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.
3 matches for
Vasiliauskas E.
Genome-wide association identifies multiple ulcerative colitis susceptibility loci
McGovern DP,
Gardet A,
Törkvist L,
Goyette P,
Essers J,
Taylor KD,
Neale BM,
Ong RT,
Lagacé C,
Li C,
Green T,
Stevens CR
and 42 more — show all
Beauchamp C,
Fleshner PR,
Carlson M,
D'Amato M,
Halfvarson J,
Hibberd ML,
Lördal M,
Padyukov L,
Andriulli A,
Colombo E,
Latiano A,
Palmieri O,
Bernard EJ,
Deslandres C,
Hommes DW,
de Jong DJ,
Stokkers PC,
Weersma RK,
Sharma Y,
Silverberg MS,
Cho JH,
Wu J,
Roeder K,
Brant SR,
Schumm LP,
Duerr RH,
Dubinsky MC,
Glazer NL,
Haritunians T,
Ippoliti A,
Melmed GY,
Siscovick DS,
Vasiliauskas EA,
Targan SR,
Annese V,
Wijmenga C,
Pettersson S,
Rotter JI,
Xavier RJ,
Daly MJ,
Rioux JD,
Seielstad M
NIDDK IBD Genetics Consortium
Nature genetics · 2010 · PMID 20228799
4 pages
Fucosyltransferase 2 (FUT2) non-secretor status is associated with Crohn's disease
McGovern DP,
Jones MR,
Taylor KD,
Marciante K,
Yan X,
Dubinsky M,
Ippoliti A,
Vasiliauskas E,
Berel D,
Derkowski C,
Dutridge D,
Fleshner P
and 9 more — show all
International IBD Genetics Consortium
Human molecular genetics · 2010 · PMID 20570966
2 pages
Comprehensive Association Analyses of Extraintestinal Manifestations in Inflammatory Bowel Disease
Khrom M,
Long M,
Dube S,
Robbins L,
Botwin GJ,
Yang S,
Mengesha E,
Li D,
Naito T,
Bonthala NN,
Ha C,
Melmed G
and 23 more — show all
Rabizadeh S,
Syal G,
Vasiliauskas E,
Ziring D,
Brant SR,
Cho J,
Duerr RH,
Rioux J,
Schumm P,
Silverberg M,
Ananthakrishnan AN,
Faubion WA,
Jabri B,
Lira SA,
Newberry RD,
Sandler RS,
Xavier RJ,
Kugathasan S,
Hercules D,
Targan SR,
Sartor RB,
Haritunians T,
McGovern DPB
Gastroenterology · 2024 · PMID 38490347
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.