Author

F. Lecoquierre

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2 papers indexed here

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Open access Jul 2026

CMIP as a novel candidate gene for neurodevelopmental and neuropsychiatric disorders

Matthias De Wachter, Mathijs B. van der Lei, Amber Declève et al. · European Journal of Human Ge... · 1 citation

Jun 2026

GIT1 loss of function causes a recognizable syndromic neurodevelopmental disorder.

Evidence is provided that biallelic GIT1 variants affecting transcript processing or causing premature termination underlie a syndromic neurodevelopmental disorder and an essential role for GIT1 in development and cognitive function is established.

P. Failla, V. Muto, Antonella Lauri et al. · Brain : a journal of neurolo... · 0 citations