Browsing by Author Bagnall, Richard

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Issue DateTitleAuthor(s)Citation
2015Comparative transcriptome profiling in human bicuspid aortic valve disease using RNA sequencingBagnall, Richard; Bannon, Paul; Padang, Ratnasari; Semsarian, Chris; Tsoutsman, Tatiana; Central Clinical School: Medicine; Central Clinical School: Surgery; Central Clinical School: Medicine; Central Clinical School: Centenary Institute; Central Clinical School: Centenary InstituteComparative transcriptome profiling in human bicuspid aortic valve disease using RNA sequencing, Physiological genomics, vol.47, 3, 2015,pp 75-87
2014Determining pathogenicity of genetic variants in hypertrophic cardiomyopathy: importance of periodic reassessmentBagnall, Richard; Das K, Jipin; Ingles, Jodie; Semsarian, Chris; Central Clinical School: Medicine; Central Clinical School: Centenary Institute; Central Clinical School: Centenary Institute; Central Clinical School: Centenary InstituteDetermining pathogenicity of genetic variants in hypertrophic cardiomyopathy: importance of periodic reassessment, Genetics in Medicine, vol.16, 4, 2014,pp 286-293
2014Exome analysis–based molecular autopsy in cases of sudden unexplained death in the youngBagnall, Richard; Das K, Jipin; Duflou, Johan; Semsarian, Chris; Central Clinical School: Medicine; Central Clinical School: Centenary Institute; Central Clinical School: Medicine; Central Clinical School: Centenary InstituteExome analysis–based molecular autopsy in cases of sudden unexplained death in the young, Heart Rhythm, vol.11, 4, 2014,pp 655-662
2014Exome sequencing identifies a mutation in the ACTN2 gene in a family with idiopathic ventricular fibrillation, left ventricular noncompaction, and sudden deathBagnall, Richard; Semsarian, Chris; Kalman, Jonathan; Molloy, Laura K.; Central Clinical School: Medicine; Central Clinical School: Centenary InstituteExome sequencing identifies a mutation in the ACTN2 gene in a family with idiopathic ventricular fibrillation, left ventricular noncompaction, and sudden death, BMC Medical Genetics, vol.15, N/A, 2014,pp 1-9
2015Exome sequencing identifies a novel mutation in the MYH6 gene in a family with early-onset sinus node dysfunction, ventricular arrhythmias, and cardiac arrestBagnall, Richard; Ingles, Jodie; Kilborn, Michael; Semsarian, Chris; Lam, Lien; Turner, Christian; Central Clinical School: Medicine; Central Clinical School: Centenary Institute; Central Clinical School: Medicine; Central Clinical School: Centenary InstituteExome sequencing identifies a novel mutation in the MYH6 gene in a family with early-onset sinus node dysfunction, ventricular arrhythmias, and cardiac arrest, HeartRhythm Case Reports, vol.1, 3, 2015,pp 141-145
2016Exome-based analysis of cardiac arrhythmia, respiratory control and epilepsy genes in sudden unexpected death in epilepsyBagnall, Richard; Cutmore, Carina; Duflou, Johan; Lam, Lien; Semsarian, Chris; Cairns, Anita; Crompton, Douglas; Dibbens, Leanne; et al, Various; Garry, Sarah I; Kivity, Sara; Petrovski, Slave; Sadleir, Lynette; Central Clinical School: Medicine; Science Faculty Admin; Central Clinical School: Medicine; Central Clinical School: Office; Central Clinical School: Centenary InstituteExome-based analysis of cardiac arrhythmia, respiratory control and epilepsy genes in sudden unexpected death in epilepsy, Annals of Neurology, vol.79, 4, 2016,pp 522-534
2011Genetic analysis of hyperpolarization-activated cyclic nucleotide-gated cation channels in sudden unexpected in epilepsy casesDuflou, Johan; Semsarian, Chris; Waterhouse, Louise; Bagnall, Richard; Tu, Emily; Central Clinical School: Medicine; Central Clinical School: Centenary Institute; Central Clinical School: MedicineGenetic analysis of hyperpolarization-activated cyclic nucleotide-gated cation channels in sudden unexpected in epilepsy cases, Brain Pathology, vol.21, 6, 2011,pp 692-698
2014Genetic analysis of PHOX2B in sudden unexpected death in epilepsy casesBagnall, Richard; Semsarian, Chris; Berkovic, Samuel F.; Crompton, Douglas; Cutmore, Carina; Regan, Bridgid; Scheffer, Ingrid; Central Clinical School: Centenary Institute; Central Clinical School: Centenary InstituteGenetic analysis of PHOX2B in sudden unexpected death in epilepsy cases, Neurology, vol.83, 11, 2014,pp 1018-1021
2012Genetic Basis of Familial Valvular Heart DiseaseBagnall, Richard; Padang, Ratnasari; Semsarian, Chris; Central Clinical School: Medicine; Central Clinical School: Medicine; Central Clinical School: Centenary InstituteGenetic Basis of Familial Valvular Heart Disease, Circulation: Cardiovascular Genetics, vol.5, 5, 2012,pp 569-580
2012Global MicroRNA Profiling of the Mouse Ventricles during Development of Severe Hypertrophic Cardiomyopathy and Heart FailureBagnall, Richard; Semsarian, Chris; Shephard, Rhian; Tsoutsman, Tatiana; Ritchie, William; Central Clinical School: Medicine; Central Clinical School: Centenary Institute; Central Clinical School: Centenary Institute; Central Clinical School: Centenary InstituteGlobal MicroRNA Profiling of the Mouse Ventricles during Development of Severe Hypertrophic Cardiomyopathy and Heart Failure, PLoS One, vol.7, 9, 2012,pp 1-8
2008Impact of multiple gene mutations in determining the severity of cardiomyopathy and heart failureSemsarian, Chris; Tsoutsman, Tatiana; Bagnall, Richard; Central Clinical School: Centenary Institute; Central Clinical School: Centenary InstituteImpact of multiple gene mutations in determining the severity of cardiomyopathy and heart failure, Clinical and Experimental Pharmacology and Physiology, vol.35, 11, 2008,pp 1349-1357
2013No association of G-protein-coupled receptor kinase 5 or β-adrenergic receptor polymorphisms with Takotsubo cardiomyopathy in a large Australian cohortAbdulla, I; Bagnall, Richard; Buchholz, Stefan; Figtree, Gemma Alexandra; Karimi Galougahi, Keyvan; Semsarian, Chris; Tan, Timothy; Ward, Michael; Yan, Warren; Horowitz, John D; Neil, Chris; Medicine; Central Clinical School: Medicine; Northern Clinical School: Medicine; Northern Clinical School: Medicine; Medicine; Central Clinical School: Centenary Institute; Concord Clinical School: Medicine; Northern Clinical School: Medicine; Northern Clinical School: MedicineNo association of G-protein-coupled receptor kinase 5 or β-adrenergic receptor polymorphisms with Takotsubo cardiomyopathy in a large Australian cohort, European Journal of Heart Failure, vol.15, 7, 2013,pp 730-733
2017Nonfamilial Hypertrophic Cardiomyopathy: Prevalence, Natural History, and Clinical ImplicationsBagnall, Richard; Burns, Charlotte; Driscoll, Timothy; Ingles, Jodie; Puranik, Rajesh; Semsarian, Chris; Atherton, John; Briffa, Thomas; Lam, L; Sarina, T; Yeates, Laura; Central Clinical School: Medicine; Central Clinical School: Centenary Institute; School of Public Health: Public Health; Central Clinical School: Centenary Institute; Central Clinical School: Medicine; Central Clinical School: Centenary InstituteNonfamilial Hypertrophic Cardiomyopathy: Prevalence, Natural History, and Clinical Implications, Circulation Cardiovascular Genetics, vol.10, 2, 2017,pp 1-11
2015NOS1AP polymorphisms modify QTc interval duration but not cardiac arrest risk in hypertrophic cardiomyopathyBagnall, Richard; Gray, Belinda; Ingles, Jodie; Semsarian, Chris; Crawford, Jackie; Earle, Nikki; Love, Donald R; Shelling, Andrew; Skinner, Jonathan R; Smith, Warren; Central Clinical School: Medicine; Central Clinical School: Medicine; Central Clinical School: Centenary Institute; Central Clinical School: Centenary InstituteNOS1AP polymorphisms modify QTc interval duration but not cardiac arrest risk in hypertrophic cardiomyopathy, Journal of Cardiovascular Electrophysiology, vol.26, 12, 2015,pp 1346-1351
2016A novel heterozygous mutation in cardiac calsequestrin causes autosomal dominant catecholaminergic polymorphic ventricular tachycardiaBagnall, Richard; Gray, Belinda; Ingles, Jodie; Lam, Lien; Semsarian, Chris; Sy, Raymond; Clancy, Colleen E; Davis, Andrew; Haan, Eric; Turner, Christian; Yang, Pei-Chi; Central Clinical School: Medicine; Central Clinical School: Medicine; Central Clinical School: Centenary Institute; Central Clinical School: Office; Central Clinical School: Centenary Institute; Concord Clinical School: MedicineA novel heterozygous mutation in cardiac calsequestrin causes autosomal dominant catecholaminergic polymorphic ventricular tachycardia, Heart Rhythm, vol.13, 8, 2016,pp 1652-1660
2016A novel heterozygous mutation in cardiac calsequestrin causes autosomal dominant catecholaminergic polymorphic ventricular tachycardiaBagnall, Richard; Gray, Belinda; Ingles, Jodie; Lam, Lien; Semsarian, Chris; Sy, Raymond; Clancy, Colleen E; Davis, Andrew; Haan, Eric; Turner, Christian; Yang, Pei-Chi; Central Clinical School: Medicine; Central Clinical School: Medicine; Central Clinical School: Centenary Institute; Central Clinical School: Office; Central Clinical School: Centenary Institute; Concord Clinical School: MedicineA novel heterozygous mutation in cardiac calsequestrin causes autosomal dominant catecholaminergic polymorphic ventricular tachycardia, Heart Rhythm, vol.13, 8, 2016,pp 1652-1660
2017Peripheral blood derived induced pluripotent stem cells (iPSCs) from a female with familial hypertrophic cardiomyopathyBagnall, Richard; Fraser, Stuart; Ross, Samantha; Semsarian, Chris; Central Clinical School: Medicine; Physiology; Geosciences; Central Clinical School: Centenary InstitutePeripheral blood derived induced pluripotent stem cells (iPSCs) from a female with familial hypertrophic cardiomyopathy, Stem Cell Research, vol.20, N/A, 2017,pp 76-79
2011A polymorphic miR-155 binding site in AGTR1 is associated with cardiac hypertrophy in Friedreich ataxiaKelly, Matthew; Semsarian, Chris; Bagnall, Richard; Corben, Louise; Delatycki, Martin B.; Donelan, Lesley; Peverill, Roger E.; Anaesthesia; Central Clinical School: Centenary InstituteA polymorphic miR-155 binding site in AGTR1 is associated with cardiac hypertrophy in Friedreich ataxia, Journal of Molecular and Cellular Cardiology, vol.51, 5, 2011,pp 848-854
2010Post-Mortem Review and Genetic Analysis of Sudden Unexpected Death in Epilepsy (SUDEP) CasesDuflou, Johan; Semsarian, Chris; Tu, Emily; Bagnall, Richard; Central Clinical School: Medicine; Central Clinical School: Centenary Institute; Central Clinical School: Centenary InstitutePost-Mortem Review and Genetic Analysis of Sudden Unexpected Death in Epilepsy (SUDEP) Cases, Brain Pathology, vol.N/A, N/A,pp 1-8
2013Postmortem review and genetic analysis in sudden infant death syndrome: an 11-year reviewBagnall, Richard; Duflou, Johan; Semsarian, Chris; Evans, Angharad; Central Clinical School: Medicine; Central Clinical School: Medicine; Central Clinical School: Centenary InstitutePostmortem review and genetic analysis in sudden infant death syndrome: an 11-year review, Human Pathology, vol.44, 9, 2013,pp 1730-1736