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Circulation. Cardiovascular genetics

Showing results (631-640 of 645) with videos related to

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Circulation. Cardiovascular Genetics|June 12, 2012
High prevalence of long QT syndrome-associated SCN5A variants in patients with early-onset lone atrial fibrillationMorten S Olesen, Lei Yuan, Bo Liang, et al.
Circulation. Cardiovascular Genetics|August 16, 2015
Functional Analysis of a Carotid Intima-Media Thickness Locus Implicates BCAR1 and Suggests a Causal VariantFreya Boardman-Pretty, Andrew J P Smith, Jackie Cooper, et al.
Circulation. Cardiovascular Genetics|June 16, 2017
Burden of Recurrent and Ancestral Mutations in Families With Hypertrophic CardiomyopathySamantha Barratt Ross, Richard D Bagnall, Jodie Ingles, et al.
Circulation. Cardiovascular Genetics|September 15, 2016
Combination of Whole Genome Sequencing, Linkage, and Functional Studies Implicates a Missense Mutation in Titin as a Cause of Autosomal Dominant Cardiomyopathy With Features of Left Ventricular NoncompactionRobert Hastings, Carin P de Villiers, Charlotte Hooper, et al.
Circulation. Cardiovascular Genetics|September 22, 2016
Epigenetic Signatures of Cigarette SmokingRoby Joehanes, Allan C Just, Riccardo E Marioni, et al.
Circulation. Cardiovascular Genetics|February 18, 2010
Investigation of variants identified in caucasian genome-wide association studies for plasma high-density lipoprotein cholesterol and triglycerides levels in Mexican dyslipidemic study samplesDaphna Weissglas-Volkov, Carlos A Aguilar-Salinas, Janet S Sinsheimer, et al.
Circulation. Cardiovascular Genetics|September 4, 2016
Decoding the Long Noncoding RNA During Cardiac Maturation: A Roadmap for Functional DiscoveryMarlin Touma, Xuedong Kang, Yan Zhao, et al.
Circulation. Cardiovascular Genetics|February 19, 2015
Common and rare variants in SCN10A modulate the risk of atrial fibrillationJavad Jabbari, Morten S Olesen, Lei Yuan, et al.
Circulation. Cardiovascular Genetics|February 19, 2015
Quantitative serum nuclear magnetic resonance metabolomics in cardiovascular epidemiology and geneticsPasi Soininen, Antti J Kangas, Peter Würtz, et al.
Circulation. Cardiovascular Genetics|June 12, 2014
Novel calmodulin mutations associated with congenital arrhythmia susceptibilityNaomasa Makita, Nobue Yagihara, Lia Crotti, et al.
Pageof 65

Showing results (631-640 of 645) with videos related to

Sort By:
Pageof 65
Circulation. Cardiovascular Genetics|June 12, 2012
High prevalence of long QT syndrome-associated SCN5A variants in patients with early-onset lone atrial fibrillationMorten S Olesen, Lei Yuan, Bo Liang, et al.
Circulation. Cardiovascular Genetics|August 16, 2015
Functional Analysis of a Carotid Intima-Media Thickness Locus Implicates BCAR1 and Suggests a Causal VariantFreya Boardman-Pretty, Andrew J P Smith, Jackie Cooper, et al.
Circulation. Cardiovascular Genetics|June 16, 2017
Burden of Recurrent and Ancestral Mutations in Families With Hypertrophic CardiomyopathySamantha Barratt Ross, Richard D Bagnall, Jodie Ingles, et al.
Circulation. Cardiovascular Genetics|September 15, 2016
Combination of Whole Genome Sequencing, Linkage, and Functional Studies Implicates a Missense Mutation in Titin as a Cause of Autosomal Dominant Cardiomyopathy With Features of Left Ventricular NoncompactionRobert Hastings, Carin P de Villiers, Charlotte Hooper, et al.
Circulation. Cardiovascular Genetics|September 22, 2016
Epigenetic Signatures of Cigarette SmokingRoby Joehanes, Allan C Just, Riccardo E Marioni, et al.
Circulation. Cardiovascular Genetics|February 18, 2010
Investigation of variants identified in caucasian genome-wide association studies for plasma high-density lipoprotein cholesterol and triglycerides levels in Mexican dyslipidemic study samplesDaphna Weissglas-Volkov, Carlos A Aguilar-Salinas, Janet S Sinsheimer, et al.
Circulation. Cardiovascular Genetics|September 4, 2016
Decoding the Long Noncoding RNA During Cardiac Maturation: A Roadmap for Functional DiscoveryMarlin Touma, Xuedong Kang, Yan Zhao, et al.
Circulation. Cardiovascular Genetics|February 19, 2015
Common and rare variants in SCN10A modulate the risk of atrial fibrillationJavad Jabbari, Morten S Olesen, Lei Yuan, et al.
Circulation. Cardiovascular Genetics|February 19, 2015
Quantitative serum nuclear magnetic resonance metabolomics in cardiovascular epidemiology and geneticsPasi Soininen, Antti J Kangas, Peter Würtz, et al.
Circulation. Cardiovascular Genetics|June 12, 2014
Novel calmodulin mutations associated with congenital arrhythmia susceptibilityNaomasa Makita, Nobue Yagihara, Lia Crotti, et al.
Pageof 65