For researchers
Is your paper here?
2,647 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.
2 matches for
Førre Ø.
Meta-analysis of shared genetic architecture across ten pediatric autoimmune diseases
Li YR,
Li J,
Zhao SD,
Bradfield JP,
Mentch FD,
Maggadottir SM,
Hou C,
Abrams DJ,
Chang D,
Gao F,
Guo Y,
Wei Z
and 54 more — show all
Connolly JJ,
Cardinale CJ,
Bakay M,
Glessner JT,
Li D,
Kao C,
Thomas KA,
Qiu H,
Chiavacci RM,
Kim CE,
Wang F,
Snyder J,
Richie MD,
Flatø B,
Førre Ø,
Denson LA,
Thompson SD,
Becker ML,
Guthery SL,
Latiano A,
Perez E,
Resnick E,
Russell RK,
Wilson DC,
Silverberg MS,
Annese V,
Lie BA,
Punaro M,
Dubinsky MC,
Monos DS,
Strisciuglio C,
Staiano A,
Miele E,
Kugathasan S,
Ellis JA,
Munro JE,
Sullivan KE,
Wise CA,
Chapel H,
Cunningham-Rundles C,
Grant SF,
Orange JS,
Sleiman PM,
Behrens EM,
Griffiths AM,
Satsangi J,
Finkel TH,
Keinan A,
Prak ET,
Polychronakos C,
Baldassano RN,
Li H,
Keating BJ,
Hakonarson H
Nature medicine · 2015 · PMID 26301688
12 pages+
Identification of multiple risk variants for ankylosing spondylitis through high-density genotyping of immune-related loci
Cortes A,
Hadler J,
Pointon JP,
Robinson PC,
Karaderi T,
Leo P,
Cremin K,
Pryce K,
Harris J,
Lee S,
Joo KB,
Shim SC
and 53 more — show all
Weisman M,
Ward M,
Zhou X,
Garchon HJ,
Chiocchia G,
Nossent J,
Lie BA,
Førre Ø,
Tuomilehto J,
Laiho K,
Jiang L,
Liu Y,
Wu X,
Bradbury LA,
Elewaut D,
Burgos-Vargas R,
Stebbings S,
Appleton L,
Farrah C,
Lau J,
Kenna TJ,
Haroon N,
Ferreira MA,
Yang J,
Mulero J,
Fernandez-Sueiro JL,
Gonzalez-Gay MA,
Lopez-Larrea C,
Deloukas P,
Donnelly P,
Bowness P,
Gafney K,
Gaston H,
Gladman DD,
Rahman P,
Maksymowych WP,
Xu H,
Crusius JB,
van der Horst-Bruinsma IE,
Chou CT,
Valle-Oñate R,
Romero-Sánchez C,
Hansen IM,
Pimentel-Santos FM,
Inman RD,
Videm V,
Martin J,
Breban M,
Reveille JD,
Evans DM,
Kim TH,
Wordsworth BP,
Brown MA
International Genetics of Ankylosing Spondylitis Consortium (IGAS) · Australo-Anglo-American Spondyloarthritis Consortium (TASC) and 4 more consortia
Nature genetics · 2013 · PMID 23749187
4 pages
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.