A genome-wide linkage and association scan reveals novel loci for autism (Q37410600)

20 August 2017

A genome-wide linkage and association scan reveals novel loci for autism (English)

1 reference

genome-wide association study

20 August 2017

0 references

0 references

4

Mark J Daly

1 reference

20 August 2017

0 references

Lauren A Weiss

1

1 reference

20 August 2017

Dan E Arking

series ordinal

2

1 reference

20 August 2017

Gene Discovery Project of Johns Hopkins & the Autism Consortium

series ordinal

3

1 reference

20 August 2017

Aravinda Chakravarti

series ordinal

5

1 reference

20 August 2017

language of work or name

English

0 references

publication date

1 October 2009

1 reference

20 August 2017

1 reference

20 August 2017

461

1 reference

20 August 2017

802-808

1 reference

20 August 2017

7265

1 reference

https://scigraph.springernature.com/pub.10.1038/nature08490

20 August 2017

0 references

cites work

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

6 September 2017

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Integrated detection and population-genetic analysis of SNPs and copy number variation

6 September 2017

1 reference

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Estimating coverage and power for genetic association studies using near-complete variation data

6 September 2017

1 reference

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Atypical recruitment of medial prefrontal cortex in autism spectrum disorders: an fMRI study of two executive function tasks

6 September 2017

1 reference

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

6 September 2017

1 reference

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Whole-genome association study of bipolar disorder

6 September 2017

1 reference

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Structural variation of chromosomes in autism spectrum disorder

6 September 2017

1 reference

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Association between microdeletion and microduplication at 16p11.2 and autism

6 September 2017

1 reference

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Molecular cytogenetic analysis and resequencing of contactin associated protein-like 2 in autism spectrum disorders

6 September 2017

1 reference

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A common genetic variant in the neurexin superfamily member CNTNAP2 increases familial risk of autism

6 September 2017

1 reference

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Linkage, association, and gene-expression analyses identify CNTNAP2 as an autism-susceptibility gene

6 September 2017

1 reference

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

6 September 2017

1 reference

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

6 September 2017

1 reference

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An Epidemiological and Diagnostic Study of Asperger Syndrome According to Four Sets of Diagnostic Criteria

6 September 2017

1 reference

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Mapping autism risk loci using genetic linkage and chromosomal rearrangements

6 September 2017

1 reference

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Childhood autism and associated comorbidities

6 September 2017

1 reference

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Population genetics models of common diseases

6 September 2017

1 reference

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A genetic variant that disrupts MET transcription is associated with autism

6 September 2017

1 reference

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Constitutional downregulation of SEMA5A expression in autism

6 September 2017

1 reference

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

6 September 2017

1 reference

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Genome-wide association studies for common diseases and complex traits

6 September 2017

1 reference

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Williams syndrome deficits in visual spatial processing linked to GTF2IRD1 and GTF2I on chromosome 7q11.23

6 September 2017

1 reference

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Undetected genotyping errors cause apparent overtransmission of common alleles in the transmission/disequilibrium test

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2772655

A genomewide screen for autism-spectrum disorders: evidence for a major susceptibility locus on chromosome 3q25-27

6 September 2017

1 reference

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Analysis of Relative Gene Expression Data Using Real-Time Quantitative PCR and the 2−ΔΔCT Method

6 September 2017

1 reference

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

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2772655

The autism genetic resource exchange: a resource for the study of autism and related neuropsychiatric conditions

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2772655

The autism diagnostic observation schedule-generic: a standard measure of social and communication deficits associated with the spectrum of autism

6 September 2017

1 reference

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Searching for genetic determinants in the new millennium

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2772655

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

6 September 2017

1 reference

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

6 September 2017

1 reference

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Autism screening questionnaire: diagnostic validity.

6 September 2017

1 reference

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Autism diagnostic interview: a standardized investigator-based instrument.

26 June 2018

1 reference

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Social language use in parents of autistic individuals

26 June 2018

1 reference

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Disruption of cerebral cortex MET signaling in autism spectrum disorder.

26 June 2018

1 reference

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Contribution of CYLN2 and GTF2IRD1 to neurological and cognitive symptoms in Williams Syndrome.

2 September 2018

1 reference

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An atypical deletion of the Williams-Beuren syndrome interval implicates genes associated with defective visuospatial processing and autism

2 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2772655

Autism spectrum disorders associated with X chromosome markers in French-Canadian males.

2 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2772655

Atypical [corrected] participation of visual cortex during word processing in autism: an fMRI study of semantic decision

2 September 2018

1 reference

Crossref

https://api.crossref.org/works/10.1038%2FNATURE08490

inferred from DOI database lookup

7 January 2021

based on heuristic

2-year-old boy who has been diagnosed with autism

1 reference

Crossref

https://api.crossref.org/works/10.1038%2FNATURE08490

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1038/NATURE08490

1 reference

20 August 2017

1 reference

20 August 2017

1 reference