Guy Rouleau Montreal Neurological Institute and Hospital McGill University Biography Publications Institution JoVE Articles Guy Rouleau has not added a biography. If you are Guy Rouleau and would like to personalize this page please email our Author Liaison for assistance. Publications Mutation Burden of Rare Variants in Schizophrenia Candidate Genes PloS One. 2015 | Pubmed ID: 26039597 Alteration of Ornithine Metabolism Leads to Dominant and Recessive Hereditary Spastic Paraplegia Brain : a Journal of Neurology. May, 2015 | Pubmed ID: 26026163 Increased Missense Mutation Burden of Fatty Acid Metabolism Related Genes in Nunavik Inuit Population PloS One. 2015 | Pubmed ID: 26010953 LRRK2 Mutations in Parkinson Disease; a Sex Effect or Lack Thereof? A Meta-analysis Parkinsonism & Related Disorders. May, 2015 | Pubmed ID: 25962553 Identification of Rare Protein Disulfide Isomerase Gene Variants in Amyotrophic Lateral Sclerosis Patients Gene. Jul, 2015 | Pubmed ID: 25913742 A Point Mutation in the Ubiquitin Ligase RNF170 That Causes Autosomal Dominant Sensory Ataxia Destabilizes the Protein and Impairs Inositol 1,4,5-Trisphosphate Receptor-mediated Ca2+ Signaling The Journal of Biological Chemistry. May, 2015 | Pubmed ID: 25882839 Defining the Genetic Connection Linking Amyotrophic Lateral Sclerosis (ALS) with Frontotemporal Dementia (FTD) Trends in Genetics : TIG. May, 2015 | Pubmed ID: 25869998 A Gain-of-function Mutation in NALCN in a Child with Intellectual Disability, Ataxia and Arthrogryposis Human Mutation. Apr, 2015 | Pubmed ID: 25864427 Genetic Markers of Restless Legs Syndrome in Parkinson Disease Parkinsonism & Related Disorders. Jun, 2015 | Pubmed ID: 25817513 Comparison of Sequencing Based CNV Discovery Methods Using Monozygotic Twin Quartets PloS One. 2015 | Pubmed ID: 25812131 PMPCA Mutations Cause Abnormal Mitochondrial Protein Processing in Patients with Non-progressive Cerebellar Ataxia Brain : a Journal of Neurology. Jun, 2015 | Pubmed ID: 25808372 Loss-of-function De Novo Mutations Play an Important Role in Severe Human Neural Tube Defects Journal of Medical Genetics. Mar, 2015 | Pubmed ID: 25805808 Exome Sequencing in Amyotrophic Lateral Sclerosis Identifies Risk Genes and Pathways Science (New York, N.Y.). Mar, 2015 | Pubmed ID: 25700176 Disruption of CLPB is Associated with Congenital Microcephaly, Severe Encephalopathy and 3-methylglutaconic Aciduria Journal of Medical Genetics. May, 2015 | Pubmed ID: 25650066 Functional Variants of POC5 Identified in Patients with Idiopathic Scoliosis The Journal of Clinical Investigation. Mar, 2015 | Pubmed ID: 25642776 Early Detection of Structural Abnormalities and Cytoplasmic Accumulation of TDP-43 in Tissue-engineered Skins Derived from ALS Patients Acta Neuropathologica Communications. 2015 | Pubmed ID: 25637145 Affected Twins in the Familial Intracranial Aneurysm Study Cerebrovascular Diseases (Basel, Switzerland). 2015 | Pubmed ID: 25571891 No Evidence for GADL1 Variation As a Bipolar Disorder Susceptibility Factor in a Caucasian Lithium-responsive Cohort The American Journal of Psychiatry. Jan, 2015 | Pubmed ID: 25553497 Deleterious Mutations in the Essential MRNA Metabolism Factor, HGle1, in Amyotrophic Lateral Sclerosis Human Molecular Genetics. Mar, 2015 | Pubmed ID: 25343993 De Novo Mutations in the Motor Domain of KIF1A Cause Cognitive Impairment, Spastic Paraparesis, Axonal Neuropathy, and Cerebellar Atrophy Human Mutation. Jan, 2015 | Pubmed ID: 25265257 Cross-disorder Genome-wide Analyses Suggest a Complex Genetic Relationship Between Tourette's Syndrome and OCD The American Journal of Psychiatry. Jan, 2015 | Pubmed ID: 25158072 Family-based Association Study of Common Variants, Rare Mutation Study and Epistatic Interaction Detection in HDAC Genes in Schizophrenia Schizophrenia Research. Dec, 2014 | Pubmed ID: 25445625 A Novel Nonsense Mutation in SCN9A in a Moroccan Child with Congenital Insensitivity to Pain Pediatric Neurology. Nov, 2014 | Pubmed ID: 25439579 A Homozygous Loss-of-function Variant in MYH11 in a Case with Megacystis-microcolon-intestinal Hypoperistalsis Syndrome European Journal of Human Genetics : EJHG. Nov, 2014 | Pubmed ID: 25407000 C9orf72 Repeat Expansions in Rapid Eye Movement Sleep Behaviour Disorder The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques. Nov, 2014 | Pubmed ID: 25377888 Exome-wide Rare Variant Analysis Identifies TUBA4A Mutations Associated with Familial ALS Neuron. Oct, 2014 | Pubmed ID: 25374358 De Novo Mutations in Moderate or Severe Intellectual Disability PLoS Genetics. Oct, 2014 | Pubmed ID: 25356899 Genome-wide Association Study of Intracranial Aneurysm Identifies a New Association on Chromosome 7 Stroke; a Journal of Cerebral Circulation. Nov, 2014 | Pubmed ID: 25256182 Increased Prevalence of Non-motor Symptoms in Essential Tremor Tremor and Other Hyperkinetic Movements (New York, N.Y.). 2014 | Pubmed ID: 25247108 Dopamine Transporter SLC6A3 Genotype Affects Cortico-striatal Activity of Set-shifts in Parkinson's Disease Brain : a Journal of Neurology. Nov, 2014 | Pubmed ID: 25212851 Meta-analysis of SHANK Mutations in Autism Spectrum Disorders: a Gradient of Severity in Cognitive Impairments PLoS Genetics. Sep, 2014 | Pubmed ID: 25188300 Linking Neocortical, Cognitive, and Genetic Variability in Autism with Alterations of Brain Plasticity: the Trigger-Threshold-Target Model Neuroscience and Biobehavioral Reviews. Nov, 2014 | Pubmed ID: 25155242 ODD Irritability is Associated with Obsessive-compulsive Behavior and Not ADHD in Chronic Tic Disorders Psychiatry Research. Dec, 2014 | Pubmed ID: 25108592 Identification of a Homozygous Splice Site Mutation in the Dynein Axonemal Light Chain 4 Gene on 22q13.1 in a Large Consanguineous Family from Pakistan with Congenital Mirror Movement Disorder Human Genetics. Nov, 2014 | Pubmed ID: 25098561 Vanishing White Matter Disease in French-Canadian Patients from Quebec Pediatric Neurology. Aug, 2014 | Pubmed ID: 25079571 Copy Number Variation in Obsessive-compulsive Disorder and Tourette Syndrome: a Cross-disorder Study Journal of the American Academy of Child and Adolescent Psychiatry. Aug, 2014 | Pubmed ID: 25062598 Genetic Association Signal Near NTN4 in Tourette Syndrome Annals of Neurology. Aug, 2014 | Pubmed ID: 25042818 Modifiers of (CAG)(n) Instability in Machado-Joseph Disease (MJD/SCA3) Transmissions: an Association Study with DNA Replication, Repair and Recombination Genes Human Genetics. Oct, 2014 | Pubmed ID: 25026993 Genome-wide Association Study in FTD: Divide to Conquer The Lancet. Neurology. Jul, 2014 | Pubmed ID: 24943334 Genetically Encoded Impairment of Neuronal KCC2 Cotransporter Function in Human Idiopathic Generalized Epilepsy EMBO Reports. Jul, 2014 | Pubmed ID: 24928908 Genetics of Essential Tremor: from Phenotype to Genes, Insights from Both Human and Mouse Studies Progress in Neurobiology. Aug-Sep, 2014 | Pubmed ID: 24820404 Mutations in DOCK7 in Individuals with Epileptic Encephalopathy and Cortical Blindness American Journal of Human Genetics. Jun, 2014 | Pubmed ID: 24814191 The Genetic Landscape of Infantile Spasms Human Molecular Genetics. Sep, 2014 | Pubmed ID: 24781210 Dissection of Genetic Factors Associated with Amyotrophic Lateral Sclerosis Experimental Neurology. Dec, 2014 | Pubmed ID: 24780888 Quantitative Trait Loci (QTL) Study Identifies Novel Genomic Regions Associated to Chiari-like Malformation in Griffon Bruxellois Dogs PloS One. 2014 | Pubmed ID: 24740420 A Blinded International Study on the Reliability of Genetic Testing for GGGGCC-repeat Expansions in C9orf72 Reveals Marked Differences in Results Among 14 Laboratories Journal of Medical Genetics. Jun, 2014 | Pubmed ID: 24706941 Molecular Aspects of Hereditary Spastic Paraplegia Experimental Cell Research. Jul, 2014 | Pubmed ID: 24631291 Genome-wide Association Study Reveals Two New Risk Loci for Bipolar Disorder Nature Communications. 2014 | Pubmed ID: 24618891 Expanding the Clinical Phenotype Associated with ELOVL4 Mutation: Study of a Large French-Canadian Family with Autosomal Dominant Spinocerebellar Ataxia and Erythrokeratodermia JAMA Neurology. Apr, 2014 | Pubmed ID: 24566826 Loss of Association of REEP2 with Membranes Leads to Hereditary Spastic Paraplegia American Journal of Human Genetics. Feb, 2014 | Pubmed ID: 24388663 Decreased Global Methylation in Patients with Bipolar Disorder Who Respond to Lithium The International Journal of Neuropsychopharmacology / Official Scientific Journal of the Collegium Internationale Neuropsychopharmacologicum (CINP). Apr, 2014 | Pubmed ID: 24345589 Exome Sequencing As a Diagnostic Tool for Pediatric-onset Ataxia Human Mutation. Jan, 2014 | Pubmed ID: 24108619 SYN2 is an Autism Predisposing Gene: Loss-of-function Mutations Alter Synaptic Vesicle Cycling and Axon Outgrowth Human Molecular Genetics. Jan, 2014 | Pubmed ID: 23956174 Deletion of C9ORF72 Results in Motor Neuron Degeneration and Stress Sensitivity in C. Elegans PloS One. 2013 | Pubmed ID: 24349511 Response Inhibition in Tic Disorders: Waiting to Respond Is Harder When ADHD Is Present Journal of Attention Disorders. Dec, 2013 | Pubmed ID: 24305059 Alterations in Phosphorylated CAMP Response Element-binding Protein (pCREB) Signaling: an Endophenotype of Lithium-responsive Bipolar Disorder? Bipolar Disorders. Dec, 2013 | Pubmed ID: 24238631 Family-based Exome-sequencing Approach Identifies Rare Susceptibility Variants for Lithium-responsive Bipolar Disorder Genome / National Research Council Canada = Génome / Conseil National De Recherches Canada. Oct, 2013 | Pubmed ID: 24237345 Partitioning the Heritability of Tourette Syndrome and Obsessive Compulsive Disorder Reveals Differences in Genetic Architecture PLoS Genetics. Oct, 2013 | Pubmed ID: 24204291 The Impact of Phenotypic and Genetic Heterogeneity on Results of Genome Wide Association Studies of Complex Diseases PloS One. 2013 | Pubmed ID: 24146854 Deficiency of Asparagine Synthetase Causes Congenital Microcephaly and a Progressive Form of Encephalopathy Neuron. Oct, 2013 | Pubmed ID: 24139043 ERBB4 Mutations That Disrupt the Neuregulin-ErbB4 Pathway Cause Amyotrophic Lateral Sclerosis Type 19 American Journal of Human Genetics. Nov, 2013 | Pubmed ID: 24119685 Whole-exome Sequencing Reveals a Rapid Change in the Frequency of Rare Functional Variants in a Founding Population of Humans PLoS Genetics. 2013 | Pubmed ID: 24086152 Recessive and Dominant Mutations in Retinoic Acid Receptor Beta in Cases with Microphthalmia and Diaphragmatic Hernia American Journal of Human Genetics. Oct, 2013 | Pubmed ID: 24075189 SYNE1 Mutations in Autosomal Recessive Cerebellar Ataxia JAMA Neurology. Oct, 2013 | Pubmed ID: 23959263 Genetic Relationship Between Five Psychiatric Disorders Estimated from Genome-wide SNPs Nature Genetics. Aug, 2013 | Pubmed ID: 23933821 Assessment of Response to Lithium Maintenance Treatment in Bipolar Disorder: A Consortium on Lithium Genetics (ConLiGen) Report PloS One. 2013 | Pubmed ID: 23840348 Differential Effect of Lithium on Spermidine/spermine N1-acetyltransferase Expression in Suicidal Behaviour The International Journal of Neuropsychopharmacology / Official Scientific Journal of the Collegium Internationale Neuropsychopharmacologicum (CINP). Nov, 2013 | Pubmed ID: 23768751 Alteration of Ganglioside Biosynthesis Responsible for Complex Hereditary Spastic Paraplegia American Journal of Human Genetics. Jul, 2013 | Pubmed ID: 23746551 Mitochondrial Damage Revealed by Immunoselection for ALS-linked Misfolded SOD1 Human Molecular Genetics. Oct, 2013 | Pubmed ID: 23736301 Potassium-chloride Cotransporter 3 Interacts with Vav2 to Synchronize the Cell Volume Decrease Response with Cell Protrusion Dynamics PloS One. 2013 | Pubmed ID: 23724134 Disruption of TBC1D7, a Subunit of the TSC1-TSC2 Protein Complex, in Intellectual Disability and Megalencephaly Journal of Medical Genetics. Nov, 2013 | Pubmed ID: 23687350 Genetic and Epigenetic Studies of Amyotrophic Lateral Sclerosis Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration. May, 2013 | Pubmed ID: 23678879 Analysis of LMNB1 Duplications in Autosomal Dominant Leukodystrophy Provides Insights into Duplication Mechanisms and Allele-specific Expression Human Mutation. Aug, 2013 | Pubmed ID: 23649844 TARDBP and FUS Mutations Associated with Amyotrophic Lateral Sclerosis: Summary and Update Human Mutation. Jun, 2013 | Pubmed ID: 23559573 Rapid EEG Activity During Sleep Dominates in Mild Traumatic Brain Injury Patients with Acute Pain Journal of Neurotrauma. Apr, 2013 | Pubmed ID: 23510169 ImmunoChip Study Implicates Antigen Presentation to T Cells in Narcolepsy PLoS Genetics. 2013 | Pubmed ID: 23459209 Comparative Analysis of the Expression Profile of Wnk1 and Wnk1/Hsn2 Splice Variants in Developing and Adult Mouse Tissues PloS One. 2013 | Pubmed ID: 23451271 Investigating the Contribution of VAPB/ALS8 Loss of Function in Amyotrophic Lateral Sclerosis Human Molecular Genetics. Jun, 2013 | Pubmed ID: 23446633 Investigation of Rare Variants in LRP1, KPNA1, ALS2CL and ZNF480 Genes in Schizophrenia Patients Reflects Genetic Heterogeneity of the Disease Behavioral and Brain Functions : BBF. 2013 | Pubmed ID: 23425335 C9orf72 Repeat Expansions Are a Rare Genetic Cause of Parkinsonism Brain : a Journal of Neurology. Feb, 2013 | Pubmed ID: 23413259 WNK1/HSN2 Mutation in Human Peripheral Neuropathy Deregulates KCC2 Expression and Posterior Lateral Line Development in Zebrafish (Danio Rerio) PLoS Genetics. 2013 | Pubmed ID: 23300475 Investigation of C9orf72 Repeat Expansions in Parkinson's Disease Neurobiology of Aging. Jun, 2013 | Pubmed ID: 23273600 Familial Intracranial Aneurysms: is Anatomic Vulnerability Heritable? Stroke; a Journal of Cerebral Circulation. Jan, 2013 | Pubmed ID: 23204049 Analysis of the Effects of Rare Variants on Splicing Identifies Alterations in GABAA Receptor Genes in Autism Spectrum Disorder Individuals European Journal of Human Genetics : EJHG. Jul, 2013 | Pubmed ID: 23169495 Mutations in SYNGAP1 Cause Intellectual Disability, Autism, and a Specific Form of Epilepsy by Inducing Haploinsufficiency Human Mutation. Feb, 2013 | Pubmed ID: 23161826 Epigenetic Regulation of Synapsin Genes in Mood Disorders Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology. Jan, 2013 | Pubmed ID: 23147482 Mutation Analysis of PFN1 in Familial Amyotrophic Lateral Sclerosis Patients Neurobiology of Aging. Apr, 2013 | Pubmed ID: 23062600 Identification and Biochemical Characterization of a Novel Mutation in DDX11 Causing Warsaw Breakage Syndrome Human Mutation. Jan, 2013 | Pubmed ID: 23033317 Mortality and Causes of Death in the Familial Intracranial Aneurysm Study International Journal of Stroke : Official Journal of the International Stroke Society. Dec, 2013 | Pubmed ID: 22928607 Genetic Analysis of SIGMAR1 As a Cause of Familial ALS with Dementia European Journal of Human Genetics : EJHG. Feb, 2013 | Pubmed ID: 22739338 H3K4 Tri-methylation in Synapsin Genes Leads to Different Expression Patterns in Bipolar Disorder and Major Depression The International Journal of Neuropsychopharmacology / Official Scientific Journal of the Collegium Internationale Neuropsychopharmacologicum (CINP). Mar, 2013 | Pubmed ID: 22571925 Rare Variants in Complex Traits: Novel Identification Strategies and the Role of De Novo Mutations Human Heredity. 2012 | Pubmed ID: 23594499 Endoplasmic Reticulum Lipid Rafts and Upper Motor Neuron Degeneration Annals of Neurology. Oct, 2012 | Pubmed ID: 23109142 The FUS About Arginine Methylation in ALS and FTLD The EMBO Journal. Nov, 2012 | Pubmed ID: 23085990 Identification of Novel Genes Involved in Migraine Headache. Oct, 2012 | Pubmed ID: 23030542 Mutations in TMEM231 Cause Joubert Syndrome in French Canadians Journal of Medical Genetics. Oct, 2012 | Pubmed ID: 23012439 De Novo Mutations in Neurological and Psychiatric Disorders: Effects, Diagnosis and Prevention Genome Medicine. 2012 | Pubmed ID: 23009675 C9orf72 Hexanucleotide Repeat Expansions As the Causative Mutation for Chromosome 9p21-linked Amyotrophic Lateral Sclerosis and Frontotemporal Dementia Archives of Neurology. Sep, 2012 | Pubmed ID: 22964911 Genome-wide Association Study of Intracranial Aneurysms Confirms Role of Anril and SOX17 in Disease Risk Stroke; a Journal of Cerebral Circulation. Nov, 2012 | Pubmed ID: 22961961 VAMP1 Mutation Causes Dominant Hereditary Spastic Ataxia in Newfoundland Families American Journal of Human Genetics. Sep, 2012 | Pubmed ID: 22958904 Nutzbarmachung Genomics ökologische Determinanten Der Erblichen Krankheit Zu Identifizieren Mutation Research. Aug, 2012 | Pubmed ID: 22935230 Exome Sequencing Identifies FUS Mutations As a Cause of Essential Tremor American Journal of Human Genetics. Aug, 2012 | Pubmed ID: 22863194 Familial ALS: Less Common Than We Think? Journal of Neurology, Neurosurgery, and Psychiatry. Dec, 2012 | Pubmed ID: 22791902 UBQLN2/ubiquilin 2 Mutation and Pathology in Familial Amyotrophic Lateral Sclerosis Neurobiology of Aging. Oct, 2012 | Pubmed ID: 22717235 UBQLN2 Mutations Are Rare in French and French-Canadian Amyotrophic Lateral Sclerosis Neurobiology of Aging. Sep, 2012 | Pubmed ID: 22560112 Unruptured Intracranial Aneurysms in the Familial Intracranial Aneurysm and International Study of Unruptured Intracranial Aneurysms Cohorts: Differences in Multiplicity and Location Journal of Neurosurgery. Jul, 2012 | Pubmed ID: 22540404 Expanding the Differential Diagnosis of Inherited Neuropathies with Non-uniform Conduction: Andermann Syndrome Journal of the Peripheral Nervous System : JPNS. Mar, 2012 | Pubmed ID: 22462673 Schizophrenia Genetics: Putting All the Pieces Together Current Neurology and Neuroscience Reports. Jun, 2012 | Pubmed ID: 22456906 Mutations in C5ORF42 Cause Joubert Syndrome in the French Canadian Population American Journal of Human Genetics. Apr, 2012 | Pubmed ID: 22425360 Loss of Neuronal Potassium/chloride Cotransporter 3 (KCC3) is Responsible for the Degenerative Phenotype in a Conditional Mouse Model of Hereditary Motor and Sensory Neuropathy Associated with Agenesis of the Corpus Callosum The Journal of Neuroscience : the Official Journal of the Society for Neuroscience. Mar, 2012 | Pubmed ID: 22423107 Association Between Schizophrenia and Genetic Variation in DCC: a Case-control Study Schizophrenia Research. May, 2012 | Pubmed ID: 22418395 CYP7B1 Mutations in French-Canadian Hereditary Spastic Paraplegia Subjects The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques. Jan, 2012 | Pubmed ID: 22384504 Synapsin II is Involved in the Molecular Pathway of Lithium Treatment in Bipolar Disorder PloS One. 2012 | Pubmed ID: 22384280 Mutant TDP-43 and FUS Cause Age-dependent Paralysis and Neurodegeneration in C. Elegans PloS One. 2012 | Pubmed ID: 22363618 Analysis of the SORT1 Gene in Familial Amyotrophic Lateral Sclerosis Neurobiology of Aging. Aug, 2012 | Pubmed ID: 22361451 Functional Analysis of Missense Variants in the TRESK (KCNK18) K Channel Scientific Reports. 2012 | Pubmed ID: 22355750 A Novel PLP1 Mutation Further Expands the Clinical Heterogeneity at the Locus The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques. Mar, 2012 | Pubmed ID: 22343157 SOD1 Mutations: More to Learn The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques. Mar, 2012 | Pubmed ID: 22343144 Erweiterte ATXN3 Frameshifting Ereignisse Sind Giftig in Drosophila Und Säugetier-Neuron-Modelle Human Molecular Genetics. Feb, 2012 | Pubmed ID: 22337953 Kennung Für Eine Neuartige In-Frame Neumutationen Im SPTAN1 in Geistiger Behinderung Und Pontozerebelläre Atrophie European Journal of Human Genetics : EJHG. Jan, 2012 | Pubmed ID: 22258530 Neuartige FUS Löschung Bei Einem Patienten Mit Juveniler Amyotrophe Lateralsklerose Archives of Neurology. Jan, 2012 | Pubmed ID: 22248478 Exome Sequenzierung Enthüllt SPG11 Mutationen Verursachen Juvenile ALS Neurobiology of Aging. Apr, 2012 | Pubmed ID: 22154821 Neurophysiologische Untersuchung Kongenitale Spiegel Bewegungen Bei Einem Patienten Mit Agenesie Des Corpus Callosum Brain Stimulation. Mar, 2011 | Pubmed ID: 22037131 Spannung-Gating Na + β1B Kanal: Eine Sezernierte Zelladhäsionsmolekül Beteiligt Menschlichen Epilepsie The Journal of Neuroscience : the Official Journal of the Society for Neuroscience. Oct, 2011 | Pubmed ID: 21994374 Eine Rolle Für Ubiquilin 2 Mutationen Im Neurodegeneration Nature Reviews. Neurology. Nov, 2011 | Pubmed ID: 21989241 Amyotrophe Lateralsklerose: Neue Gene, Neue Modelle Und Neue Mechanismen F1000 Biology Reports. 2011 | Pubmed ID: 21941597 Eine Funktionale XPNPEP2 Projektträger Haplotype Führt Zu Reduzierten Plasma Aminopeptidase P Und Erhöhtes Risiko Für ACE-Hemmer-induzierte Angioödem Human Mutation. Nov, 2011 | Pubmed ID: 21898657 Glucocerebrosidase Mutationen in Ein Französisch-kanadischer Parkinson Krankheit Kohorte The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques. Sep, 2011 | Pubmed ID: 21856586 Migräne: Rolle Des Kaliumkanals Plavi Zwei-Pore The International Journal of Biochemistry & Cell Biology. Nov, 2011 | Pubmed ID: 21855646 Brief an Die Redaktion: Kommentar Auf "Hereditäre Sensorische Und Autonome Neuropathie II Durch Neuartige Genmutation Die HSN2 in Mexikanische Familien" Journal of Neurology. Aug, 2011 | Pubmed ID: 21847616 FUS Und TARDBP Aber Nicht SOD1 Interagieren Auf Genetische Modelle Der Amyotrophen Lateralsklerose PLoS Genetics. Aug, 2011 | Pubmed ID: 21829392 KIF1A, Eine Axonale Transporter Der Synaptischen Bläschen, Ist in Hereditäre Sensorische Und Autonome Neuropathie Typ 2 Mutiert American Journal of Human Genetics. Aug, 2011 | Pubmed ID: 21820098 Frühen Einfluss Der Rs4675690 Auf Die Neurale Substrate Der Traurigkeit Journal of Affective Disorders. Dec, 2011 | Pubmed ID: 21807415 Genomweiten Assoziation Studie Identifiziert Roman Restless-Legs-Syndrom Anfälligkeit Loci Auf 2 P 14 Und 16q12.1 PLoS Genetics. Jul, 2011 | Pubmed ID: 21779176 Pathologische Merkmale Lobäres Amyotrophe Lateralsklerose/Frontotemporale Degeneration in Transgenen Mäusen Produziert Mit TDP-43 Genomische Fragmente Brain : a Journal of Neurology. Sep, 2011 | Pubmed ID: 21752789 Exonic De Novo Mutationsrate Bei Patienten Mit Schizophrenie Erhöht Nature Genetics. Sep, 2011 | Pubmed ID: 21743468 Die Laufenden Dissektion Der Genetischen Architektur Des Autistischen Spektrums-Störung Molecular Autism. 2011 | Pubmed ID: 21740537 Restless-Legs-Syndrom-assoziierten MEIS1 Risiko-Variante, Die Eisen-Homöostase Beeinflusst Annals of Neurology. Jul, 2011 | Pubmed ID: 21710629 Verband Der Langen ATXN2 CAG Wiederholen Größen Mit Einem Erhöhten Risiko Der Amyotrophen Lateralsklerose Archives of Neurology. Jun, 2011 | Pubmed ID: 21670397 Variation in Genomweiten Mutation Preise Innerhalb Und Zwischen Menschlichen Familien Nature Genetics. Jul, 2011 | Pubmed ID: 21666693 Transit Mangel Von Kalium-Chlorid-Co-transporter-3 Ist Ein Hauptmechanismus Der Pathogenen Hereditäre Motorisch -sensorische Neuropathie Mit Agenesie Des Corpus Callosum The Journal of Biological Chemistry. Aug, 2011 | Pubmed ID: 21628467 Der Fall Für Locus-spezifische Datenbanken Nature Reviews. Genetics. Jun, 2011 | Pubmed ID: 21540879 SYN1 Loss of Function-Mutationen Im Autismus Und Partialepilepsie, Dass Beeinträchtigte Synaptische Funktion Human Molecular Genetics. Jun, 2011 | Pubmed ID: 21441247 Vergleich Der Genomweiten Array Genomische Hybridisierung-Plattformen Für Den Nachweis Der Kopie Zahl Varianten in Idiopathische Geistesverlangsamung BMC Medical Genomics. 2011 | Pubmed ID: 21439053 Das Kürzen Von Mutationen in NRXN2 Und NRXN1 Im Autismus-Spektrum-Störungen Und Schizophrenie Human Genetics. Oct, 2011 | Pubmed ID: 21424692 Keine Auswirkung Auf SOD1, TARDP Oder FUS Mutationen Spleißen Archives of Neurology. Mar, 2011 | Pubmed ID: 21403029 Ein Bevölkerung Genetische Ansatz Für Neurologische Erkrankung Gene Mit Tiefen Neusequenzierung Zuordnen PLoS Genetics. Feb, 2011 | Pubmed ID: 21383861 Überschuss an De Novo Schädlichen Mutationen in Genen, Die Glutamat-Systemen in Nicht-syndromale Geistiger Behinderung Zugeordnet American Journal of Human Genetics. Mar, 2011 | Pubmed ID: 21376300 Geistiger Behinderung Ohne Epilepsie Mit STXBP1 Störung Verbunden European Journal of Human Genetics : EJHG. May, 2011 | Pubmed ID: 21364700 Neuropathie, Sensorische Und Motorische Bei Einem Patienten Mit Der Mutation A382P TDP-43 Orphanet Journal of Rare Diseases. 2011 | Pubmed ID: 21294910 Wo Sind Die Fehlenden Teile Der Schizophrenie-Genetik Puzzle? Current Opinion in Genetics & Development. Jun, 2011 | Pubmed ID: 21277191 LINGO1-Varianten in Die Kanadische Bevölkerung PloS One. 2011 | Pubmed ID: 21264305 Kennung Des Neuartigen FUS-Mutationen in Sporadischen Fällen Der Amyotrophen Lateralsklerose Amyotrophic Lateral Sclerosis : Official Publication of the World Federation of Neurology Research Group on Motor Neuron Diseases. Mar, 2011 | Pubmed ID: 21261515 TAR DNA-bindenden Protein 43 (TDP-43) Regelt Die Spannung Untermodul Dynamik über Differenzielle Verordnung Von G3BP Und TIA-1 Human Molecular Genetics. Apr, 2011 | Pubmed ID: 21257637 De Novo SYNGAP1 Mutationen Im Nicht-syndromale Geistiger Behinderung Und Autismus Biological Psychiatry. May, 2011 | Pubmed ID: 21237447 Neusequenzierung 29 Kandidatengene Bei Patienten Mit Familiären Und Sporadische Amyotrophe Lateralsklerose Archives of Neurology. May, 2011 | Pubmed ID: 21220648 Gemeinsame Varianten in P2RY11 Sind Narkolepsie Zugeordnet Nature Genetics. Jan, 2011 | Pubmed ID: 21170044 Identifizierung Von Einem FUS Spleißen Mutation in Einer Großen Familie Mit Amyotrophe Lateralsklerose Journal of Human Genetics. Mar, 2011 | Pubmed ID: 21160488 Zelluläre Ausdruck Des K +-cl--Kotransporter KCC3 Im ZNS Der Maus Brain Research. Feb, 2011 | Pubmed ID: 21147077 Eine Mutation Im RNF170-Gen Bewirkt, Dass Sensorische Ataxie Brain : a Journal of Neurology. Feb, 2011 | Pubmed ID: 21115467 Response to Treatment in Bipolar Disorder Current Opinion in Psychiatry. Jan, 2011 | Pubmed ID: 21088584 Analyse Der OPTN Als Ursächliche Gen Für Amyotrophe Lateralsklerose Neurobiology of Aging. Mar, 2011 | Pubmed ID: 21074290 Restless-Legs-Syndrom-Mütter Und Aufmerksamkeit-Defizit/Hyperaktivität-Störung-Kinder: Was Zwischen Ihnen Passiert Ist? Sleep Medicine. Jan, 2011 | Pubmed ID: 20851048 Hypomorphen Temperaturempfindliche Allele Des NSDHL Dazu Führen, Dass CK-Syndrom American Journal of Human Genetics. Dec, 2010 | Pubmed ID: 21129721 De-Novo-Mutationen Im FOXP1 in Fällen Mit Geistigen Behinderungen, Autismus Und Sprache Wertminderung American Journal of Human Genetics. Nov, 2010 | Pubmed ID: 20950788 Familiäre Migräne Mit Aura Ist Eine Dominant-negativen-Mutation in Plavi Kaliumkanals Verknüpft Nature Medicine. Oct, 2010 | Pubmed ID: 20871611 Frühe Auswirkungen Der 5-HTTLPR-Polymorphismus Auf Die Neuronalen Korreliert Der Traurigkeit Neuroscience Letters. Nov, 2010 | Pubmed ID: 20851164 Störungen Bei Der PTCHD1-Locus Auf Xp22.11 Im Autismus-Spektrum-Störung Und Des Geistigen Behinderung Science Translational Medicine. Sep, 2010 | Pubmed ID: 20844286 Chromosom 9 P 21 in Amyotrophe Lateralsklerose: Die Handlung Verdichtet Lancet Neurology. Oct, 2010 | Pubmed ID: 20801719 Direktes Maß Für Die De-Novo-Mutationsrate in Kohorten Von Autismus Und Schizophrenie American Journal of Human Genetics. Sep, 2010 | Pubmed ID: 20797689 Implication of Synapse-related Genes in Bipolar Disorder by Linkage and Gene Expression Analyses The International Journal of Neuropsychopharmacology / Official Scientific Journal of the Collegium Internationale Neuropsychopharmacologicum (CINP). Nov, 2010 | Pubmed ID: 20667171 De Novo Mutation Im Zusammenhang Mit Schizophrenie Kinesin-17 Abschneiden Biological Psychiatry. Oct, 2010 | Pubmed ID: 20646681 SOD1, ANG, VAPB, TARDBP, FUS Mutationen in Familiäre Amyotrophe Lateralsklerose: Genotyp-Phänotyp-Korrelationen Journal of Medical Genetics. Aug, 2010 | Pubmed ID: 20577002 Kognitive Beeinträchtigung in Der ARCA-1, Ein Neu Entdecktes Pure Zerebelläre Ataxie-Syndrom Cerebellum (London, England). Sep, 2010 | Pubmed ID: 20559786 Integrative Gen-Gewebe Microarray-Ansatz Zur Identifizierung Von Biomarkern Menschlicher Erkrankungen: Anwendung Auf Amyotrophe Lateralsklerose Human Molecular Genetics. Aug, 2010 | Pubmed ID: 20530642 Verband Der NPAS3 Exonic Variation Mit Schizophrenie Schizophrenia Research. Jul, 2010 | Pubmed ID: 20466522 Vier Familiäre Ahnentafeln ALS Störfaktor Für Zwei SOD1-Mutationen: Sind Alle SOD1-Mutationen Pathogenen? Journal of Neurology, Neurosurgery, and Psychiatry. May, 2010 | Pubmed ID: 20460594 Familie Studie Des Restless-Legs-Syndrom in Quebec, Kanada: Klinische Charakterisierung Von 671 Familiäre Fälle Archives of Neurology. May, 2010 | Pubmed ID: 20457962 The International Consortium on Lithium Genetics (ConLiGen): an Initiative by the NIMH and IGSLI to Study the Genetic Basis of Response to Lithium Treatment Neuropsychobiology. 2010 | Pubmed ID: 20453537 Mutationen Im DCC Führen Angeborene Spiegel Bewegungen Science (New York, N.Y.). Apr, 2010 | Pubmed ID: 20431009 Analyse Des UNC13A-Gens Als Risikofaktor Für Sporadische Amyotrophische Lateralsklerose Archives of Neurology. Apr, 2010 | Pubmed ID: 20385924 De Novo Mutationen Im Gen Für Das Synaptische Gerüstbau-Protein SHANK3 Bei Patienten, Die Für Schizophrenie Festgestellt Proceedings of the National Academy of Sciences of the United States of America. Apr, 2010 | Pubmed ID: 20385823 Nebensprechen Zwischen Kanonischer Wnt Signalisieren Und Die Sirtuine-FoxO Langlebigkeit Pathway Gegen Muskuläre Pathologie Induziert Durch Mutant PABPN1 Ausdruck in C. Elegans Zu Schützen Neurobiology of Disease. Jun, 2010 | Pubmed ID: 20227501 The Relationship Between Smoking and Replicated Sequence Variants on Chromosomes 8 and 9 with Familial Intracranial Aneurysm Stroke; a Journal of Cerebral Circulation. Jun, 2010 | Pubmed ID: 20190001 [De Novo Mutationen in SYNGAP1 Zusammenhang Mit Nicht-syndromalen Geistesverlangsamung] Médecine Sciences : M/S. Feb, 2010 | Pubmed ID: 20188038 Genomweiten TDT Analyse in Französisch-kanadischer Familien Mit Tourette-Syndrom The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques. Jan, 2010 | Pubmed ID: 20169783 Charakterisierung Der Sirtuine Inhibitoren in Nematoden, Die Ausdruck Einer Muskeldystrophie-Protein Zeigt Muskelzelle Und Verhaltensorientierten Schutz Durch Spezifische Sirtinol-Analoga Journal of Medicinal Chemistry. Feb, 2010 | Pubmed ID: 20041717 Analyse Von DPP6 Und FGGY Als Kandidatengenen Für Amyotrophe Lateralsklerose Amyotrophic Lateral Sclerosis : Official Publication of the World Federation of Neurology Research Group on Motor Neuron Diseases. Aug, 2010 | Pubmed ID: 20001489 Gewinn Und Verlust Der Funktion Des TARDBP (TDP-43) ALS Im Zusammenhang Mit Mutationen Verursachen In-vivo Motorische Defizite Human Molecular Genetics. Feb, 2010 | Pubmed ID: 19959528 Somatosensory-motor Bodily Representation Cortical Thinning in Tourette: Effects of Tic Severity, Age and Gender Cortex; a Journal Devoted to the Study of the Nervous System and Behavior. Jun, 2010 | Pubmed ID: 19733347 Chromogranin B P413L Variante Als Risikofaktor Und Modifizierer Krankheit Einstiegsalter Für Amyotrophe Lateralsklerose Proceedings of the National Academy of Sciences of the United States of America. Dec, 2009 | Pubmed ID: 20007371 Nachweis Von Pathogenen Kopie Zahl Varianten Bei Kindern Mit Idiopathischen Geistiger Behinderung Mit 500K SNP Array Genomische Hybridisierung BMC Genomics. 2009 | Pubmed ID: 19917086 Eine Mutation, Die Eine Pseudoexon Im SOD1 Erstellt Bewirkt, Dass Familiäre ALS Annals of Human Genetics. Nov, 2009 | Pubmed ID: 19847927 Genetik Von Motoneuron-Erkrankungen: Neue Einblicke in Pathogenen Mechanismen Nature Reviews. Genetics. Nov, 2009 | Pubmed ID: 19823194 Verband Der Verband Intronic Varianten Des BTBD9-Gens Mit Tourette-Syndrom Archives of Neurology. Oct, 2009 | Pubmed ID: 19822783 Quantitative Analyse der Kletter Defekte in einem Drosophila Modell von neurodegenerativen Erkrankungen Surya T. Madabattula1, Joel C. Strautman1, Andrew M. Bysice1, Julia A. O’Sullivan1, Alaura Androschuk1, Cory Rosenfelt1, Kacy Doucet1, Guy Rouleau2, Francois Bolduc1 1Department of Pediatrics, University of Alberta, 2Montreal Neurological Institute and Hospital, McGill University Neuroscience
Quantitative Analyse der Kletter Defekte in einem Drosophila Modell von neurodegenerativen Erkrankungen Surya T. Madabattula1, Joel C. Strautman1, Andrew M. Bysice1, Julia A. O’Sullivan1, Alaura Androschuk1, Cory Rosenfelt1, Kacy Doucet1, Guy Rouleau2, Francois Bolduc1 1Department of Pediatrics, University of Alberta, 2Montreal Neurological Institute and Hospital, McGill University Neuroscience