Mitsuru Emi

9.6k total citations
192 papers, 6.2k citations indexed

About

Mitsuru Emi is a scholar working on Molecular Biology, Genetics and Cancer Research. According to data from OpenAlex, Mitsuru Emi has authored 192 papers receiving a total of 6.2k indexed citations (citations by other indexed papers that have themselves been cited), including 89 papers in Molecular Biology, 58 papers in Genetics and 50 papers in Cancer Research. Recurrent topics in Mitsuru Emi's work include Genetic factors in colorectal cancer (45 papers), Cancer Genomics and Diagnostics (36 papers) and Genomic variations and chromosomal abnormalities (28 papers). Mitsuru Emi is often cited by papers focused on Genetic factors in colorectal cancer (45 papers), Cancer Genomics and Diagnostics (36 papers) and Genomic variations and chromosomal abnormalities (28 papers). Mitsuru Emi collaborates with scholars based in Japan, United States and United Kingdom. Mitsuru Emi's co-authors include Hisaki Nagai, Fujio Kasumi, Takahiro Nishide, Goi Sakamoto, Kenichi Matsubara, Jean-Marc Lalouel, Masamitsu Onda, Michio Ogawa, Takemitsu Nagahata and Masataka Yoshimoto and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nucleic Acids Research and Nature Genetics.

In The Last Decade

Mitsuru Emi

192 papers receiving 6.1k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Mitsuru Emi Japan 45 3.1k 1.4k 1.4k 1.1k 888 192 6.2k
Svetlana Pack United States 47 3.1k 1.0× 1.1k 0.8× 1.5k 1.1× 1.1k 1.0× 1.4k 1.5× 130 6.5k
Christine Perret France 48 5.4k 1.8× 1.3k 0.9× 1.8k 1.3× 1.4k 1.3× 429 0.5× 158 8.7k
Mario A. Anzano United States 31 3.8k 1.2× 974 0.7× 1.5k 1.1× 758 0.7× 552 0.6× 41 6.0k
Ralf Bützow Finland 53 3.0k 1.0× 1.1k 0.8× 1.8k 1.3× 1.6k 1.5× 770 0.9× 188 7.4k
Javier Benı́tez Spain 51 3.9k 1.3× 2.1k 1.5× 2.2k 1.6× 2.1k 1.9× 619 0.7× 243 7.6k
Yusuke Nakamura Japan 46 3.0k 1.0× 1.2k 0.8× 2.1k 1.5× 1.6k 1.5× 801 0.9× 134 6.6k
Sakari Knuutila Finland 53 3.8k 1.2× 1.4k 1.0× 1.7k 1.2× 1.4k 1.3× 1.1k 1.3× 257 8.4k
Susanne M. Gollin United States 48 4.4k 1.4× 1.3k 0.9× 2.0k 1.5× 1.6k 1.5× 549 0.6× 141 7.2k
Giuseppe Viglietto Italy 48 5.4k 1.7× 663 0.5× 2.3k 1.7× 1.6k 1.4× 803 0.9× 150 8.2k
Carl Morrison United States 45 4.2k 1.4× 865 0.6× 2.3k 1.7× 2.4k 2.2× 1.3k 1.5× 185 8.1k

Countries citing papers authored by Mitsuru Emi

Since Specialization
Citations

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

Fields of papers citing papers by Mitsuru Emi

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Mitsuru Emi

This figure shows the co-authorship network connecting the top 25 collaborators of Mitsuru Emi. A scholar is included among the top collaborators of Mitsuru Emi 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 Mitsuru Emi. Mitsuru Emi 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.
Takahashi, Yuka, Yoshiya Horimoto, Kaoru Mogushi, et al.. (2020). Short somatic alterations at the site of copy number variation in breast cancer. Cancer Science. 112(1). 444–453. 7 indexed citations
2.
Nasu, Masaki, Mitsuru Emi, Sandra Pastorino, et al.. (2015). High Incidence of Somatic BAP1 Alterations in Sporadic Malignant Mesothelioma. Journal of Thoracic Oncology. 10(4). 565–576. 216 indexed citations
3.
Yoshikawa, Yoshie, Ayuko Sato, Tohru Tsujimura, et al.. (2012). Frequent inactivation of the BAP1 gene in epithelioid‐type malignant mesothelioma. Cancer Science. 103(5). 868–874. 137 indexed citations
4.
Kato, Takeo, Chifumi Iseki, Yoshimi Takahashi, et al.. (2010). iNPH (Idiopathic normal pressure hydrocephalus) and AVIM (asymptomatic ventriculomegaly with features of iNPH on MRI). Rinsho Shinkeigaku. 50(11). 963–965. 4 indexed citations
5.
Ichikawa, Kazunobu, Tsuneo Konta, Mitsuru Emi, et al.. (2009). Genetic polymorphisms of paraoxonase-1 are associated with chronic kidney disease in Japanese women. Kidney International. 76(2). 183–189. 10 indexed citations
6.
Takabatake, Noriaki, Yoko Shibata, Shuichi Abe, et al.. (2006). A Single Nucleotide Polymorphism in the CCL1 Gene Predicts Acute Exacerbations in Chronic Obstructive Pulmonary Disease. American Journal of Respiratory and Critical Care Medicine. 174(8). 875–885. 34 indexed citations
7.
Ezura, Yoichi & Mitsuru Emi. (2005). [Genetic analysis of osteoporosis susceptibility: future perspectives on genome wide analysis].. PubMed. 15(5). 762–7. 1 indexed citations
8.
Iwasaki, Tadao, Sadao Takahashi, Mitsuaki Ishihara, et al.. (2004). The important role for βVLDLs binding at the fourth cysteine of first ligand-binding domain in the low-density lipoprotein receptor. Journal of Human Genetics. 49(11). 622–628. 4 indexed citations
9.
Watanabe, Takafumi, Issei Imoto, Akira Hirasawa, et al.. (2002). Differentially Regulated Genes as Putative Targets of Amplifications at 20q in Ovarian Cancers. Japanese Journal of Cancer Research. 93(10). 1114–1122. 46 indexed citations
10.
Ota, N., et al.. (2001). . Nippon Ronen Igakkai Zasshi Japanese Journal of Geriatrics. 38(4). 498–500. 2 indexed citations
11.
12.
Utada, Yoshihito, Shunsuke Haga, Tetsuro Kajiwara, et al.. (2000). Mapping of Target Regions of Allelic Loss in Primary Breast Cancers to 1‐cM Intervals on Genomic Contigs at 6q21 and 6q25.3. Japanese Journal of Cancer Research. 91(3). 293–300. 25 indexed citations
13.
Yokota, Takashi, Masataka Yoshimoto, Goi Sakamoto, et al.. (1999). Localization of a tumor suppressor gene associated with the progression of human breast carcinoma within a 1-cm interval of 8p22-p23.1. Cancer. 85(2). 447–452. 65 indexed citations
14.
Kawamura, Naoki, Hisaki Nagai, Satoshi Matsumoto, et al.. (1999). PTEN/MMAC1 Mutations in Hepatocellular Carcinomas: Somatic Inactivation of Both Alleles in Tumors. Japanese Journal of Cancer Research. 90(4). 413–418. 36 indexed citations
15.
Nagai, Hisaki, et al.. (1999). Localization of a Target Region of Allelic Loss to a 1‐cM Interval on Chromosome 16p.13.13 in Hepatocellular Carcinoma. Japanese Journal of Cancer Research. 90(9). 951–956. 19 indexed citations
16.
Keicho, Naoto, Katsushi Tokunaga, Koichiro Nakata, et al.. (1998). Contribution of HLA Genes to Genetic Predisposition in Diffuse Panbronchiolitis. American Journal of Respiratory and Critical Care Medicine. 158(3). 846–850. 40 indexed citations
17.
Kurose, Keisuke, Aritoshi Iida, Tsutomu Araki, et al.. (1998). Frequent Allelic Loss at 7p14‐15 Associated with Aggressive Histologic Types of Breast Cancer. Japanese Journal of Cancer Research. 89(5). 533–538. 12 indexed citations
18.
Emi, Mitsuru, Mieko Matsushima, Toyomasa Katagiri, et al.. (1998). Multiplex Mutation Screening of the BRCA1 Gene in 1000 Japanese Breast Cancers. Japanese Journal of Cancer Research. 89(1). 12–16. 18 indexed citations
19.
Komiya, Akira, Hiroyoshi Suzuki, Takeshi Ueda, et al.. (1996). Allelic losses at loci on chromosome 10 are associated with metastasis and progression of human prostate cancer. Genes Chromosomes and Cancer. 17(4). 245–253. 69 indexed citations
20.
Inoue, Satoshi, Akira Orimo, Youichi Matsuda, et al.. (1995). Chromosome mapping of human (ZNF147) and mouse genes for estrogen-responsive finger protein (efp), a member of the RING finger family. Genomics. 25(2). 581–583. 12 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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