(Q34482858)

2 August 2017

title

Identification of the semaphorin receptor PLXNA2 as a candidate for susceptibility to schizophrenia (English)

1 reference

2 August 2017

0 references

Mah S

1

1 reference

2 August 2017

Nelson MR

2

1 reference

2 August 2017

Delisi LE

3

1 reference

2 August 2017

Reneland RH

4

1 reference

2 August 2017

Markward N

5

1 reference

2 August 2017

James MR

6

1 reference

2 August 2017

Nyholt DR

7

1 reference

2 August 2017

Hayward N

8

1 reference

2 August 2017

Handoko H

9

1 reference

2 August 2017

Mowry B

10

1 reference

2 August 2017

Kammerer S

11

1 reference

2 August 2017

Braun A

12

1 reference

2 August 2017

language of work or name

English

0 references

publication date

1 May 2006

1 reference

2 August 2017

1 reference

2 August 2017

volume

11

1 reference

2 August 2017

issue

5

1 reference

2 August 2017

page(s)

471-478

1 reference

https://scigraph.springernature.com/pub.10.1038/sj.mp.4001785

2 August 2017

exact match

0 references

cites work

Is schizophrenia universal?

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001785

7 January 2021

Association and linkage analyses of RGS4 polymorphisms in schizophrenia

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001785

7 January 2021

Schizophrenia and affective disorders--cosegregation with a translocation at chromosome 1q42 that directly disrupts brain-expressed genes: clinical and P300 findings in a family.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001785

7 January 2021

Genetic variation in the 6p22.3 gene DTNBP1, the human ortholog of the mouse dysbindin gene, is associated with schizophrenia

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001785

7 January 2021

Neuregulin 1 and susceptibility to schizophrenia

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001785

7 January 2021

Genetic and physiological data implicating the new human gene G72 and the gene for D-amino acid oxidase in schizophrenia

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001785

7 January 2021

Effect of COMT Val108/158 Met genotype on frontal lobe function and risk for schizophrenia

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001785

7 January 2021

Genetic variation at the 22q11 PRODH2/DGCR6 locus presents an unusual pattern and increases susceptibility to schizophrenia

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001785

7 January 2021

Searching for schizophrenia genes

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001785

7 January 2021

Recent advances in the genetics of schizophrenia

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001785

7 January 2021

Functional SNPs in the lymphotoxin-alpha gene that are associated with susceptibility to myocardial infarction

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001785

7 January 2021

Association between a variation in the phosphodiesterase 4D gene and bone mineral density

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001785

7 January 2021

Large-scale association study identifies ICAM gene region as breast and prostate cancer susceptibility locus.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001785

7 January 2021

Association of the NuMA region on chromosome 11q13 with breast cancer susceptibility

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001785

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.4001785

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.4001785

7 January 2021

Chromosome 1 loci in Finnish schizophrenia families

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001785

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.4001785

7 January 2021

Linkage of schizophrenia with chromosome 1q loci in Taiwanese families.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001785

7 January 2021

A genome-wide scan for linkage to chromosomal regions in 382 sibling pairs with schizophrenia or schizoaffective disorder

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001785

7 January 2021

No major schizophrenia locus detected on chromosome 1q in a large multicenter sample

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001785

7 January 2021

Chromosome 1q12-q22 linkage results in eastern Québec families affected by schizophrenia

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001785

7 January 2021

Genomewide linkage scan of 409 European-ancestry and African American families with schizophrenia: suggestive evidence of linkage at 8p23.3-p21.2 and 11p13.1-q14.1 in the combined sample

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001785

7 January 2021

Diagnostic interview for genetic studies. Rationale, unique features, and training. NIMH Genetics Initiative

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001785

7 January 2021

A controlled family study of chronic psychoses. Schizophrenia and schizoaffective disorder

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001785

7 January 2021

Best estimate of lifetime psychiatric diagnosis: a methodological study.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001785

7 January 2021

Second stage of a genome scan of schizophrenia: study of five positive regions in an expanded sample

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001785

7 January 2021

Multicenter linkage study of schizophrenia loci on chromosome 22q.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001785

7 January 2021

Large-scale validation of single nucleotide polymorphisms in gene regions

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001785

7 January 2021

Association testing by DNA pooling: an effective initial screen

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001785

7 January 2021

High-throughput screening for evidence of association by using mass spectrometry genotyping on DNA pools

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001785

7 January 2021

Identification of the sources of error in allele frequency estimations from pooled DNA indicates an optimal experimental design

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001785

7 January 2021

Pedigree disequilibrium tests for multilocus haplotypes.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001785

7 January 2021

Plexin A is a neuronal semaphorin receptor that controls axon guidance

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001785

7 January 2021

Plexin-A3 mediates semaphorin signaling and regulates the development of hippocampal axonal projections

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001785

7 January 2021

In vitro and in vivo characterization of a novel semaphorin 3A inhibitor, SM-216289 or xanthofulvin.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001785

7 January 2021

Plexins are a large family of receptors for transmembrane, secreted, and GPI-anchored semaphorins in vertebrates

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001785

7 January 2021

Plexin/neuropilin complexes mediate repulsion by the axonal guidance signal semaphorin 3A.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001785

7 January 2021

Schizophrenia: diverse approaches to a complex disease

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001785

7 January 2021

The neuropathology of schizophrenia. A critical review of the data and their interpretation

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001785

7 January 2021

Schizophrenia, neurodevelopment and corpus callosum

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001785

7 January 2021

Structural and functional characteristics of the corpus callosum in schizophrenics, psychiatric controls, and normal controls. A magnetic resonance imaging and neuropsychological evaluation

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001785

7 January 2021

Shape differences in the corpus callosum in first-episode schizophrenia and first-episode psychotic affective disorder

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001785

7 January 2021

The axonal chemorepellant semaphorin 3A is increased in the cerebellum in schizophrenia and may contribute to its synaptic pathology

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001785

7 January 2021

Is schizophrenia linked to chromosome 1q?

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001785

7 January 2021

Disruption of two novel genes by a translocation co-segregating with schizophrenia

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001785

7 January 2021

A high-density genome scan detects evidence for a bipolar-disorder susceptibility locus on 13q32 and other potential loci on 1q32 and 18p11.2.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001785

7 January 2021

Evidence for shared susceptibility in bipolar disorder and schizophrenia

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001785

7 January 2021

Identifiers

DOI

10.1038/SJ.MP.4001785

1 reference

2 August 2017

1 reference