Genome-wide analysis of copy number variants in attention deficit hyperactivity disorder: the role of rare variants and duplications at 15q13.3. - Wikidata - wikimedia - TriplyDB

Genome-wide analysis of copy number variants in attention deficit hyperactivity disorder: the role of rare variants and duplications at 15q13.3.

Genome-wide analysis of copy number variants in attention deficit hyperactivity disorder: the role of rare variants and duplications at 15q13.3.

http://www.wikidata.org/entity/Q36695755

about

What have we learnt about the causes of ADHD?Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis Genetics and genomics of psychiatric disease The human CHRNA7 and CHRFAM7A genes: A review of the genetics, regulation, and function Attention deficit hyperactivity disorder CNVs: harbingers of a rare variant revolution in psychiatric genetics Nicotinic α7 receptors enhance NMDA cognitive circuits in dorsolateral prefrontal cortex Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs Nicotine increases impulsivity and decreases willingness to exert cognitive effort despite improving attention in "slacker" rats: insights into cholinergic regulation of cost/benefit decision making Polygenic transmission and complex neuro developmental network for attention deficit hyperactivity disorder: genome-wide association study of both common and rare variants.Chromosomal microarray analysis of consecutive individuals with autism spectrum disorders or learning disability presenting for genetic services.Copy number variation at 22q11.2: from rare variants to common mechanisms of developmental neuropsychiatric disorders.Genomic insights into the overlap between psychiatric disorders: implications for research and clinical practice.Biological overlap of attention-deficit/hyperactivity disorder and autism spectrum disorder: evidence from copy number variants Intellectual disability in children with attention deficit hyperactivity disorder.Genetic architectures of psychiatric disorders: the emerging picture and its implications.Large-scale genomics unveils the genetic architecture of psychiatric disorders CHRNA7 triplication associated with cognitive impairment and neuropsychiatric phenotypes in a three-generation pedigree.Investigation of 15q11-q13, 16p11.2 and 22q13 CNVs in autism spectrum disorder Brazilian individuals with and without epilepsy.Genetic risk for attention-deficit/hyperactivity disorder contributes to neurodevelopmental traits in the general population.Intragenic deletions affecting two alternative transcripts of the IMMP2L gene in patients with Tourette syndrome.Schizophrenia genetics: emerging themes for a complex disorder.Investigation of the ZNF804A gene polymorphism with genetic risk for bipolar disorder in attention deficit hyperactivity disorder Palindromic GOLGA8 core duplicons promote chromosome 15q13.3 microdeletion and evolutionary instability Genome-wide analysis of attention deficit hyperactivity disorder in Norway.Neurocognitive abilities in the general population and composite genetic risk scores for attention-deficit hyperactivity disorder.The relative contribution of common and rare genetic variants to ADHD The human clinical phenotypes of altered CHRNA7 copy number Duplicated copy of CHRNA7 increases risk and worsens prognosis of COPD and lung cancer Psychiatric gene discoveries shape evidence on ADHD's biology Duplications in ADHD patients harbour neurobehavioural genes that are co-expressed with genes associated with hyperactivity in the mouse.Application of custom-designed oligonucleotide array CGH in 145 patients with autistic spectrum disorders.Attentional switching forms a genetic link between attention problems and autistic traits in adults.Common alleles contribute to schizophrenia in CNV carriers.Distribution of disease-associated copy number variants across distinct disorders of cognitive development.Genetic influences on alcohol use across stages of development: GABRA2 and longitudinal trajectories of drunkenness from adolescence to young adulthood.15q13.3 duplication in two patients with childhood-onset schizophrenia.Genome-wide analysis of rare copy number variations reveals PARK2 as a candidate gene for attention-deficit/hyperactivity disorder.Autistic traits in children with and without ADHD.High loading of polygenic risk for ADHD in children with comorbid aggression.

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Genome-wide analysis of copy number variants in attention deficit hyperactivity disorder: the role of rare variants and duplications at 15q13.3.

http://www.wikidata.org/entity/Q36695755

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Genome-wide analysis of copy n ...... s and duplications at 15q13.3.

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American Journal of Psychiatry

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Alexandre Todorov

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Anath C Lionel

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Andreas Warnke

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Christiane Seitz

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Christine M Freitag

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Corina Shtir

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Frank Middleton

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P2860

The Worldwide Prevalence of ADHD: A Systematic Review and Metaregression Analysis

The genetics of attention deficit/hyperactivity disorder in adults, a review

Meta-analysis of genome-wide association studies of attention-deficit/hyperactivity disorder

Candidate gene studies of ADHD: a meta-analytic review

Rare chromosomal deletions and duplications increase risk of schizophrenia

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

Rare structural variants found in attention-deficit hyperactivity disorder are preferentially associated with neurodevelopmental genes

Neuronal nicotinic receptor agonists for the treatment of attention-deficit/hyperactivity disorder: focus on cognition

The bipolar disorder risk allele at CACNA1C also confers risk of recurrent major depression and of schizophrenia

Shared heritability of attention-deficit/hyperactivity disorder and autism spectrum disorder

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2

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Hans-Christoph Steinhausen

Philip Asherson

Herbert Roeyers

Michael C O'Donovan

Susanne Walitza

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2012-02-01T00:00:00Z

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221897064

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22420048

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