J. Jager

Yield of Clinical Screening for Hypertrophic Cardiomyopathy in Child First-Degree Relatives

P. Elliott, J. Ochoa, J. Kaski, 2019, Circulation.

The novel desmin variant p.Leu115Ile is associated with a unique form of biventricular Arrhythmogenic Cardiomyopathy.

M. Ashworth, P. Elliott, P. Syrris, 2020, The Canadian journal of cardiology.

Alpha-protein kinase 3 (ALPK3) truncating variants are a cause of autosomal dominant hypertrophic cardiomyopathy

P. Elliott, L. Monserrat, P. Syrris, 2021, European heart journal.

A microRNA Expression Profile as Non-Invasive Biomarker in a Large Arrhythmogenic Cardiomyopathy Cohort

D. Corrado, G. Thiene, C. Basso, 2020, International journal of molecular sciences.

Cryptic Splice-altering Variants in MYBPC3 Are a Prevalent Cause of Hypertrophic Cardiomyopathy.

P. Elliott, M. Carmo-Fonseca, L. Monserrat, 2020, Circulation. Genomic and precision medicine.

Iterative Reanalysis of Hypertrophic Cardiomyopathy Exome Data Reveals Causative Pathogenic Mitochondrial DNA Variants.

P. Elliott, P. Syrris, A. Pittman, 2021, Circulation. Genomic and precision medicine.