For researchers
Is your paper here?
2,662 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.
9 matches for
Shen M.
Genomewide association study of leprosy
Zhang FR,
Huang W,
Chen SM,
Sun LD,
Liu H,
Li Y,
Cui Y,
Yan XX,
Yang HT,
Yang RD,
Chu TS,
Zhang C
and 55 more — show all
Zhang L,
Han JW,
Yu GQ,
Quan C,
Yu YX,
Zhang Z,
Shi BQ,
Zhang LH,
Cheng H,
Wang CY,
Lin Y,
Zheng HF,
Fu XA,
Zuo XB,
Wang Q,
Long H,
Sun YP,
Cheng YL,
Tian HQ,
Zhou FS,
Liu HX,
Lu WS,
He SM,
Du WL,
Shen M,
Jin QY,
Wang Y,
Low HQ,
Erwin T,
Yang NH,
Li JY,
Zhao X,
Jiao YL,
Mao LG,
Yin G,
Jiang ZX,
Wang XD,
Yu JP,
Hu ZH,
Gong CH,
Liu YQ,
Liu RY,
Wang DM,
Wei D,
Liu JX,
Cao WK,
Cao HZ,
Li YP,
Yan WG,
Wei SY,
Wang KJ,
Hibberd ML,
Yang S,
Zhang XJ,
Liu JJ
The New England journal of medicine · 2009 · PMID 20018961
4 pages
Genome-wide association study for vitiligo identifies susceptibility loci at 6q27 and the MHC
Quan C,
Ren YQ,
Xiang LH,
Sun LD,
Xu AE,
Gao XH,
Chen HD,
Pu XM,
Wu RN,
Liang CZ,
Li JB,
Gao TW
and 55 more — show all
Zhang JZ,
Wang XL,
Wang J,
Yang RY,
Liang L,
Yu JB,
Zuo XB,
Zhang SQ,
Zhang SM,
Chen G,
Zheng XD,
Li P,
Zhu J,
Li YW,
Wei XD,
Hong WS,
Ye Y,
Zhang Y,
Wu WS,
Cheng H,
Dong PL,
Hu DY,
Li Y,
Li M,
Zhang X,
Tang HY,
Tang XF,
Xu SX,
He SM,
Lv YM,
Shen M,
Jiang HQ,
Wang Y,
Li K,
Kang XJ,
Liu YQ,
Sun L,
Liu ZF,
Xie SQ,
Zhu CY,
Xu Q,
Gao JP,
Hu WL,
Ni C,
Pan TM,
Li Y,
Yao S,
He CF,
Liu YS,
Yu ZY,
Yin XY,
Zhang FY,
Yang S,
Zhou Y,
Zhang XJ
Nature genetics · 2010 · PMID 20526339
2 pages
A genome-wide association study in Han Chinese identifies new susceptibility loci for ankylosing spondylitis
Lin Z,
Bei JX,
Shen M,
Li Q,
Liao Z,
Zhang Y,
Lv Q,
Wei Q,
Low HQ,
Guo YM,
Cao S,
Yang M
and 39 more — show all
Hu Z,
Xu M,
Wang X,
Wei Y,
Li L,
Li C,
Li T,
Huang J,
Pan Y,
Jin O,
Wu Y,
Wu J,
Guo Z,
He P,
Hu S,
Wu H,
Song H,
Zhan F,
Liu S,
Gao G,
Liu Z,
Li Y,
Xiao C,
Li J,
Ye Z,
He W,
Liu D,
Shen L,
Huang A,
Wu H,
Tao Y,
Pan X,
Yu B,
Tai ES,
Zeng YX,
Ren EC,
Shen Y,
Liu J,
Gu J
Nature genetics · 2011 · PMID 22138694
2 pages
Performance of genetic risk factors in prediction of trichloroethylene induced hypersensitivity syndrome
Dai Y,
Chen Y,
Huang H,
Zhou W,
Niu Y,
Zhang M,
Bin P,
Dong H,
Jia Q,
Huang J,
Yi J,
Liao Q
and 26 more — show all
Li H,
Teng Y,
Zang D,
Zhai Q,
Duan H,
Shen J,
He J,
Meng T,
Sha Y,
Shen M,
Ye M,
Jia X,
Xiang Y,
Huang H,
Wu Q,
Shi M,
Huang X,
Yang H,
Luo L,
Li S,
Li L,
Zhao J,
Li L,
Wang J,
Wang J,
Zheng Y
Scientific reports · 2015 · PMID 26190474 · open access
2 pages
Genome-wide association study in a Chinese Han population identifies nine new susceptibility loci for systemic lupus erythematosus
Han JW,
Zheng HF,
Cui Y,
Sun LD,
Ye DQ,
Hu Z,
Xu JH,
Cai ZM,
Huang W,
Zhao GP,
Xie HF,
Fang H
and 55 more — show all
Lu QJ,
Xu JH,
Li XP,
Pan YF,
Deng DQ,
Zeng FQ,
Ye ZZ,
Zhang XY,
Wang QW,
Hao F,
Ma L,
Zuo XB,
Zhou FS,
Du WH,
Cheng YL,
Yang JQ,
Shen SK,
Li J,
Sheng YJ,
Zuo XX,
Zhu WF,
Gao F,
Zhang PL,
Guo Q,
Li B,
Gao M,
Xiao FL,
Quan C,
Zhang C,
Zhang Z,
Zhu KJ,
Li Y,
Hu DY,
Lu WS,
Huang JL,
Liu SX,
Li H,
Ren YQ,
Wang ZX,
Yang CJ,
Wang PG,
Zhou WM,
Lv YM,
Zhang AP,
Zhang SQ,
Lin D,
Li Y,
Low HQ,
Shen M,
Zhai ZF,
Wang Y,
Zhang FY,
Yang S,
Liu JJ,
Zhang XJ
Nature genetics · 2009 · PMID 19838193
1 page
A genome-wide association study identifies two new risk loci for Graves' disease
Chu X,
Pan CM,
Zhao SX,
Liang J,
Gao GQ,
Zhang XM,
Yuan GY,
Li CG,
Xue LQ,
Shen M,
Liu W,
Xie F
and 36 more — show all
Yang SY,
Wang HF,
Shi JY,
Sun WW,
Du WH,
Zuo CL,
Shi JX,
Liu BL,
Guo CC,
Zhan M,
Gu ZH,
Zhang XN,
Sun F,
Wang ZQ,
Song ZY,
Zou CY,
Sun WH,
Guo T,
Cao HM,
Ma JH,
Han B,
Li P,
Jiang H,
Huang QH,
Liang L,
Liu LB,
Chen G,
Su Q,
Peng YD,
Zhao JJ,
Ning G,
Chen Z,
Chen JL,
Chen SJ,
Huang W,
Song HD
China Consortium for Genetics of Autoimmune Thyroid Disease
Nature genetics · 2011 · PMID 21841780
1 page
Genome-wide association study in Chinese men identifies two new prostate cancer risk loci at 9q31.2 and 19q13.4
Xu J,
Mo Z,
Ye D,
Wang M,
Liu F,
Jin G,
Xu C,
Wang X,
Shao Q,
Chen Z,
Tao Z,
Qi J
and 58 more — show all
Zhou F,
Wang Z,
Fu Y,
He D,
Wei Q,
Guo J,
Wu D,
Gao X,
Yuan J,
Wang G,
Xu Y,
Wang G,
Yao H,
Dong P,
Jiao Y,
Shen M,
Yang J,
Ou-Yang J,
Jiang H,
Zhu Y,
Ren S,
Zhang Z,
Yin C,
Gao X,
Dai B,
Hu Z,
Yang Y,
Wu Q,
Chen H,
Peng P,
Zheng Y,
Zheng X,
Xiang Y,
Long J,
Gong J,
Na R,
Lin X,
Yu H,
Wang Z,
Tao S,
Feng J,
Sun J,
Liu W,
Hsing A,
Rao J,
Ding Q,
Wiklund F,
Gronberg H,
Shu XO,
Zheng W,
Shen H,
Jin L,
Shi R,
Lu D,
Zhang X,
Sun J,
Zheng SL,
Sun Y
Nature genetics · 2012 · PMID 23023329
1 page
A genome-wide association study in Han Chinese identifies a susceptibility locus for primary Sjögren's syndrome at 7q11.23
Li Y,
Zhang K,
Chen H,
Sun F,
Xu J,
Wu Z,
Li P,
Zhang L,
Du Y,
Luan H,
Li X,
Wu L
and 64 more — show all
Li H,
Wu H,
Li X,
Li X,
Zhang X,
Gong L,
Dai L,
Sun L,
Zuo X,
Xu J,
Gong H,
Li Z,
Tong S,
Wu M,
Li X,
Xiao W,
Wang G,
Zhu P,
Shen M,
Liu S,
Zhao D,
Liu W,
Wang Y,
Huang C,
Jiang Q,
Liu G,
Liu B,
Hu S,
Zhang W,
Zhang Z,
You X,
Li M,
Hao W,
Zhao C,
Leng X,
Bi L,
Wang Y,
Zhang F,
Shi Q,
Qi W,
Zhang X,
Jia Y,
Su J,
Li Q,
Hou Y,
Wu Q,
Xu D,
Zheng W,
Zhang M,
Wang Q,
Fei Y,
Zhang X,
Li J,
Jiang Y,
Tian X,
Zhao L,
Wang L,
Zhou B,
Li Y,
Zhao Y,
Zeng X,
Ott J,
Wang J,
Zhang F
Nature genetics · 2013 · PMID 24097066
1 page
Identification of Novel T1D Risk Loci and Their Association With Age and Islet Function at Diagnosis in Autoantibody-Positive T1D Individuals: Based on a Two-Stage Genome-Wide Association Study
Zhu M,
Xu K,
Chen Y,
Gu Y,
Zhang M,
Luo F,
Liu Y,
Gu W,
Hu J,
Xu H,
Xie Z,
Sun C
and 42 more — show all
Li Y,
Sun M,
Xu X,
Hsu HT,
Chen H,
Fu Q,
Shi Y,
Xu J,
Ji L,
Liu J,
Bian L,
Zhu J,
Chen S,
Xiao L,
Li X,
Jiang H,
Shen M,
Huang Q,
Fang C,
Li X,
Huang G,
Fan J,
Jiang Z,
Jiang Y,
Dai J,
Ma H,
Zheng S,
Cai Y,
Dai H,
Zheng X,
Zhou H,
Ni S,
Jin G,
She JX,
Yu L,
Polychronakos C,
Hu Z,
Zhou Z,
Weng J,
Weng J,
Shen H,
Yang T
Diabetes care · 2019 · PMID 31152121
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.