論文・総説 - 田中 敏博
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Wataru Shimizu, Hisaki Makimoto, Kenichiro Yamagata, Tsukasa Kamakura, Mitsuru Wada, Koji Miyamoto, Yuko Inoue-Yamada, Hideo Okamura, Kohei Ishibashi, Takashi Noda, Satoshi Nagase, Aya Miyazaki, Heima Sakaguchi, Isao Shiraishi, Takeru Makiyama, Seiko Ohno, Hideki Itoh, Hiroshi Watanabe, Kenshi Hayashi, Masakazu Yamagishi, Hiroshi Morita, Masao Yoshinaga, Yoshiyasu Aizawa, Kengo Kusano, Yoshihiro Miyamoto, Shiro Kamakura, Satoshi Yasuda, Hisao Ogawa, Toshihiro Tanaka, Naotaka Sumitomo, Nobuhisa Hagiwara, Keiichi Fukuda, Satoshi Ogawa, Yoshifusa Aizawa, Naomasa Makita, Tohru Ohe, Minoru Horie, Takeshi Aiba. Association of Genetic and Clinical Aspects of Congenital Long QT Syndrome With Life-Threatening Arrhythmias in Japanese Patients. JAMA Cardiol. 2019.03; 4 (3): 246-254. ( PubMed, DOI )
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El Rouby N, McDonough CW, Gong Y, McClure LA, Mitchell BD, Horenstein RB, Talbert RL, Crawford DC; eMERGE network, Gitzendanner MA, Takahashi A, Tanaka T, Kubo M, Pepine CJ, Cooper-DeHoff RM, Benavente OR, Shuldiner AR, Johnson JA.. Genome-wide association analysis of common genetic variants of resistant hypertension. Pharmacogenomics J. 2018.09; ( DOI )
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Roselli C, Chaffin MD, Weng LC, Aeschbacher S, Ahlberg G, Albert CM, Almgren P, Alonso A, Anderson CD, Aragam KG, Arking DE, Barnard J, Bartz TM, Benjamin EJ, Bihlmeyer NA, Bis JC, Bloom HL, Boerwinkle E, Bottinger EB, Brody JA, Calkins H, Campbell A, Cappola TP, Carlquist J, Chasman DI, Chen LY, Chen YI, Choi EK, Choi SH, Christophersen IE, Chung MK, Cole JW, Conen D, Cook J, Crijns HJ, Cutler MJ, Damrauer SM, Daniels BR, Darbar D, Delgado G, Denny JC, Dichgans M, Dörr M, Dudink EA, Dudley SC, Esa N, Esko T, Eskola M, Fatkin D, Felix SB, Ford I, Franco OH, Geelhoed B, Grewal RP, Gudnason V, Guo X, Gupta N, Gustafsson S, Gutmann R, Hamsten A, Harris TB, Hayward C, Heckbert SR, Hernesniemi J, Hocking LJ, Hofman A, Horimoto ARVR, Huang J, Huang PL, Huffman J, Ingelsson E, Ipek EG, Ito K, Jimenez-Conde J, Johnson R, Jukema JW, Kääb S, Kähönen M, Kamatani Y, Kane JP, Kastrati A, Kathiresan S, Katschnig-Winter P, Kavousi M, Kessler T, Kietselaer BL, Kirchhof P, Kleber ME, Knight S, Krieger JE, Kubo M, Launer LJ, Laurikka J, Lehtimäki T, Leineweber K, Lemaitre RN, Li M, Lim HE, Lin HJ, Lin H, Lind L, Lindgren CM, Lokki ML, London B, Loos RJF, Low SK, Lu Y, Lyytikäinen LP, Macfarlane PW, Magnusson PK, Mahajan A, Malik R, Mansur AJ, Marcus GM, Margolin L, Margulies KB, März W, McManus DD5, Melander O, Mohanty S, Montgomery JA, Morley MP, Morris AP, Müller-Nurasyid M, Natale A, Nazarian S, Neumann B, Newton-Cheh C, Niemeijer MN, Nikus K, Nilsson P, Noordam R, Oellers H, Olesen MS, Orho-Melander M, Padmanabhan S, Pak HN, Paré G, Pedersen NL, Pera J, Pereira A, Porteous D, Psaty BM, Pulit SL, Pullinger CR, Rader DJ, Refsgaard L, Ribasés M, Ridker PM, Rienstra M, Risch L, Roden DM, Rosand J, Rosenberg MA, Rost N, Rotter JI, Saba S, Sandhu RK, Schnabel RB, Schramm K, Schunkert H, Schurman C, Scott SA, Seppälä I, Shaffer C, Shah S, Shalaby AA, Shim J, Shoemaker MB, Siland JE, Sinisalo J, Sinner MF, Slowik A, Smith AV, Smith BH, Smith JG, Smith JD, Smith NL, Soliman EZ, Sotoodehnia N, Stricker BH Sun A, Sun H, Svendsen JH, Tanaka T, Tanriverdi K, Taylor KD, Teder-Laving M, Teumer A, Thériault S, Trompet S Tucker NR, Tveit A, Uitterlinden AG, Van Der Harst P, Van Gelder IC, Van Wagoner DR, Verweij N, Vlachopoulou E, Völker U, Wang B, Weeke PE, Weijs B, Weiss R, Weiss S, Wells QS, Wiggins KL, Wong JA, Woo D, Worrall BB, Yang PS, Yao J, Yoneda ZT, Zeller T, Zeng L, Lubitz SA, Lunetta KL, Ellinor PT.. Multi-ethnic genome-wide association study for atrial fibrillation. Nat Genet. 2018.09; 50 (9): 1225-1233. ( DOI )
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Hirata J, Hirota T, Ozeki T, Kanai M, Sudo T, Tanaka T, Hizawa N, Nakagawa H, Sato S, Mushiroda T, Saeki H, Tamari M, Okada Y.. Variants at HLA-A, HLA-C, and HLA-DQB1 Confer Risk of Psoriasis Vulgaris in Japanese. J Invest Dermatol. 2018.03; 138 (3): 542-548. ( DOI )
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Urayama KY, Takagi M, Kawaguchi T, Matsuo K, Tanaka Y, Ayukawa Y, Arakawa Y, Hasegawa D, Yuza Y, Kaneko T, Noguchi Y, Taneyama Y, Ota S, Inukai T, Yanagimachi M, Keino D, Koike K, Toyama D, Nakazawa Y, Kurosawa H, Nakamura K, Moriwaki K, Goto H, Sekinaka Y, Morita D, Kato M, Takita J, Tanaka T, Inazawa J, Koh K, Ishida Y, Ohara A, Mizutani S, Matsuda F, Manabe A.. Regional evaluation of childhood acute lymphoblastic leukemia genetic susceptibility loci among Japanese. Sci Rep. 2018.01; 8 (1): 789. ( DOI )
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McCormack M, Gui H, Ingason A, Speed D, Wright GEB, Zhang EJ, Secolin R, Yasuda C, Kwok M, Wolking S, Becker F, Rau S, Avbersek A, Heggeli K, Leu C, Depondt C, Sills GJ, Marson AG, Auce P, Brodie MJ, Francis B, Johnson MR, Koeleman BPC, Striano P, Coppola A, Zara F, Kunz WS, Sander JW, Lerche H, Klein KM, Weckhuysen S, Krenn M, Gudmundsson LJ, Stefánsson K, Krause R, Shear N, Ross CJD, Delanty N; EPIGEN Consortium;, Pirmohamed M, Carleton BC; Canadian Pharmacogenomics Network for Drug Safety;, Cendes F, Lopes-Cendes I, Liao WP, O'Brien TJ, Sisodiya SM; EpiPGX Consortium;, Cherny S, Kwan P, Baum L; International League Against Epilepsy Consortium on Complex Epilepsies;, Cavalleri GL.. Genetic variation in CFH predicts phenytoin-induced maculopapular exanthema in European-descent patients. Neurology. . 2018.01; 90 (4): e332-e341. ( DOI )
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T Sudo, Y Okada, K Ozaki, K Urayama, M Kanai, H Kobayashi, M Gokyu, Y Izumi, T Tanaka. Association of NOD2 Mutations with Aggressive Periodontitis. J. Dent. Res.. 2017.06; 22034517715432. ( PubMed, DOI )
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Spracklen Cassandra N, Chen Peng, Kim Young Jin, Wang Xu, Cai Hui, Li Shengxu, Long Jirong, Wu Ying, Wang Ya Xing, Takeuchi Fumihiko, Wu Jer-Yuarn, Jung Keum-Ji, Hu Cheng, Akiyama Koichi, Zhang Yonghong, Moon Sanghoon, Johnson Todd A, Li Huaixing, Dorajoo Rajkumar, He Meian, Cannon Maren E, Roman Tamara S, Salfati Elias, Lin Keng-Hung, Guo Xiuqing, Sheu Wayne H H, Absher Devin, Adair Linda S, Assimes Themistocles L, Aung Tin, Cai Qiuyin, Chang Li-Ching, Chen Chien-Hsiun, Chien Li-Hsin, Chuang Lee-Ming, Chuang Shu-Chun, Du Shufa, Fan Qiao, Fann Cathy S J, Feranil Alan B, Friedlander Yechiel, Gordon-Larsen Penny, Gu Dongfeng, Gui Lixuan, Guo Zhirong, Heng Chew-Kiat, Hixson James, Hou Xuhong, Hsiung Chao Agnes, Hu Yao, Hwang Mi Yeong, Hwu Chii-Min, Isono Masato, Juang Jyh-Ming Jimmy, Khor Chiea-Chuen, Kim Yun Kyoung, Koh Woon-Puay, Kubo Michiaki, Lee I-Te, Lee Sun-Ju, Lee Wen-Jane, Liang Kae-Woei, Lim Blanche, Lim Sing-Hui, Liu Jianjun, Nabika Toru, Pan Wen-Harn, Peng Hao, Quertermous Thomas, Sabanayagam Charumathi, Sandow Kevin, Shi Jinxiu, Sun Liang, Tan Pok Chien, Tan Shu-Pei, Taylor Kent D, Teo Yik-Ying, Toh Sue-Anne, Tsunoda Tatsuhiko, van Dam Rob M, Wang Aili, Wang Feijie, Wang Jie, Wei Wen Bin, Xiang Yong-Bing, Yao Jie, Yuan Jian-Min, Zhang Rong, Zhao Wanting, Chen Yii-Der Ida, Rich Stephen S, Rotter Jerome I, Wang Tzung-Dau, Wu Tangchun, Lin Xu, Han Bok-Ghee, Tanaka Toshihiro, Cho Yoon Shin, Katsuya Tomohiro, Jia Weiping, Jee Sun-Ha, Chen Yuan-Tsong, Kato Norihiro, Jonas Jost B, Cheng Ching-Yu, Shu Xiao-Ou, He Jiang, Zheng Wei, Wong Tien-Yin, Huang Wei, Kim Bong-Jo, Tai E-Shyong, Mohlke Karen L, Sim Xueling. Association analyses of East Asian individuals and trans-ancestry analyses with European individuals reveal new loci associated with cholesterol and triglyceride levels. Hum Mol Genet. 2017.05; 26 (9): 1770-1784. ( PubMed, DOI )
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Low Siew-Kee, Takahashi Atsushi, Ebana Yusuke, Ozaki Kouichi, Christophersen Ingrid E, Ellinor Patrick T, Ogishima Soichi, Yamamoto Masayuki, Satoh Mamoru, Sasaki Makoto, Yamaji Taiki, Iwasaki Motoki, Tsugane Shoichiro, Tanaka Keitaro, Naito Mariko, Wakai Kenji, Tanaka Hideo, Furukawa Tetsushi, Kubo Michiaki, Ito Kaoru, Kamatani Yoichiro, Tanaka Toshihiro, AFGen Consortium. Identification of six new genetic loci associated with atrial fibrillation in the Japanese population. Nat Genet. 2017.04; ( PubMed, DOI )
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Christophersen Ingrid E, Rienstra Michiel, Roselli Carolina, Yin Xiaoyan, Geelhoed Bastiaan, Barnard John, Lin Honghuang, Arking Dan E, Smith Albert V, Albert Christine M, Chaffin Mark, Tucker Nathan R, Li Molong, Klarin Derek, Bihlmeyer Nathan A, Low Siew-Kee, Weeke Peter E, Muller-Nurasyid Martina, Smith J Gustav, Brody Jennifer A, Niemeijer Maartje N, Dorr Marcus, Trompet Stella, Huffman Jennifer, Gustafsson Stefan, Schurmann Claudia, Kleber Marcus E, Lyytikainen Leo-Pekka, Seppala Ilkka, Malik Rainer, Horimoto Andrea R V R, Perez Marco, Sinisalo Juha, Aeschbacher Stefanie, Theriault Sebastien, Yao Jie, Radmanesh Farid, Weiss Stefan, Teumer Alexander, Choi Seung Hoan, Weng Lu-Chen, Clauss Sebastian, Deo Rajat, Rader Daniel J, Shah Svati H, Sun Albert, Hopewell Jemma C, Debette Stephanie, Chauhan Ganesh, Yang Qiong, Worrall Bradford B, Pare Guillaume, Kamatani Yoichiro, Hagemeijer Yanick P, Verweij Niek, Siland Joylene E, Kubo Michiaki, Smith Jonathan D, Van Wagoner David R, Bis Joshua C, Perz Siegfried, Psaty Bruce M, Ridker Paul M, Magnani Jared W, Harris Tamara B, Launer Lenore J, Shoemaker M Benjamin, Padmanabhan Sandosh, Haessler Jeffrey, Bartz Traci M, Waldenberger Melanie, Lichtner Peter, Arendt Marina, Krieger Jose E, Kahonen Mika, Risch Lorenz, Mansur Alfredo J, Peters Annette, Smith Blair H, Lind Lars, Scott Stuart A, Lu Yingchang, Bottinger Erwin B, Hernesniemi Jussi, Lindgren Cecilia M, Wong Jorge A, Huang Jie, Eskola Markku, Morris Andrew P, Ford Ian, Reiner Alex P, Delgado Graciela, Chen Lin Y, Chen Yii-Der Ida, Sandhu Roopinder K, Li Man, Boerwinkle Eric, Eisele Lewin, Lannfelt Lars, Rost Natalia, Anderson Christopher D, Taylor Kent D, Campbell Archie, Magnusson Patrik K, Porteous David, Hocking Lynne J, Vlachopoulou Efthymia, Pedersen Nancy L, Nikus Kjell, Orho-Melander Marju, Hamsten Anders, Heeringa Jan, Denny Joshua C, Kriebel Jennifer, Darbar Dawood, Newton-Cheh Christopher, Shaffer Christian, Macfarlane Peter W, Heilmann-Heimbach Stefanie, Almgren Peter, Huang Paul L, Sotoodehnia Nona, Soliman Elsayed Z, Uitterlinden Andre G, Hofman Albert, Franco Oscar H, Volker Uwe, Jockel Karl-Heinz, Sinner Moritz F, Lin Henry J, Guo Xiuqing, Dichgans Martin, Ingelsson Erik, Kooperberg Charles, Melander Olle, Loos Ruth J F, Laurikka Jari, Conen David, Rosand Jonathan, van der Harst Pim, Lokki Marja-Liisa, Kathiresan Sekar, Pereira Alexandre, Jukema J Wouter, Hayward Caroline, Rotter Jerome I, Marz Winfried, Lehtimaki Terho, Stricker Bruno H, Chung Mina K, Felix Stephan B, Gudnason Vilmundur, Alonso Alvaro, Roden Dan M, Kaab Stefan, Chasman Daniel I, Heckbert Susan R, Benjamin Emelia J, Tanaka Toshihiro, Lunetta Kathryn L, Lubitz Steven A, Ellinor Patrick T, METASTROKE Consortium of the ISGC. Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation. Nat Genet. 2017.04; ( PubMed, DOI )
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Yamagata Kenichiro, Horie Minoru, Aiba Takeshi, Ogawa Satoshi, Aizawa Yoshifusa, Ohe Toru, Yamagishi Masakazu, Makita Naomasa, Sakurada Harumizu, Tanaka Toshihiro, Shimizu Akihiko, Hagiwara Nobuhisa, Kishi Ryoji, Nakano Yukiko, Takagi Masahiko, Makiyama Takeru, Ohno Seiko, Fukuda Keiichi, Watanabe Hiroshi, Morita Hiroshi, Hayashi Kenshi, Kusano Kengo, Kamakura Shiro, Yasuda Satoshi, Ogawa Hisao, Miyamoto Yoshihiro, Kapplinger Jamie D, Ackerman Michael J, Shimizu Wataru. Genotype-Phenotype Correlation of SCN5A Mutation for the Clinical and Electrocardiographic Characteristics of Probands with Brugada Syndrome: A Japanese Multicenter Registry. Circulation. 2017.03; ( PubMed, DOI )
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Nagai Akiko, Hirata Makoto, Kamatani Yoichiro, Muto Kaori, Matsuda Koichi, Kiyohara Yutaka, Ninomiya Toshiharu, Tamakoshi Akiko, Yamagata Zentaro, Mushiroda Taisei, Murakami Yoshinori, Yuji Koichiro, Furukawa Yoichi, Zembutsu Hitoshi, Tanaka Toshihiro, Ohnishi Yozo, Nakamura Yusuke, Kubo Michiaki, BioBank Japan Cooperative Hospital Group. Overview of the BioBank Japan Project: Study design and profile. J Epidemiol. 2017.03; 27 (3S): S2-S8. ( PubMed, DOI )
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Hirata Makoto, Nagai Akiko, Kamatani Yoichiro, Ninomiya Toshiharu, Tamakoshi Akiko, Yamagata Zentaro, Kubo Michiaki, Muto Kaori, Kiyohara Yutaka, Mushiroda Taisei, Murakami Yoshinori, Yuji Koichiro, Furukawa Yoichi, Zembutsu Hitoshi, Tanaka Toshihiro, Ohnishi Yozo, Nakamura Yusuke, Matsuda Koichi, BioBank Japan Cooperative Hospital Group. Overview of BioBank Japan follow-up data in 32 diseases. J Epidemiol. 2017.03; 27 (3S): S22-S28. ( PubMed, DOI )
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Hirata Makoto, Kamatani Yoichiro, Nagai Akiko, Kiyohara Yutaka, Ninomiya Toshiharu, Tamakoshi Akiko, Yamagata Zentaro, Kubo Michiaki, Muto Kaori, Mushiroda Taisei, Murakami Yoshinori, Yuji Koichiro, Furukawa Yoichi, Zembutsu Hitoshi, Tanaka Toshihiro, Ohnishi Yozo, Nakamura Yusuke, Matsuda Koichi, BioBank Japan Cooperative Hospital Group. Cross-sectional analysis of BioBank Japan clinical data: A large cohort of 200,000 patients with 47 common diseases. J Epidemiol. 2017.03; 27 (3S): S9-S21. ( PubMed, DOI )
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Ebana Yusuke, Ozaki Kouichi, Liu Lian, Hachiya Hitoshi, Hirao Kenzo, Isobe Mitsuaki, Kubo Michiaki, Tanaka Toshihiro, Furukawa Tetsushi. Clinical utility and functional analysis of variants in atrial fibrillation-associated locus 4q25. J Cardiol. 2017.01; ( PubMed, DOI )
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Chisato Shimizu, Hariklia Eleftherohorinou, Victoria J Wright, Jihoon Kim, Martin P Alphonse, James C Perry, Rolando Cimaz, David Burgner, Nagib Dahdah, Long T Hoang, Chiea Chuen Khor, Andrea Salgado, Adriana H Tremoulet, Sonia Davila, Taco W Kuijpers, Martin L Hibberd, Todd A Johnson, Atsushi Takahashi, Tatsuhiko Tsunoda, Michiaki Kubo, Toshihiro Tanaka, Yoshihiro Onouchi, Rae S M Yeung, Lachlan J M Coin, Michael Levin, Jane C Burns, . Genetic Variation in the SLC8A1 Calcium Signaling Pathway Is Associated With Susceptibility to Kawasaki Disease and Coronary Artery Abnormalities. Circ Cardiovasc Genet. 2016.12; 9 (6): 559-568. ( PubMed, DOI )
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Tumurkhuu T, Fujiwara T, Komazaki Y, Kawaguchi Y, Tanaka T, Inazawa J, Ganburged G, Bazar A, Ogawa T, Moriyama K. Association between maternal education and malocclusion in Mongolian adolescents: a cross-sectional study. BMJ Open. 2016.11; 6 (11):
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Lian Liu, Yusuke Ebana, Jun-Ichi Nitta, Yoshihide Takahashi, Shinsuke Miyazaki, Toshihiro Tanaka, Masatoshi Komura, Mitsuaki Isobe, Tetsushi Furukawa. Genetic Variants Associated With Susceptibility to Atrial Fibrillation in a Japanese Population. Can J Cardiol. 2016.11; ( PubMed, DOI )
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Tsasan Tumurkhuu, Takeo Fujiwara, Yuko Komazaki, Yoko Kawaguchi, Toshihiro Tanaka, Johji Inazawa, Ganjargal Ganburged, Amarsaikhan Bazar, Takuya Ogawa, Keiji Moriyama. Association between maternal education and malocclusion in Mongolian adolescents: a cross-sectional study. BMJ Open. 2016.11; 6 (11): e012283. ( PubMed, DOI )
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Mari Ichikawa, Takeshi Aiba, Seiko Ohno, Daichi Shigemizu, Junichi Ozawa, Keiko Sonoda, Megumi Fukuyama, Hideki Itoh, Yoshihiro Miyamoto, Tatsuhiko Tsunoda, Takeru Makiyama, Toshihiro Tanaka, Wataru Shimizu, Minoru Horie. Phenotypic Variability of ANK2 Mutations in Patients With Inherited Primary Arrhythmia Syndromes. Circ. J.. 2016.11; 80 (12): 2435-2442. ( PubMed, DOI )