(Q33699542)

28 July 2017

title

Genome-wide association scan of attention deficit hyperactivity disorder (English)

1 reference

genome-wide association study

28 July 2017

main subject

0 references

attention

1 reference

based on heuristic

inferred from title

attention deficit hyperactivity disorder

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1 reference

28 July 2017

1 reference

28 July 2017

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28 July 2017

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28 July 2017

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28 July 2017

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Aribert Rothenberger

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Edmund Sonuga-Barke

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Herbert Roeyers

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Philip Asherson

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Jan Buitelaar

1 reference

28 July 2017

Mark Daly

1 reference

Hans-Christoph Steinhausen

28 July 2017

object named as

Hans Christoph Steinhausen

1 reference

28 July 2017

Nan Laird

1 reference

28 July 2017

Benjamin M Neale

1 reference

28 July 2017

Jessica Lasky-Su

1 reference

28 July 2017

Robert D Oades

1 reference

28 July 2017

Alejandro Arias-Vásquez

object named as

Alejandro Arias Vasquez

1 reference

28 July 2017

Kaixin Zhou

1 reference

28 July 2017

Wai Chen

1 reference

28 July 2017

Joseph Sergeant

1 reference

28 July 2017

Fernando Mulas

1 reference

28 July 2017

Eric Taylor

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28 July 2017

Christoph Lange

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28 July 2017

language of work or name

English

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publication date

1 December 2008

1 reference

American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

28 July 2017

published in

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28 July 2017

volume

147B

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28 July 2017

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28 July 2017

page(s)

1337-1344

1 reference

Non-random error in genotype calling procedures: implications for family-based and case-control genome-wide association studies

28 July 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2831205

Linkage to chromosome 1p36 for attention-deficit/hyperactivity disorder traits in school and home settings

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2831205

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2831205

Whole-genome association study of bipolar disorder

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2831205

Estimation of significance thresholds for genomewide association scans

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2831205

Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2831205

Genome-wide association study identifies new susceptibility loci for Crohn disease and implicates autophagy in disease pathogenesis

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2831205

The endophenotype concept in psychiatric genetics

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2831205

The worldwide prevalence of ADHD: is it an American condition?

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2831205

The analysis of 51 genes in DSM-IV combined type attention deficit hyperactivity disorder: association signals in DRD4, DAT1 and 16 other genes

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2831205

The IMAGE project: methodological issues for the molecular genetic analysis of ADHD.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2831205

Molecular genetics of attention-deficit/hyperactivity disorder

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2831205

The scientific foundation for understanding attention-deficit/hyperactivity disorder as a valid psychiatric disorder

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2831205

Genome-wide association studies for common diseases and complex traits

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2831205

Attention-deficit/hyperactivity disorder in a population isolate: linkage to loci at 4q13.2, 5q33.3, 11q22, and 17p11.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2831205

Genetics of adult attention-deficit/hyperactivity disorder

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2831205

A whole-genome scan in 164 Dutch sib pairs with attention-deficit/hyperactivity disorder: suggestive evidence for linkage on chromosomes 7p and 15q.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2831205

Genetic linkage of attention-deficit/hyperactivity disorder on chromosome 16p13, in a region implicated in autism

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2831205

A genomewide scan for loci involved in attention-deficit/hyperactivity disorder

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2831205

High-throughput variation detection and genotyping using microarrays

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2831205

Transmission test for linkage disequilibrium: the insulin gene region and insulin-dependent diabetes mellitus (IDDM)

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2831205

A note on the application of the transmission disequilibrium test when a parent is missing.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2831205

Genetic dissection of complex traits: guidelines for interpreting and reporting linkage results

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2831205

A family study of the hyperactive child syndrome

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2831205

Conduct disorder and hyperactivity: I. Separation of hyperactivity and antisocial conduct in British child psychiatric patients.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2831205

DSM-IV combined type ADHD shows familial association with sibling trait scores: a sampling strategy for QTL linkage.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2831205

A high-density SNP linkage scan with 142 combined subtype ADHD sib pairs identifies linkage regions on chromosomes 9 and 16.

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2831205

The monoamine oxidase B gene exhibits significant association to ADHD.

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2831205

Meta-analysis shows significant association between dopamine system genes and attention deficit hyperactivity disorder (ADHD).

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2831205

Possible association of the alpha-2A adrenergic receptor gene (ADRA2A) with symptoms of attention-deficit/hyperactivity disorder.

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2831205

A genome-wide scan for attention-deficit/hyperactivity disorder in 155 German sib-pairs

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2831205

Power and sample size calculations for case-control genetic association tests when errors are present: application to single nucleotide polymorphisms

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2831205

Neurobiology of attention-deficit hyperactivity disorder

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2831205

Meta-analysis of association between a catechol-O-methyltransferase gene polymorphism and attention deficit hyperactivity disorder

30 October 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/18980221

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Guilt beyond a reasonable doubt

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/18980221

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

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

2 references

5 May 2024

https://opencitations.net/index/api/v1/citations/10.1002/AJMG.B.30867

5 May 2024

https://opencitations.net/index/api/v1/references/10.1002/AJMG.B.30866

Sequence variants in the autophagy gene IRGM and multiple other replicating loci contribute to Crohn's disease susceptibility

1 reference

5 May 2024

https://opencitations.net/index/api/v1/references/10.1002/AJMG.B.30866

Population structure, differential bias and genomic control in a large-scale, case-control association study

1 reference

5 May 2024

https://opencitations.net/index/api/v1/references/10.1002/AJMG.B.30866

Genomic control for association studies

1 reference

5 May 2024

https://opencitations.net/index/api/v1/references/10.1002/AJMG.B.30866

A genome-wide association study identifies novel risk loci for type 2 diabetes

1 reference

5 May 2024

https://opencitations.net/index/api/v1/references/10.1002/AJMG.B.30866

A variant in CDKAL1 influences insulin response and risk of type 2 diabetes

1 reference

5 May 2024

https://opencitations.net/index/api/v1/references/10.1002/AJMG.B.30866

Advances in the Genetics and Neurobiology of Attention Deficit Hyperactivity Disorder

1 reference

5 May 2024

https://opencitations.net/index/api/v1/references/10.1002/AJMG.B.30866

Linkage analysis of attention deficit hyperactivity disorder

2 references

5 May 2024

https://opencitations.net/index/api/v1/references/10.1002/AJMG.B.30866

5 May 2024

https://opencitations.net/index/api/v1/citations/10.1002/AJMG.B.30631

Nature, Nurture, and Attention Deficit Hyperactivity Disorder

1 reference

5 May 2024

https://opencitations.net/index/api/v1/references/10.1002/AJMG.B.30866

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

1 reference

5 May 2024

https://opencitations.net/index/api/v1/references/10.1002/AJMG.B.30866

Nonreplication in Genetic Association Studies of Obesity and Diabetes Research

1 reference

5 May 2024

https://opencitations.net/index/api/v1/references/10.1002/AJMG.B.30866

Identifiers

DOI

10.1002/AJMG.B.30866

1 reference

28 July 2017

1 reference

28 July 2017

1 reference