For researchers
Is your paper here?
2,660 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
Thomas G.
Common variants near TARDBP and EGR2 are associated with susceptibility to Ewing sarcoma
Postel-Vinay S,
Véron AS,
Tirode F,
Pierron G,
Reynaud S,
Kovar H,
Oberlin O,
Lapouble E,
Ballet S,
Lucchesi C,
Kontny U,
González-Neira A
and 14 more — show all
Picci P,
Alonso J,
Patino-Garcia A,
de Paillerets BB,
Laud K,
Dina C,
Froguel P,
Clavel-Chapelon F,
Doz F,
Michon J,
Chanock SJ,
Thomas G,
Cox DG,
Delattre O
Nature genetics · 2012 · PMID 22327514
4 pages
A genome-wide association study identifies novel alleles associated with hair color and skin pigmentation
Han J,
Kraft P,
Nan H,
Guo Q,
Chen C,
Qureshi A,
Hankinson SE,
Hu FB,
Duffy DL,
Zhao ZZ,
Martin NG,
Montgomery GW
and 5 more — show all
PLoS genetics · 2008 · PMID 18483556 · open access
3 pages
Genome-wide association study identifies variants in the ABO locus associated with susceptibility to pancreatic cancer
Amundadottir L,
Kraft P,
Stolzenberg-Solomon RZ,
Fuchs CS,
Petersen GM,
Arslan AA,
Bueno-de-Mesquita HB,
Gross M,
Helzlsouer K,
Jacobs EJ,
LaCroix A,
Zheng W
and 60 more — show all
Zheng W,
Albanes D,
Bamlet W,
Berg CD,
Berrino F,
Bingham S,
Buring JE,
Bracci PM,
Canzian F,
Clavel-Chapelon F,
Clipp S,
Cotterchio M,
de Andrade M,
Duell EJ,
Fox JW Jr,
Gallinger S,
Gaziano JM,
Giovannucci EL,
Goggins M,
González CA,
Hallmans G,
Hankinson SE,
Hassan M,
Holly EA,
Hunter DJ,
Hutchinson A,
Jackson R,
Jacobs KB,
Jenab M,
Kaaks R,
Klein AP,
Kooperberg C,
Kurtz RC,
Li D,
Lynch SM,
Mandelson M,
McWilliams RR,
Mendelsohn JB,
Michaud DS,
Olson SH,
Overvad K,
Patel AV,
Peeters PH,
Rajkovic A,
Riboli E,
Risch HA,
Shu XO,
Thomas G,
Tobias GS,
Trichopoulos D,
Van Den Eeden SK,
Virtamo J,
Wactawski-Wende J,
Wolpin BM,
Yu H,
Yu K,
Zeleniuch-Jacquotte A,
Chanock SJ,
Hartge P,
Hoover RN
Nature genetics · 2009 · PMID 19648918
3 pages
Interaction between ERAP1 and HLA-B27 in ankylosing spondylitis implicates peptide handling in the mechanism for HLA-B27 in disease susceptibility
Evans DM,
Spencer CC,
Pointon JJ,
Su Z,
Harvey D,
Kochan G,
Oppermann U,
Dilthey A,
Pirinen M,
Stone MA,
Appleton L,
Moutsianas L
and 81 more — show all
Leslie S,
Wordsworth T,
Kenna TJ,
Karaderi T,
Thomas GP,
Ward MM,
Weisman MH,
Farrar C,
Bradbury LA,
Danoy P,
Inman RD,
Maksymowych W,
Gladman D,
Rahman P,
Morgan A,
Marzo-Ortega H,
Bowness P,
Gaffney K,
Gaston JS,
Smith M,
Bruges-Armas J,
Couto AR,
Sorrentino R,
Paladini F,
Ferreira MA,
Xu H,
Liu Y,
Jiang L,
Lopez-Larrea C,
Díaz-Peña R,
López-Vázquez A,
Zayats T,
Band G,
Bellenguez C,
Blackburn H,
Blackwell JM,
Bramon E,
Bumpstead SJ,
Casas JP,
Corvin A,
Craddock N,
Deloukas P,
Dronov S,
Duncanson A,
Edkins S,
Freeman C,
Gillman M,
Gray E,
Gwilliam R,
Hammond N,
Hunt SE,
Jankowski J,
Jayakumar A,
Langford C,
Liddle J,
Markus HS,
Mathew CG,
McCann OT,
McCarthy MI,
Palmer CN,
Peltonen L,
Plomin R,
Potter SC,
Rautanen A,
Ravindrarajah R,
Ricketts M,
Samani N,
Sawcer SJ,
Strange A,
Trembath RC,
Viswanathan AC,
Waller M,
Weston P,
Whittaker P,
Widaa S,
Wood NW,
McVean G,
Reveille JD,
Wordsworth BP,
Brown MA,
Donnelly P
Spondyloarthritis Research Consortium of Canada (SPARCC) · Australo-Anglo-American Spondyloarthritis Consortium (TASC) and 1 more consortia
Nature genetics · 2011 · PMID 21743469
3 pages
Genome-wide association study of tanning phenotype in a population of European ancestry
Nan H,
Kraft P,
Qureshi AA,
Guo Q,
Chen C,
Hankinson SE,
Hu FB,
Thomas G,
Hoover RN,
Chanock S,
Hunter DJ,
Han J
The Journal of investigative dermatology · 2009 · PMID 19340012
2 pages
Multiple loci identified in a genome-wide association study of prostate cancer
Thomas G,
Jacobs KB,
Yeager M,
Kraft P,
Wacholder S,
Orr N,
Yu K,
Chatterjee N,
Welch R,
Hutchinson A,
Crenshaw A,
Cancel-Tassin G
and 27 more — show all
Staats BJ,
Wang Z,
Gonzalez-Bosquet J,
Fang J,
Deng X,
Berndt SI,
Calle EE,
Feigelson HS,
Thun MJ,
Rodriguez C,
Albanes D,
Virtamo J,
Weinstein S,
Schumacher FR,
Giovannucci E,
Willett WC,
Cussenot O,
Valeri A,
Andriole GL,
Crawford ED,
Tucker M,
Gerhard DS,
Fraumeni JF Jr,
Hoover R,
Hayes RB,
Hunter DJ,
Chanock SJ
Nature genetics · 2008 · PMID 18264096
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.