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Preview	Issue Date	Title	Author(s)
	2015	A recurrent de novo mutation in KCNC1 causes progressive myoclonus epilepsy	Muona, M.; Berkovic, S.; Dibbens, L.; Oliver, K.; Maljevic, S.; Bayly, M.; Joensuu, T.; Canafoglia, L.; Franceschetti, S.; Michelucci, R.; Markkinen, S.; Heron, S.; Hildebrand, M.; Andermann, E.; Andermann, F.; Gambardella, A.; Tinuper, P.; Licchetta, L.; Scheffer, I.; Criscuolo, C.; et al.
	2015	Single nucleotide variations in CLCN6 identified in patients with benign partial epilepsies in infancy and/or febrile seizures	Yamamoto, T.; Shimojima, K.; Sangu, N.; Komoike, Y.; Ishii, A.; Abe, S.; Yamashita, S.; Imai, K.; Kubota, T.; Fukasawa, T.; Okanishi, T.; Enoki, H.; Tanabe, T.; Saito, A.; Furukawa, T.; Shimizu, T.; Milligan, C.; Petrou, S.; Heron, S.; Dibbens, L.; et al.; Ishii, R.
	2010	Molecular marker survey and expression analyses of the rice submergence-tolerance gene SUB1A	Singh, N.; Dang, T.; Vergara, G.; Pandey, D.; Sanchez, D.; Neeraja, C.; Septiningsih, E.; Mendioro, M.; Tecson-Mendoza, E.; Ismail, A.; MacKill, D.; Heuer, S.
	2014	Differential, dominant activation and inhibition of Notch signalling and APP cleavage by truncations of PSEN1 in human disease	Newman, M.; Wilson, L.; Verdile, G.; Lim, A.; Khan, I.; Nik, S.; Pursglove, S.; Chapman, G.; Martins, R.; Lardelli, M.
	2013	Distinctive expansion of potential virulence genes in the genome of the oomycete fish pathogen Saprolegnia parasitica	Jiang, R.; de Bruijn, I.; Haas, B.; Belmonte, R.; Löbach, L.; Christie, J.; van den Ackerveken, G.; Bottin, A.; Bulone, V.; Díaz-Moreno, S.; Dumas, B.; Fan, L.; Gaulin, E.; Govers, F.; Grenville-Briggs, L.; Horner, N.; Levin, J.; Mammella, M.; Meijer, H.; Morris, P.; et al.; McDowell, J.
	2011	Phosphate utilization efficiency correlates with expression of low-affinity phosphate transporters and noncoding RNA, IPS1, in barley	Huang, C.; Shirley, N.; Genc, Y.; Shi, B.; Langridge, P.
	2010	Amino acid substitutions in the aryl hydrocarbon receptor ligand binding domain reveal YH439 as an atypical AhR activator	Whelan, F.; Hao, N.; Furness, S.; Whitelaw, M.; Chapman-Smith, A.
	2012	Molecular diagnosis of infantile mitochondrial disease with targeted next-generation sequencing	Calvo, S.; Compton, A.; Hershman, S.; Lim, S.; Lieber, D.; Tucker, E.; Laskowski, A.; Garone, C.; Liu, S.; Jaffe, D.; Christodoulou, J.; Fletcher, J.; Bruno, D.; Goldblatt, J.; DiMauro, S.; Thorburn, D.; Mootha, V.
	2012	CBG Santiago: a novel CBG mutation	Torpy, D.; Lundgren, B.; Ho, J.; Lewis, J.; Scott, H.; Mericq, V.
	2010	Epilepsy and mental retardation limited to females with PCDH19 mutations can present de novo or in single generation families	Hynes, K.; Tarpey, P.; Dibbens, L.; Bayly, M.; Berkovic, S.; Smith, R.; Al Raisi, Z.; Turner, S.; Brown, N.; Desai, T.; Haan, E.; Turner, G.; Christodoulou, J.; Leonard, H.; Gill, D.; Stratton, M.; Gecz, J.; Scheffer, I.