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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.
	2019	Association of chromosome 9p21 with subsequent coronary heart disease events A GENIUS-CHD study of individual participant data	Patel, R.S.; Schmidt, A.F.; Tragante, V.; McCubrey, R.O.; Holmes, M.; Howe, L.J.; Direk, K.; Akerblom, A.; Leander, K.; Virani, S.S.; Kaminski, K.A.; Muehlschlegel, J.D.; Dube, M.-P.; Allayee, H.; Almgren, P.; Alver, M.; Baranova, E.; Behlouli, H.; Boeckx, B.; Braund, P.S.; 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.
	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.
	2018	Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection	Pardiñas, A.; Holmans, P.; Pocklington, A.; Escott-Price, V.; Ripke, S.; Carrera, N.; Legge, S.; Bishop, S.; Cameron, D.; Hamshere, M.; Han, J.; Hubbard, L.; Lynham, A.; Mantripragada, K.; Rees, E.; MacCabe, J.; McCarroll, S.; Baune, B.; Breen, G.; Byrne, E.; et al.
	2020	Multitrait analysis of glaucoma identifies new risk loci and enables polygenic prediction of disease susceptibility and progression	Craig, J.E.; Han, X.; Qassim, A.; Hassall, M.; Cooke Bailey, J.N.; Kinzy, T.G.; Khawaja, A.P.; An, J.; Marshall, H.; Gharahkhani, P.; Igo, R.P.; Graham, S.L.; Healey, P.R.; Ong, J.-S.; Zhou, T.; Siggs, O.; Law, M.H.; Souzeau, E.; Ridge, B.; Hysi, P.G.; et al.
	2014	Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's disease	Nalls, M.A.; Pankratz, N.; Lill, C.M.; Do, C.B.; Hernandez, D.G.; Saad, M.; DeStefano, A.L.; Kara, E.; Bras, J.; Sharma, M.; Schulte, C.; Keller, M.F.; Arepalli, S.; Letson, C.; Edsall, C.; Stefansson, H.; Liu, X.; Pliner, H.; Lee, J.H.; Cheng, R.; 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.
	2018	A genome-wide association study of diabetic kidney disease in subjects with type 2 diabetes	Van Zuydam, N.R.; Ahlqvist, E.; Sandholm, N.; Deshmukh, H.; William Rayner, N.; Abdalla, M.; Ladenvall, C.; Ziemek, D.; Fauman, E.; Robertson, N.R.; McKeigue, P.M.; Valo, E.; Forsblom, C.; Harjutsalo, V.; Perna, A.; Rurali, E.; Loredana Marcovecchio, M.; Igo, R.P.; Salem, R.M.; Perico, N.; 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.