Kayoko Sudo

891 total citations
35 papers, 666 citations indexed

About

Kayoko Sudo is a scholar working on Molecular Biology, Clinical Biochemistry and Surgery. According to data from OpenAlex, Kayoko Sudo has authored 35 papers receiving a total of 666 indexed citations (citations by other indexed papers that have themselves been cited), including 23 papers in Molecular Biology, 9 papers in Clinical Biochemistry and 7 papers in Surgery. Recurrent topics in Kayoko Sudo's work include Metabolism and Genetic Disorders (9 papers), Biochemical and Molecular Research (7 papers) and Cancer, Hypoxia, and Metabolism (6 papers). Kayoko Sudo is often cited by papers focused on Metabolism and Genetic Disorders (9 papers), Biochemical and Molecular Research (7 papers) and Cancer, Hypoxia, and Metabolism (6 papers). Kayoko Sudo collaborates with scholars based in Japan, United States and South Korea. Kayoko Sudo's co-authors include Masato Maekawa, Takashi Kanno, Steven S.‐L. Li, Katsuhiro Fukutake, Nishio Honda, Shinji Kanda, Kazuo Kotani, Dilip Dey, Takashi Kanno and Akihiro Ohnishi and has published in prestigious journals such as Biochemical and Biophysical Research Communications, Genome Research and Human Molecular Genetics.

In The Last Decade

Kayoko Sudo

35 papers receiving 635 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Kayoko Sudo Japan 14 345 149 110 105 90 35 666
Josep M. Lluis Spain 11 619 1.8× 287 1.9× 58 0.5× 85 0.8× 26 0.3× 15 1.0k
Fanny Robbesyn France 12 292 0.8× 67 0.4× 39 0.4× 73 0.7× 40 0.4× 15 707
Kozo Ishidate Japan 16 500 1.4× 101 0.7× 94 0.9× 47 0.4× 12 0.1× 29 754
H Jamil Canada 15 705 2.0× 117 0.8× 103 0.9× 90 0.9× 17 0.2× 27 1.2k
Rosanna C. Mirabile United States 13 580 1.7× 148 1.0× 22 0.2× 155 1.5× 34 0.4× 20 1.1k
Albert L. Shroads United States 14 577 1.7× 281 1.9× 133 1.2× 71 0.7× 14 0.2× 20 908
W C King United States 11 574 1.7× 147 1.0× 22 0.2× 67 0.6× 61 0.7× 14 942
Yoshiki Amuro Japan 17 341 1.0× 87 0.6× 27 0.2× 28 0.3× 104 1.2× 52 735
Janna C. Collins United States 12 566 1.6× 48 0.3× 296 2.7× 136 1.3× 14 0.2× 24 867

Countries citing papers authored by Kayoko Sudo

Since Specialization
Citations

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

Fields of papers citing papers by Kayoko Sudo

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Kayoko Sudo

This figure shows the co-authorship network connecting the top 25 collaborators of Kayoko Sudo. A scholar is included among the top collaborators of Kayoko Sudo 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 Kayoko Sudo. Kayoko Sudo 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.
Ohnishi, Akihiro, et al.. (2004). Genetic and immunological analyses of patients with increased serum butyrylcholinesterase activity and its C5 variant form. Clinical Chemistry and Laboratory Medicine (CCLM). 42(9). 991–6. 10 indexed citations
2.
3.
Sudo, Kayoko, et al.. (1997). Human Butyrylcholinesterase L330I Mutation Belongs to a Fluoride-Resistant Gene, by Expression in Human Fetal Kidney Cells. Biochemical and Biophysical Research Communications. 240(2). 372–375. 7 indexed citations
4.
Maekawa, Masato, et al.. (1995). Genetic basis of the silent phenotype of serum butyrylcholinesterase in three compound heterozygotes. Clinica Chimica Acta. 235(1). 41–57. 21 indexed citations
5.
Sudo, Kayoko, et al.. (1994). Premature termination mutations in two patients with deficiency of lactate dehydrogenase H(B) subunit. Clinical Chemistry. 40(8). 1567–1570. 8 indexed citations
6.
7.
Maekawa, Masato, et al.. (1994). A novel deletion mutation of lactate dehydrogenase A(M) gene in the fifth family with the enzyme deficiency. Human Molecular Genetics. 3(5). 825–826. 11 indexed citations
8.
Maekawa, Masato, Kayoko Sudo, Kiyotaka Fujita, et al.. (1994). DNA analysis of slow type of electrophoretic lactate dehydrogenase B(H) variant.. SEIBUTSU BUTSURI KAGAKU. 38(1). 25–29. 2 indexed citations
9.
Maekawa, Masato, Kayoko Sudo, & Takashi Kanno. (1993). Search for improved electrophoretic conditions for PCR--single-strand conformation polymorphism analysis: is an SDS buffer condition useful.. Genome Research. 3(2). 130–132. 7 indexed citations
10.
Maekawa, Masato, et al.. (1993). Analysis of a genetic mutation in an electrophoretic variant of the human lactate dehydrogenase-B(H) subunit. Human Genetics. 91(5). 423–6. 13 indexed citations
11.
Sudo, Kayoko, Masato Maekawa, Makoto Shioya, et al.. (1992). Molecular analysis of genetic mutation in electrophoretic variant of human lactate dehydrogenase-A(M) subunit.. PubMed. 27(6). 1051–7. 4 indexed citations
12.
Sudo, Kayoko, et al.. (1992). Molecular characterization of genetic mutations in human lactate dehydrogenase (LDH) B (H) variant. Human Genetics. 89(2). 158–62. 10 indexed citations
13.
Maekawa, Masato, Kayoko Sudo, Steven S.‐L. Li, & Takashi Kanno. (1991). Analysis of genetic mutations in human lactate dehydrogenase-A(M) deficiency using DNA conformation polymorphism in combination with polyacrylamide gradient gel and silver staining. Biochemical and Biophysical Research Communications. 180(2). 1083–1090. 25 indexed citations
14.
Sudo, Kayoko, et al.. (1990). A missense mutation found in human lactate dehydrogenase-B (H) variant gene. Biochemical and Biophysical Research Communications. 168(2). 672–676. 13 indexed citations
15.
Kanno, Takashi, et al.. (1988). Lactate dehydrogenase M-subunit deficiency: a new type of hereditary exertional myopathy. Clinica Chimica Acta. 173(1). 89–98. 113 indexed citations
16.
Maekawa, Masato, et al.. (1986). A case of rheumatoid arthritis with various enzyme-immunoglobulin complexes. Clinica Chimica Acta. 157(1). 45–53. 13 indexed citations
17.
18.
Sudo, Kayoko, et al.. (1985). Immunochemical properties of immunoglobulin G conjugated with lactate dehydrogenase.. Clinical Chemistry. 31(7). 1178–1181. 11 indexed citations
19.
Sudo, Kayoko, et al.. (1980). Hereditary deficiency of lactate dehydrogenase M-subunit. Clinica Chimica Acta. 108(2). 267–276. 95 indexed citations
20.
Sudo, Kayoko, et al.. (1977). Properties of amylase-linked immunoglobulins. Clinica Chimica Acta. 76(1). 67–77. 28 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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