Sébastien Lebon
Mother Hospital(IN)University of Lausanne(CH)
Publications by Year
Research Areas
Epilepsy research and treatment, Genetics and Neurodevelopmental Disorders, Genomics and Rare Diseases, Genomic variations and chromosomal abnormalities, Diet and metabolism studies
Most-Cited Works
- → A 600 kb deletion syndrome at 16p11.2 leads to energy imbalance and neuropsychiatric disorders(2012)353 cited
- → Defining the Effect of the 16p11.2 Duplication on Cognition, Behavior, and Medical Comorbidities(2015)292 cited
- → Quantifying the Effects of 16p11.2 Copy Number Variants on Brain Structure: A Multisite Genetic-First Study(2018)91 cited
- → 16p11.2 600 kb Duplications confer risk for typical and atypical Rolandic epilepsy(2014)69 cited
- → Autosomal recessive primary microcephaly due to ASPM mutations: An update(2017)69 cited
- → Xq28 duplication including MECP2 in six unreported affected females: what can we learn for diagnosis and genetic counselling?(2016)54 cited
- → Effects of eight neuropsychiatric copy number variants on human brain structure(2021)45 cited
- → Pediatric Encephalopathy: Clinical, Biochemical and Cellular Insights into the Role of Gln52 of GNAO1 and GNAI1 for the Dominant Disease(2021)37 cited
- → Perinatal arterial ischemic stroke related to carotid artery occlusion(2016)30 cited
- → Early‐onset encephalopathy with epilepsy associated with a novel splice site mutation in SMC1A(2015)30 cited