For researchers

Is your paper here?

2,665 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.

14 matches for Gu J.

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+
rs10886810 rs1037137 rs11892008 rs6151589 rs4713343 rs78416326
Multi-ancestry genome-wide association study of kidney cancer identifies 63 susceptibility regions
BioBank Japan Project · FinnGen
Nature genetics · 2024 · PMID 38671320
12 pages+
rs6574106 rs6916760 rs4506680 rs114427493 rs12274095 rs57551109
Multi-population GWAS meta-analysis identifies bladder cancer susceptibility loci and highlights genetic regulation of smoking-related risk
UROMOL Consortium
Nature communications · 2026 · PMID 42706231 · open access
12 pages+
rs72826305 rs112204664 rs7076867 rs7937265 rs6910215 rs7145592
Genome-wide association study identifies multiple susceptibility loci for diffuse large B cell lymphoma
Nature genetics · 2014 · PMID 25261932 · open access
5 pages
rs79480871 rs116446171 rs13255292 rs4733601 Diffuse Large B Cell Lymphoma
Genome-wide association study identifies five susceptibility loci for follicular lymphoma outside the HLA region
American journal of human genetics · 2014 · PMID 25279986
5 pages
rs12195582 rs4937362 rs17749561 rs13254990 Follicular Lymphoma
Genome-wide association analyses of breast cancer in women of African ancestry identify new susceptibility loci and improve risk prediction
Nature genetics · 2024 · PMID 38741014
4 pages
rs16963205 rs2372943 rs56069439 rs61751053
Genetic variation in the prostate stem cell antigen gene PSCA confers susceptibility to urinary bladder cancer
Nature genetics · 2009 · PMID 19648920
2 pages
rs2294008 Bladder Cancer
A genome-wide association study in Han Chinese identifies new susceptibility loci for ankylosing spondylitis
Nature genetics · 2011 · PMID 22138694
2 pages
rs17095830 Ankylosing Spondylitis
Genome-wide association study identifies variants in casein kinase II (CSNK2A2) to be associated with leukocyte telomere length in a Punjabi Sikh diabetic cohort
Circulation. Cardiovascular genetics · 2014 · PMID 24795349
2 pages
rs74019828 Telomere Length and Epigenetic Age Acceleration
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
A genetic variant near the PMAIP1/Noxa gene is associated with increased bleomycin sensitivity
Human molecular genetics · 2011 · PMID 21106707
1 page
rs8093763
Rare variants of large effect in BRCA2 and CHEK2 affect risk of lung cancer
Nature genetics · 2014 · PMID 24880342 · open access
1 page
rs13314271
Distinct germline genetic susceptibility profiles identified for common non-Hodgkin lymphoma subtypes
Leukemia · 2022 · PMID 36273105
1 page
rs9258807
Case-Case Genome-Wide Analyses Identify Subtype-Informative Variants That Confer Risk for Breast Cancer
Cancer research · 2024 · PMID 38832928
1 page
rs7580240

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.