Michiko Furutani
Tokyo Women's Medical University(JP)
Publications by Year
Research Areas
Cardiac electrophysiology and arrhythmias, Cardiomyopathy and Myosin Studies, Ion channel regulation and function, Mitochondrial Function and Pathology, Cardiovascular Function and Risk Factors
Most-Cited Works
- → Germline gain-of-function mutations in RAF1 cause Noonan syndrome(2007)494 cited
- → GATA6 mutations cause human cardiac outflow tract defects by disrupting semaphorin-plexin signaling(2009)237 cited
- → Phenotypes with GATA4 or NKX2.5 mutations in familial atrial septal defect(2005)218 cited
- → Novel Mechanism Associated With an Inherited Cardiac Arrhythmia(1999)192 cited
- → Implications of Mutations of Activin Receptor-Like Kinase 1 Gene (<i>ALK1</i>) in Addition to Bone Morphogenetic Protein Receptor II Gene (<i>BMPR2</i>) in Children With Pulmonary Arterial Hypertension(2007)109 cited
- → Oxidized LDL receptor gene (OLR1) is associated with the risk of myocardial infarction(2003)107 cited
- → RAF1 mutations in childhood-onset dilated cardiomyopathy(2014)84 cited
- → Genetic Analysis of Essential Cardiac Transcription Factors in 256 Patients With Non-Syndromic Congenital Heart Defects(2012)81 cited
- → Identification of a novel TPM1 mutation in a family with left ventricular noncompaction and sudden death(2010)42 cited
- → Complete sequence of human cardiac α‐myosin heavy chain gene and amino acid comparison to other myosins based on structural and functional differences(1991)39 cited