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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.
	2017	Electrophysiological, cognitive and clinical profiles of at-risk mental state: the longitudinal minds in transition (MinT) study	Atkinson, R.J.; Fulham, W.R.; Michie, P.T.; Ward, P.B.; Todd, J.; Stain, H.; Langdon, R.; Thienel, R.; Paulik, G.; Cooper, G.; Anthes, L.; Bowen, D.; Case, V.; Clark, S.; Collins-Langworthy, J.; Curtis, J.; Ehlkes, T.; Haddow, T.; Lawrence, C.; Logan, S.; et al.; Hashimoto, K.
	2017	Epiregulin and EGFR interactions are involved in pain processing	Martin, L.J.; Smith, S.B.; Khoutorsky, A.; Magnussen, C.A.; Samoshkin, A.; Sorge, R.E.; Cho, C.; Yosefpour, N.; Sivaselvachandran, S.; Tohyama, S.; Cole, T.; Khuong, T.M.; Mir, E.; Gibson, D.G.; Wieskopf, J.S.; Sotocinal, S.G.; Austin, J.S.; Meloto, C.B.; Gitt, J.H.; Gkogkas, C.; et al.
	2014	Inactivating mutations in NPC1L1 and protection from coronary heart disease	Stitziel, N.O.; Won, H.H.; Morrison, A.C.; Peloso, G.M.; Do, R.; Lange, L.A.; Fontanillas, P.; Gupta, N.; Duga, S.; Goel, A.; Farrall, M.; Saleheen, D.; Ferrario, P.; König, I.; Asselta, R.; Merlini, P.A.; Marziliano, N.; Notarangelo, M.F.; Schick, U.; Auer, P.; et al.
	2013	Genetic variants associated with increased risk of malignant pleural mesothelioma: a genome-wide association study	Matullo, G.; Guarrera, S.; Betti, M.; Fiorito, G.; Ferrante, D.; Voglino, F.; Cadby, G.; Di Gaetano, C.; Rosa, F.; Russo, A.; Hirvonen, A.; Casalone, E.; Tunesi, S.; Padoan, M.; Giordano, M.; Aspesi, A.; Casadio, C.; Ardissone, F.; Ruffini, E.; Betta, P.; et al.; Miao, X.-P.
	2014	MicroRNA related polymorphisms and breast cancer risk	Khan, S.; Greco, D.; Michailidou, K.; Milne, R.; Muranen, T.; Heikkinen, T.; Aaltonen, K.; Dennis, J.; Bolla, M.; Liu, J.; Hall, P.; Irwanto, A.; Humphreys, K.; Li, J.; Czene, K.; Chang-Claude, J.; Hein, R.; Rudolph, A.; Seibold, P.; Flesch-Janys, D.; et al.; Zhao, Z.
	2012	A genome-wide association search for type 2 diabetes genes in African Americans	Palmer, N.; McDonough, C.; Hicks, P.; Roh, B.; Wing, M.; Sandy An, S.; Hester, J.; Cooke, J.; Bostrom, M.; Rudock, M.; Talbert, M.; Lewis, J.; DIAGRAM Consortium,; MAGIC Consortium,; Ferrara, A.; Lu, L.; Ziegler, J.; Sale, M.; Divers, J.; Shriner, D.; et al.; Kronenberg, F.
	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	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	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.