For researchers
Is your paper here?
2,662 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.
5 matches for
Orth M.
GWAS meta-analysis of psoriasis identifies new susceptibility alleles impacting disease mechanisms and therapeutic targets
Dand N,
Stuart PE,
Bowes J,
Ellinghaus D,
Nititham J,
Saklatvala JR,
Teder-Laving M,
Thomas LF,
Traks T,
Uebe S,
Assmann G,
Baudry D
and 73 more — show all
Behrens F,
Billi AC,
Brown MA,
Burkhardt H,
Capon F,
Chung R,
Curtis CJ,
Duckworth M,
Ellinghaus E,
FitzGerald O,
Gerdes S,
Griffiths CEM,
Gulliver S,
Helliwell PS,
Ho P,
Hoffmann P,
Holmen OL,
Huang ZM,
Hveem K,
Jadon D,
Köhm M,
Kraus C,
Lamacchia C,
Lee SH,
Ma F,
Mahil SK,
McHugh N,
McManus R,
Modalsli EH,
Nissen MJ,
Nöthen M,
Oji V,
Oksenberg JR,
Patrick MT,
Perez White BE,
Ramming A,
Rech J,
Rosen C,
Sarkar MK,
Schett G,
Schmidt B,
Tejasvi T,
Traupe H,
Voorhees JJ,
Wacker EM,
Warren RB,
Wasikowski R,
Weidinger S,
Wen X,
Zhang Z,
Barton A,
Chandran V,
Esko T,
Foerster J,
Franke A,
Gladman DD,
Gudjonsson JE,
Gulliver W,
Hüffmeier U,
Kingo K,
Kõks S,
Liao W,
Løset M,
Mägi R,
Nair RP,
Rahman P,
Reis A,
Smith CH,
Di Meglio P,
Barker JN,
Tsoi LC,
Simpson MA,
Elder JT
BSTOP study group · Estonian Biobank research team
Nature communications · 2025 · PMID 40021644 · open access
9 pages
Genome-wide meta-analysis implicates mediators of hair follicle development and morphogenesis in risk for severe acne
Petridis C,
Navarini AA,
Dand N,
Saklatvala J,
Baudry D,
Duckworth M,
Allen MH,
Curtis CJ,
Lee SH,
Burden AD,
Layton A,
Bataille V
and 9 more — show all
Acne Genetic Study Group
Nature communications · 2018 · PMID 30542056 · open access
3 pages
Population-specific genetic modification of Huntington's disease in Venezuela
Chao MJ,
Kim KH,
Shin JW,
Lucente D,
Wheeler VC,
Li H,
Roach JC,
Hood L,
Wexler NS,
Jardim LB,
Holmans P,
Jones L
and 5 more — show all
PLoS genetics · 2018 · PMID 29750799 · open access
2 pages
Genome-wide association study of CSF levels of 59 alzheimer's disease candidate proteins: significant associations with proteins involved in amyloid processing and inflammation
Kauwe JS,
Bailey MH,
Ridge PG,
Perry R,
Wadsworth ME,
Hoyt KL,
Staley LA,
Karch CM,
Harari O,
Cruchaga C,
Ainscough BJ,
Bales K
and 6 more — show all
Alzheimer's Disease Neuroimaging Initiative
PLoS genetics · 2014 · PMID 25340798 · open access
1 page
Comparative Genetic Analysis of Psoriatic Arthritis and Psoriasis for the Discovery of Genetic Risk Factors and Risk Prediction Modeling
Soomro M,
Stadler M,
Dand N,
Bluett J,
Jadon D,
Jalali-Najafabadi F,
Duckworth M,
Ho P,
Marzo-Ortega H,
Helliwell PS,
Ryan AW,
Kane D
and 17 more — show all
Korendowych E,
Simpson MA,
Packham J,
McManus R,
Gabay C,
Lamacchia C,
Nissen MJ,
Brown MA,
Verstappen SMM,
Van Staa T,
Barker JN,
Smith CH,
FitzGerald O,
McHugh N,
Warren RB,
Bowes J,
Barton A
BADBIR Study Group · BSTOP study group
Arthritis & rheumatology (Hoboken, N.J.) · 2022 · PMID 35507331 · 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.