Dr Trisha Dwight

Research Fellow
Kolling Institute of Medical Research, Northern Clinical School


Map

Selected grants

2012

  • The Australasian Succinate Dehydrogenase Consortium; Dwight T, Clifton-Bligh R, Benn D, Robinson B; Pheo Para Alliance/Project grant.
  • Mitochondrial Dysfunction and Hypoxic Responses: Implications for Tumorigenesis; Dwight T, Clifton-Bligh R, Benn D, Robinson B; Pheo Para Alliance/Project grant.

Selected publications

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Journals

  • Gill, A., Toon, C., Clarkson, A., Sioson, L., Chou, A., Winship, I., Robinson, B., Benn, D., Clifton-Bligh, R., Dwight, T. (2014). Succinate dehydrogenase deficiency is rare in pituitary adenomas. American Journal of Surgical Pathology, 38(4), 560-566. [More Information]
  • Dwight, T., Mann, K., Benn, D., Robinson, B., McKelvie, P., Gill, A., Winship, I., Clifton-Bligh, R. (2013). Familial SDHA Mutation Associated With Pituitary Adenoma and Pheochromocytoma/Paraganglioma. Journal of Clinical Endocrinology and Metabolism, 98(6), E1103-E1108. [More Information]
  • Dwight, T., Benn, D., Clarkson, A., Vilain, R., Lipton, L., Robinson, B., Clifton-Bligh, R., Gill, A. (2013). Loss of SDHA Expression Identifies SDHA Mutations in Succinate Dehydrogenase–deficient Gastrointestinal Stromal Tumors. The American Journal of Surgical Pathology, 37(2), 226-233. [More Information]
  • Cardinal, J., Bergman, L., Hayward, N., Sweet, A., Warner, J., Marks, L., Learoyd, D., Dwight, T., Robinson, B., Epstein, M., Smith, M., et al (2005). A report of a national mutation testing service for the MEN1 gene: clinical presentations and implications for mutation testing. Journal of Medical Genetics, 42(1), 69-74. [More Information]
  • Dwight, T., Nelson, A., Theodosopoulos, G., Richardson, A., Learoyd, D., Philips, J., Delbridge, L., Zedenius, J., Teh, B., Larsson, C., Marsh, D., Robinson, B. (2002). Independent Genetic Events Associated with the Development of Multiple Parathyroid Tumors in Patients with Primary Hyperparqathyroidism. The American Journal of Pathology: cellular and molecular biology of disease, 161(4), 1299-1306.
  • Villablanca, A., Wassif, W., Smith, T., Hoog, A., Vierimaa, O., Kassem, M., Dwight, T., Forsberg, L., Du, Q., Learoyd, D., Robinson, B., et al (2002). Involvement of the MEN1 gene locus in familial isolated hyperparathyroidism. European Journal of Endocrinology, 147(3), 313-322.

Conferences

  • Tsang, V., Parker, N., Cassano, J., Dwight, T., Sue, C., Veivers, D., Robinson, B., Benn, D., Clifton-Bligh, R. (2012). Interaction between hypoxia and mutations in the SDH subunit genes associated with phaeochromocytoma/paragangliomas. 2012 Annual Scientific Meeting of the Endocrine Society of Australia and the Society for Reproductive Biology, Gold Coast, Queensland, Australia.

2014

  • Gill, A., Toon, C., Clarkson, A., Sioson, L., Chou, A., Winship, I., Robinson, B., Benn, D., Clifton-Bligh, R., Dwight, T. (2014). Succinate dehydrogenase deficiency is rare in pituitary adenomas. American Journal of Surgical Pathology, 38(4), 560-566. [More Information]

2013

  • Dwight, T., Mann, K., Benn, D., Robinson, B., McKelvie, P., Gill, A., Winship, I., Clifton-Bligh, R. (2013). Familial SDHA Mutation Associated With Pituitary Adenoma and Pheochromocytoma/Paraganglioma. Journal of Clinical Endocrinology and Metabolism, 98(6), E1103-E1108. [More Information]
  • Dwight, T., Benn, D., Clarkson, A., Vilain, R., Lipton, L., Robinson, B., Clifton-Bligh, R., Gill, A. (2013). Loss of SDHA Expression Identifies SDHA Mutations in Succinate Dehydrogenase–deficient Gastrointestinal Stromal Tumors. The American Journal of Surgical Pathology, 37(2), 226-233. [More Information]

2012

  • Tsang, V., Parker, N., Cassano, J., Dwight, T., Sue, C., Veivers, D., Robinson, B., Benn, D., Clifton-Bligh, R. (2012). Interaction between hypoxia and mutations in the SDH subunit genes associated with phaeochromocytoma/paragangliomas. 2012 Annual Scientific Meeting of the Endocrine Society of Australia and the Society for Reproductive Biology, Gold Coast, Queensland, Australia.

2005

  • Cardinal, J., Bergman, L., Hayward, N., Sweet, A., Warner, J., Marks, L., Learoyd, D., Dwight, T., Robinson, B., Epstein, M., Smith, M., et al (2005). A report of a national mutation testing service for the MEN1 gene: clinical presentations and implications for mutation testing. Journal of Medical Genetics, 42(1), 69-74. [More Information]

2002

  • Dwight, T., Nelson, A., Theodosopoulos, G., Richardson, A., Learoyd, D., Philips, J., Delbridge, L., Zedenius, J., Teh, B., Larsson, C., Marsh, D., Robinson, B. (2002). Independent Genetic Events Associated with the Development of Multiple Parathyroid Tumors in Patients with Primary Hyperparqathyroidism. The American Journal of Pathology: cellular and molecular biology of disease, 161(4), 1299-1306.
  • Villablanca, A., Wassif, W., Smith, T., Hoog, A., Vierimaa, O., Kassem, M., Dwight, T., Forsberg, L., Du, Q., Learoyd, D., Robinson, B., et al (2002). Involvement of the MEN1 gene locus in familial isolated hyperparathyroidism. European Journal of Endocrinology, 147(3), 313-322.

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