Hiroko Nikaido

1.8k total citations
39 papers, 1.5k citations indexed

About

Hiroko Nikaido is a scholar working on Molecular Biology, Clinical Biochemistry and Physiology. According to data from OpenAlex, Hiroko Nikaido has authored 39 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 21 papers in Molecular Biology, 20 papers in Clinical Biochemistry and 13 papers in Physiology. Recurrent topics in Hiroko Nikaido's work include Metabolism and Genetic Disorders (20 papers), Diet and metabolism studies (10 papers) and Mitochondrial Function and Pathology (9 papers). Hiroko Nikaido is often cited by papers focused on Metabolism and Genetic Disorders (20 papers), Diet and metabolism studies (10 papers) and Mitochondrial Function and Pathology (9 papers). Hiroko Nikaido collaborates with scholars based in Japan and United States. Hiroko Nikaido's co-authors include Jun-ichiro Hayakawa, Ikumi Tamai, Yoshimichi Sai, Noriyoshi Hashimoto, Jun‐ichi Nezu, Akira Tsuji, Rikiya Ohashi, Miyuki Shimane, Asuka Oku and Tsutomu Koizumi and has published in prestigious journals such as Journal of Biological Chemistry, Nature Genetics and Hepatology.

In The Last Decade

Hiroko Nikaido

39 papers receiving 1.4k citations

Peers

Hiroko Nikaido
V. Ganapathy United States
Joyce E. Becker United States
Vadivel Ganapathy United States
Rahel Pfeiffer Switzerland
Anne‐Marie Lamhonwah Canada
Arno van Cruchten Netherlands
Lina Zhuang United States
Sylvia J. Downing United States
Guillermina Asins Spain
LaVell M. Henderson United States
V. Ganapathy United States
Hiroko Nikaido
Citations per year, relative to Hiroko Nikaido Hiroko Nikaido (= 1×) peers V. Ganapathy

Countries citing papers authored by Hiroko Nikaido

Since Specialization
Citations

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

Fields of papers citing papers by Hiroko Nikaido

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Hiroko Nikaido

This figure shows the co-authorship network connecting the top 25 collaborators of Hiroko Nikaido. A scholar is included among the top collaborators of Hiroko Nikaido 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 Hiroko Nikaido. Hiroko Nikaido 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.
Inano, Akihiro, Yoshimichi Sai, Hiroko Nikaido, et al.. (2003). Acetyl‐L‐carnitine permeability across the blood–brain barrier and involvement of carnitine transporter OCTN2. Biopharmaceutics & Drug Disposition. 24(8). 357–365. 65 indexed citations
2.
Xiaofei, E, Yasuhiko Wada, Miwako Dakeishi, et al.. (2002). Age-Associated Cardiomyopathy in Heterozygous Carrier Mice of a Pathological Mutation of Carnitine Transporter Gene, OCTN2. The Journals of Gerontology Series A. 57(7). B270–B278. 12 indexed citations
3.
Kido, Yasuto, Ikumi Tamai, Yoshimichi Sai, et al.. (2001). Functional relevance of carnitine transporter OCTN2 to brain distribution ofl‐carnitine and acetyl‐l‐carnitine across the blood–brain barrier. Journal of Neurochemistry. 79(5). 959–969. 142 indexed citations
4.
Yokogawa, Koiçhi, Ikumi Tamai, Rikiya Ohashi, et al.. (1999). Loss of wild-type carrier-mediated L-carnitine transport activity in hepatocytes of juvenile visceral steatosis mice. Hepatology. 30(4). 997–1001. 31 indexed citations
5.
Hashimoto, Noriyoshi, Fumio Suzuki, Ikumi Tamai, et al.. (1998). Gene-Dose Effect on Carnitine Transport Activity in Embryonic Fibroblasts of JVS Mice as a Model of Human Carnitine Transporter Deficiency. Biochemical Pharmacology. 55(10). 1729–1732. 32 indexed citations
6.
Kuwajima, Masamichi, Kangmo Lu, Masako Sei, et al.. (1998). Characteristics of Cardiac Hypertrophy in the Juvenile Visceral Steatosis Mouse with Systemic Carnitine Deficiency. Journal of Molecular and Cellular Cardiology. 30(4). 773–781. 33 indexed citations
7.
Okita, Kohei, Takashi Tokino, Hiroyuki Nishimori, et al.. (1996). Definition of the Locus Responsible for Systemic Carnitine Deficiency within a 1.6-cM Region of Mouse Chromosome 11 by Detailed Linkage Analysis. Genomics. 33(2). 289–291. 13 indexed citations
8.
Hotta, Kikuko, Masamichi Kuwajima, Akira Ono, et al.. (1996). Disordered expression of glycolytic and gluconeogenic liver enzymes of juvenile visceral steatosis mice with systemic carnitine deficiency. Diabetes Research and Clinical Practice. 32(3). 117–123. 14 indexed citations
9.
Miyagawa, Jun‐ichiro, M Kuwajima, Toshiaki Hanafusa, et al.. (1995). Mitochondrial abnormalities of muscle tissue in mice with juvenile visceral steatosis associated with systemic carnitine deficiency. Archiv für Pathologische Anatomie und Physiologie und für Klinische Medicin. 426(3). 271–9. 26 indexed citations
10.
Nikaido, Hiroko, Masahisa Horiuchi, N Hashimoto, Takeyori Saheki, & Jun-ichiro Hayakawa. (1995). Mapping of jvs (juvenile visceral steatosis) gene, which causes systemic carnitine deficiency in mice, on Chromosome 11. Mammalian Genome. 6(5). 369–370. 18 indexed citations
11.
Horiuchi, Masahisa, Keiko Kobayashi, Seiji Yamaguchi, et al.. (1994). Primary defect of juvenile visceral steatosis (jvs) mouse with systemic carnitine deficiency is probably in renal carnitine transport system. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1226(1). 25–30. 73 indexed citations
12.
Horiuchi, Masahisa, Hiroki Yoshida, Keiko Kobayashi, et al.. (1993). Cardiac hypertrophy in juvenile visceral steatosis (jvs) mice with systemic carnitine deficiency. FEBS Letters. 326(1-3). 267–271. 68 indexed citations
13.
Tomomura, Mineko, Yasushi Imamura, Masahisa Horiuchi, et al.. (1992). Abnormal expression of urea cycle enzyme genes in juvenile visceral steatosis (jvs) mice. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1138(2). 167–171. 33 indexed citations
14.
Nikaido, Hiroko, et al.. (1991). Specificity of the sex-influenced esterase (ES-SI) isozyme in rat liver. Biochemical Genetics. 29(5-6). 261–269. 1 indexed citations
15.
Morita, Atsushi, et al.. (1990). Selective purification of sex‐influenced esterase from rat serum by immunoaffinity chromatographies. European Journal of Biochemistry. 189(2). 431–435. 8 indexed citations
16.
Imamura, Yasushi, Takeyori Saheki, Hiroyuki Arakawa, et al.. (1990). Urea cycle disorder in C3H‐H‐2° mice with juvenile steatosis of viscera. FEBS Letters. 260(1). 119–121. 31 indexed citations
17.
Hayakawa, Jun-ichiro & Hiroko Nikaido. (1987). Two types of liver-specific F antigen are encoded by a locus located on chromosome 5 in mice. Immunogenetics. 26(6). 366–369. 7 indexed citations
18.
Hayakawa, Jun-ichiro, Hiroko Nikaido, & Tsutomu Koizumi. (1983). Components of major urinary proteins (MUP's) in the mouse. Journal of Heredity. 74(6). 453–456. 10 indexed citations
19.
Yamada, Junzo, et al.. (1980). Linkage analyses among five esterase loci in the laboratory rat (Rattus norvegicus). Biochemical Genetics. 18(5-6). 433–438. 15 indexed citations
20.
Yamada, Junzo, et al.. (1979). Genetic Variability within and between Outbred Wistar Strains of Rats. EXPERIMENTAL ANIMALS. 28(2). 259–265. 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by V. Ganapathy Breakdown of academic impact, for papers by Joyce E. Becker Breakdown of academic impact, for papers by Vadivel Ganapathy Breakdown of academic impact, for papers by Rahel Pfeiffer Breakdown of academic impact, for papers by Anne‐Marie Lamhonwah Breakdown of academic impact, for papers by Arno van Cruchten Breakdown of academic impact, for papers by Lina Zhuang Breakdown of academic impact, for papers by Sylvia J. Downing Breakdown of academic impact, for papers by Guillermina Asins Breakdown of academic impact, for papers by LaVell M. Henderson
Rankless by CCL
2026