For researchers

Is your paper here?

2,673 papers hold this site up. Every variant and condition page names the research it was written from, and this is that list, gathered from the pages themselves. Search your name, your journal, or a PMID.

55 matches for Pharoah P, showing the first 20.

Genome-wide association studies in oesophageal adenocarcinoma and Barrett's oesophagus: a large-scale meta-analysis
Barrett's and Esophageal Adenocarcinoma Consortium (BEACON) · Esophageal Adenocarcinoma GenEtics Consortium (EAGLE) and 1 more consortia
The Lancet. Oncology · 2016 · PMID 27527254 · open access
6 pages
rs2464469 rs17451754 rs9918259 rs1979654 rs75783973 Oesophageal Cancer
Genome-wide association study identifies multiple risk loci for renal cell carcinoma
Nature communications · 2017 · PMID 28598434 · open access
6 pages
rs4381241 rs67311347 rs11813268 rs74911261 rs4903064 Renal Cell Carcinoma
Identification of nine new susceptibility loci for endometrial cancer
Nature communications · 2018 · PMID 30093612 · open access
6 pages
rs113998067 rs1740828 rs9668337 rs10850382 rs7981863 Endometrial Cancer
A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers
GEMO Study Collaborators · EMBRACE Collaborators and 3 more consortia
Nature communications · 2021 · PMID 33597508 · open access
6 pages
rs7222250 rs60882887 rs9901834 rs12470785 rs79183898 rs736596
Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer
ABCTB Investigators · EMBRACE and 4 more consortia
Nature genetics · 2017 · PMID 29058716
5 pages
rs10995201 rs9397437 rs6562760 rs6678914 rs67397200
Identification of multiple risk loci and regulatory mechanisms influencing susceptibility to multiple myeloma
PRACTICAL consortium
Nature communications · 2018 · PMID 30213928 · open access
5 pages
rs4325816 rs6595443 rs17507636 rs58618031 Multiple Myeloma
Genetic architectures of proximal and distal colorectal cancer are partly distinct
Gut · 2021 · PMID 33632709 · open access
5 pages
rs73161913 rs62131228 rs6014965 rs61975764 rs80158569
Meta-analysis of three genome-wide association studies identifies susceptibility loci for colorectal cancer at 1q41, 3q26.2, 12q13.13 and 20q13.33
COGENT Consortium · CORGI Consortium and 2 more consortia
Nature genetics · 2010 · PMID 20972440 · open access
4 pages
rs6687758 rs4925386 rs6691170 Colorectal Cancer
Genome-wide association study of classical Hodgkin lymphoma identifies key regulators of disease susceptibility
PRACTICAL consortium
Nature communications · 2017 · PMID 29196614 · open access
4 pages
rs9482849 rs3781093 Hodgkin Lymphoma Nodular Sclerosis Hodgkin Lymphoma
Genome-wide association study of 398,238 women unveils seven loci associated with high-grade serous ovarian cancer
NPJ genomic medicine · 2025 · PMID 41266372 · open access
4 pages
rs6979 rs768719522 rs1013698558 rs528577783
Meta-analysis of genome-wide association data identifies four new susceptibility loci for colorectal cancer
COGENT Study · Colorectal Cancer Association Study Consortium and 1 more consortia
Nature genetics · 2008 · PMID 19011631
3 pages
rs4444235 rs10411210 Colorectal Cancer
Genome-wide association study identifies five new breast cancer susceptibility loci
Breast Cancer Susceptibility Collaboration (UK)
Nature genetics · 2010 · PMID 20453838
3 pages
rs10995190 rs1011970 rs614367
Identification of six new susceptibility loci for invasive epithelial ovarian cancer
EMBRACE · GEMO Study Collaborators and 6 more consortia
Nature genetics · 2015 · PMID 25581431 · open access
3 pages
rs10088218 rs8170 rs9303542
Five endometrial cancer risk loci identified through genome-wide association analysis
National Study of Endometrial Cancer Genetics Group (NSECG) · Australian National Endometrial Cancer Study Group (ANECS) and 2 more consortia
Nature genetics · 2016 · PMID 27135401 · open access
3 pages
rs11841589 rs2498796 Endometrial Cancer
Genetic overlap between endometriosis and endometrial cancer: evidence from cross-disease genetic correlation and GWAS meta-analyses
Cancer medicine · 2018 · PMID 29608257 · open access
3 pages
rs6782972 rs2218868 Endometrial Cancer
Novel Common Genetic Susceptibility Loci for Colorectal Cancer
Journal of the National Cancer Institute · 2019 · PMID 29917119
3 pages
rs10911251 rs3824999 rs17094983
Genome-wide association study implicates immune dysfunction in the development of Hodgkin lymphoma
PRACTICAL Consortium
Blood · 2018 · PMID 30194254
3 pages
rs1002658 rs7111520 Hodgkin Lymphoma
A genome-wide association study identifies a new ovarian cancer susceptibility locus on 9p22.2
Australian Cancer (Ovarian) Study · Australian Ovarian Cancer Study Group and 1 more consortia
Nature genetics · 2009 · PMID 19648919
2 pages
rs3814113 Ovarian Cancer
Genome-wide meta-analysis identifies five new susceptibility loci for cutaneous malignant melanoma
GenoMEL Consortium · Essen-Heidelberg Investigators and 4 more consortia
Nature genetics · 2015 · PMID 26237428 · open access
2 pages
rs498136 Cutaneous Malignant Melanoma
Genome-wide association studies identify susceptibility loci for epithelial ovarian cancer in east Asian women
Australian Ovarian Cancer Study Group
Gynecologic oncology · 2019 · PMID 30898391
2 pages
rs7748275 rs1934363

Showing 20 of 55 · page 2 of 3

Questions about this list

Why is my paper here? I never gave you permission.

Nothing of your paper is reproduced here. This page records that a MyGeneLog™ page cites your work, and links to the paper on PubMed — which is what a citation is. Your title and author list come from Europe PMC, the same public record a library catalogue uses.

Why are all the authors listed instead of "et al."?

Because a study that needed 622 people is a different kind of study from one that needed four, and "et al." erases that. Twelve names show and the rest are one click away. Everyone is searchable, including the 187th name on a consortium paper — that person exists and may be looking for it.

My name is misspelt, or the paper is wrong.

Tell us and it is fixed. Names come from the public record and initials are inconsistent across databases; where two people share a form of a name we cannot separate them, and we would rather be corrected than guess.

My paper is not here. Does that mean you rejected it?

No. This catalogue is assembled from what a small team could read, and it is thinnest outside European-ancestry cohorts. A paper is absent because nobody has got to it, not because it was assessed and turned down.

Which pages rest on a paper?

Each row lists them, up to six, and links to each one. The count beside a row is how many pages cite it in total.

How often does this change?

It is rebuilt from the pages every hour. A paper appears the moment a page starts resting on it and disappears if that page stops — there is no separate list to keep in step, because the citation lives on the page that makes the claim.