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Preview	Issue Date	Title	Author(s)
	2011	Spatiotemporal regulation of multiple overlapping sense and novel natural antisense transcripts at the Nrgn and Camk2n1 gene loci during mouse cerebral corticogenesis	Ling, K.; Hewitt, C.; Beissbarth, T.; Hyde, L.; Cheah, P.; Smyth, G.; Tan, S.; Hahn, C.; Thomas, T.; Thomas, P.; Scott, H.
	2014	Deciphering the secret role of Sox4 gene locus during mouse cerebral corticogenesis	Ling, K.; Lee, H.; Brautigan, P.; Moore, S.; Fraser, R.; Cheah, P.; Raison, J.; Babic, M.; Lee, Y.; Daish, T.; Mattiske, D.; Mann, J.; Adelson, D.; Thomas, P.; Hahn, C.; Scott, H.; 12th Biennial Meeting of the Asian-Pacific Society for Neurochemistry (23 Aug 2014 - 26 Aug 2014 : Kaohsiung, Taiwan)
	2013	Molecular pathology of polyalanine expansion disorders: New perspectives from mouse models	Hughes, J.; Thomas, P.
	2014	Identification of highly conserved putative developmental enhancers bound by SOX3 in neural progenitors using ChIP-Seq	McAninch, D.; Thomas, P.; Zheng, D.
	2016	In depth analysis of the Sox4 gene locus that consists of sense and natural antisense transcripts	Ling, K.; Brautigan, P.; Moore, S.; Fraser, R.; Leong, M.; Leong, J.; Zainal Abidin, S.; Lee, H.; Cheah, P.; Raison, J.; Babic, M.; Lee, Y.; Daish, T.; Mattiske, D.; Mann, J.; Adelson, D.; Thomas, P.; Hahn, C.; Scott, H.
	2012	XX male sex reversal with genital abnormalities associated with a de novo SOX3 gene duplication	Moalem, S.; Babul-Hirji, R.; Stavropolous, D.; Wherrett, D.; Bagli, D.; Thomas, P.; Chitayat, D.
	2015	SOX3 expression in the glial system of the developing and adult mouse cerebellum	Cheah, P.; Thomas, P.
	2014	SOX3 deletion in mouse and human Is associated with persistence of the craniopharyngeal canal	Alatzoglou, K.; Azriyanti, A.; Rogers, N.; Ryan, F.; Curry, N.; Noakes, C.; Bignell, P.; Hall, G.; Littooij, A.; Saunders, D.; Thomas, P.; Stewart, H.; Dattani, M.
	2013	Expression of the murine transcription factor SOX3 during embryonic and adult neurogenesis	Rogers, N.; Cheah, P.; Szarek, E.; Banerjee, K.; Schwartz, J.; Thomas, P.
	2012	Neurodevelopmental and neuropsychiatric behaviour defects arise from 14-3-3ζ deficiency	Cheah, P.; Ramshaw, H.; Thomas, P.; Toyo-oka, K.; Xu, X.; Martin, S.; Coyle, P.; Guthridge, M.; Stomski, F.; van den Buuse, M.; Wynshaw-Boris, A.; Lopez, A.; Schwarz, Q.