Y. Nakamura

1.3k total citations
23 papers, 999 citations indexed

About

Y. Nakamura is a scholar working on Molecular Biology, Cancer Research and Oncology. According to data from OpenAlex, Y. Nakamura has authored 23 papers receiving a total of 999 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 5 papers in Cancer Research and 4 papers in Oncology. Recurrent topics in Y. Nakamura's work include RNA modifications and cancer (4 papers), Genomic variations and chromosomal abnormalities (3 papers) and Cancer Genomics and Diagnostics (3 papers). Y. Nakamura is often cited by papers focused on RNA modifications and cancer (4 papers), Genomic variations and chromosomal abnormalities (3 papers) and Cancer Genomics and Diagnostics (3 papers). Y. Nakamura collaborates with scholars based in Japan, United States and United Kingdom. Y. Nakamura's co-authors include Kazuhiro Yamakawa, Jiro ISHIKAWA, Ryoji Morita, Ei Takahashi, S. Higuchi, Aritoshi Iida, Naoko Hayashi, Akihiro Sekine, S. Kawauchi and Masanobu Ogawa and has published in prestigious journals such as Nucleic Acids Research, Biochemical and Biophysical Research Communications and Environmental Health Perspectives.

In The Last Decade

Y. Nakamura

23 papers receiving 965 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Y. Nakamura Japan 13 546 342 312 185 162 23 999
F Viguié France 21 861 1.6× 302 0.9× 206 0.7× 90 0.5× 131 0.8× 45 1.6k
Yongli Guan United States 18 709 1.3× 165 0.5× 513 1.6× 124 0.7× 231 1.4× 25 1.6k
Sumiko Ohnami Japan 20 734 1.3× 352 1.0× 402 1.3× 211 1.1× 265 1.6× 54 1.3k
Jung‐Ta Chen Taiwan 20 538 1.0× 352 1.0× 246 0.8× 168 0.9× 111 0.7× 34 1.4k
E. Gebhart Germany 19 666 1.2× 209 0.6× 502 1.6× 54 0.3× 260 1.6× 93 1.3k
Erwin T. Waas Netherlands 9 629 1.2× 355 1.0× 381 1.2× 73 0.4× 86 0.5× 11 1.1k
Karin Boman Sweden 18 462 0.8× 247 0.7× 96 0.3× 138 0.7× 152 0.9× 29 1.6k
Stefanie Tauber Austria 15 614 1.1× 223 0.7× 171 0.5× 74 0.4× 103 0.6× 19 1.1k
Abul Elahi United States 17 628 1.2× 252 0.7× 361 1.2× 238 1.3× 84 0.5× 31 1.0k
Emmanuelle Gormally France 10 338 0.6× 176 0.5× 327 1.0× 96 0.5× 80 0.5× 15 710

Countries citing papers authored by Y. Nakamura

Since Specialization
Citations

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

Fields of papers citing papers by Y. Nakamura

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Y. Nakamura

This figure shows the co-authorship network connecting the top 25 collaborators of Y. Nakamura. A scholar is included among the top collaborators of Y. Nakamura 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 Y. Nakamura. Y. Nakamura 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.
Nakamura, Y., et al.. (2025). Coating and culture performance of chemically synthesized scaffold as a culture-surface platform for iPSC manufacturing. Cytotherapy. 27(5). S232–S232. 1 indexed citations
2.
Saito, Susumu, Aritoshi Iida, Akihiro Sekine, et al.. (2002). Catalog of 238 variations among six human genes encoding solute carriers (hSLCs) in the Japanese population. Journal of Human Genetics. 47(11). 576–584. 49 indexed citations
3.
Saito, Susumu, Aritoshi Iida, Akihiro Sekine, et al.. (2002). Identification of 779 genetic variations in eight genes encoding members of the ATP-binding cassette, subfamily C (ABCC/MRP/CFTR). Journal of Human Genetics. 47(4). 147–171. 105 indexed citations
4.
Williams, John G., et al.. (2001). Potential impact of Renibacterium salmoninarum on adult returns of Snake River spring/summer chinook salmon.. 55–59. 4 indexed citations
5.
6.
Isomura, Minoru, Kazushi Izawa, Yasuhiro Fujiwara, et al.. (1996). Isolation of 45 exon-like fragments from 8p22→p21.3, a region that is commonly deleted in hepatocellular, colorectal, and non-small cell lung carcinomas. Cytogenetic and Genome Research. 75(2-3). 190–196. 23 indexed citations
7.
Miura, Koh, Kazufumi Suzuki, Takashi Tokino, et al.. (1996). Detailed deletion mapping in squamous cell carcinomas of the esophagus narrows a region containing a putative tumor suppressor gene to about 200 kilobases on distal chromosome 9q.. PubMed. 56(7). 1629–34. 24 indexed citations
8.
Soejima, Hidenobu, Toshiya Tamura, Takashi Tokino, et al.. (1995). Fifty novel sequence-tagged sites (STSs) on human chromosome 11q13.4→q25 identified from microclones generated by microdissection. Cytogenetic and Genome Research. 70(1-2). 108–111. 1 indexed citations
9.
Hibi, K, Kazuhiro Yamakawa, Ryuzo Ueda, et al.. (1994). Aberrant upregulation of a novel integrin alpha subunit gene at 3p21.3 in small cell lung cancer.. PubMed. 9(2). 611–9. 42 indexed citations
10.
Westbrook, Carol A., Michelle M. Le Beau, W.L. Neuman, et al.. (1994). Physical and genetic map of 5q31: use of fluorescence in situ hybridization data to identify errors in the CEPH database. Cytogenetic and Genome Research. 67(2). 86–93. 11 indexed citations
11.
Liu, Wanguo, Viji Shridhar, Zheng Song, et al.. (1993). The isolation of a yeast artificial chromosome (YAC) contig extending for 2 megabases in the vicinity of the Von Hippel Lindau disease gene. Human Molecular Genetics. 2(8). 1177–1182. 7 indexed citations
12.
Yamakawa, Kazuhiro, Takashi Takahashi, Yoshiyuki Horio, et al.. (1993). Frequent homozygous deletions in lung cancer cell lines detected by a DNA marker located at 3p21.3-p22.. PubMed. 8(2). 327–30. 55 indexed citations
13.
Neuman, W.L., Michael J. Dixon, Rafael Espinosa, et al.. (1993). Physical localization of 70 polymorphic markers to human chromosome 5 by fluorescence in situ hybridization. Cytogenetic and Genome Research. 62(4). 207–210. 2 indexed citations
14.
Crossey, Paul A., Eamonn R. Maher, Michael H. Jones, et al.. (1993). Genetic linkage between Von Hippel—Lindau disease and three microsatellite polymorphisms refines the localisation of the VHL locus. Human Molecular Genetics. 2(3). 279–282. 43 indexed citations
15.
Morita, Ryoji, S. Saito, Jiro ISHIKAWA, et al.. (1991). Common regions of deletion on chromosomes 5q, 6q, and 10q in renal cell carcinoma.. PubMed. 51(21). 5817–20. 133 indexed citations
16.
Yamakawa, Kazuhiro, et al.. (1991). A detailed deletion mapping of the short arm of chromosome 3 in sporadic renal cell carcinoma.. PubMed. 51(17). 4707–11. 125 indexed citations
17.
Franco, Brunella, Diego E. Rincón-Limas, Y. Nakamura, Pragna I. Patel, & J.R. Lupski. (1991). AnMspI RFLP at the D17S258 locus. Nucleic Acids Research. 19(8). 1980–1980. 3 indexed citations
18.
Gatti, Richard A., et al.. (1989). Informativeness of VNTR genetic markers for detecting chimerism after bone marrow transplantation.. PubMed. 7(2). 105–12. 6 indexed citations
19.
Sadler, J. Evan, P. O’Connell, Y. Nakamura, et al.. (1987). Identification and mapping of RFLPs for human tissue factor (HTF) to chromosome 1p. Nucleic Acids Research. 15(21). 9098–9098. 6 indexed citations
20.
Tomita, Ikuyoshi, et al.. (1982). Mutagenic/carcinogenic potential of DEHP and MEHP.. Environmental Health Perspectives. 45. 119–125. 75 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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