Author

Osamu Komure

Observed names: O Komure, O. Komure, コムレ, オサム

Observed institutions: Mayo Clinic, Shiga University of Medical Science, University of Washington, VA Puget Sound Health Care System, Hôpital Rangueil, Hyogo Prefectural Amagasaki General Medical Center, Hôpital Purpan, Utano Hospital, Mayo Clinic in Florida, South Osaka Neurosurgical Hospital, Indiana University Indianapolis, Indiana University, Kobe University

OpenAlex ID: A5015662005

Mutations of optineurin in amyotrophic lateral sclerosis

2010 · Hirofumi Maruyama, Hiroyuki Morino, et al. · Nature · 1,263

Dentatorubral and pallidoluysian atrophy expansion of an unstable CAG trinucleotide on chromosome 12p

1994 · S. Nagafuchi, H. Yanagisawa, et al. · Nature Genetics · 716

Brain-derived growth factor and nerve growth factor concentrations are decreased in the substantia nigra in Parkinson's disease

1999 · Makio Mogi, Akifumi Togari, et al. · Neuroscience Letters · 392

Caspase activities and tumor necrosis factor receptor R1 (p55) level are elevated in the substantia nigra from Parkinsonian brain

2000 · M. Mogi, A. Togari, et al. · Journal of Neural Transmission · 282

DNA analysis in hereditary dentatorubral-pallidoluysian atrophy

1995 · O. Komure, A. Sano, et al. · Neurology · 141

A mutation in the microtubule-associated protein tau in pallido-nigro-luysian degeneration

1999 · M. Yasuda, T. Kawamata, et al. · Neurology · 84

SCA8 Repeat Expansion: Large CTA/CTG Repeat Alleles Are More Common in Ataxic Patients, Including Those with SCA6

2003 · Yuishin Izumi, Hirofumi Maruyama, et al. · The American Journal of Human Genetics · 81

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Somatic mosaicism of CAG repeat in dentatorubral-pallidoluysian atrophy (DRPLA)

1995 · Shu-ichi Ueno, Keiji Kondoh, et al. · Human Molecular Genetics · 79

Triggering of neuronal cell death by accumulation of activated SEK1 on nuclear polyglutamine aggregations in PML bodies

1999 · Shingo Yasuda, Kiyoshi Inoue, et al. · Genes to Cells · 64

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Clinicopathologic study on an ALS family with a heterozygous E478G optineurin mutation

2011 · Hidefumi Ito, Masataka Nakamura, et al. · Acta Neuropathologica · 61

Contribution of the interleukin‐1β gene polymorphism in multiple system atrophy

2002 · Masataka Nishimura, Hideshi Kawakami, et al. · Movement Disorders · 60

Possible Reduced Penetrance of Expansion of 44 to 47 CAG/CAA Repeats in the TATA-Binding Protein Gene in Spinocerebellar Ataxia Type 17

2004 · Masaya Oda, Hirofumi Maruyama, et al. · Archives of Neurology · 59

Increase in [3H]cAMP binding sites and decrease in Giα and Goα immunoreactivities in left temporal cortices from patients with schizophrenia

1993 · Naoki Nishino, Noboru Kitamura, et al. · Brain Research · 40

Clinical and genetic studies of families with the tau N279K mutation (FTDP-17)

2002 · Y. Tsuboi, M. Baker, et al. · Neurology · 38

Multiple Proteinopathies in Familial ALS Cases With Optineurin Mutations

2017 · Takashi Ayaki, Hidefumi Ito, et al. · Journal of Neuropathology & Experimental Neurology · 34

A single nucleotide polymorphism of dopamine transporter gene is associated with Parkinson's disease

2000 · Hiroyuki Morino, Toshitaka Kawarai, et al. · Annals of Neurology · 34

Expression of Kruppel-like factor 5 gene in human brain and association of the gene with the susceptibility to schizophrenia

2008 · Masaya Yanagi, Takeshi Hashimoto, et al. · Schizophrenia Research · 33

The Effect of tau genotype on clinical features in FTDP-17

2005 · Yasuhiko Baba, Yoshio Tsuboi, et al. · Parkinsonism & Related Disorders · 32

Anticipation in hereditary dentatorubral-pallidoluysian atrophy

1994 · Akira Sano, Noriko Yamauchi, et al. · Human Genetics · 27

Phenotypic heterogeneity within a new family with the MAPT p301s mutation

2005 · Minoru Yasuda, Yoshitsugu Nakamura, et al. · Annals of Neurology · 24

Pallidonigroluysian degeneration with iron deposition: a study of three autopsy cases

1993 · J. Kawai, M. Sasahara, et al. · Acta Neuropathologica · 23

Intra-axonal polysaccharide deposits in the peripheral nerve seen in adult polysaccharide storage myopathy

1985 · O. Komure, K. Ichikawa, et al. · Acta Neuropathologica · 19

DNA analysis of benign adult familial myoclonic epilepsy reveals associations between the pathogenic TTTCA repeat insertion in SAMD12 and the nonpathogenic TTTTA repeat expansion in TNRC6A

2020 · Akane Terasaki, Masayuki Nakamura, et al. · Journal of Human Genetics · 17

Effects of l-threo-DOPS, a noradrenaline precursor, on the long-term potentiation in the rat hippocampal mossy fiber-CA3 region

1991 · Norio Sakai, Masashi Sasa, et al. · Brain Research · 13

The loss of βII-protein kinase C in the striatum from patients with Huntington's disease

1992 · Takeshi Hashimoto, Noboru Kitamura, et al. · Brain Research · 12

Works count: 47

Citation count: 3,709

H-index: 21

I10-index: 28