(Q30496457)

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High-density SNP association study and copy number variation analysis of the AUTS1 and AUTS5 loci implicate the IMMP2L-DOCK4 gene region in autism susceptibility

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scholarly article

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Europe PubMed Central

19 October 2017

High-density SNP association study and copy number variation analysis of the AUTS1 and AUTS5 loci implicate the IMMP2L-DOCK4 gene region in autism susceptibility (English)

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Europe PubMed Central

19 October 2017

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C Toma

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author name string

E Maestrini

1

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Europe PubMed Central

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A T Pagnamenta

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J A Lamb

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E Bacchelli

4

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N H Sykes

5

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I Sousa

6

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G Barnby

8

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H Butler

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L Winchester

10

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T S Scerri

11

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F Minopoli

12

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J Reichert

13

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G Cai

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O Korvatska

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G D Schellenberg

17

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G Dawson

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A de Bildt

19

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R B Minderaa

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E J Mulder

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A P Morris

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A J Bailey

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IMGSAC

25

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19 October 2017

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publication date

28 April 2009

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19 October 2017

Molecular Psychiatry

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15

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9

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954-968

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Europe PubMed Central

19 October 2017

Identification of loci associated with schizophrenia by genome-wide association and follow-up

1 reference

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Genome-wide linkage analyses of quantitative and categorical autism subphenotypes

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Identifying autism loci and genes by tracing recent shared ancestry

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Dock4 regulates dendritic development in hippocampal neurons

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

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Likelihood-based association analysis for nuclear families and unrelated subjects with missing genotype data

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Novel submicroscopic chromosomal abnormalities detected in autism spectrum disorder

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Rare structural variants disrupt multiple genes in neurodevelopmental pathways in schizophrenia

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Phenotypically concordant and discordant monozygotic twins display different DNA copy-number-variation profiles

1 reference

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Structural variation of chromosomes in autism spectrum disorder

1 reference

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

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Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project

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

1 reference

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Strong association of de novo copy number mutations with autism

1 reference

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QuantiSNP: an Objective Bayes Hidden-Markov Model to detect and accurately map copy number variation using SNP genotyping data

1 reference

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Mapping autism risk loci using genetic linkage and chromosomal rearrangements

1 reference

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Mutations in the gene encoding the synaptic scaffolding protein SHANK3 are associated with autism spectrum disorders

1 reference

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European population substructure: clustering of northern and southern populations

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A flexible Bayesian framework for modeling haplotype association with disease, allowing for dominance effects of the underlying causative variants

1 reference

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Prevalence of disorders of the autism spectrum in a population cohort of children in South Thames: the Special Needs and Autism Project (SNAP)

1 reference

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14 July 2018

Epidemiology of autistic disorder and other pervasive developmental disorders

1 reference

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ZNF674: a new kruppel-associated box-containing zinc-finger gene involved in nonsyndromic X-linked mental retardation

1 reference

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Efficiency and power in genetic association studies

1 reference

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14 July 2018

SLC25A12 and CMYA3 gene variants are not associated with autism in the IMGSAC multiplex family sample

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2934739

14 July 2018

Identification of novel autism candidate regions through analysis of reported cytogenetic abnormalities associated with autism

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2934739

14 July 2018

A heterogeneity-based genome search meta-analysis for autism-spectrum disorders

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2934739

14 July 2018

Evolutionarily conserved elements in vertebrate, insect, worm, and yeast genomes

1 reference

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Direct analysis of unphased SNP genotype data in population-based association studies via Bayesian partition modelling of haplotypes

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2934739

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Pervasive developmental disorders in preschool children: confirmation of high prevalence

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2934739

14 July 2018

Analysis of IMGSAC autism susceptibility loci: evidence for sex limited and parent of origin specific effects.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2934739

14 July 2018

Mutation screening and association analysis of six candidate genes for autism on chromosome 7q

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2934739

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Haploview: analysis and visualization of LD and haplotype maps

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Increasing the power and efficiency of disease-marker case-control association studies through use of allele-sharing information

1 reference

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Mutations in the ZNF41 gene are associated with cognitive deficits: identification of a new candidate for X-linked mental retardation

1 reference

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Screening of nine candidate genes for autism on chromosome 2q reveals rare nonsynonymous variants in the cAMP-GEFII gene

1 reference

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Analysis of reelin as a candidate gene for autism

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1 reference

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

1 reference

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1 reference

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1 reference

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

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https://api.crossref.org/works/10.1038%2FMP.2009.34

21 January 2018

Array CGH identifies reciprocal 16p13.1 duplications and deletions that predispose to autism and/or mental retardation.

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An analysis of candidate autism loci on chromosome 2q24-q33: evidence for association to the STK39 gene

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Simple detection of genomic microdeletions and microduplications using QMPSF in patients with idiopathic mental retardation.

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https://api.crossref.org/works/10.1038%2FMP.2009.34

21 January 2018

Clinical and molecular characterization of a patient with a 2q31.2-32.3 deletion identified by array-CGH.

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Detection of known and novel genomic rearrangements by array based comparative genomic hybridisation: deletion of ZNF533 and duplication of CHARGE syndrome genes.

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Zinc finger 81 (ZNF81) mutations associated with X-linked mental retardation

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Identifiers

10.1038/MP.2009.34

1 reference

Europe PubMed Central

19 October 2017

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1 reference

Europe PubMed Central

19 October 2017

1 reference

Europe PubMed Central

19 October 2017

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Springer Nature article ID

10.1038/mp.2009.34

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