For researchers
Is your paper here?
2,651 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
Wan J.
Novel Susceptibility Loci for Moyamoya Disease Revealed by a Genome-Wide Association Study
Duan L,
Wei L,
Tian Y,
Zhang Z,
Hu P,
Wei Q,
Liu S,
Zhang J,
Wang Y,
Li D,
Yang W,
Zong R
and 25 more — show all
Xian P,
Han C,
Bao X,
Zhao F,
Feng J,
Liu W,
Cao W,
Zhou G,
Zhu C,
Yu F,
Yang W,
Meng Y,
Wang J,
Chen X,
Wang Y,
Shen B,
Zhao B,
Wan J,
Zhang F,
Zhao G,
Xu A,
Zhang X,
Liu J,
Zuo X,
Wang K
Stroke · 2018 · PMID 29273593
6 pages
A genome-wide association study in Han Chinese identifies multiple susceptibility loci for IgA nephropathy
Yu XQ,
Li M,
Zhang H,
Low HQ,
Wei X,
Wang JQ,
Sun LD,
Sim KS,
Li Y,
Foo JN,
Wang W,
Li ZJ
and 13 more — show all
Yin XY,
Tang XQ,
Fan L,
Chen J,
Li RS,
Wan JX,
Liu ZS,
Lou TQ,
Zhu L,
Huang XJ,
Zhang XJ,
Liu ZH,
Liu JJ
Nature genetics · 2011 · PMID 22197929
5 pages
Genome-wide analysis of multi-ancestry cohorts identifies new loci influencing intraocular pressure and susceptibility to glaucoma
Hysi PG,
Cheng CY,
Springelkamp H,
Macgregor S,
Bailey JNC,
Wojciechowski R,
Vitart V,
Nag A,
Hewitt AW,
Höhn R,
Venturini C,
Mirshahi A
and 79 more — show all
Ramdas WD,
Thorleifsson G,
Vithana E,
Khor CC,
Stefansson AB,
Liao J,
Haines JL,
Amin N,
Wang YX,
Wild PS,
Ozel AB,
Li JZ,
Fleck BW,
Zeller T,
Staffieri SE,
Teo YY,
Cuellar-Partida G,
Luo X,
Allingham RR,
Richards JE,
Senft A,
Karssen LC,
Zheng Y,
Bellenguez C,
Xu L,
Iglesias AI,
Wilson JF,
Kang JH,
van Leeuwen EM,
Jonsson V,
Thorsteinsdottir U,
Despriet DDG,
Ennis S,
Moroi SE,
Martin NG,
Jansonius NM,
Yazar S,
Tai ES,
Amouyel P,
Kirwan J,
van Koolwijk LME,
Hauser MA,
Jonasson F,
Leo P,
Loomis SJ,
Fogarty R,
Rivadeneira F,
Kearns L,
Lackner KJ,
de Jong PTVM,
Simpson CL,
Pennell CE,
Oostra BA,
Uitterlinden AG,
Saw SM,
Lotery AJ,
Bailey-Wilson JE,
Hofman A,
Vingerling JR,
Maubaret C,
Pfeiffer N,
Wolfs RCW,
Lemij HG,
Young TL,
Pasquale LR,
Delcourt C,
Spector TD,
Klaver CCW,
Small KS,
Burdon KP,
Stefansson K,
Wong TY,
Viswanathan A,
Mackey DA,
Craig JE,
Wiggs JL,
van Duijn CM,
Hammond CJ,
Aung T
BMES GWAS Group · NEIGHBORHOOD Consortium and 1 more consortia
Nature genetics · 2014 · PMID 25173106 · open access
4 pages
Meta-analysis of genome-wide association studies identifies two loci associated with circulating osteoprotegerin levels
Kwan JS,
Hsu YH,
Cheung CL,
Dupuis J,
Saint-Pierre A,
Eriksson J,
Handelman SK,
Aragaki A,
Karasik D,
Pramstaller PP,
Kooperberg C,
Lacroix AZ
and 13 more — show all
Larson MG,
Lau KS,
Lorentzon M,
Pichler I,
Sham PC,
Taliun D,
Vandenput L,
Kiel DP,
Hicks AA,
Jackson RD,
Ohlsson C,
Benjamin EJ,
Kung AW
Human molecular genetics · 2014 · PMID 25080503
2 pages
Genome-wide association analyses identified novel susceptibility loci for pulmonary embolism among Han Chinese population
Zhang Z,
Li H,
Weng H,
Zhou G,
Chen H,
Yang G,
Zhang P,
Zhang X,
Ji Y,
Ying K,
Liu B,
Xu Q
and 36 more — show all
Tang Y,
Zhu G,
Liu Z,
Xia S,
Yang X,
Dong L,
Zhu L,
Zeng M,
Yuan Y,
Yang Y,
Zhang N,
Xu X,
Pang W,
Zhang M,
Zhang Y,
Zhen K,
Wang D,
Lei J,
Wu S,
Shu S,
Zhang Y,
Zhang S,
Gao Q,
Huang Q,
Deng C,
Fu X,
Chen G,
Duan W,
Wan J,
Xie W,
Zhang P,
Wang S,
Yang P,
Zuo X,
Zhai Z,
Wang C
China pUlmonary Thromboembolism REgistry Study (CURES) investigators
BMC medicine · 2023 · PMID 37076872 · open access
2 pages
Genome-Wide Meta-Analysis Identifies Three Novel Susceptibility Loci and Reveals Ethnic Heterogeneity of Genetic Susceptibility for IgA Nephropathy
Li M,
Wang L,
Shi DC,
Foo JN,
Zhong Z,
Khor CC,
Lanzani C,
Citterio L,
Salvi E,
Yin PR,
Bei JX,
Wang L
and 13 more — show all
Liao YH,
Chen J,
Chen QK,
Xu G,
Jiang GR,
Wan JX,
Chen MH,
Chen N,
Zhang H,
Zeng YX,
Liu ZH,
Liu JJ,
Yu XQ
Journal of the American Society of Nephrology : JASN · 2020 · PMID 32912934
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.