Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Emelia J. Benjamin"'
Autor:
Lu-Chen Weng, Nona Sotoodehnia, Deborah A. Nickerson, Honghuang Lin, Donna M. Muzny, Elsayed Z. Soliman, Marco V Perez, Eric Boerwinkle, Steven A. Lubitz, Dan E. Arking, Emelia J. Benjamin, Nathan A. Bihlmeyer, Alvaro Alonso, Susan R. Heckbert, Joshua C. Bis, Ingrid E. Christophersen, L. Adrienne Cupples, Carolina Roselli, Kathryn L. Lunetta, Bruce M. Psaty, Patrick T. Ellinor, Jennifer A. Brody, Richard A. Gibbs, Peter J. Mohler
Publikováno v:
PLoS Genetics, Vol 12, Iss 9, p e1006284 (2016)
PLoS Genetics
PLoS Genetics
Atrial fibrillation (AF) is a morbid and heritable arrhythmia. Over 35 genes have been reported to underlie AF, most of which were described in small candidate gene association studies. Replication remains lacking for most, and therefore the contribu
Autor:
Brian E. Henderson, Hooman Allayee, Stanley L. Hazen, Myriam Fornage, Terrence Forrester, George J. Papanicolaou, Atif Qasim, Ervin R. Fox, Al Dreisbach, Thomas H. Mosley, Guillaume Lettre, Joel N. Hirschhorn, Stephen S. Rich, Dina N. Paltoo, Eric Boerwinkle, Stephen B. Kritchevsky, Emelia J. Benjamin, Mingyao Li, W.H. Wilson Tang, David S. Siscovick, Christopher Newton-Cheh, Anne B. Newman, Bruce M. Psaty, Brendan J. Keating, James B. Meigs, Russell P. Tracy, Herman A. Taylor, Jerome I. Rotter, Rainford J. Wilks, Emma K. Larkin, Franklyn I. Bennett, Susan Redline, Muredach P. Reilly, Alexander P. Reiner, Aaron R. Folsom, Susan R. Heckbert, Christopher A. Haiman, Daniel J. Rader, Jaana Hartiala, Megan E. Rudock, Stacey Gabriel, Kevin M. Waters, Kenechi Ejebe, Nick Patterson, Peter Shrader, Donald W. Bowden, Colin A. McKenzie, Cameron D. Palmer, Wendy S. Post, Liming Qu, Yang A. Meng, Sekar Kathiresan, James G. Wilson, Ramachandran S. Vasan, Richard R. Fabsitz, Yongmei Liu, Aravinda Chakravarti, Taylor Young, Deborah N. Farlow, Tamara B. Harris
Publikováno v:
PLoS Genetics, Vol 7, Iss 2, p e1001300 (2011)
PLoS Genetics
PLoS Genetics
Coronary heart disease (CHD) is the leading cause of mortality in African Americans. To identify common genetic polymorphisms associated with CHD and its risk factors (LDL- and HDL-cholesterol (LDL-C and HDL-C), hypertension, smoking, and type-2 diab
Autor:
Steven A Lubitz, Jennifer A Brody, Nathan A Bihlmeyer, Carolina Roselli, Lu-Chen Weng, Ingrid E Christophersen, Alvaro Alonso, Eric Boerwinkle, Richard A Gibbs, Joshua C Bis, NHLBI GO Exome Sequencing Project, L Adrienne Cupples, Peter J Mohler, Deborah A Nickerson, Donna Muzny, Marco V Perez, Bruce M Psaty, Elsayed Z Soliman, Nona Sotoodehnia, Kathryn L Lunetta, Emelia J Benjamin, Susan R Heckbert, Dan E Arking, Patrick T Ellinor, Honghuang Lin
Publikováno v:
PLoS Genetics, Vol 12, Iss 9, p e1006284 (2016)
Atrial fibrillation (AF) is a morbid and heritable arrhythmia. Over 35 genes have been reported to underlie AF, most of which were described in small candidate gene association studies. Replication remains lacking for most, and therefore the contribu
Externí odkaz:
https://doaj.org/article/3d79ce45b97047b7a46d869eae4ff497
Autor:
Guillaume Paré, Paul M Ridker, Lynda Rose, Maja Barbalic, Josée Dupuis, Abbas Dehghan, Joshua C Bis, Emelia J Benjamin, Dov Shiffman, Alexander N Parker, Daniel I Chasman
Publikováno v:
PLoS Genetics, Vol 7, Iss 4, p e1001374 (2011)
Soluble ICAM-1 (sICAM-1) is an endothelium-derived inflammatory marker that has been associated with diverse conditions such as myocardial infarction, diabetes, stroke, and malaria. Despite evidence for a heritable component to sICAM-1 levels, few ge
Externí odkaz:
https://doaj.org/article/7cdf24c30b454875ab3a116610ae568b
Autor:
J Gustav Smith, Jared W Magnani, Cameron Palmer, Yan A Meng, Elsayed Z Soliman, Solomon K Musani, Kathleen F Kerr, Renate B Schnabel, Steven A Lubitz, Nona Sotoodehnia, Susan Redline, Arne Pfeufer, Martina Müller, Daniel S Evans, Michael A Nalls, Yongmei Liu, Anne B Newman, Alan B Zonderman, Michele K Evans, Rajat Deo, Patrick T Ellinor, Dina N Paltoo, Christopher Newton-Cheh, Emelia J Benjamin, Reena Mehra, Alvaro Alonso, Susan R Heckbert, Ervin R Fox, Candidate-gene Association Resource (CARe) Consortium
Publikováno v:
PLoS Genetics, Vol 7, Iss 2, p e1001304 (2011)
The PR interval on the electrocardiogram reflects atrial and atrioventricular nodal conduction time. The PR interval is heritable, provides important information about arrhythmia risk, and has been suggested to differ among human races. Genome-wide a
Externí odkaz:
https://doaj.org/article/916dd9b034a04cfab045fdad07271c1b
Autor:
Guillaume Lettre, Cameron D Palmer, Taylor Young, Kenechi G Ejebe, Hooman Allayee, Emelia J Benjamin, Franklyn Bennett, Donald W Bowden, Aravinda Chakravarti, Al Dreisbach, Deborah N Farlow, Aaron R Folsom, Myriam Fornage, Terrence Forrester, Ervin Fox, Christopher A Haiman, Jaana Hartiala, Tamara B Harris, Stanley L Hazen, Susan R Heckbert, Brian E Henderson, Joel N Hirschhorn, Brendan J Keating, Stephen B Kritchevsky, Emma Larkin, Mingyao Li, Megan E Rudock, Colin A McKenzie, James B Meigs, Yang A Meng, Tom H Mosley, Anne B Newman, Christopher H Newton-Cheh, Dina N Paltoo, George J Papanicolaou, Nick Patterson, Wendy S Post, Bruce M Psaty, Atif N Qasim, Liming Qu, Daniel J Rader, Susan Redline, Muredach P Reilly, Alexander P Reiner, Stephen S Rich, Jerome I Rotter, Yongmei Liu, Peter Shrader, David S Siscovick, W H Wilson Tang, Herman A Taylor, Russell P Tracy, Ramachandran S Vasan, Kevin M Waters, Rainford Wilks, James G Wilson, Richard R Fabsitz, Stacey B Gabriel, Sekar Kathiresan, Eric Boerwinkle
Publikováno v:
PLoS Genetics, Vol 7, Iss 2, p e1001300 (2011)
Coronary heart disease (CHD) is the leading cause of mortality in African Americans. To identify common genetic polymorphisms associated with CHD and its risk factors (LDL- and HDL-cholesterol (LDL-C and HDL-C), hypertension, smoking, and type-2 diab
Externí odkaz:
https://doaj.org/article/d9f44e2061144ffba888d0850b646b15