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Results 11-20 of 68 (Search time: 0.003 seconds).
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PreviewIssue DateTitleAuthor(s)
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.
2017Discovery and functional prioritization of Parkinson's disease candidate genes from large-scale whole exome sequencingJansen, I.E.; Ye, H.; Heetveld, S.; Lechler, M.C.; Michels, H.; Seinstra, R.I.; Lubbe, S.J.; Drouet, V.; Lesage, S.; Majounie, E.; Gibbs, J.R.; Nalls, M.A.; Ryten, M.; Botia, J.A.; Vandrovcova, J.; Simon-Sanchez, J.; Castillo-Lizardo, M.; Rizzu, P.; Blauwendraat, C.; Chouhan, A.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.
2021Gene selection for the Australian Reproductive Genetic Carrier Screening Project ("Mackenzie's Mission")Kirk, E.P.; Ong, R.; Boggs, K.; Hardy, T.; Righetti, S.; Ben, K.; Roscioli, T.; Amor, D.J.; Bakshi, M.; Chung, C.W.T.; Colley, A.; Jamieson, R.; Liebelt, J.; Ma, A.; Pachter, N.; Rajagopalan, S.; Ravine, A.; Wilson, M.; Caruana, J.; Casella, R.; et al.
2020Genome-wide gene-environment analyses of major depressive disorder and reported lifetime traumatic experiences in UK BiobankColeman, J.R.I.; Peyrot, W.J.; Purves, K.L.; Davis, K.A.S.; Rayner, C.; Choi, S.W.; Hübel, C.; Gaspar, H.A.; Kan, C.; Van der Auwera, S.; Adams, M.J.; Lyall, D.M.; Choi, K.W.; Wray, N.R.; Ripke, S.; Mattheisen, M.; Trzaskowski, M.; Byrne, E.M.; Abdellaoui, A.; Adams, M.J.; 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.
2021Implementing gene curation for hereditary cancer susceptibility in Australia: achieving consensus on genes with clinical utilityTudini, E.; Davidson, A.L.; Dressel, U.; Andrews, L.; Antill, Y.; Crook, A.; Field, M.; Gattas, M.; Harris, R.; Kirk, J.; Pachter, N.; Salmon, L.; Susman, R.; Townshend, S.; Trainer, A.H.; Tucker, K.M.; Mitchell, G.; James, P.A.; Ward, R.L.; Mar Fan, H.; et al.
2020Common genetic variation indicates separate causes for periventricular and deep white matter hyperintensitiesArmstrong, N.J.; Mather, K.A.; Sargurupremraj, M.; Knol, M.J.; Malik, R.; Satizabal, C.L.; Yanek, L.R.; Wen, W.; Gudnason, V.G.; Dueker, N.D.; Elliott, L.T.; Hofer, E.; Hofer, E.; Bis, J.; Jahanshad, N.; Li, S.; Logue, M.A.; Logue, M.A.; Luciano, M.; Scholz, 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.

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