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Preview	Issue Date	Title	Author(s)
	2011	Inherited Balanced Translocation t(9;17)(q33.2;q25.3) Concomitant With a 16p13.1 Duplication in a Patient With Schizophrenia	Fullston, T.; Gabb, B.; Callen, D.; Ullmann, R.; Woollatt, E.; Bain, S.; Ropers, H.; Cooper, M.; Chandler, D.; Carter, K.; Jablensky, A.; Kalaydjieva, L.; Gecz, J.
	2011	Screening and cell-based assessment of mutations in the Aristaless-related homeobox (ARX) gene	Fullston, T.; Finnis, M.; Hackett, A.; Hodgson, B.; Brueton, L.; Baynam, G.; Norman, A.; Reish, O.; Shoubridge, C.; Gecz, J.
	2011	Hybridisation-based resequencing of 17 X-linked intellectual disability genes in 135 patients reveals novel mutations in ATRX, SLC6A8 and PQBP1	Jensen, L.; Wei, C.; Moser, B.; Lipkowitz, B.; Schroeder, C.; Musante, L.; Tzschach, A.; Kalscheuer, V.; Meloni, I.; Raynaud, M.; Van Esch, H.; Chelly, J.; de Brouwer, A.; Hackett, A.; van der Haar, S.; Henn, W.; Gecz, J.; Riess, O.; Bonin, M.; Reinhardt, R.; et al.
	2011	Functional characterization of the AFF (AF4/FMR2) family of RNA-binding proteins: insights into the molecular pathology of FRAXE intellectual disability	Melko, M.; Douguet, D.; Bensaid, M.; Zongaro, S.; Verheggen, C.; Gecz, J.; Bardoni, B.
	2011	Identification of a microRNA that activates gene expression by repressing nonsense-mediated RNA decay	Bruno, I.; Karam, R.; Huang, L.; Bhardwaj, A.; Lou, C.; Shum, E.; Song, H.; Corbett, M.; Gifford, W.; Gecz, J.; Pfaff, S.; Wilkinson, M.
	2011	"Blinders, phenotype, and fashionable genetic analysis": setting the record straight for epilepsy!	Mulley, J.C.; Heron, S.E.; Wallace, R.H.; Gecz, J.; Dibbens, L.M.