Mayumi Nishimura

1.2k total citations
68 papers, 1.0k citations indexed

About

Mayumi Nishimura is a scholar working on Molecular Biology, Radiology, Nuclear Medicine and Imaging and Oncology. According to data from OpenAlex, Mayumi Nishimura has authored 68 papers receiving a total of 1.0k indexed citations (citations by other indexed papers that have themselves been cited), including 27 papers in Molecular Biology, 26 papers in Radiology, Nuclear Medicine and Imaging and 21 papers in Oncology. Recurrent topics in Mayumi Nishimura's work include Effects of Radiation Exposure (21 papers), Radiation Therapy and Dosimetry (15 papers) and DNA Repair Mechanisms (14 papers). Mayumi Nishimura is often cited by papers focused on Effects of Radiation Exposure (21 papers), Radiation Therapy and Dosimetry (15 papers) and DNA Repair Mechanisms (14 papers). Mayumi Nishimura collaborates with scholars based in Japan, United States and China. Mayumi Nishimura's co-authors include Yoshiya Shimada, Shizuko Kakinuma, Tatsuhiko Imaoka, Kazuhiro Daino, Yukiko Nishimura, Daisuke Iizuka, Takashi Takabatake, Masaru Takabatake, Toshiaki Kokubo and Hiroshi Ueno and has published in prestigious journals such as PLoS ONE, Chemical Communications and International Journal of Radiation Oncology*Biology*Physics.

In The Last Decade

Mayumi Nishimura

68 papers receiving 983 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Mayumi Nishimura Japan	19	373	369	252	248	247	68	1.0k
C. Luccioni France	17	434 1.2×	184 0.5×	194 0.8×	178 0.7×	138 0.6×	32	864
Akihito Nishioka Japan	19	265 0.7×	260 0.7×	242 1.0×	354 1.4×	213 0.9×	88	1.1k
Tsutomu Shimura Japan	31	1.3k 3.5×	415 1.1×	439 1.7×	547 2.2×	281 1.1×	72	2.1k
Benjamin J. Blyth Australia	18	268 0.7×	529 1.4×	181 0.7×	151 0.6×	363 1.5×	59	921
Fangyu Peng United States	22	288 0.8×	261 0.7×	390 1.5×	60 0.2×	165 0.7×	60	1.3k
Zhikun Liu China	23	653 1.8×	96 0.3×	411 1.6×	394 1.6×	259 1.0×	115	1.5k
Xiaobo Li China	25	635 1.7×	109 0.3×	283 1.1×	274 1.1×	271 1.1×	68	1.6k
Jiřina Vávrová Czechia	19	656 1.8×	231 0.6×	295 1.2×	178 0.7×	99 0.4×	98	1.2k
Ravi S. Harapanhalli United States	16	410 1.1×	190 0.5×	204 0.8×	108 0.4×	151 0.6×	27	1.1k
Sha Zhu China	18	416 1.1×	102 0.3×	362 1.4×	245 1.0×	328 1.3×	88	1.2k

Countries citing papers authored by Mayumi Nishimura

Since Specialization

Citations

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

Fields of papers citing papers by Mayumi Nishimura

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Mayumi Nishimura

This figure shows the co-authorship network connecting the top 25 collaborators of Mayumi Nishimura. A scholar is included among the top collaborators of Mayumi Nishimura 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 Mayumi Nishimura. Mayumi Nishimura is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Nagata, K., Mayumi Nishimura, Kazuhiro Daino, et al.. (2024). Luminal progenitor and mature cells are more susceptible than basal cells to radiation-induced DNA double-strand breaks in rat mammary tissue. Journal of Radiation Research. 65(5). 640–650. 2 indexed citations

Nishimura, Yukiko, Daisuke Iizuka, Masaru Takabatake, et al.. (2024). Characterization of Molecular Subtypes of Rat Mammary Cancer and Their Association With Environmental Exposures. Anticancer Research. 44(10). 4261–4272. 1 indexed citations

Imaoka, Tatsuhiko, Mayumi Nishimura, Kazuhiro Daino, et al.. (2022). DOSE-RATE EFFECT OF RADIATION ON RAT MAMMARY CARCINOGENESIS AND AN EMERGING ROLE FOR STEM CELL BIOLOGY. Radiation Protection Dosimetry. 198(13-15). 1036–1046. 2 indexed citations

Nishimura, Yukiko, K. Nagata, Mayumi Nishimura, et al.. (2022). Brca1^L63X^/+ rat is a novel model of human BRCA1 deficiency displaying susceptibility to radiation‐induced mammary cancer. Cancer Science. 113(10). 3362–3375. 11 indexed citations

Nishimura, Mayumi, Tatsuhiko Imaoka, Kazuhiro Daino, et al.. (2022). Copenhagen Rats Display Dominantly Inherited Yet Non-uniform Resistance to Spontaneous, Radiation-induced, and Chemically-induced Mammary Carcinogenesis. Anticancer Research. 42(5). 2415–2423. 2 indexed citations

Nishimura, Mayumi, Kazuhiro Daino, Yukiko Nishimura, et al.. (2021). Development of mammary cancer in γ-irradiated F1 hybrids of susceptible Sprague-Dawley and resistant Copenhagen rats, with copy-number losses that pinpoint potential tumor suppressors. PLoS ONE. 16(8). e0255968–e0255968. 5 indexed citations

Daino, Kazuhiro, Atsuko Ishikawa, Tatsuhiko Imaoka, et al.. (2021). Exome of Radiation-induced Rat Mammary Carcinoma Shows Copy-number Losses and Mutations in Human-relevant Cancer Genes. Anticancer Research. 41(1). 55–70. 7 indexed citations

Morioka, Takamitsu, Benjamin J. Blyth, Tatsuhiko Imaoka, et al.. (2019). Establishing the Japan-Store house of animal radiobiology experiments (J-SHARE), a large-scale necropsy and histopathology archive providing international access to important radiobiology data. International Journal of Radiation Biology. 95(10). 1372–1377. 29 indexed citations

Imaoka, Tatsuhiko, Mayumi Nishimura, Kazuhiro Daino, et al.. (2018). Risk of second cancer after ion beam radiotherapy: insights from animal carcinogenesis studies. International Journal of Radiation Biology. 95(10). 1431–1440. 12 indexed citations

10.

Takabatake, Takashi, Shizuko Kakinuma, Kazutaka Doi, et al.. (2010). Genomic and gene expression signatures of radiation in medulloblastomas after low-dose irradiation in Ptch1 heterozygous mice. Carcinogenesis. 31(9). 1694–1701. 20 indexed citations

11.

Kokubo, Toshiaki, Shizuko Kakinuma, Toshiyuki Kobayashi, et al.. (2009). Age dependence of radiation‐induced renal cell carcinomas in an Eker rat model. Cancer Science. 101(3). 616–623. 16 indexed citations

12.

Yamaya, Taiga, Eiji Yoshida, Chie Toramatsu, et al.. (2009). Preliminary study on potential of the jPET-D4 human brain scanner for small animal imaging. Annals of Nuclear Medicine. 23(2). 183–190. 10 indexed citations

13.

Kobayashi, Shigeru, Mayumi Nishimura, Yoshiya Shimada, et al.. (2007). Existence of a threshold-like dose for γ-ray induction of thymic lymphomas and no susceptibility to radiation-induced solid tumors in SCID mice. Mutation research. Fundamental and molecular mechanisms of mutagenesis. 619(1-2). 124–133. 11 indexed citations

14.

Takabatake, Takashi, Katsuyoshi Fujikawa, Satoshi Tanaka, et al.. (2006). Array-CGH Analyses of Murine Malignant Lymphomas: Genomic Clues to Understanding the Effects of Chronic Exposure to Low-Dose-Rate Gamma Rays on Lymphomagenesis. Radiation Research. 166(1). 61–72. 10 indexed citations

15.

Kakinuma, Shizuko, Mayumi Nishimura, Junya Nagai, et al.. (2005). Frequent retention of heterozygosity for point mutations in p53 and Ikaros in N-ethyl-N-nitrosourea-induced mouse thymic lymphomas. Mutation research. Fundamental and molecular mechanisms of mutagenesis. 572(1-2). 132–141. 17 indexed citations

16.

Ogiu, Toshiaki, Mayumi Nishimura, Yasushi Ohmachi, et al.. (2003). 195 Translesion DNA polymerases and mutations induced in a plasmid with a single adduct of 3-nitrobenzanthrone in SOS-induced Escherichia coli(Mutation, Abstracts of the 46th Annual Meeting of the Japan Radiation Research Society) :. Journal of Radiation Research. 44(4). 434–435. 1 indexed citations

17.

Kakinuma, Shizuko, Mayumi Nishimura, Kazuei Mita, et al.. (2002). Spectrum of Znfn1a1 (Ikaros) Inactivation and its Association with Loss of Heterozygosity in Radiogenic T-Cell Lymphomas in Susceptible B6C3F1 Mice. Radiation Research. 157(3). 331–340. 29 indexed citations

18.

Nishimura, Mayumi, Shizuko Kakinuma, Shigeharu Wakana, et al.. (2001). Reduced sensitivity to and ras mutation spectrum of N-ethyl-N-nitrosourea-induced thymic lymphomas in adult C.B-17 scid mice. Mutation Research/DNA Repair. 486(4). 275–283. 5 indexed citations

19.

Shimada, Yoshiya, Mayumi Nishimura, Shizuko Kakinuma, et al.. (2000). Radiation-Associated Loss of Heterozygosity at theZnfn1a1(Ikaros) Locus on Chromosome 11 in Murine Thymic Lymphomas. Radiation Research. 154(3). 293–300. 46 indexed citations

20.

Ogiu, Toshiaki, Hiroko Fukami, Mayumi Nishimura, & Mutsushi Matsuyama. (1995). Genetic Regulation of Development of Thymic Lymphomas Induced by N‐Propyl‐N‐nitrosourea in the Rat. Japanese Journal of Cancer Research. 86(7). 638–644. 1 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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