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Paper ยท 17529967

Genome-wide association study identifies novel breast cancer susceptibility loci.

Easton DF and 104 others. Nature, 2007. Cited by 1,771 papers, by iCite.

11 sourcespapers-2026-11-12-0.1.0

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ConductScience Library. Genome-wide association study identifies novel breast cancer susceptibility loci. Papers, record 17529967. Release papers-2026-11-12-0.1.0, 12 Nov 2026. https://conductscience.org/library/papers/17529967

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Paper

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

Title
Genome-wide association study identifies novel breast cancer susceptibility loci.
PubMed
Journal
Nature
PubMed
Year
2007
PubMed
Publication types
Journal Article, Research Support, Non-U.S. Gov't
PubMed
Citations, by iCite
1,771
iCite
Relative citation ratio, by iCite
37.1
iCite
Revised in PubMed
2025-05-29
PubMed

Authors105

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

OrderAuthorForenameKindORCID iD
1Easton DFDouglas F
2Pooley KAKaren A
3Dunning AMAlison M
4Pharoah PDPaul D P
5Thompson DDeborah
6Ballinger DGDennis G
7Struewing JPJeffery P
8Morrison JJonathan
9Field HHelen
10Luben RRobert

1 to 10 of 105Source PubMed

See all 105 authors

Topics21

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

MeSH termMajor
Breast NeoplasmsMajor topic
Genetic Predisposition to DiseaseMajor topic
Genome, HumanMajor topic
Alleles
Apoptosis Regulatory Proteins
Asia, Southeastern
Australia
Case-Control Studies
Europe
Female
Genotype
High Mobility Group Proteins
Humans
MAP Kinase Kinase Kinase 1
Microfilament Proteins
North America
Odds Ratio
Polymorphism, Single Nucleotide
Receptor, Fibroblast Growth Factor, Type 2
Receptors, Progesterone
Trans-Activators

Source PubMed

Grants4

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 bySource
2004NOV49Breast Cancer NowUnited KingdomPubMedPubMed
A3353Cancer Research UKUnited KingdomPubMedPubMed
BREAST CANCER NOW RESEARCH CENTREBreast Cancer NowUnited KingdomPubMedPubMed
Z01SC010083NIHNIH RePORTER

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.

References39

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

OrderPMIDTitleJournalYearIn PapersSource
111,959,976Comprehensive human genome amplification using multiple displacement amplification.Proc Natl Acad Sci U S A2002https://conductscience.org/library/papers/11959976PubMed
211,967,536Low-penetrance susceptibility to breast cancer due to CHEK2(*)1100delC in noncarriers of BRCA1 or BRCA2 mutations.Nat Genet2002https://conductscience.org/library/papers/11967536PubMed
311,984,562Polygenic susceptibility to breast cancer and implications for prevention.Nat Genet2002https://conductscience.org/library/papers/11984562PubMed
412,677,558Average risks of breast and ovarian cancer associated with BRCA1 or BRCA2 mutations detected in case Series unselected for family history: a combined analysis of 22 studies.Am J Hum Genet2003https://conductscience.org/library/papers/12677558PubMed
514,557,987Polygenic inheritance of breast cancer: Implications for design of association studies.Genet Epidemiol2003https://conductscience.org/library/papers/14557987PubMed
615,122,511CHEK2*1100delC and susceptibility to breast cancer: a collaborative analysis involving 10,860 breast cancer cases and 9,065 controls from 10 studies.Am J Hum Genet2004https://conductscience.org/library/papers/15122511PubMed
715,381,934The BOADICEA model of genetic susceptibility to breast and ovarian cancer.Br J Cancer2004https://conductscience.org/library/papers/15381934PubMed
811,890,312Two-stage designs for gene-disease association studies.Biometrics2002https://conductscience.org/library/papers/11890312PubMed
911,791,212Score tests for association between traits and haplotypes when linkage phase is ambiguous.Am J Hum Genet2002https://conductscience.org/library/papers/11791212PubMed
1011,752,248The Ensembl genome database project.Nucleic Acids Res2002https://conductscience.org/library/papers/11752248PubMed

Cited by1,126

The papers in our copy of PubMed whose reference list names this one, newest first. iCite, which reads more sources, counts 1,771 citations.

PMIDTitleJournalYearIn PapersSource
42,679,042Genetic architectures of brain-related traits are shaped by strong selective constraints.Proc Natl Acad Sci U S A2026https://conductscience.org/library/papers/42679042PubMed
42,363,452Unraveling the intricate molecular mechanisms of sex hormones' roles in breast cancer pathogenesis: A review.Medicine (Baltimore)2026https://conductscience.org/library/papers/42363452PubMed
42,222,333TNNT3 as a candidate node in breast cancer mechanobiology: current evidence, mechanistic models, and key knowledge gaps.Front Cell Dev Biol2026https://conductscience.org/library/papers/42222333PubMed
42,062,290Nuclear genetic modulation of tissue-specific mitochondrial RNA processing contributes to common disease risk.Nat Commun2026https://conductscience.org/library/papers/42062290PubMed
41,983,230MMTV Virus Detection, Survival Analysis, and Prognostic Relevance of Six Tumor Genes in Patients With Breast Cancer.Int J Breast Cancer2026https://conductscience.org/library/papers/41983230PubMed
41,972,694MAP3K1: A Multifunctional Kinase at the Crossroads of Cancer Progression and Tumor Suppression.Cells2026https://conductscience.org/library/papers/41972694PubMed
41,929,205Genetic architectures of brain-related traits are shaped by strong selective constraints.bioRxiv2026https://conductscience.org/library/papers/41929205PubMed
41,849,381A transcription regulator atlas identifies TOX3 as an Atoh1 coactivator in cerebellar development and tumorigenesis.Proc Natl Acad Sci U S A2026https://conductscience.org/library/papers/41849381PubMed
41,318,657RAD51B-EZH2 axis as a potential therapeutic target for TNBC through cell fate conversion.Cell Death Dis2025https://conductscience.org/library/papers/41318657PubMed
41,146,041A systematic review of prediction models for risk of breast cancer.BMC Cancer2025https://conductscience.org/library/papers/41146041PubMed

1 to 10 of 1,126

See all 1,126 cited by

Genes20

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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