Makita, Naomasa

Top Publications

Top Publications Authored or Co-Authored by "Makita, Naomasa"

• Fibrosis, connexin-43, and conduction abnormalities in the Brugada syndrome

  Journal of the American College of Cardiology, Volume 66, No. 18, Year 2015, Citations 324
• The E1784K mutation in SCN5A is associated with mixed clinical phenotype of type 3 long QT syndrome

  Journal of Clinical Investigation, Volume 118, No. 6, Year 2008, Citations 224
• Calmodulin mutations and life-threatening cardiac arrhythmias: Insights from the International Calmodulinopathy Registry

  European Heart Journal, Volume 40, No. 35, Year 2019, Citations 97
• A novel disease gene for Brugada syndrome: Sarcolemmal membrane-associated protein gene mutations impair intracellular trafficking of hNav1.5

  Circulation: Arrhythmia and Electrophysiology, Volume 5, No. 6, Year 2012, Citations 94
• Targeted resequencing identifies TRPM4 as a major gene predisposing to progressive familial heart block type i

  International Journal of Cardiology, Volume 207, Year 2016, Citations 49