Madoka Mori‐Yoshimura

2.3k total citations
87 papers, 881 citations indexed

About

Madoka Mori‐Yoshimura is a scholar working on Molecular Biology, Epidemiology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Madoka Mori‐Yoshimura has authored 87 papers receiving a total of 881 indexed citations (citations by other indexed papers that have themselves been cited), including 54 papers in Molecular Biology, 30 papers in Epidemiology and 23 papers in Cellular and Molecular Neuroscience. Recurrent topics in Madoka Mori‐Yoshimura's work include Muscle Physiology and Disorders (42 papers), Inflammatory Myopathies and Dermatomyositis (28 papers) and Genetic Neurodegenerative Diseases (23 papers). Madoka Mori‐Yoshimura is often cited by papers focused on Muscle Physiology and Disorders (42 papers), Inflammatory Myopathies and Dermatomyositis (28 papers) and Genetic Neurodegenerative Diseases (23 papers). Madoka Mori‐Yoshimura collaborates with scholars based in Japan, United States and Italy. Madoka Mori‐Yoshimura's co-authors include Ichizo Nishino, Yasushi Oya, Yukiko Hayashi, Miho Murata, Harumasa Nakamura, En Kimura, Hirofumi Komaki, S. Noguchi, Shin’ichi Takeda and Yuji Takahashi and has published in prestigious journals such as PLoS ONE, Neurology and Scientific Reports.

In The Last Decade

Madoka Mori‐Yoshimura

78 papers receiving 875 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Madoka Mori‐Yoshimura Japan 18 522 278 213 168 156 87 881
Yasushi Oya Japan 20 829 1.6× 491 1.8× 325 1.5× 195 1.2× 247 1.6× 91 1.4k
Olavo M. Vasconcelos United States 16 610 1.2× 174 0.6× 246 1.2× 95 0.6× 288 1.8× 25 1.1k
I. Pénisson-Besnier France 21 696 1.3× 75 0.3× 324 1.5× 163 1.0× 147 0.9× 55 1.2k
Hui Xiong China 17 652 1.2× 63 0.2× 123 0.6× 239 1.4× 126 0.8× 116 1.0k
Ângela Romano Italy 16 351 0.7× 97 0.3× 99 0.5× 223 1.3× 126 0.8× 77 924
Barend P. Lotz South Africa 12 368 0.7× 380 1.4× 90 0.4× 91 0.5× 144 0.9× 31 863
Nuria Muelas Spain 18 422 0.8× 55 0.2× 148 0.7× 160 1.0× 370 2.4× 50 922
Pinki Munot United Kingdom 15 259 0.5× 56 0.2× 116 0.5× 127 0.8× 113 0.7× 51 718
Beatrijs Wokke Netherlands 14 559 1.1× 41 0.1× 147 0.7× 86 0.5× 147 0.9× 38 894
J. Franques France 21 256 0.5× 69 0.2× 91 0.4× 124 0.7× 242 1.6× 44 927

Countries citing papers authored by Madoka Mori‐Yoshimura

Since Specialization
Citations

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

Fields of papers citing papers by Madoka Mori‐Yoshimura

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Madoka Mori‐Yoshimura. 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 Madoka Mori‐Yoshimura. The network helps show where Madoka Mori‐Yoshimura may publish in the future.

Co-authorship network of co-authors of Madoka Mori‐Yoshimura

This figure shows the co-authorship network connecting the top 25 collaborators of Madoka Mori‐Yoshimura. A scholar is included among the top collaborators of Madoka Mori‐Yoshimura 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 Madoka Mori‐Yoshimura. Madoka Mori‐Yoshimura 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.
Mori‐Yoshimura, Madoka, et al.. (2024). Efficacy and safety of avalglucosidase alfa in Japanese patients with late-onset and infantile-onset Pompe diseases: A case series from clinical trials. Molecular Genetics and Metabolism Reports. 42. 101163–101163. 1 indexed citations
2.
3.
Ohkawara, Bisei, K. Nakajima, Jun‐ichi Takeda, et al.. (2024). Muscle-specific lack of Gfpt1 triggers ER stress to alleviate misfolded protein accumulation. Disease Models & Mechanisms. 17(8). 4 indexed citations
4.
Mori‐Yoshimura, Madoka, et al.. (2023). Factors influencing the decision to introduce alternative nutrition in patients with Duchenne muscular dystrophy. Muscle & Nerve. 68(5). 737–742.
5.
Mori‐Yoshimura, Madoka, Hiroyuki Yajima, Yasushi Oya, et al.. (2022). Long-term evaluation parameters in GNE myopathy: a 5-year observational follow-up natural history study. BMJ Neurology Open. 4(2). e000362–e000362. 5 indexed citations
6.
Mori‐Yoshimura, Madoka, Yasushi Oya, Michio Inoue, et al.. (2022). Myoglobinopathy affecting facial and oropharyngeal muscles. Neuromuscular Disorders. 32(6). 516–520.
7.
Noguchi, S., et al.. (2022). Advances in understanding of the natural history, mechanism, extra‐muscular manifestations and treatment of GNE myopathy. Neurology and Clinical Neuroscience. 10(6). 289–297. 1 indexed citations
8.
Ogasawara, Masashi, Nobuyuki Eura, Utako Nagaoka, et al.. (2021). Intranuclear inclusions in skin biopsies are not limited to neuronal intranuclear inclusion disease but can also be seen in oculopharyngodistal myopathy. Neuropathology and Applied Neurobiology. 48(3). e12787–e12787. 14 indexed citations
9.
Mori‐Yoshimura, Madoka, Hiroyuki Yajima, Katsuhiro Mizuno, et al.. (2021). Assessment of thrombocytopenia, sleep apnea, and cardiac involvement in GNE myopathy patients. Muscle & Nerve. 65(3). 284–290. 11 indexed citations
10.
Mori‐Yoshimura, Madoka, Yasushi Oya, Narihiro Minami, et al.. (2020). Severe cardiac involvement with preserved truncated dystrophin expression in Becker muscular dystrophy by +1G>A DMD splice-site mutation: a case report. Journal of Human Genetics. 65(10). 903–909. 4 indexed citations
11.
Saito, Yoshihiko, Atsuko Nishikawa, Aritoshi Iida, et al.. (2020). ADSSL1 myopathy is the most common nemaline myopathy in Japan with variable clinical features. Neurology. 95(11). e1500–e1511. 20 indexed citations
12.
Sato, Noriko, Yoko Shigemoto, Yukio Kimura, et al.. (2020). New MRI Findings in Fukuyama Congenital Muscular Dystrophy: Brain Stem and Venous System Anomalies. American Journal of Neuroradiology. 41(6). 1094–1098. 2 indexed citations
13.
Mori‐Yoshimura, Madoka, Jun Miki, Ryogen Sasaki, et al.. (2020). Paramyotonia Congenita with Persistent Distal and Facial Muscle Weakness: A Case Report with Literature Review. Journal of Neuromuscular Diseases. 7(2). 193–201. 5 indexed citations
14.
Matsumoto, Chihiro, Madoka Mori‐Yoshimura, S. Noguchi, et al.. (2019). Phenotype of a limb-girdle congenital myasthenic syndrome patient carrying a GFPT1 mutation. Brain and Development. 41(5). 470–473. 7 indexed citations
15.
Mori‐Yoshimura, Madoka, Sumiko Yoshida, Narihiro Minami, et al.. (2019). Psychiatric and neurodevelopmental aspects of Becker muscular dystrophy. Neuromuscular Disorders. 29(12). 930–939. 28 indexed citations
16.
Mori‐Yoshimura, Madoka, Toshiyuki Yamamoto, Yasushi Oya, et al.. (2019). Chronic sarcoid myopathy mimicking sporadic inclusion body myositis. Clinical Neurology and Neurosurgery. 182. 84–86. 6 indexed citations
17.
Inoue, Michio, Aritoshi Iida, Shinichiro Hayashi, et al.. (2018). Two novel VCP missense variants identified in Japanese patients with multisystem proteinopathy. Human Genome Variation. 5(1). 9–9. 5 indexed citations
18.
Okubo, Mariko, Kanako Goto, Hirofumi Komaki, et al.. (2017). Comprehensive analysis for genetic diagnosis of Dystrophinopathies in Japan. Orphanet Journal of Rare Diseases. 12(1). 149–149. 38 indexed citations
19.
Sugiyama, Atsuhiko, Daichi Sone, Noriko Sato, et al.. (2017). Brain gray matter structural network in myotonic dystrophy type 1. PLoS ONE. 12(11). e0187343–e0187343. 15 indexed citations
20.
Suzuki, Naoki, Madoka Mori‐Yoshimura, Satoshi Yamashita, et al.. (2016). Multicenter questionnaire survey for sporadic inclusion body myositis in Japan. Orphanet Journal of Rare Diseases. 11(1). 146–146. 31 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Yasushi Oya Breakdown of academic impact, for papers by Olavo M. Vasconcelos Breakdown of academic impact, for papers by I. Pénisson-Besnier Breakdown of academic impact, for papers by Hui Xiong Breakdown of academic impact, for papers by Ângela Romano Breakdown of academic impact, for papers by Barend P. Lotz Breakdown of academic impact, for papers by Nuria Muelas Breakdown of academic impact, for papers by Pinki Munot Breakdown of academic impact, for papers by Beatrijs Wokke Breakdown of academic impact, for papers by J. Franques
Rankless by CCL
2026