Glycaemic behaviour during breastfeeding in women with Type 1 diabetes von Achong, N., McIntyre, H. D., Callaway, L., Duncan, E. L.

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Isolation of a Candidate Human Telomerase Catalytic Subunit Gene, Which Reveals Complex Splicing Patterns in Different Cell Types von Kilian, Andrzej, Bowtell, David D.L., Abud, Helen E., Hime, Gary R., Venter, Deon J., Keese, Paul K., Duncan, Emma L., Reddel, Roger R., Jefferson, Richard A.

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Whole exome sequencing is an efficient, sensitive and specific method for determining the genetic cause of short-rib thoracic dystrophies von McInerney-Leo, A.M., Harris, J.E., Leo, P.J., Marshall, M.S., Gardiner, B., Kinning, E., Leong, H.Y., McKenzie, F., Ong, W.P., Vodopiutz, J., Wicking, C., Brown, M.A., Zankl, A., Duncan, E.L.

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Zero-point entropy in stuffed spin-ice von Freitas, R. S, Schiffer, P, Ueland, B. G, Lau, G. C, Cava, R. J, Muegge, B. D, Duncan, E. L

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Broadening the phenotypic spectrum of POP1‐skeletal dysplasias: identification of POP1 mutations in a mild and severe skeletal dysplasia von Barraza‐García, J., Rivera‐Pedroza, C.I., Hisado‐Oliva, A., Belinchón‐Martínez, A., Sentchordi‐Montané, L., Duncan, E.L., Clark, G.R., del Pozo, A., Ibáñez‐Garikano, K., Offiah, A., Prieto‐Matos, P., Cormier‐Daire, V., Heath, K.E.

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Risedronate in adults with osteogenesis imperfecta type I: increased bone mineral density and decreased bone turnover, but high fracture rate persists von Bradbury, L. A., Barlow, S., Geoghegan, F., Hannon, R. A., Stuckey, S. L., Wass, J. A. H., Russell, R. G. G., Brown, M. A., Duncan, E. L.

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‘Sink or swim’: an evaluation of the clinical characteristics of individuals with high bone mass von Gregson, C. L., Steel, S. A., O’Rourke, K. P., Allan, K., Ayuk, J., Bhalla, A., Clunie, G., Crabtree, N., Fogelman, I., Goodby, A., Langman, C. M., Linton, S., Marriott, E., McCloskey, E., Moss, K. E., Palferman, T., Panthakalam, S., Poole, K. E. S., Stone, M. D., Turton, J., Wallis, D., Warburton, S., Wass, J., Duncan, E. L., Brown, M. A., Davey-Smith, G., Tobias, J. H.

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Response to ‘Predicting the diagnosis of autism spectrum disorder using gene pathway analysis’ von Robinson, E B, Howrigan, D, Yang, J, Ripke, S, Anttila, V, Duncan, L E, Jostins, L, Barrett, J C, Medland, S E, MacArthur, D G, Breen, G, O'Donovan, M C, Wray, N R, Devlin, B, Daly, M J, Visscher, P M, Sullivan, P F, Neale, B M

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Traits and Motives: Toward an Integration of Two Traditions in Personality Research von Winter, David G, John, Oliver P, Stewart, Abigail J, Klohnen, Eva C, Duncan, Lauren E

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Next-generation sequencing: a frameshift in skeletal dysplasia gene discovery von Lazarus, S., Zankl, A., Duncan, E. L.

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Does hypertension and its pharmacotherapy affect the quality of sexual function in women? von Duncan, Laurie E, Lewis, Carol, Jenkins, Paul, Pearson, Thomas A

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Letter to the Editor: Posttraumatic stress disorder has genetic overlap with cardiometabolic traits von Sumner, J A, Duncan, L E, Wolf, E J, Amstadter, A B, Baker, D G, Beckham, J C, Gelaye, B, Hemmings, S, Kimbrel, N A, Logue, M W, Michopoulos, V, Mitchell, K S, Nievergelt, C, Rothbaum, A, Seedat, S, Shinozaki, G, Vermetten, E

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Whole‐exome sequencing for mutation detection in pediatric disorders of insulin secretion: Maturity onset diabetes of the young and congenital hyperinsulinism von Johnson, S R, Leo, P J, McInerney‐Leo, A M, Anderson, L K, Marshall, M, McGown, I, Newell, F, Brown, M A, Conwell, L S, Harris, M, Duncan, E L

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A brilliant breakthrough in OI type V von Lazarus, S., Moffatt, P., Duncan, E. L., Thomas, G. P.

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Suggestive Linkage of the Parathyroid Receptor Type 1 to Osteoporosis von Duncan, Emma L., Brown, Matthew A., Sinsheimer, Janet, Bell, John, Carr, Andrew J., Wordsworth, B. Paul, Wass, John A. H.

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The genetic associations of acute anterior uveitis and their overlap with the genetics of ankylosing spondylitis von Robinson, P C, Leo, P J, Pointon, J J, Harris, J, Cremin, K, Bradbury, L A, Stebbings, S, Harrison, A A, Evans, D M, Duncan, E L, Wordsworth, B P, Brown, M A

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COL1A1 C-propeptide cleavage site mutation causes high bone mass, bone fragility and jaw lesions: a new cause of gnathodiaphyseal dysplasia? von McInerney-Leo, A. M., Duncan, E. L., Leo, P. J., Gardiner, B., Bradbury, L. A., Harris, J. E., Clark, G. R., Brown, M. A., Zankl, A.

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Stuffed rare earth pyrochlore solid solutions von Lau, G.C., Muegge, B.D., McQueen, T.M., Duncan, E.L., Cava, R.J.

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Point mutation in p14ARF‐specific exon 1β of CDKN2A causing familial melanoma and astrocytoma von McInerney‐Leo, A. M., Wheeler, L., Sturm, R.A., Tan, J.‐M., Harris, J.E., Anderson, L., Jagirdar, K., Brown, M.A., Leo, P.J., Soyer, H.P., Duncan, E.L.

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THU0380 Patterns of Osteoporosis Medication Dispensing for Older Australian Women From 2002 to 2010: Influences of Publications, Guidelines, Marketing Activities and Policy von Peeters, G., Tett, S. E., Duncan, E. L., Mishra, G. D., Dobson, A. J.

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