Paper · 17564968

Highly sensitive method for genomewide detection of allelic composition in nonpaired, primary tumor specimens by use of affymetrix single-nucleotide-polymorphism genotyping microarrays.

Yamamoto G and 11 others. Am J Hum Genet, 2007. Cited by 221 papers, by iCite.

11 sourcespapers-2026-11-12-0.1.0

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ConductScience Library. Highly sensitive method for genomewide detection of allelic composition in nonpaired, primary tumor specimens by use of affymetrix single-nucleotide-polymorphism genotyping microarrays. Papers, record 17564968. Release papers-2026-11-12-0.1.0, 12 Nov 2026. https://conductscience.org/library/papers/17564968

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Paper

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

Title: Highly sensitive method for genomewide detection of allelic composition in nonpaired, primary tumor specimens by use of affymetrix single-nucleotide-polymorphism genotyping microarrays.; PubMed
Journal: Am J Hum Genet; PubMed
Year: 2007; PubMed
Publication types: Journal Article, Research Support, Non-U.S. Gov't; PubMed
PubMed: https://pubmed.ncbi.nlm.nih.gov/17564968/; PubMed
DOI: https://doi.org/10.1086/518809; PubMed
PMC: https://pmc.ncbi.nlm.nih.gov/articles/PMC1950910/; PubMed
The journal: https://conductscience.org/library/journal-index/0370475; PubMed
Citations, by iCite: 221; iCite
Relative citation ratio, by iCite: 4.07; iCite
Revised in PubMed: 2020-08-24; PubMed

Authors12

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

Order	Author	Forename
1	Yamamoto G	Go
2	Nannya Y	Yasuhito
3	Kato M	Motohiro
4	Sanada M	Masashi
5	Levine RL	Ross L
6	Kawamata N	Norihiko
7	Hangaishi A	Akira
8	Kurokawa M	Mineo
9	Chiba S	Shigeru
10	Gilliland DG	D Gary

1 to 10 of 12Source PubMed

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Topics15

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

MeSH term	Major
Genetic Predisposition to Disease	Major topic
Loss of Heterozygosity	Major topic
Neoplasms	Major topic
Oligonucleotide Array Sequence Analysis	Major topic
Polymorphism, Single Nucleotide	Major topic
Uniparental Disomy	Major topic
Alleles
Cell Line, Tumor
DNA Mutational Analysis
DNA, Neoplasm
Genome, Human
Genomics
Humans
Myeloproliferative Disorders
Sensitivity and Specificity

Source PubMed

Grants0

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.

None in this release.

Trials0

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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.

References26

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	10,958,631	Genome-wide detection of allelic imbalance using human SNPs and high-density DNA arrays.	Genome Res	2000	https://conductscience.org/library/papers/10958631	PubMed
2	16,787,995	PLASQ: a generalized linear model-based procedure to determine allelic dosage in cancer cells from SNP array data.	Biostatistics	2007	https://conductscience.org/library/papers/16787995	PubMed
3	11,905,807	Two genetic hits (more or less) to cancer.	Nat Rev Cancer	2001	https://conductscience.org/library/papers/11905807	PubMed
4	12,406,101	Exploring polycythaemia vera with fluorescence in situ hybridization: additional cryptic 9p is the most frequent abnormality detected.	Br J Haematol	2002	https://conductscience.org/library/papers/12406101	PubMed
5	12,816,870	Molecular characterization of the recurrent unbalanced translocation der(1;7)(q10;p10).	Blood	2003	https://conductscience.org/library/papers/12816870	PubMed
6	12,960,966	Large-scale genotyping of complex DNA.	Nat Biotechnol	2003	https://conductscience.org/library/papers/12960966	PubMed
7	14,762,065	High-resolution analysis of DNA copy number using oligonucleotide microarrays.	Genome Res	2004	https://conductscience.org/library/papers/14762065	PubMed
8	15,126,342	An integrated view of copy number and allelic alterations in the cancer genome using single nucleotide polymorphism arrays.	Cancer Res	2004	https://conductscience.org/library/papers/15126342	PubMed
9	15,290,239	Concurrent analysis of loss of heterozygosity (LOH) and copy number abnormality (CNA) for oral premalignancy progression using the Affymetrix 10K SNP mapping array.	Hum Genet	2004	https://conductscience.org/library/papers/15290239	PubMed
10	15,588,488	Whole genome DNA copy number changes identified by high density oligonucleotide arrays.	Hum Genomics	2004	https://conductscience.org/library/papers/15588488	PubMed

1 to 10 of 26

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Cited by138

The papers in our copy of PubMed whose reference list names this one, newest first. iCite, which reads more sources, counts 221 citations.

PMID	Title	Journal	Year	In Papers	Source
40,921,497	Efficacy of ciclosporin monotherapy in non-severe aplastic anaemia not requiring transfusions: Results from a multicentre phase II study.	Br J Haematol	2026	https://conductscience.org/library/papers/40921497	PubMed
38,732,046	Links among Obesity, Type 2 Diabetes Mellitus, and Osteoporosis: Bone as a Target.	Int J Mol Sci	2024	https://conductscience.org/library/papers/38732046	PubMed
38,455,392	Case Report: Tuberous sclerosis complex-associated hemihypertrophy successfully treated with mTOR inhibitor sirolimus.	Front Pediatr	2024	https://conductscience.org/library/papers/38455392	PubMed
37,696,750	PNA-Pdx: Versatile Peptide Nucleic Acid-Based Detection of Nucleic Acids and SNPs.	Anal Chem	2023	https://conductscience.org/library/papers/37696750	PubMed
34,591,292	Successful treatment of hepatosplenic T-cell lymphoma with fludarabine, high-dose cytarabine and subsequent unrelated umbilical cord blood transplantation.	Int J Hematol	2022	https://conductscience.org/library/papers/34591292	PubMed
34,129,823	Molecular classification and diagnostics of upper urinary tract urothelial carcinoma.	Cancer Cell	2021	https://conductscience.org/library/papers/34129823	PubMed
34,070,898	Delineation of Molecular Lesions in Acute Myeloid Leukemia Patients at Diagnosis: Integrated Next Generation Sequencing and Cytogenomic Studies.	Genes (Basel)	2021	https://conductscience.org/library/papers/34070898	PubMed
33,820,980	Discrimination of single-point mutations in unamplified genomic DNA via Cas9 immobilized on a graphene field-effect transistor.	Nat Biomed Eng	2021	https://conductscience.org/library/papers/33820980	PubMed
33,650,312	The prognostic significance of single-nucleotide polymorphism array-based whole-genome analysis and uniparental disomy in myelodysplastic syndrome.	Int J Lab Hematol	2021	https://conductscience.org/library/papers/33650312	PubMed
33,067,557	Genetic and clinical landscape of breast cancers with germline BRCA1/2 variants.	Commun Biol	2020	https://conductscience.org/library/papers/33067557	PubMed

1 to 10 of 138

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Genes1

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
JAK2	3,717	PubTator's text mining	https://conductscience.org/library/genes/3717

Source NCBI Gene

Drugs0

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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

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ClinicalTrials.govNo license stated
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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

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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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