E. Quinn

Deletions of specific exons of FHOD3 detected by next‐generation sequencing are associated with hypertrophic cardiomyopathy

P. Elliott, L. Monserrat, J. Ochoa, 2020, Clinical genetics.

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

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

The promise and challenges of precision medicine in dilated cardiomyopathy

B. Halliday, E. Quinn, Samantha Mason, 2021, European heart journal. Case reports.

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.