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Bulik-Sullivan, Brendan K., Albus, M, Alexander, M, Amin, F, Bacanu, SA, Begemann, M, Belliveau, RA, Bene, J, Bergen, SE, Bruggeman, R, Bevilacqua, E, Bigdeli, TB, Black, DW, Buccola, NG, Buckner, RL, Byerley, W, Cahn, W, Cai, G, Cairns, MJ, Campion, D, Cantor, RM, Carr, VJ, Carrera, N, Catts, SV, Chambert, KD, Chan, RCK, Chen, RYL, Cohen, D, Chen, EYH, Cheng, W, Cheung, EFC, Chong, SA, Cloninger, CR, Cohen, N, Cormican, P, Craddock, N, Crespo-Facorro, B, Crowley, JJ, Curtis, D, Davidson, M, Davis, KL, Degenhardt, F, Del Favero, J, Loh, Po-Ru, Michie, Patricia T., Schall, Ulrich, Scott, Rodney J., Tooney, Paul A., Wu, Jing Qin, Patterson, Nick, Daly, Mark J., Price, Alkes L., Neale, Benjamin M., Finucane, Hilary K., Ripke, Stephan, Yang, Jian, Schizophrenia Working Group of the Psychiatric Genomics Consortium,, Cairns, Murray J., Henskens, Frans A., Kelly, Brian J., Loughland, Carmel M.. Nature Publishing Group; 2015. LD score regression distinguishes confounding from polygenicity in genome-wide association studies.
Di Biase, Maria A., Geaghan, Michael P., Bouix, Sylvain, Knyazhanskaya, Evdokiya E., Lyall, Amanda E., Pasternak, Ofer, Kubicki, Marek, Rathi, Yogesh, Visco, Andrew, Gaunnac, Megan, Lv, Jinglei, Mesholam-Gately, Raquelle I., Reay, William R., Cairns, Murray J., Holt, DJ, Keshavan, MS, Pantelis, C, Öngür, D, Breier, A, Cairns, MJ, Shenton, ME, Zalesky, A, Seidlitz, Jakob, Weickert, Cynthia Shannon, Pébay, Alice, Green, Melissa J., Quidé, Yann, Atkins, Joshua R., Coleman, Michael J.. Nature Publishing Group; 2022. Cell type-specific manifestations of cortical thickness heterogeneity in schizophrenia.
Duchatel, Ryan J., Jackson, Evangeline R., Kearney, Padraic S., Jamaluddin, M. Fairuz B., Douglas, Alicia M., Beitaki, Tyrone, McEwen, Holly P., Persson, Mika L., Hocke, Emily A., Jain, Vaibhav, Aksu, Michael, Manning, Elizabeth E., Parackal, Sarah G., Murray, Heather C., Verrills, Nicole M., Hua, Susan, Cairns, Murray J., Alvaro, Frank, Dayas, Christopher V., Dun, Matthew D., Hua, S, de Bock, CE, Colino-Sanguino, Y, Kiltschewskij, Dylan, Valdes-Mora, F, Tsoli, M, Ziegler, DS, Cairns, MJ, Raabe, EH, Vitanza, NA, Hulleman, E, Phoenix, TN, Koschmann, C, Alvaro, F, Findlay, Izac J., Dayas, CV, Tinkle, CL, Wheeler, H, Whittle, JR, Eisenstat, DD, Firestein, R, Mueller, S, Valvi, S, Hansford, JR, Ashley, DM, Mannan, Abdul, Gregory, SG, Kilburn, LB, Nazarian, J, Cain, JE, Dun, MD, Staudt, Dilana E., Thomas, Bryce C., Germon, Zacary P., Laternser, Sandra. American Society for Clinical Investigation; 2024. PI3K/mTOR is a therapeutically targetable genetic dependency in diffuse intrinsic pontine glioma.
Knol, Maria J., Poot, Raymond A., van Dam-Nolen, Dianne H. K., Brunner, HG, Le Grand, Q, Sim, K, Stein, DJ, Bowden, DW, Cairns, MJ, Hariri, AR, Cheung, C-L, Andersson, S, Villringer, A, Lamballais, Sander, Paus, T, Cichon, S, Calhoun, VD, Crivello, F, Launer, LJ, White, T, Koudstaal, PJ, Houlden, H, Fornage, M, Matsuda, F, Pawlak, Mikolaj A., Grabe, HJ, Ikram, MA, Debette, S, Thompson, PM, Seshadri, S, Adams, HHH, Lewis, Cora E., Carrion-Castillo, Amaia, van Erp, Theo G. M., Reinbold, Céline S., Shin, Jean, Scholz, Markus, Håberg, Asta K., Evans, Tavia E., Kämpe, Anders, Li, GHY, Avinun, R, Atkins, Joshua R., Hsu, F-C, Amod, AR, Lam, M, Tsuchida, A, Teunissen, MWA, Aygün, N, Satizabal, Claudia L., Patel, Y, Liang, D, Beiser, AS, Beyer, F, Bis, JC, Bos, D, Bryan, RN, Bülow, R, Caspers, S, Catheline, G, Mishra, Aniket, Cecil, CAM, Dalvie, S, Dartigues, J-F, DeCarli, C, Enlund-Cerullo, M, Ford, JM, Franke, B, Freedman, BI, Friedrich, N, Green, MJ, Sargurupremraj, Muralidharan, Haworth, S, Helmer, C, Hoffmann, P, Homuth, G, Ikram, MK, Jack, CR, Jahanshad, N, Jockwitz, C, Kamatani, Y, Knodt, AR, van der Auwera, Sandra, Li, S, Lim, K, Longstreth, WT, Macciardi, F, Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium,, Enhancing NeuroImaging Genetics through Meta-Analysis (ENIGMA) Consortium,, Mäkitie, O, Mazoyer, B, Medland, SE, Miyamoto, S, Duperron, Marie-Gabrielle, Moebus, S, Mosley, TH, Muetzel, R, Mühleisen, TW, Nagata, M, Nakahara, S, Palmer, ND, Pausova, Z, Preda, A, Quidé, Y, Jian, Xueqiu, Reay, WR, Roshchupkin, GV, Schmidt, R, Schreiner, PJ, Setoh, K, Shapland, CY, Sidney, S, St Pourcain, B, Stein, JL, Tabara, Y, Hostettler, Isabel C., Teumer, A, Uhlmann, A, van der Lugt, A, Vernooij, MW, Werring, DJ, Windham, BG, Witte, AV, Wittfeld, K, Yang, Q, Yoshida, K. Cell Press; 2024. Genetic variants for head size share genes and pathways with cancer.