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
Topics22
NLM's MeSH indexing of the paper, its major topics first.
| MeSH term | Major |
|---|---|
| Chromosomes, Human | Major topic |
| DNA, Neoplasm | Major topic |
| Gene Dosage | Major topic |
| Oligonucleotide Array Sequence Analysis | Major topic |
| Pancreatic Neoplasms | Major topic |
| Polymorphism, Single Nucleotide | Major 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 it | Agency | Country | NIH project | Stated by |
|---|---|---|---|---|
| A6253 | Cancer Research UK | United Kingdom | PubMed | |
| A6438 | Cancer Research UK | United Kingdom | PubMed | |
| A6789 | Cancer Research UK | United Kingdom | PubMed |
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.
| Order | PMID | Title | Journal | Year | In Papers | Source |
|---|---|---|---|---|---|---|
| 1 | 11,830,540 | Interglandular cytogenetic heterogeneity detected by comparative genomic hybridization in pancreatic cancer. | Cancer Res | 2002 | https://conductscience.org/library/papers/11830540 | PubMed |
| 2 | 10,973,224 | Loss-of-heterozygosity analysis of small-cell lung carcinomas using single-nucleotide polymorphism arrays. | Nat Biotechnol | 2000 | https://conductscience.org/library/papers/10973224 | PubMed |
| 3 | 10,379,865 | Genomic changes defining the genesis, progression, and malignancy potential in solid human tumors: a phenotype/genotype correlation. | Genes Chromosomes Cancer | 1999 | https://conductscience.org/library/papers/10379865 | PubMed |
| 4 | 7,757,992 | Consistent chromosome abnormalities in adenocarcinoma of the pancreas. | Cancer Res | 1995 | https://conductscience.org/library/papers/7757992 | PubMed |
| 5 | 15,695,375 | Genome-wide single nucleotide polymorphism analysis reveals frequent partial uniparental disomy due to somatic recombination in acute myeloid leukemias. | Cancer Res | 2005 | https://conductscience.org/library/papers/15695375 | PubMed |
| 6 | 17,564,968 | Highly 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 Genet | 2007 | https://conductscience.org/library/papers/17564968 | PubMed |
| 7 | 17,189,270 | alpha-Synuclein stimulates differentiation of osteosarcoma cells: relevance to down-regulation of proteasome activity. | J Biol Chem | 2007 | https://conductscience.org/library/papers/17189270 | PubMed |
| 8 | 16,785,998 | Molecular karyotyping of human hepatocellular carcinoma using single-nucleotide polymorphism arrays. | Oncogene | 2006 | https://conductscience.org/library/papers/16785998 | PubMed |
| 9 | 16,774,939 | Frequent occurrence of uniparental disomy in colorectal cancer. | Carcinogenesis | 2007 | https://conductscience.org/library/papers/16774939 | PubMed |
| 10 | 16,024,607 | A robust algorithm for copy number detection using high-density oligonucleotide single nucleotide polymorphism genotyping arrays. | Cancer Res | 2005 | https://conductscience.org/library/papers/16024607 | PubMed |
1 to 10 of 32
See all 32 referencesCited by87
The papers in our copy of PubMed whose reference list names this one, newest first. iCite, which reads more sources, counts 118 citations.
| PMID | Title | Journal | Year | In Papers | Source |
|---|---|---|---|---|---|
| 42,975,825 | LC-WGS-based Chromosomal Instability Analysis of EUS-FNA Specimens for Diagnosing Solid Pancreatic Lesions. | Ann Surg Oncol | 2026 | https://conductscience.org/library/papers/42975825 | PubMed |
| 42,721,202 | Biomarker discovery and patient stratification in pancreatic cancer using incomplete multi-omics data. | PLoS Comput Biol | 2026 | https://conductscience.org/library/papers/42721202 | PubMed |
| 42,602,860 | Ultra-low-pass whole-genome sequencing of bile cfDNA in patients with biliary strictures. | eGastroenterology | 2026 | https://conductscience.org/library/papers/42602860 | PubMed |
| 41,719,404 | Evidence that extra copies of chromosome 1q play a role in the early phases of pancreatic neoplasia. | Sci Adv | 2026 | https://conductscience.org/library/papers/41719404 | PubMed |
| 40,397,745 | Genome-wide analyses of cell-free DNA for therapeutic monitoring of patients with pancreatic cancer. | Sci Adv | 2025 | https://conductscience.org/library/papers/40397745 | PubMed |
| 39,966,556 | Deletion of 17p in cancers: Guilt by (p53) association. | Oncogene | 2025 | https://conductscience.org/library/papers/39966556 | PubMed |
| 39,408,992 | Pleomorphic Parotid Adenoma in a Child Affected with Cri du Chat Syndrome: Clinical, Cytogenetic, and Molecular Analysis. | Int J Mol Sci | 2024 | https://conductscience.org/library/papers/39408992 | PubMed |
| 39,350,250 | Copy number amplification-induced overexpression of lncRNA LOC101927668 facilitates colorectal cancer progression by recruiting hnRNPD to disrupt RBM47/p53/p21 signaling. | J Exp Clin Cancer Res | 2024 | https://conductscience.org/library/papers/39350250 | PubMed |
| 38,203,561 | Copy Number Variations in Pancreatic Cancer: From Biological Significance to Clinical Utility. | Int J Mol Sci | 2023 | https://conductscience.org/library/papers/38203561 | PubMed |
| 36,535,941 | Genomic heterogeneity in pancreatic cancer organoids and its stability with culture. | NPJ Genom Med | 2022 | https://conductscience.org/library/papers/36535941 | PubMed |
1 to 10 of 87
See all 87 cited byGenes24
The genes the Gene search release ties to the paper: Swiss-Prot's references first, then PubTator's text mining.
| Gene | NCBI Gene ID | Linked by | In Genes | Source |
|---|---|---|---|---|
| CBX3 | 11,335 | PubTator's text mining | https://conductscience.org/library/genes/11335 | NCBI Gene |
| CDKN2A | 1,029 | PubTator's text mining | https://conductscience.org/library/genes/1029 | NCBI Gene |
| CDKN2B | 1,030 | PubTator's text mining | https://conductscience.org/library/genes/1030 | NCBI Gene |
| CYB5A | 1,528 | PubTator's text mining | https://conductscience.org/library/genes/1528 | NCBI Gene |
| DCC | 1,630 | PubTator's text mining | https://conductscience.org/library/genes/1630 | NCBI Gene |
| EGFR | 1,956 | PubTator's text mining | https://conductscience.org/library/genes/1956 | NCBI Gene |
| ERBB2 | 2,064 | PubTator's text mining | https://conductscience.org/library/genes/2064 | NCBI Gene |
| FBXO15 | 201,456 | PubTator's text mining | https://conductscience.org/library/genes/201456 | NCBI Gene |
| FN1 | 2,335 | PubTator's text mining | https://conductscience.org/library/genes/2335 | NCBI Gene |
| HAND1 | 9,421 | PubTator's text mining | https://conductscience.org/library/genes/9421 | NCBI Gene |
1 to 10 of 24
See all 24 genesDrugs0
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.
- 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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