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Preview	Issue Date	Title	Author(s)
	2000	Gene structure and expression study of the SEDL gene for Spondyloepiphyseal Dysplasia Tarda	Gecz, J.; Hillman, M.; Gedeon, A.; Cox, T.; Baker, E.; Mulley, J.
	2002	A novel gene, FAM11A, associated with the FRAXF CpG island is transcriptionally silent in FRAXF full mutation	Shaw, M.; Chiurazzi, P.; Romain, D.; Neri, G.; Gecz, J.
	2001	Characterization of ARHGEF6, a guanine nucleotide exchange factor for Rho GTPases and a candidate gene for x-linked mental retardation: Mutation screening in Borjeson-Forssman-Lehmann syndrome and MRX27	Lower, K.; Gecz, J.
	1999	Characterisation and expression of a large, 13.7 kb FMR2 isoform	Gecz, J.; Mulley, J.
	2006	ARX: a gene for all seasons	Gecz, J.; Cloosterman, D.; Partington, 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.
	2023	Bi-allelic variants in the neuronal cell adhesion molecule NRCAM lead to a novel neurodevelopmental disorder characterized by developmental delay, hypotonia, peripheral neuropathy or spasticity	Kurolap, A.; Kreuder, F.; Gonzaga-Jauregui, C.; Duvdevani, M.P.; Harel, T.; Tammer, L.; Xin, B.; Bakhtiari, S.; Rice, J.; van Eyk, C.; Gecz, J.; Mah, J.K.; Atkinson, D.; Cope, H.; Sullivan, J.A.; Douek, A.M.; Colquhoun, D.; Henry, J.; Wlodkowic, D.; Parman, Y.; et al.; 55th European Society of Human Genetics Conference (ESHG) (11 Jun 2022 - 14 Jun 2022 : Vienna, Austria & virtual online)
	2013	Loss of Usp9x disrupts cortical architecture, hippocampal development and TGFβ-mediated axonogenesis	Stegeman, S.; Jolly, L.; Premarathne, S.; Gecz, J.; Richards, L.; Mackay-Sim, A.; Wood, S.; Alsina, B.
	2010	A novel syndrome of paediatric cataract, dysmorphism, ectodermal features, and developmental delay in Australian Aboriginal family maps to 1p35.3-p36.32	Hattersley, K.; Laurie, K.; Liebelt, J.; Gecz, J.; Durkin, S.; Craig, J.; Burden, K.