Vincent Cantagrel
7PUBLICATIONS
49CO-AUTHORS
Get your video featured.
Publish with JoVEGet your video featured.
Publish with JoVE
Publications (7)
Sort by Publication Date:
|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
|May 05, 2022
Suleiman-El-Hattab syndrome: a histone modification disorder caused by TASP1 deficiency.Korbinian M Riedhammer, Anna L Burgemeister, Vincent Cantagrel
|Apr 07, 2022
16p13.11p11.2 triplication syndrome: a new recognizable genomic disorder characterized by optical genome mapping and whole genome sequencing.Romain Nicolle, Karine Siquier-Pernet, Marlène Rio
|May 08, 2021
Loss of function mutations in GEMIN5 cause a neurodevelopmental disorder.Sukhleen Kour, Deepa S Rajan, Tyler R Fortuna
|Mar 25, 2021
Inherited glycosylphosphatidylinositol defects cause the rare Emm-negative blood phenotype and developmental disorders.Romain Duval, Gaël Nicolas, Alexandra Willemetz
|Dec 01, 2020
MINPP1 prevents intracellular accumulation of the chelator inositol hexakisphosphate and is mutated in Pontocerebellar Hypoplasia.Ekin Ucuncu, Karthyayani Rajamani, Miranda S C Wilson
Pageof 2
Frequent Collaborators
2 joint publications
Maha S Zaki
2 joint publications
Patrick Nitschké
2 joint publications
Joseph G Gleeson
2 joint publications
Valérie Malan
2 joint publications
Marlène Rio
2 joint publications
Karine Siquier-Pernet
1 joint publications
Emilie Schlumberger
1 joint publications
Lydie Burglen
1 joint publications
Adolfo Saiardi
1 joint publications
Gaël Nicolas
