Genetic Basis of Sudden Unexpected Death in Epilepsy

od Bagnall, Richard D., Crompton, Douglas E., Semsarian, Christopher
izdano v Front Neurol (2017)

Post‐Mortem Review and Genetic Analysis of Sudden Unexpected Death in Epilepsy (SUDEP) Cases

od Tu, Emily, Bagnall, Richard D., Duflou, Johan, Semsarian, Christopher
izdano v Brain Pathol (2010)

Gene conversion and evolution of Xq28 duplicons involved in recurring inversions causing severe hemophilia A

od Bagnall, Richard D., Ayres, Karen L., Green, Peter M., Giannelli, Francesco
Izdano 2005

Exome sequencing identifies a mutation in the ACTN2 gene in a family with idiopathic ventricular fibrillation, left ventricular noncompaction, and sudden death

od Bagnall, Richard D, Molloy, Laura K, Kalman, Jonathan M, Semsarian, Christopher
izdano v BMC Med Genet (2014)

Genetic Analysis of Hyperpolarization‐Activated Cyclic Nucleotide‐Gated Cation Channels in Sudden Unexpected Death in Epilepsy Cases

od Tu, Emily, Waterhouse, Louise, Duflou, Johan, Bagnall, Richard D., Semsarian, Christopher
izdano v Brain Pathol (2011)

Global MicroRNA Profiling of the Mouse Ventricles during Development of Severe Hypertrophic Cardiomyopathy and Heart Failure

od Bagnall, Richard D., Tsoutsman, Tatiana, Shephard, Rhian E., Ritchie, William, Semsarian, Christopher
Izdano 2012

Exome sequencing identifies a novel mutation in the MYH6 gene in a family with early-onset sinus node dysfunction, ventricular arrhythmias, and cardiac arrest()

od Lam, Lien, Ingles, Jodie, Turner, Christian, Kilborn, Michael, Bagnall, Richard D., Semsarian, Christopher
izdano v HeartRhythm Case Rep (2015)

LAMP2 shines a light on cardiomyopathy in an athlete

od Martin, Sophie, Ingles, Jodie, Hunyor, Imre, Bagnall, Richard D., Puranik, Rajesh, Semsarian, Christopher
izdano v HeartRhythm Case Rep (2017)

Holt-Oram syndrome in two families diagnosed with left ventricular noncompaction and conduction disease

od Ross, Samantha Barratt, Bagnall, Richard D., Yeates, Laura, Sy, Raymond W., Semsarian, Christopher
izdano v HeartRhythm Case Rep (2018)

Sudden unexpected death in epilepsy genetics: Molecular diagnostics and prevention

od Goldman, Alica M., Behr, Elijah R., Semsarian, Christopher, Bagnall, Richard D., Sisodiya, Sanjay, Cooper, Paul N.
izdano v Epilepsia (2016)

Transcriptome Sequencing of Patients With Hypertrophic Cardiomyopathy Reveals Novel Splice-Altering Variants in MYBPC3

od Holliday, Mira, Singer, Emma S., Ross, Samantha B., Lim, Seakcheng, Lal, Sean, Ingles, Jodie, Semsarian, Christopher, Bagnall, Richard D.
izdano v Circ Genom Precis Med (2021)

Are Variants Causing Cardiac Arrhythmia Risk Factors in Sudden Unexpected Death in Epilepsy?

od Bleakley, Lauren E., Soh, Ming S., Bagnall, Richard D., Sadleir, Lynette G., Gooley, Samuel, Semsarian, Christopher, Scheffer, Ingrid E., Berkovic, Samuel F., Reid, Christopher A.
izdano v Front Neurol (2020)

A novel heterozygous mutation in cardiac calsequestrin causes autosomal dominant catecholaminergic polymorphic ventricular tachycardia

od Gray, Belinda, Bagnall, Richard D., Lam, Lien, Ingles, Jodie, Turner, Christian, Haan, Eric, Davis, Andrew, Yang, Pei-Chi, Clancy, Colleen E., Sy, Raymond W., Semsarian, Christopher
izdano v Heart Rhythm (2016)

Relations between right ventricular morphology and clinical, electrical and genetic parameters in Brugada Syndrome

od Gray, Belinda, Gnanappa, Ganesh Kumar, Bagnall, Richard D., Femia, Giuseppe, Yeates, Laura, Ingles, Jodie, Burns, Charlotte, Puranik, Rajesh, Grieve, Stuart M., Semsarian, Christopher, Sy, Raymond W.
izdano v PLoS One (2018)

Genetic architecture of left ventricular noncompaction in adults

od Ross, Samantha Barratt, Singer, Emma S., Driscoll, Elizabeth, Nowak, Natalie, Yeates, Laura, Puranik, Rajesh, Sy, Raymond W., Rajagopalan, Sulekha, Barratt, Alexandra, Ingles, Jodie, Bagnall, Richard D., Semsarian, Christopher
izdano v Hum Genome Var (2020)

Prevalence and Phenotypic Correlations of Calmodulinopathy-Causative CALM1-3 Variants Detected in a Multi-Center Molecular Autopsy Cohort of Sudden Unexplained Death Victims

od Clemens, Daniel J., Gray, Belinda, Bagnall, Richard D., Tester, David J., Giudicessi, John R., Maleszewski, Joseph J., Crotti, Lia, Schwartz, Peter J., Matthews, Emma, Semsarian, Christopher, Behr, Elijah R., Ackerman, Michael J.
izdano v Circ Genom Precis Med (2020)

Whole-Genome Sequencing as a First-Line Genetic Test in Familial Dilated Cardiomyopathy

od Minoche, Andre E., Horvat, Claire, Johnson, Renee, Gayevskiy, Velimir, Morton, Sarah U., Drew, Alexander P., Woo, Kerhan, Statham, Aaron L., Lundie, Ben, Bagnall, Richard D., Ingles, Jodie, Semsarian, Christopher, Seidman, J.G., Seidman, Christine E., Dinger, Marcel E., Cowley, Mark J., Fatkin, Diane
izdano v Genet Med (2018)

Loss‐of‐function variants in K(v)11.1 cardiac channels as a biomarker for SUDEP

od Soh, Ming S., Bagnall, Richard D., Bennett, Mark F., Bleakley, Lauren E., Mohamed Syazwan, Erlina S., Phillips, A. Marie, Chiam, Mathew D. F., McKenzie, Chaseley E., Hildebrand, Michael, Crompton, Douglas, Bahlo, Melanie, Semsarian, Christopher, Scheffer, Ingrid E., Berkovic, Samuel F., Reid, Christopher A.
izdano v Ann Clin Transl Neurol (2021)