-
Chang, Y, Wacker, J, Ingles, J, Macciocca, I, King, I, Flagship, TAGCD, Semsarian, C, McGaughran, J, Weintraub, RG, Bagnall, RD.
TBX20 loss-of-function variants in families with left ventricular non-compaction cardiomyopathy.
Journal of Medical Genetics
61(2)
:
171 -175
2024
view publication
-
Rath, A, Weintraub, R.
Overview of Cardiomyopathies in Childhood.
Frontiers in Pediatrics
9:
708732
2024
view publication
-
Tran, DL, Gibson, H, Maiorana, AJ, Verrall, CE, Baker, DW, Clode, M, Lubans, DR, Zannino, D, Bullock, A, Ferrie, S, et al.
Exercise Intolerance, Benefits, and Prescription for People Living With a Fontan Circulation: The Fontan Fitness Intervention Trial (F-FIT)—Rationale and Design.
Frontiers in Pediatrics
9:
799125
2024
view publication
-
Lesurf, R, Said, A, Akinrinade, O, Breckpot, J, Delfosse, K, Liu, T, Yao, R, Persad, G, McKenna, F, Noche, RR, et al.
Whole genome sequencing delineates regulatory, copy number, and cryptic splice variants in early onset cardiomyopathy.
npj Genomic Medicine
7(1)
:
18
2024
view publication
-
Singer, ES, Crowe, J, Holliday, M, Isbister, JC, Lal, S, Nowak, N, Yeates, L, Burns, C, Rajagopalan, S, Macciocca, I, et al.
The burden of splice-disrupting variants in inherited heart disease and unexplained sudden cardiac death.
npj Genomic Medicine
8(1)
:
29
2024
view publication