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.

8 matches for Black A.

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
rs1400482 rs1879586 rs7207826 rs11651755 rs688187 rs7902587
Genome-wide association study identifies multiple risk loci for renal cell carcinoma
Nature communications · 2017 · PMID 28598434 · open access
6 pages
rs4381241 rs67311347 rs11813268 rs74911261 rs4903064 Renal Cell Carcinoma
Identification of nine new susceptibility loci for endometrial cancer
Nature communications · 2018 · PMID 30093612 · open access
6 pages
rs113998067 rs1740828 rs9668337 rs10850382 rs7981863 Endometrial Cancer
Two susceptibility loci identified for prostate cancer aggressiveness
African Ancestry Prostate Cancer GWAS Consortium
Nature communications · 2015 · PMID 25939597 · open access
5 pages
rs71277158 rs7929962 rs17023900 rs35148638 rs16901979
A multi-stage genome-wide association study of bladder cancer identifies multiple susceptibility loci
Nature genetics · 2010 · PMID 20972438 · open access
2 pages
rs8102137 rs798766
Soluble Urokinase Plasminogen Activator Receptor: Genetic Variation and Cardiovascular Disease Risk in Black Adults
Circulation. Genomic and precision medicine · 2021 · PMID 34706549
2 pages
rs399145 rs73935023
Quarta CC et al. The amyloidogenic V122I transthyretin variant in elderly black Americans. NEJM 2015. PMID:25551524 https://europepmc.org/article/MED/25551524
· PMID 25551524
1 page
Transthyretin Amyloidosis (ATTR)
Sex specific associations in genome wide association analysis of renal cell carcinoma
European journal of human genetics : EJHG · 2019 · PMID 31231134
1 page
rs78971134

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.