Morié Ishida

667 total citations
17 papers, 443 citations indexed

About

Morié Ishida is a scholar working on Cell Biology, Molecular Biology and Physiology. According to data from OpenAlex, Morié Ishida has authored 17 papers receiving a total of 443 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Cell Biology, 13 papers in Molecular Biology and 2 papers in Physiology. Recurrent topics in Morié Ishida's work include Cellular transport and secretion (11 papers), Retinal Development and Disorders (9 papers) and CRISPR and Genetic Engineering (5 papers). Morié Ishida is often cited by papers focused on Cellular transport and secretion (11 papers), Retinal Development and Disorders (9 papers) and CRISPR and Genetic Engineering (5 papers). Morié Ishida collaborates with scholars based in Japan, United States and Switzerland. Morié Ishida's co-authors include Mitsunori Fukuda, Norihiko Ohbayashi, Juan S. Bonifacino, Yuto Maruta, David C. Gershlick, Julie R. Jones, David B. Everman, Paulina S. Wawro, Naonobu Fujita and Yuta Homma and has published in prestigious journals such as Science, Journal of Biological Chemistry and Nature Communications.

In The Last Decade

Morié Ishida

16 papers receiving 439 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Morié Ishida Japan 12 321 262 58 47 47 17 443
Emma Martínez‐Alonso Spain 14 350 1.1× 286 1.1× 59 1.0× 61 1.3× 44 0.9× 24 566
Masataka Kunii Japan 11 219 0.7× 214 0.8× 43 0.7× 21 0.4× 21 0.4× 16 380
Pierre‐Yves Gougeon Canada 6 136 0.4× 203 0.8× 41 0.7× 41 0.9× 12 0.3× 7 344
M.J. Hannah Germany 5 209 0.7× 207 0.8× 46 0.8× 79 1.7× 21 0.4× 6 369
James B. Reinecke United States 10 129 0.4× 174 0.7× 69 1.2× 13 0.3× 22 0.5× 20 324
Takuya Tomemori Japan 8 164 0.5× 314 1.2× 75 1.3× 9 0.2× 21 0.4× 14 501
Christine M. Rostosky Germany 5 81 0.3× 153 0.6× 72 1.2× 37 0.8× 35 0.7× 5 312
Katherine R. Doherty United States 7 150 0.5× 446 1.7× 80 1.4× 7 0.1× 19 0.4× 7 524
Keiko Obata Japan 8 197 0.6× 259 1.0× 48 0.8× 38 0.8× 12 0.3× 17 398
Justin D. Topp United States 8 140 0.4× 336 1.3× 41 0.7× 101 2.1× 22 0.5× 8 508

Countries citing papers authored by Morié Ishida

Since Specialization
Citations

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

Fields of papers citing papers by Morié Ishida

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Morié Ishida

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

All Works

17 of 17 papers shown
1.
Yoshii, Tatsuyuki, Morié Ishida, Eriko Kajikawa, et al.. (2025). Nematode telomerase RNA hitchhikes on introns of germline–up-regulated genes. Science. 390(6771). eads7778–eads7778.
2.
Ishida, Morié, Adriana E. Golding, Tal Keren‐Kaplan, et al.. (2024). ARMH3 is an ARL5 effector that promotes PI4KB-catalyzed PI4P synthesis at the trans-Golgi network. Nature Communications. 15(1). 10168–10168. 4 indexed citations
3.
Scaramuzza, Stefano, Morié Ishida, Chad D. Williamson, et al.. (2023). Architecture of the ESCPE-1 membrane coat. Nature Structural & Molecular Biology. 30(7). 958–969. 11 indexed citations
4.
Ishida, Morié, María Gabriela Otero, Pedro A. Sanchez‐Lara, et al.. (2022). A neurodevelopmental disorder associated with an activatingde novomissense variant inARF1. Human Molecular Genetics. 32(7). 1162–1174. 9 indexed citations
5.
Beilina, Alexandra, Luis Bonet‐Ponce, Ravindran Kumaran, et al.. (2020). The Parkinson’s Disease Protein LRRK2 Interacts with the GARP Complex to Promote Retrograde Transport to the trans-Golgi Network. Cell Reports. 31(5). 107614–107614. 50 indexed citations
6.
Ishida, Morié, et al.. (2019). The BLOC-3 subunit HPS4 is required for activation of Rab32/38 GTPases in melanogenesis, but its Rab9 activity is dispensable for melanogenesis. Journal of Biological Chemistry. 294(17). 6912–6922. 22 indexed citations
7.
Homma, Yuta, Yoshihiko Kuchitsu, Paulina S. Wawro, et al.. (2019). Comprehensive knockout analysis of the Rab family GTPases in epithelial cells. The Journal of Cell Biology. 218(6). 2035–2050. 58 indexed citations
8.
Ishida, Morié & Juan S. Bonifacino. (2019). ARFRP1 functions upstream of ARL1 and ARL5 to coordinate recruitment of distinct tethering factors to the trans-Golgi network. The Journal of Cell Biology. 218(11). 3681–3696. 25 indexed citations
9.
Gershlick, David C., et al.. (2018). A neurodevelopmental disorder caused by mutations in the VPS51 subunit of the GARP and EARP complexes. Human Molecular Genetics. 28(9). 1548–1560. 40 indexed citations
10.
Ishida, Morié, et al.. (2016). M-INK, a novel tool for visualizing melanosomes and melanocores. The Journal of Biochemistry. 161(4). mvw100–mvw100. 6 indexed citations
11.
Ishida, Morié, et al.. (2016). Multiple Types of Guanine Nucleotide Exchange Factors (GEFs) for Rab Small GTPases. Cell Structure and Function. 41(2). 61–79. 53 indexed citations
12.
Ishida, Morié, Norihiko Ohbayashi, & Mitsunori Fukuda. (2015). Rab1A regulates anterograde melanosome transport by recruiting kinesin-1 to melanosomes through interaction with SKIP. Scientific Reports. 5(1). 8238–8238. 38 indexed citations
13.
Ishida, Morié, et al.. (2014). The GTPase-deficient Rab27A(Q78L) Mutant Inhibits Melanosome Transport in Melanocytes through Trapping of Rab27A Effector Protein Slac2-a/Melanophilin in Their Cytosol. Journal of Biological Chemistry. 289(16). 11059–11067. 17 indexed citations
14.
Imai, Akane, Morié Ishida, Mitsunori Fukuda, Tomoko Nashida, & Hiromi Shimomura. (2013). MADD/DENN/Rab3GEP functions as a guanine nucleotide exchange factor for Rab27 during granule exocytosis of rat parotid acinar cells. Archives of Biochemistry and Biophysics. 536(1). 31–37. 20 indexed citations
15.
Ishida, Morié, et al.. (2012). Functional involvement of Rab1A in microtubule-dependent anterograde melanosome transport in melanocytes. Journal of Cell Science. 125(Pt 21). 5177–87. 40 indexed citations
16.
Ohbayashi, Norihiko, Yuto Maruta, Morié Ishida, & Mitsunori Fukuda. (2012). Melanoregulin regulates retrograde melanosome transport through interaction with the RILP·p150Glued complex in melanocytes. Journal of Cell Science. 125(Pt 6). 1508–18. 49 indexed citations
17.
Yamamoto, Tsunehisa, Morié Ishida, & T Nishimura. (1963). [ON THE SO-CALLED VESICULAR COMPONENTS OF SATELLITE CELLS].. PubMed. 38. 188–94. 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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