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Paper ยท 17952125

Genome-wide DNA copy number analysis in pancreatic cancer using high-density single nucleotide polymorphism arrays.

Harada T and 7 others. Oncogene, 2008. Cited by 118 papers, by iCite.

11 sourcespapers-2026-11-12-0.1.0

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ConductScience Library. Genome-wide DNA copy number analysis in pancreatic cancer using high-density single nucleotide polymorphism arrays. Papers, record 17952125. Release papers-2026-11-12-0.1.0, 12 Nov 2026. https://conductscience.org/library/papers/17952125

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Paper

PubMed's record of the paper, with iCite's citation figures. No abstract is shown.

Title
Genome-wide DNA copy number analysis in pancreatic cancer using high-density single nucleotide polymorphism arrays.
PubMed
Journal
Oncogene
PubMed
Year
2008
PubMed
Publication types
Journal Article, Research Support, Non-U.S. Gov't
PubMed
Citations, by iCite
118
iCite
Relative citation ratio, by iCite
2.27
iCite
Revised in PubMed
2025-05-29
PubMed

Authors8

The authors in the order PubMed's record lists them, with the ORCID iDs it states.

OrderAuthorForenameKindORCID iD
1Harada TT
2Chelala CC
3Bhakta VV
4Chaplin TT
5Caulee KK
6Baril PP
7Young BDB D
8Lemoine NRN R

Source PubMed

Topics22

NLM's MeSH indexing of the paper, its major topics first.

MeSH termMajor
Chromosomes, HumanMajor topic
DNA, NeoplasmMajor topic
Gene DosageMajor topic
Oligonucleotide Array Sequence AnalysisMajor topic
Pancreatic NeoplasmsMajor topic
Polymorphism, Single NucleotideMajor topic
Adenocarcinoma
Adult
Aged
Carcinoma, Pancreatic Ductal
Chromosome Aberrations
Female
Humans
In Situ Hybridization, Fluorescence
Intracellular Signaling Peptides and Proteins
Loss of Heterozygosity
Male
Microdissection
Middle Aged
Nucleic Acid Hybridization
RNA, Neoplasm
Reverse Transcriptase Polymerase Chain Reaction

Source PubMed

Grants3

Each grant PubMed's record writes, matched to the NIH project NIH's grant and paper links name for this paper, and each of those links the record does not write.

Grant, as the record writes itAgencyCountryNIH projectStated by
A6253Cancer Research UKUnited KingdomPubMed
A6438Cancer Research UKUnited KingdomPubMed
A6789Cancer Research UKUnited KingdomPubMed

Source PubMed

Trials0

The trials whose ClinicalTrials.gov record lists the paper, and the trial numbers the paper's PubMed record names.

None in this release.

Comments and corrections0

PubMed's comments and corrections, NLM's own indexing: retractions first, then expressions of concern, errata and updates, and comments last.

None in this release.

References32

The papers the reference list in PubMed's record names, those in our copy of PubMed, in the list's order.

OrderPMIDTitleJournalYearIn PapersSource
111,830,540Interglandular cytogenetic heterogeneity detected by comparative genomic hybridization in pancreatic cancer.Cancer Res2002https://conductscience.org/library/papers/11830540PubMed
210,973,224Loss-of-heterozygosity analysis of small-cell lung carcinomas using single-nucleotide polymorphism arrays.Nat Biotechnol2000https://conductscience.org/library/papers/10973224PubMed
310,379,865Genomic changes defining the genesis, progression, and malignancy potential in solid human tumors: a phenotype/genotype correlation.Genes Chromosomes Cancer1999https://conductscience.org/library/papers/10379865PubMed
47,757,992Consistent chromosome abnormalities in adenocarcinoma of the pancreas.Cancer Res1995https://conductscience.org/library/papers/7757992PubMed
515,695,375Genome-wide single nucleotide polymorphism analysis reveals frequent partial uniparental disomy due to somatic recombination in acute myeloid leukemias.Cancer Res2005https://conductscience.org/library/papers/15695375PubMed
617,564,968Highly sensitive method for genomewide detection of allelic composition in nonpaired, primary tumor specimens by use of affymetrix single-nucleotide-polymorphism genotyping microarrays.Am J Hum Genet2007https://conductscience.org/library/papers/17564968PubMed
717,189,270alpha-Synuclein stimulates differentiation of osteosarcoma cells: relevance to down-regulation of proteasome activity.J Biol Chem2007https://conductscience.org/library/papers/17189270PubMed
816,785,998Molecular karyotyping of human hepatocellular carcinoma using single-nucleotide polymorphism arrays.Oncogene2006https://conductscience.org/library/papers/16785998PubMed
916,774,939Frequent occurrence of uniparental disomy in colorectal cancer.Carcinogenesis2007https://conductscience.org/library/papers/16774939PubMed
1016,024,607A robust algorithm for copy number detection using high-density oligonucleotide single nucleotide polymorphism genotyping arrays.Cancer Res2005https://conductscience.org/library/papers/16024607PubMed

Cited by87

The papers in our copy of PubMed whose reference list names this one, newest first. iCite, which reads more sources, counts 118 citations.

PMIDTitleJournalYearIn PapersSource
42,975,825LC-WGS-based Chromosomal Instability Analysis of EUS-FNA Specimens for Diagnosing Solid Pancreatic Lesions.Ann Surg Oncol2026https://conductscience.org/library/papers/42975825PubMed
42,721,202Biomarker discovery and patient stratification in pancreatic cancer using incomplete multi-omics data.PLoS Comput Biol2026https://conductscience.org/library/papers/42721202PubMed
42,602,860Ultra-low-pass whole-genome sequencing of bile cfDNA in patients with biliary strictures.eGastroenterology2026https://conductscience.org/library/papers/42602860PubMed
41,719,404Evidence that extra copies of chromosome 1q play a role in the early phases of pancreatic neoplasia.Sci Adv2026https://conductscience.org/library/papers/41719404PubMed
40,397,745Genome-wide analyses of cell-free DNA for therapeutic monitoring of patients with pancreatic cancer.Sci Adv2025https://conductscience.org/library/papers/40397745PubMed
39,966,556Deletion of 17p in cancers: Guilt by (p53) association.Oncogene2025https://conductscience.org/library/papers/39966556PubMed
39,408,992Pleomorphic Parotid Adenoma in a Child Affected with Cri du Chat Syndrome: Clinical, Cytogenetic, and Molecular Analysis.Int J Mol Sci2024https://conductscience.org/library/papers/39408992PubMed
39,350,250Copy number amplification-induced overexpression of lncRNA LOC101927668 facilitates colorectal cancer progression by recruiting hnRNPD to disrupt RBM47/p53/p21 signaling.J Exp Clin Cancer Res2024https://conductscience.org/library/papers/39350250PubMed
38,203,561Copy Number Variations in Pancreatic Cancer: From Biological Significance to Clinical Utility.Int J Mol Sci2023https://conductscience.org/library/papers/38203561PubMed
36,535,941Genomic heterogeneity in pancreatic cancer organoids and its stability with culture.NPJ Genom Med2022https://conductscience.org/library/papers/36535941PubMed

1 to 10 of 87

See all 87 cited by

Genes24

The genes the Gene search release ties to the paper: Swiss-Prot's references first, then PubTator's text mining.

Drugs0

The drugs whose trials, in the Pipelines release, list the paper.

None in this release.

Data0

The data bank entries PubMed's record names. Trial numbers are under Trials.

None in this release.

Data dates

The date of each source this release read.

PubMed
2026-11-06
PubMed
iCite
2026-11-05
iCite
PMC's ID file
2026-11-05
PMC's ID file
NIH RePORTER's grant and paper links
2026-11-01
NIH RePORTER's grant and paper links
Trials
2026-11-12
Gene search
2026-11-11
Pipelines
2026-09-18

Sources 11

  • ChEMBL, through Open TargetsCC BY-SA 3.0
  • ClinicalTrials.govNo license stated
  • HGNCCC0
  • iCiteCC BY 4.0
  • NCBI GenePublic domain (US government)
  • NIH RePORTER's grant and paper linksPublic domain
  • Open TargetsCC0 1.0
  • PMC's ID filePublic domain (US government)
  • PubMedNLM's terms
  • PubTator 3Public domain
  • UniProtCC BY 4.0
Each source's terms
  • ChEMBL, through Open TargetsCC BY-SA 3.0, for the parts from ChEMBL. Read on 8 Nov 2026 at https://platform-docs.opentargets.org/licence
  • ClinicalTrials.govnone stated
  • HGNCCC0: https://www.genenames.org/about/license/
  • iCiteCC BY 4.0
  • NCBI GeneNone named for the file. NCBI says information created by or for the US government on its site is in the public domain, and asks that NLM be acknowledged: https://www.ncbi.nlm.nih.gov/home/about/policies/
  • NIH RePORTER's grant and paper linksPublic domain (NIH RePORTER)
  • Open TargetsCC0 1.0. Open Targets asks that users cite its latest paper: Buniello et al. 2025, Open Targets Platform: facilitating therapeutic hypotheses building in drug discovery, Nucleic Acids Research 53(D1):D1467, PMID 39657122. Read on 8 Nov 2026 at https://platform-docs.opentargets.org/licence
  • PMC's ID fileNone named for the file. NCBI says information created by or for the US government on its site is in the public domain, and asks that NLM be acknowledged: https://www.ncbi.nlm.nih.gov/home/about/policies/
  • PubMedNLM's terms
  • PubTator 3Public domain
  • UniProtCC BY 4.0. UniProt's licence file: "All databases and documents in the UniProt FTP directory may be copied and redistributed freely, without advance permission, provided that this copyright statement is reproduced with each copy." UniProt asks that users cite its latest paper: The UniProt Consortium, UniProt: the Universal Protein Knowledgebase in 2025, Nucleic Acids Research 53:D609-D617, https://doi.org/10.1093/nar/gkae1010. Read on 9 Nov 2026 at https://www.uniprot.org/help/license

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

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