|
Genetics of cardiovascular disease
Citations 251-260 of 492 total displayed.
|
Past content
(since Jan 1999):
|
- Review: Special Reports
Mutation in the KCNQ1 Gene Leading to the Short QT-Interval Syndrome
- Chloé Bellocq, Antoni C.G. van Ginneken, Connie R. Bezzina, Mariel Alders, Denis Escande, Marcel M.A.M. Mannens, Isabelle Baró, and Arthur A.M. Wilde
Circulation 2004;109:2394-2397, doi:10.1161/01.CIR.0000130409.72142.FE
[Abstract]
[Full text]
- Clinical Investigations and Reports
The Microsomal Triglyceride Transfer Protein Gene-493T Variant Lowers Cholesterol But Increases the Risk of Coronary Heart Disease
- Helena Ledmyr, Alex D. McMahon, Ewa Ehrenborg, Lars B. Nielsen, Matt Neville, Hans Lithell, Peter W. MacFarlane, Christopher J. Packard, Fredrik Karpe on behalf of the WOSCOPS executive;
Circulation 2004;109:2279-2284; published online before print as doi:10.1161/01.CIR.0000130070.96758.7b
[Abstract]
[Full text]
- Articles
The Microsomal Triglyceride Transfer Protein Gene-493T Variant Lowers Cholesterol But Increases the Risk of Coronary Heart Disease
- Helena Ledmyr, Alex D. McMahon, Ewa Ehrenborg, Lars B. Nielsen, Matt Neville, Hans Lithell, Peter W. MacFarlane, Christopher J. Packard, Fredrik Karpe on behalf of the WOSCOPS executive
Circulation published May 10, 2004, doi:10.1161/01.CIR.0000130070.96758.7b
[Abstract]
- Clinical Investigations and Reports
Genome Scan for Familial Abdominal Aortic Aneurysm Using Sex and Family History as Covariates Suggests Genetic Heterogeneity and Identifies Linkage to Chromosome 19q13
- Hidenori Shibamura, Jane M. Olson, Clarissa van Vlijmen-van Keulen, Sarah G. Buxbaum, Doreen M. Dudek, Gerard Tromp, Toru Ogata, Magdalena Skunca, Natzi Sakalihasan, Gerard Pals, Raymond Limet, Gerald L. MacKean, Olivier Defawe, Alain Verloes, Claudette Arthur, Alan G. Lossing, Marjorie Burnett, Taijiro Sueda, and Helena Kuivaniemi
Circulation 2004;109:2103-2108; published online before print as doi:10.1161/01.CIR.0000127857.77161.A1
[Abstract]
[Full text]
- Articles
Genome Scan for Familial Abdominal Aortic Aneurysm Using Sex and Family History as Covariates Suggests Genetic Heterogeneity and Identifies Linkage to Chromosome 19q13
- Hidenori Shibamura, Jane M. Olson, Clarissa van Vlijmen-van Keulen, Sarah G. Buxbaum, Doreen M. Dudek, Gerard Tromp, Toru Ogata, Magdalena Skunca, Natzi Sakalihasan, Gerard Pals, Raymond Limet, Gerald L. MacKean, Olivier Defawe, Alain Verloes, Claudette Arthur, Alan G. Lossing, Marjorie Burnett, Taijiro Sueda, and Helena Kuivaniemi
Circulation published April 19, 2004, doi:10.1161/01.CIR.0000127857.77161.A1
[Abstract]
- Special Reports
National Heart, Lung, and Blood Institute Clinical Proteomics Working Group Report
- Christopher B. Granger, Jennifer E. Van Eyk, Stephen C. Mockrin, N. Leigh Anderson on behalf of the Working Group Members
Circulation 2004;109:1697-1703, doi:10.1161/01.CIR.0000121563.47232.2A
[Abstract]
[Full text]
- Clinical Investigations and Reports
Renin-Angiotensin System Gene Polymorphisms and Atrial Fibrillation
- Chia-Ti Tsai, Ling-Ping Lai, Jiunn-Lee Lin, Fu-Tien Chiang, Juey-Jen Hwang, Marylyn D. Ritchie, Jason H. Moore, Kuan-Lih Hsu, Chuen-Den Tseng, Chiau-Suong Liau, and Yung-Zu Tseng
Circulation 2004;109:1640-1646; published online before print as doi:10.1161/01.CIR.0000124487.36586.26
[Abstract]
[Full text]
- Clinical Investigations and Reports
Endothelial Nitric Oxide Synthase Genotype and Ischemic Heart Disease: Meta-Analysis of 26 Studies Involving 23028 Subjects
- Juan P. Casas, Leonelo E. Bautista, Steve E. Humphries, and Aroon D. Hingorani
Circulation 2004;109:1359-1365; published online before print as doi:10.1161/01.CIR.0000121357.76910.A3
[Abstract]
[Full text]
- Articles
Renin-Angiotensin System Gene Polymorphisms and Atrial Fibrillation
- Chia-Ti Tsai, Ling-Ping Lai, Jiunn-Lee Lin, Fu-Tien Chiang, Juey-Jen Hwang, Marylyn D. Ritchie, Jason H. Moore, Kuan-Lih Hsu, Chuen-Den Tseng, Chiau-Suong Liau, and Yung-Zu Tseng
Circulation published March 15, 2004, doi:10.1161/01.CIR.0000124487.36586.26
[Abstract]
- Articles
Endothelial Nitric Oxide Synthase Genotype and Ischemic Heart Disease. Meta-Analysis of 26 Studies Involving 23028 Subjects
- Juan P. Casas, Leonelo E. Bautista, Steve E. Humphries, and Aroon D. Hingorani
Circulation published March 8, 2004, doi:10.1161/01.CIR.0000121357.76910.A3
[Abstract]
|
|