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.
7 matches for
Gut I.
Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease
Barrett JC,
Hansoul S,
Nicolae DL,
Cho JH,
Duerr RH,
Rioux JD,
Brant SR,
Silverberg MS,
Taylor KD,
Barmada MM,
Bitton A,
Dassopoulos T
and 49 more — show all
Datta LW,
Green T,
Griffiths AM,
Kistner EO,
Murtha MT,
Regueiro MD,
Rotter JI,
Schumm LP,
Steinhart AH,
Targan SR,
Xavier RJ,
Libioulle C,
Sandor C,
Lathrop M,
Belaiche J,
Dewit O,
Gut I,
Heath S,
Laukens D,
Mni M,
Rutgeerts P,
Van Gossum A,
Zelenika D,
Franchimont D,
Hugot JP,
de Vos M,
Vermeire S,
Louis E,
Cardon LR,
Anderson CA,
Drummond H,
Nimmo E,
Ahmad T,
Prescott NJ,
Onnie CM,
Fisher SA,
Marchini J,
Ghori J,
Bumpstead S,
Gwilliam R,
Tremelling M,
Deloukas P,
Mansfield J,
Jewell D,
Satsangi J,
Mathew CG,
Parkes M,
Georges M,
Daly MJ
NIDDK IBD Genetics Consortium · Belgian-French IBD Consortium and 1 more consortia
Nature genetics · 2008 · PMID 18587394
11 pages
Genome-wide association study identifies eight loci associated with blood pressure
Newton-Cheh C,
Johnson T,
Gateva V,
Tobin MD,
Bochud M,
Coin L,
Najjar SS,
Zhao JH,
Heath SC,
Eyheramendy S,
Papadakis K,
Voight BF
and 147 more — show all
Scott LJ,
Zhang F,
Farrall M,
Tanaka T,
Wallace C,
Chambers JC,
Khaw KT,
Nilsson P,
van der Harst P,
Polidoro S,
Grobbee DE,
Onland-Moret NC,
Bots ML,
Wain LV,
Elliott KS,
Teumer A,
Luan J,
Lucas G,
Kuusisto J,
Burton PR,
Hadley D,
McArdle WL,
Brown M,
Dominiczak A,
Newhouse SJ,
Samani NJ,
Webster J,
Zeggini E,
Beckmann JS,
Bergmann S,
Lim N,
Song K,
Vollenweider P,
Waeber G,
Waterworth DM,
Yuan X,
Groop L,
Orho-Melander M,
Allione A,
Di Gregorio A,
Guarrera S,
Panico S,
Ricceri F,
Romanazzi V,
Sacerdote C,
Vineis P,
Barroso I,
Sandhu MS,
Luben RN,
Crawford GJ,
Jousilahti P,
Perola M,
Boehnke M,
Bonnycastle LL,
Collins FS,
Jackson AU,
Mohlke KL,
Stringham HM,
Valle TT,
Willer CJ,
Bergman RN,
Morken MA,
Döring A,
Gieger C,
Illig T,
Meitinger T,
Org E,
Org E,
Pfeufer A,
Wichmann HE,
Kathiresan S,
Marrugat J,
O'Donnell CJ,
Schwartz SM,
Siscovick DS,
Subirana I,
Freimer NB,
Hartikainen AL,
McCarthy MI,
O'Reilly PF,
Peltonen L,
Pouta A,
de Jong PE,
Snieder H,
van Gilst WH,
Clarke R,
Goel A,
Hamsten A,
Peden JF,
Seedorf U,
Syvänen AC,
Tognoni G,
Lakatta EG,
Sanna S,
Scheet P,
Schlessinger D,
Scuteri A,
Dörr M,
Ernst F,
Felix SB,
Homuth G,
Lorbeer R,
Reffelmann T,
Rettig R,
Völker U,
Galan P,
Gut IG,
Hercberg S,
Lathrop GM,
Zelenika D,
Deloukas P,
Soranzo N,
Williams FM,
Zhai G,
Salomaa V,
Laakso M,
Elosua R,
Forouhi NG,
Völzke H,
Uiterwaal CS,
van der Schouw YT,
Numans ME,
Matullo G,
Navis G,
Berglund G,
Bingham SA,
Kooner JS,
Connell JM,
Bandinelli S,
Ferrucci L,
Watkins H,
Spector TD,
Tuomilehto J,
Altshuler D,
Strachan DP,
Laan M,
Meneton P,
Wareham NJ,
Uda M,
Jarvelin MR,
Mooser V,
Melander O,
Loos RJ,
Elliott P,
Abecasis GR,
Caulfield M,
Munroe PB
Wellcome Trust Case Control Consortium
Nature genetics · 2009 · PMID 19430483 · open access
4 pages
A susceptibility locus for lung cancer maps to nicotinic acetylcholine receptor subunit genes on 15q25
Hung RJ,
McKay JD,
Gaborieau V,
Boffetta P,
Hashibe M,
Zaridze D,
Mukeria A,
Szeszenia-Dabrowska N,
Lissowska J,
Rudnai P,
Fabianova E,
Mates D
and 53 more — show all
Bencko V,
Foretova L,
Janout V,
Chen C,
Goodman G,
Field JK,
Liloglou T,
Xinarianos G,
Cassidy A,
McLaughlin J,
Liu G,
Narod S,
Krokan HE,
Skorpen F,
Elvestad MB,
Hveem K,
Vatten L,
Linseisen J,
Clavel-Chapelon F,
Vineis P,
Bueno-de-Mesquita HB,
Lund E,
Martinez C,
Bingham S,
Rasmuson T,
Hainaut P,
Riboli E,
Ahrens W,
Benhamou S,
Lagiou P,
Trichopoulos D,
Holcátová I,
Merletti F,
Kjaerheim K,
Agudo A,
Macfarlane G,
Talamini R,
Simonato L,
Lowry R,
Conway DI,
Znaor A,
Healy C,
Zelenika D,
Boland A,
Delepine M,
Foglio M,
Lechner D,
Matsuda F,
Blanche H,
Gut I,
Heath S,
Lathrop M,
Brennan P
Nature · 2008 · PMID 18385738
2 pages
Novel breast cancer susceptibility locus at 9q31.2: results of a genome-wide association study
Fletcher O,
Johnson N,
Orr N,
Hosking FJ,
Gibson LJ,
Walker K,
Zelenika D,
Gut I,
Heath S,
Palles C,
Coupland B,
Broderick P
and 17 more — show all
Schoemaker M,
Jones M,
Williamson J,
Chilcott-Burns S,
Tomczyk K,
Simpson G,
Jacobs KB,
Chanock SJ,
Hunter DJ,
Tomlinson IP,
Swerdlow A,
Ashworth A,
Ross G,
dos Santos Silva I,
Lathrop M,
Houlston RS,
Peto J
Journal of the National Cancer Institute · 2011 · PMID 21263130
2 pages
Genetic variants regulating ORMDL3 expression contribute to the risk of childhood asthma
Moffatt MF,
Kabesch M,
Liang L,
Dixon AL,
Strachan D,
Heath S,
Depner M,
von Berg A,
Bufe A,
Rietschel E,
Heinzmann A,
Simma B
and 12 more — show all
Frischer T,
Willis-Owen SA,
Wong KC,
Illig T,
Vogelberg C,
Weiland SK,
von Mutius E,
Abecasis GR,
Farrall M,
Gut IG,
Lathrop GM,
Cookson WO
Nature · 2007 · PMID 17611496
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.