Year: 2018
Type: article
Source: Nature
Authors: Benjamin B. Sun, Joseph C. Maranville, James E. Peters, David Stacey, James R. Staley, James Blackshaw, Stephen Burgess, Tao Jiang, Ellie Paige, Praveen Surendran, Clare Oliver-Williams, Mihir A. Kamat, Bram P. Prins, Sheri K. Wilcox, Erik S. Zimmerman, An Chi, Narinder Bansal, Sarah L. Spain, Angela M. Wood, Nicholas W. Morrell, John R. Bradley, Nebojsa Janjic, David J. Roberts, Willem H. Ouwehand, John A. Todd, Nicole Soranzo, Karsten Suhre, Dirk S. Paul, Caroline S. Fox, Robert M. Plenge, John Danesh, Heiko Runz, Adam S. Butterworth
Institutions: University of Cambridge, Merck & Co., Inc., Rahway, NJ, USA (United States), British Heart Foundation, Addenbrooke's Hospital, MRC Biostatistics Unit, Australian National University, SomaLogic (United States), University of Bristol, Wellcome Sanger Institute, NIHR Cambridge Biomedical Research Centre, National Health Service, Churchill Hospital, John Radcliffe Hospital, University of Oxford, NIHR Oxford Biomedical Research Centre, NHS Blood and Transplant, National Institute for Health and Care Research, Centre for Human Genetics, Weill Cornell Medical College in Qatar, Weill Cornell Medicine, Biogen (United States)
Language: English
Subfield: Genetics
Domain: Life Sciences
Open Access status: green
Funders: Qatar Foundation, NHS Blood and Transplant, Wellcome Trust, National Institute for Health and Care Research, British Heart Foundation, European Commission, University of Sheffield, Cambridge University Hospitals, Weill Cornell Medical College, Weill Cornell Medicine - Qatar, Medical Research Council, NIHR Cambridge Biomedical Research Centre, National Institute of Neurological Disorders and Stroke
Awards: Genetics and causality: towards more accessible and more reliable Mendelian randomization investigations, G1332667197, G1359875377, Institutional Strategic Support Fund PHASE 2 FY2014/16, NIHR Senior Investigator Award, NIHR Senior Investigator Award, G2050459141, Identification of epigenetic markers underlying increased risk of T2D in South Asians, Collaborative pooled analysis of data on C-reactive protein gene variants and coronary disease, G2325242462, G2474488143, Institutional Strategic Support Fund PHASE 2 FY2014/16, NIHR Senior Investigator Award, Diabetes and Inflammation Laboratory., G2804450655, A BLUEPRINT of Haematopoietic Epigenomes, G3217060148, NIHR Senior Investigator Award, Epigenetics towards systems biology, G385907487, G4073969003, G4194769985, G4211044638, Investigation of gene-lifestyle interactions on risk of confirmed first-ever myocardial infarction in South Asians: a genome-wide association study in a Pakistani population., G4584873075, G4612446324, G5133619070, Large-scale studies of metabolic risk factors in coronary heart disease, G5572759459, G5618924097, G567453067, G587296758, DTG 2013 & 2014, G6467398148, Establishment of a bioresource for discovery and evaluation of genetic and other, EPIC-CVD: Individualised CVD risk assessment: tailoring targeted and cost-effective approaches to Europe's diverse populations, G6564977220, G6654704239, G6991716568, G6995430370, The BHF Chair of Epidemiology and Medicine, Large-scale integrative studies of risk factors in coronary heart disease: from discovery to application (renewal). (Joint funding with MRC), National Cohort Study of Heritable Pulmonary Arterial Hypertension, G7644601275, Using genetics to explore the pathophysiology of cerebral small vessel disease. 15, G7992221752, Research Excellence, G804990870, G8197964739, G8346449347, G8491121283, G8538723892, G8585681489, G8881768140
OpenAlex ID: W2805712258