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Barbu, MC, Zeng, Y, Shen, X, Cox, SR, Clarke, TK, Gibson, J, Adams, MJ, Johnstone, M, Haley, CS, Lawrie, SM et al (show 86 more authors) , Deary, IJ, Wray, NR, Ripke, S, Mattheisen, M, Trzaskowski, M, Byrne, EM, Abdellaoui, A, Agerbo, E, Air, TM, Andlauer, TFM, Bacanu, SA, Bækvad-Hansen, M, Beekman, ATF, Bigdeli, TB, Binder, EB, Blackwood, DHR, Bryois, J, Buttenschøn, HN, Bybjerg-Grauholm, J, Cai, N, Castelao, E, Christensen, JH, Coleman, JRI, Colodro-Conde, L, Couvy-Duchesne, B, Craddock, N, Crawford, GE, Davies, G, Degenhardt, F, Derks, EM, Direk, N, Dolan, CV, Dunn, EC, Eley, TC, Escott-Price, V, Hassan Kiadeh, FF, Finucane, HK, Forstner, AJ, Frank, J, Gaspar, HA, Gill, M, Goes, FS, Gordon, SD, Grove, J, Hall, LS, Hansen, CS, Hansen, TF, Herms, S, Hickie, IB, Hoffmann, P, Homuth, G, Horn, C, Hottenga, JJ, Hougaard, DM, Ising, M, Jansen, R, Jorgenson, E, Knowles, JA, Kohane, IS, Kraft, J, Kretzschmar, WW, Krogh, J, Kutalik, Z, Li, Y, Lind, PA, MacIntyre, DJ, MacKinnon, DF, Maier, RM, Maier, W, Marchini, J, Mbarek, H, McGrath, P, McGuffin, P, Medland, SE, Mehta, D, Middeldorp, CM, Mihailov, E, Milaneschi, Y, Milani, L, Mondimore, FM, Montgomery, GW, Mostafavi, S, Mullins, N, Nauck, M, Ng, B and Nivard, MG (2019) Association of Whole-Genome and NETRIN1 Signaling Pathway–Derived Polygenic Risk Scores for Major Depressive Disorder and White Matter Microstructure in the UK Biobank. Biological Psychiatry: Cognitive Neuroscience and Neuroimaging, 4 (01). pp. 91-100.

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Amos, CI, Dennis, J, Wang, Z, Byun, J, Schumacher, FR, Gayther, SA, Casey, G, Hunter, DJ, Sellers, TA, Gruber, SB et al (show 83 more authors) , Dunning, AM, Michailidou, K, Fachal, L, Doheny, K, Spurdle, AB, Li, Y, Xiao, X, Romm, J, Pugh, E, Coetzee, GA, Hazelett, DJ, Bojesen, SE, Caga-Anan, C, Haiman, CA, Kamal, A, Luccarini, C, Tessier, D, Vincent, D, Bacot, F, Van Den Berg, DJ, Nelson, S, Demetriades, S, Goldgar, DE, Couch, FJ, Forman, JL, Giles, GG, Conti, DV, Bickeböller, H, Risch, A, Waldenberger, M, Brüske-Hohlfeld, I, Hicks, BD, Ling, H, McGuffog, L, Lee, A, Kuchenbaecker, K, Soucy, P, Manz, J, Cunningham, JM, Butterbach, K, Kote-Jarai, Z, Kraft, P, FitzGerald, L, Lindström, S, Adams, M, McKay, JD, Phelan, CM, Benlloch, S, Kelemen, LE, Brennan, P, Riggan, M, O'Mara, TA, Shen, H, Shi, Y, Thompson, DJ, Goodman, MT, Nielsen, SF, Berchuck, A, Laboissiere, S, Schmit, SL, Shelford, T, Edlund, CK, Taylor, JA, Field, JK ORCID: 0000-0003-3951-6365, Park, SK, Offit, K, Thomassen, M, Schmutzler, R, Ottini, L, Hung, RJ, Marchini, J, Amin Al Olama, A, Peters, U, Eeles, RA, Seldin, MF, Gillanders, E, Seminara, D, Antoniou, AC, Pharoah, PDP, Chenevix-Trench, G, Chanock, SJ, Simard, J and Easton, DF (2017) The OncoArray Consortium: A Network for Understanding the Genetic Architecture of Common Cancers. Cancer Epidemiology, Biomarkers and Prevention, 26 (1). pp. 126-135.

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Kosmicki, JA, Horowitz, JE, Banerjee, N, Lanche, R, Marcketta, A, Maxwell, E, Bai, X, Sun, D, Backman, JD, Sharma, D et al (show 72 more authors) , Kang, HM, O'Dushlaine, C, Yadav, A, Mansfield, AJ, Li, AH, Watanabe, K, Gurski, L, McCarthy, SE, Locke, AE, Khalid, S, O'Keeffe, S, Mbatchou, J, Chazara, O, Huang, Y, Kvikstad, E, O'Neill, A, Nioi, P, Parker, MM, Petrovski, S, Runz, H, Szustakowski, JD, Wang, Q, Wong, E, Cordova-Palomera, A, Smith, EN, Szalma, S, Zheng, X, Esmaeeli, S, Davis, JW, Lai, Y-P, Chen, X, Justice, AE, Leader, JB, Mirshahi, T, Carey, DJ, Verma, A, Sirugo, G, Ritchie, MD, Rader, DJ, Povysil, G, Goldstein, DB, Kiryluk, K, Pairo-Castineira, E, Rawlik, K, Pasko, D, Walker, S, Meynert, A, Kousathanas, A, Moutsianas, L, Tenesa, A, Caulfield, M, Scott, R, Wilson, JF, Baillie, JK, Butler-Laporte, G, Nakanishi, T, Lathrop, M, Richards, JB, Regeneron Genetics Center, , UKB Exome Sequencing Consortium, , Jones, M, Balasubramanian, S, Salerno, W, Shuldiner, AR, Marchini, J, Overton, JD, Habegger, L, Cantor, MN, Reid, JG, Baras, A, Abecasis, GR and Ferreira, MA (2021) A catalog of associations between rare coding variants and COVID-19 outcomes. [Preprint]