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Results 1-10 of 35 (Search time: 0.003 seconds).
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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.
2017Genome-wide meta-analysis of 241,258 adults accounting for smoking behaviour identifies novel loci for obesity traitsJustice, A.; Winkler, T.; Feitosa, M.; Graff, M.; Fisher, V.; Young, K.; Barata, L.; Deng, X.; Czajkowski, J.; Hadley, D.; Ngwa, J.; Ahluwalia, T.; Chu, A.; Heard-Costa, N.; Lim, E.; Perez, J.; Eicher, J.; Kutalik, Z.; Xue, L.; Mahajan, A.; et al.
2012Colorectal cancer linkage on chromosomes 4q21, 8q13, 12q24, and 15q22Cicek, M.; Cunningham, J.; Fridley, B.; Serie, D.; Bamlet, W.; Diergaarde, B.; Haile, R.; Le Marchand, L.; Krontiris, T.; Younghusband, H.; Gallinger, S.; Newcomb, P.; Hopper, J.; Jenkins, M.; Casey, G.; Schumacher, F.; Chen, Z.; DeRycke, M.; Templeton, A.; Winship, I.; et al.; Lo, A.
2018Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selectionPardiñas, 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.
2013A pathway-based analysis provides additional support for an immune-related genetic susceptibility to Parkinsons diseaseHolmans, 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.
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.
2020Multitrait analysis of glaucoma identifies new risk loci and enables polygenic prediction of disease susceptibility and progressionCraig, 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.
2020A phenome-wide association and Mendelian Randomisation study of polygenic risk for depression in UK BiobankShen, X.; Howard, D.M.; Adams, M.J.; Hill, W.D.; Clarke, T.K.; Adams, M.J.; Clarke, T.K.; McIntosh, A.M.; Deary, I.J.; Wray, N.R.; Ripke, S.; Mattheisen, M.; Trzaskowski, M.; Byrne, E.M.; Abdellaoui, A.; Agerbo, E.; Air, T.M.; Andlauer, T.F.M.; Bacanu, S.A.; Bækvad-Hansen, M.; et al.
2014Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's diseaseNalls, 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.
2014Common variants near ABCA1, AFAP1 and GMDS confer risk of primary open-angle glaucomaGharahkhani, 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.

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