(Q33984019)

30 July 2017

title

Replication of an association of a common variant in the Reelin gene (RELN) with schizophrenia in Ashkenazi Jewish women (English)

1 reference

30 July 2017

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3

John McGrath

1 reference

30 July 2017

6

Gerald Nestadt

1 reference

30 July 2017

Yaping Liu

1

1 reference

30 July 2017

Pei-Lung Chen

2

1 reference

30 July 2017

Paula Wolyniec

4

1 reference

30 July 2017

Daniele Fallin

5

1 reference

30 July 2017

Kung-Yee Liang

7

1 reference

30 July 2017

Ann Pulver

8

1 reference

30 July 2017

David Valle

9

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30 July 2017

Dimitrios Avramopoulos

10

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30 July 2017

language of work or name

English

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publication date

1 August 2010

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30 July 2017

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30 July 2017

volume

20

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30 July 2017

issue

4

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30 July 2017

page(s)

184-186

1 reference

Genome-wide association identifies a common variant in the reelin gene that increases the risk of schizophrenia only in women

30 July 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2901865

Interstitial white matter neurons express less reelin and are abnormally distributed in schizophrenia: towards an integration of molecular and morphologic aspects of the neurodevelopmental hypothesis

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2901865

Genomewide linkage scan for schizophrenia susceptibility loci among Ashkenazi Jewish families shows evidence of linkage on chromosome 10q22.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2901865

The founder mutation MSH2*1906G-->C is an important cause of hereditary nonpolyposis colorectal cancer in the Ashkenazi Jewish population

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2901865

A highly significant association between a COMT haplotype and schizophrenia.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2901865

Schizophrenia: diverse approaches to a complex disease

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2901865

A decrease of reelin expression as a putative vulnerability factor in schizophrenia

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2901865

Familiality of novel factorial dimensions of schizophrenia

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2901865

A variant in the reelin gene increases the risk of schizophrenia and schizoaffective disorder but not bipolar disorder.

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2901865

10.1097/YPG.0B013E32833A220B

29 October 2018

Identifiers

DOI

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30 July 2017

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30 July 2017

1 reference