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Autism Research : Official Journal of the International Society for Autism Research|February 18, 2011
Behavioral profiles of mouse models for autism spectrum disordersElodie Ey, Claire S Leblond, Thomas Bourgeron
Experimental Neurology|May 1, 2014
Dissection of genetic factors associated with amyotrophic lateral sclerosisClaire S Leblond, Hannah M Kaneb, Patrick A Dion, et al.
Parkinsonism & Related Disorders|May 13, 2015
LRRK2 mutations in Parkinson disease; a sex effect or lack thereof? A meta-analysisZiv Gan-Or, Claire S Leblond, Victoria Mallett, et al.
Behavioural Brain Research|September 3, 2013
The Autism ProSAP1/Shank2 mouse model displays quantitative and structural abnormalities in ultrasonic vocalisationsElodie Ey, Nicolas Torquet, Anne-Marie Le Sourd, et al.
Neurology. Genetics|April 29, 2016
De novo FUS P525L mutation in Juvenile amyotrophic lateral sclerosis with dysphonia and diplopiaClaire S Leblond, Alina Webber, Ziv Gan-Or, et al.
Molecular and Cellular Neurosciences|May 1, 2021
Operative list of genes associated with autism and neurodevelopmental disorders based on database reviewClaire S Leblond, Thuy-Linh Le, Simon Malesys, et al.
Neurology. Genetics|May 2, 2019
Somatic expansion of the C9orf72 hexanucleotide repeat does not occur in ALS spinal cord tissuesJay P Ross, Claire S Leblond, Hélène Catoire, et al.
Scientific Reports|December 20, 2017
Heritability of the melatonin synthesis variability in autism spectrum disordersMarion Benabou, Thomas Rolland, Claire S Leblond, et al.
Neurogenetics|May 10, 2020
Oligogenicity, C9orf72 expansion, and variant severity in ALSJay P Ross, Claire S Leblond, Sandra B Laurent, et al.
Gene|April 28, 2015
Identification of rare protein disulfide isomerase gene variants in amyotrophic lateral sclerosis patientsPaloma Gonzalez-Perez, Ute Woehlbier, Ru-Ju Chian, et al.
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