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Preview	Issue Date	Title	Author(s)
	2008	Antagonism of the chemokine receptors CXCR3 and CXCR4 reduces the pathology of experimental autoimmune encephalomyelitis	Kohler, R.; Comerford, I.; Townley, S.; Haylock-Jacobs, S.; Clark-Lewis, I.; McColl, S.
	2007	Mutations in UPF3B, a member of the nonsense-mediated mRNA decay complex, cause syndromic and nonsyndromic mental retardation	Tarpey, P.; Raymond, F.; Nguyen, L.; Rodriguez, J.; Hackett, A.; Vandeleur, L.; Smith, R.; Shoubridge, C.; Edkins, S.; Stevens, C.; O'Meara, S.; Tofts, C.; Barthorpe, S.; Buck, G.; Cole, J.; Halliday, K.; Hills, K.; Jones, D.; Mironenko, T.; Perry, J.; et al.
	1998	Febrile seizures and generalised epilepsy associated with a mutation in the Na+-channel b1 subunit gene SCN1B	Wallace, R.; Wang, D.; Singh, R.; Scheffer, I.; George Jnr., A.; Phillips, H.; Saar, K.; Reis, A.; Johnson, E.; Sutherland, G.; Berkovic, S.; Mulley, J.
	1999	Identification of the gene (SEDL) causing X-linked spondyloepiphyseal dysplasia tarda	Gedeon, A.; Colley, A.; Jamieson, R.; Thompson, E.; Rogers, J.; Sillence, D.; Tiller, G.; Mulley, J.; Gecz, J.
	2015	Ancient transposable elements transformed the uterine regulatory landscape and transcriptome during the evolution of mammalian pregnancy	Lynch, V.; Nnamani, M.; Kapusta, A.; Brayer, K.; Plaza, S.; Mazur, E.; Emera, D.; Sheikh, S.; Grützner, F.; Bauersachs, S.; Graf, A.; Young, S.; Lieb, J.; DeMayo, F.; Feschotte, C.; Wagner, G.
	2009	Inhibition of CCR6 Function Reduces the Severity of Experimental Autoimmune Encephalomyelitis via Effects on the Priming Phase of the Immune Response	Liston, A.; Kohler, R.; Townley, S.; Haylock-Jacobs, S.; Comerford, I.; Caon, A.; Webster, J.; Harrison, J.; Swann, J.; Clark-Lewis, I.; Korner, H.; McColl, S.
	2014	Overexpression of piRNA pathway genes in epithelial ovarian cancer	Lim, S.; Ricciardelli, C.; Oehler, M.; De Arao Tan, I.; Russell, D.; Grützner, F.; Samant, R.
	2011	A mutation in the Golgi Qb-SNARE gene GOSR2 causes progressive myoclonus epilepsy with early ataxia	Corbett, M.; Schwake, M.; Bahlo, M.; Dibbens, L.; Lin, M.; Gandolfo, L.; Vears, D.; O'Sullivan, J.; Robertson, T.; Bayly, M.; Gardner, A.; Vlaar, A.; Korenke, G.; Bloem, B.; de Coo, I.; Verhagen, J.; Lehesjoki, A.; Gecz, J.; Berkovic, S.
	2010	A focal Eeilepsy and intellectual disability syndrome is due to a mutation in TBC1D24	Bahlo, M.; Jolly, L.; Afawi, Z.; Gardner, A.; Oliver, K.; Tan, S.; Coffey, A.; Mulley, J.; Dibbens, L.; Simri, W.; Shalata, A.; Kivity, S.; Jackson, G.; Berkovic, S.; Gecz, J.; Corbett, M.
	1999	Detection of a novel missense mutation and second recurrent mutation in the CACNA1A gene in individuals with EA-2 and FHM	Friend, K.; Crimmins, D.; Phan, T.; Sue, C.; Colley, A.; Fung, V.; Morris, J.; Sutherland, G.; Richards, R.