Jean-Louis Mandel

Publication Activity (10 Years)

Years Active: 2022-2024
Publications (10 Years): 5

Top Topics

Traumatic Brain Injury

Intellectual Disability

Autism Spectrum Disorder

Top Venues

American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics

American journal of medical genetics. Part A

EMBO molecular medicine

Molecular psychiatry

This page only lists publications with an associated author ORCID identifier.

Publications

Elana J Forbes, Lottie D Morison, Fatma Lelik, Tegan Howell, Simone Debono, Himanshu Goel, Pauline Burger, Jean-Louis Mandel, David Geneviève, David J Amor, Angela T Morgan
Speech and language in DDX3X-neurodevelopmental disorder: A call for early augmentative and alternative communication intervention. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics (2024)
Elana J Forbes, Lottie D Morison, Fatma Lelik, Tegan Howell, Simone Debono, Himanshu Goel, Pauline Burger, Jean-Louis Mandel, David Geneviève, David J Amor, Angela T Morgan
Speech and language in DDX3X-neurodevelopmental disorder: A call for early augmentative and alternative communication intervention. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 195 (6) (2024)
Jérémie Courraud, Camille Engel, Angélique Quartier, Nathalie Drouot, Ursula Houessou, Damien Plassard, Arthur Sorlin, Elise Brischoux-Boucher, Evan Gouy, Lionel Van Maldergem, Massimiliano Rossi, Gaëtan Lesca, Patrick Edery, Audrey Putoux, Frederic Bilan, Brigitte Gilbert-Dussardier, Isis Atallah, Vera M Kalscheuer, Jean-Louis Mandel, Amelie Piton
Molecular consequences of PQBP1 deficiency, involved in the X-linked Renpenning syndrome. Molecular psychiatry (2023)
Arianne Bouman, Romy N Bouwmeester, Leo A van Vlimmeren, Pauline Burger, Jean-Louis Mandel, Bert B A de Vries, Marinus de Kleuver, Willemijn M Klein, Joyce M Geelen, David A Koolen
Clinical and radiological assessment of scoliosis in Koolen-de Vries syndrome. American journal of medical genetics. Part A (2023)
Karima Habbas, Oktay Cakil, Boglárka Zámbó, Ricardos Tabet, Fabrice Riet, Doulaye Dembele, Jean-Louis Mandel, Michaël Hocquemiller, Ralph Laufer, Françoise Piguet, Hervé Moine
AAV-delivered diacylglycerol kinase DGKk achieves long-term rescue of fragile X syndrome mouse model. EMBO molecular medicine 14 (5) (2022)