KIF5B-RET fusions in lung adenocarcinoma von Kohno, Takashi, Ichikawa, Hitoshi, Totoki, Yasushi, Yasuda, Kazuki, Hiramoto, Masaki, Nammo, Takao, Sakamoto, Hiromi, Tsuta, Koji, Furuta, Koh, Shimada, Yoko, Iwakawa, Reika, Ogiwara, Hideaki, Oike, Takahiro, Enari, Masato, Schetter, Aaron J, Okayama, Hirokazu, Haugen, Aage, Skaug, Vidar, Chiku, Suenori, Yamanaka, Itaru, Arai, Yasuhito, Watanabe, Shun-ichi, Sekine, Ikuo, Ogawa, Seishi, Harris, Curtis C, Tsuda, Hitoshi, Yoshida, Teruhiko, Yokota, Jun, Shibata, Tatsuhiro

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Genetic Link Between Obesity and MMP14-Dependent Adipogenic Collagen Turnover von CHUN, Tae-Hwa, INOUE, Mayumi, MORISAKI, Hiroko, YAMANAKA, Itaru, MIYAMOTO, Yoshihiro, OKAMURA, Tomonori, SATO-KUSUBATA, Kaori, WEISS, Stephen J

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Leptin Gene and Leptin Receptor Gene Polymorphisms Are Associated with Sweet Preference and Obesity von Mizuta, Einosuke, Kokubo, Yoshihiro, Yamanaka, Itaru, Miyamoto, Yoshihiro, Okayama, Akira, Yoshimasa, Yasunao, Tomoike, Hitonobu, Morisaki, Hiroko, Morisaki, Takayuki

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Stimulation of interferon-β responses by aberrant SARS-CoV-2 small viral RNAs acting as retinoic acid-inducible gene-I agonists von Arai, Yasuha, Yamanaka, Itaru, Okamoto, Toru, Isobe, Ayana, Nakai, Naomi, Kamimura, Naoko, Suzuki, Tatsuya, Daidoji, Tomo, Ono, Takao, Nakaya, Takaaki, Matsumoto, Kazuhiko, Okuzaki, Daisuke, Watanabe, Yohei

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CDH13 gene coding t-cadherin influences variations in plasma adiponectin levels in the Japanese population von Morisaki, Hiroko, Yamanaka, Itaru, Iwai, Naoharu, Miyamoto, Yoshihiro, Kokubo, Yoshihiro, Okamura, Tomonori, Okayama, Akira, Morisaki, Takayuki

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Mutations in a TGF-β Ligand, TGFB3, Cause Syndromic Aortic Aneurysms and Dissections von Bertoli-Avella, Aida M., MD, PhD, Gillis, Elisabeth, MSc, Morisaki, Hiroko, MD, PhD, Verhagen, Judith M.A., MD, de Graaf, Bianca M., BSc, van de Beek, Gerarda, BSc, Gallo, Elena, PhD, Kruithof, Boudewijn P.T., PhD, Venselaar, Hanka, PhD, Myers, Loretha A., BSc, Laga, Steven, MD, Doyle, Alexander J., MD, PhD, Oswald, Gretchen, MS, CGC, van Cappellen, Gert W.A., PhD, Yamanaka, Itaru, PhD, van der Helm, Robert M., BSc, Beverloo, Berna, PhD, de Klein, Annelies, PhD, Pardo, Luba, MD, PhD, Lammens, Martin, MD, PhD, Evers, Christina, MD, Devriendt, Koenraad, MD, PhD, Dumoulein, Michiel, MD, Timmermans, Janneke, MD, Bruggenwirth, Hennie T., PhD, Verheijen, Frans, PhD, Rodrigus, Inez, MD, Baynam, Gareth, MD, Kempers, Marlies, MD, PhD, Saenen, Johan, MD, PhD, Van Craenenbroeck, Emeline M., MD, PhD, Minatoya, Kenji, MD, PhD, Matsukawa, Ritsu, MD, PhD, Tsukube, Takuro, MD, PhD, Kubo, Noriaki, MD, PhD, Hofstra, Robert, PhD, Goumans, Marie Jose, PhD, Bekkers, Jos A., MD, PhD, Roos-Hesselink, Jolien W., MD, PhD, van de Laar, Ingrid M.B.H., MD, PhD, Dietz, Harry C., MD, Van Laer, Lut, PhD, Morisaki, Takayuki, MD, PhD, Wessels, Marja W., MD, PhD, Loeys, Bart L., MD, PhD

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A Novel Thr56Met Mutation of the Autosomal Recessive Hypercholesterolemia Gene Associated with Hypercholesterolemia von Harada, Koji, Miyamoto, Yoshihiro, Morisaki, Hiroko, Ohta, Naotaka, Yamanaka, Itaru, Kokubo, Yoshihiro, Makino, Hisashi, Harada-Shiba, Mariko, Okayama, Akira, Tomoike, Hitonobu, Tomonori, Okamura, Saito, Yoshihiko, Yoshimasa, Yasunao, Morisaki, Takayuki

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Genetic association analysis of 77,539 genomes reveals rare disease etiologies von Greene, Daniel, Pirri, Daniela, Frudd, Karen, Sackey, Ege, Al-Owain, Mohammed, Giese, Arnaud P.J, Ramzan, Khushnooda, Riaz, Sehar, Yamanaka, Itaru, Boeckx, Nele, Thys, Chantal, Gelb, Bruce D, Brennan, Paul, Hartill, Verity, Harvengt, Julie, Kosho, Tomoki, Mansour, Sahar, Masuno, Mitsuo, Ohata, Takako, Stewart, Helen, Taibah, Khalid, Turner, Claire L.S, Imtiaz, Faiqa, Riazuddin, Saima, Morisaki, Takayuki, Ostergaard, Pia, Loeys, Bart L, Morisaki, Hiroko, Ahmed, Zubair M, Birdsey, Graeme M, Freson, Kathleen, Mumford, Andrew, Turro, Ernest

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Antisense transcripts with FANTOM2 clone set and their implications for gene regulation von Kiyosawa, Hidenori, Yamanaka, Itaru, Osato, Naoki, Kondo, Shinji, Hayashizaki, Yoshihide

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Erratum: A Novel Thr56Met Mutation of the Autosomal Recessive Hypercholesterolemia Gene Associated with Hypercholesterolemia[Journal of Atherosclerosis and Thrombosis 131-140] von Harada, Koji, Miyamoto, Yoshihiro, Morisaki, Hiroko, Ohta, Naotaka, Yamanaka, Itaru, Kokubo, Yoshihiro, Makino, Hisashi, Harada-Shiba, Mariko, Okayama, Akira, Hitonobu, Tomoike, Okamura, Tomonori, Saito, Yoshihiko, Yoshimasa, Yasunao, Morisaki, Takayuki

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Mutation of ACTA2 gene as an important cause of familial and nonfamilial nonsyndromatic thoracic aortic aneurysm and/or dissection (TAAD) von Morisaki, Hiroko, Akutsu, Koichi, Ogino, Hitoshi, Kondo, Norihiro, Yamanaka, Itaru, Tsutsumi, Yoshiaki, Yoshimuta, Tsuyoshi, Okajima, Toshiya, Matsuda, Hitoshi, Minatoya, Kenji, Sasaki, Hiroaki, Tanaka, Hiroshi, Ishibashi-Ueda, Hatsue, Morisaki, Takayuki

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Stimulation of IFN-β responses by aberrant SARS-CoV-2 small viral RNAs acting as RIG-I agonists von Arai, Yasuha, Yamanaka, Itaru, Okamoto, Toru, Isobe, Ayana, Nakai, Naomi, Kamimura, Naoko, Suzuki, Tatsuya, Daidoji, Tomo, Ono, Takao, Nakaya, Takaaki, Matsumoto, Kazuhiko, Okuzaki, Daisuke, Watanabe, Yohei

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Mutations in a TGF-[beta] Ligand, TGFB3, Cause Syndromic Aortic Aneurysms and Dissections von Bertoli-Avella, Aida M, Gillis, Elisabeth, Morisaki, Hiroko, Verhagen, Judith MA, de Graaf, Bianca M, van de Beek, Gerarda, Gallo, Elena, Kruithof, Boudewijn PT, Venselaar, Hanka, Myers, Loretha A, Laga, Steven, Doyle, Alexander J, Oswald, Gretchen, van Cappellen, Gert WA, Yamanaka, Itaru, van der Helm, Robert M, Beverloo, Berna, de Klein, Annelies, Pardo, Luba, Lammens, Martin, Evers, Christina, Devriendt, Koenraad, Dumoulein, Michiel, Timmermans, Janneke, Bruggenwirth, Hennie T, Verheijen, Frans, Rodrigus, Inez, Baynam, Gareth, Kempers, Marlies, Saenen, Johan, Van Craenenbroeck, Emeline M, Minatoya, Kenji, Matsukawa, Ritsu, Tsukube, Takuro, Kubo, Noriaki, Hofstra, Robert, Goumans, Marie Jose, Bekkers, Jos A, Roos-Hesselink, Jolien W, van de Laar, Ingrid MBH, Dietz, Harry C, Van Laer, Lut, Morisaki, Takayuki, Wessels, Marja W, Loeys, Bart L

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Mutations in a TGF-β Ligand, TGFB3, Cause Syndromic Aortic Aneurysms and Dissections von Bertoli-Avella, Aida M, Gillis, Elisabeth, Morisaki, Hiroko, Verhagen, Judith M.A, de Graaf, Bianca M, van de Beek, Gerarda, Gallo, Elena, Kruithof, Boudewijn P.T, Venselaar, Hanka, Myers, Loretha A, Laga, Steven, Doyle, Alexander J, Oswald, Gretchen, van Cappellen, Gert W.A, Yamanaka, Itaru, van der Helm, Robert M, Beverloo, Berna, de Klein, Annelies, Pardo, Luba, Lammens, Martin, Evers, Christina, Devriendt, Koenraad, Dumoulein, Michiel, Timmermans, Janneke, Bruggenwirth, Hennie T, Verheijen, Frans, Rodrigus, Inez, Baynam, Gareth, Kempers, Marlies, Saenen, Johan, Van Craenenbroeck, Emeline M, Minatoya, Kenji, Matsukawa, Ritsu, Tsukube, Takuro, Kubo, Noriaki, Hofstra, Robert, Goumans, Marie Jose, Bekkers, Jos A, Roos-Hesselink, Jolien W, van de Laar, Ingrid M.B.H, Dietz, Harry C, Van Laer, Lut, Morisaki, Takayuki, Wessels, Marja W, Loeys, Bart L

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Association study of 11β-hydroxysteroid dehydrogenase type 1 gene polymorphisms and metabolic syndrome in urban Japanese cohort von Miyamoto, Yoshihiro, Morisaki, Hiroko, Yamanaka, Itaru, Kokubo, Yoshihiro, Masuzaki, Hiroaki, Okayama, Akira, Tomoike, Hitonobu, Nakao, Kazuwa, Okamura, Tomonori, Yoshimasa, Yasunao, Morisaki, Takayuki

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Abstract B93: Gene fusions detected by whole transcriptome sequencing of lung adenocarcinoma von Kohno, Takashi, Ichikawa, Hitoshi, Totoki, Yasushi, Yasuda, Kazuki, Hiramoto, Masaki, Nammo, Takao, Sakamoto, Hiromi, Tsuta, Kohji, Furuta, Koh, Shimada, Yoko, Iwakawa, Reika, Chiku, Suenori, Yamanaka, Itaru, Watanabe, Shunichi, Sekine, Ikuo, Ogawa, Seishi, Tsuda, Hitoshi, Yoshida, Teruhiko, Yokota, Jun, Shibata, Tatsuhiro

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Mapping of 19032 mouse cDNAs on mouse chromosomes von Yamanaka, Itaru, Kiyosawa, Hidenori, Kondo, Shinji, Saito, Tetsuya, Carninci, Piero, Shinagawa, Akira, Aizawa, Katsunori, Fukuda, Shiro, Hara, Ayako, Itoh, Masayoshi, Kawai, Jun, Shibata, Kazuhiro, Arakawa, Takahiro, Ishii, Yoshiyuki, Hayashizaki, Yoshihide

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Resistin gene variations are associated with the metabolic syndrome in Japanese men von Miyamoto, Yoshihiro, Morisaki, Hiroko, Kokubo, Yoshihiro, Yamanaka, Itaru, Tomoike, Hitonobu, Okayama, Akira, Yoshimasa, Yasunao, Morisaki, Takayuki

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Introduction of RIKEN-GenoMapper, Mapping Viewer System: Figure 1 von Kiyosawa, Hidenori, Kawashima, Tsugumi, Hasegawa, Yuki, Yamanaka, Itaru, Sakai, Katsunaga, Kondo, Shinji, Hayashizaki, Yoshihide

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Genetic association analysis of 77,539 genomes reveals rare disease etiologies von Greene, Daniel, Genomics England Research Consortium, Pirri, Daniela, Frudd, Karen, Sackey, Ege, Al-Owain, Mohammed, Giese, Arnaud PJ, Ramzan, Khushnooda, Riaz, Sehar, Yamanaka, Itaru, Boeckx, Nele, Thys, Chantal, Gelb, Bruce D, Brennan, Paul, Hartill, Verity, Harvengt, Julie, Kosho, Tomoki, Mansour, Sahar, Masuno, Mitsuo, Ohata, Takako, Stewart, Helen, Taibah, Khalid, Turner, Claire LS, Imtiaz, Faiqa, Riazuddin, Saima, Morisaki, Takayuki, Ostergaard, Pia, Loeys, Bart L, Morisaki, Hiroko, Ahmed, Zubair M, Birdsey, Graeme M, Freson, Kathleen, Mumford, Andrew, Turro, Ernest

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