For researchers

Is your paper here?

2,660 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 Olson SH.

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 Meta-Analyses of Breast, Ovarian, and Prostate Cancer Association Studies Identify Multiple New Susceptibility Loci Shared by at Least Two Cancer Types
ABCTB Investigators · AOCS Study Group & Australian Cancer Study (Ovarian Cancer) and 5 more consortia
Cancer discovery · 2016 · PMID 27432226
6 pages
rs3802173 rs1469713 rs9657608 rs2628317 rs17762342 rs739704
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 meta-analysis identifies five new susceptibility loci for pancreatic cancer
Nature communications · 2018 · PMID 29422604 · open access
4 pages
rs13303010 rs1517037 rs4795218 rs2941471
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
Genome-wide association study identifies variants in the ABO locus associated with susceptibility to pancreatic cancer
Nature genetics · 2009 · PMID 19648918
3 pages
rs505922 ABO Blood Group Pancreatic Cancer
Identification of six new susceptibility loci for invasive epithelial ovarian cancer
EMBRACE · GEMO Study Collaborators and 6 more consortia
Nature genetics · 2015 · PMID 25581431 · open access
3 pages
rs10088218 rs8170 rs9303542
Common variation at 2p13.3, 3q29, 7p13 and 17q25.1 associated with susceptibility to pancreatic cancer
Nature genetics · 2015 · PMID 26098869 · open access
3 pages
rs17688601 rs9854771 Pancreatic Cancer
Three new pancreatic cancer susceptibility signals identified on chromosomes 1q32.1, 5p15.33 and 8q24.21
Oncotarget · 2016 · PMID 27579533 · open access
3 pages
rs10094872 rs35226131 Pancreatic Cancer

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.