Richard Redon

16PUBLICATIONS

270CO-AUTHORS

Gene expression (incl. microarray and other genome-wide approaches)Autonomic nervous systemNeurogeneticsEuropean history (excl. British, classical Greek and Roman)Epigenetics (incl. genome methylation and epigenomics)

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Publications (16)

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|May 11, 2026

Ventricular conduction is a marker for arrhythmic risk in SCN5A-E1784K overlap sodium channel disease.

|Mar 11, 2026

Clinical profile and prognosis of brugada syndrome SCN5A variant carriers with negative sodium channel blocker challenge.

Elodie Surget, Gael Clerici, Frédéric Sacher

|Oct 23, 2025

PERIGENOMED-CLINICS 1-the first study on feasibility, acceptability and psychosocial impact of PERIGENOMED: a pilot project aimed at providing initial concrete evidence on the relevance of panel-based genome sequencing for newborn screening (NBS) in France.

Camille Level, Christel Thauvin-Robinet, Christine Binquet

|Dec 10, 2024

SURFBAT: a surrogate family based association test building on large imputation reference panels.

Anthony F Herzig, Simone Rubinacci, Gaëlle Marenne

|Oct 11, 2024

A Rare Noncoding Enhancer Variant in <i>SCN5A</i> Contributes to the High Prevalence of Brugada Syndrome in Thailand.

Roddy Walsh, John Mauleekoonphairoj, Isabella Mengarelli

|Aug 07, 2024

Human genetic structure in Northwest France provides new insights into West European historical demography.

Isabel Alves, Joanna Giemza, Michael G B Blum

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Frequent Collaborators

Julien Barc

Christian Dina

Jean-Jacques Schott

Jan H Veldink

Elijah R Behr

Ynte M Ruigrok

Antti Lindgren

Vincent Probst

Stéphanie Debette

Philippe Amouyel

Frequent Collaborators

Julien Barc

Christian Dina

Jean-Jacques Schott

Jan H Veldink