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.

12 matches for Atkinson E.

Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function
ICBP Consortium · AGEN Consortium and 3 more consortia
Nature communications · 2016 · PMID 26831199 · open access
12 pages+
rs9682041 rs2928148 rs6795744 rs228611 rs3750082 rs10491967
Mapping genomic loci implicates genes and synaptic biology in schizophrenia
Indonesia Schizophrenia Consortium · PsychENCODE and 3 more consortia
Nature · 2022 · PMID 35396580
12 pages+
rs140365013 rs302317 rs77622099 rs619091 rs12652777 rs12476312
Genome-wide association analyses identify 95 risk loci and provide insights into the neurobiology of post-traumatic stress disorder
AURORA Study · Estonian Biobank Research Team and 2 more consortia
Nature genetics · 2024 · PMID 38637617
12 pages+
rs10992779 rs13161130 rs868754 rs2899991 rs6802567 rs2684641
Multi-trait and multi-ancestry genetic analysis of comorbid lung diseases and traits improves genetic discovery and polygenic risk prediction
Nature genetics · 2026 · PMID 41565855
12 pages+
rs924150 rs8089099 rs4791806 rs41522747 rs340121 rs2609260
An international genome-wide meta-analysis of primary biliary cholangitis: Novel risk loci and candidate drugs
PBC Consortia · Canadian PBC Consortium and 5 more consortia
Journal of hepatology · 2021 · PMID 34033851 · open access
10 pages
rs11742270 rs859767 rs6550965 rs12419634 rs742108 rs7674640
Genome-wide association study of primary sclerosing cholangitis identifies new risk loci and quantifies the genetic relationship with inflammatory bowel disease
UK-PSC Consortium · International IBD Genetics Consortium and 1 more consortia
Nature genetics · 2017 · PMID 27992413 · open access
8 pages
rs13140464 rs56258221 rs60652743 rs72837826 rs80060485 rs36023390
Genome-wide study investigating effector genes and polygenic prediction for kidney function in persons with ancestry from Africa and the Americas
Cell genomics · 2024 · PMID 38190104 · open access
6 pages
rs35790011 rs11753349 rs73392143 rs10993435 rs2016708 rs13392691
The impact of non-additive genetic associations on age-related complex diseases
FinnGen Consortium
Nature communications · 2021 · PMID 33893285 · open access
5 pages
rs10858023 rs9272521 rs55651120 rs6675912 rs13166760
New loci associated with kidney function and chronic kidney disease
Nature genetics · 2010 · PMID 20383146
4 pages
rs267734 rs10774021 rs7805747 rs6465825
Multiethnic genome-wide association study of cerebral white matter hyperintensities on MRI
Circulation. Cardiovascular genetics · 2015 · PMID 25663218
4 pages
rs7894407 rs72848980 rs7909791 rs7214628
CUBN is a gene locus for albuminuria
CKDGen Consortium
Journal of the American Society of Nephrology : JASN · 2011 · PMID 21355061
1 page
Kidney Function
Immunochip analyses identify a novel risk locus for primary biliary cirrhosis at 13q14, multiple independent associations at four established risk loci and epistasis between 1p31 and 7q32 risk variants
Italian PBC Genetics Study Group
Human molecular genetics · 2012 · PMID 22936693
1 page
rs7775055

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.