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.

15 matches for Cole J.

The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study
CHARGE Consortium · DIAGRAM Consortium and 4 more consortia
PLoS genetics · 2015 · PMID 26426971 · open access
12 pages+
rs2820443 rs12955983 rs6737082 rs2821248 rs10840060 rs4727804
Multi-ethnic genome-wide association study for atrial fibrillation
Nature genetics · 2018 · PMID 29892015
12 pages+
rs10027347 rs10165883 rs1044258 rs10479177 rs10760361 rs10842383
Comprehensive genomic analysis of dietary habits in UK Biobank identifies hundreds of genetic associations
Nature communications · 2020 · PMID 32193382 · open access
12 pages+
rs6024408 rs7921 rs11646721 rs1512914 rs9517948 rs11084734
Genome-wide association analyses of physical activity and sedentary behavior provide insights into underlying mechanisms and roles in disease prevention
Lifelines Cohort Study
Nature genetics · 2022 · PMID 36071172 · open access
12 pages+
rs58541850 rs9867121 rs114590429 rs13235840 rs4518438 rs1160545
A saturated map of common genetic variants associated with human height
23andMe Research Team · VA Million Veteran Program and 5 more consortia
Nature · 2022 · PMID 36224396 · open access
12 pages+
rs6139332 rs2014307 rs630839 rs6514424 rs6677770 rs505317
Genetic diversity fuels gene discovery for tobacco and alcohol use
23andMe Research Team · Biobank Japan Project
Nature · 2022 · PMID 36477530 · open access
12 pages+
rs60966685 rs61857945 rs62376929 rs7105506 rs73249524 rs73581416
Rare variant analyses in 51,256 type 2 diabetes cases and 370,487 controls reveal the pathogenicity spectrum of monogenic diabetes genes
Nature genetics · 2024 · PMID 39379762 · open access
12 pages+
rs61993309 rs10841867 rs7313918 rs6752053 rs2074314 rs72802352
Global multi-ancestry genome-wide analyses identify genes and biological pathways associated with thyroid cancer and benign thyroid diseases
Penn Medicine BioBank · Virtual Thyroid Biopsy Consortium and 4 more consortia
Nature genetics · 2026 · PMID 41644669 · open access
12 pages+
rs74401365 rs6085463 rs9531006 rs17242727 rs369835958 rs11221322
Genome-Wide Association Study of Diabetic Kidney Disease Highlights Biology Involved in Glomerular Basement Membrane Collagen
SUMMIT Consortium, DCCT/EDIC Research Group, GENIE Consortium
Journal of the American Society of Nephrology : JASN · 2019 · PMID 31537649
5 pages
rs142823282 rs118124843 rs77273076 rs149641852 rs115061173
Stroke genetics informs drug discovery and risk prediction across ancestries
COMPASS Consortium · INVENT Consortium and 13 more consortia
Nature · 2022 · PMID 36180795 · open access
5 pages
rs12415501 rs60401382 rs72934589 rs76110445 Cardioembolic Stroke
The impact of non-additive genetic associations on age-related complex diseases
FinnGen Consortium
Nature communications · 2021 · PMID 33893285 · open access
4 pages
rs10858023 rs9272521 rs55651120 rs6675912
Genome-wide association analyses identify 13 new susceptibility loci for generalized vitiligo
Nature genetics · 2012 · PMID 22561518 · open access
3 pages
rs1129038 rs4766578 rs10768122
Genome-Wide Association Study Reveals Multiple Loci Influencing Normal Human Facial Morphology
PLoS genetics · 2016 · PMID 27560520 · open access
3 pages
rs2424399 rs8007643 rs17106852
Genome-wide meta-analysis and omics integration identifies novel genes associated with diabetic kidney disease
GENIE Consortium
Diabetologia · 2022 · PMID 35763030 · open access
2 pages
rs116216059 rs185299109
Genetic variation at 16q24.2 is associated with small vessel stroke
METASTROKE, UK Young Lacunar DNA Study, NINDS Stroke Genetics Network, Neurology Working Group of the CHARGE Consortium · International Stroke Genetics Consortium
Annals of neurology · 2017 · PMID 27997041 · open access
1 page
rs12445022

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.