Anna Rommel-Gaertner

Bad Oeynhausen, NW, Germany

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 12 publications

Molecular autopsy and family screening in a young case of sudden cardiac death reveals an unusually severe case of FHL1 related hypertrophic cardiomyopathy.

Molecular autopsy and family screening in a young case of sudden cardiac death reveals an unusually severe case of FHL1 related hypertrophic cardiomyopathy.

Journal: Molecular genetics & genomic medicine

Published: January 11, 2019

The Translational Landscape of the Human Heart.

The Translational Landscape of the Human Heart.

Journal: Cell

Published: November 05, 2018

Functional analysis of DES-p.L398P and RBM20-p.R636C.

Functional analysis of DES-p.L398P and RBM20-p.R636C.

Journal: Genetics in medicine : official journal of the American College of Medical Genetics

Published: July 24, 2018

In vitro analysis of arrhythmogenic cardiomyopathy associated desmoglein-2 (DSG2) mutations reveals diverse glycosylation patterns.

In vitro analysis of arrhythmogenic cardiomyopathy associated desmoglein-2 (DSG2) mutations reveals diverse glycosylation patterns.

Journal: Journal of molecular and cellular cardiology

Published: June 18, 2018

Molecular insights into cardiomyopathies associated with desmin (DES) mutations.

Molecular insights into cardiomyopathies associated with desmin (DES) mutations.

Journal: Biophysical reviews

Published: April 27, 2018

FLNC (Filamin-C): A New(er) Player in the Field of Genetic Cardiomyopathies.

FLNC (Filamin-C): A New(er) Player in the Field of Genetic Cardiomyopathies.

Journal: Circulation. Cardiovascular genetics

Published: December 08, 2017

A novel desmin (DES) indel mutation causes severe atypical cardiomyopathy in combination with atrioventricular block and skeletal myopathy.

A novel desmin (DES) indel mutation causes severe atypical cardiomyopathy in combination with atrioventricular block and skeletal myopathy.

Journal: Molecular genetics & genomic medicine

Published: August 21, 2017

Arrhythmogenic cardiomyopathy related DSG2 mutations affect desmosomal cadherin binding kinetics.

Arrhythmogenic cardiomyopathy related DSG2 mutations affect desmosomal cadherin binding kinetics.

Journal: Scientific reports

Published: June 21, 2017

High proportion of genetic cases in patients with advanced cardiomyopathy including a novel homozygous Plakophilin 2-gene mutation.

High proportion of genetic cases in patients with advanced cardiomyopathy including a novel homozygous Plakophilin 2-gene mutation.

Journal: PloS one

Published: June 06, 2017

The novel αB-crystallin (CRYAB) mutation p.D109G causes restrictive cardiomyopathy.

The novel αB-crystallin (CRYAB) mutation p.D109G causes restrictive cardiomyopathy.

Journal: Human mutation

Published: February 24, 2017

Molecular autopsy of sudden unexplained deaths reveals genetic predispositions for cardiac diseases among young forensic cases.

Molecular autopsy of sudden unexplained deaths reveals genetic predispositions for cardiac diseases among young forensic cases.

Journal: Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology

Published: December 18, 2015

Myocardial expression profiles of candidate molecules in patients with arrhythmogenic right ventricular cardiomyopathy/dysplasia compared to those with dilated cardiomyopathy and healthy controls.

Myocardial expression profiles of candidate molecules in patients with arrhythmogenic right ventricular cardiomyopathy/dysplasia compared to those with dilated cardiomyopathy and healthy controls.

Journal: Heart rhythm

Published: July 29, 2015

Showing 1-12 of 12

Last Updated: 09/26/2026