Genetics of cardiac arrhythmias

di Wilde, Arthur A M, Bezzina, Connie R
Pubblicazione 2005

When genetic burden reaches threshold

di Walsh, Roddy, Tadros, Rafik, Bezzina, Connie R
Pubblicato in Eur Heart J (2020)

Next-Generation Sequencing in Post-mortem Genetic Testing of Young Sudden Cardiac Death Cases

di Lahrouchi, Najim, Behr, Elijah R., Bezzina, Connie R.
Pubblicato in Front Cardiovasc Med (2016)

Illuminating the path from genetics to clinical outcome in Brugada syndrome

di Postema, Pieter G, Walsh, Roddy, Bezzina, Connie R
Pubblicato in Eur Heart J (2021)

Genetic Basis of Ventricular Arrhythmias

di Pazoki, Raha, Wilde, Arthur A. M., Bezzina, Connie R.
Pubblicazione 2010

Beyond the “one gene-one disease” paradigm: complex genetics and pleiotropy in inheritable cardiac disorders

di Cerrone, Marina, Remme, Carol Ann, Tadros, Rafik, Bezzina, Connie R., Delmar, Mario
Pubblicato in Circulation (2019)

Genome-wide association studies of cardiac electrical phenotypes

di Glinge, Charlotte, Lahrouchi, Najim, Jabbari, Reza, Tfelt-Hansen, Jacob, Bezzina, Connie R
Pubblicato in Cardiovasc Res (2020)

Induced pluripotent stem cell derived cardiomyocytes as models for cardiac arrhythmias

di Hoekstra, Maaike, Mummery, Christine L., Wilde, Arthur A. M., Bezzina, Connie R., Verkerk, Arie O.
Pubblicazione 2012

Patch-Clamp Recording from Human Induced Pluripotent Stem Cell-Derived Cardiomyocytes: Improving Action Potential Characteristics through Dynamic Clamp

di Verkerk, Arie O., Veerman, Christiaan C., Zegers, Jan G., Mengarelli, Isabella, Bezzina, Connie R., Wilders, Ronald
Pubblicato in Int J Mol Sci (2017)

Inherited cardiac arrhythmias

di Schwartz, Peter J., Ackerman, Michael J., Antzelevitch, Charles, Bezzina, Connie R., Borggrefe, Martin, Cuneo, Bettina F., Wilde, Arthur A. M.
Pubblicato in Nat Rev Dis Primers (2020)

Inherited dilated cardiomyopathy in a large Moroccan family caused by LMNA mutation

di Adadi, Najlae, Radi, Fatima Zohra, Lahrouchi, Najim, Hara, Loubna, Ratbi, Ilham, Elalaoui, Siham Chafai, Alders, Marielle, Zarzur, Jamila, Bezzina, Connie, Sefiani, Abdelaziz
Pubblicato in Anatol J Cardiol (2018)

Sodium Channel Remodeling in Subcellular Microdomains of Murine Failing Cardiomyocytes

di Rivaud, Mathilde R., Agullo‐Pascual, Esperanza, Lin, Xianming, Leo‐Macias, Alejandra, Zhang, Mingliang, Rothenberg, Eli, Bezzina, Connie R., Delmar, Mario, Remme, Carol Ann
Pubblicato in J Am Heart Assoc (2017)

hiPSC-derived cardiomyocytes from Brugada Syndrome patients without identified mutations do not exhibit clear cellular electrophysiological abnormalities

di Veerman, Christiaan C., Mengarelli, Isabella, Guan, Kaomei, Stauske, Michael, Barc, Julien, Tan, Hanno L., Wilde, Arthur A. M., Verkerk, Arie O., Bezzina, Connie R.
Pubblicato in Sci Rep (2016)

A Heterozygous Deletion Mutation in the Cardiac Sodium Channel Gene SCN5A with Loss- and Gain-of-Function Characteristics Manifests as Isolated Conduction Disease, without Signs of...

di Zumhagen, Sven, Veldkamp, Marieke W., Stallmeyer, Birgit, Baartscheer, Antonius, Eckardt, Lars, Paul, Matthias, Remme, Carol Ann, Bhuiyan, Zahurul A., Bezzina, Connie R., Schulze-Bahr, Eric
Pubblicazione 2013

Sibling history is associated with heart failure after a first myocardial infarction

di Glinge, Charlotte, Oestergaard, Louise, Jabbari, Reza, Rossetti, Sara, Skals, Regitze, Køber, Lars, Engstrøm, Thomas, Bezzina, Connie R, Torp-Pedersen, Christian, Gislason, Gunnar, Tfelt-Hansen, Jacob
Pubblicato in Open Heart (2020)

SNPs Identified as Modulators of ECG Traits in the General Population Do Not Markedly Affect ECG Traits during Acute Myocardial Infarction nor Ventricular Fibrillation Risk in This...

di Pazoki, Raha, de Jong, Jonas S.S.G., Marsman, Roos F., Bruinsma, Nienke, Dekker, Lukas R. C., Wilde, Arthur A. M., Bezzina, Connie R., Tanck, Michael W. T.
Pubblicazione 2013

Heart failure following STEMI: a contemporary cohort study of incidence and prognostic factors

di Gho, Johannes M I H, Postema, Pieter G, Conijn, Maartje, Bruinsma, Nienke, de Jong, Jonas S S G, Bezzina, Connie R, Wilde, Arthur A M, Asselbergs, Folkert W
Pubblicato in Open Heart (2017)

Functional Consequences of the SCN5A-p.Y1977N Mutation within the PY Ubiquitylation Motif: Discrepancy between HEK293 Cells and Transgenic Mice

di Casini, Simona, Albesa, Maxime, Wang, Zizun, Portero, Vincent, Ross-Kaschitza, Daniela, Rougier, Jean-Sébastien, Marchal, Gerard A., Chung, Wendy K., Bezzina, Connie R., Abriel, Hugues, Remme, Carol Ann
Pubblicato in Int J Mol Sci (2019)

Systems Genetics Approaches in Rat Identify Novel Genes and Gene Networks Associated With Cardiac Conduction

di Adriaens, Michiel E., Lodder, Elisabeth M., Moreno‐Moral, Aida, Šilhavý, Jan, Heinig, Matthias, Glinge, Charlotte, Belterman, Charly, Wolswinkel, Rianne, Petretto, Enrico, Pravenec, Michal, Remme, Carol Ann, Bezzina, Connie R.
Pubblicato in J Am Heart Assoc (2018)

Dissection of a Quantitative Trait Locus for PR Interval Duration Identifies Tnni3k as a Novel Modulator of Cardiac Conduction

di Lodder, Elisabeth M., Scicluna, Brendon P., Milano, Annalisa, Sun, Albert Y., Tang, Hao, Remme, Carol Ann, Moerland, Perry D., Tanck, Michael W. T., Pitt, Geoffrey S., Marchuk, Douglas A., Bezzina, Connie R.
Pubblicazione 2012