artery Disease.. Journal of the American College of Cardiology. 69(7):823-836. Abstract