Investigating the contribution of common genetic variants to the risk and pathogenesis of ADHD. (Q36695747)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22420046%20AND%20SRC:MED&resulttype=core&format=json

26 January 2020

title

Investigating the contribution of common genetic variants to the risk and pathogenesis of ADHD (English)

1 reference

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26 January 2020

10

1 reference

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26 January 2020

Michael C O'Donovan

13

1 reference

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26 January 2020

Evangelia Stergiakouli

1

1 reference

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26 January 2020

Peter Holmans

3

1 reference

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26 January 2020

Kate Langley

4

1 reference

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26 January 2020

Ziarih Hawi

8

1 reference

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26 January 2020

Lindsey Kent

9

1 reference

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26 January 2020

Anita Thapar

14

1 reference

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26 January 2020

2

Marian Hamshere

1 reference

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26 January 2020

author name string

Irina Zaharieva

5

1 reference

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26 January 2020

deCODE Genetics

6

1 reference

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26 January 2020

Psychiatric GWAS Consortium

7

1 reference

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26 January 2020

Nigel Williams

11

1 reference

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26 January 2020

Michael J Owen

12

1 reference

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26 January 2020

language of work or name

English

0 references

publication date

1 February 2012

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22420046%20AND%20SRC:MED&resulttype=core&format=json

American Journal of Psychiatry

26 January 2020

number of pages

9

1 reference

based on heuristic

inferred from page(s)

published in

1 reference

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26 January 2020

volume

169

1 reference

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26 January 2020

issue

2

1 reference

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26 January 2020

page(s)

186-194

1 reference

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Genetic evidence implicates the immune system and cholesterol metabolism in the aetiology of Alzheimer's disease

26 January 2020

cites work

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

30 September 2017

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Fitting the pieces together: current research on the genetic basis of attention-deficit/hyperactivity disorder (ADHD)

30 September 2017

1 reference

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Accurately assessing the risk of schizophrenia conferred by rare copy-number variation affecting genes with brain function

30 September 2017

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Case-control genome-wide association study of attention-deficit/hyperactivity disorder

30 September 2017

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

30 September 2017

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

30 September 2017

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Single particle tracking of alpha7 nicotinic AChR in hippocampal neurons reveals regulated confinement at glutamatergic and GABAergic perisynaptic sites

30 September 2017

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

30 September 2017

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PANTHER version 7: improved phylogenetic trees, orthologs and collaboration with the Gene Ontology Consortium

30 September 2017

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A small recurrent deletion within 15q13.3 is associated with a range of neurodevelopmental phenotypes

30 September 2017

1 reference

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

30 September 2017

1 reference

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

30 September 2017

1 reference

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Gene ontology analysis of GWA study data sets provides insights into the biology of bipolar disorder

30 September 2017

1 reference

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Genome-wide association studies in ADHD.

30 September 2017

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Genomewide association studies: history, rationale, and prospects for psychiatric disorders

30 September 2017

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Genome-wide association scan of attention deficit hyperactivity disorder

30 September 2017

1 reference

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

30 September 2017

1 reference

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Microdeletion/duplication at 15q13.2q13.3 among individuals with features of autism and other neuropsychiatric disorders

30 September 2017

1 reference

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Estimation of the multiple testing burden for genomewide association studies of nearly all common variants

30 September 2017

1 reference

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The Mouse Genome Database (MGD): mouse biology and model systems

30 September 2017

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PennCNV: an integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data

30 September 2017

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Prediction of individual genetic risk to disease from genome-wide association studies

30 September 2017

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PLINK: a tool set for whole-genome association and population-based linkage analyses

30 September 2017

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

30 September 2017

1 reference

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Principal components analysis corrects for stratification in genome-wide association studies

30 September 2017

1 reference

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Molecular genetics of attention-deficit/hyperactivity disorder

30 September 2017

1 reference

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30 September 2017

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30 September 2017

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30 September 2017

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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.

30 September 2017

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Genome-wide association studies in psychiatry: lessons from early studies of non-psychiatric and psychiatric phenotypes.

5 September 2018

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5 September 2018

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The Child Attention-Deficit Hyperactivity Disorder Teacher Telephone Interview (CHATTI): reliability and validity

5 September 2018

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Association of promoter variants in the alpha7 nicotinic acetylcholine receptor subunit gene with an inhibitory deficit found in schizophrenia

5 September 2018

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

5 September 2018

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Design of Case-controls Studies with Unscreened Controls

5 September 2018

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10.1176/APPI.AJP.2011.11040551

4 December 2018

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22420046%20AND%20SRC:MED&resulttype=core&format=json

26 January 2020

1 reference

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26 January 2020

1 reference

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