Seiichi Tsujino

2.3k total citations
73 papers, 1.7k citations indexed

About

Seiichi Tsujino is a scholar working on Molecular Biology, Rheumatology and Clinical Biochemistry. According to data from OpenAlex, Seiichi Tsujino has authored 73 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 46 papers in Molecular Biology, 32 papers in Rheumatology and 20 papers in Clinical Biochemistry. Recurrent topics in Seiichi Tsujino's work include Glycogen Storage Diseases and Myoclonus (24 papers), Metabolism and Genetic Disorders (20 papers) and RNA regulation and disease (13 papers). Seiichi Tsujino is often cited by papers focused on Glycogen Storage Diseases and Myoclonus (24 papers), Metabolism and Genetic Disorders (20 papers) and RNA regulation and disease (13 papers). Seiichi Tsujino collaborates with scholars based in Japan, United States and Italy. Seiichi Tsujino's co-authors include Sara Shanske, S. DiMauro, Salvatore DiMauro, Naomi Kanazawa, Takanari Miyamoto, Saburo Sakoda, Rochelle Hirschhorn, Ikuya Nonaka, Andrew G. Engel and Paola Tonin and has published in prestigious journals such as New England Journal of Medicine, Journal of Biological Chemistry and Molecular and Cellular Biology.

In The Last Decade

Seiichi Tsujino

70 papers receiving 1.7k citations

Peers

Seiichi Tsujino

RHEUM

PHYSI

GENET

Denise Cassandrini Italy

Callum Wilson New Zealand

Helena Hůlková Czechia

Edoardo Malfatti France

Shuichi Yatsuga Japan

Shoichi Takikita United States

Luc Régal Belgium

J. Ledvinová Czechia

Sari Kiuru‐Enari Finland

Sindu Krishna United States

Denise Cassandrini Italy

Seiichi Tsujino

315 ×0.4

RHEUM

735 ×0.9

252 ×0.4

PHYSI

176 ×0.5

GENET

228 ×0.9

Citations per year, relative to Seiichi Tsujino Seiichi Tsujino (= 1×) peers Denise Cassandrini

Countries citing papers authored by Seiichi Tsujino

Since Specialization

Citations

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

Fields of papers citing papers by Seiichi Tsujino

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Seiichi Tsujino

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

Nishio, T., N Sunohara, Ikuya Nonaka, Seiichi Tsujino, & Hideo Sugie. (2009). Case report Myophosphorylase deficiency and limb-girdle muscular dystrophy in the same pedigree. Acta Neurologica Scandinavica. 98(5). 364–367.

Torisu, Hiroyuki, Ryutaro Kira, Naomi Kanazawa, et al.. (2006). A novel R275X mutation of the SLC25A15 gene in a Japanese patient with the HHH syndrome. Brain and Development. 28(5). 332–335. 5 indexed citations

Asahina, Naoko, Takayuki Okamoto, Akira Sudo, et al.. (2005). An infantile–juvenile form of Alexander disease caused by a R79H mutation in GFAP. Brain and Development. 28(2). 131–133. 9 indexed citations

Feng, Jianhua, Toshiyuki Yamamoto, Yuki Ohsaki, et al.. (2003). New GAA mutations in japanese patients with GSDII (pompe disease). Pediatric Neurology. 29(4). 284–287. 18 indexed citations

Miyamoto, Takeshi, Naomi Kanazawa, Chiemi Hayakawa, & Seiichi Tsujino. (2002). A novel mutation, P126R, in a Japanese patient with HHH syndrome. Pediatric Neurology. 26(1). 65–67. 12 indexed citations

Tsujino, Seiichi, Maryann L. Huie, Naomi Kanazawa, et al.. (2000). Frequent mutations in Japanese patients with acid maltase deficiency. Neuromuscular Disorders. 10(8). 599–603. 31 indexed citations

Tsujino, Seiichi, Nobutsune Ichihara, Hisae Kikuchi, et al.. (1998). Adenovirus-Mediated Transfer of Human Acid Maltase Gene Reduces Glycogen Accumulation in Skeletal Muscle of Japanese Quail with Acid Maltase Deficiency. Human Gene Therapy. 9(11). 1609–1616. 28 indexed citations

Tohyama, Jun, Seiichi Tsujino, Kahei Sato, et al.. (1997). Amelioration of prolidase deficiency in fibroblasts using adenovirus mediated gene transfer. The Japanese Journal of Human Genetics. 42(3). 401–408. 8 indexed citations

Nishio, Takeshi, N Sunohara, Tsuyoshi Yoshihara, et al.. (1996). Small increase in triplet repeat length of cerebellum from patients with myotonic dystrophy. Human Genetics. 98(2). 138–140. 38 indexed citations

10.

Toscano, António, Seiichi Tsujino, Giuseppe Vita, et al.. (1996). Molecular basis of muscle phosphoglycerate mutase (PGAM-M) deficiency in the Italian kindred. Muscle & Nerve. 19(9). 1134–1137. 29 indexed citations

11.

Valberg, Stephanie J., Bradford P. Smith, Sara Shanske, et al.. (1995). Myophosphorylase deficiency associated with rhabdomyolysis and exercise intolerance in 6 related charolais cattle. Muscle & Nerve. 18(7). 736–740. 37 indexed citations

12.

Tsujino, Seiichi, Sara Shanske, Ikuya Nonaka, & S. DiMauro. (1995). The molecular genetic basis of myophosphorylase deficiency (McArdle's disease). Muscle & Nerve. 18(S14). S23–S27. 41 indexed citations

13.

Tsujino, Seiichi, Sara Shanske, & Salvatore DiMauro. (1995). Molecular genetic heterogeneity of phosphoglycerate kinase (PGK) deficiency. Muscle & Nerve. 18(S14). S45–S49. 20 indexed citations

14.

Tsujino, Seiichi, Sara Shanske, Andrea Martinuzzi, Terry Heiman‐Patterson, & Salvatore DiMauro. (1995). Two novel missense mutations (E654K, L396P) in caucasian patients with myophosphorylase deficiency (McArdle's disease). Human Mutation. 6(3). 276–277. 15 indexed citations

15.

DiMauro, Salvatore, Seiichi Tsujino, Sara Shanske, & Lewis P. Rowland. (1995). Biochemistry and molecular genetics of human glycogenoses: An overview. Muscle & Nerve. 18(S14). S10–S17. 16 indexed citations

16.

Tsujino, Seiichi, Sara Shanske, Saburo Sakoda, António Toscano, & S. DiMauro. (1995). Molecular genetic studies in muscle phosphoglycerate mutase (PGAM-M) deficiency. Muscle & Nerve. 18(S14). S50–S53. 18 indexed citations

17.

Tsujino, Seiichi, Sara Shanske, A. Keith W. Brownell, Ronald G. Haller, & Salvatore DiMauro. (1994). Molecular genetic studies of muscle lactate dehydrogenase deficiency in white patients. Annals of Neurology. 36(4). 661–665. 36 indexed citations

18.

Nakatsuji, Yuji, Kyoko Hidaka, Seiichi Tsujino, et al.. (1992). A Single MEF-2 Site Is a Major Positive Regulatory Element Required for Transcription of the Muscle-Specific Subunit of the Human Phosphoglycerate Mutase Gene in Skeletal and Cardiac Muscle Cells. Molecular and Cellular Biology. 12(10). 4384–4390. 15 indexed citations

19.

Tsujino, Seiichi, et al.. (1991). Hyperornithinemia, hyperammonemia and homocitrullinuria — a case report and study of ornithine metabolism using in vivo deuterium labelling. Clinica Chimica Acta. 201(1-2). 129–133. 8 indexed citations

20.

Azuma, Tamiko, et al.. (1988). Studies of neurocirculatory effects of long-term L-threo-3, 4-dihydroxyphenylserine administration in a patient with familial amyloidotic polyneuropathy. Acta Neurologica Scandinavica. 77(5). 409–413. 7 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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