Copy number variants in German patients with schizophrenia (Q34811896)

4 August 2017

title

Copy number variants in German patients with schizophrenia (English)

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4 August 2017

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Andreas Meyer-Lindenberg

11

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4 August 2017

18

Marcella Rietschel

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Sven Cichon

20

Sven Cichon

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Manuel Mattheisen

9

Manuel Mattheisen

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Stefan Herms

Stefan Herms

5

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Markus M Nöthen

Markus M Nöthen

19

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Igor Nenadic

14

Igor Nenadic

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4 August 2017

2

Franziska Degenhardt

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4 August 2017

16

Dan Rujescu

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4 August 2017

10

Susanne Moebus

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4 August 2017

Henrik Walter

12

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ORCID Public Data File 2021

Heinrich Sauer

15

Heinrich Sauer

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4 August 2017

6

Stephanie H Witt

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4 August 2017

7

Per Hoffmann

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4 August 2017

13

Rainald Mössner

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4 August 2017

3

Jana Strohmaier

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4 August 2017

4

René Breuer

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4 August 2017

1

Lutz Priebe

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4 August 2017

Rebecca Kulbida

8

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4 August 2017

Wolfgang Maier

17

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4 August 2017

language of work or name

English

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publication date

2 July 2013

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4 August 2017

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4 August 2017

volume

8

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4 August 2017

issue

7

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4 August 2017

page(s)

e64035

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Creative Commons Attribution 4.0 International

4 August 2017

copyright license

start time

2 July 2013

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April 2022 Public Data File from Crossref

copyright status

copyrighted

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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/JOURNAL.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/JOURNAL.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/JOURNAL.PONE.0064035

10.1371/JOURNAL.PONE.0064035

21 January 2018

Identifiers

DOI

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4 August 2017

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4 August 2017

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