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Is your paper here?
2,661 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
Cheng TH.
Identification of nine new susceptibility loci for endometrial cancer
O'Mara TA,
Glubb DM,
Amant F,
Annibali D,
Ashton K,
Attia J,
Auer PL,
Beckmann MW,
Black A,
Bolla MK,
Brauch H,
Brenner H
and 114 more — show all
Brinton L,
Buchanan DD,
Burwinkel B,
Chang-Claude J,
Chanock SJ,
Chen C,
Chen MM,
Cheng THT,
Clarke CL,
Clendenning M,
Cook LS,
Couch FJ,
Cox A,
Crous-Bous M,
Czene K,
Day F,
Dennis J,
Depreeuw J,
Doherty JA,
Dörk T,
Dowdy SC,
Dürst M,
Ekici AB,
Fasching PA,
Fridley BL,
Friedenreich CM,
Fritschi L,
Fung J,
García-Closas M,
Gaudet MM,
Giles GG,
Goode EL,
Gorman M,
Haiman CA,
Hall P,
Hankison SE,
Healey CS,
Hein A,
Hillemanns P,
Hodgson S,
Hoivik EA,
Holliday EG,
Hopper JL,
Hunter DJ,
Jones A,
Krakstad C,
Kristensen VN,
Lambrechts D,
Marchand LL,
Liang X,
Lindblom A,
Lissowska J,
Long J,
Lu L,
Magliocco AM,
Martin L,
McEvoy M,
Meindl A,
Michailidou K,
Milne RL,
Mints M,
Montgomery GW,
Nassir R,
Olsson H,
Orlow I,
Otton G,
Palles C,
Perry JRB,
Peto J,
Pooler L,
Prescott J,
Proietto T,
Rebbeck TR,
Risch HA,
Rogers PAW,
Rübner M,
Runnebaum I,
Sacerdote C,
Sarto GE,
Schumacher F,
Scott RJ,
Setiawan VW,
Shah M,
Sheng X,
Shu XO,
Southey MC,
Swerdlow AJ,
Tham E,
Trovik J,
Turman C,
Tyrer JP,
Vachon C,
VanDen Berg D,
Vanderstichele A,
Wang Z,
Webb PM,
Wentzensen N,
Werner HMJ,
Winham SJ,
Wolk A,
Xia L,
Xiang YB,
Yang HP,
Yu H,
Zheng W,
Zheng W,
Pharoah PDP,
Dunning AM,
Kraft P,
De Vivo I,
Tomlinson I,
Easton DF,
Spurdle AB,
Thompson DJ
Nature communications · 2018 · PMID 30093612 · open access
6 pages
Five endometrial cancer risk loci identified through genome-wide association analysis
Cheng TH,
Thompson DJ,
O'Mara TA,
Painter JN,
Glubb DM,
Flach S,
Lewis A,
French JD,
Freeman-Mills L,
Church D,
Gorman M,
Martin L
and 76 more — show all
Hodgson S,
Webb PM,
Attia J,
Holliday EG,
McEvoy M,
Scott RJ,
Henders AK,
Martin NG,
Montgomery GW,
Nyholt DR,
Ahmed S,
Healey CS,
Shah M,
Dennis J,
Fasching PA,
Beckmann MW,
Hein A,
Ekici AB,
Hall P,
Czene K,
Darabi H,
Li J,
Dörk T,
Dürst M,
Hillemanns P,
Runnebaum I,
Amant F,
Schrauwen S,
Zhao H,
Lambrechts D,
Depreeuw J,
Dowdy SC,
Goode EL,
Fridley BL,
Winham SJ,
Njølstad TS,
Salvesen HB,
Trovik J,
Werner HM,
Ashton K,
Otton G,
Proietto T,
Liu T,
Mints M,
Tham E,
Consortium C,
Jun Li M,
Yip SH,
Wang J,
Bolla MK,
Michailidou K,
Wang Q,
Tyrer JP,
Dunlop M,
Houlston R,
Palles C,
Hopper JL,
Peto J,
Swerdlow AJ,
Burwinkel B,
Brenner H,
Meindl A,
Brauch H,
Lindblom A,
Chang-Claude J,
Couch FJ,
Giles GG,
Kristensen VN,
Cox A,
Cunningham JM,
Pharoah PDP,
Dunning AM,
Edwards SL,
Easton DF,
Tomlinson I,
Spurdle AB
National Study of Endometrial Cancer Genetics Group (NSECG) · Australian National Endometrial Cancer Study Group (ANECS) and 2 more consortia
Nature genetics · 2016 · PMID 27135401 · open access
3 pages
Genetic overlap between endometriosis and endometrial cancer: evidence from cross-disease genetic correlation and GWAS meta-analyses
Painter JN,
O'Mara TA,
Morris AP,
Cheng THT,
Gorman M,
Martin L,
Hodson S,
Jones A,
Martin NG,
Gordon S,
Henders AK,
Attia J
and 65 more — show all
McEvoy M,
Holliday EG,
Scott RJ,
Webb PM,
Fasching PA,
Beckmann MW,
Ekici AB,
Hein A,
Rübner M,
Hall P,
Czene K,
Dörk T,
Dürst M,
Hillemanns P,
Runnebaum I,
Lambrechts D,
Lambrechts D,
Amant F,
Annibali D,
Depreeuw J,
Vanderstichele A,
Goode EL,
Cunningham JM,
Dowdy SC,
Winham SJ,
Trovik J,
Hoivik E,
Werner HMJ,
Krakstad C,
Ashton K,
Otton G,
Proietto T,
Tham E,
Mints M,
Ahmed S,
Healey CS,
Shah M,
Pharoah PDP,
Dunning AM,
Dennis J,
Bolla MK,
Michailidou K,
Wang Q,
Tyrer JP,
Hopper JL,
Peto J,
Swerdlow AJ,
Burwinkel B,
Brenner H,
Meindl A,
Brauch H,
Lindblom A,
Chang-Claude J,
Couch FJ,
Giles GG,
Kristensen VN,
Cox A,
Zondervan KT,
Nyholt DR,
MacGregor S,
Montgomery GW,
Tomlinson I,
Easton DF,
Thompson DJ,
Spurdle AB
Cancer medicine · 2018 · PMID 29608257 · open access
3 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.