Key Publications - Amsterdam Center, Netherlands
- Schott JJ, Alshinawi C (= Bezzina), Kyndt F, Probst V, Hoorntje TM, Hulsbeek M, Wilde AAM, Escande D, Mannens MMAM, Le Marec H. Cardiac conduction defects associate with mutations in SCN5A. Nature Genet 1999;23:20-21.
- Wilde AAM, Roden DM. Predicting the long-QT genotype from clinical data. From sense to science. Circulation 2000;102:2796-8.
- Tan HL, Bink-Boelkens MTE, Bezzina CR, Viswanathan PC, Beaufort-Krol GCM, Van Tintelen JP, Van den Berg MP, Wilde AAM, Balser JR. A sodium-channel mutation causes isolated cardiac conduction disease. Nature 2001;409:1043-
- Viswanathan PC, Bezzina CR, George Jr AL, Roden DM, Wilde AAM, Balser JR. Gating-dependent mechanisms for flecainide action in SCN5A-linked arrhythmia syndromes. Circulation 2001;104:1200-5.
- Tan HL, Kupershmidt S, Zhang R, Stepanovic, Roden DM, Wilde AAM, Anderson ME, Balser JR. A calcium sensor in the sodium channel modulates cardiac excitability. Nature 2002;415:442-
- Wilde AAM, Antzelevitch C, Borggrefe M, Brugada J, Brugada R, Brugada P, Corrado D, Hauer RNW, Kass RS, Nademanee K, Priori SG, Towbin JA, for the Study Group on the Molecular Basis of the European Society of Cardiology. Proposed diagnostic criteria for the Brugada Syndrome. Consensus report. Circulation 2002;106:2514-9.
- Bezzina CR, Rook MB, Groenewegen WA, Herfst LJ, van der Wal AC, Lam J, Jongsma HJ, Wilde AAM, Mannens MMAM. Compound heterozygosity for mutations (W156X and R225W) in SCN5A associated with severe cardiac conduction disturbances and degenerative changes in the conduction system. Circ Res 2003;92:159-68.
- Bellocq C, van Ginneken ACG, Bezzina, CR, Alders M, Escande D, MD, Mannens MMAM, Baró I, Wilde AAM. Mutation in the KCNQ1 gene leading to the Short QT Interval Syndrome. Circulation 2004 ;109 :2394-7.
- Eckardt L, Probst V, Smits JPP, Schulze-Bahr E, Wolpert C, Schimpf R, Wichter T, Boisseau P, Breithardt G, Borggrefe M, leMarec H, Bocker D, Wilde AAM. Long-term prognosis of individuals with right precordial ST-elevation. Brugada syndrome. Circulation 2005 ;111 :257-63
- Bezzina CR, Shimizu W, Yang P, Koopmann TT, Tanck MW, Miyamoto Y, Kamakura S, Roden DM, Wilde AAM. Common sodium channel promoter haplotype in asian subjects underlies variability in cardiac conduction. Circulation. 2006;113:338-44.
- Dekker LR, Bezzina CR, Henriques JP, Tanck MW, Koch KT, Alings MW, Arnold AE, de Boer MJ, Gorgels AP, Michels HR, Verkerk A, Verheugt FW, Zijlstra F, Wilde AA. Familial sudden death is an important risk factor for primary ventricular fibrillation: a case-control study in acute myocardial infarction patients. Circulation. 2006 Sep 12;114(11):1140-5. Epub 2006 Aug 28.