Shingo Kariya

2.0k total citations
29 papers, 1.6k citations indexed

About

Shingo Kariya is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, Shingo Kariya has authored 29 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 21 papers in Molecular Biology, 12 papers in Genetics and 8 papers in Cellular and Molecular Neuroscience. Recurrent topics in Shingo Kariya's work include Neurogenetic and Muscular Disorders Research (12 papers), RNA modifications and cancer (7 papers) and Mitochondrial Function and Pathology (6 papers). Shingo Kariya is often cited by papers focused on Neurogenetic and Muscular Disorders Research (12 papers), RNA modifications and cancer (7 papers) and Mitochondrial Function and Pathology (6 papers). Shingo Kariya collaborates with scholars based in United States, Japan and Spain. Shingo Kariya's co-authors include Umrao R. Monani, Gyu-Hwan Park, Cathleen Lutz, Satoshi Ueno, Makito Hirano, Yuka Maeno-Hikichi, Marc S. Arkovitz, Lynn T. Landmesser, Diane B. Ré and Nobuyuki Takahashi and has published in prestigious journals such as Journal of Clinical Investigation, Neuron and Molecular and Cellular Biology.

In The Last Decade

Shingo Kariya

28 papers receiving 1.6k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Shingo Kariya United States 16 1.1k 916 267 265 243 29 1.6k
Andreina Bordoni Italy 29 2.0k 1.8× 406 0.4× 396 1.5× 127 0.5× 396 1.6× 73 2.6k
Matthew E.R. Butchbach United States 20 2.0k 1.8× 1.4k 1.6× 124 0.5× 467 1.8× 239 1.0× 35 2.5k
Norma B. Romero France 22 1.2k 1.1× 324 0.4× 304 1.1× 43 0.2× 291 1.2× 44 1.7k
Giulietta Riboldi Italy 19 846 0.8× 393 0.4× 432 1.6× 98 0.4× 353 1.5× 43 1.4k
Yoshihiro Nihei Japan 21 751 0.7× 238 0.3× 539 2.0× 205 0.8× 296 1.2× 42 1.5k
Aleksey Shatunov United Kingdom 26 972 0.9× 522 0.6× 917 3.4× 37 0.1× 325 1.3× 45 2.0k
Hiroyuki Ishiura Japan 25 844 0.8× 312 0.3× 627 2.3× 92 0.3× 633 2.6× 146 1.8k
A. Nascimento Spain 20 757 0.7× 184 0.2× 190 0.7× 89 0.3× 232 1.0× 94 1.2k
Jun Mitsui Japan 24 860 0.8× 214 0.2× 582 2.2× 88 0.3× 480 2.0× 115 1.7k
Soledad Matus Chile 17 497 0.4× 122 0.1× 490 1.8× 88 0.3× 255 1.0× 21 1.5k

Countries citing papers authored by Shingo Kariya

Since Specialization
Citations

This map shows the geographic impact of Shingo Kariya'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 Shingo Kariya with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Shingo Kariya more than expected).

Fields of papers citing papers by Shingo Kariya

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Shingo Kariya. 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 Shingo Kariya. The network helps show where Shingo Kariya may publish in the future.

Co-authorship network of co-authors of Shingo Kariya

This figure shows the co-authorship network connecting the top 25 collaborators of Shingo Kariya. A scholar is included among the top collaborators of Shingo Kariya 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 Shingo Kariya. Shingo Kariya 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.
Ré, Diane B., et al.. (2024). Physical Exercise Counteracts Aging-Associated White Matter Demyelination Causing Cognitive Decline. Aging and Disease. 15(5). 2136–2136. 8 indexed citations
2.
Comfort, Nicole, Chiara Parodi, Tessa R. Bloomquist, et al.. (2023). Longitudinal transcriptomic analysis of mouse sciatic nerve reveals pathways associated with age‐related muscle pathology. Journal of Cachexia Sarcopenia and Muscle. 14(3). 1322–1336. 7 indexed citations
3.
Bucchia, Monica, et al.. (2018). Limitations and Challenges in Modeling Diseases Involving Spinal Motor Neuron Degeneration in Vitro. Frontiers in Cellular Neuroscience. 12. 61–61. 21 indexed citations
4.
Harding, Brian, Shingo Kariya, Umrao R. Monani, et al.. (2014). Spectrum of Neuropathophysiology in Spinal Muscular Atrophy Type I. Journal of Neuropathology & Experimental Neurology. 74(1). 15–24. 88 indexed citations
5.
Emmanuele, Valentina, Akatsuki Kubota, Beatriz García-Díaz, et al.. (2014). Fhl1 W122S causes loss of protein function and late-onset mild myopathy. Human Molecular Genetics. 24(3). 714–726. 7 indexed citations
6.
Ré, Diane B., Virginia Le Verche, Mackenzie W. Amoroso, et al.. (2014). Necroptosis Drives Motor Neuron Death in Models of Both Sporadic and Familial ALS. Neuron. 81(5). 1001–1008. 320 indexed citations
7.
Kariya, Shingo, Diane B. Ré, Arnaud Jacquier, et al.. (2012). Mutant superoxide dismutase 1 (SOD1), a cause of amyotrophic lateral sclerosis, disrupts the recruitment of SMN, the spinal muscular atrophy protein to nuclear Cajal bodies. Human Molecular Genetics. 21(15). 3421–3434. 44 indexed citations
8.
Lutz, Cathleen, Shingo Kariya, Melissa Osborne, et al.. (2011). Postsymptomatic restoration of SMN rescues the disease phenotype in a mouse model of severe spinal muscular atrophy. Journal of Clinical Investigation. 121(8). 3029–3041. 126 indexed citations
9.
Park, Gyu-Hwan, Shingo Kariya, & Umrao R. Monani. (2010). Spinal Muscular Atrophy: New and Emerging Insights from Model Mice. Current Neurology and Neuroscience Reports. 10(2). 108–117. 44 indexed citations
10.
Kariya, Shingo, Gyu-Hwan Park, Yuka Maeno-Hikichi, et al.. (2008). Reduced SMN protein impairs maturation of the neuromuscular junctions in mouse models of spinal muscular atrophy. Human Molecular Genetics. 17(16). 2552–2569. 355 indexed citations
11.
12.
Hirano, Makito, Aya Yamamoto, Toshio Mori, et al.. (2007). DNA single‐strand break repair is impaired in aprataxin‐related ataxia. Annals of Neurology. 61(2). 162–174. 62 indexed citations
13.
Kariya, Shingo, Makito Hirano, Yoshiko Furiya, & Satoshi Ueno. (2005). Effect of humanin on decreased ATP levels of human lymphocytes harboring A3243G mutant mitochondrial DNA. Neuropeptides. 39(2). 97–101. 33 indexed citations
14.
Kariya, Shingo, Nobuyuki Takahashi, Makito Hirano, & Satoshi Ueno. (2005). Increased Vulnerability to l-DOPA Toxicity in Dopaminergic Neurons From VMAT2 Heterozygote Knockout Mice. Journal of Molecular Neuroscience. 27(3). 277–280. 15 indexed citations
15.
Kariya, Shingo, Makito Hirano, Yoshitaka Nagai, et al.. (2005). Humanin Attenuates Apoptosis Induced by DRPLA Proteins With Expanded Polyglutamine Stretches. Journal of Molecular Neuroscience. 25(2). 165–170. 30 indexed citations
16.
Kariya, Shingo, Makito Hirano, Yoshiko Furiya, Kazuma Sugie, & Satoshi Ueno. (2005). Humanin detected in skeletal muscles of MELAS patients: a possible new therapeutic agent. Acta Neuropathologica. 109(4). 367–372. 39 indexed citations
17.
Kariya, Shingo, Makito Hirano, Shinichi Uesato, et al.. (2005). Cytoprotective effect of novel histone deacetylase inhibitors against polyglutamine toxicity. Neuroscience Letters. 392(3). 213–215. 9 indexed citations
18.
19.
Hirano, Makito, et al.. (2004). Loss of function mechanism in aprataxin-related early-onset ataxia. Biochemical and Biophysical Research Communications. 322(2). 380–386. 11 indexed citations
20.
Kariya, Shingo, Nobuyuki Takahashi, Makito Hirano, & Satoshi Ueno. (2003). Humanin improves impaired metabolic activity and prolongs survival of serum-deprived human lymphocytes. Molecular and Cellular Biochemistry. 254(1-2). 83–89. 42 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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