The ATXN1 and TRIM31 genes are related to intelligence in an ADHD background: evidence from a large collaborative study totaling 4,963 subjects (Q34893127)

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English	The ATXN1 and TRIM31 genes are related to intelligence in an ADHD background: evidence from a large collaborative study totaling 4,963 subjects	scientific article

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scholarly article

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Europe PubMed Central

5 August 2017

The ATXN1 and TRIM31 genes are related to intelligence in an ADHD background: evidence from a large collaborative study totaling 4,963 subjects (English)

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5 August 2017

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Richard P. Ebstein

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George Davey Smith

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Nicholas J. Timpson

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Stephen Faraone

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Tobias Banaschewski

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Tobias Banaschewski

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Aribert Rothenberger

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Aribert Rothenberger

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Narelle Hansell

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Allison Ashley-Koch

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Margaret J. Wright

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David J. Porteous

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Nanda Rommelse

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Beate St Pourcain

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Beate St Pourcain

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Edmund Sonuga-Barke

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Edmund Sonuga-Barke

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Herbert Roeyers

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Herbert Roeyers

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Danielle Posthuma

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Danielle Posthuma

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Philip Asherson

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Philip Asherson

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Grant W. Montgomery

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Grant W Montgomery

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Ian J Deary

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Jan Buitelaar

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Hans-Christoph Steinhausen

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Hans Christoph Steinhausen

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Melanie E Garrett

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Melanie E Garrett

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Alejandro Arias-Vásquez

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Alejandro Arias-Vasquez

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John M Starr

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Robert D Oades

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Thais S Rizzi

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Dina Ruano

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Christina A Markunas

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Christina A Markunas

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Scott H Kollins

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Scott H Kollins

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Arthur D Anastopoulos

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Arthur D Anastopoulos

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Fernando Mulas

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author name string

Sophie Van der Sluis

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Sarah E Harris

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Gail Davies

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Albert Tenesa

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Joseph Sergeant

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Eric Taylor

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publication date

16 December 2010

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American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

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156

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145-157

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Common variants in the trichohyalin gene are associated with straight hair in Europeans

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3085124

8 July 2018

Genotype imputation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3085124

8 July 2018

Common variants in the region around Osterix are associated with bone mineral density and growth in childhood

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3085124

8 July 2018

SNPs in dopamine D2 receptor gene (DRD2) and norepinephrine transporter gene (NET) are associated with continuous performance task (CPT) phenotypes in ADHD children and their families

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3085124

8 July 2018

WGAViewer: software for genomic annotation of whole genome association studies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3085124

8 July 2018

Genome-wide quantitative trait locus association scan of general cognitive ability using pooled DNA and 500K single nucleotide polymorphism microarrays.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3085124

8 July 2018

Exploring the functional role of the CHRM2 gene in human cognition: results from a dense genotyping and brain expression study

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3085124

8 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3085124

8 July 2018

Association of CHRM2 with IQ: converging evidence for a gene influencing intelligence

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3085124

8 July 2018

Association between the CHRM2 gene and intelligence in a sample of 304 Dutch families

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3085124

8 July 2018

In silico method for inferring genotypes in pedigrees

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3085124

8 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3085124

8 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3085124

8 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3085124

8 July 2018

The molecular genetics of cognition: dopamine, COMT and BDNF.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3085124

8 July 2018

Joint analysis is more efficient than replication-based analysis for two-stage genome-wide association studies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3085124

8 July 2018

Genetic variation in DTNBP1 influences general cognitive ability

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3085124

8 July 2018

TRIM/RBCC, a novel class of 'single protein RING finger' E3 ubiquitin ligases

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3085124

8 July 2018

A genomewide scan for intelligence identifies quantitative trait loci on 2q and 6p.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3085124

8 July 2018

Meta-analysis of intellectual and neuropsychological test performance in 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=3085124

8 July 2018

A functional polymorphism in the succinate-semialdehyde dehydrogenase (aldehyde dehydrogenase 5 family, member A1) gene is associated with cognitive ability

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3085124

8 July 2018

Association study of a brain-derived neurotrophic factor (BDNF) Val66Met polymorphism and personality trait and intelligence in healthy young females

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3085124

8 July 2018

Genetic Power Calculator: design of linkage and association genetic mapping studies of complex traits

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3085124

8 July 2018

A comprehensive review of genetic association studies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3085124

8 July 2018

ALSPAC--the Avon Longitudinal Study of Parents and Children. I. Study methodology

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3085124

8 July 2018

A general test of association for quantitative traits in nuclear families

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3085124

8 July 2018

Cloning and characterization of a novel RING finger protein that interacts with class V myosins

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3085124

8 July 2018

Combined linkage and association sib-pair analysis for quantitative traits

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3085124

8 July 2018

Mice lacking ataxin-1 display learning deficits and decreased hippocampal paired-pulse facilitation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3085124

8 July 2018

Substantial genetic influence on cognitive abilities in twins 80 or more years old.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3085124

8 July 2018

Expansion of an unstable trinucleotide CAG repeat in spinocerebellar ataxia type 1.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3085124

8 July 2018

Expression analysis of the ataxin-1 protein in tissues from normal and spinocerebellar ataxia type 1 individuals

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3085124

8 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3085124

8 July 2018

Identification and characterization of the gene causing type 1 spinocerebellar ataxia.

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31149

21 January 2018

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1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31149

21 January 2018

Cognitive traits link to human chromosomal regions

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31149

21 January 2018

Role of the cholinergic muscarinic 2 receptor (CHRM2) gene in cognition.

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31149

21 January 2018

Linkage analyses of IQ in the collaborative study on the genetics of alcoholism (COGA) sample.

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31149

21 January 2018

The SNAP-25 gene is associated with cognitive ability: evidence from a family-based study in two independent Dutch cohorts.

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31149

21 January 2018

Catechol O-methyl transferase and dopamine D2 receptor gene polymorphisms: evidence of positive heterosis and gene-gene interaction on working memory functioning

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31149

21 January 2018

The brain-derived neurotrophic factor Val66Met polymorphism is associated with age-related change in reasoning skills.

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31149

21 January 2018

A United Kingdom population-based study of intellectual capacities in children with and without soiling, daytime wetting, and bed-wetting

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31149

21 January 2018

Co-occurrence of ADHD and low IQ has genetic origins.

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31149

21 January 2018

Genome-wide scan of IQ finds significant linkage to a quantitative trait locus on 2q.

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31149

21 January 2018

Cognitive ability at age 11 and 70 years, information processing speed, and APOE variation: the Lothian Birth Cohort 1936 study.

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31149

21 January 2018

Influence and interactions of cathepsin D, HLA-DRB1 and APOE on cognitive abilities in an older non-demented population.

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31149

21 January 2018

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1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31149

21 January 2018

Apolipoprotein E and cognitive performance: a meta-analysis.

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31149

21 January 2018

Intelligence in DSM-IV combined type attention-deficit/hyperactivity disorder is not predicted by either dopamine receptor/transporter genes or other previously identified risk alleles for attention-deficit/hyperactivity disorder

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31149

21 January 2018

Common variants underlying cognitive ability: further evidence for association between the SNAP-25 gene and cognition using a family-based study in two independent Dutch cohorts

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31149

21 January 2018

Population differences in the International Multi-Centre ADHD Gene Project

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31149

21 January 2018

Genetics and general cognitive ability

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31149

21 January 2018

Progress in the Molecular-Genetic Study of Intelligence

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31149

21 January 2018

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10.1002/AJMG.B.31149

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Europe PubMed Central

5 August 2017

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Europe PubMed Central

5 August 2017

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Europe PubMed Central

5 August 2017

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