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Adam E Locke, Bratati Kahali, Sonja I Berndt, Anne E Justice, Tune H Pers, Felix R Day, Corey Powell, Sailaja Vedantam, Martin L Buchkovich, Jian Yang, Damien C Croteau-Chonka, Tonu Esko, Tove Fall, Teresa Ferreira, Stefan Gustafsson, Zoltán Kutalik, Jian'an Luan, Reedik Mägi, Joshua C Randall, Thomas W Winkler, Andrew R Wood, Tsegaselassie Workalemahu, Jessica D Faul, Jennifer A Smith, Jing Hua Zhao, Wei Zhao, Jin Chen, Rudolf Fehrmann, Åsa K Hedman, Juha Karjalainen, Ellen M Schmidt, Devin Absher, Najaf Amin, Denise Anderson, Marian Beekman, Jennifer L Bolton, Jennifer L Bragg-Gresham, Steven Buyske, Ayse Demirkan, Guohong Deng, Georg B Ehret, Bjarke Feenstra, Mary F Feitosa, Krista Fischer, Anuj Goel, Jian Gong, Anne U Jackson, Stavroula Kanoni, Marcus E Kleber, Kati Kristiansson, Unhee Lim, Vaneet Lotay, Massimo Mangino, Irene Mateo Leach, Carolina Medina-Gomez, Sarah E Medland, Michael A Nalls, Cameron D Palmer, Dorota Pasko, Sonali Pechlivanis, Marjolein J Peters, Inga Prokopenko, Dmitry Shungin, Alena Stančáková, Rona J Strawbridge, Yun Ju Sung, Toshiko Tanaka, Alexander Teumer, Stella Trompet, Sander W van der Laan, Jessica van Setten, Jana V Van Vliet-Ostaptchouk, Zhaoming Wang, Loïc Yengo, Weihua Zhang, Aaron Isaacs, Eva Albrecht, Johan Ärnlöv, Gillian M Arscott, Antony P Attwood, Stefania Bandinelli, Amy Barrett, Isabelita N Bas, Claire Bellis, Amanda J Bennett, Christian Berne, Roza Blagieva, Matthias Blüher, Stefan Böhringer, Lori L Bonnycastle, Yvonne Böttcher, Heather A Boyd, Marcel Bruinenberg, Ida H Caspersen, Yii-Der Ida Chen, Robert Clarke, E Warwick Daw, Anton J M de Craen, Graciela Delgado, Maria Dimitriou, Alex S F Doney, Niina Eklund, Karol Estrada, Elodie Eury, Lasse Folkersen, Ross M Fraser, Melissa E Garcia, Frank Geller, Vilmantas Giedraitis, Bruna Gigante, Alan S Go, Alain Golay, Alison H Goodall, Scott D Gordon, Mathias Gorski, Hans-Jörgen Grabe, Harald Grallert, Tanja B Grammer, Jürgen Gräßler, Henrik Grönberg, Christopher J Groves, Gaëlle Gusto, Jeffrey Haessler, Per Hall, Toomas Haller, Goran Hallmans, Catharina A Hartman, Maija Hassinen, Caroline Hayward, Nancy L Heard-Costa, Quinta Helmer, Christian Hengstenberg, Oddgeir Holmen, Jouke-Jan Hottenga, Alan L James, Janina M Jeff, Åsa Johansson, Jennifer Jolley, Thorhildur Juliusdottir, Leena Kinnunen, Wolfgang Koenig, Markku Koskenvuo, Wolfgang Kratzer, Jaana Laitinen, Claudia Lamina, Karin Leander, Nanette R Lee, Peter Lichtner, Lars Lind, Jaana Lindström, Ken Sin Lo, Stéphane Lobbens, Roberto Lorbeer, Yingchang Lu, François Mach, Patrik K E Magnusson, Anubha Mahajan, Wendy L McArdle, Stela McLachlan, Cristina Menni, Sigrun Merger, Evelin Mihailov, Lili Milani, Alireza Moayyeri, Keri L Monda, Mario A Morken, Antonella Mulas, Gabriele Müller, Martina Müller-Nurasyid, Arthur W Musk, Ramaiah Nagaraja, Markus M Nöthen, Ilja M Nolte, Stefan Pilz, Nigel W Rayner, Frida Renstrom, Rainer Rettig, Janina S Ried, Stephan Ripke, Neil R Robertson, Lynda M Rose, Serena Sanna, Hubert Scharnagl, Salome Scholtens, Fredrick R Schumacher, William R Scott, Thomas Seufferlein, Jianxin Shi, Albert Vernon Smith, Joanna Smolonska, Alice V Stanton, Valgerdur Steinthorsdottir, Kathleen Stirrups, Heather M Stringham, Johan Sundström, Morris A Swertz, Amy J Swift, Ann-Christine Syvänen, Sian-Tsung Tan, Bamidele O Tayo, Barbara Thorand, Gudmar Thorleifsson, Jonathan P Tyrer, Hae-Won Uh, Liesbeth Vandenput, Frank C Verhulst, Sita H Vermeulen, Niek Verweij, Judith M Vonk, Lindsay L Waite, Helen R Warren, Dawn Waterworth, Michael N Weedon, Lynne R Wilkens, Christina Willenborg, Tom Wilsgaard, Mary K Wojczynski, Andrew Wong, Alan F Wright, Qunyuan Zhang ; 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Wen W, Zheng W, Okada Y, Takeuchi F, Tabara Y, Hwang JY, Dorajoo R, Li H, Tsai FJ, Yang X, He J, 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: Meta-analysis of genome-wide association studies in East Asian-ancestry populations identifies four new loci for body mass index. Hum Mol Genet. 2014.10; 23 (20): 5492-5504. ( PubMed , DOI )

Kolek MJ, Edwards TL, Muhammad R, Balouch A, Shoemaker MB, Blair MA, Kor KC, Takahashi A, Kubo M, Roden DM, Tanaka T, Darbar D: A genome-wide association study to identify genomic modulators of rate control therapy in patients with atrial fibrillation. Am J Cardiol. 2014.08; 114 (4): 593-600. ( PubMed , DOI )

Fukuda M, Mizutani T, Mochizuki W, Matsumoto T, Nozaki K, Sakamaki Y, Ichinose S, Okada Y, Tanaka T, Watanabe M, Nakamura T: Small intestinal stem cell identity is maintained with functional Paneth cells in heterotopically grafted epithelium onto the colon. Genes Dev. 2014.08; 28 (16): 1752-1757. ( PubMed , DOI )

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Miyamoto Y, Mabuchi A, Shi D, Kubo T, Takatori Y, Saito S, Fujioka M, Sudo A, Uchida A, Yamamoto S, Ozaki K, Takigawa M, Tanaka T, Nakamura Y, Jiang Q, Ikegawa S: A functional polymorphism in the 5' UTR of GDF5 is associated with susceptibility to osteoarthritis. Nat Genet. 2007.04; 39 (4): 529-533. ( PubMed , DOI )

Ebana Y, Ozaki K, Inoue K, Sato H, Iida A, Lwin H, Saito S, Mizuno H, Takahashi A, Nakamura T, Miyamoto Y, Ikegawa S, Odashiro K, Nobuyoshi M, Kamatani N, Hori M, Isobe M, Nakamura Y, Tanaka T: A functional SNP in ITIH3 is associated with susceptibility to myocardial infarction. J Hum Genet. 2007; 52 (3): 220-229. ( PubMed , DOI )

Ozaki K, Sato H, Iida A, Mizuno H, Nakamura T, Miyamoto Y, Takahashi A, Tsunoda T, Ikegawa S, Kamatani N, Hori M, Nakamura Y, Tanaka T: A functional SNP in PSMA6 confers risk of myocardial infarction in the Japanese population. Nat Genet. 2006.08; 38 (8): 921-925. ( PubMed , DOI )

Mizuno H, Sato H, Sakata Y, Ohnishi Y, Hishida E, Kinjo K, Nakatani D, Shimizu M, Kondo H, Tanaka T, Ozaki K, Hirayama A, Ito H, Otsu K, Hori M: Impact of atherosclerosis-related gene polymorphisms on mortality and recurrent events after myocardial infarction. Atherosclerosis. 2006.04; 185 (2): 400-405. ( PubMed , DOI )

Ishii N, Ozaki K, Sato H, Mizuno H, Saito S, Takahashi A, Miyamoto Y, Ikegawa S, Kamatani N, Hori M, Saito S, Nakamura Y, Tanaka T: Identification of a novel non-coding RNA, MIAT, that confers risk of myocardial infarction. J Hum Genet. 2006; 51 (12): 1087-1099. ( PubMed , DOI )

Tanaka T, Ozaki K: Inflammation as a risk factor for myocardial infarction. J Hum Genet. 2006; 51 (7): 595-604. ( PubMed , DOI )

Kato M, Sekine A, Ohnishi Y, Johnson TA, Tanaka T, Nakamura Y, Tsunoda T: Linkage disequilibrium of evolutionarily conserved regions in the human genome. BMC Genomics. 2006; 7 326. ( PubMed , DOI )

Ozaki K, Tanaka T: Genome-wide association study to identify single-nucleotide polymorphisms conferring risk of myocardial infarction. Methods Mol Med. 2006; 128 173-180. ( PubMed , DOI )

A haplotype map of the human genome. Nature. 2005.10; 437 (7063): 1299-1320. ( PubMed , DOI )

Ozaki K, Tanaka T: Genome-wide association study to identify SNPs conferring risk of myocardial infarction and their functional analyses. Cell Mol Life Sci. 2005.08; 62 (16): 1804-1813. ( PubMed , DOI )

Ohtsubo S, Iida A, Nitta K, Tanaka T, Yamada R, Ohnishi Y, Maeda S, Tsunoda T, Takei T, Obara W, Akiyama F, Ito K, Honda K, Uchida K, Tsuchiya K, Yumura W, Ujiie T, Nagane Y, Miyano S, Suzuki Y, Narita I, Gejyo F, Fujioka T, Nihei H, Nakamura Y: Association of a single-nucleotide polymorphism in the immunoglobulin mu-binding protein 2 gene with immunoglobulin A nephropathy. J Hum Genet. 2005; 50 (1): 30-35. ( PubMed , DOI )

Iida A, Ozaki K, Tanaka T, Nakamura Y: Fine-scale SNP map of an 11-kb genomic region at 22q13.1 containing the galectin-1 gene. J Hum Genet. 2005; 50 (1): 42-45. ( PubMed , DOI )

Onda M, Emi M, Yoshida A, Miyamoto S, Akaishi J, Asaka S, Mizutani K, Shimizu K, Nagahama M, Ito K, Tanaka T, Tsunoda T: Comprehensive gene expression profiling of anaplastic thyroid cancers with cDNA microarray of 25 344 genes. Endocr Relat Cancer. 2004.12; 11 (4): 843-854. ( PubMed , DOI )

Onda M, Emi M, Nagai H, Nagahata T, Tsumagari K, Fujimoto T, Akiyama F, Sakamoto G, Makita M, Kasumi F, Miki Y, Tanaka T, Tsunoda T, Nakamura Y: Gene expression patterns as marker for 5-year postoperative prognosis of primary breast cancers. J Cancer Res Clin Oncol. 2004.09; 130 (9): 537-545. ( PubMed , DOI )

Tsunoda T, Lathrop GM, Sekine A, Yamada R, Takahashi A, Ohnishi Y, Tanaka T, Nakamura Y: Variation of gene-based SNPs and linkage disequilibrium patterns in the human genome. Hum Mol Genet. 2004.08; 13 (15): 1623-1632. ( PubMed , DOI )

Integrating ethics and science in the International HapMap Project. Nat Rev Genet. 2004.06; 5 (6): 467-475. ( PubMed , DOI )

Ozaki K, Inoue K, Sato H, Iida A, Ohnishi Y, Sekine A, Sato H, Odashiro K, Nobuyoshi M, Hori M, Nakamura Y, Tanaka T: Functional variation in LGALS2 confers risk of myocardial infarction and regulates lymphotoxin-alpha secretion in vitro. Nature. 2004.05; 429 (6987): 72-75. ( PubMed , DOI )

Nagahata T, Onda M, Emi M, Nagai H, Tsumagari K, Fujimoto T, Hirano A, Sato T, Nishikawa K, Akiyama F, Sakamoto G, Kasumi F, Miki Y, Tanaka T, Tsunoda T: Expression profiling to predict postoperative prognosis for estrogen receptor-negative breast cancers by analysis of 25,344 genes on a cDNA microarray. Cancer Sci. 2004.03; 95 (3): 218-225. ( PubMed )

Ota T, Suzuki Y, Nishikawa T, Otsuki T, Sugiyama T, Irie R, Wakamatsu A, Hayashi K, Sato H, Nagai K, Kimura K, Makita H, Sekine M, Obayashi M, Nishi T, Shibahara T, Tanaka T, Ishii S, Yamamoto J, Saito K, Kawai Y, Isono Y, Nakamura Y, Nagahari K, Murakami K, Yasuda T, Iwayanagi T, Wagatsuma M, Shiratori A, Sudo H, Hosoiri T, Kaku Y, Kodaira H, Kondo H, Sugawara M, Takahashi M, Kanda K, Yokoi T, Furuya T, Kikkawa E, Omura Y, Abe K, Kamihara K, Katsuta N, Sato K, Tanikawa M, Yamazaki M, Ninomiya K, Ishibashi T, Yamashita H, Murakawa K, Fujimori K, Tanai H, Kimata M, Watanabe M, Hiraoka S, Chiba Y, Ishida S, Ono Y, Takiguchi S, Watanabe S, Yosida M, Hotuta T, Kusano J, Kanehori K, Takahashi-Fujii A, Hara H, Tanase TO, Nomura Y, Togiya S, Komai F, Hara R, Takeuchi K, Arita M, Imose N, Musashino K, Yuuki H, Oshima A, Sasaki N, Aotsuka S, Yoshikawa Y, Matsunawa H, Ichihara T, Shiohata N, Sano S, Moriya S, Momiyama H, Satoh N, Takami S, Terashima Y, Suzuki O, Nakagawa S, Senoh A, Mizoguchi H, Goto Y, Shimizu F, Wakebe H, Hishigaki H, Watanabe T, Sugiyama A, Takemoto M, Kawakami B, Yamazaki M, Watanabe K, Kumagai A, Itakura S, Fukuzumi Y, Fujimori Y, Komiyama M, Tashiro H, Tanigami A, Fujiwara T, Ono T, Yamada K, Fujii Y, Ozaki K, Hirao M, Ohmori Y, Kawabata A, Hikiji T, Kobatake N, Inagaki H, Ikema Y, Okamoto S, Okitani R, Kawakami T, Noguchi S, Itoh T, Shigeta K, Senba T, Matsumura K, Nakajima Y, Mizuno T, Morinaga M, Sasaki M, Togashi T, Oyama M, Hata H, Watanabe M, Komatsu T, Mizushima-Sugano J, Satoh T, Shirai Y, Takahashi Y, Nakagawa K, Okumura K, Nagase T, Nomura N, Kikuchi H, Masuho Y, Yamashita R, Nakai K, Yada T, Nakamura Y, Ohara O, Isogai T, Sugano S: Complete sequencing and characterization of 21,243 full-length human cDNAs. Nat Genet. 2004.01; 36 (1): 40-45. ( PubMed , DOI )

The International HapMap Project. Nature. 2003.12; 426 (6968): 789-796. ( PubMed , DOI )

Sasaki Y, Mita H, Toyota M, Ishida S, Morimoto I, Yamashita T, Tanaka T, Imai K, Nakamura Y, Tokino T: Identification of the interleukin 4 receptor alpha gene as a direct target for p73. Cancer Res. 2003.12; 63 (23): 8145-8152. ( PubMed )

Watanabe G, Nishimori H, Irifune H, Sasaki Y, Ishida S, Zembutsu H, Tanaka T, Kawaguchi S, Wada T, Hata J, Kusakabe M, Yoshida K, Nakamura Y, Tokino T: Induction of tenascin-C by tumor-specific EWS-ETS fusion genes. Genes Chromosomes Cancer. 2003.03; 36 (3): 224-232. ( PubMed , DOI )

Tsukada S, Iwai M, Nishiu J, Itoh M, Tomoike H, Horiuchi M, Nakamura Y, Tanaka T: Inhibition of experimental intimal thickening in mice lacking a novel G-protein-coupled receptor. Circulation. 2003.01; 107 (2): 313-319. ( PubMed )

Iida A, Ozaki K, Ohnishi Y, Tanaka T, Nakamura Y: Identification of 46 novel SNPs in the 130-kb region containing a myocardial infarction susceptibility gene on chromosomal band 6p21. J Hum Genet. 2003; 48 (9): 476-479. ( PubMed , DOI )

Obara W, Iida A, Suzuki Y, Tanaka T, Akiyama F, Maeda S, Ohnishi Y, Yamada R, Tsunoda T, Takei T, Ito K, Honda K, Uchida K, Tsuchiya K, Yumura W, Ujiie T, Nagane Y, Nitta K, Miyano S, Narita I, Gejyo F, Nihei H, Fujioka T, Nakamura Y: Association of single-nucleotide polymorphisms in the polymeric immunoglobulin receptor gene with immunoglobulin A nephropathy (IgAN) in Japanese patients. J Hum Genet. 2003; 48 (6): 293-299. ( PubMed , DOI )

Iida A, Tanaka T, Nakamura Y: High-density SNP map of human ITR, a gene associated with vascular remodeling. J Hum Genet. 2003; 48 (4): 170-172. ( PubMed , DOI )

Ozaki K, Ohnishi Y, Iida A, Sekine A, Yamada R, Tsunoda T, Sato H, Sato H, Hori M, Nakamura Y, Tanaka T: Functional SNPs in the lymphotoxin-alpha gene that are associated with susceptibility to myocardial infarction. Nat Genet. 2002.12; 32 (4): 650-654. ( PubMed , DOI )

Nishimori H, Sasaki Y, Yoshida K, Irifune H, Zembutsu H, Tanaka T, Aoyama T, Hosaka T, Kawaguchi S, Wada T, Hata J, Toguchida J, Nakamura Y, Tokino T: The Id2 gene is a novel target of transcriptional activation by EWS-ETS fusion proteins in Ewing family tumors. Oncogene. 2002.11; 21 (54): 8302-8309. ( PubMed , DOI )

Ishiguro H, Shimokawa T, Tsunoda T, Tanaka T, Fujii Y, Nakamura Y, Furukawa Y: Isolation of HELAD1, a novel human helicase gene up-regulated in colorectal carcinomas. Oncogene. 2002.09; 21 (41): 6387-6394. ( PubMed , DOI )

Inoue K, Matsuda K, Itoh M, Kawaguchi H, Tomoike H, Aoyagi T, Nagai R, Hori M, Nakamura Y, Tanaka T: Osteopenia and male-specific sudden cardiac death in mice lacking a zinc transporter gene, Znt5. Hum Mol Genet. 2002.07; 11 (15): 1775-1784. ( PubMed )

Takei T, Iida A, Nitta K, Tanaka T, Ohnishi Y, Yamada R, Maeda S, Tsunoda T, Takeoka S, Ito K, Honda K, Uchida K, Tsuchiya K, Suzuki Y, Fujioka T, Ujiie T, Nagane Y, Miyano S, Narita I, Gejyo F, Nihei H, Nakamura Y: Association between single-nucleotide polymorphisms in selectin genes and immunoglobulin A nephropathy. Am J Hum Genet. 2002.03; 70 (3): 781-786. ( PubMed , DOI )

Hirakawa M, Tanaka T, Hashimoto Y, Kuroda M, Takagi T, Nakamura Y: JSNP: a database of common gene variations in the Japanese population. Nucleic Acids Res. 2002.01; 30 (1): 158-162. ( PubMed )

Sasaki Y, Ishida S, Morimoto I, Yamashita T, Kojima T, Kihara C, Tanaka T, Imai K, Nakamura Y, Tokino T: The p53 family member genes are involved in the Notch signal pathway. J Biol Chem. 2002.01; 277 (1): 719-724. ( PubMed , DOI )

Iwasa H, Kurabayashi M, Nagai R, Nakamura Y, Tanaka T: Twenty single-nucleotide polymorphisms in four genes encoding cardiac ion channels. J Hum Genet. 2002; 47 (4): 208-212. ( PubMed , DOI )

Akiyama F, Tanaka T, Yamada R, Ohnishi Y, Tsunoda T, Maeda S, Takei T, Obara W, Ito K, Honda K, Uchida K, Tsuchiya K, Nitta K, Yumura W, Nihei H, Ujiie T, Nagane Y, Miyano S, Suzuki Y, Fujioka T, Narita I, Gejyo F, Nakamura Y: Single-nucleotide polymorphisms in the class II region of the major histocompatibility complex in Japanese patients with immunoglobulin A nephropathy. J Hum Genet. 2002; 47 (10): 532-538. ( PubMed , DOI )

Haga H, Yamada R, Ohnishi Y, Nakamura Y, Tanaka T: Gene-based SNP discovery as part of the Japanese Millennium Genome Project: identification of 190,562 genetic variations in the human genome. Single-nucleotide polymorphism. J Hum Genet. 2002; 47 (11): 605-610. ( PubMed , DOI )

Fujita M, Furukawa Y, Tsunoda T, Tanaka T, Ogawa M, Nakamura Y: Up-regulation of the ectodermal-neural cortex 1 (ENC1) gene, a downstream target of the beta-catenin/T-cell factor complex, in colorectal carcinomas. Cancer Res. 2001.11; 61 (21): 7722-7726. ( PubMed )

Lin YM, Ono K, Satoh S, Ishiguro H, Fujita M, Miwa N, Tanaka T, Tsunoda T, Yang KC, Nakamura Y, Furukawa Y: Identification of AF17 as a downstream gene of the beta-catenin/T-cell factor pathway and its involvement in colorectal carcinogenesis. Cancer Res. 2001.09; 61 (17): 6345-6349. ( PubMed )

Kihara C, Tsunoda T, Tanaka T, Yamana H, Furukawa Y, Ono K, Kitahara O, Zembutsu H, Yanagawa R, Hirata K, Takagi T, Nakamura Y: Prediction of sensitivity of esophageal tumors to adjuvant chemotherapy by cDNA microarray analysis of gene-expression profiles. Cancer Res. 2001.09; 61 (17): 6474-6479. ( PubMed )

Ishiguro H, Tsunoda T, Tanaka T, Fujii Y, Nakamura Y, Furukawa Y: Identification of AXUD1, a novel human gene induced by AXIN1 and its reduced expression in human carcinomas of the lung, liver, colon and kidney. Oncogene. 2001.08; 20 (36): 5062-5066. ( PubMed , DOI )

Suzuki Y, Tsunoda T, Sese J, Taira H, Mizushima-Sugano J, Hata H, Ota T, Isogai T, Tanaka T, Nakamura Y, Suyama A, Sakaki Y, Morishita S, Okubo K, Sugano S: Identification and characterization of the potential promoter regions of 1031 kinds of human genes. Genome Res. 2001.05; 11 (5): 677-684. ( PubMed , DOI )

Suzuki Y, Taira H, Tsunoda T, Mizushima-Sugano J, Sese J, Hata H, Ota T, Isogai T, Tanaka T, Morishita S, Okubo K, Sakaki Y, Nakamura Y, Suyama A, Sugano S: Diverse transcriptional initiation revealed by fine, large-scale mapping of mRNA start sites. EMBO Rep. 2001.05; 2 (5): 388-393. ( PubMed , DOI )

Kitahara O, Furukawa Y, Tanaka T, Kihara C, Ono K, Yanagawa R, Nita ME, Takagi T, Nakamura Y, Tsunoda T: Alterations of gene expression during colorectal carcinogenesis revealed by cDNA microarrays after laser-capture microdissection of tumor tissues and normal epithelia. Cancer Res. 2001.05; 61 (9): 3544-3549. ( PubMed )

Matsushima-Nishiu M, Unoki M, Ono K, Tsunoda T, Minaguchi T, Kuramoto H, Nishida M, Satoh T, Tanaka T, Nakamura Y: Growth and gene expression profile analyses of endometrial cancer cells expressing exogenous PTEN. Cancer Res. 2001.05; 61 (9): 3741-3749. ( PubMed )

Yamada R, Tanaka T, Unoki M, Nagai T, Sawada T, Ohnishi Y, Tsunoda T, Yukioka M, Maeda A, Suzuki K, Tateishi H, Ochi T, Nakamura Y, Yamamoto K: Association between a single-nucleotide polymorphism in the promoter of the human interleukin-3 gene and rheumatoid arthritis in Japanese patients, and maximum-likelihood estimation of combinatorial effect that two genetic loci have on susceptibility to the disease. Am J Hum Genet. 2001.03; 68 (3): 674-685. ( PubMed , DOI )

Kunishima S, Kojima T, Matsushita T, Tanaka T, Tsurusawa M, Furukawa Y, Nakamura Y, Okamura T, Amemiya N, Nakayama T, Kamiya T, Saito H: Mutations in the NMMHC-A gene cause autosomal dominant macrothrombocytopenia with leukocyte inclusions (May-Hegglin anomaly/Sebastian syndrome). Blood. 2001.02; 97 (4): 1147-1149. ( PubMed )

Kato T, Satoh S, Okabe H, Kitahara O, Ono K, Kihara C, Tanaka T, Tsunoda T, Yamaoka Y, Nakamura Y, Furukawa Y: Isolation of a novel human gene, MARKL1, homologous to MARK3 and its involvement in hepatocellular carcinogenesis. Neoplasia. 2001.01; 3 (1): 4-9. ( PubMed , DOI )

Iwasa H, Kurabayashi M, Nagai R, Nakamura Y, Tanaka T: Multiple single-nucleotide polymorphisms (SNPs) in the Japanese population in six candidate genes for long QT syndrome. J Hum Genet. 2001; 46 (3): 158-162. ( PubMed , DOI )

Iida A, Ohnishi Y, Ozaki K, Ariji Y, Nakamura Y, Tanaka T: High-density single-nucleotide polymorphism (SNP) map in the 96-kb region containing the entire human DiGeorge syndrome critical region 2 (DGCR2) gene at 22q11.2. J Hum Genet. 2001; 46 (10): 604-608. ( PubMed , DOI )

Ohnishi Y, Tanaka T, Ozaki K, Yamada R, Suzuki H, Nakamura Y: A high-throughput SNP typing system for genome-wide association studies. J Hum Genet. 2001; 46 (8): 471-477. ( PubMed , DOI )

Iwasa H, Kurabayashi M, Nagai R, Nakamura Y, Tanaka T: Genetic variations in five genes involved in the excitement of cardiomyocytes. J Hum Genet. 2001; 46 (9): 549-552. ( PubMed , DOI )

Itoh T, Kikuchi K, Odagawa Y, Takata S, Yano K, Okada S, Haneda N, Ogawa S, Nakano O, Kawahara Y, Kasai H, Nakayama T, Fukutomi T, Sakurada H, Shimizu A, Yazaki Y, Nagai R, Nakamura Y, Tanaka T: Correlation of genetic etiology with response to beta-adrenergic blockade among symptomatic patients with familial long-QT syndrome. J Hum Genet. 2001; 46 (1): 38-40. ( PubMed , DOI )

Ono K, Tanaka T, Tsunoda T, Kitahara O, Kihara C, Okamoto A, Ochiai K, Takagi T, Nakamura Y: Identification by cDNA microarray of genes involved in ovarian carcinogenesis. Cancer Res. 2000.09; 60 (18): 5007-5011. ( PubMed )

Yamauchi T, Tada M, Houkin K, Tanaka T, Nakamura Y, Kuroda S, Abe H, Inoue T, Ikezaki K, Matsushima T, Fukui M: Linkage of familial moyamoya disease (spontaneous occlusion of the circle of Willis) to chromosome 17q25. Stroke. 2000.04; 31 (4): 930-935. ( PubMed )

Yamada R, Tanaka T, Ohnishi Y, Suematsu K, Minami M, Seki T, Yukioka M, Maeda A, Murata N, Saiki O, Teshima R, Kudo O, Ishikawa K, Ueyosi A, Tateishi H, Inaba M, Goto H, Nishizawa Y, Tohma S, Ochi T, Yamamoto K, Nakamura Y: Identification of 142 single nucleotide polymorphisms in 41 candidate genes for rheumatoid arthritis in the Japanese population. Hum Genet. 2000.03; 106 (3): 293-297. ( PubMed )

Ohnishi Y, Tanaka T, Yamada R, Suematsu K, Minami M, Fujii K, Hoki N, Kodama K, Nagata S, Hayashi T, Kinoshita N, Sato H, Sato H, Kuzuya T, Takeda H, Hori M, Nakamura Y: Identification of 187 single nucleotide polymorphisms (SNPs) among 41 candidate genes for ischemic heart disease in the Japanese population. Hum Genet. 2000.03; 106 (3): 288-292. ( PubMed )

Iwasa H, Itoh T, Nagai R, Nakamura Y, Tanaka T: Twenty single nucleotide polymorphisms (SNPs) and their allelic frequencies in four genes that are responsible for familial long QT syndrome in the Japanese population. J Hum Genet. 2000; 45 (3): 182-183. ( PubMed , DOI )

Seki T, Tanaka T, Nakamura Y: Genomic structure and multiple single-nucleotide polymorphisms (SNPs) of the thiopurine S-methyltransferase (TPMT) gene. J Hum Genet. 2000; 45 (5): 299-302. ( PubMed , DOI )

Tsunoda T, Yamada R, Tanaka T, Ohnishi Y, Kamatani N: Environmental factor dependent maximum likelihood method for association study targeted to personalized medicine. Genome Inform Ser Workshop Genome Inform. 2000; 11 96-105. ( PubMed )

Nakajima T, Kurabayashi M, Ohyama Y, Kaneko Y, Furukawa T, Itoh T, Taniguchi Y, Tanaka T, Nakamura Y, Hiraoka M, Nagai R: Characterization of S818L mutation in HERG C-terminus in LQT2. Modification of activation-deactivation gating properties FEBS Lett. 2000; 481 (2): 197-203. ( PubMed )

Kunishima S, Kojima T, Tanaka T, Kamiya T, Ozawa K, Nakamura Y, Saito H: Mapping of a gene for May-Hegglin anomaly to chromosome 22q. Hum Genet. 1999.11; 105 (5): 379-383. ( PubMed )

Mikami M, Yasuda T, Terao A, Nakamura M, Ueno S, Tanabe H, Tanaka T, Onuma T, Goto Y, Kaneko S, Sano A: Localization of a gene for benign adult familial myoclonic epilepsy to chromosome 8q23.3-q24.1. Am J Hum Genet. 1999.09; 65 (3): 745-751. ( PubMed )

Tsujikawa M, Kurahashi H, Tanaka T, Nishida K, Shimomura Y, Tano Y, Nakamura Y: Identification of the gene responsible for gelatinous drop-like corneal dystrophy. Nat Genet. 1999.04; 21 (4): 420-423. ( PubMed , DOI )

Nakajima T, Furukawa T, Hirano Y, Tanaka T, Sakurada H, Takahashi T, Nagai R, Itoh T, Katayama Y, Nakamura Y, Hiraoka M: Voltage-shift of the current activation in HERG S4 mutation (R534C) in LQT2 Cardiovasc Res. 1999; 44 (2): 283-293. ( PubMed )

Tsujikawa M, Kurahashi H, Tanaka T, Okada M, Yamamoto S, Maeda N, Watanabe H, Inoue Y, Kiridoshi A, Matsumoto K, Ohashi Y, Kinoshita S, Shimomura Y, Nakamura Y, Tano Y: Homozygosity mapping of a gene responsible for gelatinous drop-like corneal dystrophy to chromosome 1p. Am J Hum Genet. 1998.10; 63 (4): 1073-1077. ( PubMed , DOI )

Itoh T, Tanaka T, Nagai R, Kikuchi K, Ogawa S, Okada S, Yamagata S, Yano K, Yazaki Y, Nakamura Y: Genomic organization and mutational analysis of KVLQT1, a gene responsible for familial long QT syndrome. Hum Genet. 1998.09; 103 (3): 290-294. ( PubMed )

Nishiu J, Tanaka T, Nakamura Y: Identification of a novel gene (ECM2) encoding a putative extracellular matrix protein expressed predominantly in adipose and female-specific tissues and its chromosomal localization to 9q22.3. Genomics. 1998.09; 52 (3): 378-381. ( PubMed , DOI )

Itoh T, Tanaka T, Nagai R, Kamiya T, Sawayama T, Nakayama T, Tomoike H, Sakurada H, Yazaki Y, Nakamura Y: Genomic organization and mutational analysis of HERG, a gene responsible for familial long QT syndrome. Hum Genet. 1998.04; 102 (4): 435-439. ( PubMed )

Nishiu J, Tanaka T, Nakamura Y: Isolation and chromosomal mapping of the human homolog of perilipin (PLIN), a rat adipose tissue-specific gene, by differential display method. Genomics. 1998.03; 48 (2): 254-257. ( PubMed , DOI )

Nakagawa H, Koyama K, Tanaka T, Miyoshi Y, Ando H, Baba S, Watatani M, Yasutomi M, Monden M, Nakamura Y: Localization of the gene responsible for Peutz-Jeghers syndrome within a 6-cM region of chromosome 19p13.3. Hum Genet. 1998.02; 102 (2): 203-206. ( PubMed )

Yamane-Tanaka Y, Kogawa K, Tanaka T, Nakamura Y, Isomura M: Heterozygosities and allelic frequencies of 358 dinucleotide-repeat marker loci in the Japanese population. J Hum Genet. 1998; 43 (3): 165-168. ( PubMed , DOI )

Itoh M, Tsukada S, Orita T, Nishiu J, Tomoike H, Nakamura Y, Tanaka T: Identification by differential display of eight known genes induced during in vivo intimal hyperplasia. J Hum Genet. 1998; 43 (1): 9-13. ( PubMed , DOI )

Nakajima T, Furukawa T, Tanaka T, Katayama Y, Nagai R, Nakamura Y, Hiraoka M: Novel mechanism of HERG current suppression in LQT2: shift in voltage dependence of HERG inactivation Circ Res. 1998; 83 (4): 415-422. ( PubMed )

Tanaka T, Nagai R, Tomoike H, Takata S, Yano K, Yabuta K, Haneda N, Nakano O, Shibata A, Sawayama T, Kasai H, Yazaki Y, Nakamura Y: Four novel KVLQT1 and four novel HERG mutations in familial long-QT syndrome. Circulation. 1997.02; 95 (3): 565-567. ( PubMed )

Tanaka T, Ogiwara A, Uchiyama I, Takagi T, Yazaki Y, Nakamura Y: Construction of a normalized directionally cloned cDNA library from adult heart and analysis of 3040 clones by partial sequencing. Genomics. 1996.07; 35 (1): 231-235. ( PubMed , DOI )

Tanaka T, Inazawa J, Nakamura Y: Molecular cloning and mapping of a human cDNA for cytosolic malate dehydrogenase (MDH1). Genomics. 1996.02; 32 (1): 128-130. ( PubMed , DOI )

Tanaka T, Inazawa J, Nakamura Y: Molecular cloning of a human cDNA encoding putative cysteine protease (PRSC1) and its chromosome assignment to 14q32.1. Cytogenet Cell Genet. 1996; 74 (1-2): 120-123. ( PubMed )

Chatterjee A, Tanaka T, Parrish JE, Herman GE: Refined mapping of caltractin in human Xq28 and in the homologous region of the mouse X chromosome places the gene within the bare patches (Bpa) and striated (Str) critical regions. Mamm Genome. 1995.11; 6 (11): 802-804. ( PubMed )

Tanaka T, Okui K, Nakamura Y: Assignment of the human caltractin gene (CALT) to Xq28 by fluorescence in situ hybridization. Genomics. 1994.12; 24 (3): 609-610. ( PubMed )

Tanaka T, Nakahara K, Kato N, Imai T, Yamazaki T, Tomita H, Shimokawa H, Matsuhashi H, Sato N, Matsui M: Genetic linkage analyses of Romano-Ward syndrome (RWS) in 13 Japanese families. Hum Genet. 1994.10; 94 (4): 380-384. ( PubMed )

Tanaka Yosuke, Kambayashi Hidetaka, Yamamoto Akiko, Onishi Iichiroh, Sugita Keisuke, Matsumura Miwa, Ishibashi Sachiko, Ikeda Masumi, Yamamoto Kouhei, Kitagawa Masanobu, Kurata Morito: Efficient Identification of the MYC Regulator with the Use of the CRISPR Library and Context-Matched Database Screenings INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES. 2022.07; 23 (14): ( PubMed , DOI )

須藤毅顕、小林宏明、青木　章、田中敏博: 全エクソーム解析による疾患遺伝子の同定-侵襲性歯周炎のNOD2遺伝子の変異の同定- 最新醫學. 2019.01; 74 (2): 207-214.

須藤　毅顕, 岡田　随象, 尾崎　浩一, 浦山　ケビン, 金井　仁弘, 小林　宏明, 御給　美沙, 和泉雄一, 田中　敏博: 侵襲性歯周炎における遺伝子変異の同定 歯界展望. 2018.12; 132 (6): 1101-1104.

Kouichi Ozaki, Toshihiro Tanaka: [Molecular genetics of coronary artery diseases]. Nippon Rinsho. 2016.06; 74 Suppl 4 Pt 1 306-313. ( PubMed )

田中敏博　: ゲノム解析テクノロジー 最新医学. 2013; 68 1520-1524.

尾崎浩一，田中敏博: 心血管疾患の遺伝的素因--GWASの成果 循環器内科. 2011; 70 210-218.

尾崎浩一，田中敏博: 虚血性心疾患感受性遺伝子の現状 日本臨床. 2011; 69 217-221-221.

尾崎浩一，田中敏博: 心筋梗塞の遺伝的リスクファクター 内科. 2010; 106 514-520.

角田達彦，田中敏博，中村祐輔: 国際HapMap・JSNPデータベースとその利用法 最新医学. 2009; 64 830-834.

田中敏博　: ハプロタイプ地図とSNP研究の将来 日本臨床 . 2009; 67 1068-1071.

尾崎浩一，田中敏博　: 心筋梗塞感受性分子の同定・解析 最新医学. 2009; 64 842-846.

田中敏博: 心筋梗塞のゲノムワイド関連解析 医学のあゆみ. 2008; 225 781-786.

田中敏博: 国際HapMap プロジェクト 実験医学. 2008; 26 998-1002.

田中敏博: 虚血性心疾患と関連遺伝子 循環器科. 2008; 63 517-522.

尾崎浩一，田中敏博: 心筋梗塞のゲノムワイド関連解析 医学のあゆみ . 2008; 225 781-786.

田中敏博: SNPとハプロタイプ地図 成人病と生活習慣病 . 2008; 38 1123-1126.

田中敏博　: 国際ハップマップ計画 実験医学. 2007; 25 199-203.

石井信明，尾崎浩一，田中敏博: 心筋梗塞原因遺伝子の解析を探る Vascular medicine . 2006; 2 113-120.

田中敏博: わが国の冠動脈疾患のSNPsのエビデンス 血管医学. 2006; 7 17-24.

尾崎浩一，田中敏博: ヒトゲノム解析と心血管疾患 日本循環器学会専門医誌 . 2006; 14 3-8.

田中敏博: 身近な疑問にこたえるサイエンスポプラディア ポプラディア. 2006; 5 38-39.

中澤誠，青見茂之，梅村敏，奥山虎之，鎌谷直之，小杉眞司，斎藤加代子，城尾邦隆，永井良三，平原史樹，福嶋義光，松岡瑠美子，松田一郎，松森昭，山岸敬幸，石上友章，今井靖，佐地勉，西尾亮介，田中敏博，東倉洋一，新川詔夫，古山順一，堀正二: 心臓血管疾患における遺伝学的検査と遺伝カウンセリングに関するガイドライン(循環器病の診断と治療に関するガイドライン(2004-2005年度合同研究班報告))　 Circulation Journal. 2006; 70 (Suppl. IV): 1377-1389.

尾崎浩一，田中敏博: 心筋梗塞とlymphotoxin-α/galectin-2遺伝子多型 ゲノム医学. 2005; 5 347-352.

田中敏博: 国際ハップマップ計画　 日本臨床. 2005; 63 29-34.

田中敏博: リンホトキシンーα結合分子ガレクチンー２と心筋梗塞 医学のあゆみ. 2005; 213 151.

田中敏博: 心筋梗塞の遺伝子解析　Annual Review2004 循環器. 2004; 53-56.

大西洋三，田中敏博: ゲノムワイドSNP解析による心筋梗塞関連遺伝子の単離 脈管学. 2004; 44 175-178.

田中敏博: Lymphotoxin-α 結合分子 galectin-2 と心筋梗塞 細胞工学. 2004; 23 1060-1061.

尾崎浩一，田中敏博: 体系的SNP解析による心筋梗塞感受性遺伝子群の同定とその機能解析--リンホトキシンα およびその結合分子ガレクチン2と心筋梗塞 蛋白質核酸酵素. 2004; 49 2215-2221.

田中敏博: 遺伝性不整脈疾患の分子遺伝学 ゲノム医学. 2003; 3 17-26.

田中敏博: ゲノム解析による心筋梗塞関連遺伝子の単離 分子細胞治療. 2003; 2 294-297.

田中敏博: ヒトゲノムプロジェクト　 Heart View. 2003; 7 8-9.

田中敏博: ゲノムワイドSNP タイピングによる疾患関連遺伝子の単離 Cardiac Practice. 2003; 14 27-30.

田中敏博: SNP解析による Common Disease 関連遺伝子単離 癌と化学療法. 2002; 29 1479-1483.

田中敏博: 体系的発現情報解析 今日の高血圧治療. 2002; 5 16-17.

田中敏博: ヒトゲノムプロジェクト　 循環器専門医. 2002; 10 89-92.

田中敏博: SNPs検出のための新しい方法（3）RCA法 CLINICAL NEUROSCIENCE 別冊. 2002; 20 10-11.

田中敏博: ヒトゲノムプロジェクト : 4.ヒトゲノムプロジェクトと心血管疾患 日本循環器学会専門医誌. 2002; 10 89-92.

田中敏博: SNPによる Pharmacogenomics　日本人標準多型収集とその基盤整備の重要性 実験医学. 2001; 19 738-742.

田中敏博: SNPタイピングによる疾患遺伝子の単離 日本循環器学会専門医誌 . 2001; 9 11-15.

田中敏博, 中村祐輔: マイクロアレイ技術を用いた発現プロファイルの解析 生体の科学. 2000; 51 74-79.

田中敏博: マイクロアレイ技術を用いた発現プロファイルの解析 生体の科学. 2000; 51 71-79.

田中敏博: 循環器疾患とヒトゲノム解析研究 —体系的遺伝子多型解析・遺伝子発現情報解析— THERAPEUTIC RESEARCH . 2000; 21 2749-2777.

田中敏博: 体系的発現情報解析 実験医学. 2000; 18 27-32.

田中敏博: マイクロアレイを利用した癌関連遺伝子の解析 実験医学. 2000; 18 119-124.

田中敏博: マイクロアレイ技術を用いた遺伝子発現プロファイルの解析 遺伝子医学. 1999; 3 701-704.

田中敏博: 家族性QT延長症候群の遺伝子解析 循環器科. 1999; 46 250-253.

田中敏博: ＤＮＡマイクロアレイ技術：ヒト遺伝子全体を総合的に解釈する手法 東京大学アイソトープ総合センターニュース . 1999; 30 (3):

田中敏博: 家族性QT延長症候群の遺伝子解析 メディカルビューポイント. 1998; 9

田中敏博: 家族性QT延長症候群の遺伝子解析 循環器NOW 分子循環器病学. 1998; 181-184.

田中敏博: 突然死症候群 内科診療ガイド‘98. 1998; 584-585.

田中敏博: QT延長症候群 循環機能検査ハンドブック . 1998; 551-554.

田中敏博: 家族性QT延長症候群の遺伝子解析 Annual Review 循環器. 1998; 126-131.

田中敏博: QT延長症候群の遺伝子解析 日本臨床. 1998; 56 532-539.

田中敏博: ゲノム解析 ラボマニュアル. 1998;

田中敏博: 家族性QT延長症候群の遺伝子解析 医学のあゆみ. 1998; 185 25-28.

田中敏博: 家族性QT延長症候群の遺伝子解析 : QT延長症候群をめぐって 日本循環器学会専門医誌. 1997; 5 253-256.

田中敏博: 家族性QT延長症候群の分子遺伝学　 プログレス6循環器疾患1. 1997; 82-90.

田中敏博: 家族性QT延長症候群の遺伝子解析 循環器 Today. 1997; 1 881-884.

田中敏博: 家族性QT延長症候群，低カルシウム血症性ビタミンＤ抵抗性くる病 Bio Science 用語ライブラリー　遺伝子病. 1996; 134-135.

田中敏博: Romano-Ward 症候群の遺伝子連鎖解析　 医学のあゆみ. 1995; 174 315-318.

田中敏博: 日本における家族性QT延長症候群（Romano-Ward 症候群）の遺伝子連鎖解析 日本心電学会誌　心電図 . 1995; 15 139-143.

田中敏博: 遺伝子連鎖解析 循環器用語解説集　基礎編 . 1995; 10-11.

中原賢一，田中敏博，永井良三，矢崎義雄，福島義光，中村祐輔　: 不整脈の遺伝的背景 -我が国の家族性QT延長症候群の連鎖解析-　 臨床病理. 1995; 43 353-357.

田中敏博: 家族性肥大型心筋症 実験医学. 1994; 12 212-213.

田中敏博: 悪性リンパ腫に合併した洞不全症候群の1例 診断と治療. 1993; 81 937-939.

田中敏博: WPW症候群に大動脈弁閉鎖不全症を合併した1例 診断と治療. 1992; 80 1273-1275.