X. Zheng

Systematic single-variant and gene-based association testing of thousands of phenotypes in 394,841 UK Biobank exomes

Jacqueline, A. Philippakis, M. Daly, 2022, Cell Genomics.

ACTN3 genotype influences muscle performance through the regulation of calcineurin signaling.

D. MacArthur, M. Lek, K. Quinlan, 2013, The Journal of clinical investigation.

A study of FHL1, BAG3, MATR3, PTRF and TCAP in Australian muscular dystrophy patients

M. Lek, Robert L L Smith, L. Waddell, 2011, Neuromuscular Disorders.

muscleresistance exercise in human skeletal Temporal response of desmin and dystrophin proteins

D. MacArthur, M. Lek, M. Hauser, 2015 .

Dysferlin, Annexin A1, and Mitsugumin 53 Are Upregulated in Muscular Dystrophy and Localize to Longitudinal Tubules of the T-System With Stretch

M. Ackerman, L. Waddell, N. Clarke, 2011, Journal of neuropathology and experimental neurology.

A study of FHL1, BAG3, MATR3, PTRF and TCAP in Australian muscular dystrophy patients

M. Lek, Robert L L Smith, L. Waddell, 2011, Neuromuscular Disorders.

Deficiency of α-actinin-3 is associated with increased susceptibility to contraction-induced damage and skeletal muscle remodeling.

D. MacArthur, M. Lek, M. Hauser, 2011, Human molecular genetics.

Evidence Based Selection of Commonly Used RT-qPCR Reference Genes for the Analysis of Mouse Skeletal Muscle

K. Quinlan, K. North, N. Yang, 2014, PloS one.