(Q48414796)

11 February 2018

title

Association between autism and variants in the wingless-type MMTV integration site family member 2 ( WNT2) gene. (English)

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11 February 2018

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Tetsuya Marui

1

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11 February 2018

Ikuko Funatogawa

2

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11 February 2018

Shinko Koishi

3

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11 February 2018

Kenji Yamamoto

4

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11 February 2018

Hideo Matsumoto

5

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11 February 2018

Ohiko Hashimoto

6

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11 February 2018

Seiichiro Jinde

7

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11 February 2018

Hisami Nishida

8

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11 February 2018

Toshiro Sugiyama

9

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11 February 2018

Kiyoto Kasai

10

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11 February 2018

Keiichiro Watanabe

11

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11 February 2018

Yukiko Kano

12

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11 February 2018

Nobumasa Kato

13

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11 February 2018

publication date

9 November 2009

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11 February 2018

The International Journal of Neuropsychopharmacology

published in

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11 February 2018

volume

13

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11 February 2018

page(s)

443-449

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11 February 2018

issue

4

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11 February 2018

The NOTCH4 locus is associated with susceptibility to schizophrenia

cites work

1 reference

https://api.crossref.org/works/10.1017%2FS1461145709990903

Mechanisms of Wnt signaling in development

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1461145709990903

Identification of a novel gene on chromosome 7q31 that is interrupted by a translocation breakpoint in an autistic individual

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1461145709990903

Xwnt-2b is a novel axis-inducing Xenopus Wnt, which is expressed in embryonic brain.

21 January 2018

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https://api.crossref.org/works/10.1017%2FS1461145709990903

Regulatory gene expression patterns reveal transverse and longitudinal subdivisions of the embryonic zebrafish forebrain

21 January 2018

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https://api.crossref.org/works/10.1017%2FS1461145709990903

The structure of haplotype blocks in the human genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1461145709990903

Genetics of austim: complex aetiology for a heterogeneous disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1461145709990903

Autism and abnormal development of brain connectivity.

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1461145709990903

Haploview: analysis and visualization of LD and haplotype maps

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1461145709990903

Molecular genetic studies of Wnt signaling in the mouse.

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1461145709990903

A genomic screen of autism: evidence for a multilocus etiology

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1461145709990903

No association between the WNT2 gene and autistic disorder.

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1461145709990903

No association of FOXP2 and PTPRZ1 on 7q31 with autism from the Japanese population

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1461145709990903

No association between the neuronal pentraxin II gene polymorphism and autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1461145709990903

Tachykinin 1 (TAC1) gene SNPs and haplotypes with autism: a case-control study.

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1461145709990903

Social interaction and sensorimotor gating abnormalities in mice lacking Dvl1

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1461145709990903

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1461145709990903

Evidence supporting WNT2 as an autism susceptibility gene.

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1461145709990903

10.1017/S1461145709990903

21 January 2018

Identifiers

DOI

1 reference

11 February 2018

PubMed ID

19895723

1 reference

11 February 2018