Satoko Kumada

2.7k total citations
86 papers, 1.4k citations indexed

About

Satoko Kumada is a scholar working on Molecular Biology, Neurology and Genetics. According to data from OpenAlex, Satoko Kumada has authored 86 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 26 papers in Molecular Biology, 24 papers in Neurology and 22 papers in Genetics. Recurrent topics in Satoko Kumada's work include Genetics and Neurodevelopmental Disorders (16 papers), Neurological disorders and treatments (13 papers) and Glycogen Storage Diseases and Myoclonus (12 papers). Satoko Kumada is often cited by papers focused on Genetics and Neurodevelopmental Disorders (16 papers), Neurological disorders and treatments (13 papers) and Glycogen Storage Diseases and Myoclonus (12 papers). Satoko Kumada collaborates with scholars based in Japan, United Kingdom and United States. Satoko Kumada's co-authors include Masaharu Hayashi, Hirotomo Saitsu, Naomichi Matsumoto, Mitsuhiro Kato, Takeshi Mizuguchi, Kazuhiro Ogata, Hitoshi Osaka, Atsuo Fukuda, Tatsuro Kumada and Kiyomi Nishiyama and has published in prestigious journals such as Nature Genetics, Neurology and Annals of Neurology.

In The Last Decade

Satoko Kumada

82 papers receiving 1.4k citations

Peers

Countries citing papers authored by Satoko Kumada

Since Specialization

Citations

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

Fields of papers citing papers by Satoko Kumada

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Satoko Kumada

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

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	The Mini-COMET Clinical Trial: Safety and Efficacy of Avalglucosidase Alfa after 97 Weeks of Treatment in Children with Infantile-Onset Pompe Disease Previously Treated with Alglucosidase Alfa 2025 ·The Journal of Pediatrics ·David Kronn, James Davison, Alexander Broomfield, Anaïs Brassier, François Labarthe, Si Houn Hahn, Satoko Kumada, Hirotaka Ohki, S. Grace Prakalapakorn, Catherine Wilson, Kristina An Haack, (unknown), Susan Richards, Susan Sparks, (unknown), Tianyue Zhou, Yin‐Hsiu Chien, Priya S. Kishnani	0
2	Efficacy and safety of avalglucosidase alfa in Japanese patients with late-onset and infantile-onset Pompe diseases: A case series from clinical trials 2024 ·Molecular Genetics and Metabolism Reports ·Madoka Mori‐Yoshimura, Hirotaka Ohki, (unknown), (unknown), Satoko Kumada, (unknown), (unknown), Masato Ikeda, Hirofumi Komaki	1
3	Issues of transition support to adulthood and the practices of pediatric-adult healthcare transition in neurological diseases 2024 ·Rinsho Shinkeigaku ·Katsuhisa Ogata, Yoko Mochizuki, Satoko Kumada, (unknown), Yoshio Sakiyama, Kenjiro Kikuchi, Mika Hayakawa, (unknown), Toshio Saito, Hideki Mochizuki	1
4	Uniparental maternal tetrasomy X co-occurrence with paternal nondisjunction: investigation of the origin of 48,XXXX 2024 ·Human Genome Variation ·(unknown), (unknown), (unknown), Satoko Kumada, Toshiyuki Yamamoto	1
5	Evidence-based diagnostic prediction score for pediatric NMDA receptor encephalitis 2024 ·European Journal of Paediatric Neurology ·Shimpei Matsuda, (unknown), Mariko Kasai, Kuniko Kohyama, Hiroya Nishida, (unknown), Ichiro Kuki, Satoko Kumada, Hirokazu Kurahashi, Sahoko Miyama, Motomasa Suzuki, Jun‐ichi Takanashi, Satoshi Usami, Satoshi Yamaguchi, Syudo Yamasaki, Atsushi Nishida, Hiroshi Sakuma	1
6	Initiatives for supporting the health care transition in various regions: activities of transitional care support centers 2024 ·Rinsho Shinkeigaku ·Yoko Mochizuki, Katsuhisa Ogata, Satoko Kumada, Tomihiro Imai, (unknown), Akiyo Hineno, (unknown), Ichiro Yabe, Hideki Mochizuki	0
7	Vagus Nerve Stimulation Therapy for Drug-Resistant Epilepsy in Children—A Literature Review 2024 ·Journal of Clinical Medicine ·Mitsumasa Fukuda, Takeshi Matsuo, (unknown), Hirofumi Kashii, Ai Hoshino, Akihiko Ishiyama, Satoko Kumada	5
8	Reduced histone H3K4 trimethylation in oral mucosa of patients with DYT-KMT2B 2024 ·Parkinsonism & Related Disorders ·Naoto Sugeno, Satoko Kumada, Hirofumi Kashii, (unknown), Toshitaka Kawarai, Takaaki Nakamura, (unknown), Shun Ishiyama, Kazuki Sato, Shun Yoshida, (unknown), Kohei Hamanaka, Satoko Miyatake, Noriko Miyake, Naomichi Matsumoto, (unknown), Kenjiro Kosaki, Hiroshi Yoshihashi, Takafumi Hasegawa, Masashi Aoki	1
9	Focal tonic seizures with asymmetrical posturing could allow voluntary movements: A lesson to not be misled for a non‐epileptic event 2023 ·Epileptic Disorders ·Mitsumasa Fukuda, (unknown), (unknown), (unknown), Hirofumi Kashii, Satoko Kumada, Kiyohide Usami, Akio Ikeda	1
10	Current practices of transition from pediatric to adult health care for patients with neurological disease: promote the cooperation between child and adult neurologists 2023 ·Rinsho Shinkeigaku ·Yoko Mochizuki, Katsuhisa Ogata, Satoko Kumada, Yasuhiro Suzuki, (unknown), Yoshio Sakiyama, Toshio Saito, Hideki Mochizuki	1
11	Loss‐of‐function mutations in SGCE found in Japanese patients with myoclonus‐dystonia 2022 ·Clinical Genetics ·Kenko Azuma, Shiro Horisawa, (unknown), Mitsumasa Fukuda, Satoko Kumada, Takakazu Kawamata, Takaomi Taira, (unknown)	1
12	Safety and efficacy of avalglucosidase alfa in individuals with infantile-onset Pompe disease enrolled in the phase 2, open-label Mini-COMET study: The 6-month primary analysis report 2022 ·Genetics in Medicine ·Priya S. Kishnani, David Kronn, Anaïs Brassier, Alexander Broomfield, James Davison, Si Houn Hahn, Satoko Kumada, François Labarthe, Hirotaka Ohki, (unknown), S. Grace Prakalapakorn, Kristina An Haack, Barbara Kittner, (unknown), Susan Sparks, Catherine Wilson, Atef Zaher, Yin‐Hsiu Chien	28
13	Nonconvulsive status epilepticus following rotavirus gastroenteritis in two pediatric patients 2021 ·Brain and Development ·(unknown), Yuji Sugawara, Ai Hoshino, (unknown), Satoko Kumada, Takeshi Hasegawa	2
14	Identification of two novel de novo TUBB variants in cases with brain malformations: case reports and literature review 2021 ·Journal of Human Genetics ·Kazuki Watanabe, Mitsuko Nakashima, Satoko Kumada, (unknown), Mikako Enokizono, Keitaro Yamada, Mitsuhiro Kato, Hirotomo Saitsu	16
15	Novel EXOSC9 variants cause pontocerebellar hypoplasia type 1D with spinal motor neuronopathy and cerebellar atrophy 2020 ·Journal of Human Genetics ·(unknown), Kazuhiro Iwama, Futoshi Sekiguchi, (unknown), Satoko Kumada, Keiko Ishigaki, Nobuhiko Okamoto, Mahdiyeh Behnam, Mohsen Ghadami, Eriko Koshimizu, Satoko Miyatake, Satomi Mitsuhashi, Takeshi Mizuguchi, Atsushi Takata, Hirotomo Saitsu, Noriko Miyake, Naomichi Matsumoto	13
16	An atypical case of KMT2B‐related dystonia manifesting asterixis and effect of deep brain stimulation of the globus pallidus 2019 ·Neurology and Clinical Neuroscience ·(unknown), Kohei Hamanaka, Satoko Kumada, (unknown), Fusako Yokochi, Makoto Taniguchi, Satoko Miyatake, Naomichi Matsumoto	3
17	Promyelocytic Leukemia Protein Is Redistributed during the Formation of Intranuclear Inclusions Independent of Polyglutamine Expansion: An Immunohistochemical Study on Marinesco Bodies 2002 ·Journal of Neuropathology & Experimental Neurology ·Satoko Kumada, Toshiki Uchihara, Masaharu Hayashi, Ayako Nakamura, (unknown), Toshio Mizutani, Masaya Oda	33
18	Oxidative Stress and Disturbed Glutamate Transport in Hereditary Nucleotide Repair Disorders 2001 ·Journal of Neuropathology & Experimental Neurology ·Masaharu Hayashi, Masahiro Itoh, Satoshi Araki, Satoko Kumada, Kei Shioda, Kimiko Tamagawa, Toshio Mizutani, Yoshio Morimatsu, (unknown), Masaya Oda	46
19	Immunohistochemical analysis of brainstem lesions in infantile spasms 2000 ·Neuropathology ·Masaharu Hayashi, Masahiro Itoh, S. Araki, Satoko Kumada, Naoyuki Tanuma, (unknown), Jun Kohyama, Yoshihide Iwakawa, J. Satoh, Yoshio Morimatsu	26
20	Cerebellar degeneration in hereditary dentatorubral-pallidoluysian atrophy and Machado-Joseph disease 2000 ·Acta Neuropathologica ·Satoko Kumada, Masaharu Hayashi, Masashi Mizuguchi, Imaharu Nakano, Yoshio Morimatsu, Masaya Oda	26

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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