Publications for Richard Bagnall
Publications for Richard Bagnall
2016
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. <a
href="http://dx.doi.org/10.1002/ana.24596">[Mo
re Information]</a>
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. <a
href="http://dx.doi.org/10.1111/epi.13232">[Mo
re Information]</a>
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. <a
href="http://dx.doi.org/10.1152/physiolgenomics
.00115.2014">[More Information]</a>
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. <a
href="http://dx.doi.org/10.1016/j.hrcr.2015.01.02
2">[More Information]</a>
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. <a
href="http://dx.doi.org/10.1038/gim.2013.138">[
More Information]</a>
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. <a
href="http://dx.doi.org/10.1016/j.hrthm.2014.01.
017">[More Information]</a>
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. <a
href="http://dx.doi.org/10.1186/s12881-014-009
9-0">[More Information]</a>
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. <a
href="http://dx.doi.org/10.1093/eurjhf/hft040">[
More Information]</a>
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. <a
href="http://dx.doi.org/10.1016/j.humpath.2013.
01.024">[More Information]</a>
2012
Padang, R., Bagnall, R., Semsarian, C. (2012).
Genetic Basis of Familial Valvular Heart
Disease. Circulation: Cardiovascular Genetics,
5(5), 569-580. <a
href="http://dx.doi.org/10.1161/CIRCGENETIC
S.112.962894">[More Information]</a>
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. <a
href="http://dx.doi.org/10.1371/journal.pone.004
4744">[More Information]</a>
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. <a
href="http://dx.doi.org/10.1016/j.yjmcc.2012.05.
009">[More Information]</a>
2011
Bagnall, R., Ingles, J., Semsarian, C. (2011).
Molecular diagnostics of cardiomyopathies: the
Publications for Richard Bagnall
future is here. Circulation Cardiovascular
Genetics, 4(2), 103-104. <a
href="http://www.ncbi.nlm.nih.gov/entrez/query.
fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract
&list_uids=21505198">[More Information]</a>