Jun Goto

10.6k total citations · 1 hit paper
64 papers, 2.6k citations indexed

About

Jun Goto is a scholar working on Neurology, Molecular Biology and Genetics. According to data from OpenAlex, Jun Goto has authored 64 papers receiving a total of 2.6k indexed citations (citations by other indexed papers that have themselves been cited), including 38 papers in Neurology, 22 papers in Molecular Biology and 15 papers in Genetics. Recurrent topics in Jun Goto's work include Amyotrophic Lateral Sclerosis Research (31 papers), Neurogenetic and Muscular Disorders Research (14 papers) and Parkinson's Disease Mechanisms and Treatments (13 papers). Jun Goto is often cited by papers focused on Amyotrophic Lateral Sclerosis Research (31 papers), Neurogenetic and Muscular Disorders Research (14 papers) and Parkinson's Disease Mechanisms and Treatments (13 papers). Jun Goto collaborates with scholars based in Japan, United States and Canada. Jun Goto's co-authors include Joan Selverstone Valentine, James A. Roe, Dale E. Bredesen, Edith Butler Gralla, Martina Wiedau‐Pazos, Edith B. Gralla, Shahrooz Rabizadeh, Michael K. Lee, Diane E. Cabelli and Thomas J. Lyons and has published in prestigious journals such as Science, Proceedings of the National Academy of Sciences and Nucleic Acids Research.

In The Last Decade

Jun Goto

64 papers receiving 2.5k citations

Hit Papers

Altered Reactivity of Superoxide Dismutase in Familial Am... 1996 2026 2006 2016 1996 100 200 300 400 500

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Jun Goto Japan 25 1.5k 879 540 515 399 64 2.6k
Lawrence J. Hayward United States 36 2.4k 1.6× 2.4k 2.7× 898 1.7× 628 1.2× 733 1.8× 52 4.5k
James A. Roe United States 14 791 0.5× 1.3k 1.4× 264 0.5× 297 0.6× 234 0.6× 17 2.3k
Jamuna R. Subramaniam India 15 694 0.5× 495 0.6× 284 0.5× 243 0.5× 317 0.8× 30 1.6k
Jacinda B. Sampson United States 19 376 0.3× 813 0.9× 376 0.7× 179 0.3× 447 1.1× 51 1.8k
Cao Huang United States 22 969 0.6× 619 0.7× 483 0.9× 358 0.7× 232 0.6× 40 1.9k
Thomas B. Bartnikas United States 20 308 0.2× 830 0.9× 421 0.8× 269 0.5× 289 0.7× 43 2.5k
Darrel Waggoner United States 24 516 0.3× 1.5k 1.7× 122 0.2× 212 0.4× 245 0.6× 65 3.2k
Yien–Ming Kuo United States 25 431 0.3× 950 1.1× 502 0.9× 304 0.6× 303 0.8× 48 3.8k
Paul J. Lockhart Australia 34 1.2k 0.8× 2.3k 2.7× 122 0.2× 463 0.9× 585 1.5× 126 5.2k
Isabel Cardoso Portugal 34 164 0.1× 2.2k 2.6× 231 0.4× 169 0.3× 1.4k 3.4× 76 3.2k

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

20 of 20 papers shown
1.
Iseki, Chifumi, Jun Miki, Hikaru Nagasawa, et al.. (2024). A novel TBK1 loss-of-function variant associated with ALS and parkinsonism phenotypes. Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration. 25(7-8). 791–794. 1 indexed citations
2.
Minami, Akira, Jun Goto, Samir Mitragotri, et al.. (2021). Enhancement of elastin expression by transdermal administration of sialidase isozyme Neu2. Scientific Reports. 11(1). 3302–3302. 9 indexed citations
3.
Goto, Jun, et al.. (2020). On the Differential Roles of Mg2+, Zn2+, and Cu2+ in the Equilibrium of β-N-Methyl-Amino-L-Alanine (BMAA) and its Carbamates. Neurotoxicity Research. 39(1). 6–16. 7 indexed citations
6.
Fujisawa, Takao, Hisae Kadowaki, H. Takahashi, et al.. (2015). A systematic immunoprecipitation approach reinforces the concept of common conformational alterations in amyotrophic lateral sclerosis-linked SOD1 mutants. Neurobiology of Disease. 82. 478–486. 7 indexed citations
7.
Park, Jin, Cory L. Brooks, José Serate, et al.. (2015). Directed Evolution of the Escherichia coli cAMP Receptor Protein at the cAMP Pocket. Journal of Biological Chemistry. 290(44). 26587–26596. 10 indexed citations
8.
Goto, Jun, et al.. (2012). The physiological effect of ingested β-N-methylamino-L-alanine on a glutamatergic synapse in an in vivo preparation. Comparative Biochemistry and Physiology Part C Toxicology & Pharmacology. 156(3-4). 171–177. 18 indexed citations
9.
Fujisawa, Takao, Kengo Homma, Hisae Kadowaki, et al.. (2012). A novel monoclonal antibody reveals a conformational alteration shared by amyotrophic lateral sclerosis‐linked SOD1 mutants. Annals of Neurology. 72(5). 739–749. 62 indexed citations
10.
Yoshida, Makiko, Yuji Takahashi, Asako Koike, et al.. (2010). A mutation database for amyotrophic lateral sclerosis. Human Mutation. 31(9). 1003–1010. 26 indexed citations
11.
Takahashi, Yuji, Hiroyuki Ishiura, Jun Mitsui, et al.. (2008). Development of a High-Throughput Microarray-Based Resequencing System for Neurological Disorders and Its Application to Molecular Genetics of Amyotrophic Lateral Sclerosis. Archives of Neurology. 65(10). 1326–32. 41 indexed citations
12.
Matsumoto, Hideyuki, Shinya Ohminami, Jun Goto, & Shoji Tsuji. (2008). Progressive Supranuclear Palsy With Walleyed Bilateral Internuclear Ophthalmoplegia Syndrome. Archives of Neurology. 65(6). 827–9. 18 indexed citations
13.
Li, Ming, Kinya Ishikawa, Shuta Toru, et al.. (2003). Physical map and haplotype analysis of 16q-linked autosomal dominant cerebellar ataxia (ADCA) type III in Japan. Journal of Human Genetics. 48(3). 111–118. 21 indexed citations
14.
Goto, Jun & Rudolph E. Tanzi. (2002). The role of the low-density lipoprotein receptor-related protein (LRP1) in alzheimer’s Aβ generation. Journal of Molecular Neuroscience. 19(1-2). 37–41. 28 indexed citations
15.
Maciel, Patrı́cia, Cláudia Gaspar, Laura Guimarães, et al.. (1999). Study of three intragenic polymorphisms in the Machado-Joseph disease gene (MJD1) in relation to genetic instability of the (CAG)n tract. European Journal of Human Genetics. 7(2). 147–156. 25 indexed citations
16.
Wiedau‐Pazos, Martina, Jun Goto, Shahrooz Rabizadeh, et al.. (1996). Cell death mechanisms in ALS. Neurology. 47(4_suppl_2). S36–8; discussion S38. 15 indexed citations
17.
Figlewicz, Denise A., Melvin G. McInnis, Jun Goto, et al.. (1994). Identification of flanking markers for the familial amyotrophic lateral sclerosis gene ALS1 on chromosome 21. Journal of the Neurological Sciences. 124. 90–95. 6 indexed citations
18.
Goto, Jun, Flora Tassone, Suzanne Demczuk, et al.. (1992). Dinucleotide repeat polymorphism at the D21S65 locus. Human Molecular Genetics. 1(5). 350–350. 4 indexed citations
19.
Goto, Jun, et al.. (1991). A Pvull RFLP at the HOX 1.4 homeobox locus (HOX1D). Nucleic Acids Research. 19(13). 3755–3755. 1 indexed citations
20.
Yamaguchi, Keizo, Hironobu Koga, Shigeru Kohno, et al.. (1986). Clinical Evaluation of SMX/TMP on Treatment of the Patients with Malaria. Kansenshogaku zasshi. 60(9). 1027–1035. 1 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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