Progress in Understanding and Treating SCN2A-Mediated DisordersStephan Sanders, Kevin J. Bender, Arthur J. Campbell et al.|Trends in Neurosciences|2018Cited by 339
Calmodulin mutations and life-threatening cardiac arrhythmias: insights from the International Calmodulinopathy RegistryLia Crotti, Peter J. Schwartz, Connie R. Bezzina et al.|European Heart Journal|2019Cited by 184
Genome-wide association study of multiple congenital heart disease phenotypes identifies a susceptibility locus for atrial septal defect at chromosome 4p16Heather J. Cordell, Bernard Keavney, Jamie Bentham et al.|Nature Genetics|2013Cited by 165
Unexpected Efficacy of a Novel Sodium Channel Modulator in Dravet SyndromeLyndsey L. Anderson, Alfred L. George|Scientific Reports|2017Cited by 74