Kei Shioda

643 total citations
25 papers, 517 citations indexed

About

Kei Shioda is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Genetics. According to data from OpenAlex, Kei Shioda has authored 25 papers receiving a total of 517 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Molecular Biology, 6 papers in Cellular and Molecular Neuroscience and 5 papers in Genetics. Recurrent topics in Kei Shioda's work include Mitochondrial Function and Pathology (6 papers), DNA Repair Mechanisms (5 papers) and Genetics and Neurodevelopmental Disorders (4 papers). Kei Shioda is often cited by papers focused on Mitochondrial Function and Pathology (6 papers), DNA Repair Mechanisms (5 papers) and Genetics and Neurodevelopmental Disorders (4 papers). Kei Shioda collaborates with scholars based in Japan, United Kingdom and United States. Kei Shioda's co-authors include Ryo Fukatsu, Masaharu Hayashi, Masaharu Hayashi, Shuki Mizutani, Kimiko Tamagawa, Masaya Oda, Satoshi Araki, Yoshio Morimatsu, Masahiro Itoh and Jun Kohyama and has published in prestigious journals such as Acta Neuropathologica, Journal of Neuropathology & Experimental Neurology and Journal of the Neurological Sciences.

In The Last Decade

Kei Shioda

25 papers receiving 512 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Kei Shioda Japan	14	274	125	83	82	81	25	517
M. T. Dotti Italy	13	309 1.1×	46 0.4×	55 0.7×	45 0.5×	82 1.0×	38	583
Chiara Aiello Italy	16	397 1.4×	91 0.7×	27 0.3×	41 0.5×	80 1.0×	34	583
Hamad Alzaidan Saudi Arabia	14	283 1.0×	55 0.4×	67 0.8×	173 2.1×	52 0.6×	39	578
Karin Seid Germany	12	245 0.9×	50 0.4×	47 0.6×	21 0.3×	168 2.1×	15	613
V. Argentiero Italy	9	109 0.4×	189 1.5×	37 0.4×	26 0.3×	96 1.2×	16	523
Yukihiko Kohda Japan	10	214 0.8×	77 0.6×	24 0.3×	20 0.2×	48 0.6×	14	474
K.L. Sikri United Kingdom	10	191 0.7×	56 0.4×	112 1.3×	43 0.5×	18 0.2×	17	465
Sinan Çomu Türkiye	8	165 0.6×	42 0.3×	38 0.5×	87 1.1×	39 0.5×	15	404
Patrick A. Lundquist United States	8	130 0.5×	238 1.9×	26 0.3×	55 0.7×	24 0.3×	16	440
Casandra M. Cartagena United States	11	179 0.7×	63 0.5×	62 0.7×	28 0.3×	39 0.5×	14	531

Countries citing papers authored by Kei Shioda

Since Specialization

Citations

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

Fields of papers citing papers by Kei Shioda

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Kei Shioda

This figure shows the co-authorship network connecting the top 25 collaborators of Kei Shioda. A scholar is included among the top collaborators of Kei Shioda 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 Kei Shioda. Kei Shioda is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Sasaki, Atsushi, Akiyoshi Kakita, Kunihiro Yoshida, et al.. (2015). Variable expression of microglial DAP12 and TREM2 genes in Nasu-Hakola disease. Neurogenetics. 16(4). 265–276. 27 indexed citations

Sasaki, Atsushi, Kei Shioda, Taku Homma, Ryo Fukatsu, & Hiroyoshi Koide. (2012). A 14‐year‐old girl with lissencephaly and craniofacial dysmorphism. Neuropathology. 32(6). 675–678. 1 indexed citations

Maruyama, Tetsuro, et al.. (2011). A RESECTED CASE OF METASTASIS TO THE SMALL INTESTINE FROM ESOPHAGEAL BASALOID CELL CARCINOMA PRESENTED WITH SMALL BOWEL OBSTRUCTION. Nihon Rinsho Geka Gakkai Zasshi (Journal of Japan Surgical Association). 72(2). 333–338. 1 indexed citations

Hayashi, Masaharu, Tatsuyuki Ohto, Kei Shioda, & Ryo Fukatsu. (2011). Lesions of cortical GABAergic interneurons and acetylcholine neurons in xeroderma pigmentosum group A. Brain and Development. 34(4). 287–292. 5 indexed citations

Miyata, Rie, et al.. (2007). Oxidative stress in neurodegeneration in dentatorubral-pallidoluysian atrophy. Journal of the Neurological Sciences. 264(1-2). 133–139. 21 indexed citations

Hayashi, Masaharu, Satoko Kumada, Kei Shioda, & Ryo Fukatsu. (2007). Neuropathological analysis of the brainstem and cerebral cortex lesions on epileptogenesis in hereditary dentatorubral-pallidoluysian atrophy. Brain and Development. 29(8). 473–481. 11 indexed citations

Hayashi, Masaharu, et al.. (2007). Mechanisms of neurodegeneration in mucopolysaccharidoses II and IIIB: analysis of human brain tissue. Acta Neuropathologica. 115(5). 547–559. 89 indexed citations

Hayashi, Masaharu, Satoshi Araki, Jun Kohyama, et al.. (2004). Brainstem and Basal Ganglia Lesions in Xeroderma Pigmentosum Group A. Journal of Neuropathology & Experimental Neurology. 63(10). 1048–1057. 17 indexed citations

Hayashi, Masaharu, Satoshi Araki, Jun Kohyama, Kei Shioda, & Ryo Fukatsu. (2004). Oxidative nucleotide damage and superoxide dismutase expression in the brains of xeroderma pigmentosum group A and Cockayne syndrome. Brain and Development. 27(1). 34–38. 46 indexed citations

10.

Hayashi, Masaharu, Masahiro Itoh, Satoshi Araki, et al.. (2001). Oxidative Stress and Disturbed Glutamate Transport in Hereditary Nucleotide Repair Disorders. Journal of Neuropathology & Experimental Neurology. 60(4). 350–356. 46 indexed citations

11.

Inoue, Tsutomu, et al.. (2001). [A case of myeloma kidney complicated by extramedullary plasmacytoma with massive bleeding].. PubMed. 43(4). 347–50. 1 indexed citations

12.

Itoh, Masahiro, Masaharu Hayashi, Kei Shioda, et al.. (1999). Neurodegeneration in hereditary nucleotide repair disorders. Brain and Development. 21(5). 326–333. 61 indexed citations

13.

Hayashi, Masaharu, et al.. (1998). Cerebellar neurodegeneration in human hereditary DNA repair disorders. Neuroscience Letters. 243(1-3). 133–136. 34 indexed citations

14.

Hokari, Shigeru, Iwao Koyama, Kei Shioda, & Yoshikatsu Sakagishi. (1994). Deoxyuridine triphosphatase in human hepatoma. International Journal of Biochemistry. 26(4). 487–490. 4 indexed citations

15.

Shioda, Kei, et al.. (1993). The Pathogenesis of Biliary Atresia. Journal of Pediatric Gastroenterology and Nutrition. 16(1). 53–60. 52 indexed citations

16.

Shioda, Kei, et al.. (1993). The Pathogenesis of Biliary Atresia. Journal of Pediatric Gastroenterology and Nutrition. 16(1). 53–60. 8 indexed citations

17.

Kato, Shinsuke, et al.. (1992). Immunohistochemical studies on the new type of astrocytic inclusions identified in a patient with brain malformation. Acta Neuropathologica. 84(4). 449–52. 14 indexed citations

18.

Shioda, Kei, et al.. (1992). Inclusion bodies in cerebral cortical astrocytes: a new change of astrocytes. Acta Neuropathologica. 84(1). 113–116. 21 indexed citations

19.

Shioda, Kei. (1990). [Neuropathological study of severely handicapped children: relationships of cortical and subcortical destructive lesions].. PubMed. 22(6). 551–9. 1 indexed citations

20.

Fujimori, Takahiro, et al.. (1981). SUBACUTE NECROTISING LYMPHADENITIS:A Clinicopathologic Study. Acta Pathologica Japonica. 31(5). 791–797. 19 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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