Genome-wide analysis of copy number variants in attention deficit hyperactivity disorder: the role of rare variants and duplications at 15q13.3. (Q36695755)

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scientific article published on February 2012

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English	Genome-wide analysis of copy number variants in attention deficit hyperactivity disorder: the role of rare variants and duplications at 15q13.3.	scientific article published on February 2012

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scholarly article

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Europe PubMed Central

PMC publication ID

15 August 2017

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

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Europe PubMed Central

PMC publication ID

15 August 2017

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based on heuristic

inferred from title

attention deficit hyperactivity disorder

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based on heuristic

inferred from title

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Michael C O'Donovan

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Nigel M Williams

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Michael J Owen

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Yanli Zhang-James

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Lu Liu

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Haukur Palmason

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Irina Zaharieva

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Josephine Elia

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publication date

1 February 2012

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American Journal of Psychiatry

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15 August 2017

169

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2

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195-204

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15 August 2017

Investigating the contribution of common genetic variants to the risk and pathogenesis of ADHD.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3601405

30 September 2017

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

1 reference

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30 September 2017

After GWAS: searching for genetic risk for schizophrenia and bipolar disorder.

1 reference

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30 September 2017

The α7 nicotinic acetylcholine receptor and the acute stress response: Maternal genotype determines offspring phenotype

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30 September 2017

Rare chromosomal deletions and duplications in attention-deficit hyperactivity disorder: a genome-wide analysis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3601405

30 September 2017

Case-Control Genome-Wide Association Study of Attention-Deficit/Hyperactivity Disorder

1 reference

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30 September 2017

Family-based genome-wide association scan of attention-deficit/hyperactivity disorder

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3601405

30 September 2017

Meta-Analysis of Genome-Wide Association Studies of Attention-Deficit/Hyperactivity Disorder

1 reference

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30 September 2017

The frequency-dependence of the nicotine-induced inhibition of dopamine is controlled by the α7 nicotinic receptor

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30 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3601405

30 September 2017

Structures and molecular mechanisms for common 15q13.3 microduplications involving CHRNA7: benign or pathological?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3601405

30 September 2017

Molecular genetics of attention deficit hyperactivity disorder

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3601405

30 September 2017

A common variant of the latrophilin 3 gene, LPHN3, confers susceptibility to ADHD and predicts effectiveness of stimulant medication

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30 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3601405

30 September 2017

The role of copy number variation in schizophrenia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3601405

30 September 2017

Microduplications of 16p11.2 are associated with schizophrenia

1 reference

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30 September 2017

Copy number variations of chromosome 16p13.1 region associated with schizophrenia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3601405

30 September 2017

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

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30 September 2017

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

1 reference

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Candidate gene studies of ADHD: a meta-analytic review

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30 September 2017

Genome-wide association studies in ADHD.

1 reference

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30 September 2017

Further delineation of the 15q13 microdeletion and duplication syndromes: a clinical spectrum varying from non-pathogenic to a severe outcome

1 reference

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30 September 2017

Gene-wide analyses of genome-wide association data sets: evidence for multiple common risk alleles for schizophrenia and bipolar disorder and for overlap in genetic risk

1 reference

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30 September 2017

Genome-wide association scan of attention deficit hyperactivity disorder

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3601405

30 September 2017

Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies

1 reference

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30 September 2017

Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations

1 reference

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30 September 2017

Integrated genotype calling and association analysis of SNPs, common copy number polymorphisms and rare CNVs

1 reference

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30 September 2017

Large recurrent microdeletions associated with schizophrenia

1 reference

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30 September 2017

Rare chromosomal deletions and duplications increase risk of schizophrenia

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30 September 2017

Structural variation of chromosomes in autism spectrum disorder

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

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The worldwide prevalence of ADHD: a systematic review and metaregression analysis

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Molecular genetics of attention-deficit/hyperactivity disorder

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Disruption of a novel member of a sodium/hydrogen exchanger family and DOCK3 is associated with an attention deficit hyperactivity disorder-like phenotype

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Rare copy number variation discovery and cross-disorder comparisons identify risk genes for ADHD.

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Most genome-wide significant susceptibility loci for schizophrenia and bipolar disorder reported to date cross-traditional diagnostic boundaries

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Genome-wide copy number variation analysis in attention-deficit/hyperactivity disorder: association with neuropeptide Y gene dosage in an extended pedigree

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5 September 2018

Correlation of a set of gene variants, life events and personality features on adult ADHD severity

1 reference

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Autism, ADHD, mental retardation and behavior problems in 100 individuals with 22q11 deletion syndrome

1 reference

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5 September 2018

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

1 reference

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5 September 2018

No association between CHRNA7 microsatellite markers and attention-deficit hyperactivity disorder

1 reference

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5 September 2018

Identifiers

10.1176/APPI.AJP.2011.11060822

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

ResearchGate publication ID

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