Common and rare genetic variation in CCR2, CCR5, or CX3CR1 and risk of atherosclerotic coronary heart disease and glucometabolic traits
Jessica R. Golbus, Nathan O. Stitziel, Wei Zhao, Chenyi Xue, Martin Farrall, Ruth Mcpherson, Jeanette Erdmann, Panos Deloukas, Hugh Watkins, Heribert Schunkert, Nilesh J. Samani, Danish Saleheen, Sekar Kathiresan, Muredach P. Reilly*
*Korrespondierende/r Autor/-in für diese Arbeit
- University of Pennsylvania
- Washington University in St. Louis
- Biostatistics and Epidemiology
- Oxford University Hospitals NHS Foundation Trust
- Wellcome Trust Centre for Human Genetics
- University of Ottawa
- Queen Mary University of London
- University of Leicester
- Center for Human Genetic Research
- Harvard University
- Broad Institute
- Columbia University in the City of New York
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