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44 matches for
Kim B,
showing the first 20.
Meta-analysis of genome-wide association studies of adult height in East Asians identifies 17 novel loci
He M,
Xu M,
Zhang B,
Liang J,
Chen P,
Lee JY,
Johnson TA,
Li H,
Yang X,
Dai J,
Liang L,
Gui L
and 79 more — show all
Qi Q,
Huang J,
Li Y,
Adair LS,
Aung T,
Cai Q,
Cheng CY,
Cho MC,
Cho YS,
Chu M,
Cui B,
Gao YT,
Go MJ,
Gu D,
Gu W,
Guo H,
Hao Y,
Hong J,
Hu Z,
Hu Y,
Huang J,
Hwang JY,
Ikram MK,
Jin G,
Kang DH,
Khor CC,
Kim BJ,
Kim HT,
Kubo M,
Lee J,
Lee J,
Lee NR,
Li R,
Li J,
Liu J,
Longe J,
Lu W,
Lu X,
Miao X,
Okada Y,
Ong RT,
Qiu G,
Seielstad M,
Sim X,
Song H,
Takeuchi F,
Tanaka T,
Taylor PR,
Wang L,
Wang W,
Wang Y,
Wu C,
Wu Y,
Xiang YB,
Yamamoto K,
Yang H,
Liao M,
Yokota M,
Young T,
Zhang X,
Kato N,
Wang QK,
Zheng W,
Zheng W,
Hu FB,
Lin D,
Shen H,
Teo YY,
Mo Z,
Wong TY,
Lin X,
Mohlke KL,
Ning G,
Tsunoda T,
Han BG,
Shu XO,
Tai ES,
Wu T,
Qi L
Human molecular genetics · 2015 · PMID 25429064
12 pages+
A comprehensive 1,000 Genomes-based genome-wide association meta-analysis of coronary artery disease
Nikpay M,
Goel A,
Won HH,
Hall LM,
Willenborg C,
Kanoni S,
Saleheen D,
Kyriakou T,
Nelson CP,
Hopewell JC,
Webb TR,
Zeng L
and 139 more — show all
Dehghan A,
Alver M,
Armasu SM,
Auro K,
Bjonnes A,
Chasman DI,
Chen S,
Ford I,
Franceschini N,
Gieger C,
Grace C,
Gustafsson S,
Huang J,
Hwang SJ,
Kim YK,
Kleber ME,
Lau KW,
Lu X,
Lu Y,
Lyytikäinen LP,
Mihailov E,
Morrison AC,
Pervjakova N,
Qu L,
Rose LM,
Salfati E,
Saxena R,
Scholz M,
Smith AV,
Tikkanen E,
Uitterlinden A,
Yang X,
Zhang W,
Zhao W,
de Andrade M,
de Vries PS,
van Zuydam NR,
Anand SS,
Bertram L,
Beutner F,
Dedoussis G,
Frossard P,
Gauguier D,
Goodall AH,
Gottesman O,
Haber M,
Han BG,
Huang J,
Jalilzadeh S,
Kessler T,
König IR,
Lannfelt L,
Lieb W,
Lind L,
Lindgren CM,
Lokki ML,
Magnusson PK,
Mallick NH,
Mehra N,
Meitinger T,
Memon FU,
Morris AP,
Nieminen MS,
Pedersen NL,
Peters A,
Rallidis LS,
Rasheed A,
Samuel M,
Shah SH,
Sinisalo J,
Stirrups KE,
Trompet S,
Wang L,
Zaman KS,
Ardissino D,
Boerwinkle E,
Borecki IB,
Bottinger EP,
Buring JE,
Chambers JC,
Collins R,
Cupples LA,
Danesh J,
Demuth I,
Elosua R,
Epstein SE,
Esko T,
Feitosa MF,
Franco OH,
Franzosi MG,
Granger CB,
Gu D,
Gudnason V,
Hall AS,
Hamsten A,
Harris TB,
Hazen SL,
Hengstenberg C,
Hofman A,
Ingelsson E,
Iribarren C,
Jukema JW,
Karhunen PJ,
Kim BJ,
Kooner JS,
Kullo IJ,
Lehtimäki T,
Loos RJF,
Melander O,
Metspalu A,
März W,
Palmer CN,
Perola M,
Quertermous T,
Rader DJ,
Ridker PM,
Ripatti S,
Roberts R,
Salomaa V,
Sanghera DK,
Schwartz SM,
Seedorf U,
Stewart AF,
Stott DJ,
Thiery J,
Zalloua PA,
O'Donnell CJ,
Reilly MP,
Assimes TL,
Thompson JR,
Erdmann J,
Clarke R,
Watkins H,
Kathiresan S,
McPherson R,
Deloukas P,
Schunkert H,
Samani NJ,
Farrall M
Nature genetics · 2015 · PMID 26343387 · open access
12 pages+
The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease
Astle WJ,
Elding H,
Jiang T,
Allen D,
Ruklisa D,
Mann AL,
Mead D,
Bouman H,
Riveros-Mckay F,
Kostadima MA,
Lambourne JJ,
Sivapalaratnam S
and 62 more — show all
Downes K,
Kundu K,
Bomba L,
Berentsen K,
Bradley JR,
Daugherty LC,
Delaneau O,
Freson K,
Garner SF,
Grassi L,
Guerrero J,
Haimel M,
Janssen-Megens EM,
Kaan A,
Kamat M,
Kim B,
Mandoli A,
Marchini J,
Martens JHA,
Meacham S,
Megy K,
O'Connell J,
Petersen R,
Sharifi N,
Sheard SM,
Staley JR,
Tuna S,
van der Ent M,
Walter K,
Wang SY,
Wheeler E,
Wilder SP,
Iotchkova V,
Moore C,
Sambrook J,
Stunnenberg HG,
Di Angelantonio E,
Kaptoge S,
Kuijpers TW,
Carrillo-de-Santa-Pau E,
Juan D,
Rico D,
Valencia A,
Chen L,
Ge B,
Vasquez L,
Kwan T,
Garrido-Martín D,
Watt S,
Yang Y,
Guigo R,
Beck S,
Paul DS,
Pastinen T,
Bujold D,
Bourque G,
Frontini M,
Danesh J,
Roberts DJ,
Ouwehand WH,
Butterworth AS,
Soranzo N
Cell · 2016 · PMID 27863252 · open access
12 pages+
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+
Interethnic analyses of blood pressure loci in populations of East Asian and European descent
Takeuchi F,
Akiyama M,
Matoba N,
Katsuya T,
Nakatochi M,
Tabara Y,
Narita A,
Saw WY,
Moon S,
Spracklen CN,
Chai JF,
Kim YJ
and 83 more — show all
Zhang L,
Wang C,
Li H,
Li H,
Wu JY,
Dorajoo R,
Nierenberg JL,
Wang YX,
He J,
Bennett DA,
Takahashi A,
Momozawa Y,
Hirata M,
Matsuda K,
Rakugi H,
Nakashima E,
Isono M,
Shirota M,
Hozawa A,
Ichihara S,
Matsubara T,
Yamamoto K,
Kohara K,
Igase M,
Han S,
Gordon-Larsen P,
Huang W,
Lee NR,
Adair LS,
Hwang MY,
Lee J,
Chee ML,
Sabanayagam C,
Zhao W,
Liu J,
Reilly DF,
Sun L,
Huo S,
Edwards TL,
Long J,
Chang LC,
Chen CH,
Yuan JM,
Koh WP,
Friedlander Y,
Kelly TN,
Bin Wei W,
Xu L,
Cai H,
Xiang YB,
Lin K,
Clarke R,
Walters RG,
Millwood IY,
Li L,
Chambers JC,
Kooner JS,
Elliott P,
van der Harst P,
Chen Z,
Sasaki M,
Shu XO,
Jonas JB,
He J,
Heng CK,
Chen YT,
Zheng W,
Zheng W,
Lin X,
Teo YY,
Tai ES,
Cheng CY,
Wong TY,
Sim X,
Mohlke KL,
Yamamoto M,
Kim BJ,
Miki T,
Nabika T,
Yokota M,
Kamatani Y,
Kubo M,
Kato N
International Genomics of Blood Pressure (iGEN-BP) Consortium
Nature communications · 2018 · PMID 30487518 · open access
12 pages+
Identification of type 2 diabetes loci in 433,540 East Asian individuals
Spracklen CN,
Horikoshi M,
Kim YJ,
Lin K,
Bragg F,
Moon S,
Suzuki K,
Tam CHT,
Tabara Y,
Kwak SH,
Takeuchi F,
Long J
and 101 more — show all
Lim VJY,
Chai JF,
Chen CH,
Nakatochi M,
Yao J,
Choi HS,
Iyengar AK,
Perrin HJ,
Brotman SM,
van de Bunt M,
Gloyn AL,
Below JE,
Boehnke M,
Bowden DW,
Chambers JC,
Mahajan A,
McCarthy MI,
Ng MCY,
Petty LE,
Zhang W,
Morris AP,
Adair LS,
Akiyama M,
Bian Z,
Chan JCN,
Chang LC,
Chee ML,
Chen YI,
Chen YT,
Chen Z,
Chuang LM,
Du S,
Gordon-Larsen P,
Gross M,
Guo X,
Guo Y,
Han S,
Howard AG,
Huang W,
Hung YJ,
Hwang MY,
Hwu CM,
Ichihara S,
Isono M,
Jang HM,
Jiang G,
Jonas JB,
Kamatani Y,
Katsuya T,
Kawaguchi T,
Khor CC,
Kohara K,
Lee MS,
Lee NR,
Li L,
Liu J,
Luk AO,
Lv J,
Okada Y,
Pereira MA,
Sabanayagam C,
Shi J,
Shin DM,
So WY,
Takahashi A,
Tomlinson B,
Tsai FJ,
van Dam RM,
Xiang YB,
Yamamoto K,
Yamauchi T,
Yoon K,
Yu C,
Yuan JM,
Zhang L,
Zheng W,
Zheng W,
Igase M,
Cho YS,
Rotter JI,
Wang YX,
Sheu WHH,
Yokota M,
Wu JY,
Cheng CY,
Wong TY,
Shu XO,
Kato N,
Park KS,
Tai ES,
Matsuda F,
Koh WP,
Ma RCW,
Maeda S,
Millwood IY,
Lee J,
Kadowaki T,
Walters RG,
Kim BJ,
Mohlke KL,
Sim X
Nature · 2020 · PMID 32499647 · open access
12 pages+
Meta-analysis of 208370 East Asians identifies 113 susceptibility loci for systemic lupus erythematosus
Yin X,
Kim K,
Suetsugu H,
Bang SY,
Wen L,
Koido M,
Ha E,
Liu L,
Sakamoto Y,
Jo S,
Leng RX,
Otomo N
and 76 more — show all
Laurynenka V,
Kwon YC,
Sheng Y,
Sugano N,
Sugano N,
Hwang MY,
Li W,
Mukai M,
Yoon K,
Cai M,
Ishigaki K,
Chung WT,
Huang H,
Takahashi D,
Lee SS,
Wang M,
Karino K,
Shim SC,
Zheng X,
Miyamura T,
Kang YM,
Ye D,
Nakamura J,
Suh CH,
Tang Y,
Motomura G,
Park YB,
Ding H,
Kuroda T,
Choe JY,
Li C,
Niiro H,
Park Y,
Shen C,
Miyamoto T,
Ahn GY,
Fei W,
Takeuchi T,
Shin JM,
Li K,
Kawaguchi Y,
Lee YK,
Wang Y,
Amano K,
Park DJ,
Yang W,
Tada Y,
Yamaji K,
Shimizu M,
Atsumi T,
Suzuki A,
Sumida T,
Okada Y,
Matsuda K,
Matsuo K,
Kochi Y,
Kottyan LC,
Weirauch MT,
Parameswaran S,
Eswar S,
Salim H,
Chen X,
Yamamoto K,
Harley JB,
Ohmura K,
Kim TH,
Yang S,
Yamamoto T,
Kim BJ,
Shen N,
Ikegawa S,
Lee HS,
Zhang X,
Terao C,
Cui Y,
Bae SC
Japanese Research Committee on Idiopathic Osteonecrosis of the Femoral Head
Annals of the rheumatic diseases · 2021 · PMID 33272962 · open access
12 pages+
The trans-ancestral genomic architecture of glycemic traits
Chen J,
Spracklen CN,
Marenne G,
Varshney A,
Corbin LJ,
Luan J,
Willems SM,
Wu Y,
Zhang X,
Horikoshi M,
Boutin TS,
Mägi R
and 393 more — show all
Waage J,
Li-Gao R,
Chan KHK,
Yao J,
Anasanti MD,
Chu AY,
Claringbould A,
Heikkinen J,
Hong J,
Hottenga JJ,
Huo S,
Kaakinen MA,
Louie T,
März W,
Moreno-Macias H,
Ndungu A,
Nelson SC,
Nolte IM,
North KE,
Raulerson CK,
Ray D,
Rohde R,
Rybin D,
Schurmann C,
Sim X,
Southam L,
Stewart ID,
Wang CA,
Wang Y,
Wu P,
Zhang W,
Ahluwalia TS,
Appel EVR,
Bielak LF,
Brody JA,
Burtt NP,
Cabrera CP,
Cade BE,
Chai JF,
Chai X,
Chang LC,
Chen CH,
Chen BH,
Chitrala KN,
Chiu YF,
de Haan HG,
Delgado GE,
Demirkan A,
Duan Q,
Engmann J,
Fatumo SA,
Gayán J,
Giulianini F,
Gong JH,
Gustafsson S,
Hai Y,
Hartwig FP,
He J,
Heianza Y,
Huang T,
Huerta-Chagoya A,
Hwang MY,
Jensen RA,
Kawaguchi T,
Kentistou KA,
Kim YJ,
Kleber ME,
Kooner IK,
Lai S,
Lange LA,
Langefeld CD,
Lauzon M,
Li M,
Ligthart S,
Liu J,
Loh M,
Long J,
Lyssenko V,
Mangino M,
Marzi C,
Montasser ME,
Nag A,
Nakatochi M,
Noce D,
Noordam R,
Pistis G,
Preuss M,
Raffield L,
Rasmussen-Torvik LJ,
Rich SS,
Robertson NR,
Rueedi R,
Ryan K,
Sanna S,
Saxena R,
Schraut KE,
Sennblad B,
Setoh K,
Smith AV,
Sparsø T,
Strawbridge RJ,
Takeuchi F,
Tan J,
Trompet S,
van den Akker E,
van der Most PJ,
Verweij N,
Vogel M,
Wang H,
Wang C,
Wang N,
Warren HR,
Wen W,
Wilsgaard T,
Wong A,
Wood AR,
Xie T,
Zafarmand MH,
Zhao JH,
Zhao W,
Amin N,
Arzumanyan Z,
Astrup A,
Bakker SJL,
Baldassarre D,
Beekman M,
Bergman RN,
Bertoni A,
Blüher M,
Bonnycastle LL,
Bornstein SR,
Bowden DW,
Cai Q,
Campbell A,
Campbell H,
Chang YC,
de Geus EJC,
Dehghan A,
Du S,
Eiriksdottir G,
Farmaki AE,
Frånberg M,
Fuchsberger C,
Gao Y,
Gjesing AP,
Goel A,
Han S,
Hartman CA,
Herder C,
Hicks AA,
Hsieh CH,
Hsueh WA,
Ichihara S,
Igase M,
Ikram MA,
Johnson WC,
Jørgensen ME,
Joshi PK,
Kalyani RR,
Kandeel FR,
Katsuya T,
Khor CC,
Kiess W,
Kolcic I,
Kuulasmaa T,
Kuusisto J,
Läll K,
Lam K,
Lawlor DA,
Lee NR,
Lemaitre RN,
Li H,
Lin SY,
Lindström J,
Linneberg A,
Liu J,
Lorenzo C,
Matsubara T,
Matsuda F,
Mingrone G,
Mooijaart S,
Moon S,
Nabika T,
Nadkarni GN,
Nadler JL,
Nelis M,
Neville MJ,
Norris JM,
Ohyagi Y,
Peters A,
Peyser PA,
Polasek O,
Qi Q,
Raven D,
Reilly DF,
Reiner A,
Rivideneira F,
Roll K,
Rudan I,
Sabanayagam C,
Sandow K,
Sattar N,
Schürmann A,
Shi J,
Stringham HM,
Taylor KD,
Teslovich TM,
Thuesen B,
Timmers PRHJ,
Tremoli E,
Tsai MY,
Uitterlinden A,
van Dam RM,
van Heemst D,
van Hylckama Vlieg A,
van Vliet-Ostaptchouk JV,
Vangipurapu J,
Vestergaard H,
Wang T,
Willems van Dijk K,
Zemunik T,
Abecasis GR,
Adair LS,
Aguilar-Salinas CA,
Alarcón-Riquelme ME,
An P,
Aviles-Santa L,
Becker DM,
Beilin LJ,
Bergmann S,
Bisgaard H,
Black C,
Boehnke M,
Boerwinkle E,
Böhm BO,
Bønnelykke K,
Boomsma DI,
Bottinger EP,
Buchanan TA,
Canouil M,
Caulfield MJ,
Chambers JC,
Chasman DI,
Chen YI,
Cheng CY,
Collins FS,
Correa A,
Cucca F,
de Silva HJ,
Dedoussis G,
Elmståhl S,
Evans MK,
Ferrannini E,
Ferrucci L,
Florez JC,
Franks PW,
Frayling TM,
Froguel P,
Gigante B,
Goodarzi MO,
Gordon-Larsen P,
Grallert H,
Grarup N,
Grimsgaard S,
Groop L,
Gudnason V,
Guo X,
Hamsten A,
Hansen T,
Hayward C,
Heckbert SR,
Horta BL,
Huang W,
Ingelsson E,
James PS,
Jarvelin MR,
Jonas JB,
Jukema JW,
Kaleebu P,
Kaplan R,
Kardia SLR,
Kato N,
Keinanen-Kiukaanniemi SM,
Kim BJ,
Kivimaki M,
Koistinen HA,
Kooner JS,
Körner A,
Kovacs P,
Kuh D,
Kumari M,
Kutalik Z,
Laakso M,
Lakka TA,
Launer LJ,
Leander K,
Li H,
Lin X,
Lind L,
Lindgren C,
Liu S,
Loos RJF,
Magnusson PKE,
Mahajan A,
Metspalu A,
Mook-Kanamori DO,
Mori TA,
Munroe PB,
Njølstad I,
O'Connell JR,
Oldehinkel AJ,
Ong KK,
Padmanabhan S,
Palmer CNA,
Palmer ND,
Pedersen O,
Pennell CE,
Porteous DJ,
Pramstaller PP,
Province MA,
Psaty BM,
Qi L,
Raffel LJ,
Rauramaa R,
Redline S,
Ridker PM,
Rosendaal FR,
Saaristo TE,
Sandhu M,
Saramies J,
Schneiderman N,
Schwarz P,
Scott LJ,
Selvin E,
Sever P,
Shu XO,
Slagboom PE,
Small KS,
Smith BH,
Snieder H,
Sofer T,
Sørensen TIA,
Spector TD,
Stanton A,
Steves CJ,
Stumvoll M,
Sun L,
Tabara Y,
Tai ES,
Timpson NJ,
Tönjes A,
Tuomilehto J,
Tusie T,
Uusitupa M,
van der Harst P,
van Duijn C,
Vitart V,
Vollenweider P,
Vrijkotte TGM,
Wagenknecht LE,
Walker M,
Wang YX,
Wareham NJ,
Watanabe RM,
Watkins H,
Wei WB,
Wickremasinghe AR,
Willemsen G,
Wilson JF,
Wong TY,
Wu JY,
Xiang AH,
Yanek LR,
Yengo L,
Yokota M,
Zeggini E,
Zheng W,
Zonderman AB,
Rotter JI,
Gloyn AL,
McCarthy MI,
Dupuis J,
Meigs JB,
Scott RA,
Prokopenko I,
Leong A,
Liu CT,
Parker SCJ,
Mohlke KL,
Langenberg C,
Wheeler E,
Morris AP,
Barroso I
Lifelines Cohort Study · Meta-Analysis of Glucose and Insulin-related Traits Consortium (MAGIC)
Nature genetics · 2021 · PMID 34059833 · open access
12 pages+
The power of genetic diversity in genome-wide association studies of lipids
Graham SE,
Clarke SL,
Wu KH,
Kanoni S,
Zajac GJM,
Ramdas S,
Surakka I,
Ntalla I,
Vedantam S,
Winkler TW,
Locke AE,
Marouli E
and 523 more — show all
Hwang MY,
Han S,
Narita A,
Choudhury A,
Bentley AR,
Ekoru K,
Verma A,
Trivedi B,
Martin HC,
Hunt KA,
Hui Q,
Klarin D,
Zhu X,
Thorleifsson G,
Helgadottir A,
Gudbjartsson DF,
Holm H,
Olafsson I,
Akiyama M,
Sakaue S,
Terao C,
Kanai M,
Zhou W,
Brumpton BM,
Rasheed H,
Ruotsalainen SE,
Havulinna AS,
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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.