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Publications by Guy A. Rouleau

LRP10 in Α-Synucleinopathies

The Lancet Neurology
Neurology
2018English

Truncating Mutations in UBAP1 Cause Hereditary Spastic Paraplegia

American Journal of Human Genetics
Genetics
2019English

De Novo Mutations in FOXP1 in Cases With Intellectual Disability, Autism, and Language Impairment

American Journal of Human Genetics
Genetics
2010English

De Novo Mutations in the Gene Encoding the Synaptic Scaffolding proteinSHANK3in Patients Ascertained for Schizophrenia

Proceedings of the National Academy of Sciences of the United States of America
Multidisciplinary
2010English

Screening of Novel Restless Legs Syndrome–associated Genes in French-Canadian Families

Neurology: Genetics
NeurologyGenetics
2018English

A Direct Interaction Between Two Restless Legs Syndrome Predisposing Genes: MEIS1 and SKOR1

Scientific Reports
Multidisciplinary
2018English

Paternal Age Explains a Major Portion of De Novo Germline Mutation Rate Variability in Healthy Individuals

PLoS ONE
Multidisciplinary
2016English

Deletion of C9ORF72 Results in Motor Neuron Degeneration and Stress Sensitivity in C. Elegans

PLoS ONE
Multidisciplinary
2013English

Genome-Wide Association Study Identifies Genetic Factors That Modify Age at Onset in Machado-Joseph Disease

2019English

Dinucleotide Repeat Polymorphism at the Human CRYB2 Gene Locus (22q11.2)

Nucleic Acids Research
Genetics
1992English
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