Sinnvolle Diagnostik: Genetik

Perceptions of genetic variant reclassification in patients with inherited cardiac disease

(2019) Eugene K. Wong et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Genetic variation at the coronary artery disease risk locus GUCY1A3 modifies cardiovascular disease prevention effects of aspirin

(2019) Kathryn T Hall et al.   EUROPEAN HEART JOURNAL

Genetic Risk Score for Coronary Disease Identifies Predispositions to Cardiovascular and Noncardiovascular Diseases

(2019) Ioanna Ntalla et al.   JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY

2019 ESC/EAS Guidelines for the management of dyslipidaemias: lipid modification to reduce cardiovascular risk

(2019) François Mach et al.   EUROPEAN HEART JOURNAL

Contemporary genetic testing in inherited cardiac disease

(2018) Francesca Girolami et al.   Journal of Cardiovascular Medicine

Genome-wide polygenic scores for common diseases identify individuals with risk equivalent to monogenic mutations

(2018) Amit V. Khera et al.   NATURE GENETICS

Genomic Risk Prediction of Coronary Artery Disease in 480,000 Adults

(2018) Michael Inouye et al.   JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY

Genetic Testing and Counseling for Hypertrophic Cardiomyopathy

(2018) Allison L. Cirino et al.   CARDIOLOGY CLINICS

Praktische Durchführung der genetischen Diagnostik in der Kardiologie

(2017) W. Reinhard et al.   HERZ

Guidelines for autopsy investigation of sudden cardiac death: 2017 update from the Association for European Cardiovascular Pathology

(2017) Cristina Basso et al.   VIRCHOWS ARCHIV

The impact of genome‐wide association studies on the pathophysiology and therapy of cardiovascular disease

(2016) Thorsten Kessler et al.   EMBO Molecular Medicine

Genetic identification of familial hypercholesterolemia within a single U.S. health care system

(2016) Noura S. Abul-Husn et al.   SCIENCE

The role of genetic testing in unexplained sudden death

(2016) Chris J. Miles et al.   Translational Research

Evaluation of the Mayo Clinic Phenotype-Based Genotype Predictor Score in Patients with Clinically Diagnosed Hypertrophic Cardiomyopathy

(2016) Sinead L. Murphy et al.   Journal of Cardiovascular Translational Research

Sudden cardiac death in the young: the molecular autopsy and a practical approach to surviving relatives

(2015) C. Semsarian et al.   EUROPEAN HEART JOURNAL

Risk prediction by genetic risk scores for coronary heart disease is independent of self-reported family history

(2015) Hayato Tada et al.   EUROPEAN HEART JOURNAL

2015 ESC Guidelines for the management of patients with ventricular arrhythmias and the prevention of sudden cardiac death

(2015) Silvia G. Priori et al.   EUROPEAN HEART JOURNAL

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

Exome analysis–based molecular autopsy in cases of sudden unexplained death in the young

(2014) Richard D. Bagnall et al.   HEART RHYTHM

Characterization of a Phenotype-Based Genetic Test Prediction Score for Unrelated Patients With Hypertrophic Cardiomyopathy

(2014) J. Martijn Bos et al.   MAYO CLINIC PROCEEDINGS

Clinical predictors of genetic testing outcomes in hypertrophic cardiomyopathy

(2013) Jodie Ingles et al.   GENETICS IN MEDICINE

Genetic Markers Enhance Coronary Risk Prediction in Men: The MORGAM Prospective Cohorts

(2012) Maria F. Hughes et al.   PLoS One

Richtlinie der Gendiagnostik-Kommission (GEKO) über die Anforderungen an die Qualifikation zur und Inhalte der genetischen Beratung gemäß 23 Abs. 2 Nr. 2a und 23 Abs. 2 Nr. 3 GenDG

(2011)   Bundesgesundheitsblatt-Gesundheitsforschung-Gesundheitsschutz

HRS/EHRA Expert Consensus Statement on the State of Genetic Testing for the Channelopathies and Cardiomyopathies: This document was developed as a partnership between the Heart Rhythm Society (HRS) and the European Heart Rhythm Association (EHRA)

(2011) M. J. Ackerman et al.   EUROPACE

Diagnosis of Arrhythmogenic Right Ventricular Cardiomyopathy/Dysplasia

(2010) Frank I. Marcus et al.   CIRCULATION

Prospective, population-based long QT molecular autopsy study of postmortem negative sudden death in 1 to 40 year olds

(2010) Jonathan R. Skinner et al.   HEART RHYTHM