Hiroyuki Ida

4.7k total citations · 1 hit paper
189 papers, 3.5k citations indexed

About

Hiroyuki Ida is a scholar working on Physiology, Molecular Biology and Epidemiology. According to data from OpenAlex, Hiroyuki Ida has authored 189 papers receiving a total of 3.5k indexed citations (citations by other indexed papers that have themselves been cited), including 122 papers in Physiology, 69 papers in Molecular Biology and 42 papers in Epidemiology. Recurrent topics in Hiroyuki Ida's work include Lysosomal Storage Disorders Research (110 papers), Carbohydrate Chemistry and Synthesis (37 papers) and Cellular transport and secretion (31 papers). Hiroyuki Ida is often cited by papers focused on Lysosomal Storage Disorders Research (110 papers), Carbohydrate Chemistry and Synthesis (37 papers) and Cellular transport and secretion (31 papers). Hiroyuki Ida collaborates with scholars based in Japan, United States and Canada. Hiroyuki Ida's co-authors include Yoshikatsu Eto, Mitsuyoshi Urashima, Toya Ohashi, Yasuyuki Wada, Mana Kurihara, M. Okazaki, Hiroshi Kobayashi, Yohta Shimada, Takashi Higuchi and Kihei Maekawa and has published in prestigious journals such as Nucleic Acids Research, SHILAP Revista de lepidopterología and PLoS ONE.

In The Last Decade

Hiroyuki Ida

185 papers receiving 3.4k citations

Hit Papers

Randomized trial of vitamin D supplementation to prevent ... 2010 2026 2015 2020 2010 200 400 600

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Hiroyuki Ida Japan 29 2.0k 982 733 729 664 189 3.5k
Vassili Valayannopoulos France 39 2.0k 1.0× 1.5k 1.5× 834 1.1× 412 0.6× 295 0.4× 125 4.7k
Kathy Nicholls Australia 37 1.9k 1.0× 555 0.6× 1.2k 1.6× 541 0.7× 358 0.5× 164 4.2k
Rossella Parini Italy 38 3.1k 1.6× 1.5k 1.5× 1.3k 1.7× 580 0.8× 308 0.5× 179 5.1k
Yeong‐Hau H. Lien United States 32 620 0.3× 953 1.0× 301 0.4× 268 0.4× 308 0.5× 85 3.1k
Dong‐Kyu Jin South Korea 33 907 0.5× 917 0.9× 631 0.9× 209 0.3× 225 0.3× 261 3.9k
Marco Spada Italy 28 1.6k 0.8× 1.1k 1.1× 700 1.0× 415 0.6× 160 0.2× 132 3.1k
Kyosuke Takeshita Japan 35 615 0.3× 1.7k 1.8× 506 0.7× 236 0.3× 214 0.3× 141 4.4k
Christian Fledelius Denmark 30 919 0.5× 1.5k 1.5× 465 0.6× 274 0.4× 331 0.5× 57 4.3k
Turgay Coşkun Türkiye 27 600 0.3× 1.1k 1.1× 155 0.2× 284 0.4× 196 0.3× 209 2.7k
Deborah Elstein Israel 34 4.3k 2.2× 1.5k 1.6× 1.6k 2.2× 2.1k 2.9× 92 0.1× 201 5.4k

Countries citing papers authored by Hiroyuki Ida

Since Specialization
Citations

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

Fields of papers citing papers by Hiroyuki Ida

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Hiroyuki Ida

This figure shows the co-authorship network connecting the top 25 collaborators of Hiroyuki Ida. A scholar is included among the top collaborators of Hiroyuki Ida 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 Hiroyuki Ida. Hiroyuki Ida 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.
Oishi, Kimihiko, et al.. (2024). Allele frequency of pathogenic variants causing acid sphingomyelinase deficiency and Gaucher disease in the general Japanese population. Human Genome Variation. 11(1). 24–24. 1 indexed citations
2.
Yamagishi, Masaaki, et al.. (2021). Sliding Aortoplasty for Severe Supravalvular Aortic Stenosis After the Lecompte Procedure. The Annals of Thoracic Surgery. 112(1). e33–e35. 3 indexed citations
3.
Ida, Hiroyuki, Toshizumi Tanabe, & Akira Tachibana. (2020). Improved cancer inhibition by miR-143 with a longer passenger strand than natural miR-143. Biochemical and Biophysical Research Communications. 524(4). 810–815. 2 indexed citations
4.
Morimoto, Satoshi, Makoto Kawai, Masahisa Kobayashi, et al.. (2019). Clinical findings of gadolinium-enhanced cardiac magnetic resonance in Fabry patients. Journal of Cardiology. 75(1). 27–33. 12 indexed citations
5.
Kobayashi, Nobuyuki, Kazuyuki Shimada, Naomi Oka, et al.. (2017). Increased interleukin-1β and basic fibroblast growth factor levels in the cerebrospinal fluid during human herpesvirus-6B (HHV-6B) encephalitis. Biochemical and Biophysical Research Communications. 486(3). 706–711. 7 indexed citations
6.
Urashima, Takashi, et al.. (2017). Pulmonary hypertension due to left heart disease causes intrapulmonary venous arterialization in rats. Journal of Thoracic and Cardiovascular Surgery. 154(5). 1742–1753.e8. 13 indexed citations
7.
Higuchi, Takashi, Yohta Shimada, Hiroshi Kobayashi, et al.. (2016). Non-myeloablative preconditioning with ACK2 (anti-c-kit antibody) is efficient in bone marrow transplantation for murine models of mucopolysaccharidosis type II. Molecular Genetics and Metabolism. 119(3). 232–238. 14 indexed citations
8.
Sato, Yohei, Hiroshi Kobayashi, Yohta Shimada, et al.. (2015). Disease modeling and lentiviral gene transfer in patient-specific induced pluripotent stem cells from late-onset Pompe disease patient. Molecular Therapy — Methods & Clinical Development. 2. 15023–15023. 37 indexed citations
9.
Akiyama, Masaharu, Kentaro Yokoi, Takashi Inoue, et al.. (2015). Paraneoplastic Syndrome of Angiomatoid Fibrous Histiocytoma May Be Caused by EWSR1-CREB1 Fusion-induced Excessive Interleukin-6 Production. Journal of Pediatric Hematology/Oncology. 37(7). 554–559. 12 indexed citations
10.
Takagi, Ken, Masahisa Kobayashi, Masako Fujiwara, et al.. (2014). Cardiac Characteristics of Fabry Disease in Japanese Children and Adolescents (Original). 61(4). 65–75. 1 indexed citations
11.
Kikuchi, Kenjiro, et al.. (2014). Efficacy of Fosphenytoin for Status Epilepticus and Cluster Seizures in Children. Journal of the Japan Epilepsy Society. 31(3). 491–497.
12.
Unno, Hirotoshi, Kyoko Futamura, Hideaki Morita, et al.. (2014). Silica and Double-Stranded RNA Synergistically Induce Bronchial Epithelial Apoptosis and Airway Inflammation. American Journal of Respiratory Cell and Molecular Biology. 51(3). 344–353. 13 indexed citations
13.
Kawano, Takeshi, Ryota Saito, Ken Sakurai, et al.. (2014). Phosphoglycerate kinase deficiency due to a novel mutation (c. 1180A>G) manifesting as chronic hemolytic anemia in a Japanese boy. International Journal of Hematology. 100(4). 393–397. 8 indexed citations
14.
OGAWA, Kiyoshi, et al.. (2013). Hypoglycemia in Children with Tetralogy of Fallot Treated with Beta-Blocker. 1(1). 61–69. 1 indexed citations
15.
OGAWA, Kiyoshi, et al.. (2013). Hypoglycemia in Children with Tetralogy of Fallot Treated with Beta-Blocker.. 29(3). 129–136. 1 indexed citations
16.
Kikuchi, Kenjiro, et al.. (2012). Efficacy and Pharmacokinetics of Intravenous Phenobarbital Maintenance Therapy for Status Epilepticus and Cluster Seizures in Childhood. Journal of the Japan Epilepsy Society. 30(1). 19–26.
17.
Kobayashi, Hiroshi, Yohta Shimada, Yoshikatsu Eto, et al.. (2011). Minimum requirement of donor cells to reduce the glycolipid storage following bone marrow transplantation in a murine model of Fabry disease. The Journal of Gene Medicine. 13(5). 262–268. 8 indexed citations
18.
Shimada, Yohta, Hiroshi Kobayashi, Takashi Higuchi, et al.. (2011). Proteasome inhibitors improve the function of mutant lysosomal α-glucosidase in fibroblasts from Pompe disease patient carrying c.546G>T mutation. Biochemical and Biophysical Research Communications. 415(2). 274–278. 18 indexed citations
19.
Kikuchi, Kenjiro, et al.. (2010). Effectiveness and safety of non-intravenous high-dose phenobarbital therapy for intractable epilepsy during childhood. Brain and Development. 33(5). 379–383. 6 indexed citations
20.
Kim, Sung Hwan, et al.. (2000). The Clinical Characteristics and Gene Analysis of Korean Gaucher Disease with Central Nervous System Involvement. Korean Journal of Pediatrics. 43(5). 611–618. 2 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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