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Marshall, CR, Marshall, CR, Howrigan, DP, Merico, D, Thiruvahindrapuram, B, Wu, W, Greer, DS, Antaki, D, Shetty, A, Holmans, PA et al (show 257 more authors) , Pinto, D, Gujral, M, Brandler, WM, Malhotra, D, Wang, Z, Fajarado, KVF, Maile, MS, Ripke, S, Agartz, I, Albus, M, Alexander, M, Amin, F, Atkins, J, Bacanu, SA, Jr, BRA, Bergen, SE, Ertalan, M, Bevilacqua, E, Bigdeli, TB, Black, DW, Bruggeman, R, Buccola, NG, Buckner, RL, Bulik-Sullivan, B, Byerley, W, Cahn, W, Cai, G, Cairns, MJ, Campion, D, Cantor, RM, Carr, VJ, Carrera, N, Catts, SV, Chambert, KD, Cheng, W, Cloninger, CR, Cohen, D, Cormican, P, Craddock, N, Crespo-Facorro, B, Crowley, JJ, Curtis, D, Davidson, M, Davis, KL, Degenhardt, F, Del Favero, J, DeLisi, LE, Dikeos, D, Dinan, T, Djurovic, S, Donohoe, G, Drapeau, E, Duan, J, Dudbridge, F, Eichhammer, P, Eriksson, J, Escott-Price, V, Essioux, L, Fanous, AH, Farh, K-H, Farrell, MS, Frank, J, Franke, L, Freedman, R, Freimer, NB, Friedman, JI, Forstner, AJ, Fromer, M, Genovese, G, Georgieva, L, Gershon, ES, Giegling, I, Giusti-Rodriguez, P, Godard, S, Goldstein, JI, Gratten, J, de Haan, L, Hamshere, ML, Hansen, M, Hansen, T, Haroutunian, V, Hartmann, AM, Henskens, FA, Herms, S, Hirschhorn, JN, Hoffinann, P, Hofman, A, Huang, H, Ikeda, M, Joa, I, Kahler, AK, Kahn, RS, Kalaydjieva, L, Karjalainen, J, Kavanagh, D, Keller, MC, Kelly, BJ, Kennedy, JL, Kim, Y, Knowles, JA, Konte, B, Laurent, C, Lee, P, Lee, SH, Legge, SE, Lerer, B, Levy, DL, Liang, K-Y, Lieberman, J, Lonnqvist, J, Loughland, CM, Magnusson, PKE, Maher, BS, Maier, W, Mallet, J, Mattheisen, M, Mattingsdal, M, McCarley, RW, McDonald, C, McIntosh, AM, Meier, S, Meijer, CJ, Melle, I, Mesholam-Gately, RI, Metspalu, A, Michie, PT, Milani, L, Milanova, V, Mokrab, Y, Morris, DW, Muller-Myhsok, B ORCID: 0000-0002-0719-101X, Murphy, KC, Murray, RM, Myin-Germeys, I, Nenadic, I, Nertney, DA, Nestadt, G, Nicodemus, KK, Nisenbaum, L, Nordin, A, O'Callaghan, E, O'Dushlaine, C, Oh, S-Y, Olincy, A, Olsen, L, O'Neill, FA, Van Os, J, Pantelis, C, Papadimitriou, GN, Parkhomenko, E, Pato, MT, Paunio, T, Perkins, DO, Pers, TH, Pietilainen, O, Pimm, J, Pocklington, AJ, Powell, J, Price, A, Pulver, AE, Purcell, SM, Quested, D, Rasmussen, HB, Reichenberg, A, Reimers, MA, Richards, AL, Roffman, JL, Roussos, P, Ruderfer, DM, Salomaa, V, Sanders, AR, Savitz, A, Schall, U, Schulze, TG, Schwab, SG, Scolnick, EM, Scott, RJ, Seidman, LJ, Shi, J, Silverman, JM, Smoller, JW, Soderman, E, Spencer, CCA, Stahl, EA, Strengman, E, Strohmaier, J, Stroup, TS, Suvisaari, J, Svrakic, DM, Szatkiewicz, JP, Thirumalai, S, Tooney, PA, Veijola, J, Visscher, PM, Waddington, J, Walsh, D, Webb, BT, Weiser, M, Wildenauer, DB, Williams, NM, Williams, S, Witt, SH, Wolen, AR, Wormley, BK, Wray, NR, Wu, JQ, Zai, CC, Adolfsson, R, Andreassen, OA, Blackwood, DHR, Bramon, E, Buxbaum, JD, Cichon, S, Collier, DA, Corvin, A, Daly, MJ, Darvasi, A, Domenici, E, Esko, T, Gejman, PV, Gill, M, Gurling, H, Hultman, CM, Iwata, N, Jablensky, AV, Jonsson, EG, Kendler, KS, Kirov, G, Knight, J, Levinson, DF, Li, QS, McCarroll, SA, McQuillin, A, Moran, JL, Mowry, BJ, Nothen, MM, Ophoff, RA, Owen, MJ, Palotie, A, Pato, CN, Petryshen, TL, Posthuma, D, Rietschel, M, Riley, BP, Rujescu, D, Sklar, P, St Clair, D, Walters, JTR, Werge, T, Siillivan, PF, O'Donovan, MC, Scherer, SW, Neale, BM, Sebat, J, CNV, , Grp, SW and Endophenotypes, P (2017) Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects. NATURE GENETICS, 49 (1). pp. 27-35.

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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]