For researchers
Is your paper here?
2,673 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.
5 matches for
Dong J.
Genetic variants at 6p21.1 and 7p15.3 are associated with risk of multiple cancers in Han Chinese
Jin G,
Ma H,
Wu C,
Dai J,
Zhang R,
Shi Y,
Lu J,
Miao X,
Wang M,
Zhou Y,
Chen J,
Li H
and 21 more — show all
Pan S,
Chu M,
Lu F,
Yu D,
Jiang Y,
Dong J,
Hu L,
Chen Y,
Xu L,
Shu Y,
Pan S,
Tan W,
Zhou B,
Lu D,
Wu T,
Zhang Z,
Chen F,
Wang X,
Hu Z,
Lin D,
Shen H
American journal of human genetics · 2012 · PMID 23103227
2 pages
Genome-wide association analysis identifies new lung cancer susceptibility loci in never-smoking women in Asia
Lan Q,
Hsiung CA,
Matsuo K,
Hong YC,
Seow A,
Wang Z,
Hosgood HD 3rd,
Chen K,
Wang JC,
Chatterjee N,
Hu W,
Wong MP
and 119 more — show all
Zheng W,
Caporaso N,
Park JY,
Chen CJ,
Kim YH,
Kim YT,
Landi MT,
Shen H,
Lawrence C,
Burdett L,
Yeager M,
Yuenger J,
Jacobs KB,
Chang IS,
Mitsudomi T,
Kim HN,
Chang GC,
Bassig BA,
Tucker M,
Wei F,
Yin Z,
Wu C,
An SJ,
Qian B,
Lee VH,
Lu D,
Liu J,
Jeon HS,
Hsiao CF,
Sung JS,
Kim JH,
Gao YT,
Tsai YH,
Jung YJ,
Guo H,
Hu Z,
Hutchinson A,
Wang WC,
Klein R,
Chung CC,
Oh IJ,
Chen KY,
Berndt SI,
He X,
Wu W,
Chang J,
Zhang XC,
Huang MS,
Zheng H,
Wang J,
Zhao X,
Li Y,
Choi JE,
Su WC,
Park KH,
Sung SW,
Shu XO,
Chen YM,
Liu L,
Kang CH,
Hu L,
Chen CH,
Pao W,
Kim YC,
Yang TY,
Xu J,
Guan P,
Tan W,
Su J,
Wang CL,
Li H,
Sihoe AD,
Zhao Z,
Chen Y,
Choi YY,
Hung JY,
Kim JS,
Yoon HI,
Cai Q,
Lin CC,
Park IK,
Xu P,
Dong J,
Kim C,
He Q,
Perng RP,
Kohno T,
Kweon SS,
Chen CY,
Vermeulen R,
Wu J,
Lim WY,
Chen KC,
Chow WH,
Ji BT,
Chan JK,
Chu M,
Li YJ,
Yokota J,
Li J,
Chen H,
Xiang YB,
Yu CJ,
Kunitoh H,
Wu G,
Jin L,
Lo YL,
Shiraishi K,
Chen YH,
Lin HC,
Wu T,
Wu YL,
Yang PC,
Zhou B,
Shin MH,
Fraumeni JF Jr,
Lin D,
Chanock SJ,
Rothman N
Nature genetics · 2012 · PMID 23143601
2 pages
Genome-wide association study identifies a novel susceptibility locus at 12q23.1 for lung squamous cell carcinoma in han chinese
Dong J,
Jin G,
Wu C,
Guo H,
Zhou B,
Lv J,
Lu D,
Shi Y,
Shu Y,
Xu L,
Chu M,
Wang C
and 37 more — show all
Zhang R,
Dai J,
Jiang Y,
Yu D,
Ma H,
Zhao X,
Yin Z,
Yang L,
Li Z,
Deng Q,
Cao S,
Qin Z,
Gong J,
Sun C,
Wang J,
Wu W,
Zhou G,
Chen H,
Guan P,
Chen Y,
Liu X,
Liu L,
Xu P,
Han B,
Bai C,
Zhao Y,
Zhang H,
Yan Y,
Liu J,
Amos CI,
Chen F,
Tan W,
Jin L,
Wu T,
Hu Z,
Lin D,
Shen H
PLoS genetics · 2013 · PMID 23341777 · open access
2 pages
Genome-Wide Association and Functional Studies Identify <i>SCML4</i> and <i>THSD7A</i> as Novel Susceptibility Genes for Coronary Artery Disease
Li Y,
Wang DW,
Chen Y,
Chen C,
Guo J,
Zhang S,
Sun Z,
Ding H,
Yao Y,
Zhou L,
Xu K,
Song C
and 30 more — show all
Yang F,
Zhao B,
Yan H,
Wang WJ,
Wu C,
Lu X,
Yang X,
Dong J,
Zheng G,
Tian S,
Cui Y,
Jin L,
Liu G,
Cui H,
Wang S,
Jiang F,
Wang C,
Erdmann J,
Zeng L,
Huang S,
Zhong J,
Ma Y,
Chen W,
Sun J,
Lei W,
Chen S,
Rao S,
Gu D,
Schunkert H,
Tian XL
Arteriosclerosis, thrombosis, and vascular biology · 2018 · PMID 29472232
2 pages
GWAS meta-analysis of 16 790 patients with Barrett's oesophagus and oesophageal adenocarcinoma identifies 16 novel genetic risk loci and provides insights into disease aetiology beyond the single marker level
Schröder J,
Chegwidden L,
Maj C,
Gehlen J,
Speller J,
Böhmer AC,
Borisov O,
Hess T,
Kreuser N,
Venerito M,
Alakus H,
May A
and 56 more — show all
Gerges C,
Schmidt T,
Thieme R,
Heider D,
Hillmer AM,
Reingruber J,
Lyros O,
Dietrich A,
Hoffmeister A,
Mehdorn M,
Lordick F,
Stocker G,
Hohaus M,
Reim D,
Kandler J,
Müller M,
Ebigbo A,
Fuchs C,
Bruns CJ,
Hölscher AH,
Lang H,
Grimminger PP,
Dakkak D,
Vashist Y,
May S,
Görg S,
Franke A,
Ellinghaus D,
Galavotti S,
Veits L,
Weismüller J,
Dommermuth J,
Benner U,
Rösch T,
Messmann H,
Schumacher B,
Neuhaus H,
Schmidt C,
Wissinowski TT,
Nöthen MM,
Dong J,
Ong JS,
Buas MF,
Thrift AP,
Vaughan TL,
Tomlinson I,
Whiteman DC,
Fitzgerald RC,
Jankowski J,
Vieth M,
Mayr A,
Gharahkhani P,
MacGregor S,
Gockel I,
Palles C,
Schumacher J
Wellcome Trust Case Control Consortium 2 (WTCCC2) · Esophageal Adenocarcinoma Genetics Consortium (EAGLE) and 1 more consortia
Gut · 2023 · PMID 35882562
2 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.