Anne Noreau

Neuroscience · Life Sciences

21h-index3.3kcitations45works0.02yr avg
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Research Topics

Genetic Neurodegenerative Diseases(12), Mitochondrial Function and Pathology(8), Neurogenetic and Muscular Disorders Research(7), Genetics and Neurodevelopmental Disorders(6), Hereditary Neurological Disorders(6)

Publications45 total

Co-construction d’activités favorisant le développement pédagogique du personnel enseignant débutant
Bibliothèque et Archives nationales du Québec (Québec government)·2023Open Access
Autosomal Recessive Cerebellar Ataxias
2021· 1 cited
Autosomal Recessive Cerebellar Ataxias
2020
SYNE1 mutations cause adult onset autosomal recessive ataxia with retained reflexes in Brazilian patients (P3.004)
Neurology·2017
Post-concussion symptoms and chronic pain after mild traumatic brain injury are modulated by multiple locus effect in the <i>BDNF</i> gene through the expression of antisense: A pilot prospective control study
Canadian Journal of Pain·2017· 3 citedOpen Access
Paternal Age Explains a Major Portion of De Novo Germline Mutation Rate Variability in Healthy Individuals
PLoS ONE·2016· 59 citedOpen Access
<i>SYNE1</i> mutations cause autosomal‐recessive ataxia with retained reflexes in Brazilian patients
Movement Disorders·2016· 16 cited
Novel SIL1 mutations cause cerebellar ataxia and atrophy in a French-Canadian family
Neurogenetics·2015· 6 cited
Parkinson’s Disease Genetic Loci in Rapid Eye Movement Sleep Behavior Disorder
Journal of Molecular Neuroscience·2015· 50 cited
Two Novel Ataxia Phenotypes in the French-Canadian Population (P2.116)
Neurology·2015
Deleterious mutations in the essential mRNA metabolism factor, hGle1, in amyotrophic lateral sclerosis
Human Molecular Genetics·2014· 128 citedOpen Access
Dopamine transporter SLC6A3 genotype affects cortico-striatal activity of set-shifts in Parkinson’s disease
Brain·2014· 31 citedOpen Access
Exome sequencing revealed PMM2 gene mutations in a French-Canadian family with congenital atrophy of the cerebellum
Cerebellum & Ataxias·2014· 2 citedOpen Access
Études génétiques de familles récessives d’ataxies et de paraplégies spastiques
Papyrus : Institutional Repository (Université de Montréal)·2014Open Access
Therapies for Ataxias
Current Treatment Options in Neurology·2014· 5 cited
Molecular aspects of hereditary spastic paraplegia
Experimental Cell Research·2014· 56 cited
Expanding the Clinical Phenotype Associated With<i>ELOVL4</i>Mutation
JAMA Neurology·2014· 128 cited
Loss of Association of REEP2 with Membranes Leads to Hereditary Spastic Paraplegia
The American Journal of Human Genetics·2014· 102 citedOpen Access
Pure hereditary spastic paraplegia due to a <i>de novo</i> mutation in the <i><scp>NIPA</scp>1</i> gene
European Journal of Neurology·2013· 9 citedOpen Access
<i>SYNE1</i>Mutations in Autosomal Recessive Cerebellar Ataxia
JAMA Neurology·2013· 56 cited
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Frequent Co-authors

Guy A. Rouleau(41), Patrick A. Dion(26), Nicolas Dupré(18), Alexandre Dionne‐Laporte(10), Dan Spiegelman(9), Simon Girard(7), Julie Gauthier(7), Jean‐Pierre Bouchard(7), Ridha Joober(6), Marie‐Odile Krebs(6), Sylvain Chouinard(6), Lan Xiong(5), Ronald G. Lafrenière(5), Fadi F. Hamdan(5), Pierre Drapeau(5), Véronique Belzil(5), Annie Levert(5), Anna Szuto(5), Édouard Henrion(4), Pascale Thibodeau(4)