- 2021 - 2024 遺伝性不整脈症候群の病原性遺伝子変異の決定とそれに基づく個別化医療の実現
- 2020 - 2024 分子疫学的コホート研究による遺伝性心血管疾患のリスク層別化・病態解明・治療薬探索
- 2018 - 2021 Gene analysis for novel causative mutations in an inherited arrhythmia and determination of the underlying mechanism of arrhythmia
- 2017 - 2020 Research in molecular and genetic epidemiology of hypertrophic cardiomyopathy and other cardiomyopathies
- 2015 - 2018 Phosphorylase phosphorylation in the heart failure development
- 2016 - 2018 Gene analysis for novel causative mutations in an inherited arrhythmia and functional study for these mutations using zebrafish(Fostering Joint International Research)
- 2014 - 2017 An examination of mutation-specific precipitation factors for ventricular tachyarrhythmias in concealed inherited arrhythmia syndromes
- 2014 - 2017 Research of the factors to contribute to the onset and the prognosis of hypertrophic cardiomyopathy by the registration study
- 2014 - 2017 Genetic analysis for inherited arrhythmia and functional study using zebrafish model
- 2013 - 2016 Searching and analysis of genes causing arrhythmia with pharmacological and non-pharmacological intervention
- 2011 - 2013 Gene analysis for the inherited arrhythmia and functional characterization of disease-causing rare variants by using zebrafish
- 2010 - 2012 Research of the tailor-maid treatment of hypertrophic and dilated cardiomyopathy by comprehensive genetic analysis
- 2010 - 2012 Gene analysis for the inherited bradyarrhythmia and characterization of cardiosphere-derived cells to create biological pacemakers
- 2007 - 2009 Molecular genetics of atrial fibrillation and evaluation of upstream therapy for atrial fibrillation
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