Florence Molinari
Marseille, France
Last Updated: 09/26/2026
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Found 19 publications
Identification of novel human microcephaly-linked protein Mtss2 that mediates cortical progenitor cell division and corticogenesis through Nedd9-RhoA.
Journal: eLife
Published: July 23, 2025
Loss of NDST1 N-sulfotransferase activity is associated with autosomal recessive intellectual disability.
Journal: Human molecular genetics
Published: July 26, 2023
NAPB and developmental and epileptic encephalopathy: Description of the electroclinical profile associated with a novel pathogenic variant.
Journal: Epilepsia
Published: November 10, 2022
TRAPPC2L-related disorder: first homozygous protein-truncating variant and further delineation of the phenotype.
Journal: Journal of medical genetics
Published: September 27, 2022
Bumetanide induces post-traumatic microglia-interneuron contact to promote neurogenesis and recovery.
Journal: Brain : a journal of neurology
Published: March 03, 2022
Biallelic variants in PCDHGC4 cause a novel neurodevelopmental syndrome with progressive microcephaly, seizures, and joint anomalies.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: March 19, 2021
High-intensity interval training is superior to moderate intensity training on aerobic capacity in rats: Impact on hippocampal plasticity markers.
Journal: Behavioural brain research
Published: July 31, 2020
A knock-in mouse model for KCNQ2-related epileptic encephalopathy displays spontaneous generalized seizures and cognitive impairment.
Journal: Epilepsia
Published: December 03, 2019
Report on three additional patients and genotype-phenotype correlation in SLC25A22-related disorders group.
Journal: European journal of human genetics : EJHG
Published: October 26, 2018
Last Updated: 09/26/2026