For researchers

Is your paper here?

2,661 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.

9 matches for Shete S.

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
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 association study of lung adenocarcinoma in East Asia and comparison with a European population
Nature communications · 2023 · PMID 37236969 · open access
5 pages
rs71467682 rs75031349 rs137884934 rs682888 rs10901793
Sex-specific glioma genome-wide association study identifies new risk locus at 3p21.31 in females, and finds sex-differences in risk at 8q24.21
GliomaScan consortium
Scientific reports · 2018 · PMID 29743610 · open access
4 pages
rs55705857 rs2297440 rs634537 Glioma
Cross-ancestry genome-wide meta-analysis of 61,047 cases and 947,237 controls identifies new susceptibility loci contributing to lung cancer
Nature genetics · 2022 · PMID 35915169
3 pages
rs11607355 rs2413932 rs12348845
Genome-wide association study identifies five susceptibility loci for glioma
Nature genetics · 2009 · PMID 19578367
2 pages
rs891835 Glioma
A Genome-Wide Association Study Identifies Two Novel Susceptible Regions for Squamous Cell Carcinoma of the Head and Neck
Cancer research · 2020 · PMID 32276964
2 pages
rs13211972 rs1265081
Genome-wide association study identifies genes associated with neuropathy in patients with head and neck cancer
Scientific reports · 2018 · PMID 29884837 · open access
1 page
rs10950641
Genome-wide association meta-analysis identifies pleiotropic risk loci for aerodigestive squamous cell cancers
PLoS genetics · 2021 · PMID 33667223 · open access
1 page
rs13204012

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.