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Is your paper here?
2,663 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
Zhou L.
Genome-wide association studies of autoimmune vitiligo identify 23 new risk loci and highlight key pathways and regulatory variants
Jin Y,
Andersen G,
Yorgov D,
Ferrara TM,
Ben S,
Brownson KM,
Holland PJ,
Birlea SA,
Siebert J,
Hartmann A,
Lienert A,
van Geel N
and 32 more — show all
Lambert J,
Luiten RM,
Wolkerstorfer A,
Wietze van der Veen JP,
Bennett DC,
Taïeb A,
Ezzedine K,
Kemp EH,
Gawkrodger DJ,
Weetman AP,
Kõks S,
Prans E,
Kingo K,
Karelson M,
Wallace MR,
McCormack WT,
Overbeck A,
Moretti S,
Colucci R,
Picardo M,
Silverberg NB,
Olsson M,
Valle Y,
Korobko I,
Böhm M,
Lim HW,
Hamzavi I,
Zhou L,
Mi QS,
Fain PR,
Santorico SA,
Spritz RA
Nature genetics · 2016 · PMID 27723757 · open access
12 pages+
Meta-analysis of gene-environment-wide association scans accounting for education level identifies additional loci for refractive error
Fan Q,
Verhoeven VJ,
Wojciechowski R,
Barathi VA,
Hysi PG,
Guggenheim JA,
Höhn R,
Vitart V,
Khawaja AP,
Yamashiro K,
Hosseini SM,
Lehtimäki T
and 142 more — show all
Lu Y,
Haller T,
Xie J,
Delcourt C,
Pirastu M,
Wedenoja J,
Gharahkhani P,
Venturini C,
Miyake M,
Hewitt AW,
Guo X,
Mazur J,
Huffman JE,
Williams KM,
Polasek O,
Campbell H,
Rudan I,
Vatavuk Z,
Wilson JF,
Joshi PK,
McMahon G,
St Pourcain B,
Evans DM,
Simpson CL,
Schwantes-An TH,
Igo RP,
Mirshahi A,
Cougnard-Gregoire A,
Bellenguez C,
Blettner M,
Raitakari O,
Kähönen M,
Seppala I,
Zeller T,
Meitinger T,
Ried JS,
Gieger C,
Portas L,
van Leeuwen EM,
Amin N,
Uitterlinden AG,
Rivadeneira F,
Hofman A,
Vingerling JR,
Wang YX,
Wang X,
Tai-Hui Boh E,
Ikram MK,
Sabanayagam C,
Gupta P,
Tan V,
Zhou L,
Ho CE,
Lim W,
Beuerman RW,
Siantar R,
Tai ES,
Vithana E,
Mihailov E,
Khor CC,
Hayward C,
Luben RN,
Foster PJ,
Klein BE,
Klein R,
Wong HS,
Mitchell P,
Metspalu A,
Aung T,
Young TL,
He M,
Pärssinen O,
van Duijn CM,
Jin Wang J,
Williams C,
Jonas JB,
Teo YY,
Mackey DA,
Oexle K,
Yoshimura N,
Paterson AD,
Pfeiffer N,
Wong TY,
Baird PN,
Stambolian D,
Wilson JE,
Cheng CY,
Hammond CJ,
Klaver CC,
Saw SM,
Rahi JS,
Korobelnik JF,
Kemp JP,
Timpson NJ,
Smith GD,
Craig JE,
Burdon KP,
Fogarty RD,
Iyengar SK,
Chew E,
Janmahasatian S,
Martin NG,
MacGregor S,
Xu L,
Schache M,
Nangia V,
Panda-Jonas S,
Wright AF,
Fondran JR,
Lass JH,
Feng S,
Zhao JH,
Khaw KT,
Wareham NJ,
Rantanen T,
Kaprio J,
Pang CP,
Chen LJ,
Tam PO,
Jhanji V,
Young AL,
Döring A,
Raffel LJ,
Cotch MF,
Li X,
Yip SP,
Yap MK,
Biino G,
Vaccargiu S,
Fossarello M,
Fleck B,
Yazar S,
Tideman JW,
Tedja M,
Deangelis MM,
Morrison M,
Farrer L,
Zhou X,
Chen W,
Mizuki N,
Meguro A,
Mäkelä KM
Consortium for Refractive Error and Myopia
Nature communications · 2016 · PMID 27020472 · open access
10 pages
Trans-ethnic genome-wide association study of blood metabolites in the Chronic Renal Insufficiency Cohort (CRIC) study
Rhee EP,
Surapaneni A,
Zheng Z,
Zhou L,
Dutta D,
Arking DE,
Zhang J,
Duong T,
Chatterjee N,
Luo S,
Schlosser P,
Mehta R
and 14 more — show all
Waikar SS,
Saraf SL,
Kelly TN,
Hamm LL,
Rao PS,
Mathew AV,
Hsu CY,
Parsa A,
Vasan RS,
Kimmel PL,
Clish CB,
Coresh J,
Feldman HI,
Grams ME
CKD Biomarkers Consortium and the Chronic Renal Insufficiency Cohort (CRIC) Study Investigators
Kidney international · 2022 · PMID 35120996
3 pages
A genome-wide association study identifies two new cervical cancer susceptibility loci at 4q12 and 17q12
Shi Y,
Li L,
Hu Z,
Li S,
Wang S,
Liu J,
Wu C,
He L,
Zhou J,
Li Z,
Hu T,
Chen Y
and 72 more — show all
Jia Y,
Wang S,
Wu L,
Cheng X,
Yang Z,
Yang R,
Li X,
Huang K,
Zhang Q,
Zhou H,
Tang F,
Chen Z,
Shen J,
Jiang J,
Ding H,
Xing H,
Zhang S,
Qu P,
Song X,
Lin Z,
Deng D,
Xi L,
Lv W,
Han X,
Tao G,
Yan L,
Han Z,
Li Z,
Miao X,
Pan S,
Shen Y,
Wang H,
Liu D,
Gong E,
Li Z,
Zhou L,
Luan X,
Wang C,
Song Q,
Wu S,
Xu H,
Shen J,
Qiang F,
Ma G,
Liu L,
Chen X,
Liu J,
Wu J,
Shen Y,
Wen Y,
Chu M,
Yu J,
Hu X,
Fan Y,
He H,
Jiang Y,
Lei Z,
Liu C,
Chen J,
Zhang Y,
Yi C,
Chen S,
Li W,
Wang D,
Wang Z,
Di W,
Shen K,
Lin D,
Shen H,
Feng Y,
Xie X,
Ma D
Nature genetics · 2013 · PMID 23817570
2 pages
Novel risk loci for rheumatoid arthritis in Han Chinese and congruence with risk variants in Europeans
Jiang L,
Yin J,
Ye L,
Yang J,
Hemani G,
Liu AJ,
Zou H,
He D,
Sun L,
Zeng X,
Li Z,
Zheng Y
and 61 more — show all
Lin Y,
Liu Y,
Fang Y,
Xu J,
Li Y,
Dai S,
Guan J,
Jiang L,
Wei Q,
Wang Y,
Li Y,
Huang C,
Zuo X,
Liu Y,
Wu X,
Zhang L,
Zhou L,
Zhang Q,
Li T,
Chen L,
Xu Z,
Yang X,
Qian F,
Xie W,
Liu W,
Guo Q,
Huang S,
Zhao J,
Li M,
Jin Y,
Gao J,
Lv Y,
Wang Y,
Lin L,
Guo A,
Danoy P,
Willner D,
Cremin C,
Hadler J,
Zhang F,
Zhao Y,
Li M,
Yue T,
Fan X,
Guo J,
Mu R,
Li J,
Wu C,
Zeng M,
Wang J,
Li S,
Jin L,
Wang B,
Wang J,
Ma X,
Sun L,
Zhang X,
Brown MA,
Visscher PM,
Su DF,
Xu H
Arthritis & rheumatology (Hoboken, N.J.) · 2014 · PMID 24782177
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
A genome wide association study identifies common variants associated with lipid levels in the Chinese population
Zhou L,
He M,
Mo Z,
Wu C,
Yang H,
Yu D,
Yang X,
Zhang X,
Wang Y,
Sun J,
Gao Y,
Tan A
and 31 more — show all
He Y,
Zhang H,
Qin X,
Zhu J,
Li H,
Lin X,
Zhu J,
Min X,
Lang M,
Li D,
Zhai K,
Chang J,
Tan W,
Yuan J,
Chen W,
Wang Y,
Wei S,
Miao X,
Wang F,
Fang W,
Liang Y,
Deng Q,
Dai X,
Lin D,
Huang S,
Guo H,
Lilly Zheng S,
Xu J,
Lin D,
Hu FB,
Wu T
PloS one · 2013 · PMID 24386095 · open access
1 page
A genome-wide association study identifies common variants influencing serum uric acid concentrations in a Chinese population
Yang B,
Mo Z,
Wu C,
Yang H,
Yang X,
He Y,
Gui L,
Zhou L,
Guo H,
Zhang X,
Yuan J,
Dai X
and 17 more — show all
Li J,
Qiu G,
Huang S,
Deng Q,
Feng Y,
Guan L,
Hu D,
Zhang X,
Wang T,
Zhu J,
Min X,
Lang M,
Li D,
Hu FB,
Lin D,
Wu T,
He M
BMC medical genomics · 2014 · PMID 24513273 · open access
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.