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Preview	Issue Date	Title	Author(s)
	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.
	2013	A pathway-based analysis provides additional support for an immune-related genetic susceptibility to Parkinsons disease	Holmans, P.; Moskvina, V.; Jones, L.; Sharma, M.; Vedernikov, A.; Buchel, F.; Sadd, M.; Bras, J.M.; Bettella, F.; Nicolaou, N.; Simon-Sanchez, J.; Mittag, F.; Gibbs, J.R.; Schulte, C.; Durr, A.; Guerreiro, R.; Hernandez, D.; Brice, A.; Stefansson, H.; Majamaa, K.; et al.
	2011	Association between common variation at the FTO locus and changes in body mass index from infancy to late childhood: the complex nature of genetic association through growth and development	Sovio, U.; Mook-Kanamori, D.; Warrington, N.; Lawrence, R.; Briollais, L.; Palmer, C.; Cecil, J.; Sandling, J.; Syvanen, A.; Kaakinen, M.; Beilin, L.; Millwood, I.; Bennett, A.; Laitneen, J.; Pouta, A.; Molitor, J.; Smith, G.; Ben-Shlomo, Y.; Jaddoe, V.; Palmer, L.; et al.; Gibson, G.
	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.
	2009	Analyses of associations with asthma in four asthma population samples from Canada and Australia	Daly, D.; Lemire, M.; Akhabir, L.; Chan-Yeung, M.; He, J.; McDonald, T.; Stanford, A.; Stefanowicz, D.; Tripp, B.; Zamar, D.; Bosse, Y.; Ferretti, V.; Montpetit, A.; Tessier, M.; Becker, A.; Kozyrskyj, A.; Beilby, J.; McCaskie, P.; Musk, A.; Warrington, N.; et al.
	2009	Sequence variants in three loci influence monocyte counts and erythrocyte volume	Ferreira, M.; Hottenga, J.; Warrington, N.; Medland, S.; Willemsen, G.; Lawrence, R.; Gordon, S.; de Geus, E.; Henders, A.; Smit, J.; Campbell, M.; Wallace, L.; Evans, D.; Wright, M.; Nyholt, D.; James, A.; Beilby, J.; Penninx, B.; Palmer, L.; Frazer, I.; et al.
	2010	The Bipolar Association case-control study (BACCS)and meta-analysis: no association with the 5,10-methylenetetrahydrofolate reductase gene and bipolar disorder	Cohen-Woods, S.; Craig, I.; Gaysina, D.; Gray, J.; Gunasinghe, C.; Craddock, N.; Elkin, A.; Jones, L.; Kennedy, J.; King, N.; Korszun, A.; Knight, J.; Owen, M.; Parikh, S.; Strauss, J.; Sterne, A.; Tozzi, F.; Perry, J.; Muglia, P.; Vincent, J.; et al.
	2013	SNP genotyping allows an in-depth characterisation of the genome of sugarcane and other complex autopolyploids	Garcia, A.; Mollinari, M.; Marconi, T.; Serang, O.; Silva, R.; Vieira, M.; Vicentini, R.; Costa, E.; Mancini, M.; Garcia, M.; Pastina, M.; Gazaffi, R.; Martins, E.; Dahmer, N.; Sforça, D.; Silva, C.; Bundock, P.; Henry, R.; Souza, G.; van Sluys, M.-A.; et al.
	2011	A genome-wide significant linkage for severe depression on chromosome 3: the depression network study	Breen, G.; Webb, B.; Butler, A.; van den Oord, E.; Tozzi, F.; Craddock, N.; Gill, M.; Korszun, A.; Maier, W.; Middleton, L.; Mors, O.; Owen, M.; Cohen-Woods, S.; Perry, J.; Galwey, N.; Upmanyu, R.; Craig, I.; Lewis, C.; Ng, M.; Brewster, S.; et al.