Dr Leigh Waddell

Research Fellow
Paediatrics & Child Health, Children's Hospital, Westmead

Telephone 9845 1455

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Selected publications

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Book Chapters

  • Waddell, L., Evesson, F., North, K., Cooper, S., Clarke, N. (2012). Diagnosis of the Muscular Dystrophies. In Madhuri Hegde & Arunkanth Ankala (Eds.), Muscular Dystrophy, (pp. 261-288). Rijeka, Croatia: InTech Publishers.

Journals

  • Clarke, N., Amburgey, K., Teener, J., Camelo-Piragua, S., Kesari, A., Punetha, J., Waddell, L., Davis, M., Laing, N., Monnier, N., North, K., et al (2013). A novel mutation expands the genetic and clinical spectrum of MYH7-related myopathies. Neuromuscular Disorders, 23(5), 432-436. [More Information]
  • Penttila, S., Palmio, J., Suominen, T., Raheem, O., Evila, A., Muelas Gomez, N., Tasca, G., Waddell, L., Clarke, N., Barboi, A., et al (2012). Eight new mutations and the expanding phenotype variability in muscular dystrophy caused by ANO5. Neurology, 78(12), 897-903. [More Information]
  • Menezes, M., Waddell, L., Evesson, F., Cooper, S., Webster, R., Jones, K., Mowat, D., Kiernan, M., Johnston, H., Corbett, A., North, K., Clarke, N., et al (2012). Importance and challenge of making an early diagnosis in LMNA-related muscular dystrophy. Neurology, 78(16), 1258-1263. [More Information]
  • Clarke, N., Waddell, L., Sie, L., van Bon, B., McLean, C., Clark, D., Kornberg, A., Lammens, M., North, K. (2012). Mutations in TPM2 and congenital fibre type disproportion. Neuromuscular Disorders, 22(11), 955-958. [More Information]
  • Tasca, G., Odgerel, Z., Monforte, M., Aurino, S., Clarke, N., Waddell, L., Udd, B., Ricci, E., Goldfarb, L. (2012). Novel FLNC mutation in a patient with myofibrillar myopathy in combination with late-onset cerebellar ataxia. Muscle and Nerve, 46(2), 275-282. [More Information]
  • Waddell, L., Tran, J., Zheng, X., Bonnemann, C., Hu, Y., Evesson, F., Lek, M., Arbuckle, S., Wang, M., Smith, R., North, K., Clarke, N. (2011). A study of FHL1, BAG3, MATR3, PTRF and TCAP in Australian muscular dystrophy patients. Neuromuscular Disorders, 21(11), 776-781. [More Information]
  • Waddell, L., Lemckert, F., Zheng, X., Tran, J., Evesson, F., Hawkes, J., Lek, A., Street, N., Lin, P., Clarke, N., North, K., Cooper, S., et al (2011). Dysferlin, Annexin A1, and Mitsugumin 53 Are Upregulated in Muscular Dystrophy and Localize to Longitudinal Tubules of the T-System With Stretch. Journal of Neuropathology and Experimental Neurology, 70(4), 302-313. [More Information]
  • Yiu, E., Klausegger, A., Waddell, L., Grasern, N., Lloyd, L., Tran, K., North, K., Bauer, J., McKelvie, P., Chow, C., et al (2011). Epidermolysis bullosa with late-onset muscular dystrophy and plectin deficiency. Muscle and Nerve, 44(1), 135-141. [More Information]
  • Waddell, L., Monnier, N., Cooper, S., North, K., Clarke, N. (2011). Using complementary DNA from MyoD-transduced fibroblasts to sequence large muscle genes. Muscle and Nerve, 44(2), 280-282. [More Information]
  • Waddell, L., Kreissl, M., Kornberg, A., Kennedy, P., McLean, C., Labarre-Vila, A., Monnier, N., North, K., Clarke, N. (2010). Evidence for a dominant negative disease mechanism in cap myopathy due to TPM3. Neuromuscular Disorders, 20(7), 464-466. [More Information]
  • Clarke, N., Waddell, L., Cooper, S., Perry, M., Smith, R., Kornberg, A., Muntoni, F., Lillis, S., Straub, V., Bushby, K., North, K., et al (2010). Recessive Mutations in RYR1 Are a Common Cause of Congenital Fiber Type Disproportion. Human Mutation, 31(7), E1544-E1550. [More Information]
  • Clarke, N., Domazetovska, A., Waddell, L., Kornberg, A., McLean, C., North, K. (2009). Cap disease due to mutation of the beta-tropomyosin gene (TPM2). Neuromuscular Disorders, 19(5), 348-351. [More Information]

2013

  • Clarke, N., Amburgey, K., Teener, J., Camelo-Piragua, S., Kesari, A., Punetha, J., Waddell, L., Davis, M., Laing, N., Monnier, N., North, K., et al (2013). A novel mutation expands the genetic and clinical spectrum of MYH7-related myopathies. Neuromuscular Disorders, 23(5), 432-436. [More Information]

2012

  • Waddell, L., Evesson, F., North, K., Cooper, S., Clarke, N. (2012). Diagnosis of the Muscular Dystrophies. In Madhuri Hegde & Arunkanth Ankala (Eds.), Muscular Dystrophy, (pp. 261-288). Rijeka, Croatia: InTech Publishers.
  • Penttila, S., Palmio, J., Suominen, T., Raheem, O., Evila, A., Muelas Gomez, N., Tasca, G., Waddell, L., Clarke, N., Barboi, A., et al (2012). Eight new mutations and the expanding phenotype variability in muscular dystrophy caused by ANO5. Neurology, 78(12), 897-903. [More Information]
  • Menezes, M., Waddell, L., Evesson, F., Cooper, S., Webster, R., Jones, K., Mowat, D., Kiernan, M., Johnston, H., Corbett, A., North, K., Clarke, N., et al (2012). Importance and challenge of making an early diagnosis in LMNA-related muscular dystrophy. Neurology, 78(16), 1258-1263. [More Information]
  • Clarke, N., Waddell, L., Sie, L., van Bon, B., McLean, C., Clark, D., Kornberg, A., Lammens, M., North, K. (2012). Mutations in TPM2 and congenital fibre type disproportion. Neuromuscular Disorders, 22(11), 955-958. [More Information]
  • Tasca, G., Odgerel, Z., Monforte, M., Aurino, S., Clarke, N., Waddell, L., Udd, B., Ricci, E., Goldfarb, L. (2012). Novel FLNC mutation in a patient with myofibrillar myopathy in combination with late-onset cerebellar ataxia. Muscle and Nerve, 46(2), 275-282. [More Information]

2011

  • Waddell, L., Tran, J., Zheng, X., Bonnemann, C., Hu, Y., Evesson, F., Lek, M., Arbuckle, S., Wang, M., Smith, R., North, K., Clarke, N. (2011). A study of FHL1, BAG3, MATR3, PTRF and TCAP in Australian muscular dystrophy patients. Neuromuscular Disorders, 21(11), 776-781. [More Information]
  • Waddell, L., Lemckert, F., Zheng, X., Tran, J., Evesson, F., Hawkes, J., Lek, A., Street, N., Lin, P., Clarke, N., North, K., Cooper, S., et al (2011). Dysferlin, Annexin A1, and Mitsugumin 53 Are Upregulated in Muscular Dystrophy and Localize to Longitudinal Tubules of the T-System With Stretch. Journal of Neuropathology and Experimental Neurology, 70(4), 302-313. [More Information]
  • Yiu, E., Klausegger, A., Waddell, L., Grasern, N., Lloyd, L., Tran, K., North, K., Bauer, J., McKelvie, P., Chow, C., et al (2011). Epidermolysis bullosa with late-onset muscular dystrophy and plectin deficiency. Muscle and Nerve, 44(1), 135-141. [More Information]
  • Waddell, L., Monnier, N., Cooper, S., North, K., Clarke, N. (2011). Using complementary DNA from MyoD-transduced fibroblasts to sequence large muscle genes. Muscle and Nerve, 44(2), 280-282. [More Information]

2010

  • Waddell, L., Kreissl, M., Kornberg, A., Kennedy, P., McLean, C., Labarre-Vila, A., Monnier, N., North, K., Clarke, N. (2010). Evidence for a dominant negative disease mechanism in cap myopathy due to TPM3. Neuromuscular Disorders, 20(7), 464-466. [More Information]
  • Clarke, N., Waddell, L., Cooper, S., Perry, M., Smith, R., Kornberg, A., Muntoni, F., Lillis, S., Straub, V., Bushby, K., North, K., et al (2010). Recessive Mutations in RYR1 Are a Common Cause of Congenital Fiber Type Disproportion. Human Mutation, 31(7), E1544-E1550. [More Information]

2009

  • Clarke, N., Domazetovska, A., Waddell, L., Kornberg, A., McLean, C., North, K. (2009). Cap disease due to mutation of the beta-tropomyosin gene (TPM2). Neuromuscular Disorders, 19(5), 348-351. [More Information]

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