Aritoshi Iida

8.5k total citations · 1 hit paper
126 papers, 4.5k citations indexed

About

Aritoshi Iida is a scholar working on Molecular Biology, Genetics and Rheumatology. According to data from OpenAlex, Aritoshi Iida has authored 126 papers receiving a total of 4.5k indexed citations (citations by other indexed papers that have themselves been cited), including 72 papers in Molecular Biology, 36 papers in Genetics and 16 papers in Rheumatology. Recurrent topics in Aritoshi Iida's work include Genetic Neurodegenerative Diseases (10 papers), Genomics and Rare Diseases (8 papers) and Cardiomyopathy and Myosin Studies (8 papers). Aritoshi Iida is often cited by papers focused on Genetic Neurodegenerative Diseases (10 papers), Genomics and Rare Diseases (8 papers) and Cardiomyopathy and Myosin Studies (8 papers). Aritoshi Iida collaborates with scholars based in Japan, China and United States. Aritoshi Iida's co-authors include Yusuke Nakamura, Akihiro Sekine, Susumu Saito, A. Sekine, Tatsuhiko Tsunoda, Toshihiro Tanaka, Kouichi Ozaki, Shiro Ikegawa, Masatsugu Hori and Hiroshi Sato and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and Nature Communications.

In The Last Decade

Aritoshi Iida

121 papers receiving 4.4k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Functional SNPs in the lymphotoxin-α gene that are associated with susceptibility to myocardial infarction

2002 696 citations Aritoshi Iida, Tatsuhiko Tsunoda et al. profile →

Peers

Countries citing papers authored by Aritoshi Iida

Since Specialization

Citations

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

Fields of papers citing papers by Aritoshi Iida

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Aritoshi Iida

This figure shows the co-authorship network connecting the top 25 collaborators of Aritoshi Iida. A scholar is included among the top collaborators of Aritoshi Iida 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 Aritoshi Iida. Aritoshi Iida 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	Two Brothers With ADSS1 Myopathy: A Report of Clinical, Radiological, and Autopsy Findings 2025 ·Neuropathology ·(unknown), Terunori Sano, Yasushi Oya, Chihiro Matsumoto, Yuji Nakayama, Yoshihiko Saito, Aritoshi Iida, Makoto Shibuya, Yuko Saito, Ichizo Nishino, Yūji Takahashi, Masaki Takao	2
2	Novel CLOCK and NR1D2 variants in 64 sighted Japanese individuals with non-24-hour sleep–wake rhythm disorder 2023 ·SLEEP ·Akiko Hida, Aritoshi Iida, (unknown), Hiroshi Kadotani, Makoto Uchiyama, Takashi Ebisawa, Yuichi Inoue, Shingo Kitamura, Kazuo Mishima	1
3	Malignant hyperthermia and cylindrical spirals in a 4-year-old boy 2022 ·Neuromuscular Disorders ·Masashi Ogasawara, Shinji Saitoh, (unknown), Shinichiro Hayashi, Aritoshi Iida, S. Noguchi, Ichizo Nishino	0
4	Myoglobinopathy affecting facial and oropharyngeal muscles 2022 ·Neuromuscular Disorders ·(unknown), Madoka Mori‐Yoshimura, (unknown), Yasushi Oya, (unknown), Michio Inoue, Aritoshi Iida, Noriko Sato, Ikuya Nonaka, Ichizo Nishino, (unknown)	0
5	Intranuclear inclusions in muscle biopsy can differentiate oculopharyngodistal myopathy and oculopharyngeal muscular dystrophy 2022 ·Acta Neuropathologica Communications ·Masashi Ogasawara, Nobuyuki Eura, Aritoshi Iida, (unknown), Narihiro Minami, Ikuya Nonaka, Shinichiro Hayashi, S. Noguchi, Ichizo Nishino	6
6	Intranuclear inclusions in skin biopsies are not limited to neuronal intranuclear inclusion disease but can also be seen in oculopharyngodistal myopathy 2021 ·Neuropathology and Applied Neurobiology ·Masashi Ogasawara, Nobuyuki Eura, Utako Nagaoka, Tatsuro Sato, Hajime Arahata, Tomohiro Hayashi, Tomoko Okamoto, Yuji Takahashi, Madoka Mori‐Yoshimura, Yasushi Oya, Akinori Nakamura, (unknown), Terunori Sano, (unknown), Narihiro Minami, Shinichiro Hayashi, S. Noguchi, Aritoshi Iida, Masaki Takao, Ichizo Nishino	14
7	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
8	ADSSL1 myopathy is the most common nemaline myopathy in Japan with variable clinical features 2020 ·Neurology ·Yoshihiko Saito, Atsuko Nishikawa, Aritoshi Iida, Madoka Mori‐Yoshimura, Yasushi Oya, Akihiko Ishiyama, Hirofumi Komaki, Seigo Nakamura, (unknown), Takashi Kanda, (unknown), (unknown), Shinichiro Hayashi, Ikuya Nonaka, S. Noguchi, Ichizo Nishino	20
9	CGG expansion in NOTCH2NLC is associated with oculopharyngodistal myopathy with neurological manifestations 2020 ·Acta Neuropathologica Communications ·Masashi Ogasawara, Aritoshi Iida, (unknown), (unknown), Yasushi Oya, H. Konishi, Akinori Nakamura, Ryu Abe, Hiroshi Takai, Ritsuko Hanajima, Hiroshi Doi, Fumiaki Tanaka, (unknown), Ikuya Nonaka, Zhaoxia Wang, Shinichiro Hayashi, S. Noguchi, Ichizo Nishino	71
10	A novel compound heterozygous variant of ECHS1 identified in a Japanese patient with Leigh syndrome 2019 ·Human Genome Variation ·(unknown), Aritoshi Iida, Atsushi Sato, Keiko Ishikawa, Masakazu Mimaki, Ichizo Nishino, Yu‐ichi Goto	12
11	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
12	A novel PAK3 pathogenic variant identified in two siblings from a Japanese family with X-linked intellectual disability: case report and review of the literature 2019 ·Molecular Case Studies ·Aritoshi Iida, Kyoko Takano, Eri Takeshita, (unknown), Shinichi Hirabayashi, Yuji Inaba, Shunichi Kosugi, Yoichiro Kamatani, Yukihide Momozawa, Michiaki Kubo, Eiji Nakagawa, Ken Inoue, Yu-ichi Goto	8
13	A novel LMNA mutation identified in a Japanese patient with LMNA-associated congenital muscular dystrophy 2018 ·Human Genome Variation ·Akihiko Ishiyama, Aritoshi Iida, Shinichiro Hayashi, Hirofumi Komaki, Masayuki Sasaki, Ikuya Nonaka, S. Noguchi, Ichizo Nishino	5
14	Two novel VCP missense variants identified in Japanese patients with multisystem proteinopathy 2018 ·Human Genome Variation ·Michio Inoue, Aritoshi Iida, Shinichiro Hayashi, Madoka Mori‐Yoshimura, (unknown), Shunsuke Yoshimura, Hirokazu Shiraishi, Akira Tsujino, Yuji Takahashi, Ikuya Nonaka, Yukiko Hayashi, S. Noguchi, Ichizo Nishino	5
15	Compound Heterozygosity for Null Mutations and a Common Hypomorphic Risk Haplotype inTBX6Causes Congenital Scoliosis 2017 ·Human Mutation ·Kazuki Takeda, Ikuyo Kou, Noriaki Kawakami, Aritoshi Iida, Masahiro Nakajima, Yoji Ogura, Eri Imagawa, Noriko Miyake, Naomichi Matsumoto, Yukuto Yasuhiko, Hideki Sudo, Toshiaki Kotani, Masaya Nakamura, Morio Matsumoto, Kota Watanabe, Shiro Ikegawa	30
16	Single nucleotide polymorphisms in the gene encoding Krüppel-like factor 7 are associated with type 2 diabetes 2005 ·Diabetologia ·Akio Kanazawa, Yumi Kawamura, Akihiro Sekine, Aritoshi Iida, Tatsuhiko Tsunoda, Atsunori Kashiwagi, Yasushi Tanaka, Tetsuya Babazono, Masafumi Matsuda, K. Kawai, (unknown), Tomoaki Fujioka, Miki Imanishi, Kohei Kaku, Yasuhiko Iwamoto, Ryuzo Kawamori, Ryuichi Kikkawa, Yusuke Nakamura, Shiro Maeda	64
17	Association analysis of SLC22A4, SLC22A5 and DLG5 in Japanese patients with Crohn disease 2004 ·Journal of Human Genetics ·Keiko Yamazaki, Masakazu Takazoe, Torao Tanaka, Toshiki Ichimori, Susumu Saito, Aritoshi Iida, Yoshihiro Onouchi, Akira Hata, Yusuke Nakamura	94
18	Identification of single-nucleotide polymorphisms (SNPs) of human N-acetyltransferase genes NAT1, NAT2, AANAT, ARD1, and L1CAM in the Japanese population 2001 ·Journal of Human Genetics ·Akihiro Sekine, S. Saito, Aritoshi Iida, (unknown), S. Higuchi, S. Harigae, Yusuke Nakamura	65
19	Catalog of 46 single-nucleotide polymorphisms (SNPs) in the microsomal glutathione S-transferase 1 (MGST1) gene 2001 ·Journal of Human Genetics ·Aritoshi Iida, S. Saito, Akihiro Sekine, S. Harigae, Satoshi Osawa, C. Mishima, Kazuhiro Kondo, Y. Kitamura, Yoshimasa Nakamura	21
20	Frequent Allelic Loss at 7p14‐15 Associated with Aggressive Histologic Types of Breast Cancer 1998 ·Japanese Journal of Cancer Research ·Keisuke Kurose, Aritoshi Iida, Tsutomu Araki, Goi Sakamoto, Fujio Kasumi, Yusuke Nakamura, Mitsuru Emi	12

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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