T Orii

658 total citations
28 papers, 538 citations indexed

About

T Orii is a scholar working on Molecular Biology, Clinical Biochemistry and Physiology. According to data from OpenAlex, T Orii has authored 28 papers receiving a total of 538 indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Molecular Biology, 12 papers in Clinical Biochemistry and 9 papers in Physiology. Recurrent topics in T Orii's work include Metabolism and Genetic Disorders (12 papers), Peroxisome Proliferator-Activated Receptors (10 papers) and Lysosomal Storage Disorders Research (5 papers). T Orii is often cited by papers focused on Metabolism and Genetic Disorders (12 papers), Peroxisome Proliferator-Activated Receptors (10 papers) and Lysosomal Storage Disorders Research (5 papers). T Orii collaborates with scholars based in Japan, United States and Netherlands. T Orii's co-authors include Nobuyuki Shimozawa, Taroh Kinoshita, Junji Takeda, Norimitsu Inoue, Yasuyuki Suzuki, Sanzo Miyazawa, Seiji Yamaguchi, Seiji Fukuda, Takashi Osumi and Takashi Hashimoto and has published in prestigious journals such as Journal of Biological Chemistry, Journal of Clinical Investigation and Nature Genetics.

In The Last Decade

T Orii

28 papers receiving 523 citations

Peers

T Orii

PHYSI

EPIDE

IMMUN

Izumi Akaboshi Japan

A Yam United States

S Tzall United States

Edwin C.J.M. de Vet Netherlands

Aikaterini Dimopoulou Greece

J. A. Barranger United States

Karin Huijben Netherlands

Martin Hasilik Germany

Carin A. F. Buskens Netherlands

Romain Péanne Belgium

Izumi Akaboshi Japan

T Orii

237 ×0.6

58 ×0.3

PHYSI

262 ×1.7

24 ×0.3

EPIDE

13 ×0.2

IMMUN

Citations per year, relative to T Orii T Orii (= 1×) peers Izumi Akaboshi

Countries citing papers authored by T Orii

Since Specialization

Citations

This map shows the geographic impact of T Orii'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 T Orii with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites T Orii more than expected).

Fields of papers citing papers by T Orii

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of T Orii

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

Fukuda, Seiji, Yasuyuki Suzuki, Nobuyuki Shimozawa, et al.. (1998). Amino acid and nucleotide sequences of human peroxisomal enoyl‐CoA hydratase : 3‐hydroxyacyl‐CoA dehydrogenase cDNA. Journal of Inherited Metabolic Disease. 21(1). 23–28. 3 indexed citations

Shimozawa, Nobuyuki, Yasuyuki Suzuki, Atsushi Imamura, et al.. (1998). Peroxisome Biogenesis Disorders: Identification of a New Complementation Group Distinct from Peroxisome-Deficient CHO Mutants and Not Complemented by Human PEX 13. Biochemical and Biophysical Research Communications. 243(2). 368–371. 19 indexed citations

Sukegawa, Kazuko, Xiang‐Qian Song, Mitsuo Masuno, et al.. (1997). Hunter disease in a girl caused by R468Q mutation in the iduronate-2-sulfatase gene and skewed inactivation of the X chromosome carrying the normal allele. Human Mutation. 10(5). 361–367. 20 indexed citations

Orii, Kenji E., Toshifumi Aoyama, Masayoshi Souri, et al.. (1996). Formation of the Enzyme Complex in Mitochondria Is Required for Function of Trifunctional β-Oxidation Protein. Biochemical and Biophysical Research Communications. 219(3). 773–777. 14 indexed citations

Suzuki, Yasuyuki, et al.. (1996). Incidence of peroxisomal disorders in Japan. The Japanese Journal of Human Genetics. 41(1). 167–175. 11 indexed citations

Fukuda, Seiji, Shunji Tomatsu, Alan Cooper, et al.. (1996). Mucopolysaccharidosis IVA (Morquio A): Three novel small deletions in the N-acetylgalactosamine-6-sulfate sulfatase gene. Human Mutation. 8(2). 187–190. 13 indexed citations

Shinnoh, Nobue, Takeshi Yamada, Hirokazu Furuya, et al.. (1995). Adrenoleukodystrophy: The Restoration of Peroxisomal β-Oxidaton by Transfection of Normal cDNA. Biochemical and Biophysical Research Communications. 210(3). 830–836. 38 indexed citations

Miura, Satoshi, Toshiki Nakai, Sadaki Yokota, et al.. (1995). Peroxisome assembly factor–2, a putative ATPase cloned by functional complementation on a peroxisome–deficient mammalian cell mutant. Nature Genetics. 11(4). 395–401. 90 indexed citations

Tomatsu, Shunji, Seiji Fukuda, Atsushi Uchiyama, et al.. (1995). Mucopolysaccharidosis IVA: polymorphic haplotypes and informative RFLPs in the Japanese population. Human Genetics. 95(3). 257–64. 18 indexed citations

10.

Imamura, Atsushi, Yumiko Komori, Osamu Fukutomi, et al.. (1994). Short latency somatosensory evoked potentials and 99mTc-HMPAO SPECT in a case of flunarizine-effective alternating hemiplegia in infancy. Brain and Development. 16(4). 325–328. 2 indexed citations

11.

Fukao, Toshiyuki, et al.. (1994). Molecular Cloning and Nucleotide Sequence of Complementary DNA for Human Hepatic Cytosolic Acetoacetyl-Coenzyme A Thiolase. Biochemical and Biophysical Research Communications. 201(1). 478–485. 34 indexed citations

12.

Maeda, Keiko, Yasuyuki Suzuki, Junichi Asano, et al.. (1992). Improvement of clinical and MM findings in a boy with adrenoleukodystrophy by dietary erucic acid therapy. Brain and Development. 14(6). 409–412. 7 indexed citations

13.

Sukegawa, Kazuko, et al.. (1991). Purification and Partial Characterization of α-N-Acetylglucosaminidase from Human Liver1. The Journal of Biochemistry. 110(5). 842–846. 11 indexed citations

14.

Tomatsu, Shunji, et al.. (1990). Molecular basis of mucopolysaccharidosis type VII: replacement of Ala619 in β-glucuronidase with Val. Gene. 89(2). 283–287. 28 indexed citations

15.

Mori, Seiji, et al.. (1990). Diabetes mellitus in a young man with Bloom's syndrome. Clinical Genetics. 38(5). 387–390. 13 indexed citations

16.

Fukao, Toshiyuki, Seiji Yamaguchi, Hiroyuki Nagasawa, et al.. (1990). Molecular cloning of cDNA for human mitochondrial acetoacetyl‐CoA thiolase and molecular analysis of 3‐ketothiolase deficiency. Journal of Inherited Metabolic Disease. 13(5). 757–760. 6 indexed citations

17.

Naritomi, Kenji, et al.. (1989). Gene assignment of Zellweger syndrome to 7q11.23: report of the second case associated with a pericentric inversion of chromosome 7. Human Genetics. 84(1). 79–80. 16 indexed citations

18.

Yamaguchi, Seiji, T Orii, Nobuo Sakura, Sanzo Miyazawa, & Takashi Hashimoto. (1988). Defect in biosynthesis of mitochondrial acetoacetyl-coenzyme A thiolase in cultured fibroblasts from a boy with 3-ketothiolase deficiency.. Journal of Clinical Investigation. 81(3). 813–817. 46 indexed citations

19.

Suzuki, Yasuyuki, Nobuyuki Shimozawa, T Orii, et al.. (1988). Molecular analysis of peroxisomal β-oxidation enzymes in infants with Zellweger syndrome and Zellweger-like syndrome: Further heterogeneity of the peroxisomal disorder. Clinica Chimica Acta. 172(1). 65–76. 37 indexed citations

20.

Shimozawa, Nobuyuki, Yasuyuki Suzuki, T Orii, & Takashi Hashimoto. (1988). Diagnosis of Zellweger syndrome by rectal biopsy: immunoblot of peroxisomal β-oxidation enzyme and activity of dihydroxyacetone phosphate acyltransferase in rectal mucosa. Clinica Chimica Acta. 175(3). 345–347. 2 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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