Impact of Mendelian inheritance in cardiovascular disease

Peripartum Cardiomyopathy as a Part of Familial Dilated Cardiomyopathy

(2010) Karin Y. van Spaendonck-Zwarts et al.   CIRCULATION

Rare Variant Mutations in Pregnancy-Associated or Peripartum Cardiomyopathy

(2010) Ana Morales et al.   CIRCULATION

Executive Summary: Heart Disease and Stroke Statistics—2010 Update

(2010) et al.   CIRCULATION

Short Communication: The Cardiac Myosin Binding Protein C Arg502Trp Mutation

(2010) Adam J. Saltzman et al.   CIRCULATION RESEARCH

A novel custom resequencing array for dilated cardiomyopathy

(2010) Rebekah S Zimmerman et al.   GENETICS IN MEDICINE

Rationale and design of a trial evaluating the effects of losartan vs. nebivolol vs. the association of both on the progression of aortic root dilation in Marfan syndrome with FBN1 gene mutations

(2010) Fabiana I Gambarin et al.   Journal of Cardiovascular Medicine

Clinical Features and Outcome of Hypertrophic Cardiomyopathy Associated With Triple Sarcomere Protein Gene Mutations

(2010) Francesca Girolami et al.   JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY

Thoracic Aortic Aneurysm

(2010) John A. Elefteriades et al.   JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY

Dilated cardiomyopathy

(2010) John Lynn Jefferies et al.   LANCET

Whole-Genome Sequencing in a Patient with Charcot–Marie–Tooth Neuropathy

(2010) James R. Lupski et al.   NEW ENGLAND JOURNAL OF MEDICINE

Analysis of Genetic Inheritance in a Family Quartet by Whole-Genome Sequencing

(2010) J. C. Roach et al.   SCIENCE

Losartan therapy in adults with Marfan syndrome: study protocol of the multi-center randomized controlled COMPARE trial

(2010) Teodora Radonic et al.   Trials

Mortality associated with adult congenital heart disease: Trends in the US population from 1979 to 2005

(2009) Priya Pillutla et al.   AMERICAN HEART JOURNAL

Mutations in Smooth Muscle Alpha-Actin (ACTA2) Cause Coronary Artery Disease, Stroke, and Moyamoya Disease, Along with Thoracic Aortic Disease

(2009) Dong-Chuan Guo et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Quality of life and psychological distress in hypertrophic cardiomyopathy mutation carriers: A cross-sectional cohort study

(2009) Imke Christiaans et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Sudden Deaths in Young Competitive Athletes

(2009) Barry J. Maron et al.   CIRCULATION

Growing Epidemic of Coronary Heart Disease in Low- and Middle-Income Countries

(2009) Thomas A. Gaziano et al.   CURRENT PROBLEMS IN CARDIOLOGY

Identification of the minimal combination of clinical features in probands for efficient mutation detection in the FBN1 gene

(2009) Chantal Stheneur et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Psychosocial impact of specialized cardiac genetic clinics for hypertrophic cardiomyopathy

(2009) Jodie Ingles et al.   GENETICS IN MEDICINE

The genetic basis of Brugada syndrome: A mutation update

(2009) Paula L. Hedley et al.   HUMAN MUTATION

The genetic basis of long QT and short QT syndromes: A mutation update

(2009) Paula L. Hedley et al.   HUMAN MUTATION

Analysis of multigenerational families with thoracic aortic aneurysms and dissections due to TGFBR1 or TGFBR2 mutations

(2009) V Tran-Fadulu et al.   JOURNAL OF MEDICAL GENETICS

Aortopathy Is Prevalent in Relatives of Bicuspid Aortic Valve Patients

(2009) Simon Biner et al.   JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY

Diagnostic, Prognostic, and Therapeutic Implications of Genetic Testing for Hypertrophic Cardiomyopathy

(2009) J. Martijn Bos et al.   JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY

Arrhythmogenic right ventricular cardiomyopathy

(2009) Cristina Basso et al.   LANCET

Myofilament Protein Gene Mutation Screening and Outcome of Patients With Hypertrophic Cardiomyopathy

(2009) Iacopo Olivotto et al.   MAYO CLINIC PROCEEDINGS

Solution hybrid selection with ultra-long oligonucleotides for massively parallel targeted sequencing

(2009) Andreas Gnirke et al.   NATURE BIOTECHNOLOGY

De novo copy number variants identify new genes and loci in isolated sporadic tetralogy of Fallot

(2009) Steven C Greenway et al.   NATURE GENETICS

Flecainide prevents catecholaminergic polymorphic ventricular tachycardia in mice and humans

(2009) Hiroshi Watanabe et al.   NATURE MEDICINE

Parental Knowledge and Attitudes Toward Hypertrophic Cardiomyopathy Genetic Testing

(2009) Sara M. Fitzgerald-Butt et al.   PEDIATRIC CARDIOLOGY

Annual Summary of Vital Statistics: 2007

(2009) M. Heron et al.   PEDIATRICS

GATA6 mutations cause human cardiac outflow tract defects by disrupting semaphorin-plexin signaling

(2009) K. Kodo et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Understanding cardiovascular disease through the lens of genome-wide association studies

(2009) Dan E. Arking et al.   TRENDS IN GENETICS

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

(2008) Sharie B. Parks et al.   AMERICAN HEART JOURNAL

National time trends in congenital heart defects, Denmark, 1977-2005

(2008) Nina Øyen et al.   AMERICAN HEART JOURNAL

Cardiomyopathic and Channelopathic Causes of Sudden Unexplained Death in Infants and Children

(2008) David J. Tester et al.   Annual Review of Medicine

Ehlers-Danlos syndromes and Marfan syndrome

(2008) Bert Callewaert et al.   BEST PRACTICE & RESEARCH IN CLINICAL RHEUMATOLOGY

Medical Management of Marfan Syndrome

(2008) Martin G. Keane et al.   CIRCULATION

Array-Based Resequencing Assay for Mutations Causing Hypertrophic Cardiomyopathy

(2008) S. Waldmuller et al.   CLINICAL CHEMISTRY

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

(2008) Ray E. Hershberger et al.   CTS-Clinical and Translational Science

Long QT Syndrome

(2008) Ilan Goldenberg et al.   CURRENT PROBLEMS IN CARDIOLOGY

NOTCH1 mutations in individuals with left ventricular outflow tract malformations reduce ligand-induced signaling

(2008) K. L. McBride et al.   HUMAN MOLECULAR GENETICS

The RAS/MAPK syndromes: novel roles of the RAS pathway in human genetic disorders

(2008) Yoko Aoki et al.   HUMAN MUTATION

A DNA resequencing array for pathogenic mutation detection in hypertrophic cardiomyopathy

(2008) Siv Fokstuen et al.   HUMAN MUTATION

The developmental genetics of congenital heart disease

(2008) Benoit G. Bruneau   NATURE

Angiotensin II Blockade and Aortic-Root Dilation in Marfan's Syndrome

(2008) Benjamin S. Brooke et al.   NEW ENGLAND JOURNAL OF MEDICINE

Shared Genetic Causes of Cardiac Hypertrophy in Children and Adults

(2008) Hiroyuki Morita et al.   NEW ENGLAND JOURNAL OF MEDICINE

Congenital long QT syndrome

(2008) Lia Crotti et al.   Orphanet Journal of Rare Diseases

Cryptic Chromosomal Abnormalities Identified in Children With Congenital Heart Disease

(2008) Ashleigh A Richards et al.   PEDIATRIC RESEARCH

Primary myopathies and the heart

(2008) Josef Finsterer et al.   SCANDINAVIAN CARDIOVASCULAR JOURNAL

Array-Based DNA Diagnostics: Let the Revolution Begin

(2007) Arthur L. Beaudet et al.   Annual Review of Medicine