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Medicine

D-Index
98
Citations
56595
World Ranking
8744
National Ranking
232

Overview

Ichizo Nishino is affiliated with Tokyo Medical University in Japan and has a robust scientific profile predominantly in the fields of Medicine and Biochemistry, Genetics and Molecular Biology. Their research spans a variety of subfields, including Molecular Biology, Epidemiology, Cellular and Molecular Neuroscience, Genetics, and Cardiology and Cardiovascular Medicine.

Their work covers several main topics, focusing extensively on inflammatory and muscular diseases as well as genetic neurodegenerative conditions. Key research areas include:

  • Inflammatory Myopathies and Dermatomyositis
  • Muscle Physiology and Disorders
  • Genetic Neurodegenerative Diseases
  • Cardiomyopathy and Myosin Studies
  • Neurogenetic and Muscular Disorders Research
  • Eosinophilic Disorders and Syndromes
  • Glycogen Storage Diseases and Myoclonus

Nishino has contributed to numerous publications in a range of prominent scientific journals. Frequent publication venues include:

  • Neuromuscular Disorders
  • Internal Medicine
  • bioRxiv (Cold Spring Harbor Laboratory)
  • Rinsho Shinkeigaku
  • Neurology

Among Nishino's recent papers are the following, illustrating an active engagement with genetic and neuromuscular research topics:

  • "Expansion of GGC Repeat in GIPC1 Is Associated with Oculopharyngodistal Myopathy" (2020) - The American Journal of Human Genetics
  • "Homozygous nonsense variant in LRIF1 associated with facioscapulohumeral muscular dystrophy" (2020) - Neurology
  • "Where are we moving in the classification of idiopathic inflammatory myopathies?" (2020) - Current Opinion in Neurology
  • "CGG expansion in NOTCH2NLC is associated with oculopharyngodistal myopathy with neurological manifestations" (2020) - Acta Neuropathologica Communications
  • "International Guideline for Idiopathic Inflammatory Myopathy-Associated Cancer Screening: an International Myositis Assessment and Clinical Studies Group (IMACS) initiative" (2023) - Nature Reviews Rheumatology

Collaboration is a significant aspect of Nishino's work. Frequent co-authors include:

  • S. Noguchi
  • Yoshihiko Saito
  • Shinichiro Hayashi
  • Yasushi Oya
  • Madoka Mori-Yoshimura

The research trajectory indicated by Nishino's publications suggests a focus on bridging clinical and molecular investigations, particularly in rare muscle disorders and related genetic mutations. This interdisciplinary approach integrates clinical neurology with molecular genetics to address complex muscle pathologies and their broader implications in neurodegenerative disease research.

Best Publications

  • Guidelines for the use and interpretation of assays for monitoring autophagy

    Daniel J. Klionsky;Fabio C. Abdalla;Hagai Abeliovich;Robert T. Abraham

  • Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition)

    Daniel J. Klionsky;Kotb Abdelmohsen;Akihisa Abe;Joynal Abedin

  • Guidelines for the use and interpretation of assays for monitoring autophagy in higher eukaryotes

    Daniel J. Klionsky;Hagai Abeliovich;Patrizia Agostinis;Devendra K. Agrawal

  • Adiponectin and AdipoR1 regulate PGC-1alpha and mitochondria by Ca(2+) and AMPK/SIRT1.

    Masato Iwabu;Toshimasa Yamauchi;Miki Okada-Iwabu;Koji Sato

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

    Ichizo Nishino;Jin Fu;Kurenai Tanji;Takeshi Yamada

  • Thymidine Phosphorylase Gene Mutations in MNGIE, a Human Mitochondrial Disorder

    Ichizo Nishino;Antonella Spinazzola;Michio Hirano

  • Post-translational disruption of dystroglycan-ligand interactions in congenital muscular dystrophies

    Daniel E. Michele;Rita Barresi;Motoi Kanagawa;Fumiaki Saito

  • Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition)

    Daniel J. Klionsky;Kotb Abdelmohsen;Akihisa Abe;Joynal Abedin

  • 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

    Yasutomi Kamei;Shinji Miura;Miki Suzuki;Yuko Kai

  • Fatal infantile cardioencephalomyopathy with COX deficiency and mutations in SCO2, a COX assembly gene

    L C Papadopoulou;C M Sue;M M Davidson;K Tanji

  • Distinctive patterns of microRNA expression in primary muscular disorders

    Iris Eisenberg;Alal Eran;Ichizo Nishino;Maurizio Moggio

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

    Yukiko K. Hayashi;Chie Matsuda;Megumu Ogawa;Kanako Goto

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

    Hiroyuki Ishiura;Shota Shibata;Jun Yoshimura;Yuta Suzuki

  • Mitochondrial neurogastrointestinal encephalomyopathy: An autosomal recessive disorder due to thymidine phosphorylase mutations

    I Nishino;A Spinazzola;A Papadimitriou;S Hammans

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

    Charlotte Fugier;Arnaud F Klein;Caroline Hammer;Stéphane Vassilopoulos

  • LARGE can functionally bypass alpha-dystroglycan glycosylation defects in distinct congenital muscular dystrophies

    Rita Barresi;Daniel E Michele;Motoi Kanagawa;Hollie A Harper

  • The sarcolemmal proteins dysferlin and caveolin-3 interact in skeletal muscle

    Chie Matsuda;Chie Matsuda;Yukiko K. Hayashi;Megumu Ogawa;Masashi Aoki

  • Clinical features and prognosis in anti-SRP and anti-HMGCR necrotising myopathy

    Yurika Watanabe;Akinori Uruha;Shigeaki Suzuki;Jin Nakahara

  • Clinicopathological features of genetically confirmed Danon disease

    K. Sugie;A. Yamamoto;K. Murayama;S. J. Oh

  • Distinctive patterns of microRNA expression in primary muscular disorders (Proceedings of the National Academy of Sciences of the United States of America (2007) 104, 43, (17016-17021) DOI: 10.1073/pnas.0708115104)

    Iris Eisenberg;Alal Eran;Ichizo Nishino;Maurizio Moggio

Frequent Co-Authors

Ikuya Nonaka
Ikuya Nonaka Tokyo Medical University
Satoru Noguchi
Satoru Noguchi Tokyo Medical University
Yu-ichi Goto
Yu-ichi Goto University of Tsukuba
Michio Hirano
Michio Hirano Columbia University
Aritoshi Iida
Aritoshi Iida Nippon Medical School
Shin'ichi Takeda
Shin'ichi Takeda National Center of Neurology and Psychiatry
Kenji Sugai
Kenji Sugai Tohoku University
Naomichi Matsumoto
Naomichi Matsumoto Yokohama City University
Tatsushi Toda
Tatsushi Toda University of Tokyo
Koji Abe
Koji Abe Okayama University

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