Overview
Background
Professor Craig Munns is the Mayne Professor of Paediatrics and Director of the Child Health Research Centre, The University of Queensland. Professor Munns is also a Senior Medical Officer in Paediatric Endocrinology and Diabetes at Queensland Children’s Hospital. He graduated from The University of Queensland, before training in paediatrics and endocrinology at The Royal Children’s Hospital, Brisbane. Professor Munns completed his PhD in paediatric growth disorders through UQ. He then undertook a post-doctoral fellowship in paediatric genetic bone disorders at The Shriners Hospital for Children, Montreal, Canada. From 2004 to 2021, Prof Munns was Senior Staff Specialist in Genetic and Metabolic Bone Disorders and Paediatric Endocrinologist at The Children’s Hospital at Westmead, Sydney. He also undertook roles as Clinical Program Director, Division of Diagnostic Services and Clinical Trials Lead at Kids Research. As Clinical Trials Lead his focus was on developing a research-intensive health system and introducing advanced therapeutics.
Professor Munns is an international expert in paediatric musculoskeletal disorders. His primary clinical and research interests are in diagnosis and management of primary and secondary bone disorders, including osteogenesis imperfecta, hypophosphataemic rickets, disuse osteoporosis and nutritional rickets. He has undertaken a wide range of investigator initiated and sponsored clinical trials, authored international consensus documents and has supervised numerous PhD and Masters students. Prof Munns is actively involved in national and international scientific societies. He was treasurer of Asia Pacific Paediatric Endocrine Society, is the inaugural treasurer of the International Society of Children’s Bone Health and has chaired the program organising committees Australasian Paediatric Endocrine Group, Australian and New Zealand Bone and Mineral Society and International Conference of Children’s Bone Health.
Availability
- Professor Craig Munns is:
- Available for supervision
- Media expert
Fields of research
Qualifications
- Bachelor of Faculty of Medicine, The University of Queensland
- Doctor of Philosophy of Paediatrics and Reproductive Medicine, The University of Queensland
- Fellow, Royal Australasian College of Physicians, Royal Australasian College of Physicians
Research interests
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Paediatric Musculoskeletal Disorders
Primary and secondary osteoporosis; Genetic rickets (X-linked hypophosphataemia); Nutritional rickets; Focal bone tumours (Giant cell granuloma, Aneurismal bone cysts); Early detection of disease; Bone density assessment
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Clinical Trials
Investigator initiated; Pharmaceutical sponsored; Gene therapy
Research impacts
Professor Munns has developed international consensus guidelines on the prevention and treatment of nutritional rickets. These guidelines have the potential to irradicate this potentially devastating, fully preventable childhood disorder. He has also developed numerous clinical guidelines for the management of paediatric bone disorders such as osteoporosis, X-linked hypophosphataemia, giant cell granuloma and aneurismal bone cysts.
Works
Search Professor Craig Munns’s works on UQ eSpace
2016
Journal Article
Global consensus recommendations on prevention and management of nutritional rickets
Munns, Craig F., Shaw, Nick, Kiely, Mairead, Specker, Bonny L., Thacher, Tom D., Ozono, Keiichi, Michigami, Toshimi, Tiosano, Dov, Mughal, M. Zulf, Mäkitie, Outi, Ramos-Abad, Lorna, Ward, Leanne, Dimeglio, Linda A., Atapattu, Navoda, Cassinelli, Hamilton, Braegger, Christian, Pettifor, John M., Seth, Anju, Idris, Hafsatu Wasagu, Bhatia, Vijayalakshmi, Fu, Junfen, Goldberg, Gail, Sävendahl, Lars, Khadgawat, Rajesh, Pludowski, Pawel, Maddock, Jane, Hyppönen, Elina, Oduwole, Abiola, Frew, Emma ... Högler, Wolfgang (2016). Global consensus recommendations on prevention and management of nutritional rickets. Hormone Research in Paediatrics, 85 (2), 83-106. doi: 10.1159/000443136
2016
Journal Article
Global consensus recommendations on prevention and management of nutrition rickets
Munns, C., Shaw, N., Kiely, M., Specker, B., Thacher, T., Ozono, K., Michigaml, T., Tiosano, D., Mughal, M., Makitie, O., Ramos-Abad, L., Ward, L., DiMeglio, L., Atapattu, N., Caassinelli, H., Braeger, C., Pettifor, G., Seth, A., Idris, H., Bhatia, V., Fu, Jm, Goldberg, G., Savendahl, L., Khadgawat, R., Pludowskl, P., Maddock, J., Hypponen, E., Oduwole, A., Frew, E. ... Hogler, W. (2016). Global consensus recommendations on prevention and management of nutrition rickets. Pediatriya, 56 (1), 60-63.
2015
Journal Article
Erratum: Vitamin D supplementation and the effects on glucose metabolism during Pregnancy: A randomized controlled trial. (Diabetes care (2014) 37 (1837-1844))
Yap, Constance, Cheung, N. Wah, Gunton, Jenny E., Athayde, Neil, Munns, Craig F., Duke, Anna and Mclean, Mark (2015). Erratum: Vitamin D supplementation and the effects on glucose metabolism during Pregnancy: A randomized controlled trial. (Diabetes care (2014) 37 (1837-1844)). Diabetes Care, 38 (10). doi: 10.2337/dc15-er10
2015
Journal Article
Quality of life prediction in children with joint hypermobility syndrome
Pacey, Verity, Tofts, Louise, Adams, Roger D., Munns, Craig F. and Nicholson, Leslie L. (2015). Quality of life prediction in children with joint hypermobility syndrome. Journal of Paediatrics and Child Health, 51 (7), 689-695. doi: 10.1111/jpc.12826
2015
Journal Article
Homozygosity for frameshift mutations in XYLT2 result in a spondylo-ocular syndrome with bone fragility, cataracts, and hearing defects
Munns, Craig F., Fahiminiya, Somayyeh, Poudel, Nabin, Munteanu, Maria Cristina, Majewski, Jacek, Sillence, David O., Metcalf, Jordan P., Biggin, Andrew, Glorieux, Francis, Fassier, François, Rauch, Frank and Hinsdale, Myron E. (2015). Homozygosity for frameshift mutations in XYLT2 result in a spondylo-ocular syndrome with bone fragility, cataracts, and hearing defects. American Journal of Human Genetics, 96 (6), 971-978. doi: 10.1016/j.ajhg.2015.04.017
2015
Journal Article
Diagnosis and Management of Osteoporosis in Children
Titmuss, Angela T., Biggin, Andrew, Korula, Sophy and Munns, Craig F (2015). Diagnosis and Management of Osteoporosis in Children. Current Pediatrics Reports, 3 (2), 187-199. doi: 10.1007/s40124-015-0082-z
2015
Journal Article
Cystic fibrosis-related bone disease in children: Examination of peripheral quantitative computed tomography (pQCT) data
Brookes, Denise S. K., Briody, Julie N., Munns, Craig F., Davies, Peter S. W. and Hill, Rebecca J. (2015). Cystic fibrosis-related bone disease in children: Examination of peripheral quantitative computed tomography (pQCT) data. Journal of Cystic Fibrosis, 14 (5) 1230, 668-677. doi: 10.1016/j.jcf.2015.04.005
2015
Journal Article
The long-term effects of switching from active intravenous bisphosphonate treatment to low-dose maintenance therapy in children with osteogenesis imperfecta
Biggin, Andrew, Zheng, Linda, Briody, Julie N., Coorey, Craig P. and Munns, Craig F. (2015). The long-term effects of switching from active intravenous bisphosphonate treatment to low-dose maintenance therapy in children with osteogenesis imperfecta. Hormone Research in Paediatrics, 83 (3), 183-189. doi: 10.1159/000369582
2015
Journal Article
Joint hypermobility syndrome subclassification in paediatrics: A factor analytic approach
Pacey, V., Adams, R. D., Tofts, L., Munns, C. and Nicholson, L. (2015). Joint hypermobility syndrome subclassification in paediatrics: A factor analytic approach. Child: Care, Health and Development, 41 (2), 335-336. doi: 10.1111/CCH.12229_3
2015
Journal Article
A Practical Approach to Children with Recurrent Fractures
Korula, Sophy, Titmuss, Angela T., Biggin, Andrew and Munns, Craig F. (2015). A Practical Approach to Children with Recurrent Fractures. Endocrine Development, 28, 210-225. doi: 10.1159/000381047
2015
Journal Article
Cystic fibrosis-related bone disease explored using a four step algorithm
Brookes, D.S.K., Briody, J.N., Munns, C.F., Davies, P.S.W. and Hill, R.J. (2015). Cystic fibrosis-related bone disease explored using a four step algorithm. Journal of Cystic Fibrosis, 14 (1), 127-134. doi: 10.1016/j.jcf.2014.07.011
2015
Journal Article
Joint hypermobility syndrome subclassification in paediatrics: A factor analytic approach
Pacey, Verity, Adams, Roger D., Tofts, Louise, Munns, Craig F. and Nicholson, Leslie L. (2015). Joint hypermobility syndrome subclassification in paediatrics: A factor analytic approach. Archives of Disease in Childhood, 100 (1), 8-13. doi: 10.1136/archdischild-2013-305304
2014
Journal Article
Mutations in SLC34A3/NPT2c are associated with kidney stones and nephrocalcinosis
Dasgupta, Debayan, Wee, Mark J., Reyes, Monica, Li, Yuwen, Simm, Peter J., Sharma, Amita, Schlingmann, Karl-Peter, Janner, Marco, Biggin, Andrew, Lazier, Joanna, Gessner, Michaela, Chrysis, Dionisios, Tuchman, Shamir, Baluarte, H. Jorge, Levine, Michael A., Tiosano, Dov, Insogna, Karl, Hanley, David A., Carpenter, Thomas O., Ichikawa, Shoji, Hoppe, Bernd, Konrad, Martin, Sävendahl, Lars, Munns, Craig F., Lee, Hang, Jüppner, Harald and Bergwitz, Clemens (2014). Mutations in SLC34A3/NPT2c are associated with kidney stones and nephrocalcinosis. Journal of the American Society of Nephrology, 25 (10), 2366-2375. doi: 10.1681/ASN.2013101085
2014
Journal Article
Proprioceptive acuity into knee hypermobile range in children with Joint Hypermobility Syndrome
Pacey, Verity, Adams, Roger D., Tofts, Louise, Munns, Craig F. and Nicholson, Leslie L. (2014). Proprioceptive acuity into knee hypermobile range in children with Joint Hypermobility Syndrome. Pediatric Rheumatology, 12 (1) 40, 1-7. doi: 10.1186/1546-0096-12-40
2014
Journal Article
The IFITM5 mutation c.-14C > T results in an elongated transcript expressed in human bone; and causes varying phenotypic severity of osteogenesis imperfecta type V
Lazarus, Syndia, McInerney-Leo, Aideen M., McKenzie, Fiona A., Baynam, Gareth, Broley, Stephanie, Cavan, Barbra V., Munns, Craig F., Pruijs, Johannes Egbertus Hans, Sillence, David, Terhal, Paulien A., Pryce, Karena, Brown, Matthew A., Zankl, Andreas, Thomas, Gethin and Duncan, Emma L. (2014). The IFITM5 mutation c.-14C > T results in an elongated transcript expressed in human bone; and causes varying phenotypic severity of osteogenesis imperfecta type V. BMC Musculoskeletal Disorders, 15 (107) 107, 1-6. doi: 10.1186/1471-2474-15-107
2014
Journal Article
The use of bisphosphonates in children: Review of the literature and guidelines for dental management
Bhatt, Reena, Hibbert, S. A. and Munns, C. F. (2014). The use of bisphosphonates in children: Review of the literature and guidelines for dental management. Australian Dental Journal, 59 (1), 9-19. doi: 10.1111/adj.12140
2014
Journal Article
Approach to the diagnosis of congenital myopathies
North, Kathryn N., Wang, Ching H., Clarke, Nigel, Jungbluth, Heinz, Vainzof, Mariz, Dowling, James J., Amburgey, Kimberly, Quijano-Roy, Susana, Beggs, Alan H., Sewry, Caroline, Laing, Nigel G., Bönnemann, Carsten G., Aloysius, Annie, Apkon, Susan, Bellini, Jonathan, Bertini, Enrico, Biancalana, Valerie, Birnkrant, David, Bushby, Kate, Connolly, Anne M., Estournet-Mathiaud, Brigitte, Ferreiro, Ana, Fitzgerald, Dominic, Florence, Julaine M., Richard Gee, P. T., Giannetti, Juliana G., Glanzman, Allan, Goebel, Hans, Guillet, Marc ... Yuan, Nanci (2014). Approach to the diagnosis of congenital myopathies. Neuromuscular Disorders, 24 (2), 97-116. doi: 10.1016/j.nmd.2013.11.003
2014
Journal Article
Vitamin D supplementation and the effects on glucose metabolism during pregnancy: A randomized controlled trial
Yap, Constance, Cheung, N. Wah, Gunton, Jenny E., Athayde, Neil, Munns, Craig F., Duke, Anna and McLean, Mark (2014). Vitamin D supplementation and the effects on glucose metabolism during pregnancy: A randomized controlled trial. Diabetes Care, 37 (7), 1837-1844. doi: 10.2337/dc14-0155
2014
Journal Article
Osteogenesis imperfecta: Diagnosis and treatment
Biggin, A. and Munns, C. F. (2014). Osteogenesis imperfecta: Diagnosis and treatment. Current Osteoporosis Reports, 12 (3), 279-288. doi: 10.1007/s11914-014-0225-0
2014
Journal Article
Fracture during intravenous bisphosphonate treatment in a child with osteogenesis imperfecta: An argument for a more frequent, low-dose treatment regimen
Biggin, Andrew, Briody, Julie N., Ormshaw, Elizabeth, Wong, Karen K.Y., Bennetts, Bruce H. and Munns, Craig F. (2014). Fracture during intravenous bisphosphonate treatment in a child with osteogenesis imperfecta: An argument for a more frequent, low-dose treatment regimen. Hormone Research in Paediatrics, 81 (3), 204-210. doi: 10.1159/000355111
Funding
Current funding
Supervision
Availability
- Professor Craig Munns is:
- Available for supervision
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Supervision history
Current supervision
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Doctor Philosophy
Urinary stem cells for diagnosis and characterisation of primary bone disorders
Principal Advisor
Other advisors: Professor Di Yu
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Doctor Philosophy
Tele-Dialysis in community settings: Is it feasible, safe and effective?
Principal Advisor
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Doctor Philosophy
Food Allergy Diagnosis and Management in Late Adolescence
Associate Advisor
Other advisors: Associate Professor Jennifer Koplin
Media
Enquiries
Contact Professor Craig Munns directly for media enquiries about:
- Paediatric Bone
- Rickets
- Vitamin D
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