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Is your paper here?
2,665 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.
8 matches for
Huang Q.
Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations
Chen MH,
Raffield LM,
Mousas A,
Sakaue S,
Huffman JE,
Moscati A,
Trivedi B,
Jiang T,
Akbari P,
Vuckovic D,
Bao EL,
Zhong X
and 98 more — show all
Manansala R,
Laplante V,
Chen M,
Lo KS,
Qian H,
Lareau CA,
Beaudoin M,
Hunt KA,
Akiyama M,
Bartz TM,
Ben-Shlomo Y,
Beswick A,
Bork-Jensen J,
Bottinger EP,
Brody JA,
van Rooij FJA,
Chitrala K,
Cho K,
Choquet H,
Correa A,
Danesh J,
Di Angelantonio E,
Dimou N,
Ding J,
Elliott P,
Esko T,
Evans MK,
Floyd JS,
Broer L,
Grarup N,
Guo MH,
Greinacher A,
Haessler J,
Hansen T,
Howson JMM,
Huang QQ,
Huang W,
Jorgenson E,
Kacprowski T,
Kähönen M,
Kamatani Y,
Kanai M,
Karthikeyan S,
Koskeridis F,
Lange LA,
Lehtimäki T,
Lerch MM,
Linneberg A,
Liu Y,
Lyytikäinen LP,
Manichaikul A,
Martin HC,
Matsuda K,
Mohlke KL,
Mononen N,
Murakami Y,
Nadkarni GN,
Nauck M,
Nikus K,
Ouwehand WH,
Pankratz N,
Pedersen O,
Preuss M,
Psaty BM,
Raitakari OT,
Roberts DJ,
Rich SS,
Rodriguez BAT,
Rosen JD,
Rotter JI,
Schubert P,
Spracklen CN,
Surendran P,
Tang H,
Tardif JC,
Trembath RC,
Ghanbari M,
Völker U,
Völzke H,
Watkins NA,
Zonderman AB,
Wilson PWF,
Li Y,
Butterworth AS,
Gauchat JF,
Chiang CWK,
Li B,
Loos RJF,
Astle WJ,
Evangelou E,
van Heel DA,
Sankaran VG,
Okada Y,
Soranzo N,
Johnson AD,
Reiner AP,
Auer PL,
Lettre G
VA Million Veteran Program
Cell · 2020 · PMID 32888493
12 pages+
Multi-ancestry genome-wide association study of major depression aids locus discovery, fine mapping, gene prioritization and causal inference
Meng X,
Navoly G,
Giannakopoulou O,
Levey DF,
Koller D,
Pathak GA,
Koen N,
Lin K,
Adams MJ,
Rentería ME,
Feng Y,
Gaziano JM
and 66 more — show all
Stein DJ,
Zar HJ,
Campbell ML,
van Heel DA,
Trivedi B,
Finer S,
McQuillin A,
Bass N,
Chundru VK,
Martin HC,
Huang QQ,
Valkovskaya M,
Chu CY,
Kanjira S,
Kuo PH,
Chen HC,
Tsai SJ,
Liu YL,
Kendler KS,
Peterson RE,
Cai N,
Fang Y,
Sen S,
Scott LJ,
Burmeister M,
Loos RJF,
Preuss MH,
Actkins KV,
Davis LK,
Uddin M,
Wani AH,
Wildman DE,
Aiello AE,
Ursano RJ,
Kessler RC,
Kanai M,
Okada Y,
Sakaue S,
Rabinowitz JA,
Maher BS,
Uhl G,
Eaton W,
Cruz-Fuentes CS,
Martinez-Levy GA,
Campos AI,
Millwood IY,
Chen Z,
Li L,
Wassertheil-Smoller S,
Jiang Y,
Tian C,
Martin NG,
Mitchell BL,
Byrne EM,
Awasthi S,
Coleman JRI,
Ripke S,
Sofer T,
Walters RG,
McIntosh AM,
Polimanti R,
Dunn EC,
Stein MB,
Gelernter J,
Lewis CM,
Kuchenbaecker K
PGC-MDD Working Group · China Kadoorie Biobank Collaborative Group and 3 more consortia
Nature genetics · 2024 · PMID 38177345 · open access
12 pages+
Genome-wide association study identifies a new susceptibility locus for cleft lip with or without a cleft palate
Sun Y,
Huang Y,
Yin A,
Pan Y,
Wang Y,
Wang C,
Du Y,
Wang M,
Lan F,
Hu Z,
Wang G,
Jiang M
and 17 more — show all
Ma J,
Zhang X,
Ma H,
Ma J,
Zhang W,
Huang Q,
Zhou Z,
Ma L,
Li Y,
Jiang H,
Xie L,
Jiang Y,
Shi B,
Cheng J,
Shen H,
Wang L,
Yang Y
Nature communications · 2015 · PMID 25775280
3 pages
A genome-wide association study identifies six novel risk loci for primary biliary cholangitis
Qiu F,
Tang R,
Zuo X,
Shi X,
Wei Y,
Zheng X,
Dai Y,
Gong Y,
Wang L,
Xu P,
Zhu X,
Wu J
and 78 more — show all
Han C,
Gao Y,
Zhang K,
Jiang Y,
Zhou J,
Shao Y,
Hu Z,
Tian Y,
Zhang H,
Dai N,
Liu L,
Wu X,
Zhao W,
Zhang X,
Zang Z,
Nie J,
Sun W,
Zhao Y,
Mao Y,
Jiang P,
Ji H,
Dong Q,
Li J,
Li Z,
Bai X,
Li L,
Lin M,
Dong M,
Li J,
Zhu P,
Wang C,
Zhang Y,
Jiang P,
Wang Y,
Jawed R,
Xu J,
Zhang Y,
Wang Q,
Yang Y,
Yang F,
Lian M,
Jiang X,
Xiao X,
Li Y,
Fang J,
Qiu D,
Zhu Z,
Qiu H,
Zhang J,
Tian W,
Chen S,
Jiang L,
Ji B,
Li P,
Chen G,
Wu T,
Sun Y,
Yu J,
Tang H,
He M,
Xia M,
Pei H,
Huang L,
Qing Z,
Wu J,
Huang Q,
Han J,
Xie W,
Sun Z,
Guo J,
He G,
Eric Gershwin M,
Lian Z,
Liu X,
Seldin MF,
Liu X,
Chen W,
Ma X
Nature communications · 2017 · PMID 28425483 · open access
2 pages
Identification of new susceptibility loci associated with rheumatoid arthritis
Leng RX,
Di DS,
Ni J,
Wu XX,
Zhang LL,
Wang XF,
Liu RS,
Huang Q,
Fan YG,
Pan HF,
Wang B,
Ye DQ
Annals of the rheumatic diseases · 2020 · PMID 32868391
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
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
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.