Resultados de búsqueda - Anders Berg Jørgensen
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Exome sequencing identifies rare LDLR and APOA5 alleles conferring risk for myocardial infarction por Ron Do, Nathan O. Stitziel, Hong‐Hee Won, Anders Berg Jørgensen, Stefano Duga, Pier Angelica Merlini, Adam Kieżun, Martin Farrall, Anuj Goel, Or Zuk, I. Guella, Rosanna Asselta, Leslie A. Lange, Gina M. Peloso, Paul L. Auer, Domenico Girelli, Nicola Martinelli, Deborah Farlow, Mark A. DePristo, Robert Roberts, Alexandre F.R. Stewart, Danish Saleheen, John Danesh, Stephen E. Epstein, Suthesh Sivapalaratnam, G. Kees Hovingh, John J.P. Kastelein, Nilesh J. Samani, Heribert Schunkert, Jeanette Erdmann, Svati H. Shah, William E. Kraus, R. W. Davies, Majid Nikpay, Christopher T. Johansen, Jian Wang, Robert A. Hegele, Eliana Hechter, Winfried März, Marcus E. Kleber, Jie Huang, Andrew D. Johnson, Mingyao Li, Greg Burke, Myron D. Gross, Yongmei Liu, Themistocles L. Assimes, Gerardo Heiss, Ethan M. Lange, Aaron R. Folsom, Herman A. Taylor, Oliviero Olivieri, Anders Hamsten, Robert Clarke, Dermot F. Reilly, Yin Wu, Manuel A. Rivas, Peter Donnelly, Jacques E. Rossouw, Bruce M. Psaty, David M. Herrington, James G. Wilson, Stephen S. Rich, Michael J. Bamshad, Russell P. Tracy, L. Adrienne Cupples, Daniel J. Rader, Muredach P. Reilly, John A. Spertus, Sharon Cresci, Jaana Hartiala, W.H. Wilson Tang, Stanley L. Hazen, Hooman Allayee, Alex P. Reiner, Christopher S. Carlson, Charles Kooperberg, Rebecca D. Jackson, Eric Boerwinkle, Eric S. Lander, Stephen M. Schwartz, David S. Siscovick, Ruth McPherson, Anne Tybjærg‐Hansen, Gonçalo R. Abecasis, Hugh Watkins, Deborah A. Nickerson, Diego Ardissino, Shamil Sunyaev, Christopher J. O’Donnell, David Altshuler, Stacey Gabriel, Sekar Kathiresan
Publicado 2014Artigo
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Materias Relacionadas
Apolipoprotein B
Biology
Cholesterol
Environmental health
Internal medicine
Medicine
Population
Allele
Bioinformatics
Cardiology
Disease
Endocrinology
Exome
Exome sequencing
Familial hypercholesterolemia
Gene
Genetics
Ischemia
Ischemic stroke
LDL receptor
Lipoprotein
Mutation
Myocardial infarction
PCSK9
Vascular disease