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Ikuya Nonaka

1980–2022 年に発表

100
論文数
22,160
被引用数
82
h 指数
100
i10 指数

被引用数

Ikuya Nonaka の年別被引用数1978 年: 被引用 1 件1981 年: 被引用 4 件1982 年: 被引用 3 件1983 年: 被引用 4 件1984 年: 被引用 1 件1985 年: 被引用 1 件1986 年: 被引用 5 件1987 年: 被引用 3 件1988 年: 被引用 11 件1989 年: 被引用 30 件1990 年: 被引用 65 件1991 年: 被引用 84 件1992 年: 被引用 97 件1993 年: 被引用 101 件1994 年: 被引用 129 件1995 年: 被引用 133 件1996 年: 被引用 122 件1997 年: 被引用 114 件1998 年: 被引用 146 件1999 年: 被引用 136 件2000 年: 被引用 172 件2001 年: 被引用 174 件2002 年: 被引用 172 件2003 年: 被引用 194 件2004 年: 被引用 193 件2005 年: 被引用 189 件2006 年: 被引用 186 件2007 年: 被引用 116 件2008 年: 被引用 167 件2009 年: 被引用 192 件2010 年: 被引用 198 件2011 年: 被引用 203 件2012 年: 被引用 190 件2013 年: 被引用 196 件2014 年: 被引用 173 件2015 年: 被引用 162 件2016 年: 被引用 148 件2017 年: 被引用 120 件2018 年: 被引用 144 件2019 年: 被引用 362 件2020 年: 被引用 360 件2021 年: 被引用 378 件2022 年: 被引用 289 件2023 年: 被引用 183 件2024 年: 被引用 253 件2025 年: 被引用 100 件1979〜1980 年は被引用が無いため表示していません

引用元

国・地域

この著者を引用した国・地域の世界地図アメリカ合衆国: 引用元論文 2,252 件、この内訳の 29%イギリス: 引用元論文 720 件、この内訳の 9.3%日本: 引用元論文 631 件、この内訳の 8.1%イタリア: 引用元論文 449 件、この内訳の 5.8%フランス: 引用元論文 415 件、この内訳の 5.3%ドイツ: 引用元論文 391 件、この内訳の 5%中国: 引用元論文 343 件、この内訳の 4.4%カナダ: 引用元論文 295 件、この内訳の 3.8%オーストラリア: 引用元論文 221 件、この内訳の 2.9%オランダ: 引用元論文 212 件、この内訳の 2.7%スペイン: 引用元論文 158 件、この内訳の 2%スウェーデン: 引用元論文 142 件、この内訳の 1.8%
0%29%その他 19.9%

機関

分野

  • Biochemistry, Genetics and Molecular Biology70.3%
  • Medicine23.6%
  • Neuroscience3.8%
  • Agricultural and Biological Sciences0.8%
  • Immunology and Microbiology0.7%
  • Engineering0.2%
  • その他0.6%

トピック

  • Mitochondrial Function and Pathology12.3%
  • Muscle Physiology and Disorders9.9%
  • Metabolism and Genetic Disorders5.9%
  • ATP Synthase and ATPases Research5.1%
  • Autophagy in Disease and Therapy3.2%
  • Cardiomyopathy and Myosin Studies3.1%
  • その他60.5%

共著者

全論文

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  1. Mitochondrial fission factor Drp1 is essential for embryonic development and synapse formation in mice

    著者: Naotada Ishihara, Masatoshi Nomura, Akihiro Jofuku, Hiroki Kato, Satoshi O. Suzuki, Keiji Masuda, Hidenori Otera, Yae Nakanishi, Ikuya Nonaka, Yu-ichi Goto, Naoko Taguchi, Hidetaka Morinaga, Maki Maeda, Ryoichi Takayanagi, Sadaki Yokota, Katsuyoshi Mihara - Nature Cell Biology 2009 被引用: 1,050

  2. A mutation in the tRNALeu(UUR) gene associated with the MELAS subgroup of mitochondrial encephalomyopathies

    著者: Yu‐ichi Goto, Ikuya Nonaka, Satoshi Horai - Nature 1990 被引用: 2,100

  3. Myogenin gene disruption results in perinatal lethality because of severe muscle defect

    著者: Yoko Nabeshima, Kazunori Hanaoka, Michiko Hayasaka, Eisaku Esuml, Shaowei Li, Ikuya Nonaka, Yo-ichi Nabeshima - Nature 1993 被引用: 972

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

    著者: 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 被引用: 947

  5. Inter-mitochondrial complementation: Mitochondria-specific system preventing mice from expression of disease phenotypes by mutant mtDNA

    著者: Kazuto Nakada, Kimiko Inoue, Tomoko Ono, Kotoyo Isobe, Atsuo Ogura, Yu‐ichi Goto, Ikuya Nonaka, Jun‐Ichi Hayashi - Nature Medicine 2001 被引用: 422

  6. Autophagic degradation of nuclear components in mammalian cells

    著者: Young-Eun Park, Yukiko Hayashi, Gisèle Bonne, Takuro Arimura, S. Noguchi, Ikuya Nonaka, Ichizo Nishino - Autophagy 2009 被引用: 221

  7. Targeted Disruption of Exon 52 in the Mouse Dystrophin Gene Induced Muscle Degeneration Similar to That Observed in Duchenne Muscular Dystrophy

    著者: Eiichi Araki, Kenji Nakamura, Kazuki Nakao, Shuhei Kameya, Osamu Kobayashi, Ikuya Nonaka, Takuro Kobayashi, Motoya Katsuki - Biochemical and Biophysical Research Communications 1997 被引用: 150

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

    著者: 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 被引用: 119

  9. Mitochondrial DNA Deletions in Progressive External Ophthalmoplegia and Kearns-Sayre Syndrome

    著者: Carlos T. Moraes, Salvatore DiMauro, Massimo Zeviani, Anne Lombès, Sara Shanske, Armand F. Miranda, Hirofumi Nakase, Eduardo Bonilla, Lineu César Werneck, Serenella Servidei, Ikuya Nonaka, Yasutoshi Koga, Alfred J. Spiro, A. Keith W. Brownell, Beny Schmidt, Donald L. Schotland, Mary L. Zupanc, Darryl C. DeVivo, Eric A. Schon, Lewis P. Rowland - New England Journal of Medicine 1989 被引用: 1,025

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

    著者: 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 被引用: 393

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

    著者: 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 被引用: 170

  12. Sialyllactose ameliorates myopathic phenotypes in symptomatic GNE myopathy model mice

    著者: Takahiro Yonekawa, May Christine V. Malicdan, Anna Cho, Yukiko Hayashi, Ikuya Nonaka, Toshiki Mine, Takeshi Yamamoto, Ichizo Nishino, S. Noguchi - Brain 2014 被引用: 75

  13. Prophylactic treatment with sialic acid metabolites precludes the development of the myopathic phenotype in the DMRV-hIBM mouse model

    著者: May Christine V. Malicdan, S. Noguchi, Yukiko Hayashi, Ikuya Nonaka, Ichizo Nishino - Nature Medicine 2009 被引用: 195

  14. Ubiquitin Ligase Cbl-b Is a Negative Regulator for Insulin-Like Growth Factor 1 Signaling during Muscle Atrophy Caused by Unloading

    著者: Reiko Nakao, Katsuya Hirasaka, Jumpei Goto, Kazumi Ishidoh, Chiharu Yamada, Ayako Ohno, Yuushi Okumura, Ikuya Nonaka, Koji Yasutomo, Kenneth M. Baldwin, Eiki Kominami, Akira Higashibata, Keisuke Nagano, Keiji Tanaka, Natsuo Yasui, Edward Mills, Shin’ichi Takeda, Takeshi Nikawa - Molecular and Cellular Biology 2009 被引用: 184

  15. Genotype and phenotype analyses in 136 patients with single large-scale mitochondrial DNA deletions

    著者: Shintaro Yamashita, Ichizo Nishino, Ikuya Nonaka, Yu‐ichi Goto - Journal of Human Genetics 2008 被引用: 98

  16. An ancient retrotransposal insertion causes Fukuyama-type congenital muscular dystrophy

    著者: Kazuhiro Kobayashi, Yutaka Nakahori, Masashi Miyake, Kiichiro Matsumura, Eri Kondo-Iida, Yoshiko Nomura, Masaya Segawa, Mieko Yoshioka, Kayoko Saito, Makiko Ōsawa, Kenzo Hamano, Youichi Sakakihara, Ikuya Nonaka, Yasuo Nakagome, Ichiro Kanazawa, Yusuke Nakamura, Katsushi Tokunaga, Tatsushi Toda - Nature 1998 被引用: 807

  17. Generation of mice with mitochondrial dysfunction by introducing mouse mtDNA carrying a deletion into zygotes

    著者: Kimiko Inoue, Kazuto Nakada, Atsuo Ogura, Kotoyo Isobe, Yu-ichi Goto, Ikuya Nonaka, Jun-Ichi Hayashi - Nature Genetics 2000 被引用: 392

  18. A Gne knockout mouse expressing human GNE D176V mutation develops features similar to distal myopathy with rimmed vacuoles or hereditary inclusion body myopathy

    著者: May Christine V. Malicdan, S. Noguchi, Ikuya Nonaka, Y. Hayashi, Ichizo Nishino - Human Molecular Genetics 2007 被引用: 160

  19. A Congenital Muscular Dystrophy with Mitochondrial Structural Abnormalities Caused by Defective De Novo Phosphatidylcholine Biosynthesis

    著者: Satomi Mitsuhashi, Aya Ohkuma, Beril Talim, Minako Karahashi, Tomoko Koumura, Chieko Aoyama, Mana Kurihara, Rosaline C. M. Quinlivan, Caroline A. Sewry, Hiroaki Mitsuhashi, Kanako Goto, Burcu Tahire Köksal, Gülsev Kale, Kazutaka Ikeda, Ryo Taguchi, S. Noguchi, Yukiko Hayashi, Ikuya Nonaka, Roger B. Sher, Hiroyuki Sugimoto, Yasuhito Nakagawa, Gregory A. Cox, Haluk Topaloğlu, Ichizo Nishino - The American Journal of Human Genetics 2011 被引用: 143

  20. A Subtype of Diabetes Mellitus Associated with a Mutation of Mitochondrial DNA

    著者: Takashi Kadowaki, Hiroko Kadowaki, Yasumichi Mori, Tobe Kazuyuki, Ryoichi Sakuta, Yoshihiko Suzuki, Yuzo Tanabe, Hiroshi Sakura, Takuya Awata, Yu‐ichi Goto, Takaki Hayakawa, Kenpei Matsuoka, Ryuzo Kawamori, Takenobu Kamada, Satoshi Horai, Ikuya Nonaka, Ryoko Hagura, Yasuo Akanuma, Yoshio Yazaki - New England Journal of Medicine 1994 被引用: 559

  21. A new mtDNA mutation associated with mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes (MELAS)

    著者: Yu‐ichi Goto, Ikuya Nonaka, Satoshi Horai - Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease 1991 被引用: 327

  22. Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke‐like episodes (MELAS)

    著者: Yu‐ichi Goto, Satoshi Horai, T. Matsuoka, Yasutoshi Koga, Keiji Nihei, Masanori Kobayashi, Ikuya Nonaka - Neurology 1992 被引用: 396

  23. Familial distal myopathy with rimmed vacuole and lamellar (myeloid) body formation

    著者: Ikuya Nonaka, N Sunohara, Shoichi Ishiura, E Satoyoshi - Journal of the Neurological Sciences 1981 被引用: 296

  24. Skeletal muscle gene expression in space‐flown rats

    著者: Takeshi Nikawa, Kazumi Ishidoh, Katsuya Hirasaka, Ibuki Ishihara, Madoka Ikemoto‐Uezumi, Mihoko Kano, Eiki Kominami, Ikuya Nonaka, Takayuki Ogawa, Gregory R. Adams, Kenneth M. Baldwin, Natsuo Yasui, Kyoichi Kishi, Shin’ichi Takeda - The FASEB Journal 2004 被引用: 208