A. Noreau

发表

Exome sequencing identifies FUS mutations as a cause of essential tremor.

G. Rouleau, J. Rivière, M. Panisset, 2012, American journal of human genetics.

Loss of association of REEP2 with membranes leads to hereditary spastic paraplegia.

A. Durr, C. Depienne, A. Brice, 2014, American journal of human genetics.

Molecular aspects of hereditary spastic paraplegia.

G. Rouleau, P. Dion, A. Noreau, 2014, Experimental cell research.

Increased exonic de novo mutation rate in individuals with schizophrenia

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

Exome sequencing revealed PMM2 gene mutations in a French-Canadian family with congenital atrophy of the cerebellum

P. Beauchemin, G. Rouleau, A. Dionne‐Laporte, 2014, Cerebellum & Ataxias.

Early impact of 5-HTTLPR polymorphism on the neural correlates of sadness

M. Beauregard, F. Lepore, M. Boivin, 2010, Neuroscience Letters.

Dopamine transporter SLC6A3 genotype affects cortico-striatal activity of set-shifts in Parkinson's disease.

A. Strafella, O. Monchi, G. Rouleau, 2014, Brain : a journal of neurology.

Early influence of the rs4675690 on the neural substrates of sadness.

M. Beauregard, F. Lepore, G. Rouleau, 2011, Journal of affective disorders.

Dopamine transporter SLC 6 A 3 genotype affects cortico-striatal activity of set-shifts in Parkinson ’ s disease

A. Strafella, O. Monchi, G. Rouleau, 2014 .

Parkinson’s Disease Genetic Loci in Rapid Eye Movement Sleep Behavior Disorder

A. Desautels, R. Postuma, J. Montplaisir, 2015, Journal of Molecular Neuroscience.

SYNE1 mutations cause autosomal‐recessive ataxia with retained reflexes in Brazilian patients

G. Rouleau, A. Dionne‐Laporte, J. Pedroso, 2016, Movement disorders : official journal of the Movement Disorder Society.

Investigation of C9orf72 repeat expansions in Parkinson's disease

N. Jodoin, G. Rouleau, S. Chouinard, 2013, Neurobiology of Aging.

Alteration of ganglioside biosynthesis responsible for complex hereditary spastic paraplegia.

A. Ferbert, A. Durr, S. Forlani, 2013, American journal of human genetics.

CYP7B1 Mutations in French-Canadian Hereditary Spastic Paraplegia Subjects

B. Brais, G. Rouleau, P. Dion, 2012, Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques.

Mutations in FUS cause FALS and SALS in French and French Canadian populations

V. Meininger, F. Salachas, J. Bouchard, 2009, Neurology.

Restless legs syndrome‐associated MEIS1 risk variant influences iron homeostasis

J. Montplaisir, G. Rouleau, G. Turecki, 2011, Annals of neurology.

Therapies for Ataxias

A. Noreau, N. Dupré, L. Martineau, 2014, Current Treatment Options in Neurology.

Novel SIL1 mutations cause cerebellar ataxia and atrophy in a French-Canadian family

B. Brais, G. Rouleau, P. Dion, 2015, neurogenetics.

SYNE1 mutations in autosomal recessive cerebellar ataxia.

A. Durr, J. Bouchard, S. Forlani, 2013, JAMA neurology.

Cadmium binding to a thiol-molecule in vacuoles of Dunaliella bioculata contaminated with CdCl2=electron probe microanalysis

A. Noreau, E. Heuillet, S. Halpern, 1986 .

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

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

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

R. Tremblay, M. Dubé, G. Rouleau, 2016, PloS one.

De novo STXBP1 mutations in mental retardation and nonsyndromic epilepsy

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

De novo mutations in the gene encoding the synaptic scaffolding protein SHANK3 in patients ascertained for schizophrenia

Marie-Pierre Dubé, Christian Néri, Marie-Odile Krebs, 2010, Proceedings of the National Academy of Sciences.

Mutations in SYNGAP1 in autosomal nonsyndromic mental retardation.

A. Addington, L. DeLisi, J. Rapoport, 2009, The New England journal of medicine.

Truncating mutations in NRXN2 and NRXN1 in autism spectrum disorders and schizophrenia

Laurent Mottron, Ann Marie Craig, Marie-Odile Krebs, 2011, Human Genetics.

Deleterious mutations in the essential mRNA metabolism factor, hGle1, in amyotrophic lateral sclerosis.

J. Bouchard, Andrew W. Folkmann, G. Rouleau, 2015, Human molecular genetics.

Autosomal Recessive Cerebellar Ataxias

J. Bouchard, G. Rouleau, P. Dion, 2013 .

J. Bouchard, G. Rouleau, A. Noreau, 2011 .

Expanding the clinical phenotype associated with ELOVL4 mutation: study of a large French-Canadian family with autosomal dominant spinocerebellar ataxia and erythrokeratodermia.

G. Rouleau, D. Nguyen, A. Noreau, 2014, JAMA neurology.

Exome sequencing reveals SPG11 mutations causing juvenile ALS

G. Rouleau, A. Dionne‐Laporte, P. Dion, 2012, Neurobiology of Aging.

Pure hereditary spastic paraplegia due to a de novo mutation in the NIPA1 gene

D. Arkadir, G. Rouleau, A. Noreau, 2014, European journal of neurology.

A new locus for autosomal dominant intracranial aneurysm, ANIB4, maps to chromosome 5p15.2-14.3

M. Dubé, D. Verlaan, G. Rouleau, 2006, Journal of Medical Genetics.

Glucocerebrosidase Mutations in a French-Canadian Parkinson's Disease Cohort

N. Jodoin, G. Rouleau, J. Rivière, 2011, Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques.

Parkinson’s Disease Genetic Loci in Rapid Eye Movement Sleep Behavior Disorder

A. Desautels, R. Postuma, J. Montplaisir, 2015, Journal of Molecular Neuroscience.

Novel SIL1 mutations cause cerebellar ataxia and atrophy in a French-Canadian family

B. Brais, G. Rouleau, P. Dion, 2015, Neurogenetics.

Autosomal Recessive Cerebellar Ataxias

J. Bouchard, G. Rouleau, P. Dion, 2021, Handbook of the Cerebellum and Cerebellar Disorders.

Post-concussion symptoms and chronic pain after mild traumatic brain injury are modulated by multiple locus effect in the BDNF gene through the expression of antisense: A pilot prospective control study

G. Lavigne, S. Khoury, G. Rouleau, 2017, Canadian journal of pain = Revue canadienne de la douleur.

Deleterious mutations in the essential mRNA metabolism factor, hGle1, in amyotrophic lateral sclerosis.

J. Bouchard, Andrew W. Folkmann, G. Rouleau, 2015, Human Molecular Genetics.

Mutations in FUS cause FALS and SALS in French and French Canadian populations

V. Meininger, F. Salachas, J. Bouchard, 2009, Neurology.

Autosomal Recessive Cerebellar Ataxias

P. Dion, A. Noreau, Ikhlass Haj Salem, 2021, Handbook of the Cerebellum and Cerebellar Disorders.

Exome sequencing identifies FUS mutations as a cause of essential tremor.

G. Rouleau, J. Rivière, M. Panisset, 2012, American journal of human genetics.

Loss of association of REEP2 with membranes leads to hereditary spastic paraplegia.

A. Durr, C. Depienne, A. Brice, 2014, American journal of human genetics.

Expanding the clinical phenotype associated with ELOVL4 mutation: study of a large French-Canadian family with autosomal dominant spinocerebellar ataxia and erythrokeratodermia.

G. Rouleau, D. Nguyen, A. Noreau, 2014, JAMA neurology.