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Preview	Issue Date	Title	Author(s)
	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.
	1996	A novel X-linked gene, G4.5. is responsible for Barth Syndrome	Bione, S.; D'Adamo, P.; Maestrini, E.; Gedeon, A.; Bolhuis, P.; Toniolo, D.
	1996	Identification of the gene FMR2, associated with FRAXE mental retardation	Gecz, J.; Gedeon, A.; Sutherland, G.; Mulley, J.
	1998	A novel gene encoding an integral membrane protein is mutated in nephropathic cystinosis.	Town, M.; Jean, G.; Cherqui, S.; Attard, M.; Forestier, L.; Whitmore, S.; Callen, D.; Gribouval, O.; Broyer, M.; Bates, G.; van't Hoff, W.; Antignac, C.
	2006	Ulocladium atrum keratitis	Badenoch, P.; Halliday, C.; Ellis, D.; Billing, K.; Mills, R.
	2009	The genome sequence of Taurine cattle: a window to ruminant biology and evolution	Bovine Genome Sequencing and Analysis Consortium,; Elsik, C.; Tellam, R.; Worley, K.; Adelson, David Louis
	2003	Sodium channel α1-subunit mutations in severe myoclonic epilepsy of infancy and infantile spasms	Wallace, R.; Hodgson, B.; Grinton, B.; Gardiner, R.; Robinson, R.; Rodriguez-Casero, V.; Sadleir, L.; Morgan, J.; Harkin, L.; Dibbens, L.; Yamamoto, T.; Andermann, E.; Mulley, J.; Berkovic, S.; Scheffer, I.
	1998	PAK3 mutation in nonsyndromic X-linked mental retardation	Allen, K.; Gleeson, J.; Bagrodia, S.; Partington, M.; MacMillan, J.; Cerione, R.; Mulley, J.; Walsh, C.
	1999	Genomic organisation and biological characterization of the novel human CC chemokine DC-CK-1/PARC/MIP-4/SCYA18	Guan, P.; Burghes, A.; Cunningham, A.; Lira, P.; Brissette, W.; Neote, K.; McColl, S.
	1998	The human dead ringer/bright homolog, DRIL1: cDNA cloning, gene structure, and mapping to D19S886, a marker on 19p13.3 that is strictly linked to the Peutz-Jeghers Syndrome.	Kortschak, R.; Reimann, H.; Zimmer, M.; Eyre, H.; Saint, R.; Jenne, D.