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Andreas Brodehl | Researchclopedia

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Andreas Brodehl

Heart and Diabetes Center North Rhine-Westphalia ORCID

76

Works

2,018

Citations

27

h-index

42

i10-index

Research Topics

Cardiomyopathy and Myosin Studies Cardiovascular Effects of Exercise Skin and Cellular Biology Research

Affiliations

Royal Netherlands Academy of Arts and Sciences2025–2025

University of Calgary2013–2019

University Hospitals of the Ruhr-University of Bochum2017–2022

Heart and Diabetes Center North Rhine-Westphalia2012–2026

University Medical Center Utrecht2025–2025

Top Works

De novo desmin-mutation N116S is associated with arrhythmogenic right ventricular cardiomyopathy

Baerbel Klauke,Sabine Kossmann,et al.

2010186 citations

Nuclear Structure and Function

Cardiac electrophysiology and arrhythmias

Mutations in<i>FLNC</i>are Associated with Familial Restrictive Cardiomyopathy

Andreas Brodehl,Raechel A. Ferrier,et al.

2015176 citations

Molecular insights into cardiomyopathies associated with desmin (DES) mutations

Andreas Brodehl,Anna Gaertner,et al.

2018152 citations

Novel Desmin Mutation p.Glu401Asp Impairs Filament Formation, Disrupts Cell Membrane Integrity, and Causes Severe Arrhythmogenic Left Ventricular Cardiomyopathy/Dysplasia

Francisco Bermúdez-Jiménez,Víctor Carriel,et al.

201798 citations

The novel αB‐crystallin ( <i>CRYAB</i> ) mutation p.D109G causes restrictive cardiomyopathy

Andreas Brodehl,Anna Gaertner,et al.

201777 citations

Transgenic mice overexpressing desmocollin-2 (DSC2) develop cardiomyopathy associated with myocardial inflammation and fibrotic remodeling

Andreas Brodehl,Darrell D. Belke,et al.

201772 citations

Human Induced Pluripotent Stem-Cell-Derived Cardiomyocytes as Models for Genetic Cardiomyopathies

Andreas Brodehl,Hans Ebbinghaus,et al.

201968 citations

The Novel Desmin Mutant p.A120D Impairs Filament Formation, Prevents Intercalated Disk Localization, and Causes Sudden Cardiac Death

Andreas Brodehl,Mareike Dieding,et al.

201366 citations

Restrictive Cardiomyopathy is Caused by a Novel Homozygous Desmin (DES) Mutation p.Y122H Leading to a Severe Filament Assembly Defect

Andreas Brodehl,Seyed Ahmad Pour Hakimi,et al.

201966 citations