Jun Goto

5.1k total citations
96 papers, 2.4k citations indexed

About

Jun Goto is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Neurology. According to data from OpenAlex, Jun Goto has authored 96 papers receiving a total of 2.4k indexed citations (citations by other indexed papers that have themselves been cited), including 55 papers in Molecular Biology, 42 papers in Cellular and Molecular Neuroscience and 27 papers in Neurology. Recurrent topics in Jun Goto's work include Genetic Neurodegenerative Diseases (34 papers), Mitochondrial Function and Pathology (25 papers) and Parkinson's Disease Mechanisms and Treatments (11 papers). Jun Goto is often cited by papers focused on Genetic Neurodegenerative Diseases (34 papers), Mitochondrial Function and Pathology (25 papers) and Parkinson's Disease Mechanisms and Treatments (11 papers). Jun Goto collaborates with scholars based in Japan, United States and Canada. Jun Goto's co-authors include Shoji Tsuji, Ichiro Kanazawa, Hideji Hashida, Jun Mitsui, Yuji Takahashi, Hiroyuki Ishiura, Osamu Onodera, Yaeko Ichikawa, Ichiro Kanazawa and Masatoyo Nishizawa and has published in prestigious journals such as Nucleic Acids Research, Nature Genetics and SHILAP Revista de lepidopterología.

In The Last Decade

Jun Goto

92 papers receiving 2.3k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Jun Goto Japan	31	1.6k	1.3k	805	348	267	96	2.4k
Ali Benomar Morocco	21	1.5k 0.9×	1.7k 1.3×	709 0.9×	346 1.0×	143 0.5×	69	2.3k
Laura Bannach Jardim Brazil	28	1.5k 1.0×	1.7k 1.3×	933 1.2×	200 0.6×	169 0.6×	144	2.6k
Paymaan Jafar‐Nejad United States	23	1.6k 1.0×	920 0.7×	610 0.8×	212 0.6×	320 1.2×	55	2.3k
Marina Kennerson Australia	27	1.5k 0.9×	1.4k 1.0×	762 0.9×	658 1.9×	262 1.0×	95	3.0k
Antonella Monticelli Italy	26	1.6k 1.0×	1.3k 1.0×	354 0.4×	158 0.5×	236 0.9×	71	2.1k
Aislinn Williams United States	16	1.2k 0.8×	763 0.6×	420 0.5×	198 0.6×	114 0.4×	35	1.8k
Emilia Bellone Italy	24	681 0.4×	1.0k 0.8×	787 1.0×	405 1.2×	176 0.7×	100	1.8k
Albena Jordanova Belgium	32	1.9k 1.2×	1.7k 1.2×	518 0.6×	638 1.8×	479 1.8×	87	3.6k
Nobutaka Arai Japan	27	841 0.5×	826 0.6×	977 1.2×	597 1.7×	117 0.4×	129	2.6k
Michael D. Kaytor United States	20	2.1k 1.3×	1.6k 1.2×	411 0.5×	92 0.3×	184 0.7×	37	2.6k

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-authorship network of co-authors of Jun Goto

This figure shows the co-authorship network connecting the top 25 collaborators of Jun Goto. A scholar is included among the top collaborators of Jun Goto based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Jun Goto. Jun Goto is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Nagashima, Yu, Tatsuo Mano, Hiroyuki Ishiura, et al.. (2021). Cerebellar Ataxia as a Common Clinical Presentation Associated with DNMT1 p.Y511H and a Review of the Literature. Journal of Molecular Neuroscience. 71(9). 1796–1801. 1 indexed citations

Ishiura, Hiroyuki, Yuji Takahashi, Toshihiro Hayashi, et al.. (2014). Molecular epidemiology and clinical spectrum of hereditary spastic paraplegia in the Japanese population based on comprehensive mutational analyses. Journal of Human Genetics. 59(3). 163–172. 49 indexed citations

Goto, Jun, et al.. (2014). Development of Power Transmitting Subsystem for MPT Ground Test Model. IEICE Technical Report; IEICE Tech. Rep.. 114(246). 71–74. 1 indexed citations

Koizumi, Hideki, et al.. (2013). PROPOSAL AND PRACTICE OF ^|^lsquo;COMMUNITY-CARE TEMPORARY-HOUSING^|^rsquo;. AIJ Journal of Technology and Design. 19(42). 671–676. 3 indexed citations

Ichikawa, Yaeko, Hiroyuki Ishiura, Jun Mitsui, et al.. (2013). Exome analysis reveals a Japanese family with spinocerebellar ataxia, autosomal recessive 1. Journal of the Neurological Sciences. 331(1-2). 158–160. 4 indexed citations

Ogawa, Naomi, Yasushi Imai, Yuji Takahashi, et al.. (2011). Evaluating Japanese Patients With the Marfan Syndrome Using High-Throughput Microarray-Based Mutational Analysis of Fibrillin-1 Gene. The American Journal of Cardiology. 108(12). 1801–1807. 16 indexed citations

Murayama, Hiroshi, Masanori Nishinaga, Jun Goto, et al.. (2011). Interactions of household composition and required care level with functional and cognitive status among disabled Japanese elderly living in a suburban apartment complex. Geriatrics and gerontology international. 12(3). 538–546. 6 indexed citations

Matsukawa, Takashi, Muriel Asheuer, Yuji Takahashi, et al.. (2010). Identification of novel SNPs of ABCD1, ABCD2, ABCD3, and ABCD4 genes in patients with X-linked adrenoleukodystrophy (ALD) based on comprehensive resequencing and association studies with ALD phenotypes. Neurogenetics. 12(1). 41–50. 21 indexed citations

Mitsui, Jun, Yuji Takahashi, Jun Goto, et al.. (2010). 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. 87(1). 75–89. 73 indexed citations

10.

Shimizu, Jun, Yuichiro Shirota, Yoshio Momose, et al.. (2009). Alien hand sign observed at the initial stage of a case of Creutzfeldt-Jakob disease. Rinsho Shinkeigaku. 49(2/3). 109–114. 2 indexed citations

11.

Wang, Kang, Yuji Takahashi, Zongliang Gao, et al.. (2009). Mitochondrial ND3 as the novel causative gene for Leber hereditary optic neuropathy and dystonia. Neurogenetics. 10(4). 337–345. 33 indexed citations

12.

Matsumoto, Hideyuki, Ritsuko Hanajima, Yasuo Terao, et al.. (2009). Efferent and afferent evoked potentials in patients with adrenomyeloneuropathy. Clinical Neurology and Neurosurgery. 112(2). 131–136. 10 indexed citations

13.

Anttonen, Anna‐Kaisa, Eija Siintola, Lisbeth Tranebjærg, et al.. (2008). Novel SIL1 mutations and exclusion of functional candidate genes in Marinesco–Sjögren syndrome. European Journal of Human Genetics. 16(8). 961–969. 31 indexed citations

14.

Takahashi, Yuji, Katsuhisa Ogata, Jun Goto, et al.. (2002). Human skeletal muscle calcium channel α1S is expressed in the basal ganglia: distinctive expression pattern among L-type Ca2+ channels. Neuroscience Research. 45(1). 129–137. 19 indexed citations

15.

Fukutake, Toshio, Hitoshi Shinotoh, Hiroshi Nishino, et al.. (2002). Homozygous Machado–Joseph disease presenting as REM sleep behaviour disorder and prominent psychiatric symptoms. European Journal of Neurology. 9(1). 97–100. 39 indexed citations

16.

Ueda, Hiroko, Jun Goto, Hideji Hashida, et al.. (2002). Enhanced SUMOylation in polyglutamine diseases. Biochemical and Biophysical Research Communications. 293(1). 307–313. 65 indexed citations

17.

Kamakura, Keiko, et al.. (1999). A Patient with Huntington’s Disease Presenting with Laryngeal Chorea. European Neurology. 41(2). 119–120. 6 indexed citations

18.

Wang, Guanghui, et al.. (1997). Machado–Joseph Disease Gene Product Identified in Lymphocytes and Brain. Biochemical and Biophysical Research Communications. 233(2). 476–479. 36 indexed citations

19.

Nakashima, Kenji, Yasuhiro Watanabe, Masayoshi Kusumi, et al.. (1996). Epidemiological and Genetic Studies of Huntington's Disease in the San-in Area of Japan. Neuroepidemiology. 15(3). 126–131. 30 indexed citations

20.

Yazawa, Ikuru, Nobuyuki Nukina, Hideji Hashida, et al.. (1995). Abnormal gene product identified in hereditary dentatorubral–pallidoluysian atrophy (DRPLA) brain. Nature Genetics. 10(1). 99–103. 125 indexed citations

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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