Kayoko Sudo

891 citations

35 papers · 666 indexed · h-index 14

Impact in

Clinical Biochemistry top 5%
- Metabolism and Genetic Disorders
Cancer Research
- Cancer, Hypoxia, and Metabolism

Papers in ⓘ

Clinical Biochemistry 9
- Metabolism and Genetic Disorders 9
Pharmacology 4
- Cholinesterase and Neurodegenerative Diseases 5

Co-authors: Masato Maekawa (26 shared papers)Takashi Kanno (13 shared papers)Steven S.‐L. Li (3 shared papers)Katsuhiro Fukutake (1 shared paper)Nishio Honda (1 shared paper)Shinji Kanda (4 shared papers)Kazuo Kotani (4 shared papers)Dilip Dey (4 shared papers)
Journals: Clinica Chimica Acta (10 papers)Clinical Chemistry (5 papers)Biochemical and Biophysical Research Communications (4 papers)Human Genetics (3 papers)Clinical Biochemistry (2 papers)
Partner nations: Japan United States South Korea

In The Last Decade

Kayoko Sudo

35 papers receiving 635 citations

Peers

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-authors

The 25 scholars most cited alongside Kayoko Sudo, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Kayoko Sudo Line = papers co-authored together Kayoko Sudo links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 35 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Lactate dehydrogenase M-subunit deficiency: a new type of hereditary exertional myopathy Clinica Chimica Acta ·Takashi Kanno, Kayoko Sudo, Masato Maekawa, Y Nishimura, Minoru UKITA, Katsuhiro Fukutake	1988	113
2	Hereditary deficiency of lactate dehydrogenase M-subunit Clinica Chimica Acta ·Kanno Takashi, Kayoko Sudo, Izumi Takeuchi, Shinji Kanda, Nishio Honda, Yoshiro Nishimura, Oyama Kunio	1980	95
3	Molecular characterization of genetic mutation in human lactate dehydrogenase-A (M) deficiency Biochemical and Biophysical Research Communications ·Masato Maekawa, Kayoko Sudo, Takashi Kanno, Steven S.‐L. Li	1990	45
4	Estimation of the gene frequency of lactate dehydrogenase subunit deficiencies. PubMed ·Masato Maekawa, Shinji Kanda, Kayoko Sudo, Takashi Kanno	1984	36
5	Properties of the amylase produced in carcinoma of the lung Clinica Chimica Acta ·Kayoko Sudo, Takashi Kanno	1976	35
6	Genetic mutations of butyrylcholine esterase identified from phenotypic abnormalities in Japan Clinical Chemistry ·Masato Maekawa, Kayoko Sudo, Dilip Dey, Jinko Ishikawa, Masakazu Izumi, Kazuo Kotani, Takashi Kanno	1997	33
7	Properties of amylase-linked immunoglobulins Clinica Chimica Acta ·Kanno Takashi, Kayoko Sudo	1977	28
8	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 ·Masato Maekawa, Kayoko Sudo, Steven S.‐L. Li, Takashi Kanno	1991	25
9	Genetic basis of the silent phenotype of serum butyrylcholinesterase in three compound heterozygotes Clinica Chimica Acta ·Masato Maekawa, Kayoko Sudo, Takashi Kanno, Kazuo Kotani, Dilip Dey, Jinko Ishikawa, Masakazu Izumi, Koki Etoh	1995	21
10	A novel in-frame deletion mutation in a case of lactate dehydrogenase (LD) H subunit deficiency showing an atypical LD isoenzyme pattern in serum and erythrocytes Clinical Biochemistry ·Kayoko Sudo, Masato Maekawa, Nobuyuki Houki, T. Okuda, Setsuko Akizuki, Tadao Magara, Kazuhiro Kawano	1999	20
11	Intestinal alkaline phosphatase linked to immunoglobulin G of the kappa type Clinica Chimica Acta ·Hiroaki Kohno, Kayoko Sudo, Kanno Takashi	1983	18
12	Sialic acid containing abnormal amylases in human sera Clinica Chimica Acta ·Kayoko Sudo, Kanno Takashi	1975	17
13	Evaluation of Cytosolic Aminopeptidase in Human Sera: Evaluation in Hepatic Disorders American Journal of Clinical Pathology ·Takashi Kanno, Masato Maekawa, Shinji Kanda, Hiroaki Kohno, Kayoko Sudo	1984	16
14	Characteristics of the complex between alkaline phosphatase and immunoglobulin A in human serum Clinica Chimica Acta ·Masato Maekawa, Kayoko Sudo, Takashi Kanno	1985	14
15	A case of rheumatoid arthritis with various enzyme-immunoglobulin complexes Clinica Chimica Acta ·Masato Maekawa, Kayoko Sudo, Takashi Kanno	1986	13
16	Analysis of a genetic mutation in an electrophoretic variant of the human lactate dehydrogenase-B(H) subunit Human Genetics ·Masato Maekawa, Kayoko Sudo, Masato Kitajima, Yukio Matsuura, StevenS.-L. Li, Takashi Kanno	1993	13
17	A missense mutation found in human lactate dehydrogenase-B (H) variant gene Biochemical and Biophysical Research Communications ·Kayoko Sudo, Masato Maekawa, Sachio Ikawa, Katsuhiko Machida, Motoshi Kitamura, Steven S.‐L. Li	1990	13
18	A novel deletion mutation of lactate dehydrogenase A(M) gene in the fifth family with the enzyme deficiency Human Molecular Genetics ·Masato Maekawa, Kayoko Sudo, Takashi Kanno, Susumu Takayasu, S. Li, Masato Kltajima, Yukio Matsuura	1994	11
19	Immunochemical properties of immunoglobulin G conjugated with lactate dehydrogenase. Clinical Chemistry ·Kayoko Sudo, Masato Maekawa, Takashi Kanno	1985	11
20	Genetic and immunological analyses of patients with increased serum butyrylcholinesterase activity and its C5 variant form Clinical Chemistry and Laboratory Medicine (CCLM) ·Setsuko Akizuki, Akihiro Ohnishi, Kazuo Kotani, Kayoko Sudo	2004	10

About Kayoko Sudo

Kayoko Sudo is a scholar working on Clinical Biochemistry, Pharmacology, Cancer Research, Pharmacology and Biotechnology, having authored 35 papers that have together received 666 indexed citations. Recurring topics across this work include Metabolism and Genetic Disorders (9 papers), Biochemical and Molecular Research (7 papers), Epigenetics and DNA Methylation (6 papers), Cancer, Hypoxia, and Metabolism (6 papers), Pancreatitis Pathology and Treatment (5 papers), Cholinesterase and Neurodegenerative Diseases (5 papers), Peptidase Inhibition and Analysis (4 papers) and Computational Drug Discovery Methods (3 papers). The work is most often cited by research in Clinical Biochemistry (110 citations), Cancer Research (149 citations), Pharmacology (90 citations), Rheumatology (78 citations) and Molecular Biology (345 citations). Kayoko Sudo has collaborated with scholars based in Japan, United States and South Korea. Frequent co-authors include Masato Maekawa, Takashi Kanno, Steven S.‐L. Li, Katsuhiro Fukutake, Nishio Honda, Shinji Kanda, Kazuo Kotani, Dilip Dey, Takashi Kanno and Katsuhiko Machida. Their work appears in journals such as Clinica Chimica Acta, Clinical Chemistry, Biochemical and Biophysical Research Communications, Human Genetics and Clinical Biochemistry.

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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