MYH7B variants cause hypertrophic cardiomyopathy by activating the CaMK-signaling pathway

Expression of Normally Repressed Myosin Heavy Chain 7b in the Mammalian Heart Induces Dilated Cardiomyopathy

(2019) Angela K. Peter et al.   Journal of the American Heart Association

MicroRNA-21 Lowers Blood Pressure in Spontaneous Hypertensive Rats by Upregulating Mitochondrial TranslationClinical Perspective

(2016) Huaping Li et al.   CIRCULATION

A novel nonsense mutation in LMNA gene identified by Exome Sequencing in an atrial fibrillation family

(2016) Jinzhao Zhao et al.   European Journal of Medical Genetics

Guidelines for diagnostic next-generation sequencing

(2015) Gert Matthijs et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Results of clinical genetic testing of 2,912 probands with hypertrophic cardiomyopathy: expanded panels offer limited additional sensitivity

(2015) Ahmed A. Alfares et al.   GENETICS IN MEDICINE

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology

(2015) Sue Richards et al.   GENETICS IN MEDICINE

Myotonic dystrophy: time for evidence-based therapy

(2014) Perry Elliott   EUROPEAN HEART JOURNAL

A Functional Variant in APOA5/A4/C3/A1 Gene Cluster Contributes to Elevated Triglycerides and Severity of CAD by Interfering With MicroRNA 3201 Binding Efficiency

(2014) Guanglin Cui et al.   JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY

Rapid molecular genetic diagnosis of hypertrophic cardiomyopathy by semiconductor sequencing

(2014) Zongzhe Li et al.   Journal of Translational Medicine

Genetic complexity in hypertrophic cardiomyopathy revealed by high-throughput sequencing

(2013) Luis R Lopes et al.   JOURNAL OF MEDICAL GENETICS

Digenic mutational inheritance of the integrin alpha 7 and the myosin heavy chain 7B genes causes congenital myopathy with left ventricular non-compact cardiomyopathy

(2013) Teresa Esposito et al.   Orphanet Journal of Rare Diseases

Production of polyclonal antibodies directed to recombinant methionyl bovine somatotropin

(2012) C. Suárez-Pantaleón et al.   ANALYTICA CHIMICA ACTA

Developmental expression and cardiac transcriptional regulation of Myh7b, a third myosin heavy chain in the vertebrate heart

(2012) Andrew S. Warkman et al.   Cytoskeleton

Early Results of Sarcomeric Gene Screening from the Egyptian National BA-HCM Program

(2012) Heba Sh. Kassem et al.   Journal of Cardiovascular Translational Research

Sarcomeric hypertrophic cardiomyopathy: Genetic profile in a Portuguese population

(2012) Dulce Brito et al.   Revista Portuguesa de Cardiologia

2011 ACCF/AHA Guideline for the Diagnosis and Treatment of Hypertrophic Cardiomyopathy: Executive Summary

(2011) Bernard J. Gersh et al.   JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY

Inherited Cardiomyopathies

(2011) Hugh Watkins et al.   NEW ENGLAND JOURNAL OF MEDICINE

Elevated miR-499 Levels Blunt the Cardiac Stress Response

(2011) Joseph T. C. Shieh et al.   PLoS One

Sudden Deaths in Young Competitive Athletes

(2009) Barry J. Maron et al.   CIRCULATION

A Family of microRNAs Encoded by Myosin Genes Governs Myosin Expression and Muscle Performance

(2009) Eva van Rooij et al.   DEVELOPMENTAL CELL

A New 15–50 MHz Array-Based Micro-Ultrasound Scanner for Preclinical Imaging

(2009) F. Stuart Foster et al.   ULTRASOUND IN MEDICINE AND BIOLOGY

Methods for Detecting Associations with Rare Variants for Common Diseases: Application to Analysis of Sequence Data

(2008) Bingshan Li et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Shared Genetic Causes of Cardiac Hypertrophy in Children and Adults

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