Frédéric Torès

Targeted Exome Sequencing Identifies PBX1 as Involved in Monogenic Congenital Anomalies of the Kidney and Urinary Tract

Laurence Heidet, Vincent Morinière, C. Henry et al. · Journal of the American Society of Nephrology · 2017 · 116 citations · Full text

Mutations in GREB1L Cause Bilateral Kidney Agenesis in Humans and Mice

Lara De Tomasi, Pierre David, Camille Humbert et al. · The American Journal of Human Genetics · 2017 · 113 citations · Full text

Urology, Developmental Biology, Medicine +7

Integrin Alpha 8 Recessive Mutations Are Responsible for Bilateral Renal Agenesis in Humans

Camille Humbert, Flora Silbermann, Bharti Morar et al. · The American Journal of Human Genetics · 2014 · 100 citations · Full text

Integrin Alpha 8, Urology, Developmental Biology +10

Convergent evidence identifying MAP/microtubule affinity-regulating kinase 1 (MARK1) as a susceptibility gene for autism

Gilles Maussion, Jérôme Carayol, Aude-Marie Lepagnol-Bestel et al. · Human Molecular Genetics · 2008 · 84 citations

Autism Spectrum Disorders, Syndromic Autism, Genetics +15

Haplotypes in the gene encoding protein kinase c-beta (PRKCB1) on chromosome 16 are associated with autism

Anne Philippi, Elke Roschmann, Frédéric Torès et al. · Molecular Psychiatry · 2005 · 77 citations

Syndromic Autism, Protein Kinase C-beta, Genetics +8