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Ikuya Nonaka

Active 1980–2022

100
Papers
22,160
Citations
82
h-index
100
i10-index

Citations

Citations per year for Ikuya Nonaka1978: 1 citations1981: 4 citations1982: 3 citations1983: 4 citations1984: 1 citations1985: 1 citations1986: 5 citations1987: 3 citations1988: 11 citations1989: 30 citations1990: 65 citations1991: 84 citations1992: 97 citations1993: 101 citations1994: 129 citations1995: 133 citations1996: 122 citations1997: 114 citations1998: 146 citations1999: 136 citations2000: 172 citations2001: 174 citations2002: 172 citations2003: 194 citations2004: 193 citations2005: 189 citations2006: 186 citations2007: 116 citations2008: 167 citations2009: 192 citations2010: 198 citations2011: 203 citations2012: 190 citations2013: 196 citations2014: 173 citations2015: 162 citations2016: 148 citations2017: 120 citations2018: 144 citations2019: 362 citations2020: 360 citations2021: 378 citations2022: 289 citations2023: 183 citations2024: 253 citations2025: 100 citations1979–1980: no citations, so these years are not shown

Citation sources

Countries

World map of the countries and regions citing this authorUnited States: 2,252 citing papers, 29% of this breakdownUnited Kingdom: 720 citing papers, 9.3% of this breakdownJapan: 631 citing papers, 8.1% of this breakdownItaly: 449 citing papers, 5.8% of this breakdownFrance: 415 citing papers, 5.3% of this breakdownGermany: 391 citing papers, 5% of this breakdownChina: 343 citing papers, 4.4% of this breakdownCanada: 295 citing papers, 3.8% of this breakdownAustralia: 221 citing papers, 2.9% of this breakdownNetherlands: 212 citing papers, 2.7% of this breakdownSpain: 158 citing papers, 2% of this breakdownSweden: 142 citing papers, 1.8% of this breakdown
0%29%Other 19.9%

Institutions

Fields

  • Biochemistry, Genetics and Molecular Biology70.3%
  • Medicine23.6%
  • Neuroscience3.8%
  • Agricultural and Biological Sciences0.8%
  • Immunology and Microbiology0.7%
  • Engineering0.2%
  • Other0.6%

Topics

  • 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%
  • Other60.5%

Coauthors

All papers

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

    Authors: 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 cited by 1,050

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

    Authors: Yu‐ichi Goto, Ikuya Nonaka, Satoshi Horai - Nature 1990 cited by 2,100

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

    Authors: Yoko Nabeshima, Kazunori Hanaoka, Michiko Hayasaka, Eisaku Esuml, Shaowei Li, Ikuya Nonaka, Yo-ichi Nabeshima - Nature 1993 cited by 972

  4. 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

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

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

  6. 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

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

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

  8. 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

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

    Authors: 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 cited by 1,025

  10. 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

  11. 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

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

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

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

    Authors: May Christine V. Malicdan, S. Noguchi, Yukiko Hayashi, Ikuya Nonaka, Ichizo Nishino - Nature Medicine 2009 cited by 195

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

    Authors: 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 cited by 184

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

    Authors: Shintaro Yamashita, Ichizo Nishino, Ikuya Nonaka, Yu‐ichi Goto - Journal of Human Genetics 2008 cited by 98

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

    Authors: 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 cited by 807

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

    Authors: Kimiko Inoue, Kazuto Nakada, Atsuo Ogura, Kotoyo Isobe, Yu-ichi Goto, Ikuya Nonaka, Jun-Ichi Hayashi - Nature Genetics 2000 cited by 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

    Authors: May Christine V. Malicdan, S. Noguchi, Ikuya Nonaka, Y. Hayashi, Ichizo Nishino - Human Molecular Genetics 2007 cited by 160

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

    Authors: 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 cited by 143

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

    Authors: 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 cited by 559

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

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

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

    Authors: Yu‐ichi Goto, Satoshi Horai, T. Matsuoka, Yasutoshi Koga, Keiji Nihei, Masanori Kobayashi, Ikuya Nonaka - Neurology 1992 cited by 396

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

    Authors: Ikuya Nonaka, N Sunohara, Shoichi Ishiura, E Satoyoshi - Journal of the Neurological Sciences 1981 cited by 296

  24. Skeletal muscle gene expression in space‐flown rats

    Authors: 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 cited by 208