(Q50301629)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17290275%20AND%20SRC:MED&resulttype=core&format=json

25 December 2019

title

Identification and characterization of the TRIP8 and REEP3 genes on chromosome 10q21.3 as novel candidate genes for autism (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17290275%20AND%20SRC:MED&resulttype=core&format=json

25 December 2019

0 references

1 reference

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25 December 2019

Joris R Vermeesch

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17290275%20AND%20SRC:MED&resulttype=core&format=json

25 December 2019

Dries Castermans

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17290275%20AND%20SRC:MED&resulttype=core&format=json

25 December 2019

Jean-Pierre Fryns

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17290275%20AND%20SRC:MED&resulttype=core&format=json

25 December 2019

Wim J M Van de Ven

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17290275%20AND%20SRC:MED&resulttype=core&format=json

25 December 2019

John W M Creemers

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17290275%20AND%20SRC:MED&resulttype=core&format=json

25 December 2019

Koen Devriendt

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17290275%20AND%20SRC:MED&resulttype=core&format=json

25 December 2019

publication date

7 February 2007

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17290275%20AND%20SRC:MED&resulttype=core&format=json

European Journal of Human Genetics

25 December 2019

published in

1 reference

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25 December 2019

volume

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25 December 2019

issue

1 reference

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25 December 2019

page(s)

422-431

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17290275%20AND%20SRC:MED&resulttype=core&format=json

Autism spectrum disorders: molecular genetic advances

25 December 2019

cites work

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Genetic influences in childhood-onset psychiatric disorders: autism and attention-deficit/hyperactivity disorder

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7 January 2021

How commonly are known medical conditions associated with autism?

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7 January 2021

Searching for ways out of the autism maze: genetic, epigenetic and environmental clues

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7 January 2021

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

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7 January 2021

A risk-factor model of epistatic interaction, focusing on autism

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7 January 2021

Chromosomal anomalies in individuals with autism: a strategy towards the identification of genes involved in autism.

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7 January 2021

Genetics of autism spectrum disorder

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7 January 2021

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

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7 January 2021

Array-based comparative genomic hybridisation identifies high frequency of cryptic chromosomal rearrangements in patients with syndromic autism spectrum disorders

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7 January 2021

The neurobeachin gene is disrupted by a translocation in a patient with idiopathic autism.

1 reference

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7 January 2021

An inversion inv(4)(p12-p15.3) in autistic siblings implicates the 4p GABA receptor gene cluster

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7 January 2021

Chromosomal disorders and autism

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7 January 2021

Infantile autism and associated autosomal chromosome abnormalities: a register-based study and a literature survey

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7 January 2021

Genetics of austim: complex aetiology for a heterogeneous disorder

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7 January 2021

Deletion of chromosome 2q37 and autism: a distinct subtype?

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7 January 2021

High-resolution molecular characterization of 15q11-q13 rearrangements by array comparative genomic hybridization (array CGH) with detection of gene dosage

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201785

7 January 2021

15q duplication associated with autism in a multiplex family with a familial cryptic translocation t(14;15)(q11.2;q13.3) detected using array-CGH.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201785

7 January 2021

Molecular karyotyping: array CGH quality criteria for constitutional genetic diagnosis.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201785

7 January 2021

Estimates of the frequency of chromosome abnormalities detectable in unselected newborns using moderate levels of banding

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201785

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201785

7 January 2021

Yop1p, the yeast homolog of the polyposis locus protein 1, interacts with Yip1p and negatively regulates cell growth

1 reference

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7 January 2021

A candidate gene for developmental dyslexia encodes a nuclear tetratricopeptide repeat domain protein dynamically regulated in brain

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7 January 2021

Sequence variants in SLITRK1 are associated with Tourette's syndrome

1 reference

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7 January 2021

JmjC: cupin metalloenzyme-like domains in jumonji, hairless and phospholipase A2β

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201785

7 January 2021

Control of thyroid hormone action in the developing rat brain

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201785

7 January 2021

Triiodothyronine (T3) concentration and therapy in autistic children

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201785

7 January 2021

A controlled crossover study of triiodothyronine in autistic children

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201785

7 January 2021

Thyroid hormone in autistic children

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201785

7 January 2021

Lack of a Relation Between Human Neonatal Thyroxine and Pediatric Neurobehavioral Disorders

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201785

7 January 2021

The TRAP220 component of a thyroid hormone receptor- associated protein (TRAP) coactivator complex interacts directly with nuclear receptors in a ligand-dependent fashion

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201785

7 January 2021

RTP family members induce functional expression of mammalian odorant receptors

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201785

7 January 2021

Specific binding to a novel and essential Golgi membrane protein (Yip1p) functionally links the transport GTPases Ypt1p and Ypt31p

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201785

7 January 2021

Rab proteins as membrane organizers

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201785

7 January 2021

The stress- and abscisic acid-induced barley gene HVA22: developmental regulation and homologues in diverse organisms

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201785

7 January 2021

Function of a plant stress-induced gene, HVA22. Synthetic enhancement screen with its yeast homolog reveals its role in vesicular traffic

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201785

7 January 2021

Long-range control of gene expression: emerging mechanisms and disruption in disease

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201785

7 January 2021

Submicroscopic deletion in patients with Williams-Beuren syndrome influences expression levels of the nonhemizygous flanking genes

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201785

7 January 2021

Position effect in human genetic disease

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201785

7 January 2021

Campomelic dysplasia translocation breakpoints are scattered over 1 Mb proximal to SOX9: evidence for an extended control region

1 reference

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7 January 2021

A long-range Shh enhancer regulates expression in the developing limb and fin and is associated with preaxial polydactyly

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7 January 2021

Schwann cells and the pathogenesis of inherited motor and sensory neuropathies (Charcot-Marie-Tooth disease).

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7 January 2021

Identifiers

DOI

10.1038/SJ.EJHG.5201785

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17290275%20AND%20SRC:MED&resulttype=core&format=json

25 December 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17290275%20AND%20SRC:MED&resulttype=core&format=json