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Preview	Issue Date	Title	Author(s)
	2016	The genetic history of Ice Age Europe	Fu, Q.; Posth, C.; Hajdinjak, M.; Petr, M.; Mallick, S.; Fernandes, D.; Furtwängler, A.; Haak, W.; Meyer, M.; Mittnik, A.; Nickel, B.; Peltzer, A.; Rohland, N.; Slon, V.; Talamo, S.; Lazaridis, I.; Lipson, M.; Mathieson, I.; Schiffels, S.; Skoglund, P.; et al.
	2013	XThe eEF2 kinase confers resistance to nutrient deprivation by blocking translation elongation	Leprivier, G.; Remke, M.; Rotblat, B.; Dubuc, A.; Mateo, A.; Kool, M.; Agnihotri, S.; El-Naggar, A.; Yu, B.; Prakash Somasekharan, S.; Faubert, B.; Bridon, G.; Tognon, C.; Mathers, J.; Thomas, R.; Li, A.; Barokas, A.; Kwok, B.; Bowden, M.; Smith, S.; 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.
	2016	A generic method of engagement to elicit regional coastal management options	Dichmont, C.; Dutra, L.; Owens, R.; Jebreen, E.; Thompson, C.; Deng, R.; van Putten, E.; Pascual, R.; Dambacher, J.; Warne, M.; Quinn, R.; Thébaud, O.; Bennett, J.; Read, M.; Wachenfeld, D.; Davies, J.; Garland, A.; Dunning, M.; Collier, C.; Waycott, M.; et al.
	2012	New susceptibility loci associated with kidney disease in type 1 diabetes	Sandholm, N.; Salem, R.; McKnight, A.; Brennan, E.; Forsblom, C.; Isakova, T.; McKay, G.; Williams, W.; Sadlier, D.; Mäkinen, V.; Swan, E.; Palmer, C.; Boright, A.; Ahlqvist, E.; Deshmukh, H.; Keller, B.; Huang, H.; Ahola, A.; Fagerholm, E.; Gordin, D.; et al.; Böger, C.A.
	2013	Rare variants in single-minded 1 (SIM1) are associated with severe obesity	Ramachandrappa, S.; Raimondo, A.; Cali, A.; Keogh, J.; Henning, E.; Saeed, S.; Thompson, A.; Garg, S.; Bochukova, E.; Brage, S.; Trowse, V.; Wheeler, E.; Sullivan, A.; Dattani, M.; Clayton, P.; Datta, V.; Bruning, J.; Wareham, N.; O'Rahilly, S.; Peet, D.; et al.
	2013	Loss-of-function mutations in SIM1 contribute to obesity and Prader-Willi-like features	Bonnefond, A.; Raimondo, A.; Stutzmann, F.; Ghoussaini, M.; Ramachandrappa, S.; Bersten, D.; Durand, E.; Vatin, V.; Balkau, B.; Lantieri, O.; Raverdy, V.; Pattou, F.; Van Hul, W.; Van Gaal, L.; Peet, D.; Weill, J.; Miller, J.; Horber, F.; Goldstone, A.; Driscoll, D.; et al.
	2015	DAT isn’t all that: cocaine reward and reinforcement require Toll-like receptor 4 signaling	Northcutt, A.; Hutchinson, M.; Wang, X.; Baratta, M.; Hiranita, T.; Cochran, T.; Pomrenze, M.; Galer, E.; Kopajtic, T.; Li, C.; Amat, J.; Larson, G.; Cooper, D.; Huang, Y.; O'Neill, C.; Yin, H.; Zahniser, N.; Katz, J.; Rice, K.; Maier, S.; et al.
	2018	BAK/BAX macropores facilitate mitochondrial herniation and mtDNA efflux during apoptosis	McArthur, K.; Whitehead, L.W.; Heddleston, J.M.; Li, L.; Padman, B.S.; Oorschot, V.; Geoghegan, N.D.; Chappaz, S.; Davidson, S.; Chin, H.S.; Lane, R.M.; Dramicanin, M.; Saunders, T.L.; Sugiana, C.; Lessene, R.; Osellame, L.D.; Chew, T.L.; Dewson, G.; Lazarou, M.; Ramm, G.; 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.