Valérie Serre

Interleukin-36–Receptor Antagonist Deficiency and Generalized Pustular Psoriasis

Slaheddine Marrakchi, Philippe Guigue, Blair R. Renshaw et al. · New England Journal of Medicine · 2011 · 965 citations · Full text

Mutation of RRM2B, encoding p53-controlled ribonucleotide reductase (p53R2), causes severe mitochondrial DNA depletion

Alice Bourdon, Limor Minai, Valérie Serre et al. · Nature Genetics · 2007 · 517 citations

Genome Instability, Mitochondrial Function, P53-controlled Ribonucleotide Reductase +10

A mitochondrial origin for frontotemporal dementia and amyotrophic lateral sclerosis through CHCHD10 involvement

Sylvie Bannwarth, Samira Ait-El-Mkadem, Annabelle Chaussenot et al. · Brain · 2014 · 490 citations · Full text

Motor Neuron Disease, Genetics, Mitochondrial Myopathy +16

CABC1 Gene Mutations Cause Ubiquinone Deficiency with Cerebellar Ataxia and Seizures

Julie Mollet, Agnès Delahodde, Valérie Serre et al. · The American Journal of Human Genetics · 2008 · 290 citations · Full text

Neurodegenerative Diseases, Molecular Neuroscience, Mendelian Disorder +11

DYNC2H1 Mutations Cause Asphyxiating Thoracic Dystrophy and Short Rib-Polydactyly Syndrome, Type III

Nathalie Dagoneau, Marie Goulet, David Geneviève et al. · The American Journal of Human Genetics · 2009 · 255 citations · Full text

Genetic Disorder, Genetics, Short Rib-polydactyly Syndrome +4