Scientists on the Spot: The complex inheritance of cardiac disorders

por Patel, Jyoti, Bezzina, Connie R
Publicado 2019

When genetic burden reaches threshold

por Walsh, Roddy, Tadros, Rafik, Bezzina, Connie R
Publicado 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 2016

Illuminating the path from genetics to clinical outcome in Brugada syndrome

por Postema, Pieter G, Walsh, Roddy, Bezzina, Connie R
Publicado 2021

Genetic Basis of Ventricular Arrhythmias

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

Genome-wide association studies of cardiac electrical phenotypes

por Glinge, Charlotte, Lahrouchi, Najim, Jabbari, Reza, Tfelt-Hansen, Jacob, Bezzina, Connie R
Publicado 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 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 2017

A diverse ancestrally-matched reference panel increases genotype imputation accuracy in a underrepresented population

por Mauleekoonphairoj, John, Tongsima, Sissades, Khongphatthanayothin, Apichai, Jurgens, Sean J., Zimmerman, Dominic S., Sutjaporn, Boosamas, Wandee, Pharawee, Bezzina, Connie R., Nademanee, Koonlawee, Poovorawan, Yong
Publicado 2023

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 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 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 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 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 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 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 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 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 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 2020

Exploring the Relationship Between Schizophrenia and Cardiovascular Disease: A Genetic Correlation and Multivariable Mendelian Randomization Study

por Veeneman, Rada R, Vermeulen, Jentien M, Abdellaoui, Abdel, Sanderson, Eleanor, Wootton, Robyn E, Tadros, Rafik, Bezzina, Connie R, Denys, Damiaan, Munafò, Marcus R, Verweij, Karin J H, Treur, Jorien L
Publicado 2021