Estelle Baron
Nantes, France
Last Updated: 09/26/2026
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Found 18 publications
Whole-genome sequencing implicates rare, low-frequency and structural non-coding variation at the SCN5A locus in Brugada syndrome.
Journal: medRxiv : the preprint server for health sciences
Published: July 17, 2026
Generation of a patient-specific induced pluripotent stem cell line carrying the DES p.R406W mutation, an isogenic control and a DES p.R406W knock-in line.
Journal: Stem cell research
Published: February 02, 2024
Human genetic structure in Northwest France provides new insights into West European historical demography.
Journal: Nature communications
Published: June 21, 2023
TAD boundary deletion causes PITX2-related cardiac electrical and structural defects.
Journal: Nature communications
Published: February 17, 2023
Author Correction: Genome-wide association analyses identify new Brugada syndrome risk loci and highlight a new mechanism of sodium channel regulation in disease susceptibility.
Journal: Nature genetics
Published: April 27, 2022
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
Genome-wide association analyses identify new Brugada syndrome risk loci and highlight a new mechanism of sodium channel regulation in disease susceptibility.
Journal: Nature genetics
Published: September 25, 2020
Genetic Association Analyses Highlight IL6, ALPL, and NAV1 As 3 New Susceptibility Genes Underlying Calcific Aortic Valve Stenosis.
Journal: Circulation. Genomic and precision medicine
Published: March 07, 2020
Dysfunction of the Voltage-Gated K+ Channel β2 Subunit in a Familial Case of Brugada Syndrome.
Journal: Journal of the American Heart Association
Published: June 12, 2016
Last Updated: 09/26/2026