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Preview	Issue Date	Title	Author(s)
	2017	Dominant protection from HLA-linked autoimmunity by antigen-specific regulatory T cells	Ooi, J.; Petersen, J.; Tan, Y.; Huynh, M.; Willett, Z.; Ramarathinam, S.; Eggenhuizen, P.; Loh, K.; Watson, K.; Gan, P.; Alikhan, M.; Dudek, N.; Handel, A.; Hudson, B.; Fugger, L.; Power, D.; Holt, S.; Coates, P.; Gregersen, J.; Purcell, A.; et al.
	2019	Tissue-specific progesterone receptor-chromatin binding and the regulation of progesterone-dependent gene expression	Dinh, D.T.; Breen, J.; Akison, L.K.; DeMayo, F.J.; Brown, H.M.; Robker, R.L.; Russell, D.L.
	2019	Recessive DES cardio/myopathy without myofibrillar aggregates: intronic splice variant silences one allele leaving only missense L190P-desmin	Riley, L.G.; Waddell, L.B.; Ghaoui, R.; Evesson, F.J.; Cummings, B.B.; Bryen, S.J.; Joshi, H.; Wang, M.X.; Brammah, S.; Kritharides, L.; Corbett, A.; MacArthur, D.G.; Cooper, S.T.
	2013	High frequency of germline TP53 mutations in a prospective adult-onset sarcoma cohort	Mitchell, G.; Ballinger, M.; Wong, S.; Hewitt, C.; James, P.; Young, M.; Cipponi, A.; Pang, T.; Goode, D.; Dobrovic, A.; Thomas, D.; Porceddu, S.; Gattas, M.; Neuhaus, S.; Suthers, G.; Tattersall, M.; Tucker, K.; Lewis, C.; Carey-Smith, R.; Toft, M.
	2010	Genome-wide identification of human FOXP3 target genes in natural regulatory T cells	Sadlon, T.; Wilkinson, B.; Pederson, S.; Brown, C.; Bresatz, S.; Gargett, T.; Melville, E.; Peng, K.; D'Andrea, R.; Glonek, G.; Goodall, G.; Zola, H.; Shannon, F.; Barry, S.
	2012	CDP-diacylglycerol synthetase-controlled phosphoinositide availability limits VEGFA signaling and vascular morphogenesis	Pan, W.; Pham, V.; Stratman, A.; Castranova, D.; Kamei, M.; Kidd, K.; Lo, B.; Shaw, K.; Torres-Vazquez, J.; Mikelis, C.; Gutkind, J.; Davis, G.; Weinstein, B.
	2014	Copy number variation in the horse genome	Ghosh, S.; Qu, Z.; Das, P.; Fang, E.; Juras, R.; Cothran, E.; McDonell, S.; Kenney, D.; Lear, T.; Adelson, D.; Chowdhary, B.; Raudsepp, T.; Barsh, G.
	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.
	2013	The genomic landscape of hypodiploid acute lymphoblastic leukemia	To, L.
	2014	Refining analyses of copy number variation identifies specific genes associated with developmental delay	Coe, B.; Witherspoon, K.; Rosenfeld, J.; van Bon, B.; Vulto-van Silfhout, A.; Bosco, P.; Friend, K.; Baker, C.; Buono, S.; Vissers, L.; Schuurs-Hoeijmakers, J.; Hoischen, A.; Pfundt, R.; Krumm, N.; Carvill, G.; Li, D.; Amaral, D.; Brown, N.; Lockhart, P.; Scheffer, I.; et al.