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Preview	Issue Date	Title	Author(s)
	2016	Early cave art and ancient DNA record the origin of European bison	Soubrier, J.; Gower, G.; Chen, K.; Richards, S.; Llamas, B.; Mitchell, K.; Ho, S.; Kosintsev, P.; Lee, M.; Baryshnikov, G.; Bollongino, R.; Bover Arbos, P.; Burger, J.; Chivall, D.; Crégut-Bonnoure, E.; Decker, J.; Doronichev, V.; Douka, K.; Fordham, D.; Fontana, F.; et al.
	2011	Genome-wide association study identifies susceptibility loci for open angle glaucoma at TMCO1 and CDKN2B-AS1	Burdon, K.; MacGregor, S.; Hewitt, A.; Sharma, S.; Chidlow, G.; Mills, R.; Danoy, P.; Casson, R.; Viswanathan, A.; Liu, J.; Landers, J.; Henders, A.; Wood, J.; Souzeau, E.; Crawford, A.; Leo, P.; Wang, J.; Rochtchina, E.; Nyholt, D.; Martin, N.; et al.
	2008	Progress and prospects in rat genetics: a community view	Aitman, T.; Critser, J.; Cuppen, E.; Dominiczak, A.; Fernandez-Suarez, X.; Flint, J.; Gauguier, D.; Geurts, A.; Gould, M.; Harris, P.; Holmdahl, R.; Hubner, N.; Izsvák, Z.; Jacob, H.; Kuramoto, T.; Kwitek, A.; Marrone, A.; Mashimo, T.; Moreno, C.; Mullins, J.; et al.
	2011	Chromosomal rearrangements maintain a polymorphic supergene controlling butterfly mimicry	Joron, M.; Frezal, L.; Jones, R.; Chamberlain, N.; Lee, S.; Haag, C.; Whibley, A.; Becuwe, M.; Baxter, S.; Ferguson, L.; Wilkinson, P.; Salazar, C.; Davidson, C.; Clark, R.; Quail, M.; Beasley, H.; Glithero, R.; Lloyd, C.; Sims, S.; Jones, M.; et al.
	2011	Heritable GATA2 mutations associated with familial myelodysplastic syndrome and acute myeloid leukemia	Hahn, C.; Chong, C.; Carmichael, C.; Wilkins, E.; Brautigan, P.; Li, X.; Babic, M.; Lin, M.; Carmagnac, A.; Lee, Y.; Kok, C.; Gagliardi, L.; Friend, K.; Ekert, P.; Butcher, C.; Brown, A.; Lewis, I.; To, L.; Timms, A.; Storek, J.; et al.
	2013	Mutations in DEPDC5 cause familial focal epilepsy with variable foci	Dibbens, L.; de Vries, B.; Donatello, S.; Heron, S.; Hodgson, B.; Chintawar, S.; Crompton, D.; Hughes, J.; Bellows, S.; Klein, K.; Callenbach, P.; Corbett, M.; Gardner, A.; Kivity, S.; Iona, X.; Regan, B.; Weller, C.; Crimmins, D.; O'Brien, T.; Guerrero-Lopez, R.; et al.
	2012	A short-term in situ CO₂ enrichment experiment on Heron Island (GBR)	Kline, D.; Teneva, L.; Schneider, K.; Miard, T.; Chai, A.; Marker, M.; Headley, K.; Opdyke, B.; Nash, M.; Valetich, M.; Caves, J.; Russell, B.; Connell, S.; Kirkwood, B.; Brewer, P.; Peltzer, E.; Silverman, J.; Caldeira, K.; Dunbar, R.; Koseff, J.; et al.
	2003	Mutations in a novel gene, NHS, cause the pleiotropic effects of Nance-Horan syndrome, including severe congenital cataract, dental anomalies, and mental retardation	Burdon, K.; McKay, J.; Sale, M.; Russell-Eggitt, I.; Mackey, D.; Wirth, G.; Elder, J.; Nicoll, A.; Clarke, M.; FitzGerald, L.; Stankovich, J.; Shaw, M.; Sharma, S.; Gajovic, S.; Gruss, P.; Ross, S.; Thomas, P.; Voss, A.; Thomas, T.; Gecz, J.; et al.
	2002	Mutations in PHF6 are associated with Börjeson-Forssman-Lehmann syndrome	Lower, K.; Turner, G.; Kerr, B.; Mathews, K.; Shaw, M.; Gedeon, A.; Schelley, S.; Hoyme, H.; White, S.; Delatycki, M.; Lampe, A.; Clayton-Smith, J.; Stewart, H.; van Ravenswaay, C.; de Vries, B.; Cox, B.; Grompe, M.; Ross, S.; Thomas, P.; Mulley, J.; et al.
	2004	The sequence and analysis of duplication-rich human chromosome 16	Martin, J.; Han, C.; Gordon, L.; Terry, A.; Prabhakar, S.; She, X.; Xie, G.; Hellsten, U.; Man, Y.; Altherr, M.; Couronne, O.; Aerts, A.; Bajorek, E.; Black, S.; Blumer, H.; Branscomb, E.; Brown, N.; Bruno, W.; Buckingham, J.; Callen, D.; et al.