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Hidden Markov Model-Based CNV Detection Algorithms for Illumina Genotyping MicroarraysRare Germline Copy Number Variations and Disease Susceptibility in Familial MelanomaLong term transcriptional reactivation of epigenetically silenced genes in colorectal cancer cells requires DNA hypomethylation and histone acetylationA survey of copy-number variation detection tools based on high-throughput sequencing data.Continuing difficulties in interpreting CNV data: lessons from a genome-wide CNV association study of Australian HNPCC/lynch syndrome patients.Copy number analysis of whole-genome data using BIC-seq2 and its application to detection of cancer susceptibility variants.The profile and contribution of rare germline copy number variants to cancer risk in Li-Fraumeni patients negative for TP53 mutations.Molecular mechanisms of gender disparity in hepatitis B virus-associated hepatocellular carcinomaCombined analysis with copy number variation identifies risk loci in lung cancer.Coregulation of FANCA and BRCA1 in human cellsIdentification of candidate predisposing copy number variants in familial and early-onset colorectal cancer patients.Li-Fraumeni-like syndrome associated with a large BRCA1 intragenic deletion.Rare copy number variants observed in hereditary breast cancer cases disrupt genes in estrogen signaling and TP53 tumor suppression networkA minimal connected network of transcription factors regulated in human tumors and its application to the quest for universal cancer biomarkersGermline DNA copy number aberrations identified as potential prognostic factors for breast cancer recurrence.Copy number variations are progressively associated with the pathogenesis of colorectal cancer in ulcerative colitisGenome-wide analysis of loss of heterozygosity in breast infiltrating ductal carcinoma distant normal tissue highlights arm specific enrichment and expansion across tumor stages.Genome-wide microarray expression and genomic alterations by array-CGH analysis in neuroblastoma stem-like cells.High Prevalence and Clinical Relevance of Genes Affected by Chromosomal Breaks in Colorectal Cancer.Duplication of CXC chemokine genes on chromosome 4q13 in a melanoma-prone family.Comparative analysis of copy number variations in ulcerative colitis associated and sporadic colorectal neoplasia.Constitutional de novo deletion of the FBXW7 gene in a patient with focal segmental glomerulosclerosis and multiple primitive tumorsGermline DNA copy number variation in familial and early-onset breast cancerMapping of three genetic determinants of susceptibility to estrogen-induced mammary cancer within the Emca8 locus on rat chromosome 5.Number of rare germline CNVs and TP53 mutation types.Genetic variation and its role in malignancyGenetic association study identifies a functional CNV in the WWOX gene contributes to the risk of intracranial aneurysms.Germline and somatic KLLN alterations in breast cancer dysregulate G2 arrest.Germline large genomic alterations on 7q in patients with multiple primary cancers.Increased genomic burden of germline copy number variants is associated with early onset breast cancer: Australian breast cancer family registry.Copy number variation in the genomes of domestic animals.Germline copy number variations and cancer predisposition.Microarray-based copy number analysis of neurofibromatosis type-1 (NF1)-associated malignant peripheral nerve sheath tumors reveals a role for Rho-GTPase pathway genes in NF1 tumorigenesis.Radiogenomics and radiotherapy response modeling.Large germline copy number variations as predisposing factor in childhood neoplasms.Germline copy number variation analysis in Finnish families with hereditary prostate cancer.Germline deletions in the tumour suppressor gene FOCAD are associated with polyposis and colorectal cancer development.Application of Machine Learning to Development of Copy Number Variation-based Prediction of Cancer RiskCNVannotator: a comprehensive annotation server for copy number variation in the human genome.Amplification of Chromosome 1q Genes Encoding the Phosphoinositide Signalling Enzymes PI4KB, AKT3, PIP5K1A and PI3KC2B in Breast Cancer.
P2860
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P2860
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on 08 April 2010
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
@da
vědecký článek
@cs
name
Germline copy number variation and cancer risk.
@en
Germline copy number variation and cancer risk.
@nl
type
label
Germline copy number variation and cancer risk.
@en
Germline copy number variation and cancer risk.
@nl
prefLabel
Germline copy number variation and cancer risk.
@en
Germline copy number variation and cancer risk.
@nl
P2093
P1476
Germline copy number variation and cancer risk.
@en
P2093
Ad Geurts van Kessel
Marjolijn J L Ligtenberg
Roland P Kuiper
P304
P356
10.1016/J.GDE.2010.03.005
P577
2010-04-08T00:00:00Z