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Clinical genetics
Contributing journals to this collection:
Hypertension,
Circulation: Heart Failure,
Stroke,
Circulation Research,
Circulation: Arrhythmia and Electrophysiology,
Circulation: Cardiovascular Genetics,
Arteriosclerosis, Thrombosis, and Vascular Biology,
Circulation: Cardiovascular Outcomes and Quality,
Circulation,
Circulation: Cardiovascular Interventions,
and Circulation: Cardiovascular Imaging
Citations 1-10 of 864 total displayed.
- Original Article
The General Cardiovascular Risk Profile Identifies Advanced Coronary Artery Calcium And Is Improved by Family History. The Multi-Ethnic Study of Atherosclerosis
- Maren T. Scheuner, Claude Messan Setodji, James S. Pankow, Roger S. Blumenthal, and Emmett Keeler
Circ Cardiovasc Genet published December 14, 2009, doi:10.1161/CIRCGENETICS.109.894527
[Abstract]
- Original Article
Association of Scavenger Receptor Class B Type I Polymorphisms with Subclinical Atherosclerosis: The Multi-Ethnic Study of Atherosclerosis
- Adam C. Naj, Michael West, Stephen S. Rich, Wendy Post, Linda Kao, Bruce A. Wasserman, David M. Herrington, and Annabelle Rodriguez
Circ Cardiovasc Genet published December 11, 2009, doi:10.1161/CIRCGENETICS.109.903195
[Abstract]
- Articles
Comparison of Clinical Presentations and Outcomes Between Patients With TGFBR2 and FBN1 Mutations in Marfan Syndrome and Related Disorders
- David Attias, Chantal Stheneur, Carine Roy, Gwenaëlle Collod-Béroud, Delphine Detaint, Laurence Faivre, Marie-Ange Delrue, Laurence Cohen, Christine Francannet, Christophe Béroud, Mireille Claustres, Franck Iserin, Philippe Khau Van Kien, Didier Lacombe, Martine Le Merrer, Stanislas Lyonnet, Sylvie Odent, Henri Plauchu, Marlène Rio, Annick Rossi, Daniel Sidi, Philippe Gabriel Steg, Philippe Ravaud, Catherine Boileau, and Guillaume Jondeau
Circulation published December 7, 2009, doi:10.1161/CIRCULATIONAHA.109.887042
[Abstract]
- Editorials
Nature’s Genetic Gradients and the Clinical Phenotype
- Ali J. Marian
Circ Cardiovasc Genet 2009;2:537-539, doi:10.1161/CIRCGENETICS.109.921940
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- Original Articles
Analysis of Dystrophin Deletion Mutations Predicts Age of Cardiomyopathy Onset in Becker Muscular Dystrophy
- Rita Wen Kaspar, Hugh D. Allen, Will C. Ray, Carlos E. Alvarez, John T. Kissel, Alan Pestronk, Robert B. Weiss, Kevin M. Flanigan, Jerry R. Mendell, and Federica Montanaro
Circ Cardiovasc Genet 2009;2:544-551; published online before print as doi:10.1161/CIRCGENETICS.109.867242
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- Original Articles
SCN5A Mutations and the Role of Genetic Background in the Pathophysiology of Brugada Syndrome
- Vincent Probst, Arthur A.M. Wilde, Julien Barc, Frederic Sacher, Dominique Babuty, Philippe Mabo, Jacques Mansourati, Solena Le Scouarnec, Florence Kyndt, Cedric Le Caignec, Pascale Guicheney, Laetitia Gouas, Juliette Albuisson, Paola G. Meregalli, Hervé Le Marec, Hanno L. Tan, and Jean-Jacques Schott
Circ Cardiovasc Genet 2009;2:552-557; published online before print as doi:10.1161/CIRCGENETICS.109.853374
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- Original Articles
Low Incidence of Sudden Cardiac Death in a Swedish Y111C Type 1 Long-QT syndrome Population
- Annika Winbo, Ulla-Britt Diamant, Eva-Lena Stattin, Steen M. Jensen, and Annika Rydberg
Circ Cardiovasc Genet 2009;2:558-564; published online before print as doi:10.1161/CIRCGENETICS.108.825547
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- Original Articles
Disruption of the Aortic Elastic Lamina and Medial Calcification Share Genetic Determinants in Mice
- Susanna S. Wang, Lisa J. Martin, Eric E. Schadt, Haijin Meng, Xuping Wang, Wei Zhao, Leslie Ingram-Drake, Martina Nebohacova, Margarete Mehrabian, Thomas A. Drake, and Aldons J. Lusis
Circ Cardiovasc Genet 2009;2:573-582; published online before print as doi:10.1161/CIRCGENETICS.109.860270
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- Original Articles
Contribution of Genome-Wide Significant Single-Nucleotide Polymorphisms and Antiretroviral Therapy to Dyslipidemia in HIV-Infected Individuals: A Longitudinal Study
- Margalida Rotger, Cornelia Bayard, Patrick Taffé, Raquel Martinez, Matthias Cavassini, Enos Bernasconi, Manuel Battegay, Bernard Hirschel, Hansjakob Furrer, Andrea Witteck, Rainer Weber, Bruno Ledergerber, Amalio Telenti, Philip E. Tarr, and the Swiss HIV Cohort Study
Circ Cardiovasc Genet 2009;2:621-628; published online before print as doi:10.1161/CIRCGENETICS.109.874412
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- Original Articles
 1-Syntrophin Mutations Identified in Sudden Infant Death Syndrome Cause an Increase in Late Cardiac Sodium Current
- Jianding Cheng, David W. Van Norstrand, Argelia Medeiros-Domingo, Carmen Valdivia, Bi-hua Tan, Bin Ye, Stacie Kroboth, Matteo Vatta, David J. Tester, Craig T. January, Jonathan C. Makielski, and Michael J. Ackerman
Circ Arrhythm Electrophysiol 2009;2:667-676; published online before print as doi:10.1161/CIRCEP.109.891440
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