CHCHD2 mutations in autosomal dominant late-onset Parkinson's disease: a genome-wide linkage and sequencing study von Funayama, Manabu, PhD, Ohe, Kenji, MD, Amo, Taku, PhD, Furuya, Norihiko, PhD, Yamaguchi, Junji, MSc, Saiki, Shinji, MD, Li, Yuanzhe, MD, Ogaki, Kotaro, MD, Ando, Maya, MD, Yoshino, Hiroyo, PhD, Tomiyama, Hiroyuki, MD, Nishioka, Kenya, MD, Hasegawa, Kazuko, MD, Saiki, Hidemoto, MD, Satake, Wataru, MD, Mogushi, Kaoru, PhD, Sasaki, Ryogen, MD, Kokubo, Yasumasa, Prof, Kuzuhara, Shigeki, Prof, Toda, Tatsushi, Prof, Mizuno, Yoshikuni, Prof, Uchiyama, Yasuo, Prof, Ohno, Kinji, Prof, Hattori, Nobutaka, Prof

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Genome-wide association study identifies zonisamide responsive gene in Parkinson's disease patients von Cha, Pei-Chieng, Satake, Wataru, Ando-Kanagawa, Yuko, Yamamoto, Ken, Murata, Miho, Toda, Tatsushi

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Genome-wide association study identifies common variants at four loci as genetic risk factors for Parkinson's disease von Kawakami, Hideshi, Nakashima, Kenji, Takeda, Atsushi, Sakoda, Saburo, Hirota, Yushi, Yamamoto, Mitsutoshi, Kawaguchi, Takahisa, Nakabayashi, Yuko, Mizuta, Ikuko, Watanabe, Masahiko, Nakamura, Yusuke, Murata, Miho, Tomiyama, Hiroyuki, Hasegawa, Kazuko, Yoshikawa, Takeo, Ito, Chiyomi, Hattori, Nobutaka, Kubo, Michiaki, Toda, Tatsushi, Tsunoda, Tatsuhiko, Obata, Fumiya, Satake, Wataru

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Variants in saposin D domain of prosaposin gene linked to Parkinson's disease von Oji, Yutaka, Hatano, Taku, Ueno, Shin-Ichi, Funayama, Manabu, Ishikawa, Kei-ichi, Okuzumi, Ayami, Noda, Sachiko, Sato, Shigeto, Satake, Wataru, Toda, Tatsushi, Li, Yuanzhe, Hino-Takai, Tomoko, Kakuta, Soichiro, Tsunemi, Taiji, Yoshino, Hiroyo, Nishioka, Kenya, Hattori, Tatsuya, Mizutani, Yasuaki, Mutoh, Tatsuro, Yokochi, Fusako, Ichinose, Yuta, Koh, Kishin, Shindo, Kazumasa, Takiyama, Yoshihisa, Hamaguchi, Tsuyoshi, Yamada, Masahito, Farrer, Matthew J., Uchiyama, Yasuo, Akamatsu, Wado, Wu, Yih-Ru, Matsuda, Junko, Hattori, Nobutaka

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Trans‐Ethnic Fine‐Mapping of the Major Histocompatibility Complex Region Linked to Parkinson's Disease von Naito, Tatsuhiko, Satake, Wataru, Ogawa, Kotaro, Suzuki, Ken, Hirata, Jun, Foo, Jia Nee, Tan, Eng‐King, Toda, Tatsushi, Okada, Yukinori

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Bardet-Biedl syndrome and related disorders in Japan von Hirano, Makito, Satake, Wataru, Moriyama, Nobuko, Saida, Ken, Okamoto, Nobuhiko, Cha, Pei-Chieng, Suzuki, Yutaka, Kusunoki, Susumu, Toda, Tatsushi

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Exome Analyses of Long QT Syndrome Reveal Candidate Pathogenic Mutations in Calmodulin-Interacting Genes von Shigemizu, Daichi, Aiba, Takeshi, Nakagawa, Hidewaki, Ozaki, Kouichi, Miya, Fuyuki, Satake, Wataru, Toda, Tatsushi, Miyamoto, Yoshihiro, Fujimoto, Akihiro, Suzuki, Yutaka, Kubo, Michiaki, Tsunoda, Tatsuhiko, Shimizu, Wataru, Tanaka, Toshihiro

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The First Nationwide Survey and Genetic Analyses of Bardet-Biedl Syndrome in Japan von Hirano, Makito, Satake, Wataru, Ihara, Kenji, Tsuge, Ikuya, Kondo, Shuji, Saida, Ken, Betsui, Hiroyuki, Okubo, Kazuhiro, Sakamoto, Hikaru, Ueno, Shuichi, Ikuno, Yasushi, Ishihara, Ryu, Iwahashi, Hiromi, Ohishi, Mitsuru, Mano, Toshiyuki, Yamashita, Toshihide, Suzuki, Yutaka, Nakamura, Yusaku, Kusunoki, Susumu, Toda, Tatsushi

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Redox states of thirteen shergottites as inferred from iron micro X-ray absorption near edge structure of maskelynite von SATAKE, WATARU, MIKOUCHI, TAKASHI, MIYAMOTO, MASAMICHI

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SPTLC2 variants are associated with early‐onset ALS and FTD due to aberrant sphingolipid synthesis von Naruse, Hiroya, Ishiura, Hiroyuki, Esaki, Kayoko, Mitsui, Jun, Satake, Wataru, Greimel, Peter, Shingai, Nanoka, Machino, Yuka, Kokubo, Yasumasa, Hamaguchi, Hirotoshi, Oda, Tetsuya, Ikkaku, Tomoko, Yokota, Ichiro, Takahashi, Yuji, Suzuki, Yuta, Matsukawa, Takashi, Goto, Jun, Koh, Kishin, Takiyama, Yoshihisa, Morishita, Shinichi, Yoshikawa, Takeo, Tsuji, Shoji, Toda, Tatsushi

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Bardet–Biedl syndrome and related disorders in Japan von Hirano, Makito, Satake, Wataru, Moriyama, Nobuko, Saida, Ken, Okamoto, Nobuhiko, Cha, Pei-Chieng, Suzuki, Yutaka, Kusunoki, Susumu, Toda, Tatsushi

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Genetic and clinical analysis in a Chinese parkinsonism-predominant spinocerebellar ataxia type 2 family von Sun, Hao, Satake, Wataru, Zhang, Changjun, Nagai, Yoshitaka, Tian, Youyong, Fu, Shouzhi, Yu, Jiankun, Qian, Yaping, Qian, Yuan, Chu, Jiayou, Toda, Tatsushi

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A case of Bardet-Biedl syndrome complicated with intracranial hypertension in a Japanese child von Saida, Ken, Inaba, Yuji, Hirano, Makito, Satake, Wataru, Toda, Tatsushi, Suzuki, Yutaka, Sudo, Asuka, Noda, Shunsuke, Hidaka, Yoshihiko, Hirabayashi, Kazutaka, Imai, Hiroki, Kurokawa, Toru, Koike, Kenichi

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Mineralogy and crystallography of some Itokawa particles returned by the Hayabusa asteroidal sample return mission von Mikouchi, Takashi, Komatsu, Mutsumi, Hagiya, Kenji, Ohsumi, Kazumasa, Zolensky, Michael E, Hoffmann, Viktor, Martinez, James, Hochleitner, Rupert, Kaliwoda, Melanie, Terada, Yasuko, Yagi, Naoto, Takata, Masaki, Satake, Wataru, Aoyagi, Yuya, Takenouchi, Atsushi, Karouji, Yuzuru, Uesugi, Masayuki, Yada, Toru

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Japanese WDR45 de novo mutation diagnosed by exome analysis: A case report von Endo, Hironobu, Uenaka, Takeshi, Satake, Wataru, Suzuki, Yutaka, Tachibana, Hisatsugu, Chihara, Norio, Ueda, Takehiro, Sekiguchi, Kenji, Mariko, Taniguchi‐Ikeda, Kowa, Hisatomo, Kanda, Fumio, Toda, Tatsushi

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Subacute Upper Motor Neuron Dysfunction Possibly Associated with the Anti-GM1 Autoantibody: A Case Report von Okubo, So, Maeda, Meiko, Katsuse, Kazuto, Ishiura, Hiroyuki, Shirota, Yuichiro, Hamada, Masashi, Satake, Wataru, Toda, Tatsushi

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TUBB3 E410K Syndrome With Childhood-Onset Nonalcoholic Steatohepatitis von Mori, Jun, Umemura, Atsushi, Satake, Wataru, Cha, Pei-Chieng, Suzuki, Yutaka, Itoh, Kyoko, Chiyonobu, Tomohiro

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A Japanese family with idiopathic basal ganglia calcification carrying a novel XPR1 variant von Orimo, Kenta, Kakumoto, Toshiyuki, Hara, Ryo, Goto, Ryoji, Ishiura, Hiroyuki, Mitsui, Jun, Yoshida, Chiharu, Uesaka, Yoshikazu, Suzuki, Yuta, Morishita, Shinichi, Satake, Wataru, Tsuji, Shoji, Toda, Tatsushi

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Trans-ethnic fine-mapping of the MHC region on Parkinson's disease identified shared genetic features associated with the risk von Naito, Tatsuhiko, Satake, Wataru, Ogawa, Kotaro, Suzuki, Ken, Hirata, Jun, Foo, Jia, Tan, Ek, Okada, Yukinori, Toda, Tatsushi

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Comprehensive research synopsis and systematic meta-analyses in Parkinson's disease genetics: The PDGene database von Lill, Christina M, Roehr, Johannes T, McQueen, Matthew B, Kavvoura, Fotini K, Bagade, Sachin, Schjeide, Brit-Maren M, Schjeide, Leif M, Meissner, Esther, Zauft, Ute, Allen, Nicole C, Liu, Tian, Schilling, Marcel, Anderson, Kari J, Beecham, Gary, Berg, Daniela, Biernacka, Joanna M, Brice, Alexis, DeStefano, Anita L, Do, Chuong B, Eriksson, Nicholas, Factor, Stewart A, Farrer, Matthew J, Foroud, Tatiana, Gasser, Thomas, Hamza, Taye, Hardy, John A, Heutink, Peter, Hill-Burns, Erin M, Klein, Christine, Latourelle, Jeanne C, Maraganore, Demetrius M, Martin, Eden R, Martinez, Maria, Myers, Richard H, Nalls, Michael A, Pankratz, Nathan, Payami, Haydeh, Satake, Wataru, Scott, William K, Sharma, Manu, Singleton, Andrew B, Stefansson, Kari, Toda, Tatsushi, Tung, Joyce Y, Vance, Jeffery, Wood, Nick W, Zabetian, Cyrus P, Young, Peter, Tanzi, Rudolph E, Khoury, Muin J, Zipp, Frauke, Lehrach, Hans, Ioannidis, John P A, Bertram, Lars

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