Oriane Trouillard
Centre National de la Recherche Scientifique(FR)Inserm(FR)Sorbonne Université(FR)Institut du Cerveau(FR)
Publications by Year
Research Areas
Epilepsy research and treatment, Genetics and Neurodevelopmental Disorders, Genomics and Rare Diseases, Neurological disorders and treatments, Axon Guidance and Neuronal Signaling
Most-Cited Works
- → Sporadic Infantile Epileptic Encephalopathy Caused by Mutations in PCDH19 Resembles Dravet Syndrome but Mainly Affects Females(2009)368 cited
- → Spectrum of SCN1A gene mutations associated with Dravet syndrome: analysis of 333 patients(2008)362 cited
- → De novo mutations in HCN1 cause early infantile epileptic encephalopathy(2014)234 cited
- → Screening for Genomic Rearrangements and Methylation Abnormalities of the 15q11-q13 Region in Autism Spectrum Disorders(2009)160 cited
- → Mechanisms for variable expressivity of inherited SCN1A mutations causing Dravet syndrome(2010)153 cited
- → Mutations and deletions in PCDH19 account for various familial or isolated epilepsies in females(2010)125 cited