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Preview	Issue Date	Title	Author(s)
	2015	Fine mapping of type 1 diabetes susceptibility loci and evidence for colocalization of causal variants with lymphoid gene enhancers	Onengut-Gumuscu, S.; Chen, W.-M.; Burren, O.; Cooper, N.J.; Quinlan, A.R.; Mychaleckyj, J.C.; Farber, E.; Bonnie, J.K.; Szpak, M.; Schofield, E.; Achuthan, P.; Guo, H.; Fortune, M.D.; Stevens, H.; Walker, N.M.; Ward, L.D.; Kundaje, A.; Kellis, M.; Daly, M.J.; Barrett, J.C.; et al.
	2015	Novel IL1RAPL1 mutations associated with intellectual disability impair synaptogenesis	Ramos-Brossier, M.; Montani, C.; Lebrun, N.; Gritti, L.; Martin, C.; Seminatore-Nole, C.; Toussaint, A.; Moreno, S.; Poirier, K.; Dorseuil, O.; Chelly, J.; Hackett, A.; Gecz, J.; Bieth, E.; Faudet, A.; Heron, D.; Kooy, R.; Loeys, B.; Humeau, Y.; Sala, C.; et al.
	2015	Fine-mapping of the HNF1B multicancer locus identifies candidate variants that mediate endometrial cancer risk	Painter, J.; O'Mara, T.; Batra, J.; Cheng, T.; Lose, F.; Dennis, J.; Michailidou, K.; Tyrer, J.; Ahmed, S.; Ferguson, K.; Healey, C.; Kaufmann, S.; Hillman, K.; Walpole, C.; Moya, L.; Pollock, P.; Jones, A.; Howarth, K.; Martin, L.; Gorman, M.; et al.
	2015	Increased STAG2 dosage defines a novel cohesinopathy with intellectual disability and behavioral problems	Kumar, R.; Corbett, M.; Van Bon, B.; Gardner, A.; Woenig, J.; Jolly, L.; Douglas, E.; Friend, K.; Tan, C.; Van Esch, H.; Holvoet, M.; Raynaud, M.; Field, M.; Leffler, M.; Budny, B.; Wisniewska, M.; Badura-Stronka, M.; Latos-Bieleńska, A.; Batanian, J.; Rosenfeld, J.; et al.
	2015	Association analysis of 29,956 individuals confirms that a low- frequency variant at CCND2 halves the risk of type 2 diabetes by enhancing insulin secretion	Yaghootkar, H.; Stancáková, A.; Freathy, R.; Vangipurapu, J.; Weedon, M.; Xie, W.; Wood, A.; Ferrannini, E.; Mari, A.; Ring, S.; Lawlor, D.; Smith, G.; Jørgensen, T.; Hansen, T.; Pedersen, O.; Steinthorsdottir, V.; Guobjartsson, D.; Thorleifsson, G.; Thorsteinsdottir, U.; Stefansson, K.; et al.
	2015	Efficacy of thiopurines and adalimumab in preventing Crohn's disease recurrence in high-risk patients - a POCER study analysis	De Cruz, P.; Kamm, M.A.; Hamilton, A.L.; Ritchie, K.J.; Krejany, E.O.; Gorelik, A.; Liew, D.; Prideaux, L.; Lawrance, I.C.; Andrews, J.M.; Bampton, P.A.; Jakobovits, S.; Florin, T.H.; Gibson, P.R.; Debinski, H.; Gearry, R.B.; Macrae, F.A.; Leong, R.W.; Kronborg, I.; Radford-Smith, G.; et al.
	2015	Genetic heritage of the balto-slavic speaking populations: a synthesis of autosomal, mitochondrial and Y-chromosomal data	Kushniarevich, A.; Utevska, O.; Chuhryaeva, M.; Agdzhoyan, A.; Dibirova, K.; Uktveryte, I.; Möls, M.; Mulahasanovic, L.; Pshenichnov, A.; Frolova, S.; Shanko, A.; Metspalu, E.; Reidla, M.; Tambets, K.; Tamm, E.; Koshel, S.; Zaporozhchenko, V.; Atramentova, L.; Kučinskas, V.; Davydenko, O.; et al.; Calafell, F.
	2015	Randomized phase II study of carboplatin and paclitaxel with either linifanib or placebo for advanced nonsquamous non–small-cell lung cancer	Ramalingam, S.S.; Shtivelband, M.; Soo, R.A.; Barrios, C.H.; Makhson, A.; Segalla, J.G.; Pittman, K.B.; Kolman, P.; Pereira, J.R.; Srkalovic, G.; Belani, C.P.; Axelrod, R.; Owonikoko, T.K.; Qin, Q.; Qian, J.; McKeegan, E.M.; Devanarayan, V.; McKee, M.D.; Ricker, J.L.; Carlson, D.M.; et al.
	2015	Causal mechanisms and balancing selection inferred from genetic associations with polycystic ovary syndrome	Day, F.; Hinds, D.; Tung, J.; Stolk, L.; Styrkarsdottir, U.; Saxena, R.; Bjonnes, A.; Broer, L.; Dunger, D.; Halldorsson, B.; Lawlor, D.; Laval, G.; Mathieson, I.; McCardle, W.; Louwers, Y.; Meun, C.; Ring, S.; Scott, R.; Sulem, P.; Uitterlinden, A.; et al.
	2015	A new antibiotic with potent activity targets MscL	Iscla, I.; Wray, R.; Blount, P.; Larkins-Ford, J.; Conery, A.; Ausubel, F.; Ramu, S.; Kavanagh, A.; Huang, J.; Blaskovich, M.; Cooper, M.; Obregon-Henao, A.; Orme, I.; Tjandra, E.; Stroeher, U.; Brown, M.; Macardle, C.; van Holst Pellekaan, N.; Ling Tong, C.; Slattery, A.; et al.