For researchers
Is your paper here?
2,657 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.
6 matches for
Cardon L.
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
Replication of genome-wide association signals in UK samples reveals risk loci for type 2 diabetes
Zeggini E,
Weedon MN,
Lindgren CM,
Frayling TM,
Elliott KS,
Lango H,
Timpson NJ,
Perry JR,
Rayner NW,
Freathy RM,
Barrett JC,
Shields B
and 14 more — show all
Morris AP,
Ellard S,
Groves CJ,
Harries LW,
Marchini JL,
Owen KR,
Knight B,
Cardon LR,
Walker M,
Hitman GA,
Morris AD,
Doney AS,
McCarthy MI,
Hattersley AT
Wellcome Trust Case Control Consortium (WTCCC)
Science (New York, N.Y.) · 2007 · PMID 17463249
3 pages
Population-based genome-wide association studies reveal six loci influencing plasma levels of liver enzymes
Yuan X,
Waterworth D,
Perry JR,
Lim N,
Song K,
Chambers JC,
Zhang W,
Vollenweider P,
Stirnadel H,
Johnson T,
Bergmann S,
Beckmann ND
and 12 more — show all
Li Y,
Ferrucci L,
Melzer D,
Hernandez D,
Singleton A,
Scott J,
Elliott P,
Waeber G,
Cardon L,
Frayling TM,
Kooner JS,
Mooser V
American journal of human genetics · 2008 · PMID 18940312
3 pages
A large-scale genome-wide association study of Asian populations uncovers genetic factors influencing eight quantitative traits
Cho YS,
Go MJ,
Kim YJ,
Heo JY,
Oh JH,
Ban HJ,
Yoon D,
Lee MH,
Kim DJ,
Park M,
Cha SH,
Kim JW
and 20 more — show all
Han BG,
Min H,
Ahn Y,
Park MS,
Han HR,
Jang HY,
Cho EY,
Lee JE,
Cho NH,
Shin C,
Park T,
Park JW,
Lee JK,
Cardon L,
Clarke G,
McCarthy MI,
Lee JY,
Lee JK,
Oh B,
Kim HL
Nature genetics · 2009 · PMID 19396169
3 pages
Genetic variants influencing circulating lipid levels and risk of coronary artery disease
Waterworth DM,
Ricketts SL,
Song K,
Chen L,
Zhao JH,
Ripatti S,
Aulchenko YS,
Zhang W,
Yuan X,
Lim N,
Luan J,
Ashford S
and 54 more — show all
Wheeler E,
Young EH,
Hadley D,
Thompson JR,
Braund PS,
Johnson T,
Struchalin M,
Surakka I,
Luben R,
Khaw KT,
Rodwell SA,
Loos RJ,
Boekholdt SM,
Inouye M,
Deloukas P,
Elliott P,
Schlessinger D,
Sanna S,
Scuteri A,
Jackson A,
Mohlke KL,
Tuomilehto J,
Roberts R,
Stewart A,
Kesäniemi YA,
Mahley RW,
Grundy SM,
McArdle W,
Cardon L,
Waeber G,
Vollenweider P,
Chambers JC,
Boehnke M,
Abecasis GR,
Salomaa V,
Järvelin MR,
Ruokonen A,
Barroso I,
Epstein SE,
Hakonarson HH,
Rader DJ,
Reilly MP,
Witteman JC,
Hall AS,
Samani NJ,
Strachan DP,
Barter P,
van Duijn CM,
Kooner JS,
Peltonen L,
Wareham NJ,
McPherson R,
Mooser V,
Sandhu MS
Wellcome Trust Case Control Consortium
Arteriosclerosis, thrombosis, and vascular biology · 2010 · PMID 20864672
3 pages
A common variant in the FTO gene is associated with body mass index and predisposes to childhood and adult obesity
Frayling TM,
Timpson NJ,
Weedon MN,
Zeggini E,
Freathy RM,
Lindgren CM,
Perry JR,
Elliott KS,
Lango H,
Rayner NW,
Shields B,
Harries LW
and 29 more — show all
Barrett JC,
Ellard S,
Groves CJ,
Knight B,
Patch AM,
Ness AR,
Ebrahim S,
Lawlor DA,
Ring SM,
Ben-Shlomo Y,
Jarvelin MR,
Sovio U,
Bennett AJ,
Melzer D,
Ferrucci L,
Loos RJ,
Barroso I,
Wareham NJ,
Karpe F,
Owen KR,
Cardon LR,
Walker M,
Hitman GA,
Palmer CN,
Doney AS,
Morris AD,
Smith GD,
Hattersley AT,
McCarthy MI
Science (New York, N.Y.) · 2007 · PMID 17434869
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.