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Preview	Issue Date	Title	Author(s)
	2014	Common variants near ABCA1, AFAP1 and GMDS confer risk of primary open-angle glaucoma	Gharahkhani, P.; Burdon, K.; Fogarty, R.; Sharma, S.; Hewitt, A.; Martin, S.; Law, M.; Cremin, K.; Bailey, J.; Loomis, S.; Pasquale, L.; Haines, J.; Hauser, M.; Viswanathan, A.; McGuffin, P.; Topouzis, F.; Foster, P.; Graham, S.; Casson, R.; Chehade, M.; 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.
	2016	A splicing-regulatory polymorphism in DRD2 disrupts ZRANB2 binding, impairs cognitive functioning and increases risk for schizophrenia in six Han Chinese samples	Cohen, O.; Weickert, T.; Hess, J.; Paish, L.; McCoy, S.; Rothmond, D.; Galletly, C.; Liu, D.; Weinberg, D.; Huang, X.; Xu, Q.; Shen, Y.; Zhang, D.; Yue, W.; Yan, J.; Wang, L.; Lu, T.; He, L.; Shi, Y.; Xu, M.; et al.
	2014	LgG4 immunostaining and its implications in orbital inflammatory disease	Wong, A.; Planck, S.; Choi, D.; Harrington, C.; Troxell, M.; Houghton, D.; Stauffer, P.; Wilson, D.; Grossniklaus, H.; Dailey, R.; Ng, J.; Steele, E.; Harris, G.; Czyz, C.; Foster, J.; White, V.; Dolman, P.; Kazim, M.; Patel, P.; Edward, D.; et al.; Wallace, G.
	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	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.
	2016	Point mutations in Exon 1B of APC reveal gastric adenocarcinoma and proximal polyposis of the stomach as a familial adenomatous polyposis variant	Li, J.; Woods, S.; Healey, S.; Beesley, J.; Chen, X.; Lee, J.; Sivakumaran, H.; Wayte, N.; Nones, K.; Waterfall, J.; Pearson, J.; Patch, A.; Senz, J.; Ferreira, M.; Kaurah, P.; MacKenzie, R.; Heravi-Moussavi, A.; Hansford, S.; Lannagan, T.; Spurdle, A.; et al.
	2015	Copy number variants in patients with intellectual disability affect the regulation of ARX transcription factor gene	Ishibashi, M.; Manning, E.; Shoubridge, C.; Krecsmarik, M.; Hawkins, T.; Giacomotto, J.; Zhao, T.; Mueller, T.; Bader, P.; Cheung, S.; Stankiewicz, P.; Bain, N.; Hackett, A.; Reddy, C.; Mechaly, A.; Peers, B.; Wilson, S.; Lenhard, B.; Bally-Cuif, L.; Gecz, J.; et al.
	2016	X chromosome dose and sex bias in autoimmune diseases: increased prevalence of 47,XXX in systemic lupus erythematosus and Sjögren's syndrome	Liu, K.; Kurien, B.; Zimmerman, S.; Kaufman, K.; Taft, D.; Kottyan, L.; Lazaro, S.; Weaver, C.; Ice, J.; Adler, A.; Chodosh, J.; Radfar, L.; Rasmussen, A.; Stone, D.; Lewis, D.; Li, S.; Koelsch, K.; Igoe, A.; Talsania, M.; Kumar, J.; et al.