Michie Shimmoto

1.1k total citations
44 papers, 918 citations indexed

About

Michie Shimmoto is a scholar working on Physiology, Molecular Biology and Genetics. According to data from OpenAlex, Michie Shimmoto has authored 44 papers receiving a total of 918 indexed citations (citations by other indexed papers that have themselves been cited), including 27 papers in Physiology, 25 papers in Molecular Biology and 10 papers in Genetics. Recurrent topics in Michie Shimmoto's work include Lysosomal Storage Disorders Research (24 papers), Muscle Physiology and Disorders (6 papers) and Cellular transport and secretion (6 papers). Michie Shimmoto is often cited by papers focused on Lysosomal Storage Disorders Research (24 papers), Muscle Physiology and Disorders (6 papers) and Cellular transport and secretion (6 papers). Michie Shimmoto collaborates with scholars based in Japan, United States and Slovakia. Michie Shimmoto's co-authors include Hitoshi Sakuraba, Yoshiyuki Suzuki, Kohji Itoh, Y Fukuhara, Akihiko Oshima, Kunihiro Yoshida, Yoshiro Nagao, Ryoichi Kase, Yoshiyuki Suzuki and Akira Satake and has published in prestigious journals such as Journal of Biological Chemistry, Journal of Clinical Investigation and Molecular and Cellular Biology.

In The Last Decade

Michie Shimmoto

43 papers receiving 898 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Michie Shimmoto Japan 15 582 407 292 231 91 44 918
Fabio Corsolini Italy 21 545 0.9× 507 1.2× 227 0.8× 245 1.1× 151 1.7× 54 1.0k
Maria Francisca Coutinho Portugal 13 437 0.8× 333 0.8× 255 0.9× 201 0.9× 102 1.1× 43 846
María Begoña Cachón-González United Kingdom 11 455 0.8× 425 1.0× 277 0.9× 184 0.8× 82 0.9× 19 896
Susanna Lualdi Italy 19 371 0.6× 376 0.9× 106 0.4× 153 0.7× 75 0.8× 25 690
Ulla Lahtinen Finland 14 342 0.6× 479 1.2× 421 1.4× 65 0.3× 22 0.2× 16 874
Hiroyuki Sonoda Japan 13 325 0.6× 305 0.7× 109 0.4× 123 0.5× 48 0.5× 37 723
Briony L. Gliddon Australia 15 267 0.5× 399 1.0× 259 0.9× 111 0.5× 26 0.3× 23 764
Teresa Occhiodoro Australia 12 260 0.4× 577 1.4× 130 0.4× 113 0.5× 57 0.6× 14 937
Elena L. Aronovich United States 19 388 0.7× 618 1.5× 119 0.4× 222 1.0× 55 0.6× 38 1.0k
Haiqing Yi United States 19 168 0.3× 533 1.3× 154 0.5× 73 0.3× 52 0.6× 34 851

Countries citing papers authored by Michie Shimmoto

Since Specialization
Citations

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

Fields of papers citing papers by Michie Shimmoto

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Michie Shimmoto

This figure shows the co-authorship network connecting the top 25 collaborators of Michie Shimmoto. A scholar is included among the top collaborators of Michie Shimmoto 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 Michie Shimmoto. Michie Shimmoto 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.
Shimmoto, Michie, et al.. (2014). Epitope analysis of Japanese cedar pollen allergen Cry j1 with the human monoclonal antibody 4701-1. Human Antibodies. 22(3-4). 73–76. 2 indexed citations
2.
3.
Shinmoto, Hiroshi, et al.. (2004). Generation of mouse–human hybridomas secreting antibodies against peanut allergen Ara h1. Cytotechnology. 46(1). 19–23. 4 indexed citations
4.
Itoh, Kohji, Yurie Satoh, Yoshito Kadota, et al.. (2003). Expression of lysosomal protective protein/cathepsin A in a stably transformed human neuroblastoma cell line during bi-directional differentiation into neuronal and Schwannian cells. Neurochemistry International. 44(6). 447–457. 4 indexed citations
5.
6.
Itoh, Kohji, et al.. (1998). Stabilizing Effect of Lysosomal β-Galactosidase on the Catalytic Activity of Protective Protein/Cathepsin A Secreted by Human Platelets. Biochemical and Biophysical Research Communications. 253(2). 228–234. 3 indexed citations
7.
Takata, T., Toshika Okumiya, Hidemasa Hayashibe, et al.. (1997). Screening and detection of gene mutations in Japanese patients with Fabry disease by non-radioactive single-stranded conformation polymorphism analysis. Brain and Development. 19(2). 111–116. 18 indexed citations
8.
Itoh, Kohji, Michie Shimmoto, Junji Nishimoto, et al.. (1997). Molecular form and subcellular distribution of acid β-galactosidase in fibroblasts from patients with GM1 gangliosidosis, Morquio B disease and galactosialidosis. Brain and Development. 19(2). 126–130. 6 indexed citations
9.
Shimmoto, Michie, Yutaka Nakahori, Ikumi Matsushita, et al.. (1996). A Human Protective Protein Gene Partially Overlaps the Gene Encoding Phospholipid Transfer Protein on the Complementary Strand of DNA. Biochemical and Biophysical Research Communications. 220(3). 802–806. 9 indexed citations
10.
Itoh, Kohji, Ryoichi Kase, Michie Shimmoto, et al.. (1995). Protective Protein as an Endogenous Endothelin Degradation Enzyme in Human Tissues. Journal of Biological Chemistry. 270(2). 515–518. 55 indexed citations
11.
Satake, Akira, Kohji Itoh, Michie Shimmoto, et al.. (1994). Distribution of Lysosomal Protective Protein in Human Tissues. Biochemical and Biophysical Research Communications. 205(1). 38–43. 39 indexed citations
12.
Shimmoto, Michie, Y Fukuhara, Kohji Itoh, et al.. (1993). Protective protein gene mutations in galactosialidosis.. Journal of Clinical Investigation. 91(6). 2393–2398. 58 indexed citations
13.
Sakuraba, Hitoshi, K Itoh, & Michie Shimmoto. (1993). [Multifunctional protective protein and its genetic deficiency 'galactosialidosis'].. PubMed. 65(7). 561–6. 1 indexed citations
14.
Nishio, Hisahide, Masafumi Matsuo, Yoshihiko Kitoh, et al.. (1993). Brain- and muscle-type promoters of the dystrophin gene are selected in peripheral lymphocytes and Epstein Barr virus-transformed lymphoplastoid cells. Journal of Neurology. 241(2). 81–86. 2 indexed citations
15.
Ishii, Keiko, Hitoshi Sakuraba, Reiko Minamikawa‐Tachino, Michie Shimmoto, & Yoshiyuki Suzuki. (1992). Carrier detection of duchenne/becker muscular dystrophy: Computer-assisted direct quantitation of gene amplification products. Brain and Development. 14(2). 80–83. 6 indexed citations
16.
Yoshida, Kunihiro, Akihiko Oshima, Michie Shimmoto, et al.. (1991). Human beta-galactosidase gene mutations in GM1-gangliosidosis: a common mutation among Japanese adult/chronic cases.. PubMed. 49(2). 435–42. 93 indexed citations
17.
Sakuraba, Hitoshi, Keiko Ishii, Michie Shimmoto, Hideo Yamada, & Yoshiyuki Suzuki. (1991). A screening for dystrophin gene deletions in Japanese patients with Duchenne/Becker muscular dystrophy by the multiplex polymerase chain reaction. Brain and Development. 13(5). 339–342. 13 indexed citations
18.
Suzuki, Yoshiyuki, Hitoshi Sakuraba, Akihiro Oshima, et al.. (1991). Clinical and Molecular Heterogeneity in Hereditary β-Galactosidase Deficiency. Developmental Neuroscience. 13(4-5). 299–303. 11 indexed citations
19.
Oshima, Akihiko, Kunihiro Yoshida, Michie Shimmoto, et al.. (1991). Human beta-galactosidase gene mutations in morquio B disease.. PubMed. 49(5). 1091–3. 65 indexed citations
20.
Shimmoto, Michie, Takako Takano, Yukiko Fukuhara, et al.. (1990). Japanese-type adult galactosialidosis. A unique and common splice junction mutation causing exon skipping in the protective protein/carboxypeptidase gene.:A Unique and Common Splice Junction Mutation Causing Exon Skipping in the Protective Protein/Carboxypeptidase Gene. Proceedings of the Japan Academy Series B. 66(10). 217–222. 6 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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