(Q34811896)

4 August 2017

Copy number variants in German patients with schizophrenia (English)

1 reference

4 August 2017

0 references

Andreas Meyer-Lindenberg

11

1 reference

4 August 2017

18

Marcella Rietschel

0 references

Sven Cichon

20

Sven Cichon

0 references

Manuel Mattheisen

9

Manuel Mattheisen

0 references

Stefan Herms

Stefan Herms

5

0 references

Markus M Nöthen

Markus M Nöthen

19

0 references

Igor Nenadic

14

Igor Nenadic

1 reference

4 August 2017

2

Franziska Degenhardt

1 reference

4 August 2017

16

Dan Rujescu

1 reference

4 August 2017

10

Susanne Moebus

1 reference

4 August 2017

Henrik Walter

12

1 reference

ORCID Public Data File 2021

Heinrich Sauer

15

Heinrich Sauer

1 reference

4 August 2017

6

Stephanie H Witt

1 reference

4 August 2017

7

Per Hoffmann

1 reference

4 August 2017

13

Rainald Mössner

1 reference

4 August 2017

3

Jana Strohmaier

1 reference

4 August 2017

4

René Breuer

1 reference

4 August 2017

1

Lutz Priebe

1 reference

4 August 2017

Rebecca Kulbida

8

1 reference

PubMed ID

23843933

4 August 2017

Wolfgang Maier

17

1 reference

PubMed ID

23843933

4 August 2017

language of work or name

English

0 references

publication date

2 July 2013

1 reference

4 August 2017

1 reference

4 August 2017

8

1 reference

4 August 2017

7

1 reference

4 August 2017

e64035

1 reference

Creative Commons Attribution 4.0 International

4 August 2017

start time

2 July 2013

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

cites work

Independent estimation of the frequency of rare CNVs in the UK population confirms their role in schizophrenia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3699619

Duplications of the neuropeptide receptor gene VIPR2 confer significant risk for schizophrenia

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3699619

Copy number variants in schizophrenia: confirmation of five previous findings and new evidence for 3q29 microdeletions and VIPR2 duplications

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3699619

Deletion 17q12 is a recurrent copy number variant that confers high risk of autism and schizophrenia

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3699619

New copy number variations in schizophrenia.

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3699619

Microdeletions of 3q29 confer high risk for schizophrenia

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3699619

Microduplications of 16p11.2 are associated with schizophrenia

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3699619

Copy number variations of chromosome 16p13.1 region associated with schizophrenia

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3699619

Neurexin 1 (NRXN1) deletions in schizophrenia

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3699619

Support for the involvement of large copy number variants in the pathogenesis of schizophrenia

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3699619

Disruption of the neurexin 1 gene is associated with schizophrenia

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3699619

Large recurrent microdeletions associated with schizophrenia

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3699619

Rare chromosomal deletions and duplications increase risk of schizophrenia

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3699619

PennCNV: an integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3699619

PLINK: a tool set for whole-genome association and population-based linkage analyses

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3699619

QuantiSNP: an Objective Bayes Hidden-Markov Model to detect and accurately map copy number variation using SNP genotyping data

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3699619

Schizophrenia as a complex trait: evidence from a meta-analysis of twin studies

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3699619

Schizophrenia susceptibility associated with interstitial deletions of chromosome 22q11.

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3699619

A polydiagnostic application of operational criteria in studies of psychotic illness. Development and reliability of the OPCRIT system

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3699619

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

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3699619

Best estimate of lifetime psychiatric diagnosis: a methodological study.

8 July 2018

1 reference

Crossref

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0064035

Association between copy number variants in 16p11.2 and major depressive disorder in a German case-control sample

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0064035

Genome-wide survey implicates the influence of copy number variants (CNVs) in the development of early-onset bipolar disorder

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0064035

10.1371/JOURNAL.PONE.0064035

21 January 2018

Identifiers

DOI

1 reference

4 August 2017

0 references

1 reference

4 August 2017

1 reference

PubMed ID

23843933