MPZL1/PZR, a novel candidate predisposing schizophrenia in Han Chinese (Q34526683)

2 August 2017

MPZL1/PZR, a novel candidate predisposing schizophrenia in Han Chinese (English)

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2 August 2017

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G He

1

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2 August 2017

X Liu

2

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2 August 2017

W Qin

3

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2 August 2017

Q Chen

4

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2 August 2017

X Wang

5

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2 August 2017

Y Yang

6

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2 August 2017

J Zhou

7

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2 August 2017

Y Xu

8

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2 August 2017

N Gu

9

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2 August 2017

G Feng

10

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2 August 2017

H Sang

11

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2 August 2017

P Wang

12

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2 August 2017

L He

13

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2 August 2017

language of work or name

English

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publication date

9 May 2006

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2 August 2017

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2 August 2017

11

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2 August 2017

8

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2 August 2017

748-751

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https://scigraph.springernature.com/pub.10.1038/sj.mp.4001841

2 August 2017

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cites work

Reporting, appraising, and integrating data on genotype prevalence and gene-disease associations

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https://api.crossref.org/works/10.1038%2FSJ.MP.4001841

The Structured Clinical Interview for DSM-III-R (SCID). I: History, rationale, and description

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.MP.4001841

Genes for schizophrenia? Recent findings and their pathophysiological implications

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.MP.4001841

7 January 2021

A genomewide screen for schizophrenia genes in an isolated Finnish subpopulation, suggesting multiple susceptibility loci

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001841

7 January 2021

Location of a major susceptibility locus for familial schizophrenia on chromosome 1q21-q22

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001841

7 January 2021

Genomewide genetic linkage analysis confirms the presence of susceptibility loci for schizophrenia, on chromosomes 1q32.2, 5q33.2, and 8p21-22 and provides support for linkage to schizophrenia, on chromosomes 11q23.3-24 and 20q12.1-11.23

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001841

7 January 2021

Fine mapping of the schizophrenia susceptibility locus on chromosome 1q22

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https://api.crossref.org/works/10.1038%2FSJ.MP.4001841

7 January 2021

Purification and cloning of PZR, a binding protein and putative physiological substrate of tyrosine phosphatase SHP-2

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001841

7 January 2021

Dissecting the interaction of SHP-2 with PZR, an immunoglobulin family protein containing immunoreceptor tyrosine-based inhibitory motifs

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001841

7 January 2021

Identification of a variant form of PZR lacking immunoreceptor tyrosine-based inhibitory motifs

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https://api.crossref.org/works/10.1038%2FSJ.MP.4001841

7 January 2021

Oligodendrocyte dysfunction in schizophrenia and bipolar disorder

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001841

7 January 2021

Problems of reporting genetic associations with complex outcomes

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001841

7 January 2021

Evidence for linkage disequilibrium between the dopamine transporter and bipolar disorder.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001841

7 January 2021

High-throughput SNP allele-frequency determination in pooled DNA samples by kinetic PCR.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001841

7 January 2021

Family-based association study of DTNBP1 in 6p22.3 and schizophrenia

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001841

7 January 2021

An extended transmission/disequilibrium test (TDT) for multi-allele marker loci.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001841

7 January 2021

A generalization of the transmission/disequilibrium test for uncertain-haplotype transmission

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001841

7 January 2021

Monte Carlo tests for associations between disease and alleles at highly polymorphic loci

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https://api.crossref.org/works/10.1038%2FSJ.MP.4001841

7 January 2021

Isolation and sequence determination of cDNA encoding the major structural protein of human peripheral myelin

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001841

7 January 2021

The major peripheral myelin protein zero gene: structure and localization in the cluster of Fc gamma receptor genes on human chromosome 1q21.3-q23

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001841

7 January 2021

Charcot-Marie-Tooth neuropathy type 1B is associated with mutations of the myelin P0 gene

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001841

7 January 2021

De novo mutation of the myelin P0 gene in Dejerine-Sottas disease (hereditary motor and sensory neuropathy type III)

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001841

7 January 2021

Genome-wide expression analysis reveals dysregulation of myelination-related genes in chronic schizophrenia

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001841

7 January 2021

Identifiers

DOI

10.1038/SJ.MP.4001841

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2 August 2017

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