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.

58 matches for Willer C, showing the first 20.

Genetic diversity fuels gene discovery for tobacco and alcohol use
23andMe Research Team · Biobank Japan Project
Nature · 2022 · PMID 36477530 · open access
12 pages+
rs56372821 rs540508277 rs6430080 rs28673808 rs78875955 rs739447
Global Biobank Meta-analysis Initiative: Powering genetic discovery across human disease
Biobank of the Americas · Biobank Japan Project and 22 more consortia
Cell genomics · 2022 · PMID 36777996 · open access
12 pages+
rs9594366 rs16856530 rs62283809 rs10854002 rs2276133 rs7748159
Multi-ancestry genome-wide association analyses improve resolution of genes and pathways influencing lung function and chronic obstructive pulmonary disease risk
China Kadoorie Biobank Collaborative Group · Qatar Genome Program Research (QGPR) Consortium
Nature genetics · 2023 · PMID 36914875 · open access
12 pages+
rs811689 rs1076135 rs980896 rs75128958 rs947350 rs1528683
Meta-analysis of genome-wide associations and polygenic risk prediction for atrial fibrillation in more than 180,000 cases
BioBank Japan Project · Regeneron Genetics Center and 1 more consortia
Nature genetics · 2025 · PMID 40050429
12 pages+
rs13019524 rs4970418 rs779029 rs1285881 rs12375999 rs2900084
Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index
MAGIC · Procardis Consortium
Nature genetics · 2010 · PMID 20935630 · open access
11 pages
rs713586 rs543874 rs10150332 rs2241423 rs2287019 rs12444979
Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension
CHARGE-Heart Failure Consortium · EchoGen Consortium and 12 more consortia
Nature genetics · 2016 · PMID 27618447 · open access
11 pages
rs16982520 rs7406910 rs34591516 rs1126930 rs10407022 rs470113
Exome-wide association study of plasma lipids in >300,000 individuals
Charge Diabetes Working Group · EPIC-InterAct Consortium and 3 more consortia
Nature genetics · 2017 · PMID 29083408 · open access
11 pages
rs10861661 rs201596848 rs900399 rs7157785 rs3927680 rs7946
Shared genetic origin of asthma, hay fever and eczema elucidates allergic disease biology
23andMe Research Team · AAGC collaborators and 2 more consortia
Nature genetics · 2017 · PMID 29083406 · open access
10 pages
rs10865050 rs1814576 rs3091307 rs55726902 rs7130753 rs17607589
Genome-wide association study of placental weight identifies distinct and shared genetic influences between placental and fetal growth
Early Growth Genetics (EGG) Consortium
Nature genetics · 2023 · PMID 37798380 · open access
10 pages
rs10486660 rs7783810 rs12529634 rs140691414 rs1434836 rs7722058
Common variants at 30 loci contribute to polygenic dyslipidemia
Nature genetics · 2009 · PMID 19060906
9 pages
rs10468017 rs12678919 rs2954029 rs7679 rs1883025 rs10401969
Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis
MAGIC investigators · GIANT Consortium
Nature genetics · 2010 · PMID 20581827
8 pages
rs1552224 rs5945326 rs11634397 rs231362 rs7957197 rs1470579
Identification of heart rate-associated loci and their effects on cardiac conduction and rhythm disorders
Global BPgen Consortium · CARDIoGRAM Consortium and 4 more consortia
Nature genetics · 2013 · PMID 23583979
8 pages
rs17287293 rs11118555 rs13030174 rs826838 rs11578508 rs4140885
Age-of-onset information helps identify 76 genetic variants associated with allergic disease
23andMe Research Team · collaborators of the SHARE study
PLoS genetics · 2020 · PMID 32603359 · open access
7 pages
rs7559046 rs7521390 rs73739621 rs2918302 rs3017289 rs61907712
Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis
Genome biology · 2022 · PMID 36575460 · open access
7 pages
rs151113194 rs762517 rs12012576 rs139120857 rs5942972 rs7063103
Novel loci for adiponectin levels and their influence on type 2 diabetes and metabolic traits: a multi-ethnic meta-analysis of 45,891 individuals
DIAGRAM+ Consortium · MAGIC Consortium and 8 more consortia
PLoS genetics · 2012 · PMID 22479202 · open access
6 pages
rs182052 rs2980879 rs6488898 rs2590838 rs4805885 Adiponectin Levels
Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes
ExomeBP Consortium · MAGIC Consortium and 1 more consortia
Nature genetics · 2018 · PMID 29632382 · open access
6 pages
rs35658696 rs16826069 rs1127787 rs7572857 rs2233580 rs56200889
Biological and clinical insights from genetics of insomnia symptoms
HUNT All In Sleep
Nature genetics · 2019 · PMID 30804566 · open access
6 pages
rs11651809 rs2296580 rs17669584 rs7711696 rs11184946 rs2062113
Genetic Architecture of Abdominal Aortic Aneurysm in the Million Veteran Program
Veterans Affairs Million Veteran Program†
Circulation · 2020 · PMID 32981348 · open access
6 pages
rs10808546 rs35254673 rs4401144 rs118039278 rs73149487 Abdominal Aortic Aneurysm
Genome-wide association study of intracranial aneurysms identifies 17 risk loci and genetic overlap with clinical risk factors
HUNT All-In Stroke · China Kadoorie Biobank Collaborative Group and 5 more consortia
Nature genetics · 2020 · PMID 33199917
6 pages
rs55965782 rs2280543 rs6997005 rs7137731 rs4705938 rs3742321
Newly identified loci that influence lipid concentrations and risk of coronary artery disease
Nature genetics · 2008 · PMID 18193043
5 pages
rs4149268 rs4775041 rs4420638 rs12286037 rs16996148

Showing 20 of 58 · 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.