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Rare Variant Mutations in Pregnancy-Associated or Peripartum Cardiomyopathy

Circulation (New York, N.Y.), 2010-05, Vol.121 (20), p.2176-2182

2010

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Genome-wide Studies of Copy Number Variation and Exome Sequencing Identify Rare Variants in BAG3 as a Cause of Dilated Cardiomyopathy

American journal of human genetics, 2011-03, Vol.88 (3), p.273-282

2011

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Coding sequence rare variants identified in MYBPC3, MYH6, TPM1, TNNC1, and TNNI3 from 312 patients with familial or idiopathic dilated cardiomyopathy

Circulation. Cardiovascular genetics, 2010-04, Vol.3 (2), p.155-161

2010

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Lamin A/C mutation analysis in a cohort of 324 unrelated patients with idiopathic or familial dilated cardiomyopathy

The American heart journal, 2008-07, Vol.156 (1), p.161-169

2008

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Evaluating pathogenicity of rare variants from dilated cardiomyopathy in the exome era

Circulation. Cardiovascular genetics, 2012-04, Vol.5 (2), p.167-174

2012

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Temporal Relationship of Conduction System Disease and Ventricular Dysfunction in LMNA Cardiomyopathy

Journal of cardiac failure, 2013-04, Vol.19 (4), p.233-239

2013

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Exome sequencing and genome-wide linkage analysis in 17 families illustrate the complex contribution of TTN truncating variants to dilated cardiomyopathy

Circulation. Cardiovascular genetics, 2013-04, Vol.6 (2), p.144-153

2013

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Mutations of Presenilin Genes in Dilated Cardiomyopathy and Heart Failure

American journal of human genetics, 2006-12, Vol.79 (6), p.1030-1039

2006

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Functional Characterization of TNNC1 Rare Variants Identified in Dilated Cardiomyopathy

The Journal of biological chemistry, 2011-09, Vol.286 (39), p.34404-34412

2011

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Unified modeling of regionally integrated energy system and application to optimization

International journal of electrical power & energy systems, 2022-01, Vol.134, p.107377, Article 107377

2022

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Desmin mutation responsible for idiopathic dilated cardiomyopathy

Circulation (New York, N.Y.), 1999-08, Vol.100 (5), p.461-464

1999

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SCN5A Rare Variants in Familial Dilated Cardiomyopathy Decrease Peak Sodium Current Depending on the Common Polymorphism H558R and Common Splice Variant Q1077del

Clinical and translational science, 2010-12, Vol.3 (6), p.287-294

2010

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Novel cardiac troponin T mutation as a cause of familial dilated cardiomyopathy

Circulation (New York, N.Y.), 2001-10, Vol.104 (18), p.2188-2193

2001

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Localization of a gene responsible for arrhythmogenic right ventricular dysplasia to chromosome 3p23

Circulation (New York, N.Y.), 1998-12, Vol.98 (25), p.2791-2795

1998

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The Locus of a Novel Gene Responsible for Arrhythmogenic Right-Ventricular Dysplasia Characterized by Early Onset and High Penetrance Maps to Chromosome 10p12-p14

American journal of human genetics, 2000-01, Vol.66 (1), p.148-156

2000

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Next-generation sequencing to identify genetic causes of cardiomyopathies

Current opinion in cardiology, 2012-05, Vol.27 (3), p.214-220

2012

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Cardiac magnetic resonance imaging of myocardial contrast uptake and blood flow in patients affected with idiopathic or familial dilated cardiomyopathy

American journal of physiology. Heart and circulatory physiology, 2008-09, Vol.295 (3), p.H1234-H1242

2008

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Genomic Organization and Isoform-Specific Tissue Expression of Human NAPOR (CUGBP2) as a Candidate Gene for Familial Arrhythmogenic Right Ventricular Dysplasia

Genomics (San Diego, Calif.), 2001-06, Vol.74 (3), p.396-401

2001

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Identification of Novel Mutations in RBM20 in Patients with Dilated Cardiomyopathy

Clinical and translational science, 2010-06, Vol.3 (3), p.90-97

2010

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Clinical and Functional Characterization of TNNT2 Mutations Identified in Patients With Dilated Cardiomyopathy

Circulation. Cardiovascular genetics, 2009-08, Vol.2 (4), p.306-313

2009

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Morphological analysis of 13 LMNA variants identified in a cohort of 324 unrelated patients with idiopathic or familial dilated cardiomyopathy

Circulation. Cardiovascular genetics, 2010-02, Vol.3 (1), p.6-14

2010

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Coding Sequence Mutations Identified in MYH7, TNNT2, SCN5A, CSRP3, LBD3, and TCAP from 313 Patients with Familial or Idiopathic Dilated Cardiomyopathy

Clinical and translational science, 2008-05, Vol.1 (1), p.21-26

2008

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Rare variant mutations identified in pediatric patients with dilated cardiomyopathy

Progress in pediatric cardiology, 2011-01, Vol.31 (1), p.39-47

2011

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Positional cloning: single-gene cardiovascular disorders

Methods in molecular medicine, 2006, Vol.128, p.125

Li, Duanxiang

2006

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MUTATIONS IN 6 GENES IDENTIFIED IN PATIENTS WITH PERIPARTUM CARDIOMYOPATHY

Journal of the American College of Cardiology, 2010-03, Vol.55 (10), p.A131.E1225-A131.E1225

2010

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Rare Variant Mutations in Pregnancy-Associated or Peripartum Cardiomyopathy

Genome-wide Studies of Copy Number Variation and Exome Sequencing Identify Rare Variants in BAG3 as a Cause of Dilated Cardiomyopathy

Coding sequence rare variants identified in MYBPC3, MYH6, TPM1, TNNC1, and TNNI3 from 312 patients with familial or idiopathic dilated cardiomyopathy

Lamin A/C mutation analysis in a cohort of 324 unrelated patients with idiopathic or familial dilated cardiomyopathy

Evaluating pathogenicity of rare variants from dilated cardiomyopathy in the exome era

Temporal Relationship of Conduction System Disease and Ventricular Dysfunction in LMNA Cardiomyopathy

Exome sequencing and genome-wide linkage analysis in 17 families illustrate the complex contribution of TTN truncating variants to dilated cardiomyopathy

Mutations of Presenilin Genes in Dilated Cardiomyopathy and Heart Failure

Functional Characterization of TNNC1 Rare Variants Identified in Dilated Cardiomyopathy

Unified modeling of regionally integrated energy system and application to optimization

Desmin mutation responsible for idiopathic dilated cardiomyopathy

SCN5A Rare Variants in Familial Dilated Cardiomyopathy Decrease Peak Sodium Current Depending on the Common Polymorphism H558R and Common Splice Variant Q1077del

Novel cardiac troponin T mutation as a cause of familial dilated cardiomyopathy

Localization of a gene responsible for arrhythmogenic right ventricular dysplasia to chromosome 3p23

The Locus of a Novel Gene Responsible for Arrhythmogenic Right-Ventricular Dysplasia Characterized by Early Onset and High Penetrance Maps to Chromosome 10p12-p14

Next-generation sequencing to identify genetic causes of cardiomyopathies

Cardiac magnetic resonance imaging of myocardial contrast uptake and blood flow in patients affected with idiopathic or familial dilated cardiomyopathy

Genomic Organization and Isoform-Specific Tissue Expression of Human NAPOR (CUGBP2) as a Candidate Gene for Familial Arrhythmogenic Right Ventricular Dysplasia

Identification of Novel Mutations in RBM20 in Patients with Dilated Cardiomyopathy

Clinical and Functional Characterization of TNNT2 Mutations Identified in Patients With Dilated Cardiomyopathy

Morphological analysis of 13 LMNA variants identified in a cohort of 324 unrelated patients with idiopathic or familial dilated cardiomyopathy

Coding Sequence Mutations Identified in MYH7, TNNT2, SCN5A, CSRP3, LBD3, and TCAP from 313 Patients with Familial or Idiopathic Dilated Cardiomyopathy

Rare variant mutations identified in pediatric patients with dilated cardiomyopathy

Positional cloning: single-gene cardiovascular disorders

MUTATIONS IN 6 GENES IDENTIFIED IN PATIENTS WITH PERIPARTUM CARDIOMYOPATHY

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