N Kanda

754 total citations
21 papers, 628 citations indexed

About

N Kanda is a scholar working on Molecular Biology, Neurology and Genetics. According to data from OpenAlex, N Kanda has authored 21 papers receiving a total of 628 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Molecular Biology, 6 papers in Neurology and 6 papers in Genetics. Recurrent topics in N Kanda's work include Neuroblastoma Research and Treatments (6 papers), DNA Repair Mechanisms (4 papers) and Microtubule and mitosis dynamics (4 papers). N Kanda is often cited by papers focused on Neuroblastoma Research and Treatments (6 papers), DNA Repair Mechanisms (4 papers) and Microtubule and mitosis dynamics (4 papers). N Kanda collaborates with scholars based in Japan, United States and Pakistan. N Kanda's co-authors include H. Kato, Yasuhiko Kaneko, M Sakurai, Nobuo Maseki, G Bruns, Ikuo Okabe, S.A. Latt, Rhona Schreck, Yumi Tsuchida and Takeo Takeda and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nucleic Acids Research and Journal of Clinical Oncology.

In The Last Decade

N Kanda

21 papers receiving 596 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
N Kanda Japan 12 344 279 123 118 89 21 628
K. L. Ying United States 12 267 0.8× 76 0.3× 252 2.0× 51 0.4× 54 0.6× 18 497
Paul J. Saxon United States 10 664 1.9× 55 0.2× 257 2.1× 200 1.7× 275 3.1× 12 1.0k
Zeng Hao Wong United Kingdom 8 389 1.1× 63 0.2× 292 2.4× 85 0.7× 116 1.3× 12 783
Denise Gibbs United States 7 1.1k 3.1× 103 0.4× 116 0.9× 63 0.5× 213 2.4× 9 1.4k
A. Behmel Austria 12 449 1.3× 69 0.2× 527 4.3× 71 0.6× 177 2.0× 18 960
Michael S. Bobola United States 18 618 1.8× 38 0.1× 50 0.4× 152 1.3× 189 2.1× 24 892
Karl Vandepoele Belgium 12 256 0.7× 40 0.1× 122 1.0× 79 0.7× 55 0.6× 23 428
Mark L. Watson United States 14 466 1.4× 29 0.1× 126 1.0× 99 0.8× 80 0.9× 23 808
Kevin R. Leiby United States 9 526 1.5× 83 0.3× 97 0.8× 35 0.3× 98 1.1× 10 855
Y Takahashi Japan 7 152 0.4× 82 0.3× 25 0.2× 24 0.2× 79 0.9× 10 412

Countries citing papers authored by N Kanda

Since Specialization
Citations

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

Fields of papers citing papers by N Kanda

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of N Kanda

This figure shows the co-authorship network connecting the top 25 collaborators of N Kanda. A scholar is included among the top collaborators of N Kanda 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 N Kanda. N Kanda 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.
Sakamaki, Kazuhiro, et al.. (2000). The eosinophil peroxidase gene forms a cluster with the genes for myeloperoxidase and lactoperoxidase on human chromosome 17. Cytogenetic and Genome Research. 88(3-4). 246–248. 19 indexed citations
2.
Nishikawa, Naoko, M Oishi, Ryoiti Kiyama, & N Kanda. (1997). Enrichment of oligo(dG){middle dot}oligo(dC)-containing fragments from human genomic DNA by Mg2+-dependent triplex affinity capture. Nucleic Acids Research. 25(9). 1701–1708. 2 indexed citations
3.
Takeda, Osamu, Masafumi Handa, Takayuki Uehara, et al.. (1996). An increased NM23H1 copy number may be a poor prognostic factor independent of LOH on 1p in neuroblastomas. British Journal of Cancer. 74(10). 1620–1626. 30 indexed citations
4.
Miwa, T., Kiyoshi Kurokawa, Shinji Kamada, et al.. (1991). Structure, chromosome location, and expression of the human smooth muscle (enteric type) gamma-actin gene: evolution of six human actin genes.. Molecular and Cellular Biology. 11(6). 3296–3306. 96 indexed citations
5.
Kaneko, Yasuhiko, N Kanda, Nobuo Maseki, et al.. (1990). Current urinary mass screening for catecholamine metabolites at 6 months of age may be detecting only a small portion of high-risk neuroblastomas: a chromosome and N-myc amplification study.. Journal of Clinical Oncology. 8(12). 2005–2013. 70 indexed citations
6.
Ikeda, Shu‐ichi, Saburo Momita, T Amagasaki, et al.. (1990). Detection of preleukemic state of adult T-cell leukemia (pre-ATL) in HTLV-1 carriers.. PubMed. 14(4). 431–5. 12 indexed citations
7.
Shimatake, Hiroyuki, et al.. (1988). Rearrangement dynamics involved in gene amplification in human neuroblastoma cells.. PubMed. 271. 121–31. 1 indexed citations
8.
Kaneko, Yasuhiko, N Kanda, Nobuo Maseki, et al.. (1987). Different karyotypic patterns in early and advanced stage neuroblastomas.. PubMed. 47(1). 311–8. 145 indexed citations
9.
Latt, S.A., Yosef Shiloh, G M Brodeur, et al.. (1986). Novel DNA rearrangement phenomena associated with DNA amplification in human neuroblastomas and neuroblastoma cell lines.. PubMed. 209A. 601–12. 2 indexed citations
10.
Latt, S.A., M. Lalande, Tim Donlon, et al.. (1986). DNA-based Detection of Chromosome Deletion and Amplification: Diagnostic and Mechanistic Significance. Cold Spring Harbor Symposia on Quantitative Biology. 51(0). 299–307. 2 indexed citations
11.
Kaneko, Yasuhiko, et al.. (1985). Possible relationship of chromosome abnormalities and gene amplification with effects of chemotherapy: a neuroblastoma xenograft study.. PubMed. 175. 171–80. 5 indexed citations
12.
Sakai, K, N Kanda, Yosef Shiloh, et al.. (1985). Molecular and cytologic analysis of DNA amplification in retinoblastoma. Cancer Genetics and Cytogenetics. 17(2). 95–112. 25 indexed citations
13.
Shiloh, Yosef, N Kanda, Louis M. Kunkel, et al.. (1985). Two RFLPs identified by a human chromosome #2 clone at 2p15–2p16 (HGM8 assignment no. D2S5). Nucleic Acids Research. 13(14). 5403–5403. 4 indexed citations
14.
Kanda, N, Rhona Schreck, Frederick W. Alt, et al.. (1983). Isolation of amplified DNA sequences from IMR-32 human neuroblastoma cells: facilitation by fluorescence-activated flow sorting of metaphase chromosomes.. Proceedings of the National Academy of Sciences. 80(13). 4069–4073. 104 indexed citations
15.
Kanda, N & H. Kato. (1980). Analysis of crossing over in mouse meiotic cells by BrdU labelling technique. Chromosoma. 78(1). 113–121. 42 indexed citations
16.
Kanda, N & H. Kato. (1979). A simple technique for in vivo observation of SCE in mouse ascites tumor and spermatogonial cells. Experimental Cell Research. 118(2). 431–434. 29 indexed citations
17.
Kanda, N & Tosihide H. YOSIDA. (1979). Identification of the facultative heterochromatic X chromosome in females of 25 rodent species. Cytogenetic and Genome Research. 23(1-2). 12–22. 6 indexed citations
18.
Kanda, N & H. Kato. (1979). In vivo sister chromatid exchange in cells of various organs of the mouse. Chromosoma. 74(3). 299–305. 19 indexed citations
19.
20.
Kanda, N. (1976). Banding pattern observed in human chromosomes by the modified BSG technique. Human Genetics. 31(3). 283–292. 11 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 K. L. Ying Breakdown of academic impact, for papers by Paul J. Saxon Breakdown of academic impact, for papers by Zeng Hao Wong Breakdown of academic impact, for papers by Denise Gibbs Breakdown of academic impact, for papers by A. Behmel Breakdown of academic impact, for papers by Michael S. Bobola Breakdown of academic impact, for papers by Karl Vandepoele Breakdown of academic impact, for papers by Mark L. Watson Breakdown of academic impact, for papers by Kevin R. Leiby Breakdown of academic impact, for papers by Y Takahashi
Rankless by CCL
2026