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Preview	Issue Date	Title	Author(s)
	2017	NAD deficiency, congenital malformations, and niacin supplementation	Shi, H.; Enriquez, A.; Rapadas, M.; Martin, E.; Wang, R.; Moreau, J.; Lim, C.; Szot, J.; Ip, E.; Hughes, J.; Sugimoto, K.; Humphreys, D.; McInerney-Leo, A.; Leo, P.; Maghzal, G.; Halliday, J.; Smith, J.; Colley, A.; Mark, P.; Collins, F.; et al.
	2019	Dietary zinc and the control of Streptococcus pneumoniae infection	Eijkelkamp, B.A.; Morey, J.R.; Neville, S.L.; Tan, A.; Pederick, V.G.; Cole, N.; Singh, P.P.; Ong, C.-L.Y.; Gonzalez de Vega, R.; Clases, D.; Cunningham, B.A.; Hughes, C.E.; Comerford, I.; Brazel, E.B.; Whittall, J.J.; Plumptre, C.D.; McColl, S.R.; Paton, J.C.; McEwan, A.G.; Doble, P.A.; et al.; Orihuela, C.J.
	2018	Plasmacytoid dendritic cells protect from viral bronchiolitis and asthma through semaphorin 4a-mediated T reg expansion	Lynch, J.; Werder, R.; Loh, Z.; Sikder, M.; Curren, B.; Zhang, V.; Rogers, M.; Lane, K.; Simpson, J.; Mazzone, S.; Spann, K.; Hayball, J.; Diener, K.; Everard, M.; Blyth, C.; Forstner, C.; Dennis, P.; Murtaza, N.; Morrison, M.; Cuív, P.; et al.
	2019	DNA hypermethylation encroachment at CpG island borders in cancer is predisposed by H3K4 monomethylation patterns	Skvortsova, K.; Masle-Farquhar, E.; Luu, P.L.; Song, J.Z.; Qu, W.; Zotenko, E.; Gould, C.M.; Du, Q.; Peters, T.J.; Colino-Sanguino, Y.; Pidsley, R.; Nair, S.S.; Khoury, A.; Smith, G.C.; Miosge, L.A.; Reed, J.H.; Kench, J.G.; Rubin, M.A.; Horvath, L.; Bogdanovic, O.; et al.
	2013	Evidence for a retroviral insertion in TRPM1 as the cause of congenital stationary night blindness and leopard complex spotting in the horse	Bellone, R.; Holl, H.; Sealuri, V.; Devi, S.; Maddodi, N.; Archer, S.; Sandmeyer, L.; Ludwig, A.; Foerster, D.; Pruvost, M.; Reissmann, M.; Bortfeldt, R.; Adelson, D.; Lim, S.; Nelson, J.; Haase, B.; Engensteiner, M.; Leeb, T.; Forsyth, G.; Mienaltowski, M.; et al.; Anderson, M.G.
	2022	BAF complex-mediated chromatin relaxation is required for establishment of X chromosome inactivation	Keniry, A.; Jansz, N.; Gearing, L.J.; Wanigasuriya, I.; Chen, J.; Nefzger, C.M.; Hickey, P.F.; Gouil, Q.; Liu, J.; Breslin, K.A.; Iminitoff, M.; Beck, T.; Tapia Del Fierro, A.; Whitehead, L.; Jarratt, A.; Kinkel, S.A.; Taberlay, P.C.; Willson, T.; Pakusch, M.; Ritchie, M.E.; et al.
	2008	Genome analysis of the platypus reveals unique signatures of evolution	Warren, W.; Hillier, L.; Graves, J.; Birney, E.; Ponting, C.; Grutzner, F.; Belov, K.; Miller, W.; Clarke, L.; Chinwall, A.; Yang, S.; Heger, A.; Locke, D.; Miethke, P.; Waters, P.; Veyrunes, F.; Fulton, L.; Fulton, B.; Graves, T.; Wallis, 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.
	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.
	2009	Genome sequence, comparative analysis, and population genetics of the domestic horse	Wade, C.; Giulotto, E.; Sigurdsson, S.; Zoli, M.; Gnerre, S.; Imsland, F.; Lear, T.; Adelson, D.; Bailey, E.; Bellone, R.; Blocker, H.; Distl, O.; Edgar, R.; Garber, M.; Leeb, T.; Mauceli, E.; Macleod, J.; PENEDO, M.; Raison, J.; Sharpe, T.; et al.