Gabriel Cáceres

A novel rare variant in SCN1Bb linked to Brugada syndrome and SIDS by combined modulation of Na 1.5 and K 4.3 channel currents

Dan Hu, Héctor Barajas-Martínez, Argelia Medeiros‐Domingo et al. · Heart Rhythm · 2011 · 103 citations

Life Sciences, Genetics, Neuroscience +17

Further Insights in the Most Common <i>SCN5A</i> Mutation Causing Overlapping Phenotype of Long QT Syndrome, Brugada Syndrome, and Conduction Defect

Christian Veltmann, Héctor Barajas-Martínez, Christian Wolpert et al. · Journal of the American Heart Association · 2016 · 58 citations · Full text

Life Sciences, Cardiology, Genetics +16

A Common Single Nucleotide Polymorphism Can Exacerbate Long-QT Type 2 Syndrome Leading to Sudden Infant Death

Eyal Nof, Jonathan M. Cordeiro, Guillermo J. Pérez et al. · Circulation Cardiovascular Genetics · 2010 · 55 citations · Full text

Medicine, Cardiology, Genetics +17

Identification of a Novel De Novo Mutation Associated with PRKAG2 Cardiac Syndrome and Early Onset of Heart Failure

Liu Yang, Rong Bai, Lin Wang et al. · PLoS ONE · 2013 · 36 citations · Full text

Medicine, Cardiology, Genetics +16

Biophysical and Molecular Characterization of a Novel De Novo <i>KCNJ2</i> Mutation Associated With Andersen-Tawil Syndrome and Catecholaminergic Polymorphic Ventricular Tachycardia Mimicry

Héctor Barajas-Martínez, Dan Hu, Gustavo Ontiveros et al. · Circulation Cardiovascular Genetics · 2010 · 34 citations · Full text

Medicine, Cardiology, Genetics +17