Shinjiro Akaboshi

854 total citations
27 papers, 592 citations indexed

About

Shinjiro Akaboshi is a scholar working on Molecular Biology, Pediatrics, Perinatology and Child Health and Physiology. According to data from OpenAlex, Shinjiro Akaboshi has authored 27 papers receiving a total of 592 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Molecular Biology, 6 papers in Pediatrics, Perinatology and Child Health and 6 papers in Physiology. Recurrent topics in Shinjiro Akaboshi's work include Metabolism and Genetic Disorders (4 papers), Lysosomal Storage Disorders Research (4 papers) and Glycosylation and Glycoproteins Research (3 papers). Shinjiro Akaboshi is often cited by papers focused on Metabolism and Genetic Disorders (4 papers), Lysosomal Storage Disorders Research (4 papers) and Glycosylation and Glycoproteins Research (3 papers). Shinjiro Akaboshi collaborates with scholars based in Japan, Italy and United States. Shinjiro Akaboshi's co-authors include Boris M. Hogema, Cornelis Jakobs, Andrea Novelletto, K. Michael Gibson, Patrizia Malaspina, Miyako Taniguchi, Kousaku Ohno, Kenzo Takeshita, Gajja S. Salomons and Toshiyuki Yamamoto and has published in prestigious journals such as Annals of Neurology, Brain Research and Epilepsia.

In The Last Decade

Shinjiro Akaboshi

27 papers receiving 566 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Shinjiro Akaboshi Japan 16 317 237 132 73 68 27 592
Paula M. Strasberg Canada 14 330 1.0× 190 0.8× 96 0.7× 59 0.8× 67 1.0× 34 543
Annette Bley Germany 14 500 1.6× 349 1.5× 115 0.9× 22 0.3× 78 1.1× 29 816
Teresa Pàmpols Spain 12 459 1.4× 267 1.1× 206 1.6× 32 0.4× 64 0.9× 27 640
Dawn Peck United States 13 329 1.0× 320 1.4× 287 2.2× 59 0.8× 28 0.4× 32 607
Auli Nuutila Finland 8 158 0.5× 156 0.7× 62 0.5× 26 0.4× 26 0.4× 9 343
Clare Beesley United Kingdom 17 288 0.9× 607 2.6× 189 1.4× 240 3.3× 108 1.6× 29 980
M. Barth France 12 217 0.7× 128 0.5× 46 0.3× 29 0.4× 140 2.1× 17 423
Jessie Zhang United States 12 499 1.6× 368 1.6× 31 0.2× 128 1.8× 37 0.5× 15 881
Colette C. Parker United States 10 331 1.0× 398 1.7× 26 0.2× 111 1.5× 50 0.7× 19 755
Agnieszka Ługowska Poland 20 428 1.4× 714 3.0× 69 0.5× 166 2.3× 44 0.6× 70 1.1k

Countries citing papers authored by Shinjiro Akaboshi

Since Specialization
Citations

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

Fields of papers citing papers by Shinjiro Akaboshi

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Shinjiro Akaboshi

This figure shows the co-authorship network connecting the top 25 collaborators of Shinjiro Akaboshi. A scholar is included among the top collaborators of Shinjiro Akaboshi 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 Shinjiro Akaboshi. Shinjiro Akaboshi 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.
Togawa, Masami, et al.. (2020). Prevalence and clinical characteristics of children with medical complexity in Tottori Prefecture, Japan: A population-based longitudinal study. Brain and Development. 42(10). 747–755. 8 indexed citations
2.
Abe, Yuichi, Tetsuro Sakai, Akihisa Okumura, et al.. (2016). Manifestations and characteristics of congenital adrenal hyperplasia-associated encephalopathy. Brain and Development. 38(7). 638–647. 16 indexed citations
3.
Shimojima, Keiko, Shino Shimada, Akiko Tamasaki, et al.. (2013). Novel compound heterozygous mutations of POLR3A revealed by whole-exome sequencing in a patient with hypomyelination. Brain and Development. 36(4). 315–321. 19 indexed citations
4.
Torisu, Hiroyuki, Toshiyuki Yamamoto, Mitsutaka Kadota, et al.. (2004). Girl with monosomy 1p36 and Angelman syndrome due to unbalanced der(1) transmission of a maternal translocation t(1;15)(p36.3;q13.1). American Journal of Medical Genetics Part A. 131A(1). 94–98. 21 indexed citations
5.
Akaboshi, Shinjiro, Boris M. Hogema, Andrea Novelletto, et al.. (2003). Mutational spectrum of the succinate semialdehyde dehydrogenase (ALDH5A1) gene and functional analysis of 27 novel disease-causing mutations in patients with SSADH deficiency. Human Mutation. 22(6). 442–450. 96 indexed citations
6.
Boyl, Pietro Pilo, Mario Ledda, Andrea Novelletto, et al.. (2002). Structure of human succinic semialdehyde dehydrogenase gene: identification of promoter region and alternatively processed isoforms. Molecular Genetics and Metabolism. 76(4). 348–362. 45 indexed citations
7.
Yamamoto, Toshiyuki, et al.. (2001). Forced normalization induced by ethosuximide therapy in a patient with intractable myoclonic epilepsy. Brain and Development. 23(1). 62–64. 12 indexed citations
8.
Akaboshi, Shinjiro, et al.. (2000). Unilateral Involuntary Movement Associated with Streptococcal Infection: Neurophysiological Investigation. Neuropediatrics. 31(2). 70–74. 6 indexed citations
9.
Akaboshi, Shinjiro, Masaki Yoshimura, Toshiro Hara, et al.. (2000). A Case of Høyeraal-Hreidarsson Syndrome: Delayed Myelination and Hypoplasia of Corpus Callosum are Other Important Signs. Neuropediatrics. 31(3). 141–144. 15 indexed citations
10.
Akaboshi, Shinjiro & Kenzo Takeshita. (2000). A case of atypical absence seizures induced by leuprolide acetate. Pediatric Neurology. 23(3). 266–268. 6 indexed citations
11.
12.
Akaboshi, Shinjiro, et al.. (2000). Case of a mentally retarded child with non‐24 hour sleep–wake syndrome caused by deficiency of melatonin secretion. Psychiatry and Clinical Neurosciences. 54(3). 379–380. 16 indexed citations
13.
Akaboshi, Shinjiro, Tatsuya Koeda, & Sadataka Houdou. (1998). 一過性 Extreme Spindle を示した亜急性マイコプラスマ脳炎の一例. Pediatrics International. 40(5). 479–482. 1 indexed citations
14.
Watanabe, Yasuhiro, Shinjiro Akaboshi, Gen Ishida, et al.. (1998). Increased levels of GM2 ganglioside in fibroblasts from a patient with juvenile Niemann–Pick disease type C. Brain and Development. 20(2). 95–97. 29 indexed citations
15.
Akaboshi, Shinjiro, Tatsuya Koeda, & Sadataka Houdou. (1998). Transient extreme spindles in a case of subacute Mycoplasma pneumoniae encephalitis. Pediatrics International. 40(5). 479–482. 7 indexed citations
16.
Toyoshima, Mitsuo, Toshiro Hara, Haidi Zhang, et al.. (1998). Ataxia‐telangiectasia without immunodeficiency: Novel point mutations within and adjacent to the phosphatidylinositol 3‐kinase‐like domain. American Journal of Medical Genetics. 75(2). 141–144. 1 indexed citations
17.
Akaboshi, Shinjiro, et al.. (1997). Peroxisomal bifunctional enzyme deficiency: serial neurophysiological examinations of a case. Brain and Development. 19(4). 295–299. 6 indexed citations
18.
Kato, Toshinori, Masami Nishina, Kazuhiro Matsushita, et al.. (1997). Increased cerebral choline-compounds in Duchenne muscular dystrophy. Neuroreport. 8(6). 1435–1437. 18 indexed citations
19.
Yano, Tamami, Miyako Taniguchi, Shinjiro Akaboshi, et al.. (1996). Accumulation of GM2 Ganglioside in Niemann-Pick Disease Type C Fibroblasts.. Proceedings of the Japan Academy Series B. 72(10). 214–219. 25 indexed citations
20.
Yuasa, Isao, et al.. (1992). The carbohydrate deficient glycoprotein syndrome in three Japanese children. Brain and Development. 14(1). 30–35. 49 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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