For researchers
Is your paper here?
2,645 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.
4 matches for
Mathieson I.
Uganda Genome Resource Enables Insights into Population History and Genomic Discovery in Africa
Gurdasani D,
Carstensen T,
Fatumo S,
Chen G,
Franklin CS,
Prado-Martinez J,
Bouman H,
Abascal F,
Haber M,
Tachmazidou I,
Mathieson I,
Ekoru K
and 45 more — show all
DeGorter MK,
Nsubuga RN,
Finan C,
Wheeler E,
Chen L,
Cooper DN,
Schiffels S,
Chen Y,
Ritchie GRS,
Pollard MO,
Fortune MD,
Mentzer AJ,
Garrison E,
Bergström A,
Hatzikotoulas K,
Adeyemo A,
Doumatey A,
Elding H,
Wain LV,
Ehret G,
Auer PL,
Kooperberg CL,
Reiner AP,
Franceschini N,
Maher D,
Montgomery SB,
Kadie C,
Widmer C,
Xue Y,
Seeley J,
Asiki G,
Kamali A,
Young EH,
Pomilla C,
Soranzo N,
Zeggini E,
Pirie F,
Morris AP,
Heckerman D,
Tyler-Smith C,
Motala AA,
Rotimi C,
Kaleebu P,
Barroso I,
Sandhu MS
Cell · 2019 · PMID 31675503
6 pages
Genome-wide analysis implicates inner ear development in Ménière disease
Shi Z,
Mandla R,
Li J,
Li X,
Zhang ZE,
Chen S,
Lapinska S,
Flynn-Carroll AO,
Pasaniuc B,
Epstein DJ,
Mathieson I
American journal of human genetics · 2026 · PMID 42302782 · open access
3 pages
Causal mechanisms and balancing selection inferred from genetic associations with polycystic ovary syndrome
Day FR,
Hinds DA,
Tung JY,
Stolk L,
Styrkarsdottir U,
Saxena R,
Bjonnes A,
Broer L,
Dunger DB,
Halldorsson BV,
Lawlor DA,
Laval G
and 15 more — show all
Mathieson I,
McCardle WL,
Louwers Y,
Meun C,
Ring S,
Scott RA,
Sulem P,
Uitterlinden AG,
Wareham NJ,
Thorsteinsdottir U,
Welt C,
Stefansson K,
Laven JSE,
Ong KK,
Perry JRB
Nature communications · 2015 · PMID 26416764 · open access
2 pages
Meta-analysis of uveal melanoma genome-wide association studies identifies novel risk loci and population effect size heterogeneity
Mies G,
Tsao NL,
Houy A,
Coupland SE,
Kalirai H,
Försti A,
Hemminki K,
Thomsen H,
Stern MH,
Shields CL,
Damrauer SM,
Ewens KG
and 2 more — show all
HGG advances · 2025 · PMID 40495383 · open access
1 page
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.