A. Giguet-Valard

Next‐generation sequencing in a series of 80 fetuses with complex cardiac malformations and/or heterotaxy

R. Touraine, N. Chassaing, P. Jouk, 2020, Human mutation.

Gossypetin Derivatives are also Putative Inhibitors of SARS-COV 2: Results of a Computational Study

R. Bellance, S. Morin, A. Giguet-Valard, 2020, Journal of Biomedical Research & Environmental Sciences.

Identification of novel pathogenic copy number variations in Charcot-Marie-Tooth disease

C. Béroud, J. Desvignes, M. Krahn, 2019, Journal of Human Genetics.

10 years of CEMARA database in the AnDDI-Rares network: a unique resource facilitating research and epidemiology in developmental disorders in France

J. Melki, A. Toutain, A. Verloes, 2021, Orphanet Journal of Rare Diseases.

SOD1-related ALS with anticipation in a large family from Martinique

T. Barnetche, C. Cazeneuve, C. Goizet, 2021, Amyotrophic lateral sclerosis & frontotemporal degeneration.

Identification of novel pathogenic copy number variations in Charcot-Marie-Tooth disease

C. Béroud, J. Desvignes, N. Lévy, 2019, Journal of Human Genetics.

A Family with a Single LMNA Mutation Illustrates Diversity in Cardiac Phenotypes Associated with Laminopathic Progeroid Syndromes

C. Vatier, A. Monfort, E. Sarrazin, 2023, Cardiogenetics.