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Yang, N, MacArthur, DG, Gulbin, JP, Hahn, AG, Beggs, AH, Easteal, S, North, K. ACTN3 Genotype Is Associated with Human Elite Athletic Performance.
American Journal of Human Genetics
73(3)
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627 -631
2003
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Yuen, M, Sandaradura, SA, Dowling, JJ, Kostyukova, AS, Moroz, N, Quinlan, KG, Lehtokari, V-L, Ravenscroft, G, Todd, EJ, Ceyhan-Birsoy, O, et al. Leiomodin-3 dysfunction results in thin filament disorganization and nemaline myopathy.
Journal of Clinical Investigation
124(11)
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4693 -4708
2014
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Garton, F, Seto, JT, North, KN, Yang, N. Validation of an automated computational method for skeletal muscle fibre morphometry analysis.
Neuromuscular Disorders
20(8)
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540 -547
2010
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North, K. Why is α-Actinin-3 Deficiency So Common in the General Population? The Evolution of Athletic Performance.
Twin Research and Human Genetics
11(4)
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384 -394
2008
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Acosta, MT, Bearden, CE, Castellanos, XF, Cutting, L, Elgersma, Y, Gioia, G, Gutmann, DH, Lee, Y, Legius, E, Muenke, M, et al. The Learning Disabilities Network (LeaDNet): Using neurofibromatosis type 1 (NF1) as a paradigm for translational research.
American Journal of Medical Genetics Part A
158A(9)
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2225 -2232
2012
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