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121 matches for
Kubo M,
showing the first 20.
Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis
Kanoni S,
Graham SE,
Wang Y,
Surakka I,
Ramdas S,
Zhu X,
Clarke SL,
Bhatti KF,
Vedantam S,
Winkler TW,
Locke AE,
Marouli E
and 527 more — show all
Zajac GJM,
Wu KH,
Ntalla I,
Hui Q,
Klarin D,
Hilliard AT,
Wang Z,
Xue C,
Thorleifsson G,
Helgadottir A,
Gudbjartsson DF,
Holm H,
Olafsson I,
Hwang MY,
Han S,
Akiyama M,
Sakaue S,
Terao C,
Kanai M,
Zhou W,
Brumpton BM,
Rasheed H,
Havulinna AS,
Veturi Y,
Pacheco JA,
Rosenthal EA,
Lingren T,
Feng Q,
Kullo IJ,
Narita A,
Takayama J,
Martin HC,
Hunt KA,
Trivedi B,
Haessler J,
Giulianini F,
Bradford Y,
Miller JE,
Campbell A,
Lin K,
Millwood IY,
Rasheed A,
Hindy G,
Faul JD,
Zhao W,
Weir DR,
Turman C,
Huang H,
Graff M,
Choudhury A,
Sengupta D,
Mahajan A,
Brown MR,
Zhang W,
Yu K,
Schmidt EM,
Pandit A,
Gustafsson S,
Yin X,
Luan J,
Zhao JH,
Matsuda F,
Jang HM,
Yoon K,
Medina-Gomez C,
Pitsillides A,
Hottenga JJ,
Wood AR,
Ji Y,
Gao Z,
Haworth S,
Yousri NA,
Mitchell RE,
Chai JF,
Aadahl M,
Bjerregaard AA,
Yao J,
Manichaikul A,
Hwu CM,
Hung YJ,
Warren HR,
Ramirez J,
Bork-Jensen J,
Kårhus LL,
Goel A,
Sabater-Lleal M,
Noordam R,
Mauro P,
Matteo F,
McDaid AF,
Marques-Vidal P,
Wielscher M,
Trompet S,
Sattar N,
Møllehave LT,
Munz M,
Zeng L,
Huang J,
Yang B,
Poveda A,
Kurbasic A,
Lamina C,
Forer L,
Scholz M,
Galesloot TE,
Bradfield JP,
Ruotsalainen SE,
Daw E,
Zmuda JM,
Mitchell JS,
Fuchsberger C,
Christensen H,
Brody JA,
Vazquez-Moreno M,
Feitosa MF,
Wojczynski MK,
Wang Z,
Preuss MH,
Mangino M,
Christofidou P,
Verweij N,
Benjamins JW,
Engmann J,
Tsao NL,
Verma A,
Slieker RC,
Lo KS,
Zilhao NR,
Le P,
Kleber ME,
Delgado GE,
Huo S,
Ikeda DD,
Iha H,
Yang J,
Liu J,
Demirkan A,
Leonard HL,
Marten J,
Frank M,
Schmidt B,
Smyth LJ,
Cañadas-Garre M,
Wang C,
Nakatochi M,
Wong A,
Hutri-Kähönen N,
Sim X,
Xia R,
Huerta-Chagoya A,
Fernandez-Lopez JC,
Lyssenko V,
Nongmaithem SS,
Bayyana S,
Stringham HM,
Irvin MR,
Oldmeadow C,
Kim HN,
Ryu S,
Timmers PRHJ,
Arbeeva L,
Dorajoo R,
Lange LA,
Prasad G,
Lorés-Motta L,
Pauper M,
Long J,
Li X,
Theusch E,
Takeuchi F,
Spracklen CN,
Loukola A,
Bollepalli S,
Warner SC,
Wang YX,
Wei WB,
Nutile T,
Ruggiero D,
Sung YJ,
Chen S,
Liu F,
Yang J,
Kentistou KA,
Banas B,
Nardone GG,
Meidtner K,
Bielak LF,
Smith JA,
Hebbar P,
Farmaki AE,
Hofer E,
Lin M,
Concas MP,
Vaccargiu S,
van der Most PJ,
Pitkänen N,
Cade BE,
van der Laan SW,
Chitrala KN,
Weiss S,
Bentley AR,
Doumatey AP,
Adeyemo AA,
Lee JY,
Petersen ERB,
Nielsen AA,
Choi HS,
Nethander M,
Freitag-Wolf S,
Southam L,
Rayner NW,
Wang CA,
Lin SY,
Wang JS,
Couture C,
Lyytikäinen LP,
Nikus K,
Cuellar-Partida G,
Vestergaard H,
Hidalgo B,
Giannakopoulou O,
Cai Q,
Obura MO,
van Setten J,
Li X,
Liang J,
Tang H,
Terzikhan N,
Shin JH,
Jackson RD,
Reiner AP,
Martin LW,
Chen Z,
Li L,
Kawaguchi T,
Thiery J,
Bis JC,
Launer LJ,
Li H,
Nalls MA,
Raitakari OT,
Ichihara S,
Wild SH,
Nelson CP,
Campbell H,
Jäger S,
Nabika T,
Al-Mulla F,
Niinikoski H,
Braund PS,
Kolcic I,
Kovacs P,
Giardoglou T,
Katsuya T,
de Kleijn D,
de Borst GJ,
Kim EK,
Adams HHH,
Ikram MA,
Zhu X,
Asselbergs FW,
Kraaijeveld AO,
Beulens JWJ,
Shu XO,
Rallidis LS,
Pedersen O,
Hansen T,
Mitchell P,
Hewitt AW,
Kähönen M,
Pérusse L,
Bouchard C,
Tönjes A,
Chen YI,
Pennell CE,
Mori TA,
Lieb W,
Franke A,
Ohlsson C,
Mellström D,
Cho YS,
Lee H,
Yuan JM,
Koh WP,
Rhee SY,
Woo JT,
Heid IM,
Stark KJ,
Zimmermann ME,
Völzke H,
Homuth G,
Evans MK,
Zonderman AB,
Polasek O,
Pasterkamp G,
Hoefer IE,
Redline S,
Pahkala K,
Oldehinkel AJ,
Snieder H,
Biino G,
Schmidt R,
Schmidt H,
Bandinelli S,
Dedoussis G,
Thanaraj TA,
Kardia SLR,
Peyser PA,
Kato N,
Schulze MB,
Girotto G,
Böger CA,
Jung B,
Joshi PK,
Bennett DA,
De Jager PL,
Lu X,
Mamakou V,
Brown M,
Caulfield MJ,
Munroe PB,
Guo X,
Ciullo M,
Jonas JB,
Samani NJ,
Kaprio J,
Pajukanta P,
Tusié-Luna T,
Aguilar-Salinas CA,
Adair LS,
Bechayda SA,
de Silva HJ,
Wickremasinghe AR,
Krauss RM,
Wu JY,
Zheng W,
Hollander AI,
Bharadwaj D,
Correa A,
Wilson JG,
Lind L,
Heng CK,
Nelson AE,
Golightly YM,
Wilson JF,
Penninx B,
Kim HL,
Attia J,
Scott RJ,
Rao DC,
Arnett DK,
Hunt SC,
Walker M,
Koistinen HA,
Chandak GR,
Mercader JM,
Costanzo MC,
Jang D,
Burtt NP,
Villalpando CG,
Orozco L,
Fornage M,
Tai E,
van Dam RM,
Lehtimäki T,
Chaturvedi N,
Yokota M,
Liu J,
Reilly DF,
McKnight AJ,
Kee F,
Jöckel KH,
McCarthy MI,
Palmer CNA,
Vitart V,
Hayward C,
Simonsick E,
van Duijn CM,
Jin ZB,
Qu J,
Hishigaki H,
Lin X,
März W,
Gudnason V,
Tardif JC,
Lettre G,
Hart LM',
Elders PJM,
Damrauer SM,
Kumari M,
Kivimaki M,
van der Harst P,
Spector TD,
Loos RJF,
Province MA,
Parra EJ,
Cruz M,
Psaty BM,
Brandslund I,
Pramstaller PP,
Rotimi CN,
Christensen K,
Ripatti S,
Widén E,
Hakonarson H,
Grant SFA,
Kiemeney LALM,
de Graaf J,
Loeffler M,
Kronenberg F,
Gu D,
Erdmann J,
Schunkert H,
Franks PW,
Linneberg A,
Jukema JW,
Khera AV,
Männikkö M,
Jarvelin MR,
Kutalik Z,
Francesco C,
Mook-Kanamori DO,
van Dijk KW,
Watkins H,
Strachan DP,
Grarup N,
Sever P,
Poulter N,
Chuang LM,
Rotter JI,
Dantoft TM,
Karpe F,
Neville MJ,
Timpson NJ,
Cheng CY,
Wong TY,
Khor CC,
Li H,
Sabanayagam C,
Peters A,
Gieger C,
Hattersley AT,
Pedersen NL,
Magnusson PKE,
Boomsma DI,
Willemsen AHM,
Cupples L,
van Meurs JBJ,
Ghanbari M,
Gordon-Larsen P,
Huang W,
Kim YJ,
Tabara Y,
Wareham NJ,
Langenberg C,
Zeggini E,
Kuusisto J,
Laakso M,
Ingelsson E,
Abecasis G,
Chambers JC,
Kooner JS,
de Vries PS,
Morrison AC,
Hazelhurst S,
Ramsay M,
North KE,
Daviglus M,
Kraft P,
Martin NG,
Whitfield JB,
Abbas S,
Saleheen D,
Walters RG,
Holmes MV,
Black C,
Smith BH,
Baras A,
Justice AE,
Buring JE,
Ridker PM,
Chasman DI,
Kooperberg C,
Tamiya G,
Yamamoto M,
van Heel DA,
Trembath RC,
Wei WQ,
Jarvik GP,
Namjou B,
Hayes MG,
Ritchie MD,
Jousilahti P,
Salomaa V,
Hveem K,
Åsvold BO,
Kubo M,
Kamatani Y,
Okada Y,
Murakami Y,
Kim BJ,
Thorsteinsdottir U,
Stefansson K,
Zhang J,
Chen Y,
Ho YL,
Lynch JA,
Rader DJ,
Tsao PS,
Chang KM,
Cho K,
O'Donnell CJ,
Gaziano JM,
Wilson PWF,
Frayling TM,
Hirschhorn JN,
Kathiresan S,
Mohlke KL,
Sun YV,
Morris AP,
Boehnke M,
Brown CD,
Natarajan P,
Deloukas P,
Willer CJ,
Assimes TL,
Peloso GM
Genome biology · 2022 · PMID 36575460 · open access
7 pages
Meta-analysis identifies multiple loci associated with kidney function-related traits in east Asian populations
Okada Y,
Sim X,
Go MJ,
Wu JY,
Gu D,
Takeuchi F,
Takahashi A,
Maeda S,
Tsunoda T,
Chen P,
Lim SC,
Wong TY
and 34 more — show all
Liu J,
Young TL,
Aung T,
Seielstad M,
Teo YY,
Kim YJ,
Lee JY,
Han BG,
Kang D,
Chen CH,
Tsai FJ,
Chang LC,
Fann SJ,
Mei H,
Rao DC,
Hixson JE,
Chen S,
Katsuya T,
Isono M,
Ogihara T,
Chambers JC,
Zhang W,
Kooner JS,
Albrecht E,
Yamamoto K,
Kubo M,
Nakamura Y,
Kamatani N,
Kato N,
He J,
Chen YT,
Cho YS,
Tai ES,
Tanaka T
KidneyGen Consortium · CKDGen Consortium and 1 more consortia
Nature genetics · 2012 · PMID 22797727
6 pages
Genome-wide association studies in the Japanese population identify seven novel loci for type 2 diabetes
Imamura M,
Takahashi A,
Yamauchi T,
Hara K,
Yasuda K,
Grarup N,
Zhao W,
Wang X,
Huerta-Chagoya A,
Hu C,
Moon S,
Long J
and 52 more — show all
Kwak SH,
Rasheed A,
Saxena R,
Ma RC,
Okada Y,
Iwata M,
Hosoe J,
Shojima N,
Iwasaki M,
Fujita H,
Suzuki K,
Danesh J,
Jørgensen T,
Jørgensen ME,
Witte DR,
Brandslund I,
Christensen C,
Hansen T,
Mercader JM,
Flannick J,
Moreno-Macías H,
Burtt NP,
Zhang R,
Kim YJ,
Zheng W,
Zheng W,
Singh JR,
Tam CH,
Hirose H,
Maegawa H,
Ito C,
Kaku K,
Watada H,
Tanaka Y,
Tobe K,
Kawamori R,
Kubo M,
Cho YS,
Chan JC,
Sanghera D,
Frossard P,
Park KS,
Shu XO,
Kim BJ,
Florez JC,
Tusié-Luna T,
Jia W,
Tai ES,
Pedersen O,
Saleheen D,
Maeda S,
Kadowaki T
Nature communications · 2016 · PMID 26818947 · open access
6 pages
Subtype-specific gout susceptibility loci and enrichment of selection pressure on <i>ABCG2</i> and <i>ALDH2</i> identified by subtype genome-wide meta-analyses of clinically defined gout patients
Nakayama A,
Nakatochi M,
Kawamura Y,
Yamamoto K,
Nakaoka H,
Shimizu S,
Higashino T,
Koyama T,
Hishida A,
Kuriki K,
Watanabe M,
Shimizu T
and 42 more — show all
Ooyama K,
Ooyama H,
Nagase M,
Hidaka Y,
Matsui D,
Tamura T,
Nishiyama T,
Shimanoe C,
Katsuura-Kamano S,
Takashima N,
Shirai Y,
Kawaguchi M,
Takao M,
Sugiyama R,
Takada Y,
Nakamura T,
Nakashima H,
Tsunoda M,
Danjoh I,
Hozawa A,
Hosomichi K,
Toyoda Y,
Kubota Y,
Takada T,
Suzuki H,
Stiburkova B,
Major TJ,
Merriman TR,
Kuriyama N,
Mikami H,
Takezaki T,
Matsuo K,
Suzuki S,
Hosoya T,
Kamatani Y,
Kubo M,
Ichida K,
Wakai K,
Inoue I,
Okada Y,
Shinomiya N,
Matsuo H
Japan Gout Genomics Consortium (Japan Gout)
Annals of the rheumatic diseases · 2020 · PMID 32238385 · open access
6 pages
A genome-wide association study in 19 633 Japanese subjects identified LHX3-QSOX2 and IGF1 as adult height loci
Okada Y,
Kamatani Y,
Takahashi A,
Matsuda K,
Hosono N,
Ohmiya H,
Daigo Y,
Yamamoto K,
Kubo M,
Nakamura Y,
Kamatani N
Human molecular genetics · 2010 · PMID 20189936
5 pages
Identification of nine novel loci associated with white blood cell subtypes in a Japanese population
Okada Y,
Hirota T,
Kamatani Y,
Takahashi A,
Ohmiya H,
Kumasaka N,
Higasa K,
Yamaguchi-Kabata Y,
Hosono N,
Nalls MA,
Chen MH,
van Rooij FJ
and 19 more — show all
Smith AV,
Tanaka T,
Couper DJ,
Zakai NA,
Ferrucci L,
Longo DL,
Hernandez DG,
Witteman JC,
Harris TB,
O'Donnell CJ,
Ganesh SK,
Matsuda K,
Tsunoda T,
Tanaka T,
Kubo M,
Nakamura Y,
Tamari M,
Yamamoto K,
Kamatani N
PLoS genetics · 2011 · PMID 21738478 · open access
5 pages
Genome-wide Trans-ethnic Meta-analysis Identifies Seven Genetic Loci Influencing Erythrocyte Traits and a Role for RBPMS in Erythropoiesis
van Rooij FJA,
Qayyum R,
Smith AV,
Zhou Y,
Trompet S,
Tanaka T,
Keller MF,
Chang LC,
Schmidt H,
Yang ML,
Chen MH,
Hayes J
and 88 more — show all
Johnson AD,
Yanek LR,
Mueller C,
Lange L,
Floyd JS,
Ghanbari M,
Zonderman AB,
Jukema JW,
Hofman A,
van Duijn CM,
Desch KC,
Saba Y,
Ozel AB,
Snively BM,
Wu JY,
Schmidt R,
Fornage M,
Klein RJ,
Fox CS,
Matsuda K,
Kamatani N,
Wild PS,
Stott DJ,
Ford I,
Slagboom PE,
Yang J,
Chu AY,
Lambert AJ,
Uitterlinden AG,
Franco OH,
Hofer E,
Ginsburg D,
Hu B,
Keating B,
Schick UM,
Brody JA,
Li JZ,
Chen Z,
Zeller T,
Guralnik JM,
Chasman DI,
Peters LL,
Kubo M,
Becker DM,
Li J,
Eiriksdottir G,
Rotter JI,
Levy D,
Grossmann V,
Patel KV,
Chen CH,
Ridker PM,
Tang H,
Launer LJ,
Rice KM,
Li-Gao R,
Ferrucci L,
Evans MK,
Choudhuri A,
Trompouki E,
Abraham BJ,
Yang S,
Takahashi A,
Kamatani Y,
Kooperberg C,
Harris TB,
Jee SH,
Coresh J,
Tsai FJ,
Longo DL,
Chen YT,
Felix JF,
Yang Q,
Psaty BM,
Boerwinkle E,
Becker LC,
Mook-Kanamori DO,
Wilson JG,
Gudnason V,
O'Donnell CJ,
Dehghan A,
Cupples LA,
Nalls MA,
Morris AP,
Okada Y,
Reiner AP,
Zon LI,
Ganesh SK
BioBank Japan Project
American journal of human genetics · 2017 · PMID 28017375
5 pages
Identification of six new genetic loci associated with atrial fibrillation in the Japanese population
Low SK,
Takahashi A,
Ebana Y,
Ozaki K,
Christophersen IE,
Ellinor PT,
Ogishima S,
Yamamoto M,
Satoh M,
Sasaki M,
Yamaji T,
Iwasaki M
and 10 more — show all
AFGen Consortium
Nature genetics · 2017 · PMID 28416822
5 pages
Genome-wide analysis of dental caries and periodontitis combining clinical and self-reported data
Shungin D,
Haworth S,
Divaris K,
Agler CS,
Kamatani Y,
Keun Lee M,
Grinde K,
Hindy G,
Alaraudanjoki V,
Pesonen P,
Teumer A,
Holtfreter B
and 26 more — show all
Sakaue S,
Hirata J,
Yu YH,
Ridker PM,
Giulianini F,
Chasman DI,
Magnusson PKE,
Sudo T,
Okada Y,
Völker U,
Kocher T,
Anttonen V,
Laitala ML,
Orho-Melander M,
Sofer T,
Shaffer JR,
Vieira A,
Marazita ML,
Kubo M,
Furuichi Y,
North KE,
Offenbacher S,
Ingelsson E,
Franks PW,
Timpson NJ,
Johansson I
Nature communications · 2019 · PMID 31235808 · open access
5 pages
Genome-wide association study of lung adenocarcinoma in East Asia and comparison with a European population
Shi J,
Shiraishi K,
Choi J,
Matsuo K,
Chen TY,
Dai J,
Hung RJ,
Chen K,
Shu XO,
Kim YT,
Landi MT,
Lin D
and 210 more — show all
Zheng W,
Yin Z,
Zhou B,
Song B,
Wang J,
Seow WJ,
Song L,
Chang IS,
Hu W,
Chien LH,
Cai Q,
Hong YC,
Kim HN,
Wu YL,
Wong MP,
Richardson BD,
Funderburk KM,
Li S,
Zhang T,
Breeze C,
Wang Z,
Blechter B,
Bassig BA,
Kim JH,
Albanes D,
Wong JYY,
Shin MH,
Chung LP,
Yang Y,
An SJ,
Zheng H,
Yatabe Y,
Zhang XC,
Kim YC,
Caporaso NE,
Chang J,
Ho JCM,
Kubo M,
Daigo Y,
Song M,
Momozawa Y,
Kamatani Y,
Kobayashi M,
Okubo K,
Honda T,
Hosgood DH,
Kunitoh H,
Patel H,
Watanabe SI,
Miyagi Y,
Nakayama H,
Matsumoto S,
Horinouchi H,
Tsuboi M,
Hamamoto R,
Goto K,
Ohe Y,
Takahashi A,
Goto A,
Minamiya Y,
Hara M,
Nishida Y,
Takeuchi K,
Wakai K,
Matsuda K,
Murakami Y,
Shimizu K,
Suzuki H,
Saito M,
Ohtaki Y,
Tanaka K,
Wu T,
Wei F,
Dai H,
Machiela MJ,
Su J,
Kim YH,
Oh IJ,
Lee VHF,
Chang GC,
Tsai YH,
Chen KY,
Huang MS,
Su WC,
Chen YM,
Seow A,
Park JY,
Kweon SS,
Chen KC,
Gao YT,
Qian B,
Wu C,
Lu D,
Liu J,
Schwartz AG,
Houlston R,
Spitz MR,
Gorlov IP,
Wu X,
Yang P,
Lam S,
Tardon A,
Chen C,
Bojesen SE,
Johansson M,
Risch A,
Bickeböller H,
Ji BT,
Wichmann HE,
Christiani DC,
Rennert G,
Arnold S,
Brennan P,
McKay J,
Field JK,
Shete SS,
Le Marchand L,
Liu G,
Andrew A,
Kiemeney LA,
Zienolddiny-Narui S,
Grankvist K,
Johansson M,
Cox A,
Taylor F,
Yuan JM,
Lazarus P,
Schabath MB,
Aldrich MC,
Jeon HS,
Jiang SS,
Sung JS,
Chen CH,
Hsiao CF,
Jung YJ,
Guo H,
Hu Z,
Burdett L,
Yeager M,
Hutchinson A,
Hicks B,
Liu J,
Zhu B,
Berndt SI,
Wu W,
Wang J,
Li Y,
Choi JE,
Park KH,
Sung SW,
Liu L,
Kang CH,
Wang WC,
Xu J,
Guan P,
Tan W,
Yu CJ,
Yang G,
Sihoe ADL,
Chen Y,
Choi YY,
Kim JS,
Yoon HI,
Park IK,
Xu P,
He Q,
Wang CL,
Hung HH,
Vermeulen RCH,
Cheng I,
Wu J,
Lim WY,
Tsai FY,
Chan JKC,
Li J,
Chen H,
Lin HC,
Jin L,
Liu J,
Sawada N,
Yamaji T,
Wyatt K,
Li SA,
Ma H,
Zhu M,
Wang Z,
Cheng S,
Li X,
Ren Y,
Chao A,
Iwasaki M,
Zhu J,
Jiang G,
Fei K,
Wu G,
Chen CY,
Chen CJ,
Yang PC,
Yu J,
Stevens VL,
Fraumeni JF Jr,
Chatterjee N,
Gorlova OY,
Hsiung CA,
Amos CI,
Shen H,
Chanock SJ,
Rothman N,
Kohno T,
Lan Q
Nature communications · 2023 · PMID 37236969 · open access
5 pages
Identification of independent risk loci for Graves' disease within the MHC in the Japanese population
Nakabayashi K,
Tajima A,
Yamamoto K,
Takahashi A,
Hata K,
Takashima Y,
Koyanagi M,
Nakaoka H,
Akamizu T,
Ishikawa N,
Kubota S,
Maeda S
and 6 more — show all
Journal of human genetics · 2011 · PMID 21900946
4 pages
A genome-wide association study identifies 2 susceptibility Loci for Crohn's disease in a Japanese population
Yamazaki K,
Umeno J,
Takahashi A,
Hirano A,
Johnson TA,
Kumasaka N,
Morizono T,
Hosono N,
Kawaguchi T,
Takazoe M,
Yamada T,
Suzuki Y
and 12 more — show all
Tanaka H,
Motoya S,
Hosokawa M,
Arimura Y,
Shinomura Y,
Matsui T,
Matsumoto T,
Iida M,
Tsunoda T,
Nakamura Y,
Kamatani N,
Kubo M
Gastroenterology · 2013 · PMID 23266558
4 pages
Multiple nonglycemic genomic loci are newly associated with blood level of glycated hemoglobin in East Asians
Chen P,
Takeuchi F,
Lee JY,
Li H,
Wu JY,
Liang J,
Long J,
Tabara Y,
Goodarzi MO,
Pereira MA,
Kim YJ,
Go MJ
and 59 more — show all
Stram DO,
Vithana E,
Khor CC,
Liu J,
Liao J,
Ye X,
Wang Y,
Lu L,
Young TL,
Lee J,
Thai AC,
Cheng CY,
van Dam RM,
Friedlander Y,
Heng CK,
Koh WP,
Chen CH,
Chang LC,
Pan WH,
Qi Q,
Isono M,
Zheng W,
Zheng W,
Cai Q,
Gao Y,
Yamamoto K,
Ohnaka K,
Takayanagi R,
Kita Y,
Ueshima H,
Hsiung CA,
Cui J,
Sheu WH,
Rotter JI,
Chen YD,
Hsu C,
Okada Y,
Kubo M,
Takahashi A,
Tanaka T,
van Rooij FJ,
Ganesh SK,
Huang J,
Huang T,
Yuan J,
Hwang JY,
Gross MD,
Assimes TL,
Miki T,
Shu XO,
Qi L,
Chen YT,
Lin X,
Aung T,
Wong TY,
Teo YY,
Kim BJ,
Kato N,
Tai ES
CHARGE Hematology Working Group
Diabetes · 2014 · PMID 24647736 · open access
4 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
Genome-wide meta-analysis identifies multiple novel loci associated with serum uric acid levels in Japanese individuals
Nakatochi M,
Kanai M,
Nakayama A,
Hishida A,
Kawamura Y,
Ichihara S,
Akiyama M,
Ikezaki H,
Furusyo N,
Shimizu S,
Yamamoto K,
Hirata M
and 38 more — show all
Okada R,
Kawai S,
Kawaguchi M,
Nishida Y,
Shimanoe C,
Ibusuki R,
Takezaki T,
Nakajima M,
Takao M,
Ozaki E,
Matsui D,
Nishiyama T,
Suzuki S,
Takashima N,
Kita Y,
Endoh K,
Kuriki K,
Uemura H,
Arisawa K,
Oze I,
Matsuo K,
Nakamura Y,
Mikami H,
Tamura T,
Nakashima H,
Nakamura T,
Kato N,
Matsuda K,
Murakami Y,
Matsubara T,
Naito M,
Kubo M,
Kamatani Y,
Shinomiya N,
Yokota M,
Wakai K,
Okada Y,
Matsuo H
Communications biology · 2019 · PMID 30993211 · open access
4 pages
Genome-wide association study identifies 14 previously unreported susceptibility loci for adolescent idiopathic scoliosis in Japanese
Kou I,
Otomo N,
Takeda K,
Momozawa Y,
Lu HF,
Kubo M,
Kamatani Y,
Ogura Y,
Takahashi Y,
Nakajima M,
Minami S,
Uno K
and 35 more — show all
Kawakami N,
Ito M,
Yonezawa I,
Watanabe K,
Kaito T,
Yanagida H,
Taneichi H,
Harimaya K,
Taniguchi Y,
Shigematsu H,
Iida T,
Demura S,
Sugawara R,
Fujita N,
Yagi M,
Okada E,
Hosogane N,
Kono K,
Nakamura M,
Chiba K,
Kotani T,
Sakuma T,
Akazawa T,
Suzuki T,
Nishida K,
Kakutani K,
Tsuji T,
Sudo H,
Iwata A,
Sato T,
Inami S,
Matsumoto M,
Terao C,
Watanabe K,
Ikegawa S
Nature communications · 2019 · PMID 31417091 · open access
4 pages
SNPs in KCNQ1 are associated with susceptibility to type 2 diabetes in East Asian and European populations
Unoki H,
Takahashi A,
Kawaguchi T,
Hara K,
Horikoshi M,
Andersen G,
Ng DP,
Holmkvist J,
Borch-Johnsen K,
Jørgensen T,
Sandbaek A,
Lauritzen T
and 18 more — show all
Hansen T,
Nurbaya S,
Tsunoda T,
Kubo M,
Babazono T,
Hirose H,
Hayashi M,
Iwamoto Y,
Kashiwagi A,
Kaku K,
Kawamori R,
Tai ES,
Pedersen O,
Kamatani N,
Kadowaki T,
Kikkawa R,
Nakamura Y,
Maeda S
Nature genetics · 2008 · PMID 18711366
3 pages
Multiple loci are associated with white blood cell phenotypes
Nalls MA,
Couper DJ,
Tanaka T,
van Rooij FJ,
Chen MH,
Smith AV,
Toniolo D,
Zakai NA,
Yang Q,
Greinacher A,
Wood AR,
Garcia M
and 81 more — show all
Gasparini P,
Liu Y,
Lumley T,
Folsom AR,
Reiner AP,
Gieger C,
Lagou V,
Felix JF,
Völzke H,
Gouskova NA,
Biffi A,
Döring A,
Völker U,
Chong S,
Wiggins KL,
Rendon A,
Dehghan A,
Moore M,
Taylor K,
Wilson JG,
Lettre G,
Hofman A,
Bis JC,
Pirastu N,
Fox CS,
Meisinger C,
Sambrook J,
Arepalli S,
Nauck M,
Prokisch H,
Stephens J,
Glazer NL,
Cupples LA,
Okada Y,
Takahashi A,
Kamatani Y,
Matsuda K,
Tsunoda T,
Tanaka T,
Kubo M,
Nakamura Y,
Yamamoto K,
Kamatani N,
Stumvoll M,
Tönjes A,
Prokopenko I,
Illig T,
Patel KV,
Garner SF,
Kuhnel B,
Mangino M,
Oostra BA,
Thein SL,
Coresh J,
Wichmann HE,
Menzel S,
Lin J,
Pistis G,
Uitterlinden AG,
Spector TD,
Teumer A,
Eiriksdottir G,
Gudnason V,
Bandinelli S,
Frayling TM,
Chakravarti A,
van Duijn CM,
Melzer D,
Ouwehand WH,
Levy D,
Boerwinkle E,
Singleton AB,
Hernandez DG,
Longo DL,
Soranzo N,
Witteman JC,
Psaty BM,
Ferrucci L,
Harris TB,
O'Donnell CJ,
Ganesh SK
PLoS genetics · 2011 · PMID 21738480 · open access
3 pages
Large-scale genome-wide association studies in East Asians identify new genetic loci influencing metabolic traits
Kim YJ,
Go MJ,
Hu C,
Hong CB,
Kim YK,
Lee JY,
Hwang JY,
Oh JH,
Kim DJ,
Kim NH,
Kim S,
Hong EJ
and 21 more — show all
Kim JH,
Min H,
Kim Y,
Zhang R,
Jia W,
Okada Y,
Takahashi A,
Kubo M,
Tanaka T,
Kamatani N,
Matsuda K,
Park T,
Oh B,
Kimm K,
Kang D,
Shin C,
Cho NH,
Kim HL,
Han BG,
Lee JY,
Cho YS
MAGIC consortium
Nature genetics · 2011 · PMID 21909109
3 pages
Meta-analysis identifies six new susceptibility loci for atrial fibrillation
Ellinor PT,
Lunetta KL,
Albert CM,
Glazer NL,
Ritchie MD,
Smith AV,
Arking DE,
Müller-Nurasyid M,
Krijthe BP,
Lubitz SA,
Bis JC,
Chung MK
and 77 more — show all
Dörr M,
Ozaki K,
Roberts JD,
Smith JG,
Pfeufer A,
Sinner MF,
Lohman K,
Ding J,
Smith NL,
Smith JD,
Rienstra M,
Rice KM,
Van Wagoner DR,
Magnani JW,
Wakili R,
Clauss S,
Rotter JI,
Steinbeck G,
Launer LJ,
Davies RW,
Borkovich M,
Harris TB,
Lin H,
Völker U,
Völzke H,
Milan DJ,
Hofman A,
Boerwinkle E,
Chen LY,
Soliman EZ,
Voight BF,
Li G,
Chakravarti A,
Kubo M,
Tedrow UB,
Rose LM,
Ridker PM,
Conen D,
Tsunoda T,
Furukawa T,
Sotoodehnia N,
Xu S,
Kamatani N,
Levy D,
Nakamura Y,
Parvez B,
Mahida S,
Furie KL,
Rosand J,
Muhammad R,
Psaty BM,
Meitinger T,
Perz S,
Wichmann HE,
Witteman JC,
Kao WH,
Kathiresan S,
Roden DM,
Uitterlinden AG,
Rivadeneira F,
McKnight B,
Sjögren M,
Newman AB,
Liu Y,
Gollob MH,
Melander O,
Tanaka T,
Stricker BH,
Felix SB,
Alonso A,
Darbar D,
Barnard J,
Chasman DI,
Heckbert SR,
Benjamin EJ,
Gudnason V,
Kääb S
Nature genetics · 2012 · PMID 22544366
3 pages
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