Mélanie Parisot

7PUBLICATIONS
48CO-AUTHORS
Epigenetics (incl. genome methylation and epigenomics)Child language acquisitionHaematological tumoursGenome structure and regulationMolecular evolution
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Publications (7)

|Jan 30, 2026
A heterozygous USB1 variant linked to immunodeficiency.

Alice Valagussa, Nidia Moreno-Corona, Chantal Lagresle-Peyrou

|Feb 13, 2025
Deciphering the genetic basis of developmental language disorder in children without intellectual disability, autism or apraxia of speech.

Clothilde Ormieres, Marion Lesieur-Sebellin, Karine Siquier-Pernet

|Jun 22, 2023
NBEAL2 deficiency in humans leads to low CTLA-4 expression in activated conventional T cells.

Laure Delage, Francesco Carbone, Quentin Riller

|Jun 22, 2022
Publisher Correction: Somatic genetic rescue of a germline ribosome assembly defect.

Shengjiang Tan, Laëtitia Kermasson, Christine Hilcenko

|Aug 20, 2021
Somatic genetic rescue of a germline ribosome assembly defect.

Shengjiang Tan, Laëtitia Kermasson, Christine Hilcenko

|Jan 12, 2020
ADAR1 mediated regulation of neural crest derived melanocytes and Schwann cell development.

Nadjet Gacem, Anthula Kavo, Lisa Zerad

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Frequent Collaborators

2 joint publications

Christine Bellanné-Chantelot

2 joint publications

Alan J Warren

2 joint publications

Peter J Bond

2 joint publications

Patrick Revy