Discover Community Create You

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

Identification and characterization of three inherited genomic copy number variations associated with familial schizophrenia.

Schizophrenia research - 1 Aug 2012

Liao Hsiao-Mei, Chao Yu-Lin, Huang Ai-Ling, Cheng Min-Chih, Chen Yann-Jang, Lee Kuei-Fang, Fang Jye-Siung, Hsu Chih-Hao, Chen Chia-Hsiang

Abstract excerpt

Schizophrenia is a complex mental disorder with high degree of genetic influence in its etiology. Several recent studies revealed that copy number variations (CNVs) of genomic DNA contributed significantly to the genetic architecture of sporadic schizophrenia. This study aimed to investigate whether CNVs also contribute to the familial forms of schizophrenia. Using array-based comparative genomic hybridization...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Taiwan
Share to Chromosomes, Human, Pair 15

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Chromosomes, Human, Pair 18

Share to Chromosomes, Human, Pair 6

Share to Comparative Genomic Hybridization

Share to Cytogenetic Analysis

Share to Gene Dosage

Share to Trisomy

Source

Identifiers

PMID: 22682706
DOI: 10.1016/j.schres.2012.05.015

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Identification and characterization of three inherited genomic copy number variations associated with familial schizophrenia.PMID 22682706Read ↗

Analysis of copy number variations at 15 schizophrenia-associated loci.Semantic proximity Read ↗

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

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

A genome-wide CNV analysis of schizophrenia reveals a potential role for a multiple-hit model.Semantic proximity Read ↗

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

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

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

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

New copy number variations in schizophrenia.Semantic proximity Read ↗

Case history and genome-wide scans for copy number variants in a family with patient having 15q11.1-q11.2 duplication and 22q11.2 deletion, and schizophrenia.Semantic proximity Read ↗

Large recurrent microdeletions associated with schizophrenia.Semantic proximity Read ↗

Copy Number Variations and Schizophrenia.Semantic proximity Read ↗

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