Professor Bruce Gregory Robinson
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Professor and Dean Medicine, Northern Clinical School Kolling Institute of Medical Research A27 - Edward Ford Building
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Professor Robinson is an Endocrinologist and has been Head of the Molecular Genetics Unit, (now Cancer Genetics Unit) at the Kolling Institute of Medical Research, Royal North Shore Hospital since 1989.
His research has focused on identifying the genetic causes contributing to the formation of tumours in endocrine glands such as the thyroid, parathyroid, adrenal and pituitary. Initially this commenced with identification of mutations in genes causing hereditary endocrine syndromes such as multiple endocrine neoplasia type 2, and subsequently hyperparathyroidism jaw tumour syndrome and the hereditary phaeochromocytoma/paraganglioma syndromes.
He recently formed the International SDH Consortium gathering families from around the world to define the relationships between phaeochromocytoma / paraganglioma and the SDH genes. In addition his lab has characterised mutations and their consequences in sporadic tumours of the thyroid adrenal and recently in brain tumours.
Since 2001 he has been the Chairman of Hoc Mai, the University of Sydney's Australia Vietnam Medical Foundation. He has supervised 25 PhD students.
His research has focused on identifying the genetic causes contributing to the formation of tumours in endocrine glands such as the thyroid, parathyroid, adrenal and pituitary. Initially this commenced with identification of mutations in genes causing hereditary endocrine syndromes such as multiple endocrine neoplasia type 2, and subsequently hyperparathyroidism jaw tumour syndrome and the hereditary phaeochromocytoma/paraganglioma syndromes.
He recently formed the International SDH Consortium gathering families from around the world to define the relationships between phaeochromocytoma / paraganglioma and the SDH genes. In addition his lab has characterised mutations and their consequences in sporadic tumours of the thyroid adrenal and recently in brain tumours.
Since 2001 he has been the Chairman of Hoc Mai, the University of Sydney's Australia Vietnam Medical Foundation. He has supervised 25 PhD students.
2008
Low, T, Delbridge, L, Sidhu, S, Learoyd, D, Robinson, B, Roach, P, Sywak, M. Lymph Node Status Influences Follow-Up Thyroglobulin Levels in Papillary Thyroid Cancer. Annals of surgical oncology. 2008 [Abstract]
Soon, P, McDonald, K, Robinson, B, Sidhu, S. Molecular markers and the pathogenesis of adrenocortical cancer. The oncologist. 2008; 13: 548-61 [Abstract]
Grodski, S, Gill, A, Robinson, B, Sidhu, S. Nonfunctioning parathyroid cancer presenting as a cervical mass. Thyroid : official journal of the American Thyroid Association. 2008; 18: 473-4 [Abstract]
Figtree, G, Grieve, S, Speller, B, Geiger, M, Robinson, B, Channon, K, Ragoussis, J, Collins, P, Watkins, H. A commonly occurring polymorphism upstream of the estrogen receptor alpha alters transcription and is associated with increased HDL. Atherosclerosis. 2008 [Abstract]
Soon, P, Libe, R, Benn, D, Gill, A, Shaw, J, Sywak, M, Groussin, L, Bertagna, X, Gicquel, C, Bertherat, J, McDonald, K, Sidhu, S, Robinson, B. Loss of heterozygosity of 17p13, with possible involvement of ACADVL and ALOX15B, in the pathogenesis of adrenocortical tumors. Annals of surgery. 2008; 247: 157-64 [Abstract]
2007
Elston, M, Gill, A, Conaglen, J, Clarkson, A, Shaw, J, Law, A, Cook, R, Little, N, Clifton-Bligh, R, Robinson, B, McDonald, K. Wnt pathway inhibitors are strongly down-regulated in pituitary tumors. Endocrinology. 2007: 1-21 [Abstract]
Learoyd, D, Robinson, B. Does genetic screening increase detection of familial medullary thyroid cancer in apparently sporadic cases?. Nature Clinical Practice Endocrinology and Metabolism.. 2007 [Abstract]
Parkinson, J, Wheeler, H, Clarkson, A, McKenzie, C, Biggs, M, Little, N, Cook, R, Messina, M, Robinson, B, McDonald, K. Variation of O(6)-methylguanine-DNA methyltransferase (MGMT) promoter methylation in serial samples in glioblastoma. Journal of neuro-oncology. 2007 [Abstract]
Lundgren, C, Delbridg, L, Learoyd, D, Robinson, B. Surgical approach to medullary thyroid cancer. Arquivos brasileiros de endocrinologia e metabologia. 2007; 51: 818-824 [Abstract]
Soon, P, Yeh, M, Delbridge, L, Bambach, C, Sywak, M, Robinson, B, Sidhu, S. Laparoscopic surgery is safe for large adrenal lesions. European journal of surgical oncology : the journal of the European Society of Surgical Oncology and the British Association of Surgical Oncology. 2007; 34: 67-70 [Abstract]
Soon, P, Benn, D, Gill, A, Robinson, B, McDonald, K. Es07 microarray gene expression analysis of human adrenocortical tumours. ANZ journal of surgery. 2007; ; [Abstract]
Yan, W, Roach, P, Bautovich, G, Learoyd, D, Robinson, B. Timing of iodine-123 scintigraphy following use of recombinant human thyrotropin in differentiated thyroid carcinoma. Clinical nuclear medicine. 2007; 32: 375-377 [Abstract]
McDonald, K, O'Sullivan, M, Parkinson, J, Shaw, J, Payne, C, Brewer, J, Young, L, Reader, D, Wheeler, H, Cook, R, Biggs, M, Little, N, Teo, C, Stone, G, Robinson, B. IQGAP1 and IGFBP2: valuable biomarkers for determining prognosis in glioma patients. Journal of neuropathology and experimental neurology. 2007; 66: 405-417 [Abstract]
Messina, M, Robinson, B. Technology insight: gene therapy and its potential role in the treatment of medullary thyroid carcinoma. Nature clinical practice. Endocrinology & metabolism. 2007; 3: 290-301 [Abstract]
Grodski, S, Stalberg, P, Robinson, B, Delbridge, L. Surgery versus Radioiodine Therapy as Definitive Management for Graves' Disease: The Role of Patient Preference. Thyroid : official journal of the American Thyroid Association. 2007; 17: 157-160 [Abstract]
Benn, D, Robinson, B. Pheochromocytoma - quo vadis?. NATURE CLINICAL PRACTICE ENDOCRINOLOGY & METABOLISM. 2007; 3: 377-377 [Abstract]
2006
Clarke, J, Patel, S, Raymond, R, Andrew, S, Robinson, B, Dressler, G, Brophy, P. Regulation of c-Ret in the developing kidney is responsive to Pax2 gene dosage. Human molecular genetics. 2006; 15: 3420-8 [Abstract]
Figtree, G, Kindmark, A, Lind, L, Grundberg, E, Speller, B, Robinson, B, Channon, K, Watkins, H. Novel estrogen receptor alpha promoter polymorphism increases ventricular hypertrophic response to hypertension. The Journal of steroid biochemistry and molecular biology. 2006 [Abstract]
Howell, V, Cardinal, J, Richardson, A, Gimm, O, Robinson, B, Marsh, D. Rapid Mutation Screening for HRPT2 and MEN1 Mutations Associated with Familial and Sporadic Primary Hyperparathyroidism. The Journal of molecular diagnostics : JMD. 2006; 8: 559-66 [Abstract]
Warusavitarne, J, Ramanathan, P, Kaufman, A, Robinson, B, Schnitzler, M. 5-Fluorouracil (5FU) treatment does not influence invasion and metastasis in microsatellite unstable (MSI-H) colorectal cancer. International journal of colorectal disease. 2006; 21: 625-31 [Abstract]
Benn, D, Robinson, B. Genetic basis of phaeochromocytoma and paraganglioma. Best practice & research. Clinical endocrinology & metabolism. 2006; 20: 435-50 [Abstract]
Benn, D, Richardson, A, Marsh, D, Robinson, B. Genetic testing in pheochromocytoma- and paraganglioma-associated syndromes. Annals of the New York Academy of Sciences. 2006; 1073: 104-11 [Abstract]
Bolland, M, Benn, D, Croxson, M, McCall, J, Shaw, J, Baillie, T, Robinson, B. Gastrointestinal stromal tumour in succinate dehydrogenase subunit B mutation-associated familial phaeochromocytoma/paraganglioma. Anz Journal of Surgery. 2006; 76: 763A-764 [Abstract]
Stewart, I, Roddie, C, Gill, A, Clarkson, A, Mirams, M, Coyle, L, Ward, C, Clifton-Bligh, P, Robinson, B, Mason, R, Clifton-Bligh, R. Elevated serum FGF23 concentrations in plasma cell dyscrasias. Bone. 2006; 39: 369-76 [Abstract]
Stalberg, P, Sidhu, S, Sywak, M, Robinson, B, Wilkinson, M, Delbridge, L. Intraoperative parathyroid hormone measurement during minimally invasive parathyroidectomy: does it "value-add" to decision-making?. Journal of the American College of Surgeons. 2006; 203: 1-6 [Abstract]
Gosnell, J, Sywak, M, Sidhu, S, Gough, I, Learoyd, D, Robinson, B, Delbridge, L. New era: prophylactic surgery for patients with multiple endocrine neoplasia-2a. ANZ journal of surgery. 2006; 76: 586-90 [Abstract]
Sundram, F, Robinson, B, Kung, A, Lim-Abrahan, M, Bay, N, Chuan, L, Chung, J, Huang, S, Hsu, L, Kamaruddin, N, Cheah, W, Kim, W, Koong, S, Da Lin, H, Mangklabruks, A, Paz-Pacheco, E, Rauff, A, Ladenson, P. Well-differentiated epithelial thyroid cancer management in the Asia Pacific region: A report and clinical practice guideline. Thyroid. 2006; 16: 461-469 [Abstract]
Giordano, T, Au, A, Kuick, R, Thomas, D, Rhodes, D, Wilhelm, K, Vinco, M, Misek, D, Sanders, D, Zhu, Z, Ciampi, R, Hanash, S, Chinnaiyan, A, Clifton-Bligh, R, Robinson, B, Nikiforov, Y, Koenig, R. Delineation, functional validation, and bioinformatic evaluation of gene expression in thyroid follicular carcinomas with the PAX8-PPARG translocation. Clinical Cancer Research. 2006; 12: 1983-1993 [Abstract]
Palazzo, F, Gosnell, J, Savio, R, Reeve, T, Sidhu, S, Sywak, M, Robinson, B, Delbridge, L. Lymphadenectomy for papillary thyroid cancer: changes in practice over four decades. European journal of surgical oncology : the journal of the European Society of Surgical Oncology and the British Association of Surgical Oncology. 2006; 32: 340-4 [Abstract]
Benn, D, Gimenez-Roqueplo, A, Reilly, J, Bertherat, J, Burgess, J, Byth, K, Croxson, M, Dahia, P, Elston, M, Gimm, O, Henley, D, Herman, P, Murday, V, Niccoli-Sire, P, Pasieka, J, Rohmer, V, Tucker, K, Jeunemaitre, X, Marsh, D, Plouin, P, Robinson, B. Clinical presentation and penetrance of pheochromocytoma/paraganglioma syndromes. Journal of Clinical Endocrinology and Metabolism. 2006; 91: 827-836 [Abstract]
Warner, J, Nyholt, D, Busfield, F, Epstein, M, Burgess, J, Stranks, S, Hill, P, Perry-Keene, D, Learoyd, D, Robinson, B, Teh, B, Prins, J, Cardinal, J. Familial isolated hyperparathyroidism is linked to a 1.7 Mb region on chromosome 2p13.3-14. Journal of Medical Genetics. 2006; 43 [Abstract]
Foukakis, T, Au, A, Wallin, G, Geli, J, Forsberg, L, Clifton-Bligh, R, Robinson, B, Lui, W, Zedenius, J, Larsson, C. The Ras effector NORE1A is suppressed in follicular thyroid carcinomas with a PAX8-PPAR gamma fusion. Journal of Clinical Endocrinology and Metabolism. 2006; 91: 1143-1149 [Abstract]
Benn, D, Gimenez-Roqueplo, A, Reilly, J, Bertherat, J, Burgess, J, Byth, K, Croxson, M, Dahia, P, Elston, M, Gimm, O, Henley, D, Herman, P, Murday, V, Niccoli-Sire, P, Pasieka, J, Rohmer, V, Tucker, K, Jeunemaitre, X, Marsh, D, Plouin, P, Robinson, B. Clinical presentation and penetrance of Pheochromocytoma/ Paraganglioma syndromes. The Journal of clinical endocrinology and metabolism. 2006; 91: 827-36 [Abstract]
Foukakis, T, Au, A, Wallin, G, Geli, J, Forsberg, L, Clifton-Bligh, R, Robinson, B, Lui, W, Zedenius, J, Larsson, C. The Ras Effector NORE1A is Suppressed in Follicular Thyroid Carcinomas with a PAX8-PPAR{gamma} Fusion. The Journal of clinical endocrinology and metabolism. 2006; 91: 1143-9 [Abstract]
Elston, M, Benn, D, Robinson, B, Conaglen, J. An apparently sporadic paraganglioma with an SDHB gene germline mutation presenting at age 68 years. Internal Medicine Journal. 2006; 36: 129-131 [Abstract]
Taylor, J, Gough, S, Hunt, P, Brix, T, Chatterjee, K, Connell, J, Franklyn, J, Hegedus, L, Robinson, B, Wiersinga, W, Wass, J, Zabaneh, D, Mackay, I, Weetman, A. A genome-wide screen in 1119 relative pairs with autoimmune thyroid disease. Journal of Clinical Endocrinology and Metabolism. 2006; 91: 646-653 [Abstract]
Au, A, McBride, C, Wilhelm, K, Koenig, R, Speller, B, Cheung, L, Messina, M, Wentworth, J, Tasevski, V, Learoyd, D, Robinson, B, Clifton-Bligh, R. PAX8-peroxisome proliferator-activated receptor gamma (PPARgamma) disrupts normal PAX8 or PPARgamma transcriptional function and stimulates follicular thyroid cell growth. Endocrinology. 2006; 147: 367-76 [Abstract]
2005
Learoyd, D, Gosnell, J, Elston, M, Saurine, T, Richardson, A, Delbridge, L, Aglen, J, Robinson, B. Experience of prophylactic thyroidectomy in multiple endocrine neoplasia type 2A kindreds with RET codon 804 mutations. Clinical endocrinology. 2005; 63: 636-41 [Abstract]
Learoyd, D, Robinson, B. Do all patients with RET mutations associated with multiple endocrine neoplasia type 2 require surgery?. Nature Clinical Practice Endocrinology & Metabolism. 2005; 1: 60-61 [Abstract]
Dechairo, B, Zabaneh, D, Collins, J, Brand, O, Dawson, G, Green, A, Mackay, I, Franklyn, J, Connell, J, Wass, J, Wiersinga, W, Hegedus, L, Brix, T, Robinson, B, Hunt, P, Weetman, A, Carey, A, Gough, S. Association of the TSHR gene with Graves'' disease: the first disease specific locus. European Journal of Human Genetics. 2005; 13: 1223-1230 [Abstract]
Savio, R, Gosnell, J, Palazzo, F, Sywak, M, Agarwal, G, Cowell, C, Shun, A, Robinson, B, Delbridge, L. The role of a more extensive surgical approach in the initial multimodality management of papillary thyroid cancer in children. Journal of pediatric surgery. 2005; 40: 1696-700 [Abstract]
Figtree, G, Robinson, B, Channon, K, Watkins, H. Novel polymorphism in estrogen receptor alpha reverses negative transcriptional regulation and is associated with improved endothelial-dependent vasodilation. Circulation. 2005; 112 [Abstract]
Stewart, I, Roddie, C, Gill, A, Clarkson, A, Mirams, M, Nelson, A, Coyle, L, Ward, C, Clifton-Bligh, P, Robinson, B, Mason, R, Clifton-Bligh, R. Elevated serum FGF23 concentrations in plasma cell dyscrasias. Journal of Bone and Mineral Research. 2005; 20 [Abstract]
Alderazi, Y, Yeh, M, Robinson, B, Benn, D, Sywak, M, Learoyd, D, Delbridge, L, Sidhu, S. Phaeochromocytoma: current concepts. Medical Journal of Australia. 2005; 183: 201-4 [Abstract]
Shaw, J, Messina, M, Both, G, Molloy, P, Robinson, B. Transcription targeted gene therapy for medullary thyroid carcinoma. Journal of Gene Medicine. 2005; 7: 1126-1127 [Abstract]
Dahia, P, Ross, K, Wright, M, Hayashida, C, Santagata, S, Barontini, M, Kung, A, Sanso, G, Powers, J, Tischler, A, Hodin, R, Heitritter, S, Moore, F, Dluhy, R, Sosa, J, Ocal, I, Benn, D, Marsh, D, Robinson, B, Schneider, K, Garber, J, Arum, S, Korbonits, M, Grossman, A, Pigny, P, Toledo, S, Nose, V, Li, C, Stiles, C. A HIF1 alpha regulatory loop links hypoxia and mitochondrial signals in pheochromocytomas. Plos Genetics. 2005; 1: 72-80 [Abstract]
Harding, J, Yeh, M, Robinson, B, Delbridge, L, Sidhu, S. Potential pitfalls in the diagnosis of phaeochromocytoma. The Medical journal of Australia. 2005; 182: 637-40 [Abstract]
Sidhu, S, Martin, E, Gicquel, C, Melki, J, Clark, S, Campbell, P, Magarey, C, Schulte, K, Röher, H, Delbridge, L, Robinson, B. Mutation and methylation analysis of TP53 in adrenal carcinogenesis. European journal of surgical oncology: the journal of the European Society of Surgical Oncology and the British Association of Surgical Oncology. 2005; 31: 549-54 [Abstract]
Henson, J, Hannay, J, McCarthy, S, Royds, J, Yeager, T, Robinson, R, Wharton, S, Jellinek, D, Arbuckle, S, Yoo, J, Robinson, B, Learoyd, D, Stalley, P, Bonar, S, Yu, D, Pollock, R, Reddel, R. A robust assay for alternative lengthening of telomeres in tumors shows the significance of alternative lengthening of telomeres in sarcomas and astrocytomas. Clinical cancer research. 2005; 11: 217-25 [Abstract]
Cardinal, J, Bergman, L, Hayward, N, Sweet, A, Warner, J, Marks, L, Learoyd, D, Dwight, T, Robinson, B, Epstein, M, Smith, M, Teh, B, Cameron, D, Prins, J. A report of a national mutation testing service for the MEN1 gene: clinical presentations and implications for mutation testing. Journal of medical genetics. 2005; 42: 69-74 [Abstract]
2004
Mirams, M, Robinson, B, Mason, R, Nelson, A. Bone as a source of FGF23: regulation by phosphate?. Bone. 2004; 35: 1192-9 [Abstract]
Haven, C, Howell, V, Eilers, P, Dunne, R, Takahashi, M, van Puijenbroek, M, Furge, K, Kievit, J, Tan, M, Fleuren, G, Robinson, B, Delbridge, L, Philips, J, Nelson, A, Krause, U, Dralle, H, Hoang-Vu, C, Gimm, O, Morreau, H, Marsh, D, Teh, B. Gene expression of parathyroid tumors: molecular subclassification and identification of the potential malignant phenotype. Cancer research. 2004; 64: 7405-11 [Abstract]
McDonnell, C, Benn, D, Marsh, D, Robinson, B, Zacharin, M. K40E: a novel succinate dehydrogenase (SDH)B mutation causing familial phaeochromocytoma and paraganglioma. Clinical endocrinology. 2004; 61: 510-4 [Abstract]
Howell, V, Zori, R, Stalker, H, Williams, C, Jesse, N, Nelson, A, Robinson, B, Marsh, D. A molecular diagnosis of hyperparathyroidism-jaw tumor syndrome in an adolescent with recurrent kidney stones. The Journal of pediatrics. 2004; 145: 567 [Abstract]
Parker, D, Robinson, B, O'Donnell, B. External ophthalmic findings in multiple endocrine neoplasia type 2B. Clinical & experimental ophthalmology. 2004; 32: 420-3 [Abstract]
Chan, S, Nery, L, McElduff, A, Wilmshurst, E, Fulcher, G, Robinson, B, Stiel, J, Gunton, J, Clifton-Bligh, P. Intravenous pamidronate in the treatment and prevention of osteoporosis. Internal medicine journal. 2004; 34: 162-6 [Abstract]
Villablanca, A, Calender, A, Forsberg, L, Höög, A, Cheng, J, Petillo, D, Bauters, C, Kahnoski, K, Ebeling, T, Salmela, P, Richardson, A, Delbridge, L, Meyrier, A, Proye, C, Carpten, J, Teh, B, Robinson, B, Larsson, C. Germline and de novo mutations in the HRPT2 tumour suppressor gene in familial isolated hyperparathyroidism (FIHP). Journal of medical genetics. 2004; 41 [Abstract]
Warner, J, Epstein, M, Sweet, A, Singh, D, Burgess, J, Stranks, S, Hill, P, Perry-Keene, D, Learoyd, D, Robinson, B, Birdsey, P, Mackenzie, E, Teh, B, Prins, J, Cardinal, J. Genetic testing in familial isolated hyperparathyroidism: unexpected results and their implications. Journal of medical genetics. 2004; 41: 155-60 [Abstract]
Sidhu, S, Sywak, M, Robinson, B, Delbridge, L. Adrenocortical cancer: recent clinical and molecular advances. Current opinion in oncology. 2004; 16: 13-8 [Abstract]
Robinson, B, Figtree, G. Estrogen receptor polymorphisms in common disease:recent developments. Current Opinion in Endocrinology and diabetes. 2004; 11: 141-146
Yamazaki, M, Straus, F, Messina, M, Robinson, B, Takeda, T, Hashizume, K, DeGroot, L. Adenovirus-mediated tumor-specific combined gene therapy using Herpes simplex virus thymidine/ganciclovir system and murine interleukin-12 induces effective antitumor activity against medullary thyroid carcinoma. Cancer gene therapy. 2004; 11: 8-15 [Abstract]
Teh, B, Howell, V, Haven, C, Kahnoski, K, Khoo, S, Petillo, D, Chen, J, Fleuren, G, Robinson, B, Delbridge, L, Philips, J, Nelson, A, Krause, U, Hammje, K, Dralle, H, Hoang-Vu, C, Gimm, O, Marsh, D, Morreau, H. Human gene mutations. Gene symbol: HRPT2. Disease: Hyperparathyroidism Jaw-tumor syndrome. Human genetics. 2004; 114: 224 [Abstract]
2003
Freeman, M, Roach, P, Robinson, B, Shields, M. Hiatal hernia in iodine-131 scintigraphy: a potential cause of false-positive midline thoracic uptake. Clinical nuclear medicine. 2003; 28: 709-10 [Abstract]
Benn, D, Croxon, M, Tucker, K, Bambach, C, Richardson, A, Delbridge, L, Pullan, P, Hammond, J, Marsh, D, Robinson, B. Novel succinate dehydrogenase subunit B (SDHB) mutations in familial phaeochromocytomas and paragangliomas, but an absence of somatic SDHB mutations in sporatid phaeochromaocytomas. Oncogene. 2003; 22: 1358-1364
Sambrook, P, Hughes, D, Nelson, A, Robinson, B, Mason, R. Osteocyte viability with glucocorticoid treatment: relation to histomorphometry. Annals Of The Rheumatic Diseases. 2003; 62: 1215-1217
Cooper, L, Clifton Bligh, R, Nery, M, Figtree, G, Hibbert, E, Twigg, S, Robinson, B. Vitamin D supplementation and bone mineral density in early postmenopausal women. American Journal Of Clinical Nutrition. 2003; 77(5): 1324-1329
Robinson, B. Gene discovery in endorinology. Current Opinion in Endocrinology and Diabetes. 2003; 10
Hammett, R, Robinson, B. Responses to access block in Australia. Medical Journal Of Australia. 2003; 178: 105-107
Barnetson, R, Eckstein, R, Robinson, B, Schnitzler, M. There is no increase in frequency of somatic mutations in metastases compared with primary colorectal carcinomas wtih microsatellite instability. Genes Chromosomes & Cancer. 2003; 38: 149-156
Sidhu, S, Giquel, C, Bambach, C, Campbell, P, Magarey, C, Robinson, B, Delbridge, L. Clinical and molecular aspects of adrenocortical tumourigenesis. Anz Journal Of Surgery. 2003; 73: 727-738
Robinson, B, Fletcher, J. Fluoropolymer coated dacron or polytetrafluoroethylene for femoropopliteal bypass grafting: a multicentre trial. Anz Journal Of Surgery. 2003; 73: 95-99
Nelson, A, Clifton Bligh, R, Mirams, M, Gill, A, Au, A, Clarkson, A, Juppner, H, Ruff, S, Stalley, P, Scolyer, R, Robinson, B, Mason, R, Bligh, P. Fibroblast growth factor 23: a new clinical marker for oncogenic osteomalacia. Journal Of Clinical Endocrinology And Metabolism. 2003; 88: 4088-4094
Howell, V, Haven, C, Kahnoski, K, Khoo, S, Petill, D, Chen, J, Fleuren, G, Robinson, B, Delbridge, L, Philips, J, Nelson, A, Krause, U, Hammje, K, Dralle, H, Hoang-Vu, C, Gimm, O, Marsh, D, Morreau, H, Teh, B. HRPT2 mutations are associated with malignancy in sporadic parathyroid tumours. Journal Of Medical Genetics. 2003; 40: 657-663
Cheung, L, Messina, M, Gill, A, Clarkson, A, Learoyd, D, Delbridge, L, Wentworth, J, Philips, J, Clifton-Bligh, R, Robinson, B. Detection of the PAX8-PPARgamma fusion oncogene in both follicular thyroid carcinomas and adenomas. Endocrinology. 2003; 88(1): 354-357
Marsh, D, Theodosopoulos, G, Martin-Schulte, K, Richardson, A, Roher, H, Philips, J, Delbridge, L, Robinson, B. Genome-wide copy number imbalances identified in familial and sproadic medullary thyroid carcinoma. Journal Of Clinical Endocrinology And Metabolism. 2003; 88(4): 1866-1872
Benn, D, Croxson, M, Tucker, K, Bambach, C, Richardson, A, Delbridge, L, Pullan, P, Hammond, J, Marsh, D, Robinson, B. Novel succinate dehydrogenase subunit B (SDHB) mutations in familial phaeochromocytomas and paragangliomas, but an absence of somatic SDHB mutations in sporadic phaeochromocytomas. Oncogene. 2003; 22: 1358-1364
Bernard, M, Sidhu, S, Berger, N, Peix, J, Marsh, D, Robinson, B, Gaston, V, Bouc, Y, Gicquel, C. A Case Report in Favor of a Multistep Adrenocortical Tumorigenesis. Endocrinology. 2003; 88: 998-1001
Nelson, A, Clifton Bligh, R, Mirams, M, Gill, A, Au, A, Clarkson, A, Juppner, H, Ruff, S, Stally, P, Scolyer, R, Robinson, B, Mason, R, Clifton Bligh, P. Fibroblast growth factor 23: a new clinical marker for oncogenic osteomalacia. Journal Of Clinical Endocrinology And Metabolism. 2003; 88(9): 4088-4094
Bernard, M, Sidhu, S, Berger, N, Peix, J, Marsh, D, Robinson, B, Gaston, V, Le Bouc, Y, Gicquel, C. A case report in favor of a multistep adrenocortical tumorigenesis. Journal Of Clinical Endocrinology And Metabolism. 2003; 88(3): 998-1001
2002
Nelson, A, Learoyd, D, Philips, J, Delbridge, L, Marsh, D, Robinson, B, Dwight, T, Theodosopoulos, G, Richardson, A, Zedenius, J, Teh, B, Larsson, C. Independent Genetic Events Associated with the Development of Multiple Parathyroid Tumors in Patients with Primary Hyperparathyroidism. American Journal Of Pathology. 2002; 161: 1299-1306
Robinson, B, Carpten, J, Robbins, C, Villablanca, A, Forsberg, L, Presciuttini, S, Bailey-Wilson, J, Simons, W, Gillanders, E, Kennedy, A, Chen, J, Agarwal, S, Sood, R, Jones, M, Moses, T, Haven, C, Petillo, D, Leotlela, P, Harding, B, Cameron, D, Pannett, A, Hoog, A, Heath III, H, James-Newton, L, Zarbo, R, Cavaco, B, Wassif, W, Perrier, N, Rosen, I, Kristoffersson, U, Turnpenny, P, Farnebo, L, Besser, G, Jackson, C, Morreau, H, Trent, J, Thakker, R, Marx, S, Teh, B. HRPT2, encoding parafibromin, is mutated in hyperparathyroidism-jaw tumor syndrome. Nature Genetics. 2002; 32: 676-680
Sidhu, S, Marsh, D, Philips, J, Bambach, C, Delbridge, L, Robinson, B, Theodosopoulos, G, Campbell, P, Magarey, C, Russell, C, Schulte, K, Roher, H. Comparative Genomic Hybridization Analysis of Adrenocortical Tumors. Journal Of Clinical Endocrinology And Metabolism. 2002; 87(7): 3467-3474
Cheung, L, Learoyd, D, Delbridge, L, Philips, J, Robinson, B, Messina, M, Gill, A, Clarkson, A, Wentworth, J, Clifton-Bligh, R. Detection of the PAX8-PPARy Fusion Oncogene in Both Follicular Thyroid Carcinomas and Adenomas. Endocrinology. 2002; 88(1): 354-357
Messina, M, Yamazaki, M, Zhang, R, Straus, F, Hashizume, K, DeGroot, L, Robinson, B. Effective gene therapy for medullary thyroid carcinoma using recombinant adenovirus inducing tumor-specific expression of interleukin-12. Gene Therapy. 2002; 9: 64-74
Dwight, T, Kytola, S, Teh, B, Theodosopoulos, G, Richardson, A, Philips, J, Twigg, S, Delbridge, L, Marsh, D, Nelson, A, Larsson, C, Robinson, B. Genetic analysis of lithium-associated parathyroid tumors. European Journal Of Endocrinology. 2002; 146: 619-627
Benn, D, Marsh, D, Robinson, B. Genetics of pheochromocytoma and paraganglioma. Current Opinion in Endocrinology & Diabetes. 2002; 9: 79-86
Nelson, A, Barden, J, Hogan, J, Mason, R, Robinson, B, Martin, E, Tasevski, V. Bioactivity of PTH/PTHrP analogs lacking the 1-14 N-terminal domain. Molecular And Cellular Endocrinology. 2002; 189: 37-49
Yu, M, Robinson, B, Messina, M, Both, G, Molloy, P. Calcitonin-Specific Transcription and Splicing Targets Gene-Directed Enqyme Prodrug Therapy to Medullary Thyroid Carcinoma Cells. Endocrinology. 2002; 88(3): 1310-1318
Sidhu, S, Bambach, C, Reeve, T, Stokes, G, Robinson, B, Delbridge, L, Pillinger, S. Changing Pattern of Adrenalectomy at a Tertiary Referral Centre 1970-2000. Anz Journal Of Surgery. 2002; 72: 463-466
Delhanty, P, Marsh, D, Robinson, B, Andrew, S, Capes-Davis, A, Mulligan, L. Transcriptional repression of the RET proto-oncogene by a mitogen activated protein kinase-dependent signalling pathway. Gene. 2002; 298: 9-19
Nelson, A, Marsh, D, Robinson, B, Dwight, T, Teh, B, Larsson, C. Parathyroid tumorigenesis in association with primary hyperparathyroidism. Current Opinion in Endocrinology &Diabetes. 2002; 9: 51-60
Delbridge, L, Barraclough, B, Robinson, B, Philips, J, Parkyn, R. Minimally Invasive Follicular Thyroid Carcinoma: Completion Thyroidectomy or Not?. Anz Journal Of Surgery. 2002; 72: 844-845
Delbridge, L, Parkyn, R, Philips, J, Barraclough, B, Robinson, B. Minimally invasive follicular thyroid carcinoma: Completion Thyroidectomy or not. Anz Journal Of Surgery. 2002; 72: 844-845
Barakate, M, Agarwal, G, Reeves, T, Barraclough, B, Robinson, B, Delbridge, L. Total Thyroidectomy is now the preferred option for the Surgical Management of Graves' Disease. Anz Journal Of Surgery. 2002; 72: 321-432
Nelson, A, Learoyd, D, Philips, J, Delbridge, L, Marsh, D, Robinson, B, Dwight, T, Theodosopoulos, G, Richardson, A, Zedenius, J, Teh, B, Larsson, C. Independent Genetic Events Associated with the Development of Multiple Parathyroid Tumors in Patients with Primary Hyperparqathyroidism. American Journal Of Pathology. 2002; 161: 1299-1306
Learoyd, D, Robinson, B, Villablanca, A, Wassif, S, Smith, T, Hoog, A, Vierimaa, O, Kassem, M, Dwight, T, Forsberg, L, Du, Q, Jones, K, Stranks, S, Juhlin, C, Teh, B, Carling, T, Larsson, C. Involvement of the MEN1 gene locus in familial isolated hyperparathyroidism. European Journal Of Endocrinology. 2002; 147: 313-322
Barraclough, B, Robinson, B, Reeve, T, Delbridge, L, Agarwal, G. Minimally Invasive Parathyroidectomy using the 'Focused' Lateral Approach. 1. Results of the First 100 Consecutive Cases. Anz Journal Of Surgery. 2002; 72: 100-104
Robinson, B, Clifton-Bligh, P, Reeve, T, Barraclough, B, Delbridge, L, Sywak, M, Fick, G. Increase in presentations and procedure rates for hyperparathyroidism in Northern Sydney and New South Wales. Medical Journal Of Australia. 2002; 177: 246-249
2001
Nelson, A, Mason, R, Robinson, B, Hogan, J, Martin, E, Ahlström, H, Aström, G, Larsson, T, Jonsson, K, Wibell, L, Ljunggren, O. Diagnosis of a patient with oncogenic osteomalacia using a phosphate uptake bioassay of serum and magnetic resonance imaging. European journal of endocrinology / European Federation of Endocrine Societies. 2001; 145: 469-76 [Abstract]
Sambrook, P, Raj, A, Hunter, D, Naganathan, V, Mason, R, Robinson, B. Osteoporosis with low dose corticosteroids: contribution of underlying disease effects and discriminatory ability of ultrasound versus bone densitometry. The Journal of rheumatology. 2001; 28: 1063-7 [Abstract]
Nelson, A, Holm, I, Robinson, B, Mason, R, Hogan, J. Phosphate wasting in oncogenic osteomalacia: PHEX Is normal and the tumor-derived factor has unique properties. Bone. 2001; 64: 1247-1254
Nelson, A, Hogan, J, Holm, I, Robinson, B, Mason, R. Phosphate wasting in oncogenic osteomalacia: PHEX is normal and the tumor-derived factor has unique properties. Bone. 2001; 66: 677-680
Marsh, D, Theodosopoulos, G, Howell, V, Richardson, A, Benn, D, Proos, A, Eng, C, Robinson, B. Rapid mutation scanning of genes associated with familial cancer syndromes using denaturing high-performance liquid chromatography. Neoplasia. 2001; 55 (6): 641-648
Holm, I, Nelson, A, Robinson, B, Mason, R, Marsh, D, Cowell, C, Carpenter, T. Mutational analysis and genotype-phenotype correlation of the PHEX gene in X-linked hypophosphatemic rickets. Journal of Clinical Endocrinology and Metabolism. 2001; 20: 177-192
Holm, I, Nelson, A, Robinson, B, Mason, R, Marsh, D, Cowell, C, Carpenter, T. Mutational analysis and genotype-phenotype correlation of the PHEX gene in X-Linked hypophosphphatiemic rickets. Endocrinology. 2001; 17(6): 567-577
Agarwal, G, Barakate, M, Robinson, B, Wilkinson, M, Barraclough, B, Reeve, T, Delbridge, L. Intraoperative quick parathyroid hormone versus same-day parathyroid hormone testing for minimally invasive parathyroidectomy: a cost effectiveness study. Surgery. 2001; Vienna Austria; 2001
Fackenthal, J, Marsh, D, Richardson, A, Cummings, S, Eng, C, Robinson, B, Olopade, O. Male breast cancer in Cowden syndrome patients with germline PTEN mutations. Journal of Medical Genetics. 2001: 139-140
Kjellman, P, Learoyd, D, Messina, M, Weber, G, Hoog, A, Wallin, G, Larsson, C, Robinson, B, Zedenius, J. Expression of the RET proto-oncogene in papullary thyroid carcinoma and its correlation with clinical outcome. British Journal of Surgery. 2001; 174: 29-32
Messina, M, Learoyd, D, Both, G, Molloy, P, Robinson, B. Gene therapy for endocrine tumors: strategies and progress. Current Opinion in Endocrinology & Diabetes. 2001; 9: 108-112
Gauger, P, Agarwal, G, England, B, Delbridge, L, Matz, K, Wilkinson, M, Robinson, B, Thompson, N. Intraoperative parathyroid hormone monitoring fails to detect double parathyroid adenomas: a 2-institution experience. Surgery. 2001; 164: 455-459
Gauger, P, Agarwal, G, England, B, Delbridge, L, Matz, K, Wilkinson, M, Robinson, B, Thompson, N. Intraoperative parathyroid hormone monitoring fails to detect double parathyroid adenomas: a 2-institution experience. Surgery. 2001; 50: 312-320
Sutherland, J, Robinson, B, Delbridge, L. Anaesthesia for Amiodarone-induced thyrotoxicosis: a case review. Anaesthesia and Intensive Care. 2001; 54: 399-400
2000
Gimm, O, Perren, A, Weng, L, Marsh, D, Yeh, Z, Ziebold, U, Gill, E, Hinze, R, Delbridge, L, Lees, J, Mutter, G, Robinson, B, Komminoth, P, Dralle, H, Eng, C. Differential nuclear and cytoplasmic expression of PTEN in normal thyroid tissue, and benign and malignant epithelial thyroid tumors. American Journal of Pathology. 2000; 156: 1693-1700
Barnetson, R, Symons, P, Robinson, B, Schnitzler, M. Genetic analysis of multiple sporadic colon carcinomas from a single patient. International Journal of Colorectal Disease. 2000; 15: 83-86
Messina, M, Yu, D, Learoyd, D, Both, G, Molloy, P, Robinson, B. High level, tissue-specific expression of a modified calcitonin/calcitonin gene-related peptide promoter in a human medullary thyroid carcinoma cell line. Molecular and Cellular Endocrinology. 2000; 164: 219-224
Dwight, T, Twigg, S, Delbridge, L, Wong, F, Farnebo, F, Richardson, A, Nelson, A, Zedenius, J, Philips, J, Larsson, C, Teh, B, Robinson, B. Loss of heterozygosity in sporadic parathyroid tumours: involvement iin chromosome 1 and the MEN1 gene locus in 11q13. Clinical Endocrinology. 2000; 53: 85-92
Dwight, T, Twigg, S, Delbridge, L, Wong, F, Farnebo, F, Richardson, A, Nelson, A, Zedenius, J, Philips, J, Larsson, C, Teh, B, Robinson, B. Loss of heterozygosity in sporadic parathyroid tumours: involvement of chromosome 1 and the MEN1 gene locus in 11q13. Clinical Endocrinology. 2000; 53: 85-`92
Delbridge, L, Dolan, S, Hop, T, Robinson, B, Wilkinson, M, Reeve, T. Minimally invasive parathyroidectomy: 50 consecutive cases. Medical Journal of Australia. 2000; 172: 418-422
Learoyd, D, Messina, M, Zedenius, J, Robinson, B. Molecular genetics and thyroid tumors and surgical decision-making. World Journal of Surgery. 2000; 24: 923-933
Gimm, O, Perren, A, Weng, L, Marsh, D, Yeh, J, Ziebold, U, Gil, E, Hinze, R, Delbridge, L, Lees, J, Mutter, G, Robinson, B, Komminoth, P, Dralle, H, Eng, C. Differential nuclear and cytoplasmic expression of PTEN in normal thyroid tissue, and benign and malignant epithelial thyroid tumors. American Journal of Pathology. 2000; 156: 1693-1700
Dominello, A, Guinea, A, Reeve, T, Robinson, B, Delbridge, L. Progressive increase in thyroid dysfunction after subtotal thyroidectomy for Graves' disease. Asian Journal of Surgery. 2000; 23: 131-135
Andrew, D, Delhanty, P, Mulligan, L, Robinson, B. Sp1 and Sp3 transactivate the RET proto-oncogene promoter. Gene. 2000; 256: 283-291
Benn, D, Dwight, T, Richardson, A, Delbridge, L, Bambach, C, Stowasser, M, Gordon, R, Marsh, D, Robinson, B. Sporadic and familial pheochromocytomas are associated with loss of at least two discrete intervals on chromosome 1p. Cancer Research. 2000; 60: 7048-7051
Gunton, J, McElduff, A, Sulway, M, Stiel, J, Kelso, I, Boyce, S, Fulcher, G, Robinson, B, Clifton-Bligh, P, Wilmshurst, E. Outcome of pregnancies complicated by pre-gestational diabetes mellitus. Australian and New Zealand Journal of Obstetrics & Gynaecology. 2000; 40: 38-43
Learoyd, D, Delbridge, L, Robinson, B. Multiple endocrine neoplasia. Australian and New Zealand Journal of Medicine. 2000; 30: 675-682
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Proteins; Mutation; Thyroid Neoplasms; Bone Density; Osteoporosis; Diphosphonates; Bone and Bones; Fibroblast Growth Factors; Hyperparathyroidism; Proto-Oncogene Proteins; Adrenal Gland Neoplasms; Gene Therapy; Germ-Line Mutation; Parathyroid Neoplasms; Receptors, Calcium-Sensing; Pheochromocytoma; Telomere; Interleukin-12; Phosphates; Sarcoma; Adrenal Cortex Neoplasms; Adrenalectomy; Microscopy, Fluorescence; Ganciclovir; Kidney Calculi; Paraganglioma; Carcinoma, Medullary; Catecholamines; Astrocytoma; In Situ Hybridization, Fluorescence; Multiple Endocrine Neoplasia Type 2a; Proto-Oncogene Proteins c-ret; Protein Subunits; Succinate Dehydrogenase; Blepharoptosis; Ectropion; Multiple Endocrine Neoplasia Type 2b; Thymidine Kinase [Hide keywords]