Adeline Goudal - Publications

LDLR-3'UTR Deletions Identified as a Genetic Cause of Hypobetalipoproteinemia: Evidence From Familial and Population-Based Studies.

Journal: Arteriosclerosis, thrombosis, and vascular biology

Published: June 04, 2026

Is there an effect of gender on phenotypical expression of genetically mediated sinus node dysfunction?

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: April 07, 2026

Dilated cardiomyopathy in patients with PRDM16 haploinsufficiency.

Journal: Journal of molecular medicine (Berlin, Germany)

Published: February 24, 2025

Impact of Prior Exercise Practice on Disease Characteristics in Desmoplakin-Related Arrhythmogenic Left Ventricular Cardiomyopathy.

Journal: JACC. Clinical electrophysiology

Published: November 19, 2024

Titin-related familial dilated cardiomyopathy: factors associated with disease onset.

Journal: European heart journal

Published: September 18, 2024

Phenotypic spectrum of cardiac conduction disturbance and cardiomyopathy linked to titin canonical splice-site variants.

Journal: Cardiovascular research

Published: June 11, 2024

Prevalence and phenotypes associated with ALPK3 null variants in a large French multicentric cohort: Confirming its involvement in hypertrophic cardiomyopathy.

Journal: Clinical genetics

Published: December 06, 2023

Description of the Two-Dimensional Layer-Specific Strain Echocardiography Phenotype of Arrhythmogenic Left Ventricular Cardiomyopathy.

Journal: Journal of the American Society of Echocardiography : official publication of the American Society of Echocardiography

Published: November 19, 2023

Burden of rare variants in arrhythmogenic cardiomyopathy with right dominant form-associated genes provides new insights for molecular diagnosis and clinical management.

Journal: Human mutation

Published: December 09, 2021