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Preview	Issue Date	Title	Author(s)
	1999	Characterization and chromosomal localization of USP3, a novel human ubiquitin-specific protease	Sloper-Mould, K.; Eyre, H.; Wang, X.W.; Sutherland, G.; Baker, R.
	2007	Multicentre search for genetic susceptibility loci in sporadic epilepsy syndrome and seizure types: a case-control study	Cavalleri, G.; Weale, M.; Shianna, K.; Singh, R.; Lynch, J.; Grinton, B.; Szoeke, C.; Murphy, K.; Kinirons, P.; O'Rourke, D.; Ge, D.; Depondt, C.; Claeys, K.; Pandolfo, M.; Gumbs, C.; Walley, N.; McNamara, J.; Mulley, J.; Linney, K.; Sheffield, L.; et al.
	2009	A systematic, large-scale resequencing screen of X-chromosome coding exons in mental retardation	Tarpey, P.; Smith, R.; Pleasance, E.; Whibley, A.; Edkins, S.; Hardy, C.; O'Meara, S.; Latimer, C.; Dicks, E.; Menzies, A.; Stephens, P.; Blow, M.; Greenman, C.; Xue, Y.; Tyler-Smith, C.; Thompson, D.; Gray, K.; Andrews, J.; Barthorpe, S.; Buck, G.; et al.
	1998	Molecular characterization, pharmacological properties and chromosomal localization of the human GALR2 galanin receptor	Fathi, Z.; Battaglino, P.; Iben, L.; Li, H.; Baker, E.; Zhang, D.; McGovern, R.; Mahle, C.; Sutherland, G.; Iismaa, T.; Dickinson, K.; Antal Zimanyi, I.
	1997	Isolation and identification of homeobox genes from the human placenta including a novel member of the Distal-less family, DLX4	Quinn, L.; Johnson, B.; Nicholl, J.; Sutherland, G.; Kalionis, B.
	1999	Molecular cloning and characterization of a cDNA encoding the human leucocyte vacuolar protein sorting (h1Vps45)	Rajasekariah, P.; Eyre, H.; Stanley, K.; Walls, R.; Sutherland, G.
	1997	The gene for the human interleukin-11 receptor alpha chain locus is highly homologous to the murine gene and contains alternatively spliced first exons	Nandurkar, H.; Robb, L.; Nicholl, J.; Hilton, D.; Sutherland, G.; Begley, C.
	1998	Complex organisation of the 5'-end of the human glycine tRNA synthetase gene	Mudge, S.; Williams, J.; Eyre, H.; Sutherland, G.; Cowan, P.; Power, D.
	1999	X-inactivation and marker studies in three families with incontinentia pigmenti: implications for counselling and gene localisation	Woffendin, H.; Jakins, T.; Jouet, M.; Stewart, H.; Landy, S.; Haan, E.; Harris, A.; Donnai, D.; Read, A.; Kenwrick, S.
	1995	Simple tandem DNA repeats and human genetic disease	Sutherland, G.; Richards, R.