For researchers

Is your paper here?

2,657 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.

17 matches for Cunningham J.

Association analysis identifies 65 new breast cancer risk loci
NBCS Collaborators · ABCTB Investigators and 1 more consortia
Nature · 2017 · PMID 29059683 · open access
12 pages+
rs71557345 rs6904031 rs56387622 rs11624333 rs1895062 rs13294895
Genome-wide association study of more than 40,000 bipolar disorder cases provides new insights into the underlying biology
HUNT All-In Psychiatry
Nature genetics · 2021 · PMID 34002096 · open access
12 pages+
rs78308718 rs6875495 rs55706012 rs6993953 rs11137399 rs4748468
Multitrait analyses identify genetic variants associated with aortic valve function and aortic stenosis risk
FinnGen
Nature genetics · 2026 · PMID 41419685 · open access
12 pages+
rs78444298 rs113193866 rs7802179 rs7644014 rs60281171 rs12154315
Identification of 12 new susceptibility loci for different histotypes of epithelial ovarian cancer
AOCS study group · EMBRACE Study and 4 more consortia
Nature genetics · 2017 · PMID 28346442
9 pages
rs1879586 rs7207826 rs11651755 rs688187 rs7902587 rs9886651
Genome-Wide Meta-Analyses of Breast, Ovarian, and Prostate Cancer Association Studies Identify Multiple New Susceptibility Loci Shared by at Least Two Cancer Types
ABCTB Investigators · AOCS Study Group & Australian Cancer Study (Ovarian Cancer) and 5 more consortia
Cancer discovery · 2016 · PMID 27432226
6 pages
rs2628317 rs17762342 rs739704 rs3802173 rs1469713 rs9657608
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
Common sequence variants on 2p15 and Xp11.22 confer susceptibility to prostate cancer
Nature genetics · 2008 · PMID 18264098
3 pages
rs721048 rs5945572 Prostate Cancer
Genome-wide association study identifies multiple risk loci for chronic lymphocytic leukemia
Nature genetics · 2013 · PMID 23770605 · open access
3 pages
rs13401811 rs17483466 rs11636802
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
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 association study of follicular lymphoma identifies a risk locus at 6p21.32
Nature genetics · 2010 · PMID 20639881 · open access
2 pages
rs10484561 Follicular Lymphoma
Meta-analysis of genome-wide association studies discovers multiple loci for chronic lymphocytic leukemia
Nature communications · 2016 · PMID 26956414 · open access
2 pages
rs9270750 rs72742684
Genome-wide association study identifies a novel susceptibility locus at 6p21.3 among familial CLL
Blood · 2011 · PMID 21131588
1 page
rs674313
Genome-wide association study identifies multiple loci associated with both mammographic density and breast cancer risk
Nature communications · 2014 · PMID 25342443 · open access
1 page
rs12642133
Pharmacogenomic study of heart failure and candesartan response from the CHARM programme
ESC heart failure · 2022 · PMID 35736394 · open access
1 page
rs664669

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.