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.

175 matches for An K, showing the first 20.

The major genetic determinants of HIV-1 control affect HLA class I peptide presentation
International HIV Controllers Study
Science (New York, N.Y.) · 2010 · PMID 21051598
6 pages
rs4418214 rs2523590 rs2255221 rs2395029 rs9262632 HIV-1 Viral Control
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
rs16826069 rs1127787 rs7572857 rs2233580 rs56200889 rs35658696
Large-scale genome-wide association study of coronary artery disease in genetically diverse populations
Regeneron Genetics Center · CARDIoGRAMplusC4D Consortium and 2 more consortia
Nature medicine · 2022 · PMID 35915156
6 pages
rs7884019 rs56210063 rs78532451 rs1867073 rs7622417 rs2715879
Multi-Omics Integrative Analysis Identifies the NK Cell-STAT3 Axis as a Shared Immunogenetic Hub Underlying the Comorbidity of Primary Sclerosing Cholangitis and Ulcerative Colitis
Life (Basel, Switzerland) · 2026 · PMID 42355477 · open access
6 pages
rs9607629 rs11578418 rs368699386 rs10916666 rs6967184 rs148170789
A genome-wide association study of optic disc parameters
PLoS genetics · 2010 · PMID 20548946 · open access
5 pages
rs1362756 rs1547014 rs1900004 rs17146964 Glaucoma
Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk
International Consortium for Blood Pressure Genome-Wide Association Studies · CARDIoGRAM consortium and 4 more consortia
Nature · 2011 · PMID 21909115 · open access
5 pages
rs6015450 rs11191548 rs7129220 rs1173771 rs13139571
Genome-wide association study identifies multiple susceptibility loci for pulmonary fibrosis
Nature genetics · 2013 · PMID 23583980 · open access
5 pages
rs1278769 rs2609255 rs11191865 rs1981997 Interstitial Lung Disease
Genome-wide association study identifies multiple susceptibility loci for pancreatic cancer
Nature genetics · 2014 · PMID 25086665 · open access
5 pages
rs9581943 rs2736098 rs6971499 rs7190458 Pancreatic Cancer
Genome-wide association meta-analysis identifies five modifier loci of lung disease severity in cystic fibrosis
Nature communications · 2015 · PMID 26417704 · open access
5 pages
rs117230773 rs7879546 rs5952223 rs546131 rs7929679
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
Genome-wide association analyses of post-traumatic stress disorder and its symptom subdomains in the Million Veteran Program
Department of Veterans Affairs Cooperative Studies Program (no. 575B) · VA Million Veteran Program
Nature genetics · 2021 · PMID 33510476 · open access
5 pages
rs3800872 rs251350 rs1496246 rs2314662 rs11760633
Genetic architectures of proximal and distal colorectal cancer are partly distinct
Gut · 2021 · PMID 33632709 · open access
5 pages
rs73161913 rs62131228 rs6014965 rs61975764 rs80158569
Whole-genome sequencing reveals host factors underlying critical COVID-19
GenOMICC investigators · 23andMe investigators and 1 more consortia
Nature · 2022 · PMID 35255492 · open access
5 pages
rs8178521 rs28368148 rs3848456 rs9271609 rs2532300
Multi-ancestry, trans-generational GWAS meta-analysis of gestational diabetes and glycaemic traits during pregnancy reveals limited evidence of pregnancy-specific genetic effects
Estonian Biobank Research Team · Genes & Health Research Team
Nature communications · 2026 · PMID 42225636 · open access
5 pages
rs613937 rs72964564 rs77864822 rs7933420 rs10036439
New loci associated with kidney function and chronic kidney disease
Nature genetics · 2010 · PMID 20383146
4 pages
rs267734 rs10774021 rs7805747 rs6465825
Genome-wide association identifies three new susceptibility loci for Paget's disease of bone
Genetic Determinants of Paget's Disease (GDPD) Consortium
Nature genetics · 2011 · PMID 21623375
4 pages
rs10498635 rs10494112 rs1561570 Paget's Disease of Bone
Genome-wide association and large-scale follow up identifies 16 new loci influencing lung function
International Lung Cancer Consortium · GIANT consortium
Nature genetics · 2011 · PMID 21946350 · open access
4 pages
rs1036429 rs2798641 rs12447804 rs6903823
Variants at multiple loci implicated in both innate and adaptive immune responses are associated with Sjögren's syndrome
UK Primary Sjögren's Syndrome Registry
Nature genetics · 2013 · PMID 24097067 · open access
4 pages
rs115575857 rs17339836 rs6579837 Sjögren's Syndrome
Genome-wide association analysis identifies six new loci associated with forced vital capacity
Nature genetics · 2014 · PMID 24929828
4 pages
rs1430193 rs6923462 rs2863171 rs6501431

Showing 20 of 175 · page 4 of 9

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.