Whole-genome mutational landscape and characterization of noncoding and structural mutations in liver cancer von Fujimoto, Akihiro, Furuta, Mayuko, Totoki, Yasushi, Tsunoda, Tatsuhiko, Kato, Mamoru, Shiraishi, Yuichi, Tanaka, Hiroko, Taniguchi, Hiroaki, Kawakami, Yoshiiku, Ueno, Masaki, Gotoh, Kunihito, Ariizumi, Shun-ichi, Wardell, Christopher P, Hayami, Shinya, Nakamura, Toru, Aikata, Hiroshi, Arihiro, Koji, Boroevich, Keith A, Abe, Tetsuo, Nakano, Kaoru, Maejima, Kazuhiro, Sasaki-Oku, Aya, Ohsawa, Ayako, Shibuya, Tetsuo, Nakamura, Hiromi, Hama, Natsuko, Hosoda, Fumie, Arai, Yasuhito, Ohashi, Shoko, Urushidate, Tomoko, Nagae, Genta, Yamamoto, Shogo, Ueda, Hiroki, Tatsuno, Kenji, Ojima, Hidenori, Hiraoka, Nobuyoshi, Okusaka, Takuji, Kubo, Michiaki, Marubashi, Shigeru, Yamada, Terumasa, Hirano, Satoshi, Yamamoto, Masakazu, Ohdan, Hideki, Shimada, Kazuaki, Ishikawa, Osamu, Yamaue, Hiroki, Chayama, Kazuki, Miyano, Satoru, Aburatani, Hiroyuki, Shibata, Tatsuhiro, Nakagawa, Hidewaki

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Genetic abnormalities in myelodysplasia and secondary acute myeloid leukemia: impact on outcome of stem cell transplantation von Yoshizato, Tetsuichi, Nannya, Yasuhito, Atsuta, Yoshiko, Shiozawa, Yusuke, Iijima-Yamashita, Yuka, Yoshida, Kenichi, Shiraishi, Yuichi, Suzuki, Hiromichi, Nagata, Yasunobu, Sato, Yusuke, Kakiuchi, Nobuyuki, Matsuo, Keitaro, Onizuka, Makoto, Kataoka, Keisuke, Chiba, Kenichi, Tanaka, Hiroko, Ueno, Hiroo, Nakagawa, Masahiro M., Przychodzen, Bartlomiej, Haferlach, Claudia, Kern, Wolfgang, Aoki, Kosuke, Itonaga, Hidehiro, Kanda, Yoshinobu, Sekeres, Mikkael A., Maciejewski, Jaroslaw P., Haferlach, Torsten, Miyazaki, Yasushi, Horibe, Keizo, Sanada, Masashi, Miyano, Satoru, Makishima, Hideki, Ogawa, Seishi

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Landscape and function of multiple mutations within individual oncogenes von Saito, Yuki, Koya, Junji, Araki, Mitsugu, Kogure, Yasunori, Shingaki, Sumito, Tabata, Mariko, McClure, Marni B., Yoshifuji, Kota, Matsumoto, Shigeyuki, Isaka, Yuta, Tanaka, Hiroko, Kanai, Takanori, Miyano, Satoru, Shiraishi, Yuichi, Okuno, Yasushi, Kataoka, Keisuke

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Action-projection in Japanese conversation: topic particles wa, mo, and tte for triggering categorization activities von Tanaka, Hiroko

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Stacked antiaromatic porphyrins von Nozawa, Ryo, Tanaka, Hiroko, Cha, Won-Young, Hong, Yongseok, Hisaki, Ichiro, Shimizu, Soji, Shin, Ji-Young, Kowalczyk, Tim, Irle, Stephan, Kim, Dongho, Shinokubo, Hiroshi

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A comprehensive characterization of cis -acting splicing-associated variants in human cancer von Shiraishi, Yuichi, Kataoka, Keisuke, Chiba, Kenichi, Okada, Ai, Kogure, Yasunori, Tanaka, Hiroko, Ogawa, Seishi, Miyano, Satoru

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Associations with oral health indices for obesity risk among Japanese men and women: results from the baseline data of a cohort study von Tanaka, Hiroko, Nakano, Mirei, Kuriki, Kiyonori

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Integrated genetic and epigenetic analysis defines novel molecular subgroups in rhabdomyosarcoma von Seki, Masafumi, Nishimura, Riki, Yoshida, Kenichi, Shimamura, Teppei, Shiraishi, Yuichi, Sato, Yusuke, Kato, Motohiro, Chiba, Kenichi, Tanaka, Hiroko, Hoshino, Noriko, Nagae, Genta, Shiozawa, Yusuke, Okuno, Yusuke, Hosoi, Hajime, Tanaka, Yukichi, Okita, Hajime, Miyachi, Mitsuru, Souzaki, Ryota, Taguchi, Tomoaki, Koh, Katsuyoshi, Hanada, Ryoji, Kato, Keisuke, Nomura, Yuko, Akiyama, Masaharu, Oka, Akira, Igarashi, Takashi, Miyano, Satoru, Aburatani, Hiroyuki, Hayashi, Yasuhide, Ogawa, Seishi, Takita, Junko

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The landscape of somatic mutations in Down syndrome–related myeloid disorders von Yoshida, Kenichi, Toki, Tsutomu, Okuno, Yusuke, Kanezaki, Rika, Shiraishi, Yuichi, Sato-Otsubo, Aiko, Sanada, Masashi, Park, Myoung-ja, Terui, Kiminori, Suzuki, Hiromichi, Kon, Ayana, Nagata, Yasunobu, Sato, Yusuke, Wang, RuNan, Shiba, Norio, Chiba, Kenichi, Tanaka, Hiroko, Hama, Asahito, Muramatsu, Hideki, Hasegawa, Daisuke, Nakamura, Kazuhiro, Kanegane, Hirokazu, Tsukamoto, Keiko, Adachi, Souichi, Kawakami, Kiyoshi, Kato, Koji, Nishimura, Ryosei, Izraeli, Shai, Hayashi, Yasuhide, Miyano, Satoru, Kojima, Seiji, Ito, Etsuro, Ogawa, Seishi

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Hand, foot, and mouth disease caused by coxsackievirus A6, Japan, 2011 von Fujimoto, Tsuguto, Iizuka, Setsuko, Enomoto, Miki, Abe, Katsuhiko, Yamashita, Kazuyo, Hanaoka, Nozomu, Okabe, Nobuhiko, Yoshida, Hiromu, Yasui, Yoshinori, Kobayashi, Masaaki, Fujii, Yoshiki, Tanaka, Hiroko, Yamamoto, Miwako, Shimizu, Hiroyuki

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Integrated molecular profiling of juvenile myelomonocytic leukemia von Murakami, Norihiro, Okuno, Yusuke, Yoshida, Kenichi, Shiraishi, Yuichi, Nagae, Genta, Suzuki, Kyogo, Narita, Atsushi, Sakaguchi, Hirotoshi, Kawashima, Nozomu, Wang, Xinan, Xu, Yinyan, Chiba, Kenichi, Tanaka, Hiroko, Hama, Asahito, Sanada, Masashi, Ito, Masafumi, Hirayama, Masashi, Watanabe, Arata, Ueno, Toshihide, Kojima, Seiji, Aburatani, Hiroyuki, Mano, Hiroyuki, Miyano, Satoru, Ogawa, Seishi, Takahashi, Yoshiyuki, Muramatsu, Hideki

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Genetic Analysis of Pheochromocytoma and Paraganglioma Complicating Cyanotic Congenital Heart Disease von Ogasawara, Tatsuki, Fujii, Yoichi, Kakiuchi, Nobuyuki, Shiozawa, Yusuke, Sakamoto, Ryuichi, Ogawa, Yoshihiro, Ootani, Katsuki, Ito, Etsuro, Tanaka, Tomoaki, Yoshida, Yusaku, Kimura, Noriko, Shiraishi, Yuichi, Chiba, Kenichi, Tanaka, Hiroko, Miyano, Satoru, Ogawa, Seishi

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Recurrent somatic mutations underlie corticotropin-independent Cushing's syndrome von Sato, Yusuke, Maekawa, Shigekatsu, Ishii, Ryohei, Sanada, Masashi, Morikawa, Teppei, Shiraishi, Yuichi, Yoshida, Kenichi, Nagata, Yasunobu, Sato-Otsubo, Aiko, Yoshizato, Tetsuichi, Suzuki, Hiromichi, Shiozawa, Yusuke, Kataoka, Keisuke, Kon, Ayana, Aoki, Kosuke, Chiba, Kenichi, Tanaka, Hiroko, Kume, Haruki, Miyano, Satoru, Fukayama, Masashi, Nureki, Osamu, Homma, Yukio, Ogawa, Seishi

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Clonal evolution in myelodysplastic syndromes von da Silva-Coelho, Pedro, Kroeze, Leonie I., Yoshida, Kenichi, Koorenhof-Scheele, Theresia N., Knops, Ruth, van de Locht, Louis T., de Graaf, Aniek O., Massop, Marion, Sandmann, Sarah, Dugas, Martin, Stevens-Kroef, Marian J., Cermak, Jaroslav, Shiraishi, Yuichi, Chiba, Kenichi, Tanaka, Hiroko, Miyano, Satoru, de Witte, Theo, Blijlevens, Nicole M. A., Muus, Petra, Huls, Gerwin, van der Reijden, Bert A., Ogawa, Seishi, Jansen, Joop H.

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ACTN1 Mutations Cause Congenital Macrothrombocytopenia von Kunishima, Shinji, Okuno, Yusuke, Yoshida, Kenichi, Shiraishi, Yuichi, Sanada, Masashi, Muramatsu, Hideki, Chiba, Kenichi, Tanaka, Hiroko, Miyazaki, Koji, Sakai, Michio, Ohtake, Masatoshi, Kobayashi, Ryoji, Iguchi, Akihiro, Niimi, Gen, Otsu, Makoto, Takahashi, Yoshiyuki, Miyano, Satoru, Saito, Hidehiko, Kojima, Seiji, Ogawa, Seishi

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Mutations in the Gene Encoding the E2 Conjugating Enzyme UBE2T Cause Fanconi Anemia von Hira, Asuka, Yoshida, Kenichi, Sato, Koichi, Okuno, Yusuke, Shiraishi, Yuichi, Chiba, Kenichi, Tanaka, Hiroko, Miyano, Satoru, Shimamoto, Akira, Tahara, Hidetoshi, Ito, Etsuro, Kojima, Seiji, Kurumizaka, Hitoshi, Ogawa, Seishi, Takata, Minoru, Yabe, Hiromasa, Yabe, Miharu

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Scrofuloderma arising from spermatic cord tuberculosis von Matsuda, Kazuki M., Tanaka‐Mizutsugu, Hiroko, Kishi, Yuriko, Chuman, Kumiko, Hino, Haruko, Kagami, Shinji

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Acquired initiating mutations in early hematopoietic cells of CLL patients von Damm, Frederik, Mylonas, Elena, Cosson, Adrien, Yoshida, Kenichi, Della Valle, Véronique, Mouly, Enguerran, Diop, M'boyba, Scourzic, Laurianne, Shiraishi, Yuichi, Chiba, Kenichi, Tanaka, Hiroko, Miyano, Satoru, Kikushige, Yoshikane, Davi, Frederick, Lambert, Jérôme, Gautheret, Daniel, Merle-Béral, Hélène, Sutton, Laurent, Dessen, Philippe, Solary, Eric, Akashi, Koichi, Vainchenker, William, Mercher, Thomas, Droin, Nathalie, Ogawa, Seishi, Nguyen-Khac, Florence, Bernard, Olivier A

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Unbiased Detection of Driver Mutations in Extramammary Paget Disease von Ishida, Yoshihiro, Kakiuchi, Nobuyuki, Yoshida, Kenichi, Inoue, Yoshikage, Irie, Hiroyuki, Kataoka, Tatsuki R, Hirata, Masahiro, Funakoshi, Takeru, Matsushita, Shigeto, Hata, Hiroo, Uchi, Hiroshi, Yamamoto, Yuki, Fujisawa, Yasuhiro, Fujimura, Taku, Saiki, Ryunosuke, Takeuchi, Kengo, Shiraishi, Yuichi, Chiba, Kenichi, Tanaka, Hiroko, Otsuka, Atsushi, Miyano, Satoru, Kabashima, Kenji, Ogawa, Seishi

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Abnormal hematopoiesis and autoimmunity in human subjects with germline IKZF1 mutations von Hoshino, Akihiro, MD, PhD, Okada, Satoshi, MD, PhD, Yoshida, Kenichi, MD, PhD, Nishida, Naonori, MD, PhD, Okuno, Yusuke, MD, PhD, Ueno, Hiroo, MD, Yamashita, Motoi, MD, Okano, Tsubasa, MD, Tsumura, Miyuki, PhD, Nishimura, Shiho, MD, Sakata, Sonoko, MD, Kobayashi, Masao, MD, PhD, Nakamura, Haruna, MD, Kamizono, Junji, MD, PhD, Mitsui-Sekinaka, Kanako, MD, Ichimura, Takuya, MD, Ohga, Shouichi, MD, PhD, Nakazawa, Yozo, MD, PhD, Takagi, Masatoshi, MD, PhD, Imai, Kohsuke, MD, PhD, Shiraishi, Yuichi, MD, PhD, Chiba, Kenichi, BA, Tanaka, Hiroko, BS, Miyano, Satoru, PhD, Ogawa, Seishi, MD, PhD, Kojima, Seiji, MD, PhD, Nonoyama, Shigeaki, MD, PhD, Morio, Tomohiro, MD, PhD, Kanegane, Hirokazu, MD, PhD

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