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.

50 matches for Amos C, showing the first 20.

Large-scale association analysis identifies new lung cancer susceptibility loci and heterogeneity in genetic susceptibility across histological subtypes
SpiroMeta Consortium
Nature genetics · 2017 · PMID 28604730 · open access
12 pages+
rs116826541 rs139244745 rs115870917 rs147680653 rs116480994 rs116418332
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+
rs71557345 rs6904031 rs56387622 rs11624333 rs1895062 rs13294895
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
Genome-wide association meta-analyses combining multiple risk phenotypes provide insights into the genetic architecture of cutaneous melanoma susceptibility
GenoMEL Consortium · Q-MEGA and QTWIN Investigators and 7 more consortia
Nature genetics · 2020 · PMID 32341527 · open access
12 pages+
rs111595456 rs13283146 rs2857482 rs75570604 rs55797833 rs10873172
Discovery and fine-mapping of height loci via high-density imputation of GWASs in individuals of African ancestry
American journal of human genetics · 2021 · PMID 33713608
12 pages+
rs10071837 rs4899520 rs75823898 rs112226333 rs2553033 rs7905296
Multi-ancestry genome-wide association analyses identify novel genetic mechanisms in rheumatoid arthritis
BioBank Japan Project
Nature genetics · 2022 · PMID 36333501
12 pages+
rs6495979 rs73005423 rs798000 rs56750287 rs16903108 rs6681482
Multi-ancestry GWAS meta-analyses of lung cancer reveal susceptibility loci and elucidate smoking-independent genetic risk
VA Million Veteran Program
Nature communications · 2024 · PMID 39366959 · open access
12 pages+
rs9267123 rs459961 rs11778371 rs41309931 rs7859886 rs1715422
Multi-trait and multi-ancestry genetic analysis of comorbid lung diseases and traits improves genetic discovery and polygenic risk prediction
Nature genetics · 2026 · PMID 41565855
12 pages+
rs924150 rs8089099 rs4791806 rs41522747 rs340121 rs2609260
Novel Association of Genetic Markers Affecting CYP2A6 Activity and Lung Cancer Risk
Cancer research · 2016 · PMID 27488534
10 pages
rs113029345 rs76935404 rs10425738 rs11878604 rs7247903 rs2316205
Genome-wide association study of glioma subtypes identifies specific differences in genetic susceptibility to glioblastoma and non-glioblastoma tumors
GliomaScan Consortium
Nature genetics · 2017 · PMID 28346443
10 pages
rs12752552 rs3751667 rs11233250 rs2235573 rs4252707 rs12076373
Genome-wide association study identifies HLA 8.1 ancestral haplotype alleles as major genetic risk factors for myositis phenotypes
Myositis Genetics Consortium
Genes and immunity · 2015 · PMID 26291516
9 pages
rs114388793 rs115146037 rs114012716 rs116088953 rs114771815 rs115902351
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
An international genome-wide meta-analysis of primary biliary cholangitis: Novel risk loci and candidate drugs
PBC Consortia · Canadian PBC Consortium and 5 more consortia
Journal of hepatology · 2021 · PMID 34033851 · open access
9 pages
rs589446 rs11742270 rs859767 rs6550965 rs12419634 rs742108
Genetic Analysis of Lung Cancer and the Germline Impact on Somatic Mutation Burden
ILCCO consortium
Journal of the National Cancer Institute · 2022 · PMID 35511172 · open access
7 pages
rs11571815 rs72905558 rs3129813 rs78062588 rs9258381 rs6457312
Cross-Cancer Genome-Wide Analysis of Lung, Ovary, Breast, Prostate, and Colorectal Cancer Reveals Novel Pleiotropic Associations
Ovarian Cancer Association Consortium (OCAC) · PRACTICAL Consortium and 3 more consortia
Cancer research · 2016 · PMID 27197191
6 pages
rs11844632 rs4808075 rs56084662 rs11571833 rs186507655 rs148883465
Comprehensive functional annotation of susceptibility variants identifies genetic heterogeneity between lung adenocarcinoma and squamous cell carcinoma
Frontiers of medicine · 2021 · PMID 32889700
6 pages
rs465498 rs1200399 rs2517873 rs4573350 rs1264308 rs17038564
Genome-wide meta-analysis across East Asian and European populations provides insights into the molecular basis of lung cancer
Genome medicine · 2026 · PMID 42152146 · open access
6 pages
rs4887067 rs13167280 rs4291686 rs36108040 rs1039766 rs12822733
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 study of lung adenocarcinoma in East Asia and comparison with a European population
Nature communications · 2023 · PMID 37236969 · open access
5 pages
rs75031349 rs137884934 rs682888 rs10901793 rs71467682
High-density genetic mapping identifies new susceptibility loci for rheumatoid arthritis
Biologics in Rheumatoid Arthritis Genetics and Genomics Study Syndicate · Wellcome Trust Case Control Consortium
Nature genetics · 2012 · PMID 23143596 · open access
4 pages
rs13397 rs13426947 rs59466457 rs2834512

Showing 20 of 50 · page 1 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.