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Consortia

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  • The copy number variation and stroke (CaNVAS) risk and outcome study

    John W. Cole, Taiwo Adigun, Rufus Akinyemi, Onoja Matthew Akpa, Steven Bell, Bowang Chen, Jordi Jimenez Conde, Uxue Lazcano Dobao, Israel Fernandez, Myriam Fornage, Cristina Gallego-Fabrega, Christina Jern, Michael Krawczak, Arne Lindgren, Hugh S. Markus, Olle Melander, Mayowa Owolabi, Kristina Schlicht, Martin Söderholm, Vinodh Srinivasasainagendra, Carolina Soriano Tárraga, Martin Stenman, Hemant Tiwari, Margaret Corasaniti, Natalie Fecteau, Beth Guizzardi, Haley Lopez, Kevin Nguyen, Brady Gaynor, Timothy O’Connor, O. Colin Stine, Steven J. Kittner, Patrick McArdle, Braxton D. Mitchell, Huichun Xu, Caspar Grond-Ginsbach

    published 19 Apr 2021

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  • Detecting SARS-CoV-2 variants with SNP genotyping

    Helen Harper, Amanda Burridge, Mark Winfield, Adam Finn, Andrew Davidson, David Matthews, Stephanie Hutchings, Barry Vipond, Nisha Jain, The COVID-19 Genomics UK (COG-UK) Consortium , Keith Edwards, Gary Barker

    published 24 Feb 2021

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  • Genetic loci associated with prevalent and incident myocardial infarction and coronary heart disease in the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium

    Julie Hahn, Yi-Ping Fu, Michael R. Brown, Joshua C. Bis, Paul S. de Vries, Mary F. Feitosa, Lisa R. Yanek, Stefan Weiss, Franco Giulianini, Albert Vernon Smith, Xiuqing Guo, Traci M. Bartz, Diane M. Becker, Lewis C. Becker, Eric Boerwinkle, Jennifer A. Brody, Yii-Der Ida Chen, Oscar H. Franco, Megan Grove, Tamara B. Harris, Albert Hofman, Shih-Jen Hwang, Brian G. Kral, Lenore J. Launer, Marcello R. P. Markus, Kenneth M. Rice, Stephen S. Rich, Paul M. Ridker, Fernando Rivadeneira, Jerome I. Rotter, Nona Sotoodehnia, Kent D. Taylor, André G. Uitterlinden, Uwe Völker, Henry Völzke, Jie Yao, Daniel I. Chasman, Marcus Dörr, Vilmundur Gudnason, Rasika A. Mathias, Wendy Post, Bruce M. Psaty, Abbas Dehghan, Christopher J. O’Donnell, Alanna C. Morrison

    published 13 Nov 2020

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