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PreviewIssue DateTitleAuthor(s)
2015Fine mapping of type 1 diabetes susceptibility loci and evidence for colocalization of causal variants with lymphoid gene enhancersOnengut-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.
2017Relations between lipoprotein(a) concentrations, LPA genetic variants, and the risk of mortality in patients with established coronary heart disease: a molecular and genetic association studyZewinger, S.; Kleber, M.E.; Tragante, V.; McCubrey, R.O.; Schmidt, A.F.; Direk, K.; Laufs, U.; Werner, C.; Koenig, W.; Rothenbacher, D.; Mons, U.; Breitling, L.P.; Brenner, H.; Jennings, R.T.; Petrakis, I.; Triem, S.; Klug, M.; Filips, A.; Blankenberg, S.; Waldeyer, C.; et al.
2019GWAS on longitudinal growth traits reveals different genetic factors influencing infant, child, and adult BMIAlves, A.C.; De Silva, N.M.G.; Karhunen, V.; Sovio, U.; Das, S.; Rob Taal, H.; Warrington, N.M.; Lewin, A.M.; Kaakinen, M.; Cousminer, D.L.; Thiering, E.; Timpson, N.J.; Bond, T.A.; Lowry, E.; Brown, C.D.; Estivill, X.; Lindi, V.; Bradfield, J.P.; Geller, F.; Speed, D.; et al.
2011Association 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 developmentSovio, 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.
2013Population genomics of cardiometabolic traits: design of the University College London-London School of Hygiene and Tropical Medicine-Edinburgh-Bristol (UCLEB) ConsortiumShah, T.; Engmann, J.; Dale, C.; Shah, S.; White, J.; Giambartolomei, C.; McLachlan, S.; Zabaneh, D.; Cavadino, A.; Finan, C.; Wong, A.; Amuzu, A.; Ong, K.; Gaunt, T.; Holmes, M.; Warren, H.; Davies, T.; Drenos, F.; Cooper, J.; Sofat, R.; et al.; Zeller, T.
2015Single nucleotide variations in CLCN6 identified in patients with benign partial epilepsies in infancy and/or febrile seizuresYamamoto, T.; Shimojima, K.; Sangu, N.; Komoike, Y.; Ishii, A.; Abe, S.; Yamashita, S.; Imai, K.; Kubota, T.; Fukasawa, T.; Okanishi, T.; Enoki, H.; Tanabe, T.; Saito, A.; Furukawa, T.; Shimizu, T.; Milligan, C.; Petrou, S.; Heron, S.; Dibbens, L.; et al.; Ishii, R.
2014Refining analyses of copy number variation identifies specific genes associated with developmental delayCoe, B.; Witherspoon, K.; Rosenfeld, J.; van Bon, B.; Vulto-van Silfhout, A.; Bosco, P.; Friend, K.; Baker, C.; Buono, S.; Vissers, L.; Schuurs-Hoeijmakers, J.; Hoischen, A.; Pfundt, R.; Krumm, N.; Carvill, G.; Li, D.; Amaral, D.; Brown, N.; Lockhart, P.; Scheffer, I.; et al.
2010The Bipolar Association case-control study (BACCS)and meta-analysis: no association with the 5,10-methylenetetrahydrofolate reductase gene and bipolar disorderCohen-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.

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