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Preview	Issue Date	Title	Author(s)
	2002	A mutation in the gene TNFRSF11B encoding osteoprotegerin causes an idiopathic hyperphosphatasia phenotype	Cundy, T.; Hegde, M.; Naot, D.; Chong, B.; King, A.; Wallace, R.; Mulley, J.; Love, D.; Seidel, J.; Fawkner, M.; Banovic, T.; Callon, K.; Grey, A.; Reid, I.; Middleton-Hardie, C.; Cornish, J.
	2005	A community-based intervention to reduce antibiotic use for upper respiratory tract infections in regional South Australia	Dollman, W.; LeBlanc, V.; Stevens, L.; O'Connor, P.; Turnidge, J.
	2019	GJB2 and GJB6 mutations in hereditary recessive non-syndromic hearing impairment in Cameroon	Tingang Wonkam, E.; Chimusa, E.; Noubiap, J.J.; Adadey, S.M.; F Fokouo, J.V.; Wonkam, A.
	2013	Erythrocyte-binding antigens of Plasmodium falciparum are targets of human inhibitory antibodies and function to evade naturally acquired immunity	Persson, K.; Fowkes, F.; McCallum, F.; Gicheru, N.; Reiling, L.; Richards, J.; Wilson, D.; Lopaticki, S.; Cowman, A.; Marsh, K.; Beeson, J.
	2023	The effects of age and biological sex on the association between I-wave recruitment and the response to cTBS: an exploratory study	Van Dam, J.M.; Graetz, L.; Pitcher, J.B.; Goldsworthy, M.R.
	2004	Benign familial neonatal-infantile seizures: Characterization of a new sodium channelopathy	Berkovic, S.; Heron, S.; Giordano, L.; Marini, C.; Guerrini, R.; Kaplan, R.; Gambardella, A.; Steinlein, O.; Grinton, B.; Dean, J.; Bordo, L.; Hodgson, B.; Yamamoto, T.; Mulley, J.; Zara, F.; Scheffer, I.
	2003	X-linked mild non-syndromic mental retardation with neuropsychiatric problems and the missense mutation A365E in PAK3	Gedeon, A.; Nelson, J.; Gecz, J.; Mulley, J.
	2011	MLVA and phage typing as complementary tools in the epidemiological investigation of Salmonella enterica serovar typhimurium clusters	Ross, I.; Davos, D.; Mwanri, L.; Raupach, J.; Heuzenroeder, M.
	2003	Dietry intakes and food sources of omega-6 and omega-3 polyunsaturated fatty acids	Meyer, B.; Mann, N.; Lewis, J.; Milligan, G.; Sinclair, A.; Howe, P.
	2013	Mutations in DEPDC5 cause familial focal epilepsy with variable foci	Dibbens, L.; de Vries, B.; Donatello, S.; Heron, S.; Hodgson, B.; Chintawar, S.; Crompton, D.; Hughes, J.; Bellows, S.; Klein, K.; Callenbach, P.; Corbett, M.; Gardner, A.; Kivity, S.; Iona, X.; Regan, B.; Weller, C.; Crimmins, D.; O'Brien, T.; Guerrero-Lopez, R.; et al.