Yoann Vial

15PUBLICATIONS
178CO-AUTHORS
Haematological tumoursEpigenetics (incl. genome methylation and epigenomics)Medical infection agents (incl. prions)Neurology and neuromuscular diseasesRespiratory diseases
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Publications (15)

|Jul 28, 2026
Cup-Like Nuclei Is a Hallmark of DUX4/ERG Acute Lymphoblastic Leukemia and Reveals Cytoplasmic Mitochondria Accumulation.

|Jun 06, 2026
Novel Variants in PUS7 Associated With Intellectual Disability and Growth Retardation: Expanding the Clinical Spectrum in 13 Patients.

|Oct 03, 2025
Myeloid neoplasms risks for germline DDX41 pathogenic variants carriers.

Marie-Charlotte Villy, Youenn Drouet, Lise Larcher

|May 16, 2025
Dominant variants in major spliceosome U4 and U5 small nuclear RNA genes cause neurodevelopmental disorders through splicing disruption.

Caroline Nava, Benjamin Cogne, Amandine Santini

|Apr 16, 2025
De novo variants in KDM2A cause a syndromic neurodevelopmental disorder.

Eric N Anderson, Stephan Drukewitz, Sukhleen Kour

|Apr 11, 2024
Mcph1, mutated in primary microcephaly, is also crucial for erythropoiesis.

Yoann Vial, Jeannette Nardelli, Adeline A Bonnard

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Frequent Collaborators

5 joint publications

Hélène Cave

3 joint publications

Séverine Drunat

3 joint publications

Sandrine Passemard

3 joint publications

Alain Verloes