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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 )

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

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 )

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 )

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 )

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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, 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 )

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, 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 )

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 )

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 )

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 )

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 )

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 )

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 )

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 )

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 )

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 )

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 )

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 )

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 )

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 )

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 )

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 )

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 )

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 )

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 )

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. 2000.09; 481 (2): 197-203. ( PubMed )

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 )

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 )

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 )

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 )

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 )

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. 1999.11; 44 (2): 283-293. ( 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 )

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 )

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, 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 )

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. 1998.08; 83 (4): 415-422. ( PubMed )

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 )

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 )

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. 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. 心筋梗塞の遺伝的リスクファクター 内科. 2010; 106 514-520.

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.

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

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.

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.

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.

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.

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. 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.

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. 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.

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

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

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. 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. 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. 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. 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. 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, 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. 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. 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. 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. 体系的発現情報解析 実験医学. 2000; 18 27-32.

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 循環器科. 1999; 46 250-253.

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. 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 メディカルビューポイント. 1998; 9

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. 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. ゲノム解析 ラボマニュアル. 1998;

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. 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. 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. 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 : 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，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. 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. 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. 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. 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.

Onouchi Y, Nakagawa H, Shigemizu D, Ozaki K, Nakamura Y, Asami Y, Seki M, Kobayashi T, Kochi Y, Toda T, Satake W, Hata A, Tsunoda T, Tanaka T, Japan Kawasaki Disease Genome Consortium. Search for genetic variations responsible for giant coronary aneurysms in Kawasaki disease patients by whole exome sequencing. ICHG2016 2016.04.04

Takeaki Sudo, Yukinori Okada, Hiroaki Kobayashi, Misa Gokyu, Yuichi Izumi, Toshihiro Tanaka. Whole-exome sequencing reveals a novel gene as a cause of Aggressive periodontitis in Japanese consanguineous families. The 13th International Congress of Human Genetics 2016.04.04

El Rouby N, McDonough CW, Gong Y, McClure LA, Mitchell BD, Horenstein RB, Talbert RL, Takahashi A, Tanaka T, Kubo M, Pepine CJ, Cooper-DeHoff RM, Benavente OR, Shuldiner AR, Johnson JA. Novel genetic loci for resistant hypertension discovered through a genome-wide association approach (GWAS) in the INternational VErapamil SR-Trandolapril STudy (INVEST) and the Secondary Prevention of Subcortical Strokes (SPS3) Study. American Society of Human Genetics 2015.10

Higuchi C, Tanaka T and Okada Y. Systematic comparison of machine learning methods for identification of miRNA species as disease biomarkers. The IWBBIO 2015 (3rd International Work-Conference on Bioinformatics and Biomedical Engineering) 2015.04 Spain Granada

Aiba T, Makimoto H, Makiyama T, Watanabe H, Hayashi K, Nakano Y, Miyauchi Y, Morita H, Aonuma K, Hagiwara N, Fukuda K, Yoshinaga M, Horigome H, Sumitomo N, Tanaka T, Sekine A, Shiraishi I, Kusano K, Miyamoto Y, Kamakura S, Yasuda S, Ogawa H, Makita N, Horie M, Shimizu W. Diverse gender difference of arrhythmic risk in patients with congenital Long QT Syndrome: from Japanese congenital LQTS multicenter registry. AHA 2014 2014.11 Chicago

Ozaki K, Sakata Y, Suna S, Onouchi Y, Tsunoda T, Kubo M, Komuro I, Tanaka T. A replication study for fifteen coronary artery disease susceptible loci in a Japanese population. ASHG 2014 2014.10 San Diego

Rouby N, McDonough C, Gong Y, Pepine C, Takahashi A, Tanaka T, Kubo M, Cooper-DeHoff R, Johnson J. Genome-wide association study of resistant hypertension in INVEST. ASHG 2014 2014.10 San Diego

Johnson T, Boroevich K, Tanaka T, Qi L, He, Xu M, Wu T, Kubo M, Tsunoda T. Integrated analysis of known height association signals with novel signals from an East Asian GWAS decodes the genetic architecture of height through in silico functional candidate prioritization and gene network analysis. ASHG 2014 2014.10 San Diego

Ozaki K, Morizono T, Onouchi Y, Takahashi A, Tsunoda T, Kubo M, Nakamura Y, Tanaka T. . Genome-wide association study for arteriosclerosis obliterans in a Japanese population. American Society of Human Genetics . ASHG 2013 2013.10

Onouchi Y, Fukazawa R, Ozaki K, Terai M, Hamada H, Honda T, Suzuki H, Suenaga T, Takeuchi T, Yasukawa K, Ebata R, Higashi K, Saji T, Kemmotsu Y, Takatsuki S, Ouchi K, Kishi F, Yoshikawa T, Nagai T, Hamamoto K, Sato Y, Abe J, Seki M, Kobayashi T, Takahashi A, Tsunoda T, Kubo M, Nakamura Y, Hata A, Tanaka T.. Variations in ORAI1 gene associated with Kawasaki disease. . ASHG 2013 2013.10

Ozaki K, and Tanaka T. Whole genome association study for atrial fibrillation in a Japanese population. ISHR 2013 2013.07

Ozaki K, Morizono T, Tsunoda T, Kubo M, Nakamura Y, Tanaka T. . Genetic risk factors for atrial fibrillation in the Japanese population.. ESHG2013 2013.06

Onouchi Y, Ozaki K, Terai M, Hamada H, Suzuki H, Suenaga T, Suzuki Y, Yasukawa K, Ebata R, Saji T, Kemmotsu Y, Ouchi K, Kishi F, Yoshikawa T, Nagai T, Hamamoto K, Sato Y, Sasago K, Takahashi A, Kubo M, Tsunoda T, Hata A, Nakamura Y, Tanaka T. . A fine mapping of the genetic variation influencing the ratio of alternatively spliced CD40 transcripts and conferring susceptibility to Kawasaki disease. . ASHG 2012 2012.11

Ozaki K, Kubo M, Tsunoda T, Onouchi Y, Kamatani N, Nakamura Y, Tanaka T. . Six chromosome loci for atrial fibrillation susceptibility identified in Japanese.. AHA 2012 2012.11

Ozaki K, Onouchi Y, Kamatani N, Tsunoda T, Kubo M, Nakamura Y, Tanaka T. . Genome-wide association study for atrial fibrillation in the Japanese population. . ASHG 2012 2012.11

Ozaki K, Tanaka T. . Identification of protein that interact BRAP, encoded by a gene associated with myocardial infarction susceptibility.. World Congress of Cardiology Scientific Sessions 2012.04

Onouchi Y, Ozaki K, Suzuki H, Terai M, Hata A, Tanaka T. . ITPKC and CASP3 polymorphisms and risks for IVIG unresponsiveness and coronary artery lesion formation in Kawasaki disease. . Human Genome Meeting 2012.03

Ozaki K, Onouchi Y, Nakamura Y, Tanaka T. . BRAP, encoded by a gene associated with myocardial infarction, binds several key inflammatory molecules.. ICHG 2011 2011.10

Onouchi Y, Ozaki K, Burns J.C, Shimizu C, Terai M, Hamada H, Suzuki H, Suenaga T, Suzuki Y, Yasukawa K, Ebata R, Saji T, Kemmotsu Y, Ouchi K, Kishi F,Yoshikawa T, Nagai T, Hamamoto K, Sato Y, Sasago K, Takahashi A, Kamatani N, Kubo M, Tsunoda T, Hata A, Nakamura Y, Tanaka T.. Genome-wide association study identified new susceptibility loci for Kawasaki disease. . ICHG 2011 2011.10

Tanaka T.. Genetic Epidemiology~Understanding the human diversity towards personalized medicine~. . The 6th International Syompsium of Nagasaki University Global COE program 2011.10

Tanaka T.. BioBank Japan. . KOGO satellite session 2011.09

Todd J, 田中敏博, 久保充明, 中村祐輔, 角田達彦 . Analyzing contiguous homozygosity to quantify haplotype structure differences between case and control samples. 日本人類遺伝学会第55回大会 2010.10

Yamagata K, Horie M, Ogawa S, Aizawa Y, Kusano K, Ohe T, Yamagishi M, Makita N, Tanaka T, Makiyama T, Akao M, Hagiwara N, Kishi R, Miyamoto Y, Kamakura S, Shimizu W. . Clinical Phenotype and Prognosis of Probands with Brugada Syndrome in Relation to SCN5A Mutation. . 第74回日本循環器学会総会・学術集会 2010.03

Makimoto H, Yamagata K, Horie M, Ogawa S, Aizawa Y, Kusano K, Ohe T, Yamagishi M, Makita N, Tanaka T, Makiyama T, Akao M, Yoshinaga M, Miyamoto Y, Kamakura S, Shimizu W. . Clinical Features of Long QT Syndrome in Pre-Elementary Age.. 第74回日本循環器学会総会・学術集会 2010.03

Ozaki K, Sato H, Inoue K, Tsunoda T, Sakata Y, Mizuno H, Onouchi Y, Odashiro K, Nobuyoshi M, Juo H S-H, Hori H, Nakamura Y, Tanaka T. . SNPs in Genes Encoding an Inflammatory Cascade Confer Risk of Myocardial Infarction.. 第74回日本循環器学会総会・学術集会 2010.03

Yamagata K, Horie M, Ogawa S, Aizawa Y, Kusano K, Ohe T, Yamagishi M, Makita N, Tanaka T, Akao M, Yoshinaga M, Okamura H, Noda T, Miyamoto Y, Kamakura S, Shimizu W.. Clinical Phenotype of Japanese LQT3 Form of Congenital Long QT Syndrome by Location of Mutation from Japanese Multicenter Registry. . 第73回日本循環器学会総会・学術集会 2009.03

Yamagata K, Horie M, Ogawa S, Aizawa Y, Kusano K, Ohe T, Yamagishi M, Makita N, Tanaka T, Akao M, Kishi R, Okamura H, Noda T, Satomi K, Suyama K, Kurita T, Aihara N, Kamaukura S, Miyamoto Y, Shimizu W. . Clinical and Electrocardiographic Characteristics of Japanese Probands with Brugada Syndrome with an SCN5A Mutation from Japanese Multicenter Registry. . 第73回日本循環器学会総会・学術集会 2009.03

Ozaki K, Sato H, Inoue K, Tsunoda T, Sakata Y, Mizuno H, Aoki A, Odashiro K, Nobuyoshi M, Juo H S-H, Hori M, Nakamura Y, Tanaka T. . A Functional Variation in a Gene Encoding One of Galectin-2 Binding Proteins Confers Risk of Myocardial Infarction in Asian Populations.. 第73回日本循環器学会総会・学術集会 2009.03

Ozaki K, Sato H, Inoue K, Mizuno H, Sakata Y, Odashiro K, Nobuyoshi M, Hori M, Nakamura Y, Tanaka T. . Large Scale SNPs Association Study to Identify Genes Confer Risk of Myocardial Infarction. . 第73回日本循環器学会総会・学術集会 2009.03

Aoki A, Ozaki K, Sato H, Takahashi A, Kubo M, Sakata Y, Mizuno H, Kamatani N, Tsunoda T, Takano H, Yasutake M, Mizuno K, Hori M, Nakamura Y, Tanaka T.. Identification of a Locus on Chromosome 5p that Confers Risk of Coronary Artery Disease by Genome Wide Association Study. . 第73回日本循環器学会総会・学術集会 2009.03

Kato M, Miya F, Kanemura Y, Tanaka T, Nakamura Y, Tsunoda T. . Patterns of high-resolution recombination rates in human genes.. HGM 2008 2008.09

Tanaka T.. Genetic background of myocardial infarction.. Mendel Symposium II Genes and the Heart 2008.09

Ozaki K, Sato H, Ishii N, Ebana Y, Iida A, Mizuno H, Hori M, Nakamura Y, and Tanaka T. . Large scale SNPs association study to identify genes confer risk of myocardial infarction. . 14th World Congress on Heart Disease 2008.07

Tanaka T.. Genetic backgrounds of myocardial infarction. . The 2008 EAUHGS Symposium and the 8th EAUHGS Annual Meeting 2008.07

Yamagata K, Horie M, Ogawa S, Aizawa Y, Ohe T, Yamagishi M, Makita N, Tanaka T, Akao M, Yoshinaga M, Okamura H, Noda T, Miyamoto Y, Kamakura S, Shimizu W. . Clinical Phenotype of Japanese LQT1 form of congenital long QT syndrome by location and coding type from Japanese multicenter registry. . 第72回日本循環器学会総会・学術集会 2008.03

Tanaka T.. Single-Nucleotide Polymorphisms Confer Risk of Myocardial infarction. . AHA 2007 2007.11

Ozaki K, Sato H, Iida A, Mizuno H, Takahashi A, Nakamura T, Lwin H, Ikegawa S, Hri M, Nakamura Y, Tanaka T. . 52,608 gene-based SNPs association study to identify genes related to myocardial infarction. . ASHG 2007 2007.10

Tanaka T.. Biobank Japan.. International Society for Biological and Environmental Repositories 2007.05

Ozaki K, Sato H, Iida A, Mizuno H, Hori M, Nakamura Y, and Tanaka T. . A functional SNP in the proteasome subunit alpha type 6 gene confers risk of myocardial infarction in Japanese population. . 第71回日本循環器学会総会・学術集会 2007.03

Ozaki K, Ishii N, Sato H, Mizuno H, Hori M, Saito S, Nakamura Y, and Tanaka T.. Identification of a novel non-coding RNA, MIAT, that confers risk of myocardial Infarction. . 第71回日本循環器学会総会・学術集会 2007.03

Tanaka T.. Identification of genes associated with common diseases by large-scale genetic association study-Studies on myocardial infarction. . The 2nd annual international symposium of genomic medicine and pharmacogenomics 2007.03

Tanaka T.. Identification of genes associated with common diseases by large-scale genetic association study-Studies on myocardial infarction. . Medical Science Seminar Series 2007.03

Ozaki K, Sato H, Iida A, Mizuno H, Hori M, Nakamura Y, and Tanaka T. . Association study in search for genetic backgrounds of myocardial infarction, focused on SNPs in genes encoding molecules that belong to lymphotoxin-a signaling cascade. . ASHG 2006 2006.10

Ozaki K, Inoue K, Odashiro M, Nobuyoshi M, Nakamura Y, Tanaka T. . Identification of proteins that bind galectin-2, encoded by a gene associated with myocardial infarction using tandem affinity purification method. . ASHG 2005 2005.11

Tanaka T.. BioBank Japan: Toward Personalized Medicine. . NCI Symposium: International Harmonization of Biorepository Practices 2005.11

Tanaka T.. From SNPs to Disease Risk –Towards predictive and personalized medicine.. 3rd World Congress of Nephrology 2005.06

Tanaka T.. Towards Personalized Medicine.. HUGO's 10th Human Genome Meeting (HGM2005) 2005.04

Tanaka T.. Recent Advance in Genomics for Diagnosis and Treatment of Cardiovascular Diseases.. The 69th Annual Science Meeting of the Japanese Circulation Society 2005.03

Tanaka T.. Functional variations in two genes encoding functionally associated proteins, lymphotoxin-α and galectin-2, confer risk of myocardial infarction.. The 13th Takeda Science Foundation Symposium on Bioscience 2004.12

Tanaka T.. The Japanese Biobank.. ESHG 2004 2004.06

Ozaki K, Ohnishi Y, Iida A, Yamada R, Tsunoda T, Sato H, Sato H, Hori M, Nakamura Y, Tanaka T. . Functional SNPs in the lymphotoxin- gene that are associated with susceptibility to myocardial infarction. . ASHG 2003 2003.11

Tanaka T.. Genome-wide association study identifies functional SNPs in the lymphotoxin- gene as associated with susceptibility to myocardial infarction.. Mendel Symposium 2003.08

Ozaki K, Ohnishi Y, Iida A, Yamada R, Tsunoda T, Sato H, Sato H, Hori M, Nakamura Y, Tanaka T. . Functional SNPs in the lymphotoxin- gene that are associated with susceptibility to myocardial infarction. . 3rd World Congress on Heart Disease 2003.07

Tanaka T, Tsukada S, Iwai M, Nishiu J, Itoh M, Tomoike H, Horiuchi M, Nakamura Y. . Inhibition of experimental intimal thickening in mice lacking a novel G-protein-coupled receptor. . 3rd World Congress on Heart Disease 2003.07

Tanaka T.. SNP projects in Japan. . The 5th International Workshop on Advanced Genomics 2003.06

Ohnishi Y, Tanaka T, Ozaki K, Sekine A, Nakamura Y. . A high-throughput SNP typing system for genome-wide association studies in patients with myocardial infarction. . ASHG 2002 2002.10

Ozaki K, Ohnishi Y, Iida A, Yamada R, Tsunoda T, Sekine A, Sato H, Sato H, Hori M, Nakamura Y, Tanaka T. . Genome-wide association study to identify genes related to myocardial infarction. . ASHG 2002 2002.10

Tanaka T.. SNP projects in Japan. . Osong International Symposium 2002.09

Tanaka T.. SNP projects in Japan. . Medical Genomics in Asia 2002.01

Inoue K, Tanaka T, Itoh M, Tomoike H, Yonekura K, Aoyagi T, Nagai R, Hori M, Nakamura Y.. Male-specific sudden cardiac death in mice with deficiency of a novel gene (OSR) related to ozidative stress resistance. . 第65回日本循環器学会・学術集会 2001.03

Yamada R, Tanaka T, Ohnishi Y, Yamamoto K, Nakamura Y. . An efficient SNP discovery procedure used in our association studies of rheumatoid arthritis. . ASHG 2000 2000.10

Ohnishi Y, Tanaka T, Yamada R, Hori M, Nakamura Y. . Systematic survey of SNPs (single nucleotide polymorphisms) in the candidate responsible genes for myocardial infarction in the Japanese population.. ASHG 2000 2000.10

Tanaka T, Ohnishi Y, Yamada R, Nakamura Y. . Large-scale SNP (single nucleotide polymorphism) discovery project in Japan. . ASHG 2000 2000.10

Tanaka T.. Microarray Analysis of Human Cancer; Toward Personalized Medicine.. Topic from Human Genome Project 2000.01

Ono K, Tanaka T, Kitahara O, Shiraishi N, Kihara C, Seki T, Yanagawa R, Ogasawara H, Okamoto T, Ohnishi Y, Kuzuya K, Tsunoda T, Takagi T, Nakamura Y.. Gene expression profiles of ovarian cancer using T7 based RNA amplification and cDNA microarray technology. . ASHG 1999 1999.10

Kihara C, Tanaka T, Furukawa Y, Ono K, Kitahara O, Shiraishi N, Yanagawa R, Ogasawara H, Seki T, Yamana H, Tsunoda T, Hirata K, Takagi T, Nakamura Y. . Gene expression profiles of esophageal cancer patients using cDNA microarray technology.. ASHG 1999 1999.10

Tanaka T, Ito T, Nagai R, Yazaki Y, Nakamura Y. . Mutational analysis of familiar long QT syndrome in Japan. . The 15th Annual Meeting of the Japanese Section 1998.12

Tanaka T, Itoh T, Nagai R, Yazaki Y, Nakamura Y. . Genomic organization of KVLQT1 and mutational analysis of familial long QT syndrome in Japan: further evidence for genotype/phenotype relationship. . ASHG 1998 1998.10

Tanaka T, Itoh T, Nagai R, Yazaki Y, Nakamura Y. . Mutational analysis of familial long QT syndrome; implication of correlation between mutated gene and response to beta-adrenergic blocking agent.. ASHG 1997 1997.10

Tanaka T, Nakamura Y. . Genetic analysis of long QT syndrome in Japan. . International Symposium on potassium ion channels; their molecular structure, function and diseases 1997.09

Tanaka T.. Genetic analysis of long QT syndrome in Japan. . International Symposium on potassium ion channels; their molecular structure, function and diseases. 1997.09

Tanaka T, Itoh M, Tsukada S, Orita T, Nishiu J, Tomoike H, Nakamura Y. . Isolation and characterization of novel genes related to endothelial proliferation by differential display method. . HUGO's Human Genome Meeting 1997.03

Tanaka T, Itoh M, Tsukada S, Orita T, Tomoike H, Nakamura Y. . Isolation of novel genes related to endothelial proliferation by differential mRNA display method.. ASHG 1996 1996.10

Tanaka T, Ogiwara A, Uchiyama I, Takagi T, Nakamura Y. . Construction of a normalized directionally-cloned cDNA library from adult heart and analysis of 3040 clones by partial sequencing. . HGM 1996 1996.03

Tanaka T, Nakamura Y.. A large scale cDNA sequencing of a normalized directionally-cloned cDNA library from adult heart. . ASHG 1995 1995.10

中野 雄二郎, 吉本 貴宣, 渡邉 亮, 村上 正憲, 藤井 靖久, 田中 敏博, 山田 哲也, 成瀬 光栄, 小川 佳宏. アルドステロン産生腺腫におけるmiRNAを利用した新規バイオマーカーの探索. 第94回日本内分泌学会学術総会 2021.04.22

田中敏博. コモンSNPと希少不整脈疾患. 第66回日本不整脈心電学会学術大会 2019.07.25

田中敏博. ゲノム医学・ゲノム医療. 公益財団法人 中谷医工計測技術振興財団　キックオフシンポジウム～「生体5次元情報」を解読する医工計測技術を創出する「知・もの・人」づくり計画～ 2019.05.16

田中　敏博. 循環器疾患とゲノム医療. 仙台心臓血管研究会 2017.06.28

田中　敏博. 循環器の薬理学. 岡山大学大学院講義 2017.01.25

田中敏博. 不整脈のゲノム医療ー現状と展望ー. 第63回日本不整脈心電学会学術大会　第5回不整脈薬物治療サミット～超高齢化社会に向けた不整脈治療を考える～ 2016.07.16 札幌コンベンションセンター

須藤毅顕、岡田随象、小林宏明、御給美沙、田中敏博、和泉雄一. 大規模並列シークエンサーを用いた侵襲性歯周炎のゲノム解析. 第143回日本歯科保存学会 2015.11.13

金井仁弘、田中敏博、岡田随象. 1000 Genomes Projectデータを用いたゲノムワイド有意水準の経験的推定. 日本人類遺伝学会第60回大会 2015.10.17 京王プラザホテル（新宿）

須藤毅顕、岡田随象、小林宏明、御給美沙、和泉雄一、田中敏博. 侵襲性歯周炎の全エクソーム解析による候補遺伝子の同定. 日本人類遺伝学会第60回大会 2015.10.16 京王プラザホテル（新宿）

吹田直政、金井仁弘、樋口千洋、田中敏博、岡田随象. 大規模ゲノムワイド関連解析研究23報告の包括的パスウェイ解析. 日本人類遺伝学会第60回大会 2015.10.16 京王プラザホテル（新宿）

石川欽也、 田中敏博、 荒木昭博、 吉田雅幸、 田中雄二郎、 稲澤譲治. 健康維持に関連するゲノム情報の提供　東京医科歯科大学での取り組みから. 日本人類遺伝学会第60回大会 2015.10.16 京王プラザホテル（新宿）

尾崎浩一、 坂田泰彦、 砂真一郎、 尾内善広、 小室一成、 久保充明、 田中敏博. 新規虚血性心疾患感受性分子BTRCの同定と解析. 日本人類遺伝学会第60回大会 2015.10.15 京王プラザホテル（新宿）

樋口千洋、田中敏博、岡田随象. 機械学習によるヒト由来miRNA 発現情報データの包括解析. 日本人類遺伝学会第60回大会 2015.10.15 京王プラザホテル（新宿）

末吉国誉、田中敏博、岡田随象. 組織間 discordant directional eQTL の同定と評価. 日本人類遺伝学会第60回大会 2015.10.15 京王プラザホテル（新宿）

Ebana Y, Ozaki K, Okada Y, Tanaka T, Isobe M, Furukawa T. SY19-1Arrhythmia, A Post-GWAS Analysis, MAGENT, Identified Novel Pathways for Atrial Fibrillation. 第79回日本循環器学会総会・学術集会 2015.04.26 大阪　中之島

Aiba T, Makimoto H, Makiyama T, Watanabe H, Hayashi K, Nakano Y, Morita H, Aonuma K, Hagiwara N, Fukuda K, Yoshinaga M, Horigome H, Sumitomo N, Tanaka T, Sekine A, Kamakura S, Miyamoto Y, Kusano K, Makita N, Horie M, Shimizu W. FRS-117Arrhythmia, Diverse Gender Difference of Arrhythmic Risk in Patients with Congenital Long QT Syndrome: From Japanese Congenital LQTS Multicenter Registry. 第79回日本循環器学会総会・学術集会 2015.04.26 大阪　中之島

Ozaki K,　Ebana Y, Furukawa T, Kubo M, Tanaka T. Identification and Analyses of Novel Atrial Fibrillation Susceptible Molecules. 第79回日本循環器学会総会・学術集会 2015.04.25 大阪　中之島

金井仁弘,山根健治,樋口千洋,田中敏博,岡田随象. ゲノムワイド関連解析ソフトウェアPLINKの次期バージョン1.90における性能評価. 日本人類遺伝学会第59回大会 2014.11

重水大智, 尾崎浩一, 藤本明洋, 宮冬樹, 秋山真太郎, ボロエビッチ キース, 安部哲雄, 中野かおる, 高地雄太, 佐竹渉, 戸田達史, 相庭武司, 宮本恵宏, 清水渉, 中川英刀, 角田達彦, 田中敏博. QT延長症候群の35家系全エクソーム解析によるカルモジュリン結合遺伝子での候補変異の解析. 日本人類遺伝学会第59回大会 2014.11

尾崎浩一, 久保充明, 森園隆, 尾内善広, 角田達彦, 田中敏博. 新規心房細動感受性遺伝子 NEURL の解析. 日本人類遺伝学会第59回大会 2014.11

樋口千洋, 田中敏博, 岡田随象. miRNA 発現情報の正則化最小二乗法・MARS 解析による疾患関連バイオマーカーの同定. 日本人類遺伝学会第59回大会 2014.11

佐竹渉, 重水大智, 鈴木穣, 山本健, 富山弘幸, 高橋篤, 村田美穂, 服部信孝, 田中敏博, 角田達彦, 久保充明, 辻省次, 松本直道, 菅野純夫, 戸田達史 . 孤発性パーキンソン病のエクソーム関連解析と第2期 SNP-GWAS. 日本人類遺伝学会第59回大会 2014.11

Ozaki K, and Tanaka T. Identification and functional analysis of a novel atrial fibrillation susceptible molecule, NEURL. The 31st Annual Meeting of the International Society for Heart Research Japanese Section 2014.11 名古屋

尾崎浩一, 坂田泰彦, 砂真一郎, 小室一成, 田中敏博. 新規心筋梗塞感受性分子の同定と解析. 第62回日本心臓病学会学術集会 2014.09

尾崎浩一, 秋山慎太郎, 坂田泰彦, 砂真一郎, 尾内善広, 角田達彦, 久保充明, 小室一成, 中村祐輔, 田中敏博. 欧米人において同定された15 個の新規虚血性心疾患感受性座位の日本人における再検証解析. 日本人類遺伝学会第58回大会 2013.11

尾内善広, 深澤隆治, 尾崎浩一, 寺井勝, 濱田洋通, 本田隆文, 鈴木啓之, 末永智浩, 武内崇, 安川久美, 江畑亮太, 東浩二, 佐地勉, 監物靖,　高月晋一, 尾内一信, 岸文雄, 吉川哲史, 永井敏郎, 濱本邦洋, 佐藤吉壮, 安部淳, 関満, 小林徹, 高橋篤, 角田達彦, 久保充明, 中村祐輔, 羽田明, 田中敏博. ORAI1 遺伝子の多型と川崎病との関連. 日本人類遺伝学会第58回大会 2013.11

尾崎浩一, 坂田泰彦, 尾内善広, 砂真一郎, 久保充明, 小室一成, 中村祐輔, 田中敏博. 心筋梗塞関連分子BRAP に結合する分子の心筋梗塞との関連. 日本人類遺伝学会第58回大会 2013.11

尾内善広, 深澤隆治, 寺井勝, 濱田洋通, 本田隆文, 鈴木啓之, 末永智浩, 武内崇, 安川久美, 江畑亮太, 東浩二, 佐地　勉, 監物　靖, 高月晋一, 濱本邦洋, 阿部淳, 関　満, 小林徹, 羽田明, 田中敏博. ORAI1遺伝子の多型と川崎病との関連. 第33回日本川崎病学会・学術集会 2013.09

田中敏博. ゲノム疫学. 動脈硬化Update2013 2013.09

田中敏博. ゲノム情報を診断ツールへ. クリニカルサミット 2013.08

尾内善広， 尾崎浩一， 鈴木洋一， 田中敏博， 羽田明 . ゲノムワイド関連解析による新規川崎病感受性遺伝子領域の同定 . 日本人類遺伝学会第57回大会 2012.10

尾崎浩一, 久保充明, 森園隆, 尾内善広, 角田達彦, 鎌谷直之, 中村祐輔, 田中敏博. 日本人における6個の心房細動感受性染色体座位の同定と解析. 日本人類遺伝学会第57回大会 2012.10

田中敏博. 遺伝因子と環境因子の相互作用の解明～ゲノム疫学の立場から～. 第3回 Molecular Cardiovascular Conference II 2012.09

尾内善広, 尾崎浩一, 鈴木陽一, 田中敏博, 羽田　明. ゲノムワイド関連解析による新規川崎病感受性遺伝子領域の同定. 第19回日本遺伝子診療学会大会 2012.07

相庭武司, 牧元久樹, 山形研一郎, 中島育太郎, 宮本康二, 山田優子, 岡村英夫, 野田崇, 里見和浩, 堀江稔, 小川聡, 相澤義房, 大江透, 草野研吾, 山岸正和, 蒔田直昌, 田中敏博, 牧山武, 吉永正夫, 萩原誠久, 住友直方, 石原正治, 安斉俊久, 安田聡, 小川久雄, 鎌倉史郎, 宮本恵宏, 清水渉. 先天性QT延長症候群における遺伝子変異領域と予後・治療の選択. 第27回日本不整脈学会学術大会 2012.07

田中敏博. ゲノム疫学. 創薬薬理フォーラム 2012.06

田中敏博. Common disease のゲノム疫学. 第49回日本臨床分子医学会学術集会 2012.04

田中敏博. ゲノム疫学～ヒト多様性の理解からオーダーメイド医療へ～. 愛媛大学プロテオ医学研究センター第2回学術シンポジウム 2012.02

田中敏博. 疾患ゲノム研究の現状と近未来. 筑波大学 Current Topics Lecture 2011.12

高橋弘, 中島正宏, 尾崎浩一, 田中敏博, 鎌谷直之, 池川志郎. 遺伝的要因と環境的要因を考慮した変形性膝関節症の発症予測モデルの開発と検証. 日本人類遺伝学会第56回大会 2011.11

尾内善広, 尾崎浩一, 鈴木啓之, 寺井勝, 安川久美, 濱田洋通, 本田隆文, 末永智浩, 武内崇, 笹子久美子, 鈴木洋一, 田中敏博, 羽田明. ITPKC及びCASP3遺伝子の多型と川崎病患児の治療抵抗性および冠動脈病変合併リスクとの関連. 日本人類遺伝学会第56回大会 2011.11

尾崎浩一, 久保充明, 森園隆, 尾内善広, 高橋篤, 角田達彦, 鎌谷直之, 中村祐輔, 田中敏博. 閉塞性動脈硬化症の全ゲノム関連解析. 日本人類遺伝学会第56回大会 2011.11

尾崎浩一, 江花有亮, 久保充明, 森園隆, 尾内善広, 高橋篤, 磯部光章, 古川哲史, 角田達彦, 鎌谷直之, 中村祐輔, 田中敏博. 心房細動の全ゲノム関連解析. 日本人類遺伝学会第56回大会 2011.11

尾崎浩一, Yi-Chu Liao, 佐藤洋, 尾内善広, 坂田泰彦, 堀正二, Juo Suh-Hang Hank, 小室一成, 中村祐輔, 田中敏博. 心筋梗塞感受性分子BRAPの機能解析と新規結合分子の同定. 日本人類遺伝学会第56回大会 2011.11

田中敏博. ゲノム疫学〜ヒト多様性の解明〜. 千葉循環器フロンティア研究会 2011.10

田中敏博. ゲノム疫学. 血管の科学セミナー2011 2011.06

尾内善広, 尾崎浩一, 角田達彦, 羽田明, 中村祐輔, 田中敏博. 川崎病罹患感受性と相関するCASP3遺伝子多型の同定. 日本人類遺伝学会第55回大会 2010.10

尾崎浩一, 佐藤洋, 尾内善広, 坂田泰彦, 堀正二, 中村祐輔, 田中敏博. Identification of proteins that bind BRAP, encoded by a gene associated with myocardial infarction using an S-protein tag pull down method.. 日本人類遺伝学会第55回大会 2010.10

田中敏博. ゲノム情報. 第58回日本心臓病学会学術集会　教育講演 2010.09

田中敏博. 心筋梗塞の遺伝的背景. Meet the Clinical Expert 2010.07

尾崎浩一, 佐藤洋, 井上勝美, 角田達彦, 坂田泰彦, 尾内善広, 池川志郎, 卓夙航, 堀正二, 中村祐輔, 田中敏博 . 新規心筋梗塞感受性分子BRAPの同定と解析. 日本人類遺伝学会第54回大会 2009.09

尾内善広, 尾崎浩一, 鈴木啓之, 寺井勝, 鈴木洋一, 羽田明, 中村祐輔, 田中敏博. 川崎病とITPKC遺伝子多型との相関. 日本人類遺伝学会第54回大会 2009.09

尾崎浩一, 青木亜佐子, 佐藤洋, 高橋篤, 久保充明, 坂田泰彦, 尾内善広, 角田達彦, 鎌谷直之, 堀正二, 中村祐輔, 田中敏博 . 全ゲノム関連解析による虚血性心疾患感受性5番染色体短縮領域の同定 . 日本人類遺伝学会第54回大会 2009.09

加藤護，宮冬樹，金村米博，田中敏博，中村祐輔，角田達彦. Patterns of high-resolution recombination rates in human genes　. 第31回日本分子生物学会年会・第81回日本生化学会大会合同大会 2008.12

青木亜佐子，尾崎浩一，高橋篤，斎藤督，久保充明，角田達彦，安武正弘，鎌谷直之，中村祐輔，田中敏博 . 不安定狭心症の25万SNPを用いた全ゲノム関連解析. 日本人類遺伝学会第53回大会 2008.09

加藤護, 宮冬樹, 金村米博, 田中敏博, 中村祐輔, 角田達彦. ヒト遺伝子における高精度組み換え率のパターン. 日本人類遺伝学会第53回大会 2008.09

尾崎浩一, 佐藤洋, 角田達彦, 坂田泰彦, 堀正二, 中村祐輔, 田中敏博. リンホトキシン-αによって冠動脈血管内皮細胞から誘導される分子の同定, 解析. 日本人類遺伝学会第53回大会 2008.09

田中敏博. 私の研究: Genetic Backgrounds of Myocardial Infarction. 第31回心筋代謝研究会 2008.07

Haraoka K, Morita H, Nakamura K, Miura D, Kusano K, Tanaka T, Ohe T. . Multiple congenital and acquired predisposing factors aggravates secondary long QT syndrome. . 第72回日本循環器学会総会・学術集会 2008.03

Noda T, Horie M, Ogawa S, Aizawa Y, Ohe T, Yamagishi M, Makita N, Tanaka T, Akao M, Yoshinaga M, Okamura H, Miyamoto Y, Kamakura S, Shimizu W. . Impact of frameshift mutation and nonsense-mediated mRNA decay on clinical phenotype in LQT2 form of congenital long QT syndrome. . 第72回日本循環器学会総会・学術集会 2008.03

田中敏博. ゲノム解析と生活習慣病：心筋梗塞を中心として. 第8回Tokyo Diabetes Seminar: New Genes New Therapy 2008.02

田中敏博, 井上勝美, 中村祐輔, 尾崎浩一. 心筋梗塞感受性分子ガレクチン-2と相互作用する分子の同定, 解析. 日本人類遺伝学会第52回大会 2007.09

26. 石井信明, 尾崎浩一, 佐藤洋, 水野裕八, 斎藤督, 高橋篤, 中村好宏, 池川志郎, 鎌谷直之, 斉藤 穎, 堀正二, 中村祐輔, 田中敏博. 大規模SNPケースコントロール関連解析による心筋梗塞感受性新規RNA分子MIATの同定. 日本人類遺伝学会第52回大会 2007.09

江花有亮, 尾崎浩一, 井上勝美, 佐藤洋, 飯田有俊, 斎藤督, HTAYLWIN, 高橋篤, 中村好宏, 池川志郎, 鎌谷直之, 磯部光章, 堀正二, 中村祐輔, 田中敏博. 大規模SNPケースコントロール関連解析による心筋梗塞感受性分子ITIH3の同定. 日本人類遺伝学会第52回大会 2007.09

尾崎浩一, 佐藤洋, 飯田有俊, 水野裕八, 高橋篤, 中村好宏, 池川志郎, 鎌谷直之, 堀正二, 中村祐輔, 田中敏博. ケースコントロール関連解析による心筋梗塞感受性分子PSMA6の同定. 日本人類遺伝学会第52回大会 2007.09

テイルイン, 尾崎浩一, 佐藤洋, 水野裕八, 池川志郎, 堀正二, 中村祐輔, 田中敏博. 国際ハップマッププロジェクトからtagSNPsを用いたホモシステイン関連遺伝子と心筋梗塞の関連. 日本人類遺伝学会第52回大会 2007.09

田中敏博. SNP Analysis. 第11回日本心不全学会学術集会 2007.09

田中敏博. ゲノム解析による疾患関連遺伝子の同定～オーダーメイド医療を目指して～. 第21回循環器エキスパートカンファレンス 2007.05

Ozaki K, Sato H, Iida A, Mizuno H, Hori M, Nakamura Y, Tanaka T. . A functional SNP in the proteasome subunit alpha type 6 gene confers risk of myocardial infarction in Japanese population.. 第71回日本循環器学会総会・学術集会 2007.03

Ozaki K, Ishii N, Sato H, Mizuno H, Saitoh S, Hori M, Nakamura Y, Tanaka T. . Identification of a novel non-coding RNA, MIAT, that confers risk of myocardial infarction. . 第71回日本循環器学会・学術集会 2007.03

田中敏博. 心筋梗塞の遺伝的背景. 大阪大学大学院医学系研究科臨床遺伝講座セミナー　 2006.12

田中敏博. オーダーメイド医療実現化プロジェクト. 東京女子医科大学第2回IREIIMS公開シンポジウム 2006.12

田中敏博. ゲノム解析を用いた臨床研究の実際. 国立循環器病センター第9回NCVC臨床研究セミナー　 2006.12

田中敏博. 心筋梗塞の遺伝的背景 . Bayer Symposium on Cardiovascular Risk Management 2006.10

田中敏博. ゲノムで変わる, 病気へのアプローチ. 理化学研究所横浜研究所・横浜市立大学鶴見キャンパス一般公開 2006.06

田中敏博. 心臓病のゲノム解析. お茶の水女子大学　再教育講座 2006.06

田中敏博. 国際ハップマッププロジェクトの現況 . 第18回日本アレルギー学会春季臨床大会 2006.05

田中敏博. ゲノム情報に基づく新たな冠危険因子の同定 . 第70回記念日本循環器学会学術集会　特別セッション 2006.03

田中敏博. ゲノム解析による疾患関連遺伝子の単離. 第4回 Circulation Forum in Hiroshima 2006.01

田中敏博. ゲノム情報からオーダーメイド医療実現へ. 大阪府立成人病センターセミナー 2005.11

田中敏博. ゲノム情報からオーダーメイド医療実現へ. 第14回リサーチカンファレンス 2005.11

田中敏博. 研究者の視点から：オーダーメイド医療を実現するための研究. 先端医学研究等普及啓発セミナー 2005.10

田中敏博. 体系的ゲノム解析に基づく心筋梗塞関連遺伝子の同定. 東京心臓の会 2005.06

田中敏博. ゲノム情報に基づく疾患遺伝子解析. 創薬薬理フォーラム 2005.06

田中敏博. ゲノム解析による心筋梗塞関連遺伝子群の同定とその機能解析. Japan Heart Colloquium 2005.06

田中敏博. 心臓病のゲノム解析. お茶の水女子大学　再教育講座 2005.05

田中敏博. 循環器疾患におけるオーダーメイド医療―臨床応用へのアプローチ―. 第69回日本循環器学会学術集会 2005.03

田中敏博. ゲノム情報に基づく疾患解析. 第6回関東甲信地区遺伝子・染色体検査セミナー 2005.03

田中敏博. ゲノム情報に基づく心筋梗塞関連遺伝子の同定と機能解析 . 第3回広島高血圧若手フォーラム 2005.02

田中敏博. ゲノム医科学：ゲノム情報に基づくオーダーメイド医療. 神奈川科学技術アカデミー教育講座 2005.02

田中敏博. 体系的SNP解析による心筋梗塞関連遺伝子群の単離. 循環器最新医療フォーラム 2005.01

田中敏博. ゲノム情報に基づくオーダーメイド医療の実現に向けて. 第21回国際心臓研究学会日本支部総会　ランチョンセミナー 2004.11

田中敏博. 体系的ゲノム情報に基づく疾患関連遺伝子の単離 . 第5回SRL遺伝子診断フォーラム 2004.11

田中敏博. ゲノム情報に基づく心筋梗塞関連遺伝子群の単離とその機能解析. BioJapan2004 2004.09

田中敏博. 体系的ゲノム解析に基づく疾患関連遺伝子群単離とその機能解析. 東北インスリン研究会 2004.09

田中敏博. ゲノム情報に基づく疾患関連遺伝子の同定. 河口湖心臓討論会 2004.07

田中敏博. Genetic Backgrounds of Myocardial Infarction　. 第13回武田科学振興財団生命科学シンポジウム 2004.02

尾崎浩一，大西洋三，飯田有俊，関根章博，山田亮，角田達彦，佐藤洋，佐藤秀幸，堀正二，中村祐輔，田中敏博. 全ゲノム相関解析による心筋梗塞感受性遺伝子リンホトキシン-α (LTA) の同定. 日本人類遺伝学会第48回大会 2003.10

大西洋三，尾崎浩一，飯田有俊，関根章博，角田達彦，佐藤洋，佐藤秀幸，堀正二，中村祐輔，田中敏博. 全ゲノム相関解析による心筋梗塞感受性遺伝子の同定. 日本人類遺伝学会第48回大会 2003.10

田中敏博. 多因子疾患の SNP 研究　SNP 解析による心筋梗塞関連遺伝子の単離 . 日本人類遺伝学会第48回大会 2003.10

田中敏博. ゲノム解析による疾患関連遺伝子の単離. Molecular Cardiovascular Conference 2003.09

田中敏博. 心筋梗塞の遺伝子解析 . 第40回日本臨床分子医学会 2003.07

田中敏博. SNP解析による心筋梗塞関連遺伝子の単離. 第13回 Medical Genetics 研究会 2003.06

田中敏博. ゲノム医科学：ゲノム医科学の課題. 神奈川科学技術アカデミー教育講座 2003.05

田中敏博. ゲノム解析によるオーダーメイド医療 . 日本人類遺伝学会第47回大会 2002.11

Ozaki K, Ohnishi Y, Iida A, Yamada R, Tsunoda T, Sekine A, Sato H, Satoh H, Hori M, Nakamura Y, Tanaka T.. Genome-wide association study to identify genes related to myocardial infarction. . 第66回日本循環器学会学術集会 2002.04

Ohnishi Y, Tanaka T, Ozaki K, Yamada R, Sekine A, Suzuki H, Sato H, Satoh H, Hori M, Nakamura Y. . A high-throughput SNP typing system for genome-wide association studies in patients with myocardial infarction.. 第66回日本循環器学会学術集会 2002.04

田中敏博. ポストゲノムにおける心血管病への遺伝的アプローチー日本におけるSNPプロジェクトー. 第66回日本循環器学会学術集会 2002.04

田中敏博. ゲノム医科学の新局面　体系的解析によるオーダーメイド医療. 千里ライフサイエンスセミナー 2002.02

佐々木泰史，森本一郎，石田勢津子，今井浩三，鬼原史，田中敏博，中村祐輔，時の隆至. p53 類似遺伝子 p73, p63/p51 の標的遺伝子の検索　. 第60回日本癌学会総会 2001.10

渡邊吾一，西森博幸，入船秀仁，佐々木泰史，前仏均，田中敏博，吉田幸一，石井清一，中村祐輔，時野隆至. EWS-ETS family 融合遺伝子の標的遺伝子の発現解析　. 第60回日本癌学会総会 2001.10

高橋めい子，田中敏博，角田達彦，中村祐輔，古川洋一. 癌抑制遺伝子によって発現の減弱する新規遺伝子の単離とその解析. 第60回日本癌学会総会 2001.10

林裕民，岡部寛，長谷川傑，北原治，柳川練平，角田達彦，田中敏博，中村祐輔，古川洋一. cDNA マイクロアレーを用いた大腸腫瘍の遺伝子解析. 第60回日本癌学会総会 2001.10

古川洋一，林裕民，石黒秀行，藤田学，三輪晋智，高橋めい子，浜本隆二，柳生隆一郎，下川卓志，田中敏博，角田達彦，中村祐輔. cDNA Microarray を用いたβ-カテニン下流遺伝子の同定とその機能解析. 第60回日本癌学会総会 2001.10

加藤達史，古川洋一，佐藤誠二，岡部寛，長谷川傑，渡辺武志，下川卓志，田中敏博，角田達彦，山岡義生，中村祐輔. cDNA Microarray を用いた新規β-カテニン下流遺伝子 MARKL1 の単離とその解析. 第60回日本癌学会総会 2001.10

岡部寛，加藤達史，長谷川傑，渡辺武志，古川洋一，田中敏博，角田達彦，山岡義生，中村祐輔. cDNA マイクロアレイによる新規肝癌関連遺伝子の同定. 第60回日本癌学会総会 2001.10

浜本隆二，柳生隆一郎，岡部寛，田中敏博，角田達彦，中村祐輔，古川洋一. 肝癌組織で発現が上昇する新規遺伝子 ZNFN3A1 の同定と機能解析. 第60回日本癌学会総会 2001.10

柳生隆一郎，浜本隆二，岡部寛，田中敏博，角田達彦，中村祐輔，古川洋一. 肝癌組織で発現が増加する新規遺伝子 VANGL1 の同定とその機能解析. 第60回日本癌学会総会 2001.10

石黒秀行，藤田学，三輪晋智，林裕民，高橋めい子，田中敏博，角田達彦，藤井義敬，中村祐輔，古川洋一. cDNA microarray を用いた AXIN により発現の増強する新規遺伝子 AXUD1 の単離とその解析. 第60回日本癌学会総会 2001.10

藤田学，石黒秀行，三輪晋智，林裕民，高橋めい子，浜本隆二，柳生隆一郎，田中敏博，角田達彦，小川道雄，中村祐輔，古川洋一. cDNA Microarray を用いたβ—カテニン下流遺伝子 A3966 の同定とその機能解析. 第60回日本癌学会総会 2001.10

三輪晋智，石黒秀行，藤田学，林裕民，高橋めい子，浜本隆二，柳生隆一郎，下川卓志，田中敏博，角田達彦，新川詔夫，中村祐輔，古川洋一. cDNA Microarray を用いたβ-αカテニン下流遺伝子 A6069 の同定とその解析. 第60回日本癌学会総会 2001.10

飯坂正義，林裕民，田中敏博，角田達彦，小川道雄，中村祐輔，古川洋一. cDNA Microarray を用いた非ステロイド系抗炎症薬（NSAID）の大腸菌細胞に対する増殖抑制に関与する遺伝子群の探索. 第60回日本癌学会総会 2001.10

長谷川傑，古川洋一，岡部寛，渡辺武志，田中敏博，角田達彦，山岡義生，中村祐輔. cDNA マイクロアレイを用いた分化型胃癌臨床検体の遺伝子発現プロファイルの解析. 第60回日本癌学会総会 2001.10

田中敏博. 高血圧領域におけるゲノム新時代　心臓の立場から. 第11回東京高血圧研究会プログラム 2001.09

田中敏博. 体系的情報解析—ゲノム解析，トランスクリプトーム解析—によるオーダーメイド医療. 第41回日本呼吸器学会総会 2001.04

大田恵子，森田宏，竹中志保，中村一文，赤木達，草野研吾，松原広己，大江透，岩佐泰靖，田中敏博. KvLQT1の遺伝子異常を有する先天性QT延長症候群の一例. 第77回日本循環器学会中国四国地方会 2000.12

新田マルセロ英治，北原治，古川洋一，角田達彦，田中敏博，柳川練平，奥津潤一，前仏均，中村祐輔. LCM と cDNA マイクロアレイを用いた大腸癌に関与する遺伝子の同定. 第59回日本癌学会総会 2000.10

吉田幸一，佐々木泰史，梅沢明弘，秦順一，鬼原史，田中敏博，中村祐輔，時野隆至. Ewing 肉腫特異的な EWS-ETS 融合転写因子の標的遺伝子. 第59回日本癌学会総会 2000.10

佐々木泰史，森本一郎，中谷宇一郎，石田勢津子，山下利春，今井浩三，鬼原史，田中敏博，中村祐輔，時野隆至. p53 類似遺伝子 p73, p51 の抗腫瘍効果についての検討. 第59回日本癌学会総会 2000.10

前仏均，鬼原史，角田達彦，田中敏博，山名秀明，古川洋一，小野賢司，北原治，平田公一，高木利久，中村祐輔. マイクロアレイによる遺伝子発現プロファイルに基づく食道癌の抗癌剤感受性予測. 第59回日本癌学会総会 2000.10

小野賢司，田中敏博，角田達彦，北原治，鬼原史，柳川練平，岡本愛光，落合和徳，高木利久，中村祐輔. マイクロアレイを用いた卵巣癌における遺伝子発現プロファイルの解析. 第59回日本癌学会総会 2000.10

三輪晋智，古川洋一，小野賢司，石黒秀行，佐藤誠二，田中敏博，角田達彦，高木利久，新川詔夫，中村祐輔. Microarray を用いたカテニン下流遺伝子の単離と機能解析. 第59回日本癌学会総会 2000.10

鬼原史，田中敏博，古川洋一，荒川博文，中村祐輔. マイクロアレイによる遺伝子発現プロファイルに基づく癌の個性診断. 第59回日本癌学会総会 2000.10

鵜木元香，松島—西宇美恵子，小野賢司，角田達彦，水口剛雄，西岡嘉宏，田中敏博，中村祐輔. 子宮体癌細胞株において Ad-PTEN 導入により誘導される遺伝子のマイクロアレイを用いた発現プロファイル. 第59回日本癌学会総会 2000.10

北原治，古川洋一，田中敏博，鬼原史，小野賢司，柳川練平，ニタマルセロ，高木利久，中村祐輔，角田達彦. LCM とマイクロアレイを用いた大腸癌臨床検体の遺伝子発現プロファイルの解析. 第59回日本癌学会総会 2000.10

古川洋一，小野賢司，西脇忠，石黒秀行，藤田学，佐藤誠二，三輪晋智，林裕民，田中敏博，角田達彦，高木利久，中村祐輔. Microarray を用いたβ-カテニン下流遺伝子の単離. 第59回日本癌学会総会 2000.10

飯坂正義，明石浩史，韓恵程，古川洋一，田中敏博，角田達彦，高木利久，小川道雄，中村祐輔. 非ステロイド系抗炎症薬（NSAID）の大腸癌細胞に対する増殖抑制に関与する遺伝子の探索. 第59回日本癌学会総会 2000.10

加藤達史，古川洋一，田中敏博，佐藤誠二，岡部寛，角田達彦，高木利久，山岡義生，中村祐輔. イクロアレイを用いた肝癌臨床検体の遺伝子発現プロファイルの解析. 第59回日本癌学会総会 2000.10

柳川練平，古川洋一，角田達彦，田中敏博，新田マルセロ英治，北原治，小野賢司，鬼原史，高木利久，中村祐輔. 大腸癌肝転移症例の遺伝子発現プロファイル. 第59回日本癌学会総会 2000.10

石黒秀行，古川洋一，小野賢司，佐藤誠二，三輪晋智，田中敏博，角田達彦，高木利久，中村祐輔. Microarray を用いたβ-カテニン新規下流遺伝子の単離と機能解析. 第59回日本癌学会総会 2000.10

林裕民，古川洋一，小野賢司，佐藤誠二，石黒秀行，三輪晋智，田中敏博，角田達彦，高木利久，中村祐輔. Microarray を用いたβ-カテニン下流遺伝子の単離と機能解析. 第59回日本癌学会総会 2000.10

田中敏博. 我が国におけるSNPプロジェクト. 日本人類遺伝学会第45回大会 2000.10

田中敏博. 体系的解析によるオーダーメイド医療 . 第48回日本臨床検査医学会総会　イブニングセミナー 2000.08

吉田幸一，佐々木泰史，梅沢明弘，秦順一，鬼原史，田中敏博，中村祐輔，時野隆至. Ewing 肉腫 / PNET に特異的 EWS-ETS 融合転写因子の標的遺伝子. 第1回DNAチップ技術研究会 2000.06

Kitahara O, Furukawa Y, Tanaka T, Kihara C, Ono K, Yanagawa R, Nita E.M, Ogasawara H, Okutsu J, Zenbutsu H, Shiraishi N, Takagi T, Nakamura Y, Tsunoda T.. Identification by cDNA Microarray of Genes Involved in Overian Carcinogenesis.. 第1回DNAチップ技術研究会 2000.06

田中敏博，中村祐輔. SNP解析によるオーダーメイド医療. 第1回DNAチップ技術研究会 2000.06

田中敏博. ゲノム解析とトランススプリクトーム解析によるオーダーメイド医療 . Genomics & Proteomics 2000 2000.06

田中敏博. DNAチップ. 第64回日本循環器学会学術集会 2000.04

中島忠，金古善明，伊藤敏夫，谷口靖広，間仁田守，大山良雄，倉林正彦，永井良三，田中敏博，中村祐輔，平岡昌和，古川哲史. LQT2-家系で認めたHERG C端cNBD内のミスセンス変異の新たな機能異常. 第64回日本循環器学会学術集会 2000.03

大西洋三，田中敏博，中村祐輔，佐藤洋，佐藤秀幸，葛谷恒彦，堀正二. 本邦における心筋梗塞のSingle Nucleotide Polymorphism(SNP)解析. 第64回日本循環器学会学術集会 2000.03

田中敏博. DNAマイクロアレイ技術 . 第62回日本血液学会総会 2000.03

田中敏博. チップテクノロジーを用いた遺伝子発現プロファイル解析. 第64回日本循環器学会学術集会 2000.03

田中敏博. DNAマイクロアレイ技術を用いた癌の“個性”診断 . 文部省特定領域研究・がんミニシンポジウム 2000.01

田中敏博. DNAマイクロアレイ技術 . 日本人類遺伝学会第44回大会 1999.11

田中敏博. 遺伝子チップ：量的変化（発現プロフィール）と質的変化（SNP；一塩基多型）. 第27回日本マス・スクリーニング学会 1999.10

北原治，田中敏博，小野賢司，白石紀彦，鬼原史，関豊和，柳川練平，高木利久，菅野純夫，中村祐輔. イクロアレイを用いた大腸癌臨床検体の遺伝子発現プロファイルの解析. 第58回日本癌学会総会 1999.09

白石紀彦，田中敏博，北原治，小野賢司，鬼原史，関豊和，柳川練平，菅野純夫，高木利久，矢守隆夫，中村祐輔. マイクロアレイを用いた各種ヒト腫瘍細胞株の発現プロファイルと抗癌剤感受性の解析. 第58回日本癌学会総会 1999.09

小野賢司，田中敏博，北原治，白石紀彦，鬼原史，関豊和，柳川練平，岡本知光，大西義孝，葛谷和夫，中村祐輔. T7 based RNA amplification 法およびマイクロアレイを用いた微量腫瘍組織検体の遺伝子発現プロファイルの解析. 第58回日本癌学会総会 1999.09

鬼原史，田中敏博，小野賢司，北原治，白石紀彦，関豊和，柳川練平，山名秀明，高木利久，菅野純夫，平田公一，中村祐輔. マイクロアレイを用いた食道癌臨床検体における遺伝子発現プロファイルの検討. 第58回日本癌学会総会 1999.09

中島忠，古川哲史，平岡昌和，伊藤敏夫，田中敏博，中村祐輔，高橋玉奈，桜田春水，永井良三. LQT2で認めるS4領域R534C変異の新たなHERG電流抑制機構 : 脱活性化の促進. 第63回日本循環器学会学術集会 1999.03

田中敏博. DNAマイクロアレイ技術. ゲノム医科学フォーラム 1999.02

辻川元一，倉橋浩樹，田中敏博，下村嘉一，田野保雄，中村祐輔. ホモ接合性マッピング法による膠様滴状角膜変性症の原因遺伝子座の限局化. 日本人類遺伝学会第43回大会 1998.10

伊藤敏夫，田中敏博，永井良三，中村祐輔. 家族性QT延長症候群の遺伝子変異の解析. 日本人類遺伝学会第43回大会 1998.10

田中敏博. 家族性QT延長症候群の遺伝子解析 . 第9回東京ベイ心臓カンファレンス 1998.06

中島忠，平岡昌和，古川哲史，田中敏博，中村祐輔，永井良三. 本邦LQT2における変異部位により異なったHERG電流抑制メカニズム. 第62回日本循環器学会学術集会 1998.03

平岡昌和, 中島忠, 古川哲史, 田中敏博, 中村祐輔. 本邦症例のHERGチャネル遺伝子変異に見られた機能発現異常. 第62回日本循環器学会学術集会 1998.03

田中敏博. 家族性QT延長症候群の遺伝子解析 . 第61回日本循環器学会学術集会 1998.03

伊藤誠，田中敏博，塚田修市，折田匠哉，西宇淳，友池仁暢，中村祐輔. ディファレンシャルディスプレイ法による血管内膜肥厚に関連する8つの遺伝子の同定. 日本人類遺伝学会第42回大会 1997.10

田中敏博. 家族性QT延長症候群の遺伝子解析. 第61回日本循環器学会総会学術集会 1997.04

菱垣晴次，北野景彦，田中敏博，中村祐輔，高木利久. DNA配列情報データベースGENOTK. 第18回日本分子生物学会年会 1995.12

田中敏博，中原賢一，山崎力，福島義光，中村祐輔，永井良三，矢崎義雄　. 我が国における家族性QT延長症候群の連鎖解析. 第58回日本循環器学会学術集会 1994.03

大滝英二，田中敏博，高橋直之，水野健彦，安藤博之，堀内規，菊池正，石井康宏，宇野元規，三枝広文，長田和裕，北原公一，諏訪二郎，鈴木紳. 血管内エコー法から見た冠動脈ステントの問題点. 第57回日本循環器学会学術集会 1993.03

石井康宏，三枝広文，菊池正，安藤博之，宇野元規，堀内規，田中敏博，高橋直之，水野健彦，長田和裕，北原公一，諏訪二郎，大滝英二，鈴木紳. 再PTCA断念例の検討. 第57回日本循環器学会学術集会 1993.03

三枝広文，水野健彦，田中敏博，高橋直之，堀内規，石井康宏，宇野元規，菊池正，安藤博之，長田和裕，諏訪二郎，北原公一，大滝英二，鈴木紳. Strecker coronary stentの初期治療成績と術後中期成績の検討. 第57回日本循環器学会学術集会 1993.03

堀内規，大滝英二，松本貢一，三枝広文，水野健彦，菊池正，高橋直之，石井康宏，春田昭二，田中敏博，安藤博之，長田和裕，北原公一，諏訪二郎，鈴木紳. 術後9年経過した静脈グラフトへのステント植え込み術後, 合併した大動脈弁狭窄症で死亡した1剖検例. 日本循環器学会第145回関東甲信越地方会 1992.09

田中敏博，森保道，塩島一朗，盛田俊介，前村浩二，山崎力，西村敬史，方勞哲，栗原裕基，世古義規，山沖和秀，永井良三，矢崎義雄，古瀬彰. 感染性心内膜炎による大動脈弁閉鎖不全症を合併したWPW症候群に対し同時手術を行った1例. 日本循環器学会第141回関東甲信越地方会 1991.10