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2,673 papers hold this site up. Every variant and condition page names
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Search your name, your journal, or a PMID.
4 matches for
Wang TD.
Association analyses of East Asian individuals and trans-ancestry analyses with European individuals reveal new loci associated with cholesterol and triglyceride levels
Spracklen CN,
Chen P,
Kim YJ,
Wang X,
Cai H,
Li S,
Long J,
Wu Y,
Wang YX,
Takeuchi F,
Wu JY,
Jung KJ
and 103 more — show all
Hu C,
Akiyama K,
Zhang Y,
Moon S,
Johnson TA,
Li H,
Dorajoo R,
He M,
Cannon ME,
Roman TS,
Salfati E,
Lin KH,
Guo X,
Sheu WHH,
Absher D,
Adair LS,
Assimes TL,
Aung T,
Cai Q,
Chang LC,
Chen CH,
Chien LH,
Chuang LM,
Chuang SC,
Du S,
Fan Q,
Fann CSJ,
Feranil AB,
Friedlander Y,
Gordon-Larsen P,
Gu D,
Gui L,
Guo Z,
Heng CK,
Hixson J,
Hou X,
Hsiung CA,
Hu Y,
Hwang MY,
Hwu CM,
Isono M,
Juang JJ,
Khor CC,
Kim YK,
Koh WP,
Kubo M,
Lee IT,
Lee SJ,
Lee WJ,
Liang KW,
Lim B,
Lim SH,
Liu J,
Nabika T,
Pan WH,
Peng H,
Quertermous T,
Sabanayagam C,
Sandow K,
Shi J,
Sun L,
Tan PC,
Tan SP,
Taylor KD,
Teo YY,
Toh SA,
Tsunoda T,
van Dam RM,
Wang A,
Wang F,
Wang J,
Wei WB,
Xiang YB,
Yao J,
Yuan JM,
Zhang R,
Zhao W,
Chen YI,
Rich SS,
Rotter JI,
Wang TD,
Wu T,
Lin X,
Han BG,
Tanaka T,
Cho YS,
Katsuya T,
Jia W,
Jee SH,
Chen YT,
Kato N,
Jonas JB,
Cheng CY,
Shu XO,
He J,
Zheng W,
Zheng W,
Wong TY,
Huang W,
Kim BJ,
Tai ES,
Mohlke KL,
Sim X
Human molecular genetics · 2017 · PMID 28334899
12 pages+
Identification of new susceptibility loci for type 2 diabetes and shared etiological pathways with coronary heart disease
Zhao W,
Rasheed A,
Tikkanen E,
Lee JJ,
Butterworth AS,
Howson JMM,
Assimes TL,
Chowdhury R,
Orho-Melander M,
Damrauer S,
Small A,
Asma S
and 78 more — show all
Imamura M,
Yamauch T,
Chambers JC,
Chen P,
Sapkota BR,
Shah N,
Jabeen S,
Surendran P,
Lu Y,
Zhang W,
Imran A,
Abbas S,
Majeed F,
Trindade K,
Qamar N,
Mallick NH,
Yaqoob Z,
Saghir T,
Rizvi SNH,
Memon A,
Rasheed SZ,
Memon FU,
Mehmood K,
Ahmed N,
Qureshi IH,
Tanveer-Us-Salam,
Iqbal W,
Malik U,
Mehra N,
Kuo JZ,
Sheu WH,
Guo X,
Hsiung CA,
Juang JJ,
Taylor KD,
Hung YJ,
Lee WJ,
Quertermous T,
Lee IT,
Hsu CC,
Bottinger EP,
Ralhan S,
Teo YY,
Wang TD,
Alam DS,
Di Angelantonio E,
Epstein S,
Nielsen SF,
Nordestgaard BG,
Tybjaerg-Hansen A,
Young R,
Benn M,
Frikke-Schmidt R,
Kamstrup PR,
Jukema JW,
Sattar N,
Smit R,
Chung RH,
Liang KW,
Anand S,
Sanghera DK,
Ripatti S,
Loos RJF,
Kooner JS,
Tai ES,
Rotter JI,
Chen YI,
Frossard P,
Maeda S,
Kadowaki T,
Reilly M,
Pare G,
Melander O,
Salomaa V,
Rader DJ,
Danesh J,
Voight BF,
Saleheen D
CHD Exome+ Consortium · EPIC-CVD Consortium and 2 more consortia
Nature genetics · 2017 · PMID 28869590 · open access
11 pages
Meta-analysis of genome-wide association studies in East Asian-ancestry populations identifies four new loci for body mass index
Wen W,
Zheng W,
Zheng W,
Okada Y,
Takeuchi F,
Tabara Y,
Hwang JY,
Dorajoo R,
Li H,
Tsai FJ,
Yang X,
He J
and 98 more — show all
Wu Y,
He M,
Zhang Y,
Liang J,
Guo X,
Sheu WH,
Delahanty R,
Guo X,
Kubo M,
Yamamoto K,
Ohkubo T,
Go MJ,
Liu JJ,
Gan W,
Chen CC,
Gao Y,
Li S,
Lee NR,
Wu C,
Zhou X,
Song H,
Yao J,
Lee IT,
Long J,
Tsunoda T,
Akiyama K,
Takashima N,
Cho YS,
Ong RT,
Lu L,
Chen CH,
Tan A,
Rice TK,
Adair LS,
Gui L,
Allison M,
Lee WJ,
Cai Q,
Isomura M,
Umemura S,
Kim YJ,
Seielstad M,
Hixson J,
Xiang YB,
Isono M,
Kim BJ,
Sim X,
Lu W,
Nabika T,
Lee J,
Lim WY,
Gao YT,
Takayanagi R,
Kang DH,
Wong TY,
Hsiung CA,
Wu IC,
Juang JM,
Shi J,
Choi BY,
Aung T,
Hu F,
Kim MK,
Lim WY,
Wang TD,
Shin MH,
Lee J,
Ji BT,
Lee YH,
Young TL,
Shin DH,
Chun BY,
Cho MC,
Han BG,
Hwu CM,
Assimes TL,
Absher D,
Yan X,
Kim E,
Kuo JZ,
Kwon S,
Taylor KD,
Chen YD,
Rotter JI,
Qi L,
Zhu D,
Wu T,
Mohlke KL,
Gu D,
Mo Z,
Wu JY,
Lin X,
Miki T,
Tai ES,
Lee JY,
Kato N,
Shu XO,
Tanaka T
Human molecular genetics · 2014 · PMID 24861553
4 pages
Multi-ancestry genome-wide gene-smoking interaction study of 387,272 individuals identifies new loci associated with serum lipids
Bentley AR,
Sung YJ,
Brown MR,
Winkler TW,
Kraja AT,
Ntalla I,
Schwander K,
Chasman DI,
Lim E,
Deng X,
Guo X,
Liu J
and 290 more — show all
Lu Y,
Cheng CY,
Sim X,
Vojinovic D,
Huffman JE,
Musani SK,
Li C,
Feitosa MF,
Richard MA,
Noordam R,
Baker J,
Chen G,
Aschard H,
Bartz TM,
Ding J,
Dorajoo R,
Manning AK,
Rankinen T,
Smith AV,
Tajuddin SM,
Zhao W,
Graff M,
Alver M,
Boissel M,
Chai JF,
Chen X,
Divers J,
Evangelou E,
Gao C,
Goel A,
Hagemeijer Y,
Harris SE,
Hartwig FP,
He M,
Horimoto ARVR,
Hsu FC,
Hung YJ,
Jackson AU,
Kasturiratne A,
Komulainen P,
Kühnel B,
Leander K,
Lin KH,
Luan J,
Lyytikäinen LP,
Matoba N,
Nolte IM,
Pietzner M,
Prins B,
Riaz M,
Robino A,
Said MA,
Schupf N,
Scott RA,
Sofer T,
Stancáková A,
Takeuchi F,
Tayo BO,
van der Most PJ,
Varga TV,
Wang TD,
Wang Y,
Ware EB,
Wen W,
Xiang YB,
Yanek LR,
Zhang W,
Zhao JH,
Adeyemo A,
Afaq S,
Amin N,
Amini M,
Arking DE,
Arzumanyan Z,
Aung T,
Ballantyne C,
Barr RG,
Bielak LF,
Boerwinkle E,
Bottinger EP,
Broeckel U,
Brown M,
Cade BE,
Campbell A,
Canouil M,
Charumathi S,
Chen YI,
Christensen K,
Concas MP,
Connell JM,
de las Fuentes L,
de Silva HJ,
de Vries PS,
Doumatey A,
Duan Q,
Eaton CB,
Eppinga RN,
Faul JD,
Floyd JS,
Forouhi NG,
Forrester T,
Friedlander Y,
Gandin I,
Gao H,
Ghanbari M,
Gharib SA,
Gigante B,
Giulianini F,
Grabe HJ,
Gu CC,
Harris TB,
Heikkinen S,
Heng CK,
Hirata M,
Hixson JE,
Ikram MA,
Jia Y,
Joehanes R,
Johnson C,
Jonas JB,
Justice AE,
Katsuya T,
Khor CC,
Kilpeläinen TO,
Koh WP,
Kolcic I,
Kooperberg C,
Krieger JE,
Kritchevsky SB,
Kubo M,
Kuusisto J,
Lakka TA,
Langefeld CD,
Langenberg C,
Launer LJ,
Lehne B,
Lewis CE,
Li Y,
Liang J,
Lin S,
Liu CT,
Liu J,
Liu K,
Loh M,
Lohman KK,
Louie T,
Luzzi A,
Mägi R,
Mahajan A,
Manichaikul AW,
McKenzie CA,
Meitinger T,
Metspalu A,
Milaneschi Y,
Milani L,
Mohlke KL,
Momozawa Y,
Morris AP,
Murray AD,
Nalls MA,
Nauck M,
Nelson CP,
North KE,
O'Connell JR,
Palmer ND,
Papanicolau GJ,
Pedersen NL,
Peters A,
Peyser PA,
Polasek O,
Poulter N,
Raitakari OT,
Reiner AP,
Renström F,
Rice TK,
Rich SS,
Robinson JG,
Rose LM,
Rosendaal FR,
Rudan I,
Schmidt CO,
Schreiner PJ,
Scott WR,
Sever P,
Shi Y,
Sidney S,
Sims M,
Smith JA,
Snieder H,
Starr JM,
Strauch K,
Stringham HM,
Tan NYQ,
Tang H,
Taylor KD,
Teo YY,
Tham YC,
Tiemeier H,
Turner ST,
Uitterlinden AG,
van Heemst D,
Waldenberger M,
Wang H,
Wang L,
Wang L,
Wei WB,
Williams CA,
Wilson G Sr,
Wojczynski MK,
Yao J,
Young K,
Yu C,
Yuan JM,
Zhou J,
Zonderman AB,
Becker DM,
Boehnke M,
Bowden DW,
Chambers JC,
Cooper RS,
de Faire U,
Deary IJ,
Elliott P,
Esko T,
Farrall M,
Franks PW,
Freedman BI,
Froguel P,
Gasparini P,
Gieger C,
Horta BL,
Juang JJ,
Kamatani Y,
Kammerer CM,
Kato N,
Kooner JS,
Laakso M,
Laurie CC,
Lee IT,
Lehtimäki T,
Magnusson PKE,
Oldehinkel AJ,
Penninx BWJH,
Pereira AC,
Rauramaa R,
Redline S,
Samani NJ,
Scott J,
Shu XO,
van der Harst P,
Wagenknecht LE,
Wang JS,
Wang YX,
Wareham NJ,
Watkins H,
Weir DR,
Wickremasinghe AR,
Wu T,
Zeggini E,
Zheng W,
Zheng W,
Bouchard C,
Evans MK,
Gudnason V,
Kardia SLR,
Liu Y,
Psaty BM,
Ridker PM,
van Dam RM,
Mook-Kanamori DO,
Fornage M,
Province MA,
Kelly TN,
Fox ER,
Hayward C,
van Duijn CM,
Tai ES,
Wong TY,
Loos RJF,
Franceschini N,
Rotter JI,
Zhu X,
Bierut LJ,
Gauderman WJ,
Rice K,
Munroe PB,
Morrison AC,
Rao DC,
Rotimi CN,
Cupples LA
COGENT-Kidney Consortium · EPIC-InterAct Consortium and 2 more consortia
Nature genetics · 2019 · PMID 30926973 · 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.