Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Analysis of copy number variations at 15 schizophrenia-associated loci.

The British journal of psychiatry : the journal of mental science - 1 Feb 2014

Rees Elliott, Walters James T R, Georgieva Lyudmila, Isles Anthony R, Chambert Kimberly D, Richards Alexander L, Mahoney-Davies Gerwyn, Legge Sophie E, Moran Jennifer L, McCarroll Steven A, O'Donovan Michael C, Owen Michael J, Kirov George

Abstract excerpt

BACKGROUND: A number of copy number variants (CNVs) have been suggested as susceptibility factors for schizophrenia. For some of these the data remain equivocal, and the frequency in individuals with schizophrenia is uncertain. AIMS: To determine the contribution of CNVs at 15 schizophrenia-associated loci (a) using a large new data-set of patients with schizophrenia (n = 6882) and controls (n = 6316), and (b)...

Topics

Join the communities discussing this publication.

Genotyping Techniques
Angelman Syndrome
Chromosome Deletion
DNA Copy Number Variations

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Genomic Imprinting

Prader-Willi Syndrome

Source

Open in PubMed Open full text

Identifiers

PMID: 24311552
DOI: 10.1192/bjp.bp.113.131052
PMCID: PMC3909838

Genes

NRXN1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 1 Sept 2026.

Community interpretation

Discuss the evidence

Ask a question, add context or challenge an interpretation. Community activity is separate from scientific evidence strength.

0

discussions

0

replies

Citations encouraged

Claims remain attributable.

No discussion yet

Be the first to add a careful, cited interpretation.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Analysis of copy number variations at 15 schizophrenia-associated loci.PMID 24311552Read ↗

Copy Number Variations in Schizophrenia: Critical Review and New Perspectives on Concepts of Genetics and DiseaseSemantic proximity Read ↗

Copy number variants of schizophrenia susceptibility loci are associated with a spectrum of speech and developmental delays and behavior problems.Semantic proximity Read ↗

Genome-wide Analysis of the Role of Copy Number Variation in Schizophrenia Risk in Chinese.Semantic proximity Read ↗

Independent estimation of the frequency of rare CNVs in the UK population confirms their role in schizophrenia.Semantic proximity Read ↗

Genomic copy number variations: A breakthrough in our knowledge on schizophrenia etiology?Semantic proximity Read ↗

New copy number variations in schizophrenia.Semantic proximity Read ↗

Support for the involvement of large copy number variants in the pathogenesis of schizophrenia.Semantic proximity Read ↗

A genome-wide investigation of SNPs and CNVs in schizophrenia.Semantic proximity Read ↗

The role of DNA copy number variation in schizophrenia.Semantic proximity Read ↗

Identification and characterization of three inherited genomic copy number variations associated with familial schizophrenia.Semantic proximity Read ↗

Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects.Semantic proximity Read ↗

Rare chromosomal deletions and duplications increase risk of schizophrenia.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.