Véronique Pingault

10PUBLICATIONS
40CO-AUTHORS
French languageLinguistics not elsewhere classifiedRadio frequency engineeringDevelopmental genetics (incl. sex determination)Gene mapping
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Publications (10)

|May 27, 2026
COCH-Related Hearing Loss in a French Cohort: Novel Variants and Genotype-Phenotype Correlations.

|Feb 07, 2025
Unilateral, bilateral symmetric or asymmetric isolated hearing loss in patients with heterozygous KITLG variants.

Margaux Serey-Gaut, Ralyath Balogoun, Laurence Jonard

|Dec 17, 2024
Overexpression of Egr1 Transcription Regulator Contributes to Schwann Cell Differentiation Defects in Neural Crest-Specific Adar1 Knockout Mice.

Lisa Zerad, Nadjet Gacem, Fanny Gayda

|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

|Feb 23, 2024
Waardenburg Syndrome: The Contribution of Next-Generation Sequencing to the Identification of Novel Causative Variants.

William Bertani-Torres, Karina Lezirovitz, Danillo Alencar-Coutinho

|Aug 03, 2023
A 22q13.1 duplication in mosaicism including SOX10.

William Bertani-Torres, Margaux Serey-Gaut, Judite de Oliveira

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Frequent Collaborators

3 joint publications

Margaux Serey-Gaut

3 joint publications

Sandrine Marlin

2 joint publications

Nadège Bondurand

2 joint publications

William Bertani-Torres