Dr Richard Bagnall

BSc (Hons), PhD
Senior Lecturer, Sydney Medical School, University of Sydney
Senior Research Officer, Molecular Cardiology Program, Centenary Institute

Telephone +61 2 9565 6295
Fax +61 2 9565 6101

Map

Selected grants

2016

  • Clinical application of whole genome studies in patients with inherited cardiomyopathies; Semsarian C, Fatkin D, Dinger M, Bagnall R, Ingles J, Cowley M, Turner C, Colley A, Berman Y, Ronan A; NSW Ministry of Health, Office for Health and Medical Research/Genomics Collaborative Grants Program.

2013

  • QIAxcel high throughput automated DNA, RNA and protein capillary electrophoresis system; Weninger W, Fazekas de St Groth B, Feng C, Jolly C, Semsarian C, Vadas M, Bertolino P, McCaughan G, Shackel N, Bagnall R, Shklovskaya E, Bailey C; National Health and Medical Research Council (NHMRC)/Equipment Grants.
  • Neuro-Cardiac Genetic Basis of Sudden Unexpected Death in Epilepsy; Semsarian C, Crompton D, Bagnall R; National Health and Medical Research Council (NHMRC)/Project Grants.

2012

  • Genetic Basis of Valvular Heart Disease; Semsarian C, Weintraub R, Winlaw D, Bagnall R; National Health and Medical Research Council (NHMRC)/Project Grants.

Selected publications

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Journals

  • Gray, B., Bagnall, R., Lam, L., Ingles, J., Turner, C., Haan, E., Davis, A., Yang, P., Clancy, C., Sy, R., Semsarian, C. (2016). A novel heterozygous mutation in cardiac calsequestrin causes autosomal dominant catecholaminergic polymorphic ventricular tachycardia. Heart Rhythm, 13(8), 1652-1660. [More Information]
  • Bagnall, R., Weintraub, R., Ingles, J., Duflou, J., Yeates, L., Lam, L., Davis, A., Thompson, T., Connell, V., Wallace, J., Puranik, R., Semsarian, C., et al (2016). A Prospective Study of Sudden Cardiac Death among Children and Young Adults. The New England Journal of Medicine, 374(25), 2441-2452. [More Information]
  • Bagnall, R., Crompton, D., Petrovski, S., Lam, L., Cutmore, C., Garry, S., Sadleir, L., Dibbens, L., Cairns, A., Kivity, S., Duflou, J., Semsarian, C., et al (2016). Exome-based analysis of cardiac arrhythmia, respiratory control and epilepsy genes in sudden unexpected death in epilepsy. Annals of Neurology, 79(4), 522-534. [More Information]
  • Goldman, A., Behr, E., Semsarian, C., Bagnall, R., Sisodiya, S., Cooper, P. (2016). Sudden unexpected death in epilepsy genetics: Molecular diagnostics and prevention. Epilepsia, 57(Suppl 1), 17-25. [More Information]
  • Semsarian, C., Bagnall, R. (2016). The authors reply. New England Journal of Medicine, 375(13), 1301-1302. [More Information]
  • Padang, R., Bagnall, R., Tsoutsman, T., Bannon, P., Semsarian, C. (2015). Comparative transcriptome profiling in human bicuspid aortic valve disease using RNA sequencing. Physiological Genomics, 47(3), 75-87. [More Information]
  • Lam, L., Ingles, J., Turner, C., Kilborn, M., Bagnall, R., Semsarian, C. (2015). Exome 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, 1(3), 141-145. [More Information]
  • Earle, N., Ingles, J., Bagnall, R., Gray, B., Crawford, J., Smith, W., Shelling, A., Love, D., Semsarian, C., Skinner, J. (2015). NOS1AP polymorphisms modify QTc interval duration but not cardiac arrest risk in hypertrophic cardiomyopathy. Journal of Cardiovascular Electrophysiology.
  • Das K, J., Ingles, J., Bagnall, R., Semsarian, C. (2014). Determining pathogenicity of genetic variants in hypertrophic cardiomyopathy: importance of periodic reassessment. Genetics in Medicine, 16(4), 286-293. [More Information]
  • Bagnall, R., Das K, J., Duflou, J., Semsarian, C. (2014). Exome analysis–based molecular autopsy in cases of sudden unexplained death in the young. Heart Rhythm, 11(4), 655-662. [More Information]
  • Bagnall, R., Molloy, L., Kalman, J., Semsarian, C. (2014). Exome sequencing identifies a mutation in the ACTN2 gene in a family with idiopathic ventricular fibrillation, left ventricular noncompaction, and sudden death. BMC Medical Genetics, 15, 1-9. [More Information]
  • Bagnall, R., Ingles, J., Semsarian, C. (2014). Illumina TruSight Cardiomyopathy Sequencing Panel: Application to hypertrophic cardiomyopathy. Heart, Lung and Circulation, 23(S2), e5.
  • Figtree, G., Bagnall, R., Abdulla, I., Buchholz, S., Galougahi, K., Yan, W., Tan, T., Neil, C., Horowitz, J., Semsarian, C., Ward, M. (2013). No 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, 15(7), 730-733. [More Information]
  • Evans, A., Bagnall, R., Duflou, J., Semsarian, C. (2013). Postmortem review and genetic analysis in sudden infant death syndrome: an 11-year review. Human Pathology, 44(9), 1730-1736. [More Information]
  • Padang, R., Bagnall, R., Semsarian, C. (2012). Genetic Basis of Familial Valvular Heart Disease. Circulation: Cardiovascular Genetics, 5(5), 569-580. [More Information]
  • Bagnall, R., Tsoutsman, T., Shephard, R., Ritchie, W., Semsarian, C. (2012). Global MicroRNA Profiling of the Mouse Ventricles during Development of Severe Hypertrophic Cardiomyopathy and Heart Failure. PloS One, 7(9), 1-8. [More Information]
  • Padang, R., Bagnall, R., Richmond, D., Bannon, P., Semsarian, C. (2012). Rare non-synonymous variations in the transcriptional activation domains of GATA5 in bicuspid aortic valve disease. Journal of Molecular and Cellular Cardiology, 53(2), 277-281. [More Information]
  • Kelly, M., Bagnall, R., Peverill, R., Donelan, L., Corben, L., Delatycki, M., Semsarian, C. (2011). A polymorphic miR-155 binding site in AGTR1 is associated with cardiac hypertrophy in Friedreich ataxia. Journal of Molecular and Cellular Cardiology, 51(5), 848-854. [More Information]
  • Tu, E., Waterhouse, L., Duflou, J., Bagnall, R., Semsarian, C. (2011). Genetic Analysis of Hyperpolarization-Activated Cyclic Nucleotide-Gated Cation Channels in Sudden Unexpected in Epilepsy Cases. Brain Pathology, 21(6), 692-698. [More Information]
  • Bagnall, R., Ingles, J., Semsarian, C. (2011). Molecular diagnostics of cardiomyopathies: the future is here. Circulation Cardiovascular Genetics, 4(2), 103-104. [More Information]
  • Chiu, C., Bagnall, R., Ingles, J., Yeates, L., Kennerson, M., Donald, J., Jormakka, M., Lind, J., Semsarian, C. (2010). Mutations in Alpha-Actinin-2 Cause Hypertrophic Cardiomyopathy: A Genome-Wide Analysis. Journal of the American College of Cardiology, 55(11), 1127-1135. [More Information]
  • Tu, E., Bagnall, R., Duflou, J., Lynch, M., Twigg, S., Semsarian, C. (2010). Post-mortem pathologic and genetic studies in "dead in bed syndrome" cases in type 1 diabetes mellitus. Human Pathology, 41(3), 392-400. [More Information]
  • Tu, E., Bagnall, R., Duflou, J., Semsarian, C. (2010). Post-Mortem Review and Genetic Analysis of Sudden Unexpected Death in Epilepsy (SUDEP) Cases. Brain Pathology, , 1-8. [More Information]
  • Tsoutsman, T., Bagnall, R., Semsarian, C. (2008). Impact of multiple gene mutations in determining the severity of cardiomyopathy and heart failure. Clinical and Experimental Pharmacology and Physiology, 35(11), 1349-1357. [More Information]

2016

  • Gray, B., Bagnall, R., Lam, L., Ingles, J., Turner, C., Haan, E., Davis, A., Yang, P., Clancy, C., Sy, R., Semsarian, C. (2016). A novel heterozygous mutation in cardiac calsequestrin causes autosomal dominant catecholaminergic polymorphic ventricular tachycardia. Heart Rhythm, 13(8), 1652-1660. [More Information]
  • Bagnall, R., Weintraub, R., Ingles, J., Duflou, J., Yeates, L., Lam, L., Davis, A., Thompson, T., Connell, V., Wallace, J., Puranik, R., Semsarian, C., et al (2016). A Prospective Study of Sudden Cardiac Death among Children and Young Adults. The New England Journal of Medicine, 374(25), 2441-2452. [More Information]
  • Bagnall, R., Crompton, D., Petrovski, S., Lam, L., Cutmore, C., Garry, S., Sadleir, L., Dibbens, L., Cairns, A., Kivity, S., Duflou, J., Semsarian, C., et al (2016). Exome-based analysis of cardiac arrhythmia, respiratory control and epilepsy genes in sudden unexpected death in epilepsy. Annals of Neurology, 79(4), 522-534. [More Information]
  • Goldman, A., Behr, E., Semsarian, C., Bagnall, R., Sisodiya, S., Cooper, P. (2016). Sudden unexpected death in epilepsy genetics: Molecular diagnostics and prevention. Epilepsia, 57(Suppl 1), 17-25. [More Information]
  • Semsarian, C., Bagnall, R. (2016). The authors reply. New England Journal of Medicine, 375(13), 1301-1302. [More Information]

2015

  • Padang, R., Bagnall, R., Tsoutsman, T., Bannon, P., Semsarian, C. (2015). Comparative transcriptome profiling in human bicuspid aortic valve disease using RNA sequencing. Physiological Genomics, 47(3), 75-87. [More Information]
  • Lam, L., Ingles, J., Turner, C., Kilborn, M., Bagnall, R., Semsarian, C. (2015). Exome 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, 1(3), 141-145. [More Information]
  • Earle, N., Ingles, J., Bagnall, R., Gray, B., Crawford, J., Smith, W., Shelling, A., Love, D., Semsarian, C., Skinner, J. (2015). NOS1AP polymorphisms modify QTc interval duration but not cardiac arrest risk in hypertrophic cardiomyopathy. Journal of Cardiovascular Electrophysiology.

2014

  • Das K, J., Ingles, J., Bagnall, R., Semsarian, C. (2014). Determining pathogenicity of genetic variants in hypertrophic cardiomyopathy: importance of periodic reassessment. Genetics in Medicine, 16(4), 286-293. [More Information]
  • Bagnall, R., Das K, J., Duflou, J., Semsarian, C. (2014). Exome analysis–based molecular autopsy in cases of sudden unexplained death in the young. Heart Rhythm, 11(4), 655-662. [More Information]
  • Bagnall, R., Molloy, L., Kalman, J., Semsarian, C. (2014). Exome sequencing identifies a mutation in the ACTN2 gene in a family with idiopathic ventricular fibrillation, left ventricular noncompaction, and sudden death. BMC Medical Genetics, 15, 1-9. [More Information]
  • Bagnall, R., Ingles, J., Semsarian, C. (2014). Illumina TruSight Cardiomyopathy Sequencing Panel: Application to hypertrophic cardiomyopathy. Heart, Lung and Circulation, 23(S2), e5.

2013

  • Figtree, G., Bagnall, R., Abdulla, I., Buchholz, S., Galougahi, K., Yan, W., Tan, T., Neil, C., Horowitz, J., Semsarian, C., Ward, M. (2013). No 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, 15(7), 730-733. [More Information]
  • Evans, A., Bagnall, R., Duflou, J., Semsarian, C. (2013). Postmortem review and genetic analysis in sudden infant death syndrome: an 11-year review. Human Pathology, 44(9), 1730-1736. [More Information]

2012

  • Padang, R., Bagnall, R., Semsarian, C. (2012). Genetic Basis of Familial Valvular Heart Disease. Circulation: Cardiovascular Genetics, 5(5), 569-580. [More Information]
  • Bagnall, R., Tsoutsman, T., Shephard, R., Ritchie, W., Semsarian, C. (2012). Global MicroRNA Profiling of the Mouse Ventricles during Development of Severe Hypertrophic Cardiomyopathy and Heart Failure. PloS One, 7(9), 1-8. [More Information]
  • Padang, R., Bagnall, R., Richmond, D., Bannon, P., Semsarian, C. (2012). Rare non-synonymous variations in the transcriptional activation domains of GATA5 in bicuspid aortic valve disease. Journal of Molecular and Cellular Cardiology, 53(2), 277-281. [More Information]

2011

  • Kelly, M., Bagnall, R., Peverill, R., Donelan, L., Corben, L., Delatycki, M., Semsarian, C. (2011). A polymorphic miR-155 binding site in AGTR1 is associated with cardiac hypertrophy in Friedreich ataxia. Journal of Molecular and Cellular Cardiology, 51(5), 848-854. [More Information]
  • Tu, E., Waterhouse, L., Duflou, J., Bagnall, R., Semsarian, C. (2011). Genetic Analysis of Hyperpolarization-Activated Cyclic Nucleotide-Gated Cation Channels in Sudden Unexpected in Epilepsy Cases. Brain Pathology, 21(6), 692-698. [More Information]
  • Bagnall, R., Ingles, J., Semsarian, C. (2011). Molecular diagnostics of cardiomyopathies: the future is here. Circulation Cardiovascular Genetics, 4(2), 103-104. [More Information]

2010

  • Chiu, C., Bagnall, R., Ingles, J., Yeates, L., Kennerson, M., Donald, J., Jormakka, M., Lind, J., Semsarian, C. (2010). Mutations in Alpha-Actinin-2 Cause Hypertrophic Cardiomyopathy: A Genome-Wide Analysis. Journal of the American College of Cardiology, 55(11), 1127-1135. [More Information]
  • Tu, E., Bagnall, R., Duflou, J., Lynch, M., Twigg, S., Semsarian, C. (2010). Post-mortem pathologic and genetic studies in "dead in bed syndrome" cases in type 1 diabetes mellitus. Human Pathology, 41(3), 392-400. [More Information]
  • Tu, E., Bagnall, R., Duflou, J., Semsarian, C. (2010). Post-Mortem Review and Genetic Analysis of Sudden Unexpected Death in Epilepsy (SUDEP) Cases. Brain Pathology, , 1-8. [More Information]

2008

  • Tsoutsman, T., Bagnall, R., Semsarian, C. (2008). Impact of multiple gene mutations in determining the severity of cardiomyopathy and heart failure. Clinical and Experimental Pharmacology and Physiology, 35(11), 1349-1357. [More Information]

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