Richard Redon

INSERM

France

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Articles (10)

Year:

2025

Year:

2025

Year:

2025

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2025

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2025

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2024

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2024

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2024

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2024

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2024

Collaborators (12)

Isabel Alves

Assistant Professor

University of Strasbourg

FRANCE

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Donald Conrad

Chief & Associate Professor

Oregon Health & Science University

UNITED STATES

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Paul Kuentz

Professeur des Universités-Praticien Hospitalier

Centre Hospitalier Universitaire Vaudois

FRANCE

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Louise-Marie CHEVALIER

Institut de Cancérologie de l'Ouest

FRANCE

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Caroline Rooryck

University of Bordeaux

FRANCE

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Eric Pasmant

Head

Institut Curie

FRANCE

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Sarah Baer

Chief of resident

Hôpitaux universitaires de Strasbourg

FRANCE

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Pierre Vande Perre

Institut Claudius Regaud

FRANCE

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Hélène Cavé

PUPH, Head of the molecular Genetics unit

Hôpital Robert-Debré

FRANCE

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Robert Olaso

Head Lab

Commissariat à l'Énergie Atomique et aux Énergies Alternatives

FRANCE

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Rafik Tadros

Université de Montréal

CANADA

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julien barc

INSERM

FRANCE

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Richard Redon

Research Interests

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Articles (10)

<i>PFMG2025</i>-integrating genomic medicine into the national healthcare system in France.

A Rare Noncoding Enhancer Variant in SCN5A Contributes to the High Prevalence of Brugada Syndrome in Thailand

Benchmark of computational methods to detect digenism in sequencing data

Identification of Hepatic-like EPO as a Cause of Polycythemia

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

Brugada syndrome in Japan and Europe: a genome-wide association study reveals shared genetic architecture and new risk loci

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

How local reference panels improve imputation in French populations

Exploring the origins of neurodevelopmental proteasomopathies associated with cardiac malformations: are neural crest cells central to certain pathological mechanisms?

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

Collaborators (12)

Isabel Alves

Donald Conrad

Paul Kuentz

Louise-Marie CHEVALIER

Caroline Rooryck

Eric Pasmant

Sarah Baer

Pierre Vande Perre

Hélène Cavé

Robert Olaso

Rafik Tadros

julien barc

Make your next move.

Richard Redon

Research Interests

Explore related searches

Contact this professor

Articles (10)

&lt;i&gt;PFMG2025&lt;/i&gt;-integrating genomic medicine into the national healthcare system in France.

A Rare Noncoding Enhancer Variant in SCN5A Contributes to the High Prevalence of Brugada Syndrome in Thailand

Benchmark of computational methods to detect digenism in sequencing data

Identification of Hepatic-like EPO as a Cause of Polycythemia

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

Brugada syndrome in Japan and Europe: a genome-wide association study reveals shared genetic architecture and new risk loci

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

How local reference panels improve imputation in French populations

Exploring the origins of neurodevelopmental proteasomopathies associated with cardiac malformations: are neural crest cells central to certain pathological mechanisms?

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

Collaborators (12)

Isabel Alves

Donald Conrad

Paul Kuentz

Louise-Marie CHEVALIER

Caroline Rooryck

Eric Pasmant

Sarah Baer

Pierre Vande Perre

Hélène Cavé

Robert Olaso

Rafik Tadros

julien barc

Make your next move.

<i>PFMG2025</i>-integrating genomic medicine into the national healthcare system in France.