Sotabase

Career

· Lecturer, Ulster University2023–
· Research Fellow, Queen's University Belfast2020–2023
· Doctor of Philosophy - PhD, Bioinformatics, Queen's University Belfast2017–2021
· Master’s Degree, Bioinformatics, Commendation classification, Queen's University Belfast2016–2017
· Production Associate, Intelesens2015–2016
· Biomedical Engineering, Bioengineering and Biomedical Engineering, 2.1 classification with Honours, University of Ulster2011–2015

Publications (98)

Mutations in Cypher/ZASP in patients with dilated cardiomyopathy and left ventricular non-compaction.
Journal of the American College of Cardiology · 2003
541
cited
Natural history and familial characteristics of isolated left ventricular non-compaction.
European Heart Journal · 2005
483
cited
Idiopathic restrictive cardiomyopathy is part of the clinical expression of cardiac troponin I mutations.
Journal of Clinical Investigation · 2003
365
cited
Mutations in the muscle LIM protein and alpha-actinin-2 genes in dilated cardiomyopathy and endocardial fibroelastosis.
Molecular Genetics and Metabolism · 2003
295
cited
Severe disease expression of cardiac troponin C and T mutations in patients with idiopathic dilated cardiomyopathy.
Journal of the American College of Cardiology · 2004
257
cited
Subclinical anthracycline- and trastuzumab-induced cardiotoxicity in the long-term follow-up of asymptomatic breast cancer survivors: a speckle tracking echocardiographic study
Heart · 2010
249
cited
Tissue synchronization imaging and optimal left ventricular pacing site in cardiac resynchronization therapy.
American Journal of Cardiology · 2006
205
cited
Novel mutation in cardiac troponin I in recessive idiopathic dilated cardiomyopathy
The Lancet · 2004
184
cited
Adenosine monophosphate-activated protein kinase disease mimicks hypertrophic cardiomyopathy and Wolff-Parkinson-White syndrome: natural history.
Journal of the American College of Cardiology · 2005
173
cited
Prospective Familial Assessment in Dilated Cardiomyopathy: Cardiac Autoantibodies Predict Disease Development in Asymptomatic Relatives
Circulation · 2006
173
cited
Echocardiographic Evaluation in Asymptomatic Relatives of Patients with Dilated Cardiomyopathy Reveals Preclinical Disease
Annals of Internal Medicine · 2005
170
cited
Mitral valve abnormalities in hypertrophic cardiomyopathy: echocardiographic features and surgical outcomes.
Annals of Thoracic Surgery · 2008
156
cited
Frequency and clinical expression of cardiac troponin I mutations in 748 consecutive families with hypertrophic cardiomyopathy.
Journal of the American College of Cardiology · 2004
154
cited
Prevalence and clinical significance of systolic impairment in hypertrophic cardiomyopathy
Heart · 2005
153
cited
Pregnancy related complications in women with hypertrophic cardiomyopathy
Heart · 2003
133
cited
ANKRD1, the gene encoding cardiac ankyrin repeat protein, is a novel dilated cardiomyopathy gene.
Journal of the American College of Cardiology · 2009
129
cited
Molecular basis for clinical heterogeneity in inherited cardiomyopathies due to myopalladin mutations.
Human Molecular Genetics · 2012
101
cited
Nebulette mutations are associated with dilated cardiomyopathy and endocardial fibroelastosis.
Journal of the American College of Cardiology · 2010
97
cited
Isolated left ventricular noncompaction is rarely caused by mutations in G4.5, alpha-dystrobrevin and FK Binding Protein-12.
Molecular Genetics and Metabolism · 2004
83
cited
Progressive left ventricular remodeling in patients with hypertrophic cardiomyopathy and severe left ventricular hypertrophy.
Journal of the American College of Cardiology · 2004
70
cited
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Ross Murphy | Researcher Profile | Sotabase | Sotabase