Objects
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.
Huckins, Laura M., Buccola, NG, Buckner, RL, Byerley, W, Cahn, W, Cai, G, Campion, D, Cantor, RM, Carr, VJ, Carrera, N, Catts, SV, Chambert, KD, Chan, RCK, Chen, RYL, Chen, EYH, Cheng, W, Cheung, EFC, Chong, SA, Cloninger, CR, Cohen, D, Cohen, N, Cormican, P, Craddock, N, Crowley, JJ, Curtis, D, Davidson, M, Davis, KL, Degenhardt, F, Del Favero, J, Demontis, D, Dikeos, D, Dinan, T, Djurovic, S, Donohoe, G, Drapeau, E, Duan, J, Dudbridge, F, Durmishi, N, Eichhammer, P, Eriksson, J, Dobbyn, Amanda, Boocock, James, Roussos, Panos, Fromer, Menachem, Kramer, Robin, Domenici, Enrico, Gamazon, Eric R., Purcell, Shaun, Johnson, Jessica S., Shah, Hardik R., Klein, Lambertus L., Ruderfer, Douglas M., Henskens, Frans A., Loughland, Carmel M., Schall, Ulrich, Michie, Patricia T., Scott, Rodney J., Gur, RE, Hahn, CG, Schadt, E, Lewis, DA, Haroutunian, V, Hoffman, Gabriel, Peters, MA, Lipska, BK, Buxbaum, JD, Hirai, K, Perumal, TM, Essioux, L, Ripke, S, Neale, BM, Corvin, A, Walters, JTR, Wang, Weiqing, Farh, KH, Holmans, PA, Lee, P, Bulik-Sullivan, B, Collier, DA, Huang, H, Pers, TH, Agartz, I, Agerbo, E, Albus, M, Pardiñas, Antonio F., Alexander, M, Amin, F, Bacanu, SA, Begemann, M, Belliveau, RA, Bene, J, Henskens, FA, Loughland, CM, Michie, PT, Schall, U, Rajagopal, Veera M., Scott, RJ, Als, Thomas D., Nguyen, Hoang T., Girdhar, Kiran. Nature Publishing Group; 2019. Gene expression imputation across multiple brain regions provides insights into schizophrenia risk.
Ni, Guiyan, Gratten, Jacob, Lee, Phil, Bulik-Sullivan, Brendan, Collier, David A., Huang, Hailiang, Pers, Tune H., Agartz, Ingrid, Agerbo, Esben, Albus, Margot, Alexander, Madeline, Amin, Farooq, Wray, Naomi R., Henskens, Frans A., Loughland, Carmel M., Michie, Patricia T., Schall, Ulrich, Scott, Rodney J., Bevilacqua, E, Bigdeli, TB, Black, DW, Bruggeman, R, Buccola, NG, Lee, Sang Hong, Buckner, RL, Byerley, W, Cahn, W, Cai, G, Campion, D, Cantor, RM, Carr, VJ, Carrera, N, Catts, SV, Chambert, KD, Ripke, Stephan, Chan, RCK, Chen, RYL, Chen, EYH, Cheng, W, Cheung, EFC, Chong, SA, Cloninger, CR, Cohen, D, Cohen, N, Cormican, P, Neale, Benjamin M., Craddock, N, Crowley, JJ, Curtis, D, Davidson, M, Davis, KL, Degenhardt, F, Del Favero, J, Demontis, D, Dikeos, D, Dinan, T, Corvin, Aiden, Djurovic, S, Donohoe, G, Drapeau, E, Walters, James T. R., Farh, Kai-How, Holmans, Peter A.. Springer; 2018. Age at first birth in women is genetically associated with increased risk of schizophrenia.
Ballinger, Mandy L., Pattnaik, Swetansu, van der Graaf, Winette T. A., Fennelly, V, Wicht, A, Zielony, B, Galligan, E, Glavich, G, Stoeckert, J, Williams, L, Djandjgava, L, Buettner, I, Osinki, C, Puri, Ajay, Stephens, S, Rogasik, M, Bouclier, L, Girodet, M, Charreton, A, Fayet, Y, Crasto, S, Sandupatla, B, Yoon, Y, Je, N, Duffaud, Florence, Thompson, L, Fowler, T, Johnson, B, Petrikova, G, Hambridge, T, Hutchins, A, Bottero, D, Scanlon, D, Stokes-Denson, J, Génin, E, Le Cesne, Axel, Campion, D, Dartigues, J-F, Deleuze, J-F, Lambert, J-C, Redon, R, Ludwig, T, Grenier-Boley, B, Letort, S, Lindenbaum, P, Meyer, V, Seddon, Beatrice, Quenez, O, Dina, C, Bellenguez, C, Le Clézio, CC, Giemza, J, Chatel, S, Férec, C, Le Marec, H, Letenneur, L, Nicolas, G, Chandrasekar, Coonoor, Rouault, K, Schiffman, Joshua D., Brohl, Andrew S., James, Paul A., Kurtz, Jean-Emmanuel, Mundra, Piyushkumar A., Penel, Nicolas, Myklebost, Ola, Meza-Zepeda, LA, Pickett, H, Kansara, M, Waddell, N, Kondrashova, O, Pearson, JV, Barbour, AP, Li, S, Zaheed, Milita, Nguyen, TL, Fatkin, D, Graham, RM, Giannoulatou, E, Green, MJ, Kaplan, W, Ravishankar, S, Copty, J, Powell, JE, Cuppen, E, Rath, Emma, van Eijk, K, Veldink, J, Ahn, J-H, Kim, JE, Randall, RL, Tucker, K, Judson, I, Sarin, R, Ludwig, T, Genin, E, Priestley, Peter, Deleuze, J-F, French Exome Project Consortium,, Haber, M, Marshall, G, Cairns, Murray J., Blay, J-Y, International Sarcoma Kindred Study,, Thomas, DM, Tattersall, M, Neuhaus, S, Baber, Jonathan, Lewis, C, Tucker, K, Carey-Smith, R, Wood, D, Porceddu, S, Dickinson, I, Thorne, H, James, P, Ray-Coquard, I, Blay, J-Y, Ray-Coquard, Isabelle, Cassier, P, Le Cesne, A, Duffaud, F, Penel, N, Isambert, N, Kurtz, J-E, Puri, A, Sarin, R, Ahn, J-H, Kim, JE, Isambert, Nicholas, Ward, I, Judson, I, van der Graaf, W, Seddon, B, Chandrasekar, C, Rickar, R, Hennig, I, Schiffman, J, Randall, RL, Silvestri, A, Causeret, Sylvain, Zaratzian, A, Tayao, M, Walwyn, K, Niedermayr, E, Mang, D, Clark, R, Thorpe, T, MacDonald, J, Riddell, K, Mar, J. American Association for the Advancement of Science (AAAS); 2023. Heritable defects in telomere and mitotic function selectively predispose to sarcomas.