Frédéric Leprêtre

Genomewide Search for Type 2 Diabetes–Susceptibility Genes in French Whites: Evidence for a Novel Susceptibility Locus for Early-Onset Diabetes on Chromosome 3q27-qter and Independent Replication of a Type 2–Diabetes Locus on Chromosome 1q21–q24

Nathalie Vionnet, El Habib Hani, S. Dupont et al. · The American Journal of Human Genetics · 2000 · 679 citations · Full text

Genome-wide Association Study, Genetic Determinant, Genotype-phenotype Association +11

Translation Initiator EIF4G1 Mutations in Familial Parkinson Disease

Marie‐Christine Chartier‐Harlin, Justus C. Dächsel, Carles Vilariño‐Güell et al. · The American Journal of Human Genetics · 2011 · 299 citations · Full text

Familial Parkinson Disease, Mendelian Disorder, Genetic Disorder +5

Genomic Landscape of <i>CXCR4</i> Mutations in Waldenström Macroglobulinemia

Stéphanie Poulain, Christophe Roumier, Aurélie Venet-Caillault et al. · Clinical Cancer Research · 2015 · 120 citations

Transcriptional profile of Parkinson blood mononuclear cells with LRRK2 mutation

Eugénie Mutez, Lydie Larvor, Frédéric Leprêtre et al. · Neurobiology of Aging · 2010 · 95 citations

Transcriptional Regulation, Systems Biology, Autophagy +4

Mutation screening of the PPARalpha gene in type 2 diabetes associated with coronary heart disease.

Corinne Lacquemant, Frédéric Leprêtre, Inès Pineda‐Torra et al. · PubMed · 2000 · 85 citations