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Preview	Issue Date	Title	Author(s)
	2013	Variability of human corticospinal excitability tracks the state of action preparation	Klein-Flugge, M.; Nobbs, D.; Pitcher, J.; Bestmann, S.
	2011	Impact of body mass index on seminal oxidative stress	Tunc, O.; Bakos, H.; Tremellen, K.
	2010	Small volumes of feed can trigger transient lower esophageal sphincter relaxation and gastroesophageal reflux in the right lateral position in infants	van Wijk, M.; Benninga, M.; Davidson, G.; Haslam, R.; Omari, T.
	2010	Lynch syndrome-associated breast cancers: Clinicopathologic characteristics of a case series from the colon cancer family registry	Walsh, M.; Buchanan, D.; Cummings, M.; Pearson, S.; Arnold, S.; Clendenning, M.; Walters, R.; McKeone, D.; Spurdle, A.; Hopper, J.; Jenkins, M.; Phillips, K.; Suthers, G.; George, J.; Goldblatt, J.; Muir, A.; Tucker, K.; Pelzer, E.; Gattas, M.; Woodall, S.; et al.
	2004	1024C>T (R342X) is a recurrent RHF6 mutation also found in the original Börjeson-Forssman-Lehmann syndrome family	Lower, K.; Solders, G.; Bondeson, M.; Nelson, J.; Brun, A.; Crawford, J.; Malm, G.; Borjeson, M.; Turner, G.; Partington, M.; Gecz, J.
	1998	Molecular heterogeneity in mucopolysaccharidosis IVA in Australia and Northern Ireland: nine novel mutations including T312S, a common allele that confers a mild phenotype	Yamada, N.; Fukuda, S.; Tomatsu, S.; Muller, V.; Hopwood, J.; Nelson, J.; Kato, Z.; Yamagishi, A.; Sukegawa, K.; Kondo, M.; Orii, T.
	2012	Broadening the phenotype associated with mutations in UPF3B: two further cases with renal dysplasia and variable developmental delay	Lynch, S.; Nguyen, L.; Ng, L.; Waldron, M.; McDonald, D.; Gecz, J.
	2003	Relation between pancreatic lipase activity and gastric emptying rate in children with cystic fibrosis	Symonds, E.; Omari, T.; Webster, J.; Davidson, G.; Butler, R.
	2012	BRIDGE Study warrants critique	Allen, D.; Parry, P.; Purssey, R.; Spielmans, G.; Jureidini, J.; Rosenlicht, N.; Healy, D.; Feinberg, I.
	2012	A noncoding, regulatory mutation implicates HCFC1 in nonsyndromic intellectual disability	Huang, L.; Jolly, L.; Willis-Owen, S.; Gardner, A.; Sharma, R.; Douglas, E.; Shoubridge, C.; Wieczorek, D.; Tzschach, A.; Cohen, M.; Hackett, A.; Field, M.; Froyen, G.; Hu, H.; Haas, S.; Ropers, H.; Kalscheuer, V.; Corbett, M.; Gecz, J.