(Q34273759)

1 August 2017

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

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1 August 2017

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12

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1 August 2017

E Bonora

5

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author name string

E Bacchelli

1

1 reference

1 August 2017

F Blasi

2

1 reference

1 August 2017

M Biondolillo

3

1 reference

1 August 2017

J A Lamb

4

1 reference

1 August 2017

G Barnby

6

1 reference

1 August 2017

J Parr

7

1 reference

1 August 2017

K S Beyer

8

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1 August 2017

S M Klauck

9

1 reference

1 August 2017

A Poustka

10

1 reference

1 August 2017

A J Bailey

11

1 reference

1 August 2017

E Maestrini

13

1 reference

1 August 2017

International Molecular Genetic Study of Autism Consortium (IMGSAC)

14

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1 August 2017

language of work or name

English

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publication date

1 November 2003

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1 August 2017

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1 August 2017

8

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1 August 2017

11

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1 August 2017

916-924

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https://scigraph.springernature.com/pub.10.1038/sj.mp.4001340

1 August 2017

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cites work

Autism: in search of susceptibility genes

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001340

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001340

Finding specific genes that cause autism: a combination of approaches will be needed to maximize power.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001340

A genomic screen of autism: evidence for a multilocus etiology

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001340

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/10.1038%2FSJ.MP.4001340

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001340

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001340

A genomewide screen for autism susceptibility loci

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001340

Genomic screen and follow-up analysis for autistic disorder.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001340

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001340

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001340

T-brain-1: a homolog of Brachyury whose expression defines molecularly distinct domains within the cerebral cortex

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001340

Nuclear translocation and transcription regulation by the membrane-associated guanylate kinase CASK/LIN-2

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001340

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001340

Analysis of reelin as a candidate gene for autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001340

Tbr1 regulates differentiation of the preplate and layer 6.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001340

A clinicopathological study of autism.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001340

Coordinated expression of Hoxa2, Hoxd1 and Pax6 in the developing diencephalon

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001340

Loss of BETA2/NeuroD leads to malformation of the dentate gyrus and epilepsy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001340

A cDNA for a human cyclic AMP response element-binding protein which is distinct from CREB and expressed preferentially in brain

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001340

ATF-2 has intrinsic histone acetyltransferase activity which is modulated by phosphorylation

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001340

Cloning and characterization of two members of the vertebrate Dlx gene family

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001340

Two genes encode distinct glutamate decarboxylases

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001340

Glutamic acid decarboxylase 65 and 67 kDa proteins are reduced in autistic parietal and cerebellar cortices

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001340

A family of cAMP-binding proteins that directly activate Rap1

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001340

cAMP-GEFII is a direct target of cAMP in regulated exocytosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001340

Alpha 2-chimerin, an SH2-containing GTPase-activating protein for the ras-related protein p21rac derived by alternate splicing of the human n-chimerin gene, is selectively expressed in brain regions and testes

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001340

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001340

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/10.1038%2FSJ.MP.4001340

A test for linkage and association in general pedigrees: the pedigree disequilibrium test

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001340

Mutations in NEUROD1 are associated with the development of type 2 diabetes mellitus

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001340

Are rare variants responsible for susceptibility to complex diseases?

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001340

A highly conserved enhancer in the Dlx5/Dlx6 intergenic region is the site of cross-regulatory interactions between Dlx genes in the embryonic forebrain.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001340

inferred from DOI database lookup

7 January 2021

based on heuristic

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

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001340

inferred from DOI database lookup

7 January 2021

based on heuristic

GOLD--graphical overview of linkage disequilibrium

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001340

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1038/SJ.MP.4001340

1 reference

1 August 2017

1 reference