Center-Authored Papers

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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
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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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Shungin D, Winkler TW, Croteau-Chonka DC, Ferreira T, Locke AE, Mägi R, Strawbridge RJ, Pers TH, Fischer K, Justice AE et al..  2015.  New genetic loci link adipose and insulin biology to body fat distribution.. Nature. 518(7538):187-96. Abstract
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Sabater-Lleal M, Huang J, Chasman D, Naitza S, Dehghan A, Johnson AD, Teumer A, Reiner AP, Folkersen L, Basu S et al..  2013.  Multiethnic meta-analysis of genome-wide association studies in >100 000 subjects identifies 23 fibrinogen-associated Loci but no strong evidence of a causal association between circulating fibrinogen and cardiovascular disease.. Circulation. 128(12):1310-24. Abstract
Lanktree MB, Guo Y, Murtaza M, Glessner JT, Bailey SD, Onland-Moret CN, Lettre G, Ongen H, Rajagopalan R, Johnson T et al..  2011.  Meta-analysis of Dense Genecentric Association Studies Reveals Common and Uncommon Variants Associated with Height.. American journal of human genetics. 88(1):6-18. Abstract
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Malik R, Traylor M, Pulit SL, Bevan S, Hopewell JC, Holliday EG, Zhao W, Abrantes P, Amouyel P, Attia JR et al..  2016.  Low-frequency and common genetic variation in ischemic stroke: The METASTROKE collaboration.. Neurology. 86(13):1217-26. 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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Stitziel NO, Won H-H, Morrison AC, Peloso GM, Do R, Lange LA, Fontanillas P, Gupta N, Duga S, Goel A et al..  2014.  Inactivating mutations in NPC1L1 and protection from coronary heart disease.. The New England journal of medicine. 371(22):2072-82. Abstract
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Huang J, Sabater-Lleal M, Asselbergs FW, Tregouet D, Shin S-Y, Ding J, Baumert J, Oudot-Mellakh T, Folkersen L, Johnson AD et al..  2012.  Genome-wide association study for circulating levels of plasminogen activator inhibitor-1 (PAI-1) provides novel insights into the regulation of PAI-1.. Blood. 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
Locke AE, Kahali B, Berndt SI, Justice AE, Pers TH, Day FR, Powell C, Vedantam S, Buchkovich ML, Yang J et al..  2015.  Genetic studies of body mass index yield new insights for obesity biology.. Nature. 518(7538):197-206. Abstract
Traylor M, Farrall M, Holliday EG, Sudlow C, Hopewell JC, Cheng Y-C, Fornage M, Ikram AM, Malik R, Bevan S et al..  2012.  Genetic risk factors for ischaemic stroke and its subtypes (the METASTROKE Collaboration): a meta-analysis of genome-wide association studies.. Lancet neurology. 11(11):951-962. Abstract
Manichaikul A, Wang X-Q, Zhao W, Wojczynski MK, Siebenthall K, Stamatoyannopoulos JA, Saleheen D, Borecki IB, Reilly MP, Rich SS et al..  2016.  Genetic association of long-chain acyl-CoA synthetase 1 variants with fasting glucose, diabetes, and subclinical atherosclerosis.. Journal of lipid research. 57(3):433-42. Abstract
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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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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Do R, Stitziel NO, Won H-H, Jørgensen AB, Duga S, Merlini PA, Kiezun A, Farrall M, Goel A, Zuk O et al..  2015.  Exome sequencing identifies rare LDLR and APOA5 alleles conferring risk for myocardial infarction.. Nature. 518(7537):102-6. Abstract
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Wood AR, Esko T, Yang J, Vedantam S, Pers TH, Gustafsson S, Chu AY, Estrada K, Luan J'an, Kutalik Z et al..  2014.  Defining the role of common variation in the genomic and biological architecture of adult human height.. Nature genetics. 46(11):1173-86. Abstract