about
Partitioning the heritability of Tourette syndrome and obsessive compulsive disorder reveals differences in genetic architectureGenome-wide association study of Tourette's syndromeFunctional Evaluations of Genes Disrupted in Patients with Tourette's Disorder.Genetic susceptibility and neurotransmitters in Tourette syndromeLocalization of a gene for myoclonus-dystonia to chromosome 7q21-q31Investigation of polymorphisms in the CREM gene in panic disorderRare missense neuronal cadherin gene (CDH2) variants in specific obsessive-compulsive disorder and Tourette disorder phenotypesThe Tourette International Collaborative Genetics (TIC Genetics) study, finding the genes causing Tourette syndrome: objectives and methodsNew Jersey Center for Tourette Syndrome sharing repository: methods and sample description.Control of Alzheimer's amyloid beta toxicity by the high molecular weight immunophilin FKBP52 and copper homeostasis in DrosophilaL-histidine decarboxylase and Tourette's syndrome.Evaluation of depression risk in LGI1 mutation carriers.Copy number variation in obsessive-compulsive disorder and tourette syndrome: a cross-disorder studyNumeracy and framing bias in epilepsy.Evaluation of duration of epilepsy prior to temporal lobe epilepsy surgery during the past two decades.A linkage search for joint panic disorder/bipolar genes.Cross-disorder genome-wide analyses suggest a complex genetic relationship between Tourette's syndrome and OCD.Interstitial cystitis and panic disorder: a potential genetic syndrome.Rare copy number variants in tourette syndrome disrupt genes in histaminergic pathways and overlap with autismEvidence for a two-stage model of dependence using the NESARC and its implications for genetic association studies.Seizure remission and relapse in adults with intractable epilepsy: a cohort study.Obsessive-compulsive disorder is not a clinical manifestation of the DYT1 dystonia gene.Mutations in THAP1 (DYT6) in early-onset dystonia: a genetic screening study.Seizure remission in adults with long-standing intractable epilepsy: an extended follow-up.Common and rare alleles of the serotonin transporter gene, SLC6A4, associated with Tourette's disorder.Targeted Re-Sequencing Approach of Candidate Genes Implicates Rare Potentially Functional Variants in Tourette Syndrome EtiologyGDNF gene is associated with tourette syndrome in a family studyAn Analytic Solution to the Computation of Power and Sample Size for Genetic Association Studies under a Pleiotropic Mode of Inheritance.Pre- and perinatal complications in relation to Tourette syndrome and co-occurring obsessive-compulsive disorder and attention-deficit/hyperactivity disorder.A unified approach for quantifying, testing and correcting population stratification in case-control association studies.Drug-resistant epilepsy in adults: Outcome trajectories after failure of two medications.An improved delta-centralization method for population stratification.Myoclonus dystonia: possible association with obsessive-compulsive disorder and alcohol dependence.Evidence for genetic linkage between a polymorphism in the adenosine 2A receptor and panic disorder.De Novo Coding Variants Are Strongly Associated with Tourette Disorder.Investigation of previously implicated genetic variants in chronic tic disorders: a transmission disequilibrium test approach.Comments on: review and evaluation of methods correcting for population stratification with a focus on underlying statistical principles.Mood disorders in familial epilepsy: A test of shared etiology.The PNKD gene is associated with Tourette Disorder or Tic disorder in a multiplex family.In response: Drug-resistant epilepsy in adults: outcome trajectories after failure of two medications.
P50
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P50
description
researcher
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wetenschapper
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հետազոտող
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name
Gary A Heiman
@ast
Gary A Heiman
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Gary A Heiman
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Gary A Heiman
@nl
Gary A Heiman
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type
label
Gary A Heiman
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Gary A Heiman
@en
Gary A Heiman
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Gary A Heiman
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Gary A Heiman
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prefLabel
Gary A Heiman
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Gary A Heiman
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Gary A Heiman
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Gary A Heiman
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Gary A Heiman
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P1053
K-2366-2018
P106
P1153
57204027096
P21
P31
P4012
P496
0000-0001-5859-0259