CNV Publication Archive

Copy number variation in human health, disease, and evolution.

Zhang et al.

Annu Rev Genomics Hum Genet.

Genomic profile of copy number  variants on the short arm of human chromosome 8.

Yu et al.

Eur J Hum Genet.

Rare deletions at 16p13.11 predispose to a diverse spectrum of sporadic epilepsy syndromes.

Heinzen et al.

Am J Hum Genet.

Genome-wide copy number variation analysis in attention-deficit/hyperactivity disorder: association with neuropeptide Y gene dosage in an extended pedigree.

Lesch et al.

Mol Psychiatry.

The clinical context of copy number variation in the human genome.

Lee et al.

Expert Rev Mol Med.

Whole Genome Survey of Copy Number Variation in the Spontaneously Hypertensive Rat. Relationship to Quantitative Trait Loci, Gene Expression, and Blood Pressure.

Charchar et al.

Hypertension.

The impact of human copy number variation on a new era of genetic testing.

Choy et al.

BJOG

The role of genetics in the etiology of schizophrenia.

Gejman et al.

Psychiatr Clin North Am.

Genetic variation of genes involved in dihydrotestosterone metabolism and the risk of prostate cancer.

Setlur et al.

Cancer Epidemol Biomarkers Prev.

Genetic copy number variants in sib pairs both affected with schizophrenia.

Lee et al.

J Biomed Sci.

Structural variation in the human genome and its role in disease.

Stankiewicz et al.

Annu Rev Med.

The pitfalls of platform comparison: DNA copy number array technologies assessed.

Curtis et al.

BMC genomics

Genomic microarrays in mental retardation: from CNV to gene, from research to diagnosis.

Vissers et a.

Journal of medical genetics

Large, rare chromosomal deletions associated with severe early-onset obesity.

Bochukova et al.

Nature.

High resolution discovery and confirmation of copy number variants in 90 Yoruba Nigerians.
Matsuzaki et al.

Genome Biology

Copy number variation upstream of PMP22 in Charcot-Marie-Tooth disease

Weterman et al.

European Journal of Human Genetics

Microduplications of 16p11.2 are associated with schizophrenia

McCarthy et al.

Nature Genetics

What have the genomics ever done for the psychoses?

Gill, Donohoe, Corvin.

Psychological Medicine.

Integrated Analysis of Copy Number Alterations and Gene Expression: A Bivariate Assessment of Equally Directed Abnormalities.

Schafer et al.

Bioinformatics.

Population diversity and antibody selective pressure to Plasmodium falciparum MSP1 block2 locus in an African malaria-endemic setting.

Noranate et al.

BMC Microbiology.

Microarray-Based Comparative Genomic Hybridization Using Sex-Matched Reference DNA Provides Greater Sensitivity for Detection of Sex Chromosome Imbalances than Array-Comparative Genomic Hybridization with Sex-Mismatched Reference DNA.

Yatsenko et al.

Journal of Molecular Diagnostics.