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Anne Noreau

Showing results (11-20 of 23) with videos related to

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Annals of Neurology|June 29, 2011
Restless legs syndrome-associated MEIS1 risk variant influences iron homeostasisHélène Catoire, Patrick A Dion, Lan Xiong, et al.
Neurobiology of Aging|January 1, 2013
Investigation of C9orf72 repeat expansions in Parkinson's diseaseHussein Daoud, Anne Noreau, Daniel Rochefort, et al.
JAMA Neurology|August 21, 2013
SYNE1 mutations in autosomal recessive cerebellar ataxiaAnne Noreau, Cynthia V Bourassa, Anna Szuto, et al.
Plos One|October 11, 2016
Paternal Age Explains a Major Portion of De Novo Germline Mutation Rate Variability in Healthy IndividualsSimon L Girard, Cynthia V Bourassa, Louis-Philippe Lemieux Perreault, et al.
Annals of Neurology|June 27, 2009
De novo STXBP1 mutations in mental retardation and nonsyndromic epilepsyFadi F Hamdan, Amélie Piton, Julie Gauthier, et al.
Human Genetics|March 23, 2011
Truncating mutations in NRXN2 and NRXN1 in autism spectrum disorders and schizophreniaJulie Gauthier, Tabrez J Siddiqui, Peng Huashan, et al.
Human Molecular Genetics|October 26, 2014
Deleterious mutations in the essential mRNA metabolism factor, hGle1, in amyotrophic lateral sclerosisHannah M Kaneb, Andrew W Folkmann, Véronique V Belzil, et al.
Nature Genetics|July 12, 2011
Increased exonic de novo mutation rate in individuals with schizophreniaSimon L Girard, Julie Gauthier, Anne Noreau, et al.
American Journal of Human Genetics|August 7, 2012
Exome sequencing identifies FUS mutations as a cause of essential tremorNancy D Merner, Simon L Girard, Hélène Catoire, et al.
American Journal of Human Genetics|January 7, 2014
Loss of association of REEP2 with membranes leads to hereditary spastic paraplegiaTyphaine Esteves, Alexandra Durr, Emeline Mundwiller, et al.
Pageof 3

Showing results (11-20 of 23) with videos related to

Sort By:
Pageof 3
Annals of Neurology|June 29, 2011
Restless legs syndrome-associated MEIS1 risk variant influences iron homeostasisHélène Catoire, Patrick A Dion, Lan Xiong, et al.
Neurobiology of Aging|January 1, 2013
Investigation of C9orf72 repeat expansions in Parkinson's diseaseHussein Daoud, Anne Noreau, Daniel Rochefort, et al.
JAMA Neurology|August 21, 2013
SYNE1 mutations in autosomal recessive cerebellar ataxiaAnne Noreau, Cynthia V Bourassa, Anna Szuto, et al.
Plos One|October 11, 2016
Paternal Age Explains a Major Portion of De Novo Germline Mutation Rate Variability in Healthy IndividualsSimon L Girard, Cynthia V Bourassa, Louis-Philippe Lemieux Perreault, et al.
Annals of Neurology|June 27, 2009
De novo STXBP1 mutations in mental retardation and nonsyndromic epilepsyFadi F Hamdan, Amélie Piton, Julie Gauthier, et al.
Human Genetics|March 23, 2011
Truncating mutations in NRXN2 and NRXN1 in autism spectrum disorders and schizophreniaJulie Gauthier, Tabrez J Siddiqui, Peng Huashan, et al.
Human Molecular Genetics|October 26, 2014
Deleterious mutations in the essential mRNA metabolism factor, hGle1, in amyotrophic lateral sclerosisHannah M Kaneb, Andrew W Folkmann, Véronique V Belzil, et al.
Nature Genetics|July 12, 2011
Increased exonic de novo mutation rate in individuals with schizophreniaSimon L Girard, Julie Gauthier, Anne Noreau, et al.
American Journal of Human Genetics|August 7, 2012
Exome sequencing identifies FUS mutations as a cause of essential tremorNancy D Merner, Simon L Girard, Hélène Catoire, et al.
American Journal of Human Genetics|January 7, 2014
Loss of association of REEP2 with membranes leads to hereditary spastic paraplegiaTyphaine Esteves, Alexandra Durr, Emeline Mundwiller, et al.
Pageof 3