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.

27 matches for Riboli E, showing the first 7.

Plasma Vitamin C and Type 2 Diabetes: Genome-Wide Association Study and Mendelian Randomization Analysis in European Populations
Diabetes care · 2021 · PMID 33203707 · open access
2 pages
rs13028225 rs117885456
Seven prostate cancer susceptibility loci identified by a multi-stage genome-wide association study
UK Genetic Prostate Cancer Study Collaborators/British Association of Urological Surgeons' Section of Oncology · UK ProtecT Study Collaborators, The Australian Prostate Cancer BioResource and 1 more consortia
Nature genetics · 2011 · PMID 21743467
1 page
rs2242652
A meta-analysis of genome-wide association studies of breast cancer identifies two novel susceptibility loci at 6q14 and 20q11
Australian Breast Cancer Tissue Bank Investigators · Familial Breast Cancer Study and 1 more consortia
Human molecular genetics · 2012 · PMID 22976474
1 page
rs9383938
A meta-analysis of genome-wide association studies to identify prostate cancer susceptibility loci associated with aggressive and non-aggressive disease
UK Genetic Prostate Cancer Study Collaborators/British Association of Urological Surgeons' Section of Oncology · UK ProtecT Study Collaborators and 2 more consortia
Human molecular genetics · 2013 · PMID 23065704
1 page
rs11672691
Rare variants of large effect in BRCA2 and CHEK2 affect risk of lung cancer
Nature genetics · 2014 · PMID 24880342 · open access
1 page
rs13314271
Sex specific associations in genome wide association analysis of renal cell carcinoma
European journal of human genetics : EJHG · 2019 · PMID 31231134
1 page
rs78971134
Distinct germline genetic susceptibility profiles identified for common non-Hodgkin lymphoma subtypes
Leukemia · 2022 · PMID 36273105
1 page
rs9258807

Showing 7 of 27 · page 2 of 2

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.