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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.
	2012	Lack of cross-protection against Bordetella holmesii after pertussis vaccination	Zhang, X.; Weyrich, L.; Lavine, J.; Karanikas, A.; Harvill, E.
	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.
	2012	Efficient measurement of opsonising antibodies to plasmodium falciparum merozoites	Hill, D.; Eriksson, E.; Carmagnac, A.; Wilson, D.; Cowman, A.; Hansen, D.; Schofield, L.; Braga, E.M.
	2008	Antibody-mediated growth inhibition of Plasmodium falciparum: Relationship to age and protection from parasitemia in Kenyan children and adults	Dent, A.; Bergmann-Leitner, E.; Wilson, D.; Tisch, D.; Kimmel, R.; Vulule, J.; Sumba, P.; Beeson, J.; Angov, E.; Moormann, A.; Kazura, J.; Sutherland, C.J.
	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.
	2013	Loss-of-function mutations in SIM1 contribute to obesity and Prader-Willi-like features	Bonnefond, A.; Raimondo, A.; Stutzmann, F.; Ghoussaini, M.; Ramachandrappa, S.; Bersten, D.; Durand, E.; Vatin, V.; Balkau, B.; Lantieri, O.; Raverdy, V.; Pattou, F.; Van Hul, W.; Van Gaal, L.; Peet, D.; Weill, J.; Miller, J.; Horber, F.; Goldstone, A.; Driscoll, D.; et al.
	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.