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Muscle & Nerve|July 15, 2011
Using complementary DNA from MyoD-transduced fibroblasts to sequence large muscle genesLeigh B Waddell, Nicole Monnier, Sandra T Cooper, et al.
Muscle & Nerve|July 19, 2012
Novel FLNC mutation in a patient with myofibrillar myopathy in combination with late-onset cerebellar ataxiaGiorgio Tasca, Zagaa Odgerel, Mauro Monforte, et al.
Neuromuscular Disorders : NMD|June 18, 2010
Evidence for a dominant negative disease mechanism in cap myopathy due to TPM3Leigh B Waddell, Michaela Kreissl, Andrew Kornberg, et al.
Neuromuscular Disorders : NMD|June 26, 2016
TOR1AIP1 as a cause of cardiac failure and recessive limb-girdle muscular dystrophyRoula Ghaoui, Tatiana Benavides, Monkol Lek, et al.
Neuromuscular Disorders : NMD|July 27, 2012
Mutations in TPM2 and congenital fibre type disproportionNigel F Clarke, Leigh B Waddell, Lilian T L Sie, et al.
Frontiers in Neurology|February 13, 2023
Case report: Adult-onset limb girdle muscular dystrophy in sibling pair due to novel homozygous LAMA2 missense variantMatthew Katz, Leigh B Waddell, Michaela Yuen, et al.
Muscle & Nerve|June 16, 2011
Epidermolysis bullosa with late-onset muscular dystrophy and plectin deficiencyEppie M Yiu, Alfred Klausegger, Leigh B Waddell, et al.
Neuromuscular Disorders : NMD|August 10, 2022
A genetic basis is identified in 74% cases of paediatric hyperCKaemia without weakness presenting to a tertiary paediatric neuromuscular centreWui-Kwan Wong, Samantha J Bryen, Adam Bournazos, et al.
Neuromuscular Disorders : NMD|June 21, 2011
A study of FHL1, BAG3, MATR3, PTRF and TCAP in Australian muscular dystrophy patientsLeigh B Waddell, Jenny Tran, Xi F Zheng, et al.
European Journal of Human Genetics : EJHG|November 7, 2013
Recessive myosin myopathy with external ophthalmoplegia associated with MYH2 mutationsHoma Tajsharghi, Simon Hammans, Christopher Lindberg, et al.
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