Vincent Meyer

Mutational signatures reveal the dynamic interplay of risk factors and cellular processes during liver tumorigenesis

Éric Letouzé, Jayendra Shinde, Victor Renault et al. · Nature Communications · 2017 · 303 citations · Full text

Mutation allele burden remains unchanged in chronic myelomonocytic leukaemia responding to hypomethylating agents

Jane Merlevede, Nathalie Droin, Tingting Qin et al. · Nature Communications · 2016 · 211 citations · Full text

Mixed-phenotype Acute Leukemia, Genetics, Dna Methylation +21

Integrative and comparative genomic analyses identify clinically relevant pulmonary carcinoid groups and unveil the supra-carcinoids

Nicolas Alcala, Noémie Leblay, Alice‐Agnes Gabriel et al. · Nature Communications · 2019 · 205 citations · Full text

Unstable TTTTA/TTTCA expansions in MARCH6 are associated with Familial Adult Myoclonic Epilepsy type 3

Rahel T. Florian, Florian Kraft, Elsa Leitão et al. · Nature Communications · 2019 · 161 citations · Full text

KIF1A missense mutations in SPG30, an autosomal recessive spastic paraplegia: distinct phenotypes according to the nature of the mutations

Stephan Klebe, Alexander Lossos, Hamid Azzedine et al. · European Journal of Human Genetics · 2012 · 153 citations · Full text

Biology, Mendelian Disorder, Kif1a Missense Mutations +8