Alex V. Postma
Amsterdam University Medical Centers(NL)
Publications by Year
Research Areas
Congenital heart defects research, Congenital Heart Disease Studies, Cardiomyopathy and Myosin Studies, Cardiac electrophysiology and arrhythmias, Ion channel regulation and function
Most-Cited Works
- → A Single Na + Channel Mutation Causing Both Long-QT and Brugada Syndromes(1999)638 cited
- → Absence of Calsequestrin 2 Causes Severe Forms of Catecholaminergic Polymorphic Ventricular Tachycardia(2002)400 cited
- → Catecholaminergic polymorphic ventricular tachycardia: RYR2 mutations, bradycardia, and follow up of the patients(2005)300 cited
- → Expanding Spectrum of Human RYR2 -Related Disease(2007)244 cited
- → HCN4 Mutations in Multiple Families With Bradycardia and Left Ventricular Noncompaction Cardiomyopathy(2014)196 cited
- → Whole Exome Sequencing Reveals the Major Genetic Contributors to Nonsyndromic Tetralogy of Fallot(2019)193 cited
- → Mutations in the Sarcomere Gene MYH7 in Ebstein Anomaly(2010)187 cited
- → A Gain-of-Function TBX5 Mutation Is Associated With Atypical Holt–Oram Syndrome and Paroxysmal Atrial Fibrillation(2008)186 cited
- → Truncating Titin Mutations are Associated with a Mild and Treatable form of Dilated Cardiomyopathy(2016)173 cited
- → Genome-wide association study of multiple congenital heart disease phenotypes identifies a susceptibility locus for atrial septal defect at chromosome 4p16(2013)165 cited