Taisuke Ishikawa

2.3k total citations
38 papers, 843 citations indexed

About

Taisuke Ishikawa is a scholar working on Cardiology and Cardiovascular Medicine, Molecular Biology and Radiology, Nuclear Medicine and Imaging. According to data from OpenAlex, Taisuke Ishikawa has authored 38 papers receiving a total of 843 indexed citations (citations by other indexed papers that have themselves been cited), including 33 papers in Cardiology and Cardiovascular Medicine, 19 papers in Molecular Biology and 8 papers in Radiology, Nuclear Medicine and Imaging. Recurrent topics in Taisuke Ishikawa's work include Cardiac electrophysiology and arrhythmias (18 papers), Cardiomyopathy and Myosin Studies (12 papers) and Ion channel regulation and function (11 papers). Taisuke Ishikawa is often cited by papers focused on Cardiac electrophysiology and arrhythmias (18 papers), Cardiomyopathy and Myosin Studies (12 papers) and Ion channel regulation and function (11 papers). Taisuke Ishikawa collaborates with scholars based in Japan, United States and Italy. Taisuke Ishikawa's co-authors include Takuro Arimura, Akinori Kimura, Naomasa Makita, Shinichi Nunoda, Sachio Kawai, Shuji Suzuki, Harumizu Sakurada, Ryuji Fukushima, Ryou Tanaka and Yukiomi Tsuji and has published in prestigious journals such as Journal of Biological Chemistry, PLoS ONE and The Journal of Physiology.

In The Last Decade

Taisuke Ishikawa

36 papers receiving 826 citations

Peers

Taisuke Ishikawa

CCM

RNMI

CMN

Ralph J. Barker United States

D. Wray United Kingdom

Sandra Pierobon‐Bormioli Italy

Yasuhiro Saito Japan

Giedrius Kanaporis United States

Xiurong Sun United States

Hadas Lahat Israel

Alex J. Fay United States

T. Jarry‐Guichard France

Ralph J. Barker United States

Taisuke Ishikawa

144 ×0.2

CCM

537 ×1.0

20 ×0.2

RNMI

25 ×0.3

CMN

39 ×0.7

Citations per year, relative to Taisuke Ishikawa Taisuke Ishikawa (= 1×) peers Ralph J. Barker

Countries citing papers authored by Taisuke Ishikawa

Since Specialization

Citations

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

Fields of papers citing papers by Taisuke Ishikawa

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Taisuke Ishikawa

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

Ohta‐Ogo, Keiko, Taisuke Ishikawa, Makoto Araki, et al.. (2025). Cardiomyopathy Associated with Subclinical Becker Muscular Dystrophy in a Patient Presenting with Anesthesia-induced Rhabdomyolysis. Internal Medicine.

Murakami, Haruka, Yoko Tanimoto, Kojiro Tanimoto, et al.. (2022). Arrhythmogenic right ventricular cardiomyopathy in a Japanese patient with a homozygous founder variant of DSG2 in the East Asian population. Human Genome Variation. 9(1). 28–28. 1 indexed citations

Matsushita, Yuki, et al.. (2020). A Case Report: Two Young Children with Long QT Syndrome Type-2 Diagnosed by Presymptomatic Genetic Testing. Journal of Pediatric Genetics. 11(4). 313–316.

Hata, Yukiko, Hironori Izumi, Ryo Nagaoka, et al.. (2020). TBX5 R264K acts as a modifier to develop dilated cardiomyopathy in mice independently of T-box pathway. PLoS ONE. 15(4). e0227393–e0227393. 6 indexed citations

Saito, Yuki, Daisuke Fukamachi, Koichi Nagashima, et al.. (2020). Desmin-Related Myopathy Characterized by Non-Compaction Cardiomyopathy, Cardiac Conduction Defect, and Coronary Artery Dissection. ESC Heart Failure. 7(3). 1338–1343. 8 indexed citations

Oshima, Yuki, Takuma Yamamoto, Taisuke Ishikawa, et al.. (2017). Postmortem genetic analysis of sudden unexpected death in infancy: neonatal genetic screening may enable the prevention of sudden infant death. Journal of Human Genetics. 62(11). 989–995. 14 indexed citations

Ishikawa, Taisuke, Seiko Ohno, Takashi Murakami, et al.. (2017). Sick sinus syndrome with HCN4 mutations shows early onset and frequent association with atrial fibrillation and left ventricular noncompaction. Heart Rhythm. 14(5). 717–724. 33 indexed citations

Takahashi, Kazuhiro, et al.. (2016). A novel de novo calmodulin mutation in a 6-year-old boy who experienced an aborted cardiac arrest. HeartRhythm Case Reports. 3(1). 69–72. 17 indexed citations

Ashihara, Takashi, Taisuke Ishikawa, Andrea Mazzanti, et al.. (2015). Genotype-dependent differences in age of manifestation and arrhythmia complications in short QT syndrome. International Journal of Cardiology. 190. 393–402. 40 indexed citations

10.

Ishikawa, Taisuke, Yukiomi Tsuji, & Naomasa Makita. (2015). Inherited bradyarrhythmia: A diverse genetic background. Journal of Arrhythmia. 32(5). 352–358. 24 indexed citations

11.

Sasano, Tetsuo, Wataru Kimura, Yoshihiro Miyamoto, et al.. (2015). Genetic defects in a His-Purkinje system transcription factor,IRX3, cause lethal cardiac arrhythmias. European Heart Journal. 37(18). 1469–1475. 43 indexed citations

12.

Tsuji, Yukiomi, Taisuke Ishikawa, & Naomasa Makita. (2014). Molecular mechanisms of heart failure progression associated with implantable cardioverter‐defibrillator shocks for ventricular tachyarrhythmias. Journal of Arrhythmia. 30(4). 235–241. 1 indexed citations

13.

Ishikawa, Taisuke, Akinori Sato, Cherisse A. Marcou, et al.. (2012). A Novel Disease Gene for Brugada Syndrome. Circulation Arrhythmia and Electrophysiology. 5(6). 1098–1107. 80 indexed citations

14.

Suzuki, Shuji, Ryuji Fukushima, Taisuke Ishikawa, et al.. (2012). Comparative effects of amlodipine and benazepril on Left Atrial Pressure in Dogs with experimentally-induced Mitral Valve Regurgitation. BMC Veterinary Research. 8(1). 166–166. 7 indexed citations

15.

Suzuki, Shuji, Ryuji Fukushima, Taisuke Ishikawa, et al.. (2011). The Effect of Pimobendan on Left Atrial Pressure in Dogs with Mitral Valve Regurgitation. Journal of Veterinary Internal Medicine. 25(6). 1328–1333. 44 indexed citations

16.

Arimura, Takuro, Taisuke Ishikawa, Shinichi Nunoda, Sachio Kawai, & Akinori Kimura. (2011). Dilated cardiomyopathy-associatedBAG3mutations impair Z-disc assembly and enhance sensitivity to apoptosis in cardiomyocytes. Human Mutation. 32(12). 1481–1491. 104 indexed citations

17.

Suzuki, Shuji, Taisuke Ishikawa, Lina Hamabe, et al.. (2011). The Effect of Furosemide on Left Atrial Pressure in Dogs with Mitral Valve Regurgitation. Journal of Veterinary Internal Medicine. 25(2). 244–250. 17 indexed citations

18.

Ishikawa, Taisuke, Ryou Tanaka, Shuji Suzuki, et al.. (2010). The Effect of Angiotensin-Converting Enzyme Inhibitors of Left Atrial Pressure in Dogs with Mitral Valve Regurgitation. Journal of Veterinary Internal Medicine. 24(2). 342–347. 17 indexed citations

19.

Ishikawa, Taisuke, et al.. (2009). Daily Rhythms of Left Atrial Pressure in Beagle Dogs with Mitral Valve Regurgitation. Journal of Veterinary Internal Medicine. 23(4). 824–831. 11 indexed citations

20.

Fujimoto, Shinji, et al.. (1999). Early Onset of X-Linked Emery-Dreifuss Muscular Dystrophy in a Boy with Emerin Gene Deletion. Neuropediatrics. 30(3). 161–163. 2 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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