Kanako Goto

2.7k total citations
62 papers, 2.0k citations indexed

About

Kanako Goto is a scholar working on Molecular Biology, Genetics and Cardiology and Cardiovascular Medicine. According to data from OpenAlex, Kanako Goto has authored 62 papers receiving a total of 2.0k indexed citations (citations by other indexed papers that have themselves been cited), including 47 papers in Molecular Biology, 17 papers in Genetics and 15 papers in Cardiology and Cardiovascular Medicine. Recurrent topics in Kanako Goto's work include Muscle Physiology and Disorders (38 papers), Neurogenetic and Muscular Disorders Research (17 papers) and Genetic Neurodegenerative Diseases (14 papers). Kanako Goto is often cited by papers focused on Muscle Physiology and Disorders (38 papers), Neurogenetic and Muscular Disorders Research (17 papers) and Genetic Neurodegenerative Diseases (14 papers). Kanako Goto collaborates with scholars based in Japan, United States and Singapore. Kanako Goto's co-authors include Kiichi Arahata, Yukiko Hayashi, Ikuya Nonaka, Ichizo Nishino, Megumu Ogawa, Satomi Mitsuhashi, S. Noguchi, Chie Matsuda, Je Hyeon Lee and Ritsuko Koga and has published in prestigious journals such as Journal of Clinical Investigation, Journal of Clinical Oncology and PLoS ONE.

In The Last Decade

Kanako Goto

60 papers receiving 2.0k citations

Peers

Kanako Goto

CCM

CMN

GENET

B. Eymard France

C. Jimenez‐Mallebrera Spain

Sebahattin Çirak United Kingdom

Ikuya Nonaka Japan

Anna Fidziańska Poland

Kumaraswamy Sivakumar United States

Andrei B. Borisov United States

Federica Montanaro United States

Andreas Roos Germany

Susana Quijano‐Roy France

B. Eymard France

Kanako Goto

1.5k ×0.9

771 ×1.7

CCM

439 ×1.2

CMN

272 ×0.8

GENET

245 ×0.8

Citations per year, relative to Kanako Goto Kanako Goto (= 1×) peers B. Eymard

Countries citing papers authored by Kanako Goto

Since Specialization

Citations

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

Fields of papers citing papers by Kanako Goto

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Kanako Goto

This figure shows the co-authorship network connecting the top 25 collaborators of Kanako Goto. A scholar is included among the top collaborators of Kanako Goto 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 Kanako Goto. Kanako Goto 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

Iida, Satoshi, Kanako Goto, Masako Mizoguchi, et al.. (2024). [A Case of Colorectal Cancer with Interstitial Pneumonia during Monotherapy with S-1].. PubMed. 51(13). 1600–1602.

Katayama, Keisho, Joshua R. Smith, Kanako Goto, et al.. (2018). Elevated sympathetic vasomotor outflow in response to increased inspiratory muscle activity during exercise is less in young women compared with men. Experimental Physiology. 103(4). 570–580. 32 indexed citations

Shimizu, Kaori, Kanako Goto, Kōji Ishida, et al.. (2017). Blood pressure response during normocapnic hyperpnoea is blunted in young women compared to men. Respiratory Physiology & Neurobiology. 247. 52–56. 10 indexed citations

Goto, Kanako, et al.. (2017). Gait characteristics in women's safety shoes. Applied Ergonomics. 65. 163–167. 10 indexed citations

Okubo, Mariko, Narihiro Minami, Kanako Goto, et al.. (2016). Genetic diagnosis of Duchenne/Becker muscular dystrophy using next-generation sequencing: validation analysis of DMD mutations. Journal of Human Genetics. 61(6). 483–489. 76 indexed citations

Sugiura, Tomoko, Yasushi Kawaguchi, Kanako Goto, et al.. (2014). Association between a C8orf13–BLK Polymorphism and Polymyositis/Dermatomyositis in the Japanese Population: An Additive Effect with STAT4 on Disease Susceptibility. PLoS ONE. 9(3). e90019–e90019. 8 indexed citations

Goto, Kanako, Keiko Ishigaki, S. Noguchi, et al.. (2014). Congenital fiber type disproportion myopathy caused by LMNA mutations. Journal of the Neurological Sciences. 340(1-2). 94–98. 12 indexed citations

Chen, Tai‐Heng, Yu‐Hung Lai, Jong‐Hau Hsu, et al.. (2013). Infantile facioscapulohumeral muscular dystrophy revisited: Expansion of clinical phenotypes in patients with a very short EcoRI fragment. Neuromuscular Disorders. 23(4). 298–305. 36 indexed citations

Tominaga, Kayo, Yukiko Hayashi, Kanako Goto, et al.. (2010). Congenital myotonic dystrophy can show congenital fiber type disproportion pathology. Acta Neuropathologica. 119(4). 481–486. 11 indexed citations

10.

Shalaby, S. W., Yukiko Hayashi, Kanako Goto, et al.. (2008). Rigid spine syndrome caused by a novel mutation in four-and-a-half LIM domain 1 gene (FHL1). Neuromuscular Disorders. 18(12). 959–961. 39 indexed citations

11.

Shalaby, S. W., Yukiko Hayashi, Kanako Goto, et al.. (2007). C.P.4.06 A novel myotilin mutation in exon 9: The first LGMD1A identified in Japan. Neuromuscular Disorders. 17(9-10). 880–880. 4 indexed citations

12.

Liang, Wen‐Chen, Chung‐Yee Yuo, Chee‐Siong Lee, et al.. (2007). Novel LMNA Mutation in a Taiwanese Family with Autosomal Dominant Emery-Dreifuss Muscular Dystrophy. Journal of the Formosan Medical Association. 106(2). S27–S31. 7 indexed citations

13.

Yamada, Hiroshi, Nobuhiko Takai, Yoko Saito, et al.. (2005). Informed Consent Training with Simulated Patients for Clinical Research Coordinator Trainees. Rinsho yakuri/Japanese Journal of Clinical Pharmacology and Therapeutics. 36(4). 209–213. 2 indexed citations

14.

Yamanaka, Gaku, Kanako Goto, Tadayuki Ishihara, et al.. (2004). FSHD-like patients without 4q35 deletion. Journal of the Neurological Sciences. 219(1-2). 89–93. 15 indexed citations

15.

Goto, Kanako, et al.. (2004). Very low penetrance in 85 Japanese families with facioscapulohumeral muscular dystrophy 1A. Journal of Medical Genetics. 41(1). e12–e12. 27 indexed citations

16.

Matsumura, Tsuyoshi, Kanako Goto, Gaku Yamanaka, et al.. (2002). Chromosome 4q;10q translocations; Comparison with different ethnic populations and FSHD patients. BMC Neurology. 2(1). 7–7. 19 indexed citations

17.

Yamanaka, Gaku, Kanako Goto, Tsuyoshi Matsumura, et al.. (2001). Tongue atrophy in facioscapulohumeral muscular dystrophy. Neurology. 57(4). 733–735. 33 indexed citations

18.

Kumagai, Toshiyuki, et al.. (1998). Two Cases of Chromosome 4q35-Linked Early Onset Facioscapulohumeral Muscular Dystrophy with Mental Retardation and Epilepsy. Neuropediatrics. 29(5). 239–240. 43 indexed citations

19.

Arikawa‐Hirasawa, Eri, Ritsuko Koga, Toshifumi Tsukahara, et al.. (1995). A severe muscular dystrophy patient with an internally deleted very short (110 kD) Dystrophin: Presence of the binding site for dystrophin-associated glycoprotein (DAG) may not be enough for physiological function of dystrophin. Neuromuscular Disorders. 5(5). 429–438. 11 indexed citations

20.

Hayashi, Yukiko, Eva Engvall, Eri Arikawa‐Hirasawa, et al.. (1993). Abnormal localization of laminin subunits in muscular dystrophies. Journal of the Neurological Sciences. 119(1). 53–64. 142 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.

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