Tetsuyuki Kitamoto

13.0k total citations · 2 hit papers
286 papers, 8.8k citations indexed

About

Tetsuyuki Kitamoto is a scholar working on Molecular Biology, Neurology and Nutrition and Dietetics. According to data from OpenAlex, Tetsuyuki Kitamoto has authored 286 papers receiving a total of 8.8k indexed citations (citations by other indexed papers that have themselves been cited), including 264 papers in Molecular Biology, 126 papers in Neurology and 63 papers in Nutrition and Dietetics. Recurrent topics in Tetsuyuki Kitamoto's work include Prion Diseases and Protein Misfolding (250 papers), Neurological diseases and metabolism (124 papers) and Trace Elements in Health (63 papers). Tetsuyuki Kitamoto is often cited by papers focused on Prion Diseases and Protein Misfolding (250 papers), Neurological diseases and metabolism (124 papers) and Trace Elements in Health (63 papers). Tetsuyuki Kitamoto collaborates with scholars based in Japan, United States and United Kingdom. Tetsuyuki Kitamoto's co-authors include Jun Tateishi, Ryong‐Woon Shin, Katsumi Doh‐ura, Tamaki Muramoto, Koji Ogomori, Stanley B. Prusiner, Shirou Mohri, Atsushi Kobayashi, Masahito Yamada and Yasushi Iwasaki and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and Journal of Biological Chemistry.

In The Last Decade

Tetsuyuki Kitamoto

279 papers receiving 8.7k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Ultrasensitive human prion detection in cerebrospinal fluid by real-time quaking-induced conversion

2011 427 citations Ryuichiro Atarashi, Katsuya Satoh et al. profile →
Formic acid pretreatment enhances immunostaining of cerebral and systemic amyloids.

1987 427 citations Tetsuyuki Kitamoto, Jun Tateishi et al. PubMed profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Tetsuyuki Kitamoto Japan	49	6.7k	3.8k	2.1k	2.1k	1.5k	286	8.8k
Jun Tateishi Japan	48	5.2k 0.8×	2.6k 0.7×	1.5k 0.7×	1.7k 0.8×	1.3k 0.9×	208	7.7k
H. A. Kretzschmar Germany	41	4.2k 0.6×	2.1k 0.6×	1.1k 0.5×	1.1k 0.5×	1.3k 0.9×	99	5.6k
Andréa C. LeBlanc Canada	44	4.5k 0.7×	1.4k 0.4×	758 0.4×	2.6k 1.3×	408 0.3×	103	6.9k
Efrat Levy United States	45	3.8k 0.6×	1.1k 0.3×	407 0.2×	3.9k 1.9×	789 0.5×	105	7.5k
Kinuko Suzuki United States	53	3.8k 0.6×	1.9k 0.5×	292 0.1×	3.4k 1.7×	720 0.5×	170	9.3k
M. L. Cuzner United Kingdom	52	2.7k 0.4×	2.6k 0.7×	208 0.1×	1.0k 0.5×	1.0k 0.7×	133	9.2k
Tsuneya Ikezu United States	51	4.8k 0.7×	3.1k 0.8×	132 0.1×	3.1k 1.5×	662 0.4×	132	9.2k
Bogdan A. Stoica United States	56	4.4k 0.6×	2.4k 0.6×	172 0.1×	793 0.4×	2.5k 1.7×	113	9.4k
Makoto Michikawa Japan	42	2.9k 0.4×	806 0.2×	309 0.1×	3.1k 1.5×	326 0.2×	155	6.2k
Christian Kaltschmidt Germany	39	3.4k 0.5×	1.5k 0.4×	203 0.1×	1.1k 0.5×	279 0.2×	97	8.0k

Countries citing papers authored by Tetsuyuki Kitamoto

Since Specialization

Citations

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

Fields of papers citing papers by Tetsuyuki Kitamoto

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Tetsuyuki Kitamoto

This figure shows the co-authorship network connecting the top 25 collaborators of Tetsuyuki Kitamoto. A scholar is included among the top collaborators of Tetsuyuki Kitamoto 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 Tetsuyuki Kitamoto. Tetsuyuki Kitamoto 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

Hamada, Shinsuke, Katsuya Satoh, Tetsuyuki Kitamoto, et al.. (2023). Genetic Creutzfeldt‒Jakob disease with 5-octapeptide repeats presented as frontotemporal dementia. Human Genome Variation. 10(1). 10–10. 2 indexed citations

Teruya, Kenta, Atsuko Takeuchi, Yoshikazu Nakamura, et al.. (2023). Preventive or promotive effects of PRNP polymorphic heterozygosity on the onset of prion disease. Heliyon. 9(3). e13974–e13974. 3 indexed citations

Hasegawa, Masato, Takeo Koyama, Akio Akagi, et al.. (2022). An autopsy case of MV2K‐type sporadic Creutzfeldt‐Jakob disease presenting with characteristic clinical, radiological, and neuropathological findings. Neuropathology. 42(3). 245–253. 2 indexed citations

Kosami, Koki, Ryusuke Ae, Tsuyoshi Hamaguchi, et al.. (2022). Methionine homozygosity for PRNP polymorphism and susceptibility to human prion diseases. Journal of Neurology Neurosurgery & Psychiatry. 93(7). 779–784. 8 indexed citations

Kobayashi, Atsushi, Tetsuya Hirata, Takashi Nishikaze, et al.. (2020). α2,3 linkage of sialic acid to a GPI anchor and an unpredicted GPI attachment site in human prion protein. Journal of Biological Chemistry. 295(22). 7789–7798. 11 indexed citations

Kobayashi, Atsushi, Yasushi Iwasaki, Masaki Takao, et al.. (2019). A Novel Combination of Prion Strain Co-Occurrence in Patients with Sporadic Creutzfeldt-Jakob Disease. American Journal Of Pathology. 189(6). 1276–1283. 8 indexed citations

Takeuchi, Atsuko, Shirou Mohri, Akira Tamaoka, et al.. (2019). Two distinct prions in fatal familial insomnia and its sporadic form. Brain Communications. 1(1). fcz045–fcz045. 12 indexed citations

Sanjo, Nobuo, Makoto Tomita, Ryuichiro Atarashi, et al.. (2014). Clinical features of genetic Creutzfeldt-Jakob disease with V180I mutation in the prion protein gene. BMJ Open. 4(5). e004968–e004968. 37 indexed citations

Barria, Marcelo A., Aru Balachandran, Masanori Morita, et al.. (2013). Molecular Barriers to Zoonotic Transmission of Prions. Emerging infectious diseases. 20(1). 88–97. 43 indexed citations

10.

Xiao, Xiangzhu, Jue Yuan, Stéphane Haı̈k, et al.. (2013). Glycoform-Selective Prion Formation in Sporadic and Familial Forms of Prion Disease. PLoS ONE. 8(3). e58786–e58786. 31 indexed citations

11.

Xiao, Xiangzhu, Jue Yuan, Ignazio Calì, et al.. (2013). Correction: Glycoform-Selective Prion Formation in Sporadic and Familial Forms of Prion Disease. PLoS ONE. 8(10). 17 indexed citations

12.

Nishimoto, Yoshinori, Daisuke Ito, Shigeaki Suzuki, et al.. (2011). Slow-progressive ataxia with a methionine-to-arginine point mutation in codon 232 in the prion protein gene (PRNP). Clinical Neurology and Neurosurgery. 113(8). 696–698. 2 indexed citations

13.

Kobayashi, Atsushi, et al.. (2008). Thr but Asn of the N-glycosylation sites of PrP is indispensable for its misfolding. Biochemical and Biophysical Research Communications. 369(4). 1195–1198. 13 indexed citations

14.

Niimi, Yoshiki, Yasushi Iwasaki, Toshitaka Umemura, et al.. (2008). MM2‐cortical‐type sporadic Creutzfeldt‐Jakob disease with early stage cerebral cortical pathology presenting with a rapidly progressive clinical course. Neuropathology. 28(6). 645–651. 7 indexed citations

15.

Nakamura, Naoto, Mariko Shimokawa, Shirou Mohri, et al.. (2003). Generation of Antibodies Against Prion Protein by Scrapie-Infected Cell Immunization of PrP ^0/0 Mice. PubMed. 22(4). 263–266. 13 indexed citations

16.

Ishizawa, Keisuke, Takashi Komori, Tomokazu Shimazu, et al.. (2002). Hyperphosphorylated tau deposition parallels prion protein burden in a case of Gerstmann-Sträussler-Scheinker syndrome P102L mutation complicated with dementia. Acta Neuropathologica. 104(4). 342–350. 39 indexed citations

17.

Muramoto, Tamaki, et al.. (2000). Analyses of Gerstmann–Straussler syndrome with 102Leu219Lys using monoclonal antibodies that specifically detect human prion protein with 219Glu. Neuroscience Letters. 288(3). 179–182. 20 indexed citations

18.

Nakamura, Yosikazu, Hiroshi Yanagawa, Tetsuyuki Kitamoto, & Takeshi Sato. (2000). Epidemiologic features of 65 Creutzfeldt–Jakob disease patients with a history of cadaveric dura mater transplantation in Japan. Epidemiology and Infection. 125(1). 201–205. 4 indexed citations

19.

Tateishi, Jun, Tetsuyuki Kitamoto, Gen Ishikawa, & Sei‐ichi Manabe. (1993). Removal of causative agent of Creutzfeldt-Jakob disease(CJD) through membrane filtration method.. MEMBRANE. 18(6). 357–362. 25 indexed citations

20.

Kitamoto, Tetsuyuki, et al.. (1991). Immunoreactivity of cerebral amyloidosis is enhanced by protein denaturation treatments. Acta Neuropathologica. 82(4). 260–265. 24 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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