Mariko Okubo

574 total citations
24 papers, 280 citations indexed

About

Mariko Okubo is a scholar working on Molecular Biology, Genetics and Cardiology and Cardiovascular Medicine. According to data from OpenAlex, Mariko Okubo has authored 24 papers receiving a total of 280 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Molecular Biology, 7 papers in Genetics and 5 papers in Cardiology and Cardiovascular Medicine. Recurrent topics in Mariko Okubo's work include Muscle Physiology and Disorders (10 papers), Neurogenetic and Muscular Disorders Research (6 papers) and Cardiomyopathy and Myosin Studies (5 papers). Mariko Okubo is often cited by papers focused on Muscle Physiology and Disorders (10 papers), Neurogenetic and Muscular Disorders Research (6 papers) and Cardiomyopathy and Myosin Studies (5 papers). Mariko Okubo collaborates with scholars based in Japan, Italy and France. Mariko Okubo's co-authors include Ichizo Nishino, S. Noguchi, Satomi Mitsuhashi, Kanako Goto, Narihiro Minami, Yu‐ichi Goto, Hirofumi Komaki, Harumasa Nakamura, Eiji Nakagawa and Shinichiro Hayashi and has published in prestigious journals such as Journal of Biological Chemistry, Scientific Reports and Human Mutation.

In The Last Decade

Mariko Okubo

23 papers receiving 279 citations

Peers

Countries citing papers authored by Mariko Okubo

Since Specialization

Citations

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

Fields of papers citing papers by Mariko Okubo

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Mariko Okubo

This figure shows the co-authorship network connecting the top 25 collaborators of Mariko Okubo. A scholar is included among the top collaborators of Mariko Okubo 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 Mariko Okubo. Mariko Okubo 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	A Unique Case of MBD5 and CCM2 Deletions Leading to a Severe Neurological Phenotype With Prolonged Status Epilepticus 2025 ·Clinical Genetics ·(unknown), Viviana Venegas, (unknown), (unknown), (unknown), (unknown), (unknown), Mariko Okubo, Sanami Takada, Noriko Miyake	1
2	Molecular genetics of dystrophinopathy 2025 ·Journal of Human Genetics ·Mariko Okubo	1
3	A 53‐year‐old man with a 16‐year history of asymmetrical proximal muscle weakness, facial muscle weakness, and scapular winging 2023 ·Brain Pathology ·Jantima Tanboon, Rasha El Sherif, Michio Inoue, Mariko Okubo, Edoardo Malfatti, Ichizo Nishino	1
4	O03 In vivo gene therapy for striated muscle laminopathy 2023 ·Neuromuscular Disorders ·Mariko Okubo, Astrid Brull, Maud Beuvin, Nathalie Mougenot, Valérie Paradis, Gisèle Bonne, (unknown)	0
5	Hepatic veno-occlusive disease accompanied by thrombotic microangiopathy developed during treatment of juvenile dermatomyositis and macrophage activation syndrome: A case report 2022 ·Modern Rheumatology Case Reports ·(unknown), (unknown), Eriko Tanaka, (unknown), Mariko Okubo, Michio Inoue, Tomohiro Morio, Masaki Shimizu, Ichizo Nishino, Naoko Okiyama, Masaaki Mori	3
6	Multidimensional analyses of the pathomechanism caused by the non-catalytic GNE variant, c.620A>T, in patients with GNE myopathy 2022 ·Scientific Reports ·(unknown), Aritoshi Iida, Kyuto Sonehara, Kazuki Yamamoto, Yasushi Oya, Madoka Mori‐Yoshimura, Takashi Kurashige, Mariko Okubo, Megumu Ogawa, Fumihiko Matsuda, Koichiro Higasa, Shinichiro Hayashi, Harumasa Nakamura, Masakazu Sekijima, (unknown), S. Noguchi, Ichizo Nishino	6
7	Becker Muscular Dystrophy Accompanied by Anti-HMGCR Antibody-positive Immune-mediated Necrotizing Myopathy 2022 ·Internal Medicine ·(unknown), Yutaka Ohsawa, Mariko Okubo, (unknown), Hirotake Nishimura, Ichizo Nishino, Yoshihide Sunada	2
8	Deep convolutional neural network-based algorithm for muscle biopsy diagnosis 2021 ·Laboratory Investigation ·(unknown), Mariko Okubo, (unknown), (unknown), Michio Inoue, Masashi Ogasawara, Yoshihiko Saito, Jantima Tanboon, (unknown), (unknown), Yen‐Lin Chen, (unknown), Shinichiro Hayashi, (unknown), Yusuke Takeuchi, (unknown), Atsushi Takano, Fumihiko Matsuda, Ichizo Nishino	13
9	TNNI1 Mutated in Autosomal Dominant Proximal Arthrogryposis 2021 ·Neurology Genetics ·(unknown), Aritoshi Iida, Masashi Ogasawara, Mariko Okubo, (unknown), Makoto Kinoshita, Kazuma Sugie, S. Noguchi, Ichizo Nishino	3
10	Mutant BIN1-Dynamin 2 complexes dysregulate membrane remodeling in the pathogenesis of centronuclear myopathy 2021 ·Journal of Biological Chemistry ·(unknown), Mariko Okubo, Tadashi Abe, Hiroshi Yamada, Ichizo Nishino, S. Noguchi, Kohji Takei, Tetsuya Takeda	23
11	Mild form of Danon disease: two case reports 2021 ·Neuromuscular Disorders ·(unknown), Utako Nagaoka, Yasushi Oya, Akinori Uruha, (unknown), (unknown), (unknown), Shiro Matsubara, (unknown), Kazushi Takahashi, Michio Inoue, Mariko Okubo, Kazuma Sugie, Ichizo Nishino	2
12	Imaging‐based evaluation of pathogenicity by novel DNM2 variants associated with centronuclear myopathy 2021 ·Human Mutation ·(unknown), Mariko Okubo, Tadashi Abe, Hiroshi Yamada, Kohji Takei, Ichizo Nishino, Tetsuya Takeda, S. Noguchi	3
13	Duchenne muscular dystrophy–like phenotype in an LGMD2I patient with novel FKRP gene variants 2020 ·Human Genome Variation ·Tetsuya Okazaki, (unknown), (unknown), Kaori Adachi, Masachika Kai, Mariko Okubo, Ichizo Nishino, Eiji Nanba, Yoshihiro Maegaki	5
14	Exon skipping induced by nonsense/frameshift mutations in DMD gene results in Becker muscular dystrophy 2020 ·Human Genetics ·Mariko Okubo, S. Noguchi, Shinichiro Hayashi, Harumasa Nakamura, Hirofumi Komaki, Masafumi Matsuo, Ichizo Nishino	27
15	Three novel MTM1 pathogenic variants identified in Japanese patients with X‐linked myotubular myopathy 2019 ·Molecular Genetics & Genomic Medicine ·Atsuko Nishikawa, Aritoshi Iida, Shinichiro Hayashi, Mariko Okubo, Yasushi Oya, Gaku Yamanaka, Ikuko Takahashi, Ikuya Nonaka, S. Noguchi, Ichizo Nishino	3
16	Association of inattention with slow-spindle density in sleep EEG of children with attention deficit-hyperactivity disorder 2019 ·Brain and Development ·Yoshihiko Saito, (unknown), Eiji Nakagawa, Mariko Okubo, (unknown), (unknown), (unknown), Masumi Inagaki	23
17	Characteristic findings of skeletal muscle MRI in caveolinopathies 2018 ·Neuromuscular Disorders ·(unknown), Takahiro Nakayama, Masaru Yoshioka, Terumi Murakami, (unknown), (unknown), Takatoshi Sato, Naomi Hino‐Fukuyo, Satoshi Kuru, Makiko Ōsawa, Satoru Nagata, Mariko Okubo, Nobuyuki Murakami, Yukiko Hayashi, Ichizo Nishino, Keiko Ishigaki	6
18	Comprehensive analysis for genetic diagnosis of Dystrophinopathies in Japan 2017 ·Orphanet Journal of Rare Diseases ·Mariko Okubo, Kanako Goto, Hirofumi Komaki, Harumasa Nakamura, Madoka Mori‐Yoshimura, Yukiko Hayashi, Satomi Mitsuhashi, S. Noguchi, En Kimura, Ichizo Nishino	38
19	Genetic diagnosis of Duchenne/Becker muscular dystrophy using next-generation sequencing: validation analysis of DMD mutations 2016 ·Journal of Human Genetics ·Mariko Okubo, Narihiro Minami, Kanako Goto, Yu‐ichi Goto, S. Noguchi, Satomi Mitsuhashi, Ichizo Nishino	76
20	A family of distal arthrogryposis type 5 due to a novel PIEZO2 mutation 2015 ·American Journal of Medical Genetics Part A ·Mariko Okubo, Atsushi Fujita, Yoshiaki Saito, Hirofumi Komaki, Akihiko Ishiyama, Eri Takeshita, (unknown), Reiko Koichihara, (unknown), Eiji Nakagawa, Kenji Sugai, Hiroko Yamazaki, (unknown), Hiroshi Tanaka, Noriko Miyake, Naomichi Matsumoto, Masayuki Sasaki	36

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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