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Preview	Issue Date	Title	Author(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.
	2011	Tmprss3, a transmembrane serine protease deficient in human DFNB8/10 deafness, is critical for cochlear hair cell survival at the onset of hearing	Fasquelle, L.; Scott, H.; Lenoir, M.; Wang, J.; Rebillard, G.; Gaboyard, S.; Venteo, S.; Francois, F.; Masset-Bonnefont, A.; Antonarakis, S.; Neidhart, E.; Chabbert, C.; Puel, J.; Guipponi, M.; Delprat, B.
	2008	Islet-1: A potentially important role for an islet cell gene in visceral fat	Li, H.; Heilbronn, L.; Hu, D.; Poynten, A.; Blackburn, M.; Shirkhedkar, D.; Kaplan, W.; Kriketos, A.; Ye, J.; Chisholm, D.
	2010	Myc-modulated miR-9 makes more metastases	Khew-Goodall, Y.; Goodall, G.
	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.
	2007	A pneumococcal MerR-like regulator and S-nitrosoglutathione reductase are required for systemic virulence	Stroeher, U.; Kidd, S.; Stafford, S.; Jennings, M.; Paton, J.; McEwan, A.
	2006	Production and characterization of monoclonal antibodies against insulin-like growth factor type 1 receptor	Keyhanfar, M.; Forbes, B.; Cosgrove, L.; Wallace, J.; Booker, G.
	2004	A functional autoantibody in narcolepsy	Smith, A.; Jackson, M.; Neufing, P.; McEvoy, R.; Gordon, T.
	2002	Mutations in PHF6 are associated with Börjeson-Forssman-Lehmann syndrome	Lower, K.; Turner, G.; Kerr, B.; Mathews, K.; Shaw, M.; Gedeon, A.; Schelley, S.; Hoyme, H.; White, S.; Delatycki, M.; Lampe, A.; Clayton-Smith, J.; Stewart, H.; van Ravenswaay, C.; de Vries, B.; Cox, B.; Grompe, M.; Ross, S.; Thomas, P.; Mulley, J.; et al.
	2002	Mutations in the human ortholog of Aristaless cause X-linked mental retardation and epilepsy	Stromme, P.; Mangelsdorf, M.; Shaw, M.; Lower, K.; Lewis, S.; Bruyere, H.; Lutcherath, V.; Gedeon, A.; Wallace, R.; Scheffer, I.; Turner, G.; Partington, M.; Frints, S.; Fryns, J.; Sutherland, G.; Mulley, J.; Gecz, J.