Gael Nicolas
Rouen, 76000, France
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 197 publications
Eating behaviour phenotype in the MYT1L-related neurodevelopmental disorder: a deep phenotyping study using standardized questionnaires.
Journal: Orphanet journal of rare diseases
Published: July 21, 2026
Exome analysis of 22,319 individuals links extremely rare copy-number variants and 22q11.21 dosage to Alzheimer risk.
Journal: American journal of human genetics
Published: April 20, 2026
Non-microglial downregulation of PLCG2 impairs synaptic function and elicits Alzheimer disease-related hallmarks.
Journal: bioRxiv : the preprint server for biology
Published: April 03, 2026
APOE and genetic risk variants influence Alzheimer's disease onset in carriers of an extra copy of APP, with and without Down syndrome.
Journal: Alzheimer's & dementia : the journal of the Alzheimer's Association
Published: March 10, 2026
Genomics link obesity and type 2 diabetes to Alzheimer's disease to unveil novel biological insights.
Journal: medRxiv : the preprint server for health sciences
Published: February 23, 2026
Genomics link obesity and type 2 diabetes to Alzheimer's disease to unveil novel biological insights.
Journal: medRxiv : the preprint server for health sciences
Published: February 23, 2026
Regulation of Aldosterone Secretion by Substance P and the Neurokinin Type 1 Receptor in Aldosterone-Producing Adenomas.
Journal: Journal of the American Heart Association
Published: January 14, 2026
Pathogenic variants in the cohesin loader subunit MAU2 lead to a new Cornelia de Lange Syndrome subtype.
Journal: medRxiv : the preprint server for health sciences
Published: December 03, 2025
Comprehensive Analysis of the Placenta-Cortex Transcriptomic Database Reveals a Neuroactive Ligand-Receptor Dysregulation After Prenatal Alcohol Exposure.
Journal: International journal of molecular sciences
Published: November 19, 2025
The clinical and molecular spectrum of the KDM6B-related neurodevelopmental disorder.
Journal: American journal of human genetics
Published: October 19, 2025
Pathogenic variants in the cohesin loader subunit MAU2 underlie a distinct Cornelia de Lange Syndrome subtype.
Journal: Nature communications
Published: October 17, 2025
Genetic Modifiers of ABCA1 Activity Interact with APOE Isoforms to Mediate Alzheimer's Disease Risk.
Genetic Modifiers of ABCA1 Activity Interact with APOE Isoforms to Mediate Alzheimer's Disease Risk.
Journal: Annals of neurology
Published: October 16, 2025
Last Updated: 09/26/2026