Margaux Serey-Gaut (Margaux Serey Gaut)

Publication Activity (10 Years)

Years Active: 2020-2024
Publications (10 Years): 5

Top Topics

Autism Spectrum Disorder

Genome Wide Identification

Computed Tomography

Top Venues

American journal of medical genetics. Part A

Clinical genetics

Audiology research

This page only lists publications with an associated author ORCID identifier.

Publications

Nicolas Rive Le Gouard, Valentin Lafond-Rive, Laurence Jonard, Natalie Loundon, Sophie Achard, Laurence Heidet, Isabelle Mosnier, Stanislas Lyonnet, Frederic Brioude, Margaux Serey-Gaut, Sandrine Marlin
HDR syndrome: Large cohort and systematic review. Clinical genetics (2024)
William Bertani-Torres, Margaux Serey-Gaut, Judite de Oliveira, Christine Bole, Mélanie Parisot, Patrick Nistschké, Marie-Laure Maurin, Jean-Michel Lapierre, Natalie Loundon, Kahina Belhous, Nadège Bondurand, Sandrine Marlin, Véronique Pingault
A 22q13.1 duplication in mosaicism including SOX10. American journal of medical genetics. Part A (2023)
Laurence Jonard, Davide Brotto, Miguel Angel Moreno-Pelayo, Ignacio Del Castillo, Hannie Kremer, Ronald J E Pennings, Helena Caria, Graça Fialho, An Boudewyns, Guy Van Camp, Monika Ołdak, Dominika Oziębło, Naïma Deggouj, Romolo Daniele De Siati, Paolo Gasparini, Giorgia Girotto, Margriet Verstreken, Silvia Dossena, Sebastian Roesch, Saba Battelino, Katarina Trebušak Podkrajšek, Athanasia Warnecke, Thomas Lenarz, Anke Lesinski-Schiedat, Michel Mondain, Anne-Françoise Roux, Françoise Denoyelle, Natalie Loundon, Margaux Serey-Gaut, Patrizia Trevisi, Elisa Rubinato, Alessandro Martini, Sandrine Marlin
Genetic Evaluation of Prelingual Hearing Impairment: Recommendations of an European Network for Genetic Hearing Impairment. Audiology research 13 (3) (2023)
Godelieve Morel, Sylvain Ernest, Margaux Serey-Gaut, Laurence Jonard, Abeke Ralyath Balogoun, Marine Parodi, Natalie Loundon, Sophie Achard, Sandrine Marlin
RIPOR2: A new gene of non-syndromic cochleovestibular dysfunction, discrepancy between human pathology and animal models. Clinical genetics (2023)
Margaux Serey-Gaut, Marcello Scala, Bruno Reversade, Lyse Ruaud, Christelle Cabrol, Francesco Musacchia, Annalaura Torella, Andrea Accogli, Nathalie Escande-Beillard, Jean Langlais, Gianluca Piatelli, Alessandro Consales, Vincenzo Nigro, Valeria Capra, Lionel Van Maldergem
Congenital posterior cervical spine malformation due to biallelic c.240-4T>G RIPPLY2 variant: A discrete entity. American journal of medical genetics. Part A 182 (6) (2020)