Publications by authors named "Jenny Cornaton"

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Germline variants in tumor suppressor FBXW7 lead to impaired ubiquitination and a neurodevelopmental syndrome.
Sarah E M Stephenson, Gregory Costain, Laura E R Blok, Michael A Silk, Thanh Binh Nguyen, Jenny Cornaton

Am J Hum Genet· April 2022

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Care management in a French cohort with Down syndrome from the AnDDI-Rares/CNSA study.
Pierre-Henri Roux-Levy, Damien Sanlaville, Bénédicte De Freminville, Renaud Touraine, Alice Masurel, Jenny Cornaton

Eur J Med Genet· October 2021

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Clinical and neuroimaging findings in 33 patients with MCAP syndrome: A survey to evaluate relevant endpoints for future clinical trials.
Aurore Garde, Laurent Guibaud, Alice Goldenberg, Florence Petit, Rodolphe Dard, Jenny Cornaton

Clin Genet· May 2021

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Neuropsychological study in 19 French patients with White-Sutton syndrome and POGZ mutations.
Aurore Garde, Jenny Cornaton, Arthur Sorlin, Sébastien Moutton, Claire Nicolas

Clin Genet· March 2021

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Associations between cognitive performance and the rehabilitation, medical care and social support provided to French children with Prader-Willi syndrome.
Pierre-Henri Roux-Levy, Marie Bournez, Alice Masurel, Nolwenn Jean, Sophie Chancenotte, Jenny Cornaton

Eur J Med Genet· December 2020

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