Genetics of cardiac arrhythmias

Por Wilde, Arthur A M, Bezzina, Connie R
Publicado em 2005

When genetic burden reaches threshold

Por Walsh, Roddy, Tadros, Rafik, Bezzina, Connie R
Publicado no Eur Heart J (2020)

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

Por Lahrouchi, Najim, Behr, Elijah R., Bezzina, Connie R.
Publicado no Front Cardiovasc Med (2016)

Genetic Basis of Ventricular Arrhythmias

Por Pazoki, Raha, Wilde, Arthur A. M., Bezzina, Connie R.
Publicado em 2010

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

Por Cerrone, Marina, Remme, Carol Ann, Tadros, Rafik, Bezzina, Connie R., Delmar, Mario
Publicado no Circulation (2019)

Genome-wide association studies of cardiac electrical phenotypes

Por Glinge, Charlotte, Lahrouchi, Najim, Jabbari, Reza, Tfelt-Hansen, Jacob, Bezzina, Connie R
Publicado no Cardiovasc Res (2020)

Induced pluripotent stem cell derived cardiomyocytes as models for cardiac arrhythmias

Por Hoekstra, Maaike, Mummery, Christine L., Wilde, Arthur A. M., Bezzina, Connie R., Verkerk, Arie O.
Publicado em 2012

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

Por Verkerk, Arie O., Veerman, Christiaan C., Zegers, Jan G., Mengarelli, Isabella, Bezzina, Connie R., Wilders, Ronald
Publicado no Int J Mol Sci (2017)

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

Por Adadi, Najlae, Radi, Fatima Zohra, Lahrouchi, Najim, Hara, Loubna, Ratbi, Ilham, Elalaoui, Siham Chafai, Alders, Marielle, Zarzur, Jamila, Bezzina, Connie, Sefiani, Abdelaziz
Publicado no Anatol J Cardiol (2018)

Sodium Channel Remodeling in Subcellular Microdomains of Murine Failing Cardiomyocytes

Por Rivaud, Mathilde R., Agullo‐Pascual, Esperanza, Lin, Xianming, Leo‐Macias, Alejandra, Zhang, Mingliang, Rothenberg, Eli, Bezzina, Connie R., Delmar, Mario, Remme, Carol Ann
Publicado no J Am Heart Assoc (2017)

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

Por Veerman, Christiaan C., Mengarelli, Isabella, Guan, Kaomei, Stauske, Michael, Barc, Julien, Tan, Hanno L., Wilde, Arthur A. M., Verkerk, Arie O., Bezzina, Connie R.
Publicado no 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...

Por 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
Publicado em 2013

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

Por 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
Publicado no 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...

Por 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.
Publicado em 2013

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

Por 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
Publicado no Open Heart (2017)

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

Por 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
Publicado no Int J Mol Sci (2019)

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

Por 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.
Publicado no J Am Heart Assoc (2018)

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

Por 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.
Publicado em 2012

SARS-CoV-2, COVID-19, and inherited arrhythmia syndromes

Por Wu, Cheng-I, Postema, Pieter G., Arbelo, Elena, Behr, Elijah R., Bezzina, Connie R., Napolitano, Carlo, Robyns, Tomas, Probst, Vincent, Schulze-Bahr, Eric, Remme, Carol Ann, Wilde, Arthur A.M.
Publicado no Heart Rhythm (2020)

The role of renin–angiotensin–aldosterone system polymorphisms in phenotypic expression of MYBPC3-related hypertrophic cardiomyopathy

Por Kolder, Iris CRM, Michels, Michelle, Christiaans, Imke, Ten Cate, Folkert J, Majoor-Krakauer, Danielle, Danser, Alexander HJ, Lekanne Deprez, Robert H, Tanck, Michael WT, Wilde, Arthur AM, Bezzina, Connie R, Dooijes, Dennis
Publicado em 2012