(Q34089144)

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Identifying loci for the overlap between attention-deficit/hyperactivity disorder and autism spectrum disorder using a genome-wide QTL linkage approach

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scholarly article

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30 July 2017

Identifying loci for the overlap between attention-deficit/hyperactivity disorder and autism spectrum disorder using a genome-wide QTL linkage approach (English)

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30 July 2017

autism spectrum disorder

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inferred from title

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Richard P. Ebstein

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Stephen Faraone

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Tobias Banaschewski

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Hans-Christoph Steinhausen

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Hans-Christoph Steinhausen

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Aribert Rothenberger

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Aribert Rothenberger

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Luise Poustka

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Herbert Roeyers

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Herbert Roeyers

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Jan K Buitelaar

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Edmund Sonuga-Barke

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Edmund J S Sonuga-Barke

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Pieter J Hoekstra

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Pieter J Hoekstra

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Catharina A Hartman

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Catharina A Hartman

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Robert D Oades

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Richard J L Anney

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Alejandro Arias-Vásquez

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Alejandro Arias-Vásquez

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Ellen A Fliers

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Marieke E Altink

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Marieke E Altink

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Cathelijne J M Buschgens

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Cathelijne J M Buschgens

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Judith S Nijmeijer

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Judith S Nijmeijer

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Philip Asherson

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Philip Asherson

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Ruud B Minderaa

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object named as

Ruud B Minderaa

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author name string

Nanda N J Rommelse

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Joseph A Sergeant

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Fernando Mulas

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publication date

20 May 2010

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30 July 2017

Journal of the American Academy of Child and Adolescent Psychiatry

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49

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7

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675-685

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30 July 2017

The paradox of cognitive flexibility in autism

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2929476

5 July 2018

Evidence for shared genetic influences on self-reported ADHD and autistic symptoms in young adult Australian twins

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2929476

5 July 2018

The ‘Fractionable Autism Triad’: A Review of Evidence from Behavioural, Genetic, Cognitive and Neural Research

1 reference

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5 July 2018

Autism symptoms in Attention-Deficit/Hyperactivity Disorder: a familial trait which correlates with conduct, oppositional defiant, language and motor disorders

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2929476

5 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2929476

5 July 2018

Advances in autism genetics: on the threshold of a new neurobiology

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2929476

5 July 2018

Structural variation of chromosomes in autism spectrum disorder

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2929476

5 July 2018

Heritability of autistic traits in the general population

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2929476

5 July 2018

Characterization of a recurrent 15q24 microdeletion syndrome.

1 reference

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5 July 2018

Mapping autism risk loci using genetic linkage and chromosomal rearrangements

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2929476

5 July 2018

A review of gene linkage, association and expression studies in autism and an assessment of convergent evidence

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2929476

5 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=2929476

5 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=2929476

5 July 2018

Genetic heterogeneity between the three components of the autism spectrum: a twin study

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2929476

5 July 2018

Support for the homeobox transcription factor gene ENGRAILED 2 as an autism spectrum disorder susceptibility locus

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2929476

5 July 2018

Handling marker-marker linkage disequilibrium: pedigree analysis with clustered markers

1 reference

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5 July 2018

A genome-wide search for alleles and haplotypes associated with autism and related pervasive developmental disorders on the Faroe Islands

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2929476

5 July 2018

Linkage and association studies identify a novel locus for Alzheimer disease at 7q36 in a Dutch population-based sample

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2929476

5 July 2018

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=2929476

5 July 2018

PEDSTATS: descriptive statistics, graphics and quality assessment for gene mapping data

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2929476

5 July 2018

Genetic investigation of quantitative traits related to autism: use of multivariate polygenic models with ascertainment adjustment

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2929476

5 July 2018

Using self-report to identify the broad phenotype in parents of children with autistic spectrum disorders: a study using the Autism-Spectrum Quotient

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2929476

5 July 2018

Attention deficit hyperactivity disorder: fine mapping supports linkage to 5p13, 6q12, 16p13, and 17p11.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2929476

5 July 2018

Association of the homeobox transcription factor, ENGRAILED 2, 3, with autism spectrum disorder

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2929476

5 July 2018

Genome-wide scan for loci of Asperger syndrome

1 reference

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A genomewide screen of 345 families for autism-susceptibility loci

1 reference

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5 July 2018

A genomewide scan for attention-deficit/hyperactivity disorder in an extended sample: suggestive linkage on 17p11

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2929476

5 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2929476

5 July 2018

Powerful regression-based quantitative-trait linkage analysis of general pedigrees

1 reference

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A high-resolution recombination map of the human genome

1 reference

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

1 reference

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Evidence for a language quantitative trait locus on chromosome 7q in multiplex autism families

1 reference

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5 July 2018

Merlin--rapid analysis of dense genetic maps using sparse gene flow trees

1 reference

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5 July 2018

A genomewide screen for autism: strong evidence for linkage to chromosomes 2q, 7q, and 16p.

1 reference

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A genomewide screen for autism susceptibility loci

1 reference

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Genetic structure of reciprocal social behavior

1 reference

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Improved inference of relationship for pairs of individuals

1 reference

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Autism screening questionnaire: diagnostic validity.

1 reference

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Genome-wide scan for autism susceptibility genes. Paris Autism Research International Sibpair Study

1 reference

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PedCheck: a program for identification of genotype incompatibilities in linkage analysis

1 reference

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Multipoint quantitative-trait linkage analysis in general pedigrees

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Autism Diagnostic Interview-Revised: a revised version of a diagnostic interview for caregivers of individuals with possible pervasive developmental disorders

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Childhood hyperactivity

1 reference

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PDD symptoms in ADHD, an independent familial trait?

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Evidence for overlapping genetic influences on autistic and ADHD behaviours in a community twin sample

1 reference

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Autistic traits in a population-based ADHD twin sample.

1 reference

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Evidence for multiple loci from a genome scan of autism kindreds.

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Psychostimulant-induced attenuation of hyperactivity and prepulse inhibition deficits in Adcyap1-deficient mice

1 reference

https://pubmed.ncbi.nlm.nih.gov/20610137

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The genetics of attention deficit hyperactivity disorder

1 reference

https://pubmed.ncbi.nlm.nih.gov/20610137

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1097/00004583-201007000-00008

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

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