Sylvain Hanein

4PUBLICATIONS
24CO-AUTHORS
Genetic immunologyDevelopmental genetics (incl. sex determination)Vision scienceGene expression (incl. microarray and other genome-wide approaches)
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Publications (4)

|Jul 30, 2026
FOXP3 deep intronic variant underlying IPEX.

|Sep 27, 2024
Chromatin assembly factor subunit CHAF1A as a monogenic cause for oculo-auriculo-vertebral spectrum.

Véronique Pingault, Cécilia Neiva-Vaz, Judite de Oliveira

|Jun 19, 2024
Four Unique Genetic Variants in Three Genes Account for 62.7% of Early-Onset Severe Retinal Dystrophy in Chile: Diagnostic and Therapeutic Consequences.

Rene Moya, Clémentine Angée, Sylvain Hanein

|Mar 06, 2021
Whole Locus Sequencing Identifies a Prevalent Founder Deep Intronic RPGRIP1 Pathologic Variant in the French Leber Congenital Amaurosis Cohort.

Isabelle Perrault, Sylvain Hanein, Xavier Gérard

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Frequent Collaborators

2 joint publications

Isabelle Perrault

2 joint publications

Jean-Michel Rozet

1 joint publications

Béatrice Bocquet

1 joint publications

Lucas Fares Taie