Rare copy number variants in tourette syndrome disrupt genes in histaminergic pathways and overlap with autism - Wikidata - wikimedia - TriplyDB

Rare copy number variants in tourette syndrome disrupt genes in histaminergic pathways and overlap with autism

Rare copy number variants in tourette syndrome disrupt genes in histaminergic pathways and overlap with autism

http://www.wikidata.org/entity/Q35764564

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Genome-wide association study of Tourette's syndrome Pediatric Autoimmune Disorders Associated with Streptococcal Infections and Tourette's Syndrome in Preclinical Studies.Functional Evaluations of Genes Disrupted in Patients with Tourette's Disorder.Histamine and the striatum International Union of Basic and Clinical Pharmacology. XCVIII. Histamine Receptors A genetic model for neurodevelopmental disease Genetic susceptibility and neurotransmitters in Tourette syndrome A research strategy to discover the environmental causes of autism and neurodevelopmental disabilities Using mice to model Obsessive Compulsive Disorder: From genes to circuits.Histidine decarboxylase knockout mice, a genetic model of Tourette syndrome, show repetitive grooming after induced fear.Animal models of tic disorders: a translational perspective.Histidine decarboxylase deficiency causes tourette syndrome: parallel findings in humans and mice Brain mechanisms for prepulse inhibition in adults with Tourette syndrome: initial findings The Tourette International Collaborative Genetics (TIC Genetics) study, finding the genes causing Tourette syndrome: objectives and methods The genetic variability and commonality of neurodevelopmental disease.Genetics of obsessive-compulsive disorder and related disorders.An inherited small microdeletion at 15q13.3 in a patient with early-onset obsessive-compulsive disorder Copy number variation in obsessive-compulsive disorder and tourette syndrome: a cross-disorder study Histaminergic system in brain disorders: lessons from the translational approach and future perspectives.CNV analysis in Tourette syndrome implicates large genomic rearrangements in COL8A1 and NRXN1.The Inheritance of Tourette Disorder: A review Urinary amino acid alterations in 3-year-old children with neurodevelopmental effects due to perinatal dioxin exposure in Vietnam: a nested case-control study for neurobiomarker discovery.Both rare and de novo copy number variants are prevalent in agenesis of the corpus callosum but not in cerebellar hypoplasia or polymicrogyria Transcriptome Analysis of the Human Striatum in Tourette Syndrome.No evidence for association of autism with rare heterozygous point mutations in Contactin-Associated Protein-Like 2 (CNTNAP2), or in Other Contactin-Associated Proteins or Contactins.A national profile of Tourette syndrome, 2011-2012.Tourette's syndrome and translational clinical science.Reduced GABAergic inhibition and abnormal sensory symptoms in children with Tourette syndrome.Investigation of a Possible Role for the Histidine Decarboxylase Gene in Tourette Syndrome in the Chinese Han Population: A Family-Based Study Tourette Syndrome: Bridging the Gap between Genetics and Biology Mouse models of neurodevelopmental disease of the basal ganglia and associated circuits.What Makes You Tic? A New Lead in Tourette Syndrome Genetics.Systematic review: pharmacological treatment of tic disorders--efficacy of antipsychotic and alpha-2 adrenergic agonist agents.The Genetic Etiology of Tourette Syndrome: Large-Scale Collaborative Efforts on the Precipice of Discovery.Histamine is required for H₃ receptor-mediated alcohol reward inhibition, but not for alcohol consumption or stimulation TS-EUROTRAIN: A European-Wide Investigation and Training Network on the Etiology and Pathophysiology of Gilles de la Tourette Syndrome Genome-wide association study of autistic-like traits in a general population study of young adults.Targeted Re-Sequencing Approach of Candidate Genes Implicates Rare Potentially Functional Variants in Tourette Syndrome Etiology Exome sequencing of extended families with autism reveals genes shared across neurodevelopmental and neuropsychiatric disorders.Balance within the Neurexin Trans-Synaptic Connexus Stabilizes Behavioral Control.

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Rare copy number variants in tourette syndrome disrupt genes in histaminergic pathways and overlap with autism

http://www.wikidata.org/entity/Q35764564

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J.BIOPSYCH.2011.09.034

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Biological Psychiatry

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A Gulhan Ercan-Sencicek

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Bernie Devlin

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Daniel O Fishman

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Hakon Hakonarson

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Ilana R Yurkiewicz

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James F Leckman

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Joseph Glessner

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Matthew W State

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Melanie J Raubeson

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Murat Günel

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Rare chromosomal deletions and duplications increase risk of schizophrenia

Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls

Functional impact of global rare copy number variation in autism spectrum disorders

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

Recurrent rearrangements in synaptic and neurodevelopmental genes and shared biologic pathways in schizophrenia, autism, and mental retardation

Autism genome-wide copy number variation reveals ubiquitin and neuronal genes

Strong association of de novo copy number mutations with autism

Microduplications of 16p11.2 are associated with schizophrenia

Recurrent reciprocal 1q21.1 deletions and duplications associated with microcephaly or macrocephaly and developmental and behavioral abnormalities

Large recurrent microdeletions associated with schizophrenia

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Thomas V. Fernandez

Jay A. Tischfield

Stephan J. Sanders

Donald L. Gilbert

Katsuhito Yasuno

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2011-12-14T00:00:00Z

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51877920

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