Genomic copy number variation, human health, and disease.
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A preliminary study of copy number variation in TibetansHuman genetics and genomics a decade after the release of the draft sequence of the human genomeRevealing the genetic basis of multiple sclerosis: are we there yet?Genetic variations in human glutathione transferase enzymes: significance for pharmacology and toxicologyChild development and molecular genetics: 14 years laterGenetic determinants of depression: recent findings and future directionsFast Bayesian Inference of Copy Number Variants using Hidden Markov Models with Wavelet CompressionFunctional impact of the human mobilomeThe emergence of human-evolutionary medical genomicsCopy number variation, chromosome rearrangement, and their association with recombination during avian evolutionGenome-wide association study of copy number variations (CNVs) with opioid dependence.The genetic basis of music abilityMeet me halfway: when genomics meets structural bioinformatics.The role of copy number variation in susceptibility to amyotrophic lateral sclerosis: genome-wide association study and comparison with published loci.Determining multiallelic complex copy number and sequence variation from high coverage exome sequencing dataEpigenetic transgenerational actions of vinclozolin on promoter regions of the sperm epigenomeIdentification of de novo copy number variants associated with human disorders of sexual development.An evaluation of copy number variation detection tools for cancer using whole exome sequencing data.Analyses of copy number variation of GK rat reveal new putative type 2 diabetes susceptibility loci.Alzheimer's Disease Neuroimaging Initiative biomarkers as quantitative phenotypes: Genetics core aims, progress, and plans.The application of gene co-expression network reconstruction based on CNVs and gene expression microarray data in breast cancer.Genetic determinants of pubertal timing in the general population.Molecular genetic analysis of Chd3 and polytene chromosome region 76B-D in Drosophila melanogaster.Genetics of hypertrophic cardiomyopathy.Application of genetic/genomic approaches to allergic disorders.Evaluation of 172 candidate polymorphisms for association with oligozoospermia or azoospermia in a large cohort of men of European descent.Building genetic scores to predict risk of complex diseases in humans: is it possible?Gene duplication of endothelin 3 is closely correlated with the hyperpigmentation of the internal organs (Fibromelanosis) in silky chickensRare chromosomal deletions and duplications in attention-deficit hyperactivity disorder: a genome-wide analysis.A hemocyte gene expression signature correlated with predictive capacity of oysters to survive Vibrio infectionsAnalysis of copy number variations in the sheep genome using 50K SNP BeadChip arrayGenetics of complex respiratory diseases: implications for pathophysiology and pharmacology studiesGenetics and clinical destiny: improving care in hypertrophic cardiomyopathyCCL3L1 copy number, HIV load, and immune reconstitution in sub-Saharan Africans.A 7.5-Mb duplication at chromosome 11q21-11q22.3 is associated with a novel spastic ataxia syndrome.Short copy number variations potentially associated with tonic immobility responses in newly hatched chicks.Pathogenesis of contact lens-associated microbial keratitisIdentification of rare germline copy number variations over-represented in five human cancer types.Differential quantification of CYP2D6 gene copy number by four different quantitative real-time PCR assaysEvolution of the rapidly mutating human salivary agglutinin gene (DMBT1) and population subsistence strategy.
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Genomic copy number variation, human health, and disease.
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on 15 June 2009
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
@da
vědecký článek
@cs
name
Genomic copy number variation, human health, and disease.
@en
Genomic copy number variation, human health, and disease.
@nl
type
label
Genomic copy number variation, human health, and disease.
@en
Genomic copy number variation, human health, and disease.
@nl
prefLabel
Genomic copy number variation, human health, and disease.
@en
Genomic copy number variation, human health, and disease.
@nl
P1433
P1476
Genomic copy number variation, human health, and disease.
@en
P2093
John A L Armour
P304
P356
10.1016/S0140-6736(09)60249-X
P407
P577
2009-06-15T00:00:00Z