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Clinical genetics
Citations 1-10 of 38 total displayed.
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Most recent content
(9 Oct 2009):
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- Editorials
Cardiac Metabolic State and Brugada Syndrome: A Link Revealed
- Mohamed Chahine
Circ. Res. 2009;105:721-723, doi:10.1161/CIRCRESAHA.109.208405
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Past content
(since Mar 2000):
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- Clinical Research
A Missense Mutation in the CHRM2 Gene Is Associated With Familial Dilated Cardiomyopathy
- Lin Zhang, Aihua Hu, Haixin Yuan, Liang Cui, Guobin Miao, Xinchun Yang, Lefeng Wang, Jinchun Liu, Xiulan Liu, Shuyan Wang, Zhiyong Zhang, Lisheng Liu, Rongrui Zhao, and Yan Shen
Circ. Res. 2008;102:1426-1432; published online before print as doi:10.1161/CIRCRESAHA.107.167783
[Abstract]
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- Clinical Research
A Gain-of-Function TBX5 Mutation Is Associated With Atypical Holt–Oram Syndrome and Paroxysmal Atrial Fibrillation
- Alex V. Postma, Judith B.A. van de Meerakker, Inge B. Mathijssen, Phil Barnett, Vincent M. Christoffels, Aho Ilgun, Jan Lam, Arthur A.M. Wilde, Ronald H. Lekanne Deprez, and Antoon F.M. Moorman
Circ. Res. 2008;102:1433-1442; published online before print as doi:10.1161/CIRCRESAHA.107.168294
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- Articles
A Gain-of-Function TBX5 Mutation Is Associated With Atypical Holt–Oram Syndrome and Paroxysmal Atrial Fibrillation
- Alex V. Postma, Judith B.A. vd Meerakker, Inge B. Mathijssen, Phil Barnett, Vincent M. Christoffels, Aho Ilgun, Jan Lam, Arthur A.M. Wilde, Ronald H. Lekanne Deprez, and Antoon F.M. Moorman
Circ. Res. published May 1, 2008, doi:10.1161/CIRCRESAHA.107.168294
[Abstract]
- Articles
A Missense Mutation in the CHRM2 Gene Is Associated With Familial Dilated Cardiomyopathy
- Lin Zhang, Aihua Hu, Haixin Yuan, Liang Cui, Guobin Miao, Xinchun Yang, Lefeng Wang, Jinchun Liu, Xiulan Liu, Shuyan Wang, Zhiyong Zhang, Lisheng Liu, Rongrui Zhao, and Yan Shen
Circ. Res. published May 1, 2008, doi:10.1161/CIRCRESAHA.107.167783
[Abstract]
- Clinical Research
Association of ATP1A1 and Dear Single-Nucleotide Polymorphism Haplotypes With Essential Hypertension: Sex-Specific and Haplotype-Specific Effects
- Nicola Glorioso, Victoria L.M. Herrera, Pia Bagamasbad, Fabiana Filigheddu, Chiara Troffa, Giuseppe Argiolas, Emanuela Bulla, Julius L. Decano, and Nelson Ruiz-Opazo
Circ. Res. 2007;100:1522-1529; published online before print as doi:10.1161/01.RES.0000267716.96196.60
[Abstract]
[Full text]
- Articles
Association of ATP1A1 and Dear Single-Nucleotide Polymorphism Haplotypes With Essential Hypertension and Sex-Specific and Haplotype-Specific Effects
- Nicola Glorioso, Victoria L.M. Herrera, Pia Bagamasbad, Fabiana Filigheddu, Chiara Troffa, Giuseppe Argiolas, Emanuela Bulla, Julius L. Decano, and Nelson Ruiz-Opazo
Circ. Res. published April 19, 2007, doi:10.1161/01.RES.0000267716.96196.60
[Abstract]
- Reports
Myozenin 2 Is a Novel Gene for Human Hypertrophic Cardiomyopathy
- Adriana Osio, Lily Tan, Suet N. Chen, Raffaella Lombardi, Sherif F. Nagueh, Sanjay Shete, Robert Roberts, James T. Willerson, and Ali J. Marian
Circ. Res. 2007;100:766-768; published online before print as doi:10.1161/01.RES.0000263008.66799.aa
[Abstract]
[Full text]
- Articles
Myozenin 2 Is a Novel Gene for Human Hypertrophic Cardiomyopathy
- Adriana Osio, Lily Tan, Suet N. Chen, Raffaella Lombardi, Sherif F. Nagueh, Sanjay Shete, Robert Roberts, James T. Willerson, and Ali J. Marian
Circ. Res. published March 8, 2007, doi:10.1161/01.RES.0000263008.66799.aa
[Abstract]
- UltraRapid Communications
Mechanisms of Abnormal Calcium Homeostasis in Mutations Responsible for Catecholaminergic Polymorphic Ventricular Tachycardia
- Vivek Iyer, Roger J. Hajjar, and Antonis A. Armoundas
Circ. Res. 2007;100:e22-31e; published online before print as doi:10.1161/01.RES.0000258468.31815.42
[Abstract]
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