É. Henrion

发表

Loss-of-function de novo mutations play an important role in severe human neural tube defects

Guy A Rouleau, Dan Spiegelman, G. Rouleau, 2015, Journal of Medical Genetics.

De Novo Mutations in Moderate or Severe Intellectual Disability

Edouard Henrion, Guy A. Rouleau, Fadi F. Hamdan, 2014, PLoS genetics.

Direct measure of the de novo mutation rate in autism and schizophrenia cohorts.

Alexander R. Griffing, A. Addington, J. Rapoport, 2010, American journal of human genetics.

Increased exonic de novo mutation rate in individuals with schizophrenia

S. Lok, A. Tong, B. Millet, 2011, Nature Genetics.

Excess of de novo deleterious mutations in genes associated with glutamatergic systems in nonsyndromic intellectual disability.

R. Huganir, J. Lacaille, G. Rouleau, 2011, American journal of human genetics.

Rare mutations in N-methyl-D-aspartate glutamate receptors in autism spectrum disorders and schizophrenia

L. DeLisi, J. Rapoport, E. Fombonne, 2011, Translational Psychiatry.

Systematic resequencing of X-chromosome synaptic genes in autism spectrum disorder and schizophrenia

J L Rapoport, A. Addington, L. DeLisi, 2011, Molecular Psychiatry.

A Population Genetic Approach to Mapping Neurological Disorder Genes Using Deep Resequencing

Edouard Henrion, Julie Hussin, Carlos D. Bustamante, 2011, PLoS genetics.

De novo STXBP1 mutations in mental retardation and nonsyndromic epilepsy

E. Fombonne, J. Lacaille, F. Dubeau, 2009, Annals of neurology.

Increased Missense Mutation Burden of Fatty Acid Metabolism Related Genes in Nunavik Inuit Population

G. Rouleau, A. Dionne‐Laporte, D. Spiegelman, 2015, PloS one.

GenPipes: an open-source framework for distributed and scalable genomic analyses

Rola Dali, Kuang Chung Chen, Louis Letourneau, 2018, bioRxiv.

Resequencing of 29 candidate genes in patients with familial and sporadic amyotrophic lateral sclerosis.

G. Rouleau, D. Spiegelman, É. Henrion, 2011, Archives of neurology.

De Novo Truncating Mutation in Kinesin 17 Associated with Schizophrenia

L. DeLisi, J. Rapoport, E. Fombonne, 2010, Biological Psychiatry.

Whole exome sequencing identifies novel predisposing genes in neural tube defects

G. Rouleau, A. Dionne‐Laporte, P. Lemay, 2018, Molecular genetics & genomic medicine.