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2015 Conference Publication Prevalence of Maturity Onset Diabetes of the young in a Western Australian paediatric diabetes clinic using targeted Massively Parallel SequencingJohnson, Stephanie R., Davis, Elizabeth, Conwell, Louise S., Harris, Mark and Duncan, Emma L. (2015). Prevalence of Maturity Onset Diabetes of the young in a Western Australian paediatric diabetes clinic using targeted Massively Parallel Sequencing. International Society of Paediatric and Adolescent Diabetes / Australasian Paediatric Endocrine Group Annual Scientific Meeting, Brisbane, Queensland, Australia: University of Queensland, October 2015. |
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2015 Conference Publication Prevalence of Maturity Onset Diabetes of the Young in a Western Australia paediatric diabetes clinic using targeted Massively Parallel SequencingJohnson, Stephanie R., Davis, Elizabeth, Conwell, Louise S., Harris, Mark and Duncan, Emma L. (2015). Prevalence of Maturity Onset Diabetes of the Young in a Western Australia paediatric diabetes clinic using targeted Massively Parallel Sequencing. Children's Health Queensland Research Conference, Brisbane Qld Australia, December 2015. |
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2015 Conference Publication Exomewide association study of ankylosing spondylitis identifies additional coding region genetic associations with as and strengthens evidence of shared genetic background with inflammatory bowel diseaseRobinson, P., Leo, P., Pointon, J., Harris, J., Cremin, K., Bradbury, L., Stebbings, S., Harrison, A., Duncan, E., Wordsworth, P. and Brown, M. (2015). Exomewide association study of ankylosing spondylitis identifies additional coding region genetic associations with as and strengthens evidence of shared genetic background with inflammatory bowel disease. Australian Rheumatology Associationin conjunction with Rheumatology Health Professionals Association, 56th Annual Scientific Meeting, Adelaide, South Australia, Australia, 23–26 May 2015. Richmond, Australia: Wiley-Blackwell Publishing Asia. doi: 10.1111/imj.12752 |
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2014 Conference Publication Next generation sequencing to identify a novel INS gene mutation in a family with Maturity Onset Diabetes of the Young (MODY)Johnson, Stephanie R., McGown, Ivan N., Conwell, Louise S., Harris, Mark and Duncan, Emma L. (2014). Next generation sequencing to identify a novel INS gene mutation in a family with Maturity Onset Diabetes of the Young (MODY). APPES & APEG 2014: Asia Pacific Paediatric Endocrine Society & Australasian Paediatric Endocrine Group Joint Annual Scientific Meeting, Darwin, NT, Australia, 29 October-1 November, 2014. |
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2014 Conference Publication Next generation sequencing for maturity onset diabetes of the youngJohnson, Stephanie R., Conwell, Louise S., Harris, Mark and Duncan, Emma L. (2014). Next generation sequencing for maturity onset diabetes of the young. ISPAD 2014: 40th Annual Meeting of the International Society of Pediatric and Adolescent Diabetes, Toronto, ON, Canada, 3-6 September, 2014. Berlin, Germany: K.I.T. Group. |
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2014 Conference Publication Next generation sequencing for maturity onset diabetes of the youngJohnson, Stephanie R., Conwell, Louise S., Harris, Mark and Duncan, Emma L. (2014). Next generation sequencing for maturity onset diabetes of the young. APPES & APEG 2014: Asia Pacific Paediatric Endocrine Society & Australasian Paediatric Endocrine Group Joint Annual Scientific Meeting, Darwin, NT, Australia, 29 October-1 November, 2014. |
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2013 Conference Publication Hepatic osteodystrophy in chronic liver diseaseGonsalkorala, E. S., Tallis, C., Stuart, K. A. and Duncan, E. (2013). Hepatic osteodystrophy in chronic liver disease. Australian Gastroenterology Week 2013, Melbourne, Australia, 7-9 October 2013. Richmond, Australia: Wiley-Blackwell Publishing Asia. doi: 10.1111/jgh.12365_5 |
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2013 Conference Publication Next-generation sequencing (NGS) to identify a novel INS gene mutation in a family with maturity onset diabetes of the young (MODY)Johnson, Stephanie R., McGown, Ivan N., Conwell, Louise S., Harris, Mark and Duncan, Emma L. (2013). Next-generation sequencing (NGS) to identify a novel INS gene mutation in a family with maturity onset diabetes of the young (MODY). LWPES/ESPE 9th Joint Meeting Global Care in Pediatric Endocrinology in collaboration with APEG, APPES, JSPE and SLEP, Milan, Italy, 19-22 September, 2013. Basel, Switzerland: S. Karger. doi: 10.1159/isbn.978-3-318-02505-7 |
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2012 Conference Publication The 7Q31 locus, containing WNT16, is associated with bone mineral density, osteoporotic fracture and bone strengthZheng, H.-F., Duncan, E., Eriksson, J., Bergstrom, U., Yerges-Armstrong, L., Leo, P., Vandenput, L., Nicholson, G., Ladouceur, M., Prince, R., Leslie, W., Eisman, J., Goltzman, D., Jones, G., Xiao, Y., Liu, J., Reid, I., Sambrook, P., Dennison, E., Danoy, P., Wilson, S., McCloskey, E., Eastell, R., Spector, T., Mitchell, B., Streeten, E., Brommage, R., Lorentzon, M., Pettersson, U. ... GEnetic Factors OSteoporosis (2012). The 7Q31 locus, containing WNT16, is associated with bone mineral density, osteoporotic fracture and bone strength. 39th Annual Congress of the European-Calcified-Tissue-Society (ECTS), Stockholm, Sweden, 19-23 May 2012. Philadelphia, PA, United States: Elsevier. doi: 10.1016/j.bone.2012.02.086 |
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2012 Conference Publication Multi-stage genome-wide association meta-analyses identified gender-specific loci associated with bone mineral densityZhang, Lei, Li, Jian, Pei, Yu-Fang, Lin, Yong, Shen, Hui, Estrada, Karol, Rivadeneira, Fernando, Guitterlinden, Andre, Shin, Chan Soo, Choi, Hyung Jin, Duncan, Emma L., Leo, Paul J., Brown, Matthew A., Liu, Yao-Zhong, Liu, Yongjun, Zhang, Ji-Gang, Tian, Qing, Wang, Yu-Ping, Zhu, Xue-Zhen, Wu, Shuyan, Papasian, Christopher J. and Deng, Hong-Wen (2012). Multi-stage genome-wide association meta-analyses identified gender-specific loci associated with bone mineral density. Ninth Annual NIH Interdisciplinary Women’s Health Research Symposium, Bethesda, MD, United States, 15 November 2012. New Rochelle, NY, United States: Mary Ann Liebert. doi: 10.1089/jwh.2012.ab02 |
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2012 Conference Publication Next generation sequencing identifies mutations clustering in the amino-terminal transcriptional activation domain of Mafb in multicentric carpotarsal osteolysisMcInerney-Leo, A., Zankl, A., Duncan, E., Clark, G., Leo, P., Glasov, E. and Brown, M. (2012). Next generation sequencing identifies mutations clustering in the amino-terminal transcriptional activation domain of Mafb in multicentric carpotarsal osteolysis. Australian Rheumatology Association in conjunction with Rheumatology Health Professionals 53rd Annual Scientific Meeting, Canberra, Australia, 12-15 May 2012. Richmond, VIC, Australia: Wiley-Blackwell Publishing Asia. doi: 10.1111/j.1445-5994.2012.02759.x |
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2012 Conference Publication Wnt16 Is associated with bone mineral density, osteoporotic fracture and bone strength: a Large-Scale Meta-Analysis of Genomewide Association StudiesZheng, Hou-Feng, Duncan, Emma, Eriksson, Joel, Bergstrom, Ulrica, Yerges-Armstrong, Laura M., Leo, Paul J., Vandenput, Liesbeth, Nicholson, Geoffrey, Ladouceur, Martin, Prince, Richard L., Leslie, William D., Eisman, John A., Goltzman, David, Jones, Graeme, Xiao, Yongjun, Liu, Jeff, Reid, Lanr, Sambrook, Philip N., Dennison, Elaine M., Danoy, Patrick, Wilson, Scott G., McCloskey, Eugene, Eastell, Richard, Spector, Tim, Mitchell, Braxton D., Streeten, Elizabeth A., Brommage, Robert, Lorentzon, Mattias, Pettersson, Ulrika ... Richards, J. Brent (2012). Wnt16 Is associated with bone mineral density, osteoporotic fracture and bone strength: a Large-Scale Meta-Analysis of Genomewide Association Studies. IOF-ECCEO European Congress on Osteoporosis and Osteoarthritis / 2nd IOF-ESCEO Pre-Clinical Symposium, Bordeaux France, 21-24 March 2012. London, United Kingdom: Springer U K. doi: 10.1007/s00198-012-1924-y |
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2011 Conference Publication Complete Exome Sequencing for Marfan Syndrome, Osteogenesis Imperfecta and Stickler Syndrome: a New EraMcInerney-Leo, A., Glasov, E., Duncan, E. and Zankl, A. (2011). Complete Exome Sequencing for Marfan Syndrome, Osteogenesis Imperfecta and Stickler Syndrome: a New Era. Rheumatology Health Professionals Association 52nd Annual Scientific Meeting, Brisbane, Queensland, 14-17 May 2011. Richmond, VIC, Australia: Wiley-Blackwell. doi: 10.1111/j.1445-5994.2010.02467.x |
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2011 Conference Publication Association analyses of 47,500 individuals identifies six fracture loci and 82 BMD loci clustering in biological pathways that regulate osteoblast and osteoclast activityEstrada, K, Evangelou, E, Hsu, YH, Styrkarsdottir, U, Liu, CT, Moayyeri, A, Kaptoge, S, Duncan, E, Amin, N, Kiel, D, Karasik, D, Albagha, OM, Brown, M, Spector, TD, Zillikens, MC, Ohlsson, C, Thorleifsson, G, Reeve, J, Vandenput, L, Pettersson, U, O'Neill, T, Riancho, JA, Ijunggren, O, Rousseau, F, Leslie, WD, Obermayer-Pietsch, B, Alonso, N, Langdahl, B, Nogues, X ... GENOMOS Consortia (2011). Association analyses of 47,500 individuals identifies six fracture loci and 82 BMD loci clustering in biological pathways that regulate osteoblast and osteoclast activity. 3rd Joint Meeting of the European-Calcified-Tissue-Society/International-Bone-and-Mineral-Society, Athens Greece, May 07-11, 2011. NEW YORK: ELSEVIER SCIENCE INC. doi: 10.1016/j.bone.2011.03.070 |
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2011 Conference Publication A Population Study to Optimize the Role of Serology and Genetics in the Diagnosis of Celiac Disease (CD)Costa, M, Henry, M, Taylor, R, Duncan, E, Kotowicz, M, Pasco, JA, Tye-Din, JA, Pollock, W, Toh, BH, Brown, MA, Nicholson, GC and Anderson, RP (2011). A Population Study to Optimize the Role of Serology and Genetics in the Diagnosis of Celiac Disease (CD). Conference on Digestive Disease Week 2011, Chicago Il, May 07-10, 2011. PHILADELPHIA: W B SAUNDERS CO-ELSEVIER INC. |
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2010 Conference Publication Prevalence and diagnosis of coeliac disease in an age-stratified random sample of Australian adultsAnderson, R. P., Henry, M., Taylor, R., Costa, M., Danoy, P., Varney, M., Tye-Din, J., Pasco, J, Pollock, W., Toh, B. H., Kotowicz, Duncan, E., Brown, M., Binder, W. and Nicolson, G. (2010). Prevalence and diagnosis of coeliac disease in an age-stratified random sample of Australian adults. Australian Gastroenterology Week 2010, Gold Coast, QLD, Australia, 20-23 October 2010. Richmond, VIC, Australia: Wiley-Blackwell Publishing Asia. doi: 10.1111/j.1440-1746.2010.06451.x |
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2009 Conference Publication Mutations in LRP5 and SOST are a rare cause of high bone mass in the general populationDuncan, E. L., Gregson, C. L., Addison, K., Brugmans, M., Pointon, J. J., Appleton, L. H., Tobias, J. H. and Brown, M. A. (2009). Mutations in LRP5 and SOST are a rare cause of high bone mass in the general population. 36th European Symposium on Calcified Tissues, Vienna, Austria, May 23-27, 2009. New York, United States: Elsevier. doi: 10.1016/j.bone.2009.03.142 |
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2008 Conference Publication Prevalence and Risk Factors for Vitamin D Deficiency in Patients with Chronic Kidney Disease in a Subtropical ClimateSiva, B., Duncan, E., Hawley, C. and Isbel, N. (2008). Prevalence and Risk Factors for Vitamin D Deficiency in Patients with Chronic Kidney Disease in a Subtropical Climate. HOBOKEN: WILEY-BLACKWELL. |
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2008 Conference Publication Phased genome-wide association study identifies new gene affecting bone mineral densityDuncan, E. L., Addison, K., Brugmans, M., Irwin, D., Evans, D., Eisman, J., Jones, G., Nicholson, G., Prince, R., Seeman, E., Uitterlinden, A., Wark, J., Ralston, S. and Brown, M. A. (2008). Phased genome-wide association study identifies new gene affecting bone mineral density. American Society for Bone and Mineral Research (ASBMR) 30th Annual Meeting, Montreal,Canada, 12 - 16 September 2008. Malden, MA, United States: Wiley-Blackwell. doi: 10.1002/jbmr.5650231306 |
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2008 Conference Publication Genome-wide association study identifies klotho and other novel loci as contributors to BMD variation in postmenopausal womenDuncan, E. L., Rivadeneira, F., Sims, A., Dowling, A., Doan, T., Arp, P. P., Jhamai, M., Moorhouse, M., Evans, D., Eisman, J., Jones, G., Nicholson, G., Prince, R., Seeman, E., Wass, J. A. H., Hofman, A., Pols, H. A., Brown, M. A. and Uitterlinden, A. G. (2008). Genome-wide association study identifies klotho and other novel loci as contributors to BMD variation in postmenopausal women. 35th European Symposium on Calcified Tissues, Barcelona, Spain, 24-28 May 2008. New York, United States: Springer. |
