For researchers

Is your paper here?

2,663 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.

18 matches for Wolk A.

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+
rs6904031 rs56387622 rs11624333 rs1895062 rs13294895 rs2223621
Association analyses of more than 140,000 men identify 63 new prostate cancer susceptibility loci
Profile Study · Australian Prostate Cancer BioResource (APCB) and 7 more consortia
Nature genetics · 2018 · PMID 29892016
12 pages+
rs684232 rs182314334 rs2121875 rs17021918 rs11859370 rs2788524
Discovery of common and rare genetic risk variants for colorectal cancer
Nature genetics · 2019 · PMID 30510241 · open access
12 pages+
rs116353863 rs117079142 rs11884596 rs12708491 rs4901473 rs6469654
Trans-ancestry genome-wide association meta-analysis of prostate cancer identifies new susceptibility loci and informs genetic risk prediction
Nature genetics · 2021 · PMID 33398198 · open access
12 pages+
rs2028900 rs339351 rs9306894 rs28441558 rs76765083 rs4714485
Genetic insights into biological mechanisms governing human ovarian ageing
Biobank-based Integrative Omics Study (BIOS) Consortium · eQTLGen Consortium and 6 more consortia
Nature · 2021 · PMID 34349265
12 pages+
rs2844466 rs140353819 rs540836853 rs2736609 rs9438982 rs117146677
Deciphering colorectal cancer genetics through multi-omic analysis of 100,204 cases and 154,587 controls of European and east Asian ancestries
Nature genetics · 2023 · PMID 36539618
12 pages+
rs117042741 rs35564340 rs1919364 rs11108175 rs78341008 rs9983528
Characterizing prostate cancer risk through multi-ancestry genome-wide discovery of 187 novel risk variants
Biobank Japan Project
Nature genetics · 2023 · PMID 37945903
12 pages+
rs78416326 rs17804499 rs72725734 rs11228580 rs7336001 rs77541621
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
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
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
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
5 pages
rs12470785 rs79183898 rs736596 rs7222250 rs60882887
Genetic architectures of proximal and distal colorectal cancer are partly distinct
Gut · 2021 · PMID 33632709 · open access
5 pages
rs73161913 rs62131228 rs6014965 rs61975764 rs80158569
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 identifies 32 novel breast cancer susceptibility loci from overall and subtype-specific analyses
kConFab Investigators · ABCTB Investigators and 2 more consortia
Nature genetics · 2020 · PMID 32424353 · open access
2 pages
rs11065822 rs17743054
Sex specific associations in genome wide association analysis of renal cell carcinoma
European journal of human genetics : EJHG · 2019 · PMID 31231134
1 page
rs78971134
Identification of Novel Loci and New Risk Variant in Known Loci for Colorectal Cancer Risk in East Asians
Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology · 2020 · PMID 31826910
1 page
rs10795668

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.