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Ichizo Nishino

Active 1997–2026

188
Papers
21,915
Citations
87
h-index
178
i10-index

Citations

Citations per year for Ichizo Nishino1997: 1 citations1998: 1 citations1999: 9 citations2000: 34 citations2001: 65 citations2002: 66 citations2003: 123 citations2004: 122 citations2005: 116 citations2006: 115 citations2007: 111 citations2008: 162 citations2009: 148 citations2010: 184 citations2011: 226 citations2012: 170 citations2013: 223 citations2014: 198 citations2015: 169 citations2016: 184 citations2017: 150 citations2018: 203 citations2019: 568 citations2020: 687 citations2021: 754 citations2022: 682 citations2023: 416 citations2024: 707 citations2025: 257 citations2026: 6 citations

Citation sources

Countries

World map of the countries and regions citing this authorUnited States: 2,123 citing papers, 24.3% of this breakdownChina: 723 citing papers, 8.3% of this breakdownUnited Kingdom: 686 citing papers, 7.8% of this breakdownJapan: 551 citing papers, 6.3% of this breakdownItaly: 534 citing papers, 6.1% of this breakdownFrance: 518 citing papers, 5.9% of this breakdownGermany: 415 citing papers, 4.7% of this breakdownCanada: 365 citing papers, 4.2% of this breakdownAustralia: 261 citing papers, 3% of this breakdownSpain: 232 citing papers, 2.7% of this breakdownNetherlands: 218 citing papers, 2.5% of this breakdownBelgium: 148 citing papers, 1.7% of this breakdown
0%24.3%Other 22.5%

Institutions

Fields

  • Biochemistry, Genetics and Molecular Biology48.5%
  • Medicine41.4%
  • Neuroscience6.8%
  • Nursing1.1%
  • Immunology and Microbiology0.9%
  • Agricultural and Biological Sciences0.3%
  • Other1%

Topics

  • Muscle Physiology and Disorders8%
  • Mitochondrial Function and Pathology5.3%
  • Inflammatory Myopathies and Dermatomyositis3.6%
  • Autophagy in Disease and Therapy3.5%
  • Adipose Tissue and Metabolism3.4%
  • Genetic Neurodegenerative Diseases3.3%
  • Other72.9%

Coauthors

All papers

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  1. Adiponectin and AdipoR1 regulate PGC-1α and mitochondria by Ca2+ and AMPK/SIRT1

    Authors: Masato Iwabu, Toshimasa Yamauchi, Miki Okada‐Iwabu, Koji Sato, Tatsuro Nakagawa, Masaaki Funata, Mamiko Yamaguchi, Shigeyuki Namiki, Ryo Nakayama, Mitsuhisa Tabata, Hitomi Ogata, Naoto Kubota, Iseki Takamoto, Yukiko Hayashi, Naoko Yamauchi, Hironori Waki, Masashi Fukayama, Ichizo Nishino, Kumpei Tokuyama, Kohjiro Ueki, Yuichi Oike, Satoshi Ishii, Kenzo Hirose, Takao Shimizu, Kazushige Touhara, Takashi Kadowaki - Nature 2010 cited by 973

  2. 224th ENMC International Workshop:

    Authors: Yves Allenbach, Andrew L. Mammen, Olivier Benvéniste, Werner Stenzel, Yves Allenbach, Anthony A. Amato, Audrey Aussey, Olivier Benvéniste, Jan De Bleecker, Ingrid de Groot, Marianne de Visser, Hans H. Goebel, B. Hervier, Norina Fischer, David Hilton‐Jones, Janice Lamb, Ingrid E. Lundberg, Andrew L. Mammen, Tahseen Mozaffar, Ichizo Nishino, Alan Pestronk, Ulrike Schara, Werner Stenzelr - Neuromuscular Disorders 2017 cited by 554

  3. Noncoding CGG repeat expansions in neuronal intranuclear inclusion disease, oculopharyngodistal myopathy and an overlapping disease

    Authors: Hiroyuki Ishiura, Shota Shibata, Jun Yoshimura, Yuta Suzuki, Wei Qü, Koichiro Doi, Mohammad Almansour, Junko Kanda Kikuchi, Makiko Taira, Jun Mitsui, Yuji Takahashi, Yaeko Ichikawa, Tatsuo Mano, Atsushi Iwata, Yasuo Harigaya, Miho Matsukawa, Takashi Matsukawa, Masaki Tanaka, Yuichiro Shirota, Ryo Ohtomo, Hisatomo Kowa, Hidetoshi Date, Aki Mitsue, Hiroyuki Hatsuta, Satoru Morimoto, Shigeo Murayama, Yasushi Shiio, Yuko Saito, Akihiko Mitsutake, M. KAWAI, Takuya Sasaki, Yusuke Sugiyama, Masashi Hamada, Gaku Ohtomo, Yasuo Terao, Yoshihiko Nakazato, Akitoshi Takeda, Yoshio Sakiyama, Yumi Umeda‐Kameyama, Jun Shinmi, Katsuhisa Ogata, Yutaka Kohno, Shen‐Yang Lim, Ai Huey Tan, Jun Shimizu, Jun Goto, Ichizo Nishino, Tatsushi Toda, Shinichi Morishita, Shoji Tsuji - Nature Genetics 2019 cited by 447

  4. 239th ENMC International Workshop: Classification of dermatomyositis, Amsterdam, the Netherlands, 14–16 December 2018

    Authors: Andrew L. Mammen, Yves Allenbach, Werner Stenzel, Olivier Benvéniste, Yves Allenbach, Olivier Benveniste, Jan De Bleecker, Olivier Boyer, Livia Casciola‐Rosen, Lisa Christopher‐Stine, Jan Damoiseaux, Cyril Gitiaux, Manabu Fujimoto, Janine A. Lamb, Océane Landon‐Cardinal, Ingrid E. Lundberg, Andrew L. Mammen, Ichizo Nishino, Josefine Radke, Albert Selva-O’Callaghan, Werner Stenzel, Jiří Vencovský, Werner Stenzel, Guochun Wang, Lucy R. Wedderburn, Victoria P. Werth, Lucy R. Wedderburn, Victoria P. Werth - Neuromuscular Disorders 2019 cited by 299

  5. Identification and characterization of PDGFRα+ mesenchymal progenitors in human skeletal muscle

    Authors: Akiyoshi Uezumi, So‐ichiro Fukada, Naoki Yamamoto, Madoka Ikemoto‐Uezumi, Masashi Nakatani, Mitsuhiro Morita, Asami Yamaguchi, Hirotsugu Yamada, Ichizo Nishino, Y. Hamada, Kunihiro Tsuchida - Cell Death and Disease 2014 cited by 304

  6. International Guideline for Idiopathic Inflammatory Myopathy-Associated Cancer Screening: an International Myositis Assessment and Clinical Studies Group (IMACS) initiative

    Authors: Alexander Oldroyd, Jeffrey P. Callen, Hector Chinoy, Leland W.K. Chung, David Fiorentino, Patrick Gordon, Pedro Machado, Neil McHugh, Albert Selva-O’Callaghan, Jens Schmidt, Sarah Tansley, Ruth Ann Vleugels, Victoria P. Werth, Anthony A. Amato, Helena Andersson, Lilia Andrade-Ortega, Dana P. Ascherman, Olivier Benvéniste, Lorenzo Cavagna, Christina Charles-Shoeman, Benjamin F. Chong, Lisa Christopher‐Stine, Jennie T. Clarke, Emma J. Crosbie, Philip Crosbie, Sonye K. Danoff, Maryam Dastmalchi, Marianne De Visser, Paul F. Dellaripa, Louise Pyndt Diederichsen, Mazen M. Dimachkie, Erik Ensrud, Floranne C. Ernste, D. Gareth Evans, Manabu Fujimoto, Ignacio García‐De La Torre, Abraham García-Kutzbach, Zoltán Griger, Latika Gupta, Marie Hudson, Florenzo Iannone, David Isenberg, Joseph L. Jorizzo, Helen Kurtz, Masataka Kuwana, Vidya Limaye, Ingrid E. Lundberg, Andrew L. Mammen, H. Mann, Frank Mastaglia, Lorna McWilliams, Christopher A. Mecoli, Federica Meloni, Frederick W. Miller, Siamak Moghadam‐Kia, Sergey Moiseev, Yoshinao Muro, Melinda Nagy‐Vincze, Clive Nayler, Merrilee Needham, Ichizo Nishino, Chester V. Oddis, Julie J. Paik, Joost Raaphorst, Lisa G. Rider, Jorge Rojas‐Serrano, Lesley Ann Saketkoo, Adam Schiffenbauer, Samuel Katsuyuki Shinjo, Vineeta Shobha, Yeong‐Wook Song, Tania Tillett, Yves Troyanov, Anneke J. van der Kooi, Mónica Vázquez-Del Mercado, Jiří Vencovský, Qian Wang, Steven R. Ytterberg, Rohit Aggarwal - Nature Reviews Rheumatology 2023 cited by 139

  7. Mutations in DNMT3B Modify Epigenetic Repression of the D4Z4 Repeat and the Penetrance of Facioscapulohumeral Dystrophy

    Authors: Marlinde L. van den Boogaard, Richard J.L.F. Lemmers, Judit Balog, Mariëlle Wohlgemuth, Mari Auranen, Satomi Mitsuhashi, Patrick J. van der Vliet, Kirsten R. Straasheijm, Rob F. P. van den Akker, Marjolein Kriek, Marlies E.Y. Laurense-Bik, Vered Raz, Monique M. van Ostaijen-ten Dam, Kerstin Hansson, E.L. van der Kooi, Sari Kiuru‐Enari, B. Udd, Maarten J. D. van Tol, Ichizo Nishino, Rabi Tawil, Stephen J. Tapscott, Baziel G.M. van Engelen, Silvère M. van der Maarel - The American Journal of Human Genetics 2016 cited by 272

  8. Expansion of GGC Repeat in GIPC1 Is Associated with Oculopharyngodistal Myopathy

    Authors: Jianwen Deng, Jiaxi Yu, Pidong Li, Xinghua Luan, Li Cao, Juan Zhao, Meng Yu, Wei Zhang, He Lv, Zhiying Xie, Lingchao Meng, Yiming Zheng, Yawen Zhao, Qiang Gang, Qingqing Wang, Jing Liu, Min Zhu, Xueyu Guo, Yanan Su, Liang Yu, Fan Liang, Tomohiro Hayashi, Meiko Hashimoto Maeda, Tatsuro Sato, Shigehisa Ura, Yasushi Oya, Masashi Ogasawara, Aritoshi Iida, Ichizo Nishino, Zhou Chang, Chuanzhu Yan, Yun Yuan, Daojun Hong, Zhaoxia Wang - The American Journal of Human Genetics 2020 cited by 157

  9. Clinical features and prognosis in anti-SRP and anti-HMGCR necrotising myopathy

    Authors: Yurika Watanabe, Akinori Uruha, Shigeaki Suzuki, Jin Nakahara, Kohei Hamanaka, K. Takayama, Norihiro Suzuki, Ichizo Nishino - Journal of Neurology Neurosurgery & Psychiatry 2016 cited by 318

  10. Homozygous nonsense variant in LRIF1 associated with facioscapulohumeral muscular dystrophy

    Authors: Kohei Hamanaka, Darina Šikrová, Satomi Mitsuhashi, Hiroki Masuda, Yukari Sekiguchi, Atsuhiko Sugiyama, Kazumoto Shibuya, Richard J.L.F. Lemmers, Remko Goossens, Megumu Ogawa, Koji Nagao, Chikashi Obuse, S. Noguchi, Yukiko Hayashi, Satoshi Kuwabara, Judit Balog, Ichizo Nishino, Silvère M. van der Maarel - Neurology 2020 cited by 151

  11. Safety and efficacy of intravenous bimagrumab in inclusion body myositis (RESILIENT): a randomised, double-blind, placebo-controlled phase 2b trial

    Authors: Michael G. Hanna, Umesh A. Badrising, Olivier Benvéniste, Thomas E. Lloyd, Merrilee Needham, Hector Chinoy, Masashi Aoki, Pedro Machado, Christina Liang, Katrina Reardon, Marianne de Visser, Dana P. Ascherman, Richard J. Barohn, Mazen M. Dimachkie, James Miller, John T. Kissel, Björn Oskarsson, Nanette C. Joyce, Peter Van den Bergh, Jonathan Baets, Jan De Bleecker, Chafic Karam, William S. David, Massimiliano Mirabella, Sharon Nations, Hans H. Jung, Elena Pegoraro, Lorenzo Maggi, Carmelo Rodolico, Massimiliano Filosto, Aziz Shaibani, Kumaraswamy Sivakumar, Namita Goyal, Madoka Mori‐Yoshimura, Satoshi Yamashita, Naoki Suzuki, Masahisa Katsuno, Kenya Murata, Hiroyuki Nodera, Ichizo Nishino, Carla D Romano, Valerie Williams, John Vissing, Lixin Zhang Auberson, Min Wu, Ana de Vera, Dimitris A. Papanicolaou, Anthony A. Amato - The Lancet Neurology 2019 cited by 133

  12. 272nd ENMC international workshop: 10 Years of progress - revision of the ENMC 2013 diagnostic criteria for inclusion body myositis and clinical trial readiness. 16–18 June 2023, Hoofddorp, The Netherlands

    Authors: James B Lilleker, Elie Naddaf, Christiaan G. J. Saris, Jens Schmidt, Marianne de Visser, Conrad C. Weihl, Helene Alexanderson, Lindsay N. Alfano, Yves Allenbach, Umesh A. Badrising, Olivier Benvéniste, Salman Bhai, Jan De Bleecker, Marie Christine Breeveld, Hector Chinoy, Louise Pyndt Diederichsen, Mazen M. Dimachkie, Steven A. Greenberg, Mridul Johari, James B Lilleker, Ulrika Lindgren, Tom Lloyd, Pedro Machado, Tahseen Mozaffar, Roland Mischke, Elie Naddaf, Merrilee Needham, Ichizo Nishino, Anders Oldfors, Christiaan G. J. Saris, Jens Schmidt, Werner Stenzel, Giorgio Tasca, Marianne de Visser, Conrad C. Weihl - Neuromuscular Disorders 2024 cited by 88

  13. Primary LAMP-2 deficiency causes X-linked vacuolar cardiomyopathy and myopathy (Danon disease)

    Authors: Ichizo Nishino, Jin Fu, Kurenai Tanji, Takeshi Yamada, Sadatomo Shimojo, Tateo Koori, Marina Mora, Jack E. Riggs, Shin J. Oh, Yasutoshi Koga, Carolyn M. Sue, Ayaka Yamamoto, Nobuyuki Murakami, Sara Shanske, Edward Byrne, Eduardo Bonilla, Ikuya Nonaka, Salvatore DiMauro, Michio Hirano - Nature 2000 cited by 947

  14. Skeletal Muscle FOXO1 (FKHR) Transgenic Mice Have Less Skeletal Muscle Mass, Down-regulated Type I (Slow Twitch/Red Muscle) Fiber Genes, and Impaired Glycemic Control

    Authors: Yasutomi Kamei, Shinji Miura, Miki Suzuki, Yuko Kai, Junko Mizukami, Tomoyasu Taniguchi, Keiji Mochida, T. Hata, Junichiro Matsuda, Hiroyuki Aburatani, Ichizo Nishino, Osamu Ezaki - Journal of Biological Chemistry 2004 cited by 567

  15. Misregulated alternative splicing of BIN1 is associated with T tubule alterations and muscle weakness in myotonic dystrophy

    Authors: Charlotte Fugier, Arnaud F. Klein, Caroline Hammer, Stéphane Vassilopoulos, Ylva Ivarsson, Anne Toussaint, Valérie Tosch, Alban Vignaud, Arnaud Ferry, Nadia Messaddeq, Yosuke Kokunai, R. Tsuburaya, Pierre de la Grange, Doulaye Dembélé, Virginie François, Guillaume Précigout, Charlotte Boulade-Ladame, Marie-Christine Hummel, Adolfo López de Munaín, Nicolas Sergeant, Annie Laquerrière, Christelle Thibault-Carpentier, François Deryckère, Didier Auboeuf, Luis García, Pascale Zimmermann, Bjarne Udd, Benedikt Schoser, Masanori Takahashi, Ichizo Nishino, Guillaume Bassez, Jocelyn Laporte, Denis Furling, Nicolas Charlet‐Berguerand - Nature Medicine 2011 cited by 330

  16. Autophagic degradation of nuclear components in mammalian cells

    Authors: Young-Eun Park, Yukiko Hayashi, Gisèle Bonne, Takuro Arimura, S. Noguchi, Ikuya Nonaka, Ichizo Nishino - Autophagy 2009 cited by 221

  17. Sarcoplasmic MxA expression

    Authors: Akinori Uruha, Atsuko Nishikawa, R. Tsuburaya, Kohei Hamanaka, Masataka Kuwana, Yurika Watanabe, Shigeaki Suzuki, Norihiro Suzuki, Ichizo Nishino - Neurology 2016 cited by 162

  18. CGG expansion in NOTCH2NLC is associated with oculopharyngodistal myopathy with neurological manifestations

    Authors: Masashi Ogasawara, Aritoshi Iida, Theerawat Kumutpongpanich, Ayami Ozaki, Yasushi Oya, H. Konishi, Akinori Nakamura, Ryu Abe, Hiroshi Takai, Ritsuko Hanajima, Hiroshi Doi, Fumiaki Tanaka, Hisayoshi Nakamura, Ikuya Nonaka, Zhaoxia Wang, Shinichiro Hayashi, S. Noguchi, Ichizo Nishino - Acta Neuropathologica Communications 2020 cited by 119

  19. Dermatomyositis

    Authors: Jantima Tanboon, Michio Inoue, Yoshihiko Saito, Hisateru Tachimori, Shinichiro Hayashi, S. Noguchi, Naoko Okiyama, Manabu Fujimoto, Ichizo Nishino - Neurology 2021 cited by 82

  20. Cellular senescence-mediated exacerbation of Duchenne muscular dystrophy

    Authors: Hidetoshi Sugihara, Naomi Teramoto, Katsuyuki Nakamura, Takanori Shiga, Taku Shirakawa, Masafumi Matsuo, Masashi Ogasawara, Ichizo Nishino, Takashi Matsuwaki, Masugi Nishihara, Keitaro Yamanouchi - Scientific Reports 2020 cited by 78

  21. Human PTRF mutations cause secondary deficiency of caveolins resulting in muscular dystrophy with generalized lipodystrophy

    Authors: Yukiko Hayashi, Chie Matsuda, Megumu Ogawa, Kanako Goto, Kayo Tominaga, Satomi Mitsuhashi, Young Eun Park, Ikuya Nonaka, Naomi Hino‐Fukuyo, Kazuhiro Haginoya, Hisashi Sugano, Ichizo Nishino - Journal of Clinical Investigation 2009 cited by 393

  22. Dominant mutations in ORAI1 cause tubular aggregate myopathy with hypocalcemia via constitutive activation of store-operated Ca2+ channels

    Authors: Yukari Endo, S. Noguchi, Yuji Hara, Yukiko Hayashi, Kazushi Motomura, Satoko Miyatake, Nobuyuki Murakami, Satsuki Tanaka, Sumimasa Yamashita, Rika Kizu, Masahiro Bamba, Yu‐ichi Goto, Naomichi Matsumoto, Ikuya Nonaka, Ichizo Nishino - Human Molecular Genetics 2014 cited by 170

  23. N‐WASP is required for Amphiphysin‐2/BIN1‐dependent nuclear positioning and triad organization in skeletal muscle and is involved in the pathophysiology of centronuclear myopathy

    Authors: Sestina Falcone, William Roman, Karim Hnia, Vincent Gache, Nathalie Didier, Jeanne Lainé, Frédéric Aurade, Isabelle Marty, Ichizo Nishino, Nicolas Charlet‐Berguerand, Norma B. Romero, Giovanna Marazzi, David Sassoon, Jocelyn Laporte, Edgar R. Gomes - EMBO Molecular Medicine 2014 cited by 115

  24. Muscle pathology of antisynthetase syndrome according to antibody subtypes

    Authors: Jantima Tanboon, Michio Inoue, Shinya Hirakawa, Hisateru Tachimori, Shinichiro Hayashi, S. Noguchi, Naoko Okiyama, Manabu Fujimoto, Shigeaki Suzuki, Ichizo Nishino - Brain Pathology 2023 cited by 47