For researchers

Is your paper here?

2,655 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.

11 matches for Ahmed S.

Genome-wide association analysis of more than 120,000 individuals identifies 15 new susceptibility loci for breast cancer
BOCS · kConFab Investigators and 3 more consortia
Nature genetics · 2015 · PMID 25751625 · open access
12 pages+
rs2012709 rs12048493 rs72755295 rs4593472 rs13267382 rs745570
Identification of 23 new prostate cancer susceptibility loci using the iCOGS custom genotyping array
COGS–Cancer Research UK GWAS–ELLIPSE (part of GAME-ON) Initiative · Australian Prostate Cancer Bioresource and 3 more consortia
Nature genetics · 2013 · PMID 23535732
7 pages
rs3850699 rs1894292 rs2273669 rs1270884 rs11650494 rs1218582
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 identifies five new breast cancer susceptibility loci
Breast Cancer Susceptibility Collaboration (UK)
Nature genetics · 2010 · PMID 20453838
3 pages
rs10995190 rs1011970 rs614367
Five endometrial cancer risk loci identified through genome-wide association analysis
National Study of Endometrial Cancer Genetics Group (NSECG) · Australian National Endometrial Cancer Study Group (ANECS) and 2 more consortia
Nature genetics · 2016 · PMID 27135401 · open access
3 pages
rs11841589 rs2498796 Endometrial Cancer
Multiplex genomewide association analysis of breast milk fatty acid composition extends the phenotypic association and potential selection of <i>FADS1</i> variants to arachidonic acid, a critical infant micronutrient
Journal of medical genetics · 2018 · PMID 29514873 · open access
3 pages
rs12535041 rs7198595 rs12583793
Genetic overlap between endometriosis and endometrial cancer: evidence from cross-disease genetic correlation and GWAS meta-analyses
Cancer medicine · 2018 · PMID 29608257 · open access
3 pages
rs6782972 rs2218868 Endometrial Cancer
Genome-wide association study identifies novel breast cancer susceptibility loci
SEARCH collaborators · kConFab and 1 more consortia
Nature · 2007 · PMID 17529967
1 page
rs3817198
A common variant at the TERT-CLPTM1L locus is associated with estrogen receptor-negative breast cancer
Gene Environment Interaction and Breast Cancer in Germany (GENICA) Consortium
Nature genetics · 2011 · PMID 22037553
1 page
rs10069690
Meta-analysis of Genome Wide Association Studies Identifies Genetic Markers of Late Toxicity Following Radiotherapy for Prostate Cancer
Radiogenomics Consortium
EBioMedicine · 2016 · PMID 27515689 · open access
1 page
rs17599026
The Genetic Architecture of Parkinson Disease in Spain: Characterizing Population-Specific Risk, Differential Haplotype Structures, and Providing Etiologic Insight
American Genome Center · International Parkinson Disease Genomics Consortium
Movement disorders : official journal of the Movement Disorder Society · 2019 · PMID 31660654
1 page
rs190807041

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.