Rixa Woitschach

Hamburg, HH, Germany

Last Updated: 09/26/2026

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Found 8 publications

Myocardial Inflammation Reveals a Genetic Desmosomal Cardiomyopathy in an Athlete.

Myocardial Inflammation Reveals a Genetic Desmosomal Cardiomyopathy in an Athlete.

Journal: JACC. Case reports
Published: December 02, 2025

Lower left ventricular ejection time in MYBPC3 variant carriers with overt or subclinical hypertrophic cardiomyopathy.

Lower left ventricular ejection time in MYBPC3 variant carriers with overt or subclinical hypertrophic cardiomyopathy.

Journal: ESC heart failure
Published: January 20, 2025

Evaluating genome sequencing strategies: trio, singleton, and standard testing in rare disease diagnosis.

Evaluating genome sequencing strategies: trio, singleton, and standard testing in rare disease diagnosis.

Journal: Genome medicine
Published: December 20, 2024

Multimodal characterization of dilated cardiomyopathy: Geno- And Phenotyping of PrImary Cardiomyopathy (GrAPHIC).

Multimodal characterization of dilated cardiomyopathy: Geno- And Phenotyping of PrImary Cardiomyopathy (GrAPHIC).

Journal: ESC heart failure
Published: April 11, 2023

LMNA Mutation in a Family with a Strong History of Sudden Cardiac Death.

LMNA Mutation in a Family with a Strong History of Sudden Cardiac Death.

Journal: Genes
Published: December 20, 2021

Genome sequencing in families with congenital limb malformations.

Genome sequencing in families with congenital limb malformations.

Journal: Human genetics
Published: March 18, 2021

A second cohort of CHD3 patients expands the molecular mechanisms known to cause Snijders Blok-Campeau syndrome.

A second cohort of CHD3 patients expands the molecular mechanisms known to cause Snijders Blok-Campeau syndrome.

Journal: European journal of human genetics : EJHG
Published: October 19, 2019

Next-generation sequencing of 32 genes associated with hereditary aortopathies and related disorders of connective tissue in a cohort of 199 patients.

Next-generation sequencing of 32 genes associated with hereditary aortopathies and related disorders of connective tissue in a cohort of 199 patients.

Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: October 25, 2018
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Last Updated: 09/26/2026