Center-Authored Papers

Filters: Author is Voight, Benjamin F  [Clear All Filters]
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Wild PS, Zeller T, Schillert A, Szymczak S, Sinning CR, Deiseroth A, Schnabel RB, Lubos E, Keller T, Eleftheriadis MS et al..  2011.  A Genome-Wide Association Study Identifies LIPA as a Susceptibility Gene for Coronary Artery Disease.. Circulation. Cardiovascular genetics. 4(4):403-12. Abstract
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Soranzo N, Spector TD, Mangino M, Kühnel B, Rendon A, Teumer A, Willenborg C, Wright B, Chen L, Li M et al..  2009.  A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium.. Nature genetics. 41(11):1182-90. Abstract
Saxena R, Elbers CC, Guo Y, Peter I, Gaunt TR, Mega JL, Lanktree MB, Tare A, Castillo BA, Li YR et al..  2012.  Large-scale gene-centric meta-analysis across 39 studies identifies type 2 diabetes loci.. American journal of human genetics. 90(3):410-25. Abstract
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O'Donnell CJ, Kavousi M, Smith AV, Kardia SLR, Feitosa MF, Hwang S-J, Sun YV, Province MA, Aspelund T, Dehghan A et al..  2011.  Genome-Wide Association Study for Coronary Artery Calcification With Follow-Up in Myocardial Infarction.. Circulation. 124(25):2855-2864. Abstract
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Kraja AT, Chasman DI, North KE, Reiner AP, Yanek LR, Kilpeläinen TO, Smith JA, Dehghan A, Dupuis J, Johnson AD et al..  2014.  Pleiotropic genes for metabolic syndrome and inflammation.. Molecular genetics and metabolism. Abstract
Kathiresan S, Voight BF, Purcell S, Musunuru K, Ardissino D, Mannucci PM, Anand S, Engert JC, Samani NJ, Schunkert H et al..  2009.  Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants.. Nature genetics. 41(3):334-41. Abstract
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Johansen CT, Wang J, Lanktree MB, McIntyre AD, Ban MR, Martins RA, Kennedy BA, Hassell RG, Visser ME, Schwartz SM et al..  2011.  An increased burden of common and rare lipid-associated risk alleles contributes to the phenotypic spectrum of hypertriglyceridemia.. Arteriosclerosis, thrombosis, and vascular biology. 31(8):1916-26. Abstract
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Fuchsberger C, Flannick J, Teslovich TM, Mahajan A, Agarwala V, Gaulton KJ, Ma C, Fontanillas P, Moutsianas L, McCarthy DJ et al..  2016.  The genetic architecture of type 2 diabetes.. Nature. 536(7614):41-7. Abstract
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Erdmann J, Grosshennig A, Braund PS, König IR, Hengstenberg C, Hall AS, Linsel-Nitschke P, Kathiresan S, Wright B, Trégouët D-A et al..  2009.  New susceptibility locus for coronary artery disease on chromosome 3q22.3.. Nature genetics. 41(3):280-2. Abstract
Ehret GB, Munroe PB, Rice KM, Bochud M, Johnson AD, Chasman DI, Smith AV, Tobin MD, Verwoert GC, Hwang S-J et al..  2011.  Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk.. Nature. 478(7367):103-9. Abstract
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Buyske S, Wu Y, Carty CL, Cheng I, Assimes TL, Dumitrescu L, Hindorff LA, Mitchell S, Ambite JL, Boerwinkle E et al..  2012.  Evaluation of the metabochip genotyping array in African Americans and implications for fine mapping of GWAS-identified loci: the PAGE study.. PloS one. 7(4):e35651. Abstract
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Assimes TL, Hólm H, Kathiresan S, Reilly MP, Thorleifsson G, Voight BF, Erdmann J, Willenborg C, Vaidya D, Xie C et al..  2010.  Lack of association between the Trp719Arg polymorphism in kinesin-like protein-6 and coronary artery disease in 19 case-control studies.. Journal of the American College of Cardiology. 56(19):1552-63. Abstract