Heritable defects in telomere and mitotic function selectively predispose to sarcomas

- 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, Genin, E, Priestley, Peter, 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, Carey-Smith, R, Wood, D, Porceddu, S, Dickinson, I, Thorne, H, James, P, Ray-Coquard, I, Ray-Coquard, Isabelle, Cassier, P, Le Cesne, A, Duffaud, F, Penel, N, Isambert, N, Kurtz, J-E, Puri, A, Isambert, Nicholas, Ward, I, van der Graaf, W, Seddon, B, Chandrasekar, C, Rickar, R, Hennig, I, Schiffman, J, Silvestri, A, Causeret, Sylvain, Zaratzian, A, Tayao, M, Walwyn, K, Niedermayr, E, Mang, D, Clark, R, Thorpe, T, MacDonald, J, Riddell, K, Mar, J

Gene expression imputation across multiple brain regions provides insights into schizophrenia risk

- 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

Age at first birth in women is genetically associated with increased risk of schizophrenia

- 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.

LD score regression distinguishes confounding from polygenicity in genome-wide association studies

- 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.