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성함이나 학술지명, PMID로 찾아보십시오.
Terao C에 대해
35건, 그중 15건 표시.
Genetic study identifies novel genes in developmental dysplasia of the hip
Yoshino S,
Chen S,
Yamaguchi R,
Kurakazu T,
Hatzikotoulas K,
Koike Y,
Inoue D,
Kohno Y,
Sasaki K,
Choe H,
Baba S,
Hara T
외 31명 — 모두 보기
Ito J,
Okuzu Y,
Shiomoto K,
Nakamura T,
Koyano G,
Shimizu T,
Kinoshita K,
Takahashi E,
Utsunomiya T,
Hara D,
Sato T,
Kawahara S,
Kaneuji A,
Yamamoto T,
Takahashi D,
Jinno T,
Kawano T,
Goto K,
Takagi M,
Mawatari T,
Inaba Y,
Nakamura T,
Kabata T,
Hamai S,
Motomura G,
Southam L,
Wilkinson JM,
Zeggini E,
Ikegawa S,
Nakashima Y,
Terao C
Bone research · 2026 · PMID 41912496 · open access
페이지 9개
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
외 527명 — 모두 보기
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
페이지 8개
Meta-analysis identifies nine new loci associated with rheumatoid arthritis in the Japanese population
Okada Y,
Terao C,
Ikari K,
Kochi Y,
Ohmura K,
Suzuki A,
Kawaguchi T,
Stahl EA,
Kurreeman FA,
Nishida N,
Ohmiya H,
Myouzen K
외 39명 — 모두 보기
Takahashi M,
Sawada T,
Nishioka Y,
Yukioka M,
Matsubara T,
Wakitani S,
Teshima R,
Tohma S,
Takasugi K,
Shimada K,
Murasawa A,
Honjo S,
Matsuo K,
Tanaka H,
Tajima K,
Suzuki T,
Iwamoto T,
Kawamura Y,
Tanii H,
Okazaki Y,
Sasaki T,
Gregersen PK,
Padyukov L,
Worthington J,
Siminovitch KA,
Lathrop M,
Taniguchi A,
Takahashi A,
Tokunaga K,
Kubo M,
Nakamura Y,
Kamatani N,
Mimori T,
Plenge RM,
Yamanaka H,
Momohara S,
Yamada R,
Matsuda F,
Yamamoto K
Nature genetics · 2012 · PMID 22446963
페이지 7개
Novel Risk Loci Identified in a Genome-Wide Association Study of Urolithiasis in a Japanese Population
Tanikawa C,
Kamatani Y,
Terao C,
Usami M,
Takahashi A,
Momozawa Y,
Suzuki K,
Ogishima S,
Shimizu A,
Satoh M,
Matsuo K,
Mikami H
외 12명 — 모두 보기
Naito M,
Wakai K,
Yamaji T,
Sawada N,
Iwasaki M,
Tsugane S,
Kohri K,
Yu ASL,
Yasui T,
Murakami Y,
Kubo M,
Matsuda K
Journal of the American Society of Nephrology : JASN · 2019 · PMID 30975718
페이지 7개
GWAS for systemic sclerosis identifies six novel susceptibility loci including one in the Fcγ receptor region
Ishikawa Y,
Tanaka N,
Asano Y,
Kodera M,
Shirai Y,
Akahoshi M,
Hasegawa M,
Matsushita T,
Saito K,
Motegi SI,
Yoshifuji H,
Yoshizaki A
외 60명 — 모두 보기
Kohmoto T,
Takagi K,
Oka A,
Kanda M,
Tanaka Y,
Ito Y,
Nakano K,
Kasamatsu H,
Utsunomiya A,
Sekiguchi A,
Niiro H,
Jinnin M,
Makino K,
Makino T,
Ihn H,
Yamamoto M,
Suzuki C,
Takahashi H,
Nishida E,
Morita A,
Yamamoto T,
Fujimoto M,
Kondo Y,
Goto D,
Sumida T,
Ayuzawa N,
Yanagida H,
Horita T,
Atsumi T,
Endo H,
Shima Y,
Kumanogoh A,
Hirata J,
Otomo N,
Suetsugu H,
Koike Y,
Tomizuka K,
Yoshino S,
Liu X,
Ito S,
Hikino K,
Suzuki A,
Momozawa Y,
Ikegawa S,
Tanaka Y,
Ishikawa O,
Takehara K,
Torii T,
Sato S,
Okada Y,
Mimori T,
Matsuda F,
Matsuda K,
Amariuta T,
Imoto I,
Matsuo K,
Kuwana M,
Kawaguchi Y,
Ohmura K,
Terao C
Nature communications · 2024 · PMID 38296975 · open access
페이지 7개
Genome-wide association studies for pelvic organ prolapse in the Japanese population
Matsunami M,
Imamura M,
Ashikari A,
Liu X,
Tomizuka K,
Hikino K,
Miwa K,
Kadekawa K,
Suda T,
Matsuda K,
Miyazato M,
Terao C
외 1명 — 모두 보기
Biobank Japan project
Communications biology · 2024 · PMID 39349682 · open access
페이지 7개
Genome-wide association study of intracranial aneurysms identifies 17 risk loci and genetic overlap with clinical risk factors
Bakker MK,
van der Spek RAA,
van Rheenen W,
Morel S,
Bourcier R,
Hostettler IC,
Alg VS,
van Eijk KR,
Koido M,
Akiyama M,
Terao C,
Matsuda K
외 62명 — 모두 보기
Walters RG,
Lin K,
Li L,
Millwood IY,
Chen Z,
Rouleau GA,
Zhou S,
Rannikmäe K,
Sudlow CLM,
Houlden H,
van den Berg LH,
Dina C,
Naggara O,
Gentric JC,
Shotar E,
Eugène F,
Desal H,
Winsvold BS,
Børte S,
Johnsen MB,
Brumpton BM,
Sandvei MS,
Willer CJ,
Hveem K,
Zwart JA,
Verschuren WMM,
Friedrich CM,
Hirsch S,
Schilling S,
Dauvillier J,
Martin O,
Jones GT,
Bown MJ,
Ko NU,
Kim H,
Coleman JRI,
Breen G,
Zaroff JG,
Klijn CJM,
Malik R,
Dichgans M,
Sargurupremraj M,
Tatlisumak T,
Amouyel P,
Debette S,
Rinkel GJE,
Worrall BB,
Pera J,
Slowik A,
Gaál-Paavola EI,
Niemelä M,
Jääskeläinen JE,
von Und Zu Fraunberg M,
Lindgren A,
Broderick JP,
Werring DJ,
Woo D,
Redon R,
Bijlenga P,
Kamatani Y,
Veldink JH,
Ruigrok YM
HUNT All-In Stroke · China Kadoorie Biobank Collaborative Group 외 컨소시엄 5곳
Nature genetics · 2020 · PMID 33199917
페이지 6개
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
외 35명 — 모두 보기
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
페이지 4개
Genetic determinants and an epistasis of <i>LILRA3</i> and HLA-B*52 in Takayasu arteritis
Terao C,
Yoshifuji H,
Matsumura T,
Naruse TK,
Ishii T,
Nakaoka Y,
Kirino Y,
Matsuo K,
Origuchi T,
Shimizu M,
Maejima Y,
Amiya E
외 29명 — 모두 보기
Tamura N,
Kawaguchi T,
Takahashi M,
Setoh K,
Ohmura K,
Watanabe R,
Horita T,
Atsumi T,
Matsukura M,
Miyata T,
Kochi Y,
Suda T,
Tanemoto K,
Meguro A,
Okada Y,
Ogimoto A,
Yamamoto M,
Takahashi H,
Nakayamada S,
Saito K,
Kuwana M,
Mizuki N,
Tabara Y,
Ueda A,
Komuro I,
Kimura A,
Isobe M,
Mimori T,
Matsuda F
Proceedings of the National Academy of Sciences of the United States of America · 2018 · PMID 30498034
페이지 3개
Genetic variants of calcium and vitamin D metabolism in kidney stone disease
Howles SA,
Wiberg A,
Goldsworthy M,
Bayliss AL,
Gluck AK,
Ng M,
Grout E,
Tanikawa C,
Kamatani Y,
Terao C,
Takahashi A,
Kubo M
외 4명 — 모두 보기
Nature communications · 2019 · PMID 31729369 · open access
페이지 3개
Novel susceptibility loci for steroid-associated osteonecrosis of the femoral head in systemic lupus erythematosus
Suetsugu H,
Kim K,
Yamamoto T,
Bang SY,
Sakamoto Y,
Shin JM,
Sugano N,
Kim JS,
Mukai M,
Lee YK,
Ohmura K,
Park DJ
외 43명 — 모두 보기
Takahashi D,
Ahn GY,
Karino K,
Kwon YC,
Miyamura T,
Kim J,
Nakamura J,
Motomura G,
Kuroda T,
Niiro H,
Miyamoto T,
Takeuchi T,
Ikari K,
Amano K,
Tada Y,
Yamaji K,
Shimizu M,
Atsumi T,
Seki T,
Tanaka Y,
Kubo T,
Hisada R,
Yoshioka T,
Yamazaki M,
Kabata T,
Kajino T,
Ohta Y,
Okawa T,
Naito Y,
Kaneuji A,
Yasunaga Y,
Ohzono K,
Tomizuka K,
Koido M,
Matsuda K,
Okada Y,
Suzuki A,
Kim BJ,
Kochi Y,
Lee HS,
Ikegawa S,
Bae SC,
Terao C
Human molecular genetics · 2022 · PMID 34850884
페이지 2개
Population-specific reference panel improves imputation quality for genome-wide association studies conducted on the Japanese population
Flanagan J,
Liu X,
Ortega-Reyes D,
Tomizuka K,
Matoba N,
Akiyama M,
Koido M,
Ishigaki K,
Ashikawa K,
Takata S,
Shi M,
Aoi T
외 8명 — 모두 보기
Biobank Japan Project
Communications biology · 2024 · PMID 39702642 · open access
페이지 2개
Large-scale blood pressure GWAS accounting for gene-depression interactions in 564,680 individuals from diverse populations
Lee S,
Miller CL,
Bentley AR,
Brown MR,
Nagarajan P,
Noordam R,
Morrison JL,
Schwander K,
Westerman K,
Kho M,
Kraja AT,
de Vries PS
외 137명 — 모두 보기
Ammous F,
Aschard H,
Bartz TM,
Do A,
Dupont CT,
Feitosa MF,
Gudmundsdottir V,
Guo X,
Harris SE,
Hikino K,
Huang Z,
Lefevre C,
Lyytikäinen LP,
Milaneschi Y,
Nardone GG,
Santin A,
Schmidt H,
Shen B,
Sofer T,
Sun Q,
Tan YA,
Tang J,
Thériault S,
van der Most PJ,
Ware EB,
Weiss S,
Xing WY,
Yu C,
Zhao W,
Ansari MAY,
Anugu P,
Attia JR,
Bazzano LA,
Bis JC,
Breyer M,
Cade B,
Chen G,
Collins S,
Corley J,
Davies G,
Dörr M,
Du J,
Edwards TL,
Faquih T,
Faul JD,
Fohner AE,
Fretts AM,
Gangireddy S,
Gepner A,
Graff M,
Hofer E,
Homuth G,
Hood MM,
Jie X,
Kähönen M,
Kardia SLR,
Karvonen-Gutierrez CA,
Launer LJ,
Levy D,
Maheshwari M,
Martin LW,
Matsuda K,
McNeil JJ,
Nolte IM,
Okochi T,
Raffield LM,
Raitakari OT,
Risch L,
Risch M,
Roux AD,
Ruiz-Narvaez EA,
Russ TC,
Saito T,
Schreiner PJ,
Scott RJ,
Shikany J,
Smith JA,
Snieder H,
Spedicati B,
Tai ES,
Taylor AM,
Taylor KD,
Tesolin P,
van Dam RM,
Wang R,
Wenbin W,
Xie T,
Yao J,
Young KL,
Zhang R,
Zonderman AB,
Concas MP,
Conen D,
Cox SR,
Evans MK,
Fox ER,
de Las Fuentes L,
Giri A,
Girotto G,
Grabe HJ,
Gu C,
Gudnason V,
Harlow SD,
Holliday E,
Jost JB,
Lacaze P,
Lee S,
Lehtimäki T,
Li C,
Liu CT,
Morrison AC,
North KE,
Penninx BWJH,
Peyser PA,
Province MM,
Psaty BM,
Redline S,
Rosendaal FR,
Rotimi CN,
Rotter JI,
Schmidt R,
Sim X,
Terao C,
Weir DR,
Zhu X,
Franceschini N,
O'Connell JR,
Jaquish CE,
Wang H,
Manning A,
Munroe PB,
Rao DC,
Chen H,
Gauderman WJ,
Bierut LJ,
Winkler TW,
Fornage M
Biobank Japan Project · Lifelines Cohort Study,
HGG advances · 2026 · PMID 41520179 · open access
페이지 2개
The human AIRE gene at chromosome 21q22 is a genetic determinant for the predisposition to rheumatoid arthritis in Japanese population
Terao C,
Yamada R,
Ohmura K,
Takahashi M,
Kawaguchi T,
Kochi Y,
Okada Y,
Nakamura Y,
Yamamoto K,
Melchers I,
Lathrop M,
Mimori T
외 1명 — 모두 보기
Human Disease Genomics Working Group · RA Clinical and Genetic Study Consortium
Human molecular genetics · 2011 · PMID 21505073
페이지 1개
A genome-wide association study identified AFF1 as a susceptibility locus for systemic lupus eyrthematosus in Japanese
Okada Y,
Shimane K,
Kochi Y,
Tahira T,
Suzuki A,
Higasa K,
Takahashi A,
Horita T,
Atsumi T,
Ishii T,
Okamoto A,
Fujio K
외 32명 — 모두 보기
Hirakata M,
Amano H,
Kondo Y,
Ito S,
Takada K,
Mimori A,
Saito K,
Kamachi M,
Kawaguchi Y,
Ikari K,
Mohammed OW,
Matsuda K,
Terao C,
Ohmura K,
Myouzen K,
Hosono N,
Tsunoda T,
Nishimoto N,
Mimori T,
Matsuda F,
Tanaka Y,
Sumida T,
Yamanaka H,
Takasaki Y,
Koike T,
Horiuchi T,
Hayashi K,
Kubo M,
Kamatani N,
Yamada R,
Nakamura Y,
Yamamoto K
PLoS genetics · 2012 · PMID 22291604 · open access
페이지 1개
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