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2,657 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
Yao C.
Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals
Surendran P,
Feofanova EV,
Lahrouchi N,
Ntalla I,
Karthikeyan S,
Cook J,
Chen L,
Mifsud B,
Yao C,
Kraja AT,
Cartwright JH,
Hellwege JN
and 269 more — show all
Giri A,
Tragante V,
Thorleifsson G,
Liu DJ,
Prins BP,
Stewart ID,
Cabrera CP,
Eales JM,
Akbarov A,
Auer PL,
Bielak LF,
Bis JC,
Braithwaite VS,
Brody JA,
Daw EW,
Warren HR,
Drenos F,
Nielsen SF,
Faul JD,
Fauman EB,
Fava C,
Ferreira T,
Foley CN,
Franceschini N,
Gao H,
Giannakopoulou O,
Giulianini F,
Gudbjartsson DF,
Guo X,
Harris SE,
Havulinna AS,
Helgadottir A,
Huffman JE,
Hwang SJ,
Kanoni S,
Kontto J,
Larson MG,
Li-Gao R,
Lindström J,
Lotta LA,
Lu Y,
Luan J,
Mahajan A,
Malerba G,
Masca NGD,
Mei H,
Menni C,
Mook-Kanamori DO,
Mosen-Ansorena D,
Müller-Nurasyid M,
Paré G,
Paul DS,
Perola M,
Poveda A,
Rauramaa R,
Richard M,
Richardson TG,
Sepúlveda N,
Sim X,
Smith AV,
Smith JA,
Staley JR,
Stanáková A,
Sulem P,
Thériault S,
Thorsteinsdottir U,
Trompet S,
Varga TV,
Velez Edwards DR,
Veronesi G,
Weiss S,
Willems SM,
Yao J,
Young R,
Yu B,
Zhang W,
Zhao JH,
Zhao W,
Zhao W,
Evangelou E,
Aeschbacher S,
Asllanaj E,
Blankenberg S,
Bonnycastle LL,
Bork-Jensen J,
Brandslund I,
Braund PS,
Burgess S,
Cho K,
Christensen C,
Connell J,
Mutsert R,
Dominiczak AF,
Dörr M,
Eiriksdottir G,
Farmaki AE,
Gaziano JM,
Grarup N,
Grove ML,
Hallmans G,
Hansen T,
Have CT,
Heiss G,
Jørgensen ME,
Jousilahti P,
Kajantie E,
Kamat M,
Käräjämäki A,
Karpe F,
Koistinen HA,
Kovesdy CP,
Kuulasmaa K,
Laatikainen T,
Lannfelt L,
Lee IT,
Lee WJ,
Linneberg A,
Martin LW,
Moitry M,
Nadkarni G,
Neville MJ,
Palmer CNA,
Papanicolaou GJ,
Pedersen O,
Peters J,
Poulter N,
Rasheed A,
Rasmussen KL,
Rayner NW,
Mägi R,
Renström F,
Rettig R,
Rossouw J,
Schreiner PJ,
Sever PS,
Sigurdsson EL,
Skaaby T,
Sun YV,
Sundstrom J,
Thorgeirsson G,
Esko T,
Trabetti E,
Tsao PS,
Tuomi T,
Turner ST,
Tzoulaki I,
Vaartjes I,
Vergnaud AC,
Willer CJ,
Wilson PWF,
Witte DR,
Yonova-Doing E,
Zhang H,
Aliya N,
Almgren P,
Amouyel P,
Asselbergs FW,
Barnes MR,
Blakemore AI,
Boehnke M,
Bots ML,
Bottinger EP,
Buring JE,
Chambers JC,
Chen YI,
Chowdhury R,
Conen D,
Correa A,
Davey Smith G,
Boer RA,
Deary IJ,
Dedoussis G,
Deloukas P,
Di Angelantonio E,
Elliott P,
Felix SB,
Ferrières J,
Ford I,
Fornage M,
Franks PW,
Franks S,
Frossard P,
Gambaro G,
Gaunt TR,
Groop L,
Gudnason V,
Harris TB,
Hayward C,
Hennig BJ,
Herzig KH,
Ingelsson E,
Tuomilehto J,
Järvelin MR,
Jukema JW,
Kardia SLR,
Kee F,
Kooner JS,
Kooperberg C,
Launer LJ,
Lind L,
Loos RJF,
Majumder AAS,
Laakso M,
McCarthy MI,
Melander O,
Mohlke KL,
Murray AD,
Nordestgaard BG,
Orho-Melander M,
Packard CJ,
Padmanabhan S,
Palmas W,
Polasek O,
Porteous DJ,
Prentice AM,
Province MA,
Relton CL,
Rice K,
Ridker PM,
Rolandsson O,
Rosendaal FR,
Rotter JI,
Rudan I,
Salomaa V,
Samani NJ,
Sattar N,
Sheu WH,
Smith BH,
Soranzo N,
Spector TD,
Starr JM,
Sebert S,
Taylor KD,
Lakka TA,
Timpson NJ,
Tobin MD,
van der Harst P,
van der Meer P,
Ramachandran VS,
Verweij N,
Virtamo J,
Völker U,
Weir DR,
Zeggini E,
Charchar FJ,
Wareham NJ,
Langenberg C,
Tomaszewski M,
Butterworth AS,
Caulfield MJ,
Danesh J,
Edwards TL,
Holm H,
Hung AM,
Lindgren CM,
Liu C,
Manning AK,
Morris AP,
Morrison AC,
O'Donnell CJ,
Psaty BM,
Saleheen D,
Stefansson K,
Boerwinkle E,
Chasman DI,
Levy D,
Newton-Cheh C,
Munroe PB,
Howson JMM
LifeLines Cohort Study · EPIC-CVD and 3 more consortia
Nature genetics · 2020 · PMID 33230300 · open access
12 pages+
Genome-wide association study in Chinese identifies novel loci for blood pressure and hypertension
Lu X,
Wang L,
Lin X,
Huang J,
Charles Gu C,
He M,
Shen H,
He J,
Zhu J,
Li H,
Hixson JE,
Wu T
and 37 more — show all
Dai J,
Lu L,
Shen C,
Chen S,
He L,
Mo Z,
Hao Y,
Mo X,
Yang X,
Li J,
Cao J,
Chen J,
Fan Z,
Li Y,
Zhao L,
Li H,
Lu F,
Yao C,
Yu L,
Xu L,
Mu J,
Wu X,
Deng Y,
Hu D,
Zhang W,
Ji X,
Guo D,
Guo Z,
Zhou Z,
Yang Z,
Wang R,
Yang J,
Zhou X,
Yan W,
Sun N,
Gao P,
Gu D
Human molecular genetics · 2015 · PMID 25249183
5 pages
GWAS of Chronic Spontaneous Urticaria Reveals Genetic Overlap with Autoimmune Diseases, Not Atopic Diseases
Zhang L,
Qiu L,
Wu J,
Qi Y,
Gao X,
He C,
Qi R,
Wang H,
Yao X,
Zhu H,
Li Y,
Hao S
and 33 more — show all
Lu Q,
Long H,
Lian S,
Zhu W,
Zhang H,
Lai W,
Su X,
Lu R,
Guo Z,
Li J,
Li M,
Liu Q,
Wang H,
He L,
Nong X,
Li F,
Li Y,
Yao C,
Xu J,
Tang H,
Wang D,
Li Z,
Yu H,
Xiao S,
An J,
Pu X,
Yu S,
Zhang J,
Chen X,
Wang H,
Huang W,
Chen H,
Xiao T
The Journal of investigative dermatology · 2023 · PMID 35933036
4 pages
Genome-wide mapping of plasma protein QTLs identifies putatively causal genes and pathways for cardiovascular disease
Yao C,
Chen G,
Song C,
Keefe J,
Mendelson M,
Huan T,
Sun BB,
Laser A,
Maranville JC,
Wu H,
Ho JE,
Courchesne P
and 12 more — show all
Lyass A,
Larson MG,
Gieger C,
Graumann J,
Johnson AD,
Danesh J,
Runz H,
Hwang SJ,
Liu C,
Butterworth AS,
Suhre K,
Levy D
Nature communications · 2018 · PMID 30111768 · open access
2 pages
Genetic Landscape of the ACE2 Coronavirus Receptor
Yang Z,
Macdonald-Dunlop E,
Chen J,
Zhai R,
Li T,
Richmond A,
Klarić L,
Pirastu N,
Ning Z,
Zheng C,
Wang Y,
Huang T
and 57 more — show all
He Y,
Guo H,
Ying K,
Gustafsson S,
Prins B,
Ramisch A,
Dermitzakis ET,
Png G,
Eriksson N,
Haessler J,
Hu X,
Zanetti D,
Boutin T,
Hwang SJ,
Wheeler E,
Pietzner M,
Raffield LM,
Kalnapenkis A,
Peters JE,
Viñuela A,
Gilly A,
Elmståhl S,
Dedoussis G,
Petrie JR,
Polašek O,
Folkersen L,
Chen Y,
Yao C,
Võsa U,
Pairo-Castineira E,
Clohisey S,
Bretherick AD,
Rawlik K,
Esko T,
Enroth S,
Johansson Å,
Gyllensten U,
Langenberg C,
Levy D,
Hayward C,
Assimes TL,
Kooperberg C,
Manichaikul AW,
Siegbahn A,
Wallentin L,
Lind L,
Zeggini E,
Schwenk JM,
Butterworth AS,
Michaëlsson K,
Pawitan Y,
Joshi PK,
Baillie JK,
Mälarstig A,
Reiner AP,
Wilson JF,
Shen X
GenOMICC Consortium† · IMI-DIRECT Consortium†
Circulation · 2022 · PMID 35387486 · open access
2 pages
Genome-wide association study in Han Chinese identifies four new susceptibility loci for coronary artery disease
Lu X,
Wang L,
Chen S,
He L,
Yang X,
Shi Y,
Cheng J,
Zhang L,
Gu CC,
Huang J,
Wu T,
Ma Y
and 68 more — show all
Li J,
Cao J,
Chen J,
Ge D,
Fan Z,
Li Y,
Zhao L,
Li H,
Zhou X,
Chen L,
Liu D,
Chen J,
Duan X,
Hao Y,
Wang L,
Lu F,
Liu Z,
Yao C,
Shen C,
Pu X,
Yu L,
Fang X,
Xu L,
Mu J,
Wu X,
Zheng R,
Wu N,
Zhao Q,
Li Y,
Liu X,
Wang M,
Yu D,
Hu D,
Ji X,
Guo D,
Sun D,
Wang Q,
Yang Y,
Liu F,
Mao Q,
Liang X,
Ji J,
Chen P,
Mo X,
Li D,
Chai G,
Tang Y,
Li X,
Du Z,
Liu X,
Dou C,
Yang Z,
Meng Q,
Wang D,
Wang R,
Yang J,
Schunkert H,
Samani NJ,
Kathiresan S,
Reilly MP,
Erdmann J,
Peng X,
Wu X,
Liu D,
Yang Y,
Chen R,
Qiang B,
Gu D
Coronary ARtery DIsease Genome-Wide Replication And Meta-Analysis (CARDIoGRAM) Consortium
Nature genetics · 2012 · PMID 22751097
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.