F. Rousseau

Instability of a 550-Base Pair DNA Segment and Abnormal Methylation in Fragile X Syndrome

I. Oberlé, F. Rousseau, Dominique Heitz et al. · Science · 1991 · 1.5K citations

Life Sciences, Genetics, Molecular Genetics +16

Altered calcium homeostasis in autism-spectrum disorders: evidence from biochemical and genetic studies of the mitochondrial aspartate/glutamate carrier AGC1

Luigi Palmieri, Veruska Papaleo, Vito Porcelli et al. · Molecular Psychiatry · 2008 · 206 citations · Full text

Life Sciences, Genetics, Neuroscience +13

Common mutations in the fibroblast growth factor receptor 3 (FGFR3) gene account for achondroplasia, hypochondroplasia, and thanatophoric dwarfism

Jacky Bonaventure, F. Rousseau, Laurence Legeai‐Mallet et al. · American Journal of Medical Genetics · 1996 · 135 citations

Life Sciences, Genetics, Molecular Genetics +15

Clinical and genetic heterogeneity of hypochondroplasia.

F. Rousseau, Jacky Bonaventure, Laurence Legeai‐Mallet et al. · Journal of Medical Genetics · 1996 · 134 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

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

Life Sciences, Genetics, Molecular Genetics +17