(Q34329016)

1 August 2017

title

Systematic genotype-phenotype analysis of autism susceptibility loci implicates additional symptoms to co-occur with autism (English)

1 reference

1 August 2017

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9

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1 August 2017

8

Herman van Engeland

1 reference

1 August 2017

Lude Franke

2

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Chantal Kemner

series ordinal

5

object named as

Chantal Kemner

1 reference

1 August 2017

6

Roel A Ophoff

1 reference

1 August 2017

7

Jacob As Vorstman

1 reference

1 August 2017

4

Emma van Daalen

1 reference

Jacobine E Buizer-Voskamp

1 August 2017

series ordinal

1

object named as

Jacobine E Buizer-Voskamp

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1 August 2017

3

Wouter G Staal

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1 August 2017

publication date

25 November 2009

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European Journal of Human Genetics

1 August 2017

published in

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1 August 2017

volume

18

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1 August 2017

issue

5

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1 August 2017

page(s)

588-595

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Large recurrent microdeletions associated with schizophrenia

1 August 2017

cites work

1 reference

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

6 July 2018

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Genome-wide association analysis identifies 20 loci that influence adult height

6 July 2018

1 reference

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Many sequence variants affecting diversity of adult human height

6 July 2018

1 reference

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Structural variation of chromosomes in autism spectrum disorder

6 July 2018

1 reference

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

6 July 2018

1 reference

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A unified genetic theory for sporadic and inherited autism

6 July 2018

1 reference

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Strong association of de novo copy number mutations with autism

6 July 2018

1 reference

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A human phenome-interactome network of protein complexes implicated in genetic disorders

6 July 2018

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Prevalence of autism spectrum disorders--autism and developmental disabilities monitoring network, 14 sites, United States, 2002.

6 July 2018

1 reference

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Informative phenotypes for genetic studies of psychiatric disorders

6 July 2018

1 reference

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The genetics of autistic disorders and its clinical relevance: a review of the literature

6 July 2018

1 reference

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Epilepsy in autism spectrum disorders

6 July 2018

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)

6 July 2018

1 reference

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Endophenotypes for psychiatric disorders: ready for primetime?

6 July 2018

1 reference

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Autism and environmental genomics

6 July 2018

1 reference

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Current perspectives on the genetic analysis of autism.

6 July 2018

1 reference

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Autism spectrum disorders: molecular genetic advances

6 July 2018

1 reference

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Creation and implications of a phenome-genome network

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2987310

Gastrointestinal Factors in Autistic Disorder: A Critical Review

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2987310

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

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2987310

Mapping phenotypes to language: a proposal to organize and standardize the clinical descriptions of malformations

6 July 2018

1 reference

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Integration of text- and data-mining using ontologies successfully selects disease gene candidates

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2987310

Autism associated with conditions characterized by developmental errors in early embryogenesis: a mini review

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2987310

6 July 2018

The teratology of autism

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2987310

The search for autism disease genes

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2987310

Molecular genetics of autism spectrum disorder.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2987310

6 July 2018

The genetics of autism

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2987310

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2987310

How common are gastrointestinal disorders in children with autism?

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2987310

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

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2987310

Perinatal risk factors for infantile autism

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2987310

Genetics of austim: complex aetiology for a heterogeneous disorder

6 July 2018

1 reference

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

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2987310

Gastrointestinal abnormalities in children with autistic disorder

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2987310

From impasse to insight in autism research: from behavioral symptoms to biological explanations

6 July 2018

1 reference

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Autism, mental retardation, multiple exostoses and short stature in a female with 46,X,t(X;8)(p22.13;q22.1).

6 July 2018

2 references

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2987310

6 July 2018

https://api.crossref.org/works/10.1038%2FEJHG.2009.206

Sizing up human height variation

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2009.206

CNTNAP2 gene dosage variation is associated with schizophrenia and epilepsy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2009.206

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/10.1038%2FEJHG.2009.206

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/10.1038%2FEJHG.2009.206

On macrocephaly, epilepsy, autism, specific facial features, and mental retardation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2009.206

Contiguous gene syndrome due to an interstitial deletion in Xp22.3 in a boy with ichthyosis, chondrodysplasia punctata, mental retardation and ADHD.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2009.206

Deletions of VCX-A and NLGN4: a variable phenotype including normal intellect.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2009.206

Epilepsy in young adults with autism: a prospective population-based follow-up study of 120 individuals diagnosed in childhood.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2009.206

An MRI study of minor physical anomalies in autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2009.206

Medical disorders among inpatients with autism in Denmark according to ICD-8: a nationwide register-based study.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2009.206

2003 Warkany Lecture: Autism as a birth defect

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2009.206

Congenital anomalies associated with autism spectrum disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2009.206

Parental report of health conditions and health care use among children with and without autism: National Survey of Children's Health.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2009.206

Case of Myhre syndrome with autism and peculiar skin histological findings.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2009.206

Developmental, behavioural and somatic factors in pervasive developmental disorders: preliminary analysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2009.206

Identification of low bone mass in a developmental center: finger bone mineral density measurement in 562 residents

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2987310

A text-mining analysis of the human phenome

27 October 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/19935830

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Normal values for morphological abnormalities in school children

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/19935830

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1038/EJHG.2009.206

1 reference

1 August 2017

1 reference

1 August 2017

1 reference