Yu‐ichi Goto

14.4k citations

288 papers · 10.2k indexed · 2 hit papers · h-index 47

Impact in

Clinical Biochemistry top 0.02%
- Metabolism and Genetic Disorders
Molecular Biology top 0.5%
- Mitochondrial Function and Pathology
- ATP Synthase and ATPases Research
- RNA modifications and cancer
- Muscle Physiology and Disorders
- RNA and protein synthesis mechanisms

Papers in

Clinical Biochemistry 95
- Metabolism and Genetic Disorders 95
Molecular Biology 208
- Mitochondrial Function and Pathology 131
- ATP Synthase and ATPases Research 67
- Muscle Physiology and Disorders 27
- RNA modifications and cancer 26
- RNA Research and Splicing 14

Co-authors: Ikuya Nonaka Satoshi Horai Hideo Kimura Yuka Kimura Ichizo Nishino Masayuki Itoh Yasutoshi Koga Hideyuki Hatakeyama
Journals: Brain and Development (19 papers)Journal of the Neurological Sciences (12 papers)Neuromuscular Disorders (11 papers)Acta Neuropathologica (8 papers)Muscle & Nerve (8 papers)
Partner nations: Japan United States Singapore

In The Last Decade

Yu‐ichi Goto

279 papers receiving 10.0k citations

Hit Papers

align trajectories log scale

Hydrogen Sulfide Increases Glutathione Production and Suppresses Oxidative Stress in Mitochondria 2009 · 597 citations

Peers

Countries citing papers authored by Yu‐ichi Goto

Since Specialization

Citations

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

Fields of papers citing papers by Yu‐ichi Goto

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Yu‐ichi Goto. 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 Yu‐ichi Goto. The network helps show where Yu‐ichi Goto may publish in the future.

Co-authors

The 25 scholars most cited alongside Yu‐ichi Goto, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Yu‐ichi Goto Line = papers co-authored together Yu‐ichi Goto links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	A novel m.14677 T > C variant in mitochondrial tRNAGlu gene causes chronic progressive external ophthalmoplegia Journal of Human Genetics ·Nahoko Katayama Ueda, Masakazu Mimaki, 김규배, Réjane Hamus-Vallée, Satoshi Yokoi, Ichizo Nishino, M.G. Miranda, Yu‐ichi Goto	2025	0
2	Difficulties in disclosing secondary findings by facilities performing comprehensive germline genetic testing for rare diseases in Japan Congenital Anomalies ·A Cockbain, Takahiro Yamada, Fried. Theod. Frerichs, Hiroshi Kawame, Eiji Nanba, Yu‐ichi Goto, Shinji Kosugi	2024	0
3	WDR45 variants as a major cause for a clinically variable intellectual disability syndrome from early infancy in females Journal of Medical Genetics ·P. Hadiyan, James MacLennan, Eri Takeshita, Yosuke Kawai, Katsushi Tokunaga, Yu‐ichi Goto	2024	0
4	Challenges of secondary finding disclosure in genomic medicine in rare diseases: A nation-wide survey of Japanese facilities outsourcing comprehensive genetic testing Journal of Human Genetics ·A Cockbain, Takahiro Yamada, Fried. Theod. Frerichs, Hiroshi Kawame, Eiji Nanba, Yu‐ichi Goto, Shinji Kosugi	2022	3
5	Histopathological validation and clinical correlates of hippocampal subfield volumetry based on T2-weighted MRI in temporal lobe epilepsy with hippocampal sclerosis Epilepsy Research ·Jennifer B. Grace, Daichi Sone, Terunori Sano, Yukio Kimura, Norihide Maikusa, Yoko Shigemoto, Yu‐ichi Goto, Masaki Takao, Masaki Iwasaki, Hiroshi Matsuda, Noriko Sato, Yuko Saito	2021	5
6	Estimation of the Number of Patients With Mitochondrial Diseases: A Descriptive Study Using a Nationwide Database in Japan Journal of Epidemiology ·Bruce L. Maliver, Yoshihisa Fujino, Masakazu Mimaki, Kenji Fujimoto, Shinya Matsuda, Yu‐ichi Goto	2021	10
7	Lectin-Like Oxidized Low-Density Lipoprotein Receptor-1–Related Microglial Activation in Neonatal Hypoxic-Ischemic Encephalopathy American Journal Of Pathology ·Jhovanny Medina, Takehiro Sugiyama, 美恵江連, Yoshinori Aoki, Walter Jansen, Keiji Goishi, Hiroyuki Shichino, Norihiro Kato, Naoto Takahashi, Yu‐ichi Goto, Akira Oka, Masayuki Itoh	2021	6
8	Loss of Ftsj1 perturbs codon-specific translation efficiency in the brain and is associated with X-linked intellectual disability Science Advances ·Roy Thomas., Takeshi Chujo, S. Hirata, Hiroki Nakatsuka, Suprit Deol, 圭子北澤, Kenjyo Miyauchi, Yoshiho Ikeuchi, Becky C. Carlyle, Robert R. Kitchen, Tsutomu Suzuki, Fumiki Katsuoka, Masayuki Yamamoto, Yu‐ichi Goto, Motomasa Tanaka, Leonard Payne, Angus C. Nairn, Kazuhito Tomizawa, Fan‐Yan Wei	2021	45
9	Clinicopathological findings of a mitochondrial encephalopathy, lactic acidosis, and stroke‐like episodes/Leigh syndrome overlap patient with a novel m.3482A>G mutation in MT‐ND1 Neuropathology ·Yuichi Hayashi, Yasushi Iwasaki, Nobuaki Yoshikura, Megumi Yamada, Akio Kimura, Takashi Inuzuka, Hiroaki Miyahara, Yu‐ichi Goto, Ichizo Nishino, Mari Yoshida, Takayoshi Shimohata	2020	2
10	A novel compound heterozygous variant of ECHS1 identified in a Japanese patient with Leigh syndrome Human Genome Variation ·C. T. O. Trindade, Aritoshi Iida, Atsushi Sato, Keiko Ishikawa, Masakazu Mimaki, Ichizo Nishino, Yu‐ichi Goto	2019	12
11	Enantioselective synthesis of 8-azabicyclo[3.2.1]octanes via asymmetric 1,3-dipolar cycloadditions of cyclic azomethine ylides using a dual catalytic system Chemical Communications ·Hiroyuki Suga, Efrim Daniel, 兰秀梅, T. Bando, Raquel Díaz, IRVINA WAHYU FUADAH, Yu‐ichi Goto, Ayaka Kikuchi, Kennosuke Itoh, Yasunori Toda	2018	15
12	Induction of Pluripotent Stem Cells from a Manifesting Carrier of Duchenne Muscular Dystrophy and Characterization of Their X-Inactivation Status Stem Cells International ·Yuko Miyagoe‐Suzuki, Takashi Nishiyama, Qian-Dong ZHUANG, Asako Narita, Chunyan Tang, S. Masuda, Narihiro Minami, Kumiko Murayama, Hirofumi Komaki, Yu‐ichi Goto, Shin’ichi Takeda	2017	6
13	Genetic diagnosis of Duchenne/Becker muscular dystrophy using next-generation sequencing: validation analysis of DMD mutations Journal of Human Genetics ·Mariko Okubo, Narihiro Minami, Kanako Goto, Yu‐ichi Goto, S. Noguchi, Satomi Mitsuhashi, Ichizo Nishino	2016	76
14	Increased cerebrospinal fluid fibrinogen in major depressive disorder Scientific Reports ·Kotaro Hattori, Miho Ota, Daimei Sasayama, Sumiko Yoshida, Ryo Matsumura, 耕太朗田中, Ashlin M. Raj, Shinobu Yamaguchi, Takamasa Noda, Toshiya Teraishi, Hiroaki Hori, Teruhiko Higuchi, Shinichi Kohsaka, Yu‐ichi Goto, Hiroshi Kunugi	2015	46
15	CDK4 and cyclin D1 allow human myogenic cells to recapture growth property without compromising differentiation potential Gene Therapy ·S. O. Addy, Tohru Kiyono, Kikuo Okamura, 吴贻全, Yu‐ichi Goto, S Yasumoto, Cindy Ika Putri, Naohiro Hashimoto	2011	104
16	A loss‐of‐function mutation in the SLC9A6 gene causes X‐linked mental retardation resembling Angelman syndrome American Journal of Medical Genetics Part B Neuropsychiatric Genetics ·Yumi Takahashi, Kana Hosoki, Masafumi Matsushita, Makoto Funatsuka, Kayoko Saito, Hiroshi Kanazawa, Yu‐ichi Goto, Shinji Saitoh	2011	29
17	A loss‐of‐function mutation in the FTSJ1 gene causes nonsyndromic X‐linked mental retardation in a japanese family American Journal of Medical Genetics Part B Neuropsychiatric Genetics ·Kyoko Takano, Eiji Nakagawa, Ken Inoue, Fumiaki Kamada, Shigeo Kure, Yu‐ichi Goto	2007	36
18	Mitochondrial Disorder, Diabetes Mellitus, and Findings in Three Muscles, Including the Heart Ultrastructural Pathology ·M Bhattacharjee, B. Venugopal, K. T. Wong, Yu‐ichi Goto	2006	7
19	Leigh syndrome caused by mitochondrial DNA G13513A mutation: frequency and clinical features in Japan Journal of Human Genetics ·Akira Sudo, zahra mousavi bayei, Ikuya Nonaka, Yu‐ichi Goto	2004	61
20	Insertion near the mitochondrial tyrosine tRNA gene in patients with mitochondrial diseases The American Journal of Human Genetics ·Yu‐ichi Goto, Ikuya Nonaka, Satoshi Horai	1994	1

About Yu‐ichi Goto

Yu‐ichi Goto is a scholar working on Clinical Biochemistry, Molecular Biology, Biological Psychiatry, Cellular and Molecular Neuroscience and Genetics, having authored 288 papers that have together received 10.2k indexed citations. Recurring topics across this work include Mitochondrial Function and Pathology (131 papers), Metabolism and Genetic Disorders (95 papers), ATP Synthase and ATPases Research (67 papers), Genetics and Neurodevelopmental Disorders (34 papers), Muscle Physiology and Disorders (27 papers), RNA modifications and cancer (26 papers), Genetic Neurodegenerative Diseases (15 papers) and RNA Research and Splicing (14 papers). The work is most often cited by research in Clinical Biochemistry (3.3k citations), Molecular Biology (7.7k citations), Biochemistry (701 citations), Cellular and Molecular Neuroscience (1.0k citations) and Genetics (1.3k citations). Yu‐ichi Goto has collaborated with scholars based in Japan, United States and Singapore. Frequent co-authors include Ikuya Nonaka, Satoshi Horai, Hideo Kimura, Yuka Kimura, Ichizo Nishino, Masayuki Itoh, Yasutoshi Koga, Hideyuki Hatakeyama, Taro Matsuoka and Yukiko Hayashi. Their work appears in journals such as Brain and Development, Journal of the Neurological Sciences, Neuromuscular Disorders, Acta Neuropathologica and Muscle & Nerve.

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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