Jun Goto

5.2k citations

96 papers · 2.4k · h-index 31

Impact in

Cellular and Molecular Neuroscience top 1%
- Genetic Neurodegenerative Diseases
- Hereditary Neurological Disorders
Neurology top 1%
- Parkinson's Disease Mechanisms and Treatments
- Neurological diseases and metabolism
- Neurological disorders and treatments

Papers in

Molecular Biology 47
- Mitochondrial Function and Pathology 22
- Muscle Physiology and Disorders 5
- RNA regulation and disease 5
Cellular and Molecular Neuroscience 41
- Genetic Neurodegenerative Diseases 33

Co-authors: Shoji Tsuji (46 shared papers)Ichiro Kanazawa (21 shared papers)Hideji Hashida (11 shared papers)Jun Mitsui (23 shared papers)Yuji Takahashi (25 shared papers)Hiroyuki Ishiura (27 shared papers)Osamu Onodera (4 shared papers)Yaeko Ichikawa (15 shared papers)
Journals: Biochemical and Biophysical Research Communications (6 papers)Neurogenetics (5 papers)Journal of the Neurological Sciences (5 papers)Annals of Neurology (4 papers)Neurology (3 papers)
Partner nations: Japan United States Canada

In The Last Decade

Jun Goto

93 papers receiving 2.4k citations

Peers

Countries citing papers authored by Jun Goto

Since Specialization

Citations

This map shows the geographic impact of Jun Goto's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Jun Goto with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Jun Goto more than expected).

Fields of papers citing papers by Jun Goto

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Jun Goto. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Jun Goto. The network helps show where Jun Goto may publish in the future.

Co-authors

The 25 scholars most cited alongside Jun Goto, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Jun Goto Line = papers co-authored together Jun Goto links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 96 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Mutations for Gaucher Disease Confer High Susceptibility to Parkinson Disease Archives of Neurology ·Jun Mitsui, Ikuko Mizuta, Atsushi Toyoda, Ryo Ashida, Yūji Takahashi, Jun Goto, Y. Fukuda, Hidetoshi Date, Atsushi Iwata, Mitsutoshi Yamamoto, Nobutaka Hattori, Miho Murata, Tatsushi Toda, Shoji Tsuji	2009	150
2	DNA haplotype analysis of Huntington disease reveals clues to the origins and mechanisms of CAG expansion and reasons for geographic variations of prevalence Human Molecular Genetics ·Ferdinando Squitieri, Susan E. Andrew, Y. Paul Goldberg, B Kremer, Niamh Spence, J. Zelsler, K. Nichol, Jane Theilmann, Jacquie Greenberg, Jun Goto, Ichiro Kanazawa, J. Vesa, Leena Peltonen, E. Almqvist, Maria Anvret, H. Telenius, Binshan Lin, G. Napolitano, Kenneth Morgan, Michael R. Hayden	1994	148
3	Abnormal gene product identified in hereditary dentatorubral–pallidoluysian atrophy (DRPLA) brain Nature Genetics ·Ikuru Yazawa, Nobuyuki Nukina, Hideji Hashida, Jun Goto, Masao Yamada, Ichiro Kanazawa	1995	126
4	Sporadic ataxias in Japan – a population-based epidemiological study The Cerebellum ·Shoji Tsuji, Osamu Onodera, Jun Goto, Masatoyo Nishizawa, (unknown)	2008	104
5	Total deletion and a missense mutation of ITPR1 in Japanese SCA15 families Neurology ·Kenju Hara, Atsushi Shiga, Hiroaki Nozaki, Jun Mitsui, Yukihiro Takahashi, Hitomi Ishiguro, Harumi Yomono, Hiroshi Kurisaki, Jun Goto, Takeshi Ikeuchi, Shoji Tsuji, M Nishizawa, Osamu Onodera	2008	104
6	Multiplex Families With Multiple System Atrophy Archives of Neurology ·Kenju Hara, Yoshio Momose, S. Tokiguchi, Mitsuteru Shimohata, Kenshi Terajima, Osamu Onodera, Akiyoshi Kakita, Mitsunori Yamada, Hitoshi Takahashi, Motoyuki Hirasawa, Yoshikuni Mizuno, Katsuhisa Ogata, Jun Goto, Ichiro Kanazawa, Masatoyo Nishizawa, Shoji Tsuji	2007	90
7	Formic Acid Dissolves Aggregates of an N-Terminal Huntingtin Fragment Containing an Expanded Polyglutamine Tract: Applying to Quantification of Protein Components of the Aggregates Biochemical and Biophysical Research Communications ·Noriko Hazeki, Tadashi Tukamoto, Jun Goto, Ichiro Kanazawa	2000	82
8	Mechanisms of Genomic Instabilities Underlying Two Common Fragile-Site-Associated Loci, PARK2 and DMD, in Germ Cell and Cancer Cell Lines The American Journal of Human Genetics ·Jun Mitsui, Yuji Takahashi, Jun Goto, Hiroyuki Tomiyama, Shunpei Ishikawa, Hiroyo Yoshino, Narihiro Minami, (unknown), Suzanne Lesage, Hiroyuki Aburatani, Ichizo Nishino, Alexis Brice, Nobutaka Hattori, Shoji Tsuji	2010	75
9	Enhanced SUMOylation in polyglutamine diseases Biochemical and Biophysical Research Communications ·Hiroko Ueda, Jun Goto, Hideji Hashida, Xia Lin, Kiyomitsu Oyanagi, Hitoshi Kawano, Huda Y. Zoghbi, Ichiro Kanazawa, Hitoshi Okazawa	2002	65
10	A homozygous mutation of C12orf65 causes spastic paraplegia with optic atrophy and neuropathy (SPG55) Journal of Medical Genetics ·Haruo Shimazaki, Yoshihisa Takiyama, Hiroyuki Ishiura, Chika Sakai, Yuichi Matsushima, Hideyuki Hatakeyama, Junko Honda, Kumi Sakoe, Tametou Naoi, Michito Namekawa, Y. Fukuda, Yuji Takahashi, Jun Goto, Shoji Tsuji, Yu‐ichi Goto, Imaharu Nakano	2012	64
11	Ancestral differences in the distribution of the Δ2642 glutamic acid polymorphism is associated with varying CAG repeat lengths on normal chromosomes: insights into the genetic evolution of Huntington disease Human Molecular Genetics ·E. Almqvist, Niamh Spence, K. Nichol, Susan E. Andrew, J. Vesa, Leena Peltonen, Maria Anvret, Jun Goto, Ichiro Kanazawa, Y. Paul Goldberg, Michael R. Hayden	1995	59
12	The genomic structure and expression of MJD, the Machado-Joseph disease gene Journal of Human Genetics ·Yaeko Ichikawa, Jun Goto, Masahira Hattori, Atsushi Toyoda, Kazuo Ishii, Seung‐Yong Jeong, Hideji Hashida, Naoki Masuda, Katsuhisa Ogata, Fumio Kasai, Miho Hirai, Patrı́cia Maciel, Guy A. Rouleau, Yoshiyuki Sakaki, I. Kanazawa	2001	58
13	Brain regional differences in the expansion of a CAG repeat in the spinocerebellar ataxias: Dentatorubral‐pallidoluysian atrophy, machado‐joseph disease, and spinocerebellar ataxia type 1 Annals of Neurology ·Hideji Hashida, Jun Goto, Hiroshi Kurisaki, Hidehiro Mizusawa, Ichiro Kanazawa	1997	49
14	Molecular epidemiology and clinical spectrum of hereditary spastic paraplegia in the Japanese population based on comprehensive mutational analyses Journal of Human Genetics ·Hiroyuki Ishiura, Yuji Takahashi, Toshihiro Hayashi, Kayoko Saito, Hirokazu Furuya, Masao Watanabe, Murata Miho, Mikiya Suzuki, Akira Sugiura, Setsu Sawai, Kazumoto Shibuya, Naohisa Ueda, Yaeko Ichikawa, Ichiro Kanazawa, Jun Goto, Shoji Tsuji	2014	49
15	A novel ferritin light chain gene mutation in a Japanese family with neuroferritinopathy: Description of clinical features and implications for genotype–phenotype correlations Movement Disorders ·Akatsuki Kubota, Ayumi Hida, Yaeko Ichikawa, Yoshio Momose, Jun Goto, Yukifusa Igeta, Hideji Hashida, Kunihiro Yoshida, Syu‐Ichi Ikeda, Ichiro KANAZAWA, Shoji Tsuji	2009	47
16	Rapid detection of expanded short tandem repeats in personal genomics using hybrid sequencing Bioinformatics ·Koichiro Doi, Taku Monjo, Pham Huy Hoang, Jun Yoshimura, Hideaki Yurino, Jun Mitsui, Hiroyuki Ishiura, Yuji Takahashi, Yaeko Ichikawa, Jun Goto, Shoji Tsuji, Shinichi Morishita	2013	42
17	Single cell analysis of CAG repeat in brains of dentatorubral-pallidoluysian atrophy (DRPLA) Journal of the Neurological Sciences ·Hideji Hashida, Jun Goto, Takashi Suzuki, Seon-Yong Jeong, Naoki Masuda, Tomonori Ooie, Yoshiaki Tachiiri, Hiroshi Tsuchiya, Ichiro Kanazawa	2001	40
18	Posterior column ataxia with retinitis pigmentosa in a Japanese family with a novel mutation in FLVCR1 Neurogenetics ·Hiroyuki Ishiura, Y. Fukuda, Jun Mitsui, Yasuo Nakahara, Budrul Ahsan, Yuji Takahashi, Yaeko Ichikawa, Jun Goto, Tetsuo Sakai, Shoji Tsuji	2011	39
19	Homozygous Machado–Joseph disease presenting as REM sleep behaviour disorder and prominent psychiatric symptoms European Journal of Neurology ·Toshio Fukutake, Hitoshi Shinotoh, Hiroshi Nishino, Yaeko Ichikawa, Jun Goto, Ichiro Kanazawa, Takaaki Hattori	2002	39
20	TRPM7 is not associated with amyotrophic lateral sclerosis‐parkinsonism dementia complex in the Kii peninsula of Japan American Journal of Medical Genetics Part B Neuropsychiatric Genetics ·Kenju Hara, Yasumasa Kokubo, Hiroyuki Ishiura, Yuko Fukuda, Akinori Miyashita, Ryozo Kuwano, Ryogen Sasaki, Jun Goto, Masatoyo Nishizawa, Shigeki Kuzuhara, Shoji Tsuji	2009	39

About Jun Goto

Jun Goto is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience, Neurology, Genetics and Neurology, having authored 96 papers that have together received 2.4k indexed citations. Recurring topics across this work include Genetic Neurodegenerative Diseases (33 papers), Mitochondrial Function and Pathology (22 papers), Neurological disorders and treatments (8 papers), Neurological diseases and metabolism (7 papers), Parkinson's Disease Mechanisms and Treatments (7 papers), Amyotrophic Lateral Sclerosis Research (5 papers), Muscle Physiology and Disorders (5 papers) and RNA regulation and disease (5 papers). The work is most often cited by research in Cellular and Molecular Neuroscience (1.3k citations), Neurology (694 citations), Neurology (305 citations), Molecular Biology (1.4k citations) and Cell Biology (213 citations). Jun Goto has collaborated with scholars based in Japan, United States and Canada. Frequent co-authors include Shoji Tsuji, Ichiro Kanazawa, Hideji Hashida, Jun Mitsui, Yuji Takahashi, Hiroyuki Ishiura, Osamu Onodera, Yaeko Ichikawa, Ichiro Kanazawa and Masatoyo Nishizawa. Their work appears in journals such as Biochemical and Biophysical Research Communications, Neurogenetics, Journal of the Neurological Sciences, Annals of Neurology and Neurology.

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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Jun Goto

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Jun Goto

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