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Genetics of cardiovascular disease
Citations 11-20 of 95 total displayed.
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Past content
(since Oct 2008):
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- Methods in Genetics and Clinical Interpretation
Single-Nucleotide Polymorphism Bioinformatics: A Comprehensive Review of Resources
- Andrew D. Johnson
Circ Cardiovasc Genet 2009;2:530-536, doi:10.1161/CIRCGENETICS.109.872010
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- Original Article
Genetic Ancestry is Associated with Subclinical Cardiovascular Disease in African Americans and Hispanics from the Multi-Ethnic Study of Atherosclerosis (MESA)
- Christina L. Wassel, James S. Pankow, Carmen A. Peralta, Shweta Choudhry, Michael F. Seldin, and Donna K. Arnett
Circ Cardiovasc Genet published September 19, 2009, doi:10.1161/CIRCGENETICS.109.876243
[Abstract]
- Original Article
Association of AHSG Gene Polymorphisms with Fetuin-A Plasma Levels and Cardiovascular Diseases in the EPIC-Potsdam Study
- Eva Fisher, Norbert Stefan, Kathrin Saar, Dagmar Drogan, Matthias B. Schulze, Andreas Fritsche, Hans-Georg Joost, Hans-Ulrich Häring, Norbert Huebner, Heiner Boeing, and Cornelia Weikert
Circ Cardiovasc Genet published September 5, 2009, doi:10.1161/CIRCGENETICS.109.870410
[Abstract]
- Original Article
Single nucleotide polymorphisms in homocysteine metabolism pathway genes: Association of CHDH A119C and MTHFR C677T with hyperhomocysteinemia.
- Jitender Kumar, Gaurav Garg, Arun Kumar, Elayanambi Sundaramoorthy, Krishna Rao Sanapala, Saurabh Ghosh, Ganesan Karthikeyan, Lakshmy Ramakrishnan, Indian Genome Variation Consortium, and Shantanu Sengupta
Circ Cardiovasc Genet published September 5, 2009, doi:10.1161/CIRCGENETICS.108.841411
[Abstract]
- Original Article
EPH Receptor B4 (EPHB4) Gene Polymorphisms and Risk of Intracranial Hemorrhage in Patients with Brain Arteriovenous Malformations
- Shantel Weinsheimer, Helen Kim, Ludmila Pawlikowska, Yongmei Chen, Michael T. Lawton, Stephen Sidney, Pui-Yan Kwok, Charles E. McCulloch, and William L. Young
Circ Cardiovasc Genet published August 22, 2009, doi:10.1161/CIRCGENETICS.109.883595
[Abstract]
- Original Article
Genetic Variation at the Proprotein Convertase Subtilisin/Kexin Type 5 Gene Modulates HDL Cholesterol Levels
- Iulia Iatan, Zari Dastani, Ron Do, Daphna Weissglas-Volkov, Isabelle Ruel, Jenny C. Lee, Adriana Huertas-Vazquez, Marja-Riitta Taskinen, Annik Prat, Nabil G. Seidah, Päivi Pajukanta, James C. Engert, and Jacques Genest
Circ Cardiovasc Genet published August 22, 2009, doi:10.1161/CIRCGENETICS.109.877811
[Abstract]
- Original Article
A Common Copy Number Variation on Chromosome 6 Association with the Gene Expression Level of Endothelin 1 in Transformed B-Lymphocytes from Three Racial Groups
- Yan V. Sun, Patricia A. Peyser, and Sharon L.R. Kardia
Circ Cardiovasc Genet published August 2, 2009, doi:10.1161/CIRCGENETICS.109.848754
[Abstract]
- Original Articles
Clinical and Functional Characterization of TNNT2 Mutations Identified in Patients With Dilated Cardiomyopathy
- Ray E. Hershberger, Jose Renato Pinto, Sharie B. Parks, Jessica D. Kushner, Duanxiang Li, Susan Ludwigsen, Jason Cowan, Ana Morales, Michelle S. Parvatiyar, and James D. Potter
Circ Cardiovasc Genet 2009;2:306-313; published online before print as doi:10.1161/CIRCGENETICS.108.846733
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- Original Articles
Genome-Wide Association Scan Identifies Variants near Matrix Metalloproteinase (MMP) Genes on Chromosome 11q21–22 Strongly Associated With Serum MMP-1 Levels
- Yu-Ching Cheng, Wen-Hong L. Kao, Braxton D. Mitchell, Jeffrey R. O'Connell, Haiqing Shen, Patrick F. McArdle, Quince Gibson, Kathleen A. Ryan, Alan R. Shuldiner, and Toni I. Pollin
Circ Cardiovasc Genet 2009;2:329-337; published online before print as doi:10.1161/CIRCGENETICS.108.834986
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- Original Articles
9p21 is a Shared Susceptibility Locus Strongly for Coronary Artery Disease and Weakly for Ischemic Stroke in Chinese Han Population
- Hu Ding, Yujun Xu, Xiaojing Wang, Qi Wang, Lan Zhang, Yuanchao Tu, Jiangtao Yan, Wei Wang, Rutai Hui, Cong-Yi Wang, and Dao Wen Wang
Circ Cardiovasc Genet 2009;2:338-346; published online before print as doi:10.1161/CIRCGENETICS.108.810226
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