Skip to menu Skip to content Skip to footer
Professor Craig Munns
Professor

Craig Munns

Email: 
Phone: 
+61 7 3069 7362

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

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

  • 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

  • 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

190 works between 2000 and 2025

81 - 100 of 190 works

2019

Journal Article

Skeletal and extraskeletal actions of vitamin D: Current evidence and outstanding questions

Bouillon, Roger, Marcocci, Claudio, Carmeliet, Geert, Bikle, Daniel, White, John H., Dawson-Hughes, Bess, Lips, Paul, Munns, Craig F., Lazaretti-Castro, Marise, Giustina, Andrea and Bilezikian, John (2019). Skeletal and extraskeletal actions of vitamin D: Current evidence and outstanding questions. Endocrine Reviews, 40 (4), 1109-1151. doi: 10.1210/er.2018-00126

Skeletal and extraskeletal actions of vitamin D: Current evidence and outstanding questions

2019

Journal Article

Bone marrow transplantation for treatment of the Col1a2+/G610C osteogenesis imperfecta mouse model

Lee, Lucinda R., Peacock, Lauren, Ginn, Samantha L., Cantrill, Laurence C., Cheng, Tegan L., Little, David G., Munns, Craig F. and Schindeler, Aaron (2019). Bone marrow transplantation for treatment of the Col1a2+/G610C osteogenesis imperfecta mouse model. Calcified Tissue International, 104 (4), 426-436. doi: 10.1007/s00223-018-0504-3

Bone marrow transplantation for treatment of the Col1a2+/G610C osteogenesis imperfecta mouse model

2019

Journal Article

Long-term outcomes of adolescent anorexia nervosa on bone

Mumford, Jessica, Kohn, Michael, Briody, Julie, Miskovic-Wheatley, Jane, Madden, Sloane, Clarke, Simon, Biggin, Andrew, Schindeler, Aaron and Munns, Craig (2019). Long-term outcomes of adolescent anorexia nervosa on bone. Journal of Adolescent Health, 64 (3), 305-310. doi: 10.1016/j.jadohealth.2018.07.025

Long-term outcomes of adolescent anorexia nervosa on bone

2019

Journal Article

A comparison of subtraction MRI with the standard contrast-enhanced imaging in Perthes’ disease

Jamil, K., Walker, T., Onikul, E., Munns, C. F. and Little, D. G. (2019). A comparison of subtraction MRI with the standard contrast-enhanced imaging in Perthes’ disease. Journal of Children's Orthopaedics, 13 (1), 82-88. doi: 10.1302/1863-2548.13.180136

A comparison of subtraction MRI with the standard contrast-enhanced imaging in Perthes’ disease

2019

Journal Article

Differential diagnosis of perinatal hypophosphatasia: radiologic perspectives

Offiah, Amaka C., Vockley, Jerry, Munns, Craig F. and Murotsuki, Jun (2019). Differential diagnosis of perinatal hypophosphatasia: radiologic perspectives. Pediatric Radiology, 49 (1), 3-22. doi: 10.1007/s00247-018-4239-0

Differential diagnosis of perinatal hypophosphatasia: radiologic perspectives

2018

Journal Article

Variations in the management of acute illness in children with congenital adrenal hyperplasia: An audit of three paediatric hospitals

Chrisp, Georgina L., Maguire, Ann M., Quartararo, Maria, Falhammar, Henrik, King, Bruce R., Munns, Craig F., Torpy, David J., Hameed, Shihab and Rushworth, R. Louise (2018). Variations in the management of acute illness in children with congenital adrenal hyperplasia: An audit of three paediatric hospitals. Clinical Endocrinology, 89 (5), 577-585. doi: 10.1111/cen.13826

Variations in the management of acute illness in children with congenital adrenal hyperplasia: An audit of three paediatric hospitals

2018

Journal Article

Management of endocrine disease: Therapeutics of Vitamin D

Ebeling, P. R., Adler, R. A., Jones, G., Liberman, U. A., Mazziotti, G., Minisola, S., Munns, C. F., Napoli, N., Pittas, A. G., Giustina, A., Bilezikian, J. P. and Rizzoli, R. (2018). Management of endocrine disease: Therapeutics of Vitamin D. European Journal of Endocrinology, 179 (5), R239-R259. doi: 10.1530/EJE-18-0151

Management of endocrine disease: Therapeutics of Vitamin D

2018

Journal Article

Diagnosis of recurrent fracture in a pediatric cohort

Fiscaletti, M., Coorey, C. P., Biggin, A., Briody, J., Little, D. G., Schindeler, A. and Munns, C. F. (2018). Diagnosis of recurrent fracture in a pediatric cohort. Calcified Tissue International, 103 (5), 529-539. doi: 10.1007/s00223-018-0449-6

Diagnosis of recurrent fracture in a pediatric cohort

2018

Journal Article

Vitamin D assays and the definition of hypovitaminosis D: results from the First International Conference on Controversies in Vitamin D

Sempos, Christopher T., Heijboer, Annemieke C., Bikle, Daniel D., Bollerslev, Jens, Bouillon, Roger, Brannon, Patsy M., DeLuca, Hector F., Jones, Glenville, Munns, Craig F., Bilezikian, John P., Giustina, Andrea and Binkley, Neil (2018). Vitamin D assays and the definition of hypovitaminosis D: results from the First International Conference on Controversies in Vitamin D. British Journal of Clinical Pharmacology, 84 (10), 2194-2207. doi: 10.1111/bcp.13652

Vitamin D assays and the definition of hypovitaminosis D: results from the First International Conference on Controversies in Vitamin D

2018

Journal Article

Novel variant in Sp7/Osx associated with recessive osteogenesis imperfecta with bone fragility and hearing impairment

Fiscaletti, Melissa, Biggin, Andrew, Bennetts, Bruce, Wong, Karen, Briody, Julie, Pacey, Verity, Birman, Catherine and Munns, Craig F. (2018). Novel variant in Sp7/Osx associated with recessive osteogenesis imperfecta with bone fragility and hearing impairment. Bone, 110, 66-75. doi: 10.1016/j.bone.2018.01.031

Novel variant in Sp7/Osx associated with recessive osteogenesis imperfecta with bone fragility and hearing impairment

2018

Journal Article

Consensus guidelines on the use of bisphosphonate therapy in children and adolescents

Simm, Peter J., Biggin, Andrew, Zacharin, Margaret R., Rodda, Christine P., Tham, Elaine, Siafarikas, Aris, Jefferies, Craig, Hofman, Paul L., Jensen, Diane E., Woodhead, Helen, Brown, Justin, Wheeler, Benjamin J., Brookes, Denise, Lafferty, Antony, Munns, Craig F. and APEG Bone Mineral Working Group (2018). Consensus guidelines on the use of bisphosphonate therapy in children and adolescents. Journal of Paediatrics and Child Health, 54 (3), 223-233. doi: 10.1111/jpc.13768

Consensus guidelines on the use of bisphosphonate therapy in children and adolescents

2018

Book Chapter

Juvenile osteoporosis

Glorieux, Francis H. and Munns, Craig (2018). Juvenile osteoporosis. Primer on the Metabolic Bone Diseases and Disorders of Mineral Metabolism. (pp. 419-423) wiley. doi: 10.1002/9781119266594.ch53

Juvenile osteoporosis

2018

Journal Article

A novel CASR mutation (p.Glu757lys) causing autosomal dominant hypocalcaemia type 1

Kwan, Benjamin, Champion, Bernard, Boyages, Steven, Munns, Craig F., Clifton-Bligh, Roderick, Luxford, Catherine and Crawford, Bronwyn (2018). A novel CASR mutation (p.Glu757lys) causing autosomal dominant hypocalcaemia type 1. Endocrinology, Diabetes and Metabolism Case Reports, 2018 (1) 18-0107, 1-4. doi: 10.1530/EDM-18-0107

A novel CASR mutation (p.Glu757lys) causing autosomal dominant hypocalcaemia type 1

2017

Journal Article

Protocol for a randomised control trial of bisphosphonate (zoledronic acid) treatment in childhood femoral head avascular necrosis due to Perthes disease

Jamil, Kamal, Zacharin, Margaret, Foster, Bruce, Donald, Geoffrey, Hassall, Timothy, Siafarikas, Aris, Johnson, Michael, Tham, Elaine, Whitewood, Colin, Gebski, Val, Cowell, Chris T, Little, David Graham and Munns, Craig Frank (2017). Protocol for a randomised control trial of bisphosphonate (zoledronic acid) treatment in childhood femoral head avascular necrosis due to Perthes disease. BMJ Paediatrics Open, 1 (1) e000084, e000084. doi: 10.1136/bmjpo-2017-000084

Protocol for a randomised control trial of bisphosphonate (zoledronic acid) treatment in childhood femoral head avascular necrosis due to Perthes disease

2017

Journal Article

Long-term bisphosphonate therapy in osteogenesis imperfecta

Biggin, A. and Munns, C. F. (2017). Long-term bisphosphonate therapy in osteogenesis imperfecta. Current Osteoporosis Reports, 15 (5), 412-418. doi: 10.1007/s11914-017-0401-0

Long-term bisphosphonate therapy in osteogenesis imperfecta

2017

Journal Article

Monitoring guidance for patients with hypophosphatasia treated with asfotase alfa

Kishnani, Priya S., Rush, Eric T., Arundel, Paul, Bishop, Nick, Dahir, Kathryn, Fraser, William, Harmatz, Paul, Linglart, Agnès, Munns, Craig F., Nunes, Mark E., Saal, Howard M., Seefried, Lothar and Ozono, Keiichi (2017). Monitoring guidance for patients with hypophosphatasia treated with asfotase alfa. Molecular Genetics and Metabolism, 122 (1-2), 4-17. doi: 10.1016/j.ymgme.2017.07.010

Monitoring guidance for patients with hypophosphatasia treated with asfotase alfa

2017

Journal Article

Combination sclerostin antibody and zoledronic acid treatment outperforms either treatment alone in a mouse model of osteogenesis imperfecta

Little, David G., Peacock, Lauren, Mikulec, Kathy, Kneissel, Michaela, Kramer, Ina, Cheng, Tegan L., Schindeler, Aaron and Munns, Craig (2017). Combination sclerostin antibody and zoledronic acid treatment outperforms either treatment alone in a mouse model of osteogenesis imperfecta. Bone, 101, 96-103. doi: 10.1016/j.bone.2017.04.016

Combination sclerostin antibody and zoledronic acid treatment outperforms either treatment alone in a mouse model of osteogenesis imperfecta

2017

Journal Article

The importance of vitamin D in maternal and child health: A global perspective

Fiscaletti, M., Stewart, P. and Munns, C. F. (2017). The importance of vitamin D in maternal and child health: A global perspective. Public Health Reviews, 38 (1) 19. doi: 10.1186/s40985-017-0066-3

The importance of vitamin D in maternal and child health: A global perspective

2016

Journal Article

Response to the letter by Sugiyama and Oda

Mughal, M. Z., Thacher, T. D., Specker, B. L., Shaw, N. J., Kiely, M., Munns, C. F. and Högler, W. (2016). Response to the letter by Sugiyama and Oda. Journal of Clinical Endocrinology and Metabolism, 101 (10), L97-L98. doi: 10.1210/jc.2016-3059

Response to the letter by Sugiyama and Oda

2016

Journal Article

Central adrenal insufficiency is not a common feature in CHARGE syndrome: A cross-sectional study in 2 cohorts

Wong, Monica T.Y., van Ravenswaaij-Arts, Conny M.A., Munns, Craig F., Hsu, Peter, Mehr, Sam and Bocca, Gianni (2016). Central adrenal insufficiency is not a common feature in CHARGE syndrome: A cross-sectional study in 2 cohorts. Journal of Pediatrics, 176, 150-155. doi: 10.1016/j.jpeds.2016.05.065

Central adrenal insufficiency is not a common feature in CHARGE syndrome: A cross-sectional study in 2 cohorts

Funding

Current funding

  • 2024 - 2026
    The 360-Kids community Network to support children with neurodevelopment challenges (HERA 2.0 partnership)
    Health and Wellbeing Queensland
    Open grant
  • 2024 - 2028
    Klinefelter Syndrome Registry
    William Ivers Memorial Fund
    Open grant
  • 2023 - 2027
    Australian Cerebral Palsy Musculoskeletal Health Network
    NHMRC MRFF EPCDR - Chronic Musculoskeletal Conditions in Children and Adolescents
    Open grant
  • 2022 - 2026
    Children with Lower Limb Pain (CLLiP): Working with families, community and health care provider's to improve outcomes (MRFF Chronic Musculoskeletal administered by Monash University)
    Monash University
    Open grant

Supervision

Availability

Professor Craig Munns is:
Available for supervision

Before you email them, read our advice on how to contact a supervisor.

Supervision history

Current supervision

  • Doctor Philosophy

    Tele-Dialysis in community settings: Is it feasible, safe and effective?

    Principal Advisor

  • Doctor Philosophy

    Urinary stem cells for diagnosis and characterisation of primary bone disorders

    Principal Advisor

    Other advisors: Professor Di Yu

  • 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

Need help?

For help with finding experts, story ideas and media enquiries, contact our Media team:

communications@uq.edu.au