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Circulation: Cardiovascular Genetics
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Clinical genetics

Citations 1-10 of 50 total displayed.

Most recent content (17 Nov 2009):

Original Article
Morphological Analysis of 13 LMNA Variants Identified in a Cohort of 324 Unrelated Patients with Idiopathic or Familial Dilated Cardiomyopathy
Jason Cowan, Duanxiang Li, Jorge Gonzalez–Quintana, Ana Morales, and Ray E. Hershberger
Circ Cardiovasc Genet published November 17, 2009, doi:10.1161/CIRCGENETICS.109.905422 [Abstract]  

Past content (since Oct 2008):

Original Article
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 published October 19, 2009, doi:10.1161/CIRCGENETICS.109.860270 [Abstract]  

Editorial
Desmosome Mutations in Arrhythmogenic Right Ventricular Cardiomyopathy: Important Insight but Only Part of the Picture
Jeffrey E. Saffitz
Circ Cardiovasc Genet 2009;2:415-417, doi:10.1161/CIRCGENETICS.109.909366 [Full text]  

Original Articles
Desmoglein-2 and Desmocollin-2 Mutations in Dutch Arrhythmogenic Right Ventricular Dysplasia/Cardiomypathy Patients: Results From a Multicenter Study
Zahurul A. Bhuiyan, Jan D.H. Jongbloed, Jasper van der Smagt, Paola M. Lombardi, Ans C.P. Wiesfeld, Marcel Nelen, Meyke Schouten, Roselie Jongbloed, Moniek G.P.J. Cox, Marleen van Wolferen, Luz M. Rodriguez, Isabelle C. van Gelder, Hennie Bikker, Albert J.H. Suurmeijer, Maarten P. van den Berg, Marcel M.A.M. Mannens, Richard N.W. Hauer, Arthur A.M. Wilde, and J. Peter van Tintelen
Circ Cardiovasc Genet 2009;2:418-427; published online before print as doi:10.1161/CIRCGENETICS.108.839829 [Abstract] [Full text]  

Original Articles
Comprehensive Desmosome Mutation Analysis in North Americans With Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy
A. Dénise den Haan, Boon Yew Tan, Michelle N. Zikusoka, Laura Ibañez Lladó, Rahul Jain, Amy Daly, Crystal Tichnell, Cynthia James, Nuria Amat-Alarcon, Theodore Abraham, Stuart D. Russell, David A. Bluemke, Hugh Calkins, Darshan Dalal, and Daniel P. Judge
Circ Cardiovasc Genet 2009;2:428-435; published online before print as doi:10.1161/CIRCGENETICS.109.858217 [Abstract] [Full text]  

Original Articles
Prevalence of Sarcomere Protein Gene Mutations in Preadolescent Children With Hypertrophic Cardiomyopathy
Juan Pablo Kaski, Petros Syrris, Maria Teresa Tome Esteban, Sharon Jenkins, Antonios Pantazis, John E. Deanfield, William J. McKenna, and Perry M. Elliott
Circ Cardiovasc Genet 2009;2:436-441; published online before print as doi:10.1161/CIRCGENETICS.108.821314 [Abstract] [Full text]  

Original Articles
Sarcomere Mutations in Cardiomyopathy With Left Ventricular Hypertrabeculation
Lisa M. Dellefave, Peter Pytel, Stephanie Mewborn, Bassem Mora, Deborah L. Guris, Savitri Fedson, Darrel Waggoner, Ivan Moskowitz, and Elizabeth M. McNally
Circ Cardiovasc Genet 2009;2:442-449; published online before print as doi:10.1161/CIRCGENETICS.109.861955 [Abstract] [Full text]  

Original Articles
Variation in the 4q25 Chromosomal Locus Predicts Atrial Fibrillation After Coronary Artery Bypass Graft Surgery
Simon C. Body, Charles D. Collard, Stanton K. Shernan, Amanda A. Fox, Kuang-Yu Liu, Marylyn D. Ritchie, Tjörvi E. Perry, Jochen D. Muehlschlegel, Sary Aranki, Brian S. Donahue, Mias Pretorius, Juan-Carlos Estrada, Patrick T. Ellinor, Christopher Newton-Cheh, Christine E. Seidman, J.G. Seidman, Daniel S. Herman;, Peter Lichtner, Thomas Meitinger, Arne Pfeufer, Stefan Kääb, Nancy J. Brown, Dan M. Roden, and Dawood Darbar
Circ Cardiovasc Genet 2009;2:499-506; published online before print as doi:10.1161/CIRCGENETICS.109.849075 [Abstract] [Full text]  

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 [Full text]  

Original Article
Analysis of Dystrophin Deletion Mutations Predicts Age of Cardiomyopathy Onset in Becker Muscular Dystrophy
Rita WenKaspar, 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 published September 30, 2009, doi:10.1161/CIRCGENETICS.109.867242 [Abstract]  

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