Frédéric Brioude

Beckwith-Wiedemann Syndrome: Growth Pattern and Tumor Risk according to Molecular Mechanism, and Guidelines for Tumor Surveillance

Frédéric Brioude, Alix M.B. Lacoste, Irène Netchine et al. · Hormone Research in Paediatrics · 2013 · 157 citations

Life Sciences, Genetics, Molecular Genetics +16

SEMA3A deletion in a family with Kallmann syndrome validates the role of semaphorin 3A in human puberty and olfactory system development

Jacques Young, Corinne Métay, Jérôme Bouligand et al. · Human Reproduction · 2012 · 141 citations · Full text

Life Sciences, Genetics, Molecular Genetics +12

Genetic disruption of the oncogenic HMGA2–PLAG1–IGF2 pathway causes fetal growth restriction

Walid Abi Habib, Frédéric Brioude, Thomas Édouard et al. · Genetics in Medicine · 2017 · 137 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

<i>CDKN1C</i> mutation affecting the PCNA-binding domain as a cause of familial Russell Silver syndrome

Frédéric Brioude, Isabelle Oliver‐Petit, A. Blaise et al. · Journal of Medical Genetics · 2013 · 132 citations

Medicine, Genetics, Molecular Genetics +16

Mutations of the Imprinted<i>CDKN1C</i>Gene as a Cause of the Overgrowth Beckwith-Wiedemann Syndrome: Clinical Spectrum and Functional Characterization

Frédéric Brioude, Irène Netchine, Françoise Praz et al. · Human Mutation · 2015 · 87 citations

Life Sciences, Genetics, Molecular Genetics +17