(Q28244222)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17764594%20AND%20SRC:MED&resulttype=core&format=json

4 January 2020

review article

1 reference

title

Autism: the quest for the genes (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17764594%20AND%20SRC:MED&resulttype=core&format=json

4 January 2020

0 references

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17764594%20AND%20SRC:MED&resulttype=core&format=json

4 January 2020

author name string

Nuala H Sykes

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17764594%20AND%20SRC:MED&resulttype=core&format=json

4 January 2020

language of work or name

English

0 references

publication date

3 September 2007

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17764594%20AND%20SRC:MED&resulttype=core&format=json

Expert Reviews in Molecular Medicine

4 January 2020

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17764594%20AND%20SRC:MED&resulttype=core&format=json

4 January 2020

volume

9

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17764594%20AND%20SRC:MED&resulttype=core&format=json

4 January 2020

issue

24

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17764594%20AND%20SRC:MED&resulttype=core&format=json

4 January 2020

page(s)

1-15

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17764594%20AND%20SRC:MED&resulttype=core&format=json

Lack of evidence for an association between WNT2 and RELN polymorphisms and autism

4 January 2020

cites work

1 reference

https://api.crossref.org/works/10.1017/S1462399407000452

Confirmation of association between autism and the mitochondrial aspartate/glutamate carrier SLC25A12 gene on chromosome 2q31

20 April 2017

1 reference

https://api.crossref.org/works/10.1017/S1462399407000452

Linkage and association of the mitochondrial aspartate/glutamate carrier SLC25A12 gene with autism

20 April 2017

1 reference

https://api.crossref.org/works/10.1017/S1462399407000452

Molecular cloning of Aralar, a new member of the mitochondrial carrier superfamily that binds calcium and is present in human muscle and brain

20 April 2017

1 reference

https://api.crossref.org/works/10.1017/S1462399407000452

Mapping autism risk loci using genetic linkage and chromosomal rearrangements

20 April 2017

1 reference

https://api.crossref.org/works/10.1017/S1462399407000452

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

20 April 2017

1 reference

https://api.crossref.org/works/10.1017/S1462399407000452

Analysis of the RELN gene as a genetic risk factor for autism

20 April 2017

1 reference

https://api.crossref.org/works/10.1017/S1462399407000452

Genome-wide and Ordered-Subset linkage analyses provide support for autism loci on 17q and 19p with evidence of phenotypic and interlocus genetic correlates

20 April 2017

1 reference

https://api.crossref.org/works/10.1017/S1462399407000452

Genome-wide expression profiling of lymphoblastoid cell lines distinguishes different forms of autism and reveals shared pathways

20 April 2017

1 reference

https://api.crossref.org/works/10.1017/S1462399407000452

MECP2 mutations in sporadic cases of Rett syndrome are almost exclusively of paternal origin

20 April 2017

1 reference

https://api.crossref.org/works/10.1017/S1462399407000452

Replication of autism linkage: fine-mapping peak at 17q21.

20 April 2017

1 reference

https://api.crossref.org/works/10.1017/S1462399407000452

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

20 April 2017

1 reference

https://api.crossref.org/works/10.1017/S1462399407000452

Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2

20 April 2017

1 reference

https://api.crossref.org/works/10.1017/S1462399407000452

Imprinting, the X-chromosome, and the male brain: explaining sex differences in the liability to autism

20 April 2017

1 reference

https://api.crossref.org/works/10.1017/S1462399407000452

DNA methylation profiling of human chromosomes 6, 20 and 22

20 April 2017

1 reference

https://api.crossref.org/works/10.1017/S1462399407000452

Strong association of de novo copy number mutations with autism

20 April 2017

1 reference

https://api.crossref.org/works/10.1017/S1462399407000452

High frequency of neurexin 1beta signal peptide structural variants in patients with autism

20 April 2017

1 reference

https://api.crossref.org/works/10.1017/S1462399407000452

A genomewide screen of 345 families for autism-susceptibility loci

20 April 2017

1 reference

https://api.crossref.org/works/10.1017/S1462399407000452

A full genome screen for autism with evidence for linkage to a region on chromosome 7q. International Molecular Genetic Study of Autism Consortium

20 April 2017

1 reference

https://api.crossref.org/works/10.1017/S1462399407000452

Global variation in copy number in the human genome

20 April 2017

1 reference

https://api.crossref.org/works/10.1017/S1462399407000452

Structural variation in the human genome

20 April 2017

1 reference

https://api.crossref.org/works/10.1017/S1462399407000452

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

20 April 2017

1 reference

https://api.crossref.org/works/10.1017/S1462399407000452

Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes

20 April 2017

1 reference

https://api.crossref.org/works/10.1017/S1462399407000452

The International HapMap Project

20 April 2017

1 reference

https://api.crossref.org/works/10.1017/S1462399407000452

Finishing the euchromatic sequence of the human genome

20 April 2017

1 reference

https://api.crossref.org/works/10.1017/S1462399407000452

A genomic screen of autism: evidence for a multilocus etiology

20 April 2017

1 reference

https://api.crossref.org/works/10.1017/S1462399407000452

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

20 April 2017

1 reference

https://api.crossref.org/works/10.1017/S1462399407000452

Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism

20 April 2017

1 reference

https://api.crossref.org/works/10.1017/S1462399407000452

A twin study of autism in Denmark, Finland, Iceland, Norway and Sweden

20 April 2017

1 reference

https://api.crossref.org/works/10.1017/S1462399407000452

Allelic heterogeneity at the serotonin transporter locus (SLC6A4) confers susceptibility to autism and rigid-compulsive behaviors

20 April 2017

1 reference

https://api.crossref.org/works/10.1017/S1462399407000452

Subset of individuals with autism spectrum disorders and extreme macrocephaly associated with germline PTEN tumour suppressor gene mutations

20 April 2017

1 reference

https://api.crossref.org/works/10.1017/S1462399407000452

Time to give up on a single explanation for autism

20 April 2017

1 reference

https://api.crossref.org/works/10.1017/S1462399407000452

Autism and the serotonin transporter: the long and short of it

20 April 2017

1 reference

https://api.crossref.org/works/10.1017/S1462399407000452

Infantile autism: a genetic study of 21 twin pairs

20 April 2017

1 reference

https://api.crossref.org/works/10.1017/S1462399407000452

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

20 April 2017

1 reference

https://api.crossref.org/works/10.1017/S1462399407000452

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

20 April 2017

1 reference

https://api.crossref.org/works/10.1017/S1462399407000452

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

20 April 2017

2 references

https://api.crossref.org/works/10.1017/S1462399407000452

20 April 2017

https://api.crossref.org/works/10.1017%2FS1462399407000452

Reelin gene alleles and susceptibility to autism spectrum disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399407000452

Absence of association between a polymorphic GGC repeat in the 5' untranslated region of the reelin gene and autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399407000452

Alleles of a reelin CGG repeat do not convey liability to autism in a sample from the CPEA network

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399407000452

Analysis of reelin as a candidate gene for autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399407000452

Reelin gene alleles and haplotypes as a factor predisposing to autistic disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399407000452

Lack of Association Between Autism and SLC25A12

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399407000452

Mapping complex disease loci in whole-genome association studies

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399407000452

Power to detect linkage based on multiple sets of data in the presence of locus heterogeneity: comparative evaluation of model-based linkage methods for affected sib pair data.

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399407000452

Neurochemical correlates of autistic disorder: a review of the literature

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399407000452

Evidence for sex-specific risk alleles in autism spectrum disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399407000452

Phenotypic homogeneity provides increased support for linkage on chromosome 2 in autistic disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399407000452

Autism spectrum disorders: molecular genetic advances

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399407000452

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399407000452

Parental origin of de novo MECP2 mutations in Rett syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399407000452

Genomic screen and follow-up analysis for autistic disorder.

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399407000452

Linkage analysis for autism in a subset families with obsessive-compulsive behaviors: evidence for an autism susceptibility gene on chromosome 1 and further support for susceptibility genes on chromosome 6 and 19.

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399407000452

Imbalanced genomic imprinting in brain development: an evolutionary basis for the aetiology of autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399407000452

A genomewide screen for autism susceptibility loci

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399407000452

Evidence for a susceptibility gene for autism on chromosome 2 and for genetic heterogeneity

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399407000452

Parent reports of sensory symptoms in toddlers with autism and those with other developmental disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399407000452

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399407000452

A comprehensive analysis of common copy-number variations in the human genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399407000452

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399407000452

MMR-vaccine and regression in autism spectrum disorders: negative results presented from Japan

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399407000452

Completing the map of human genetic variation

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399407000452

MMR vaccination and pervasive developmental disorders: a case-control study

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399407000452

Highly parallel genomic assays

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399407000452

Maternal infection: window on neuroimmune interactions in fetal brain development and mental illness

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399407000452

Maternal administration of thalidomide or valproic acid causes abnormal serotonergic neurons in the offspring: implication for pathogenesis of autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399407000452

Prenatal, perinatal, and neonatal factors in autism, pervasive developmental disorder-not otherwise specified, and the general population

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399407000452

Autism: the phenotype in relatives.

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399407000452

Genetics and child psychiatry: II Empirical research findings

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399407000452

Overcoming the winner's curse: estimating penetrance parameters from case-control data

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399407000452

Establishment of genetic associations for complex diseases is independent of early study findings

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399407000452

The complex interplay among factors that influence allelic association.

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399407000452

5-HTTLPR variants not associated with autistic spectrum disorders.

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399407000452

Increasing knowledge of PTEN germline mutations: Two additional patients with autism and macrocephaly.

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399407000452

Mutation screening of the PTEN gene in patients with autism spectrum disorders and macrocephaly

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399407000452

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399407000452

The endophenotype concept in psychiatric genetics

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399407000452

Proteomic approach for the elucidation of biological defects in autism.

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399407000452

Evidence for an association with the serotonin transporter promoter region polymorphism and autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399407000452

Serotonin transporter (5-HTT) gene variants associated with autism?

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399407000452

Serotonin transporter gene and autism: a haplotype analysis in an Irish autistic population

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399407000452

Linkage and association analysis at the serotonin transporter (SLC6A4) locus in a rigid-compulsive subset of autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399407000452

Evidence of linkage between the serotonin transporter and autistic disorder.

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399407000452

Reelin signaling is impaired in autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399407000452

Polymorphic GGC repeat differentially regulates human reelin gene expression levels

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399407000452

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399407000452

The economic impact of autism in Britain.

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399407000452

The serotonin system in autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399407000452

Shaking the tree: mapping complex disease genes with linkage disequilibrium

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399407000452

7 January 2021

A proteomic study of serum from children with autism showing differential expression of apolipoproteins and complement proteins

1 reference

https://api.crossref.org/works/10.1017%2FS1462399407000452

7 January 2021

The hyper-systemizing, assortative mating theory of autism

1 reference

https://api.crossref.org/works/10.1017%2FS1462399407000452

7 January 2021

Lack of association between autism and SLC25A12

1 reference

https://api.crossref.org/works/10.1017%2FS1462399407000452

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1017%2FS1462399407000452

7 January 2021

5-HTTLPR Genotype-Specific Phenotype in Children and Adolescents With Autism

1 reference

https://api.crossref.org/works/10.1017%2FS1462399407000452

7 January 2021

Lack of evidence for association of the serotonin transporter gene SLC6A4 with autism.

1 reference

https://api.crossref.org/works/10.1017%2FS1462399407000452

7 January 2021

Serotonin transporter (5-HTT) and gamma-aminobutyric acid receptor subunit beta3 (GABRB3) gene polymorphisms are not associated with autism in the IMGSA families. The International Molecular Genetic Study of Autism Consortium.

1 reference

https://api.crossref.org/works/10.1017%2FS1462399407000452

7 January 2021

Epigenetic variation and inheritance in mammals

1 reference

https://api.crossref.org/works/10.1017%2FS1462399407000452

7 January 2021

Accumulating quantitative trait linkage evidence across multiple datasets using the posterior probability of linkage

1 reference

https://api.crossref.org/works/10.1017%2FS1462399407000452

7 January 2021

Autism as a disorder of neural information processing: directions for research and targets for therapy

1 reference

https://api.crossref.org/works/10.1017%2FS1462399407000452

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1017%2FS1462399407000452

7 January 2021

Autism spectrum disorders: early detection, intervention, education, and psychopharmacological management

1 reference

https://api.crossref.org/works/10.1017%2FS1462399407000452

7 January 2021

Autism as a strongly genetic disorder: evidence from a British twin study

1 reference

https://api.crossref.org/works/10.1017%2FS1462399407000452

7 January 2021

Autism in thalidomide embryopathy: a population study.

1 reference

https://api.crossref.org/works/10.1017%2FS1462399407000452

7 January 2021

10.1017/S1462399407000452

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17764594%20AND%20SRC:MED&resulttype=core&format=json

OpenCitations bibliographic resource ID

4 January 2020

3537325

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

2 references

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

3537325