What is he best known for?
The fields of study he is best known for:
- Internal medicine
- Gene
- Enzyme
Minoru Horie mainly investigates Internal medicine, Cardiology, Endocrinology, QT interval and Long QT syndrome.
Many of his studies on Internal medicine apply to Anesthesia as well.
His Cardiology research incorporates elements of Predictive value of tests and Hazard ratio.
He interconnects Regulation of gene expression, Patch clamp and Cell biology in the investigation of issues within Endocrinology.
His research integrates issues of Mutation, Proband, Repolarization and Mutation in his study of QT interval.
Minoru Horie has included themes like Genetics, Genetic heterogeneity, Pediatrics and Torsades de pointes in his Long QT syndrome study.
His most cited work include:
- HRS/EHRA/APHRS expert consensus statement on the diagnosis and management of patients with inherited primary arrhythmia syndromes: document endorsed by HRS, EHRA, and APHRS in May 2013 and by ACCF, AHA, PACES, and AEPC in June 2013. (1123 citations)
- Executive summary: HRS/EHRA/APHRS expert consensus statement on the diagnosis and management of patients with inherited primary arrhythmia syndromes (430 citations)
- Cloning and Functional Characterization of a Novel ATP-sensitive Potassium Channel Ubiquitously Expressed in Rat Tissues, including Pancreatic Islets, Pituitary, Skeletal Muscle, and Heart (374 citations)
What are the main themes of his work throughout his whole career to date?
The scientist’s investigation covers issues in Internal medicine, Cardiology, Endocrinology, Heart failure and Long QT syndrome.
Minoru Horie connects Internal medicine with In patient in his research.
His Cardiology research is multidisciplinary, relying on both Anesthesia and Catecholaminergic polymorphic ventricular tachycardia.
His studies link Patch clamp with Endocrinology.
In his study, which falls under the umbrella issue of Long QT syndrome, Mutant is strongly linked to Mutation.
His work deals with themes such as Proband and Sudden death, which intersect with QT interval.
He most often published in these fields:
- Internal medicine (71.48%)
- Cardiology (53.70%)
- Endocrinology (17.78%)
What were the highlights of his more recent work (between 2015-2021)?
- Internal medicine (71.48%)
- Cardiology (53.70%)
- Long QT syndrome (14.32%)
In recent papers he was focusing on the following fields of study:
His main research concerns Internal medicine, Cardiology, Long QT syndrome, Brugada syndrome and Catecholaminergic polymorphic ventricular tachycardia.
His Internal medicine study frequently draws connections to other fields, such as Endocrinology.
He has researched Long QT syndrome in several fields, including Phenotype, Pediatrics, Mutation and Induced pluripotent stem cell.
In his study, Mutant, Calmodulin, Molecular biology and Cohort is inextricably linked to Mutation, which falls within the broad field of Phenotype.
His biological study spans a wide range of topics, including Genetics, Sudden death, Proband and Sodium channel.
His work focuses on many connections between Proband and other disciplines, such as Gene mutation, that overlap with his field of interest in Arrhythmogenic right ventricular dysplasia and Pathology.
Between 2015 and 2021, his most popular works were:
- J-Wave syndromes expert consensus conference report: Emerging concepts and gaps in knowledge. (287 citations)
- The genetics underlying acquired long QT syndrome: impact for genetic screening (92 citations)
- Splicing misregulation of SCN5A contributes to cardiac-conduction delay and heart arrhythmia in myotonic dystrophy (90 citations)
In his most recent research, the most cited papers focused on:
- Internal medicine
- Gene
- Enzyme
Minoru Horie spends much of his time researching Internal medicine, Cardiology, Long QT syndrome, Brugada syndrome and Atrial fibrillation.
His Internal medicine research incorporates themes from Endocrinology and Proband.
Minoru Horie combines subjects such as Allele, Induced pluripotent stem cell and Medical genetics with his study of Long QT syndrome.
His work carried out in the field of Brugada syndrome brings together such families of science as Genetics, EARLY REPOLARIZATION SYNDROME, Expert consensus and Missense mutation.
His Atrial fibrillation research is multidisciplinary, incorporating elements of Adverse effect, Ablation and Inward-rectifier potassium ion channel.
The concepts of his QT interval study are interwoven with issues in Molecular pathogenesis and Delayed rectifier.
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