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.
Finucane, Hilary K., Bulik-Sullivan, Brendan, Ripke, Stephan, Day, Felix R., ReproGen Consortium,, Schizophrenia Working Group of the Psychiatric Genomics Consortium,, The RACI Consortium,, Purcell, Shaun, Stahl, Eli, Lindstrom, Sara, Perry, John R. B., Okada, Yukinori, Gusev, Alexander, Raychaudhuri, Soumya, Daly, Mark J., Patterson, Nick, Neale, Benjamin M., Price, Alkes L., Henskens, Frans A., Loughland, Carmel M., Michie, Patricia T., Schall, Ulrich, Scott, Rodney J., Trynka, Gosia, Tooney, Paul A., Wu, Jing Qin, Reshef, Yakir, Loh, Po-Ru, Anttila, Verneri, Xu, Han, Zang, Chongzhi, Farh, Kyle. Nature Publishing; 2015. Partitioning heritability by functional annotation using genome-wide association summary statistics.
Gusev, Alexander, Lee, S. Hong, Kähler, Anna K., Hultman, Christina M., Purcell, Shaun M., McCarroll, Steven A., Daly, Mark, Pasaniuc, Bogdan, Sullivan, Patrick F., Neale, Benjamin M., Wray, Naomi R., Raychaudhuri, Soumya, Trynka, Gosia, Price, Alkes L., Finucane, Hilary, Vilhjálmsson, Bjarni J., Xu, Han, Zang, Chongzhi, Ripke, Stephan, Bulik-Sullivan, Brendan, Stahl, Eli. Cell Press; 2014. Partitioning heritability of regulatory and cell-type-specific variants across 11 common diseases.
Gusev, Alexander, Mancuso, Nicholas, Ophoff, Roel A., O'Donovan, Miuchael C., Crawford, Gregory E., Geschwind, Daniel H., Katsanis, Nicholas, Sullivan, Patrick F., Pasaniuc, Bogdan, Price, Alkes L., Henskens, Frans A., Loughland, Carmel M., Won, Hyejung, Michie, Patricia T., Schall, Ulrich, Scott, Rodney J., Kousi, Maria, Finucane, Hilary K., Reshef, Yakir, Song, Lingyun, Safi, Alexias, McCarroll, Steven, Neale, Benjamin M.. Nature Publishing Group; 2018. Transcriptome-wide association study of schizophrenia and chromatin activity yields mechanistic disease insights.
Loh, Po-Ro, Bhatia, Gaurav, Kendler, Kenneth S., O'Donovan, Michael, Neale, Benjamin M., Patterson, Nick, Price, Alkes L., Henskens, Frans A., Loughland, Carmel M., Michie, Patricia T., Schall, Ulrich, Scott, Rodney J., Gusev, Alexander, Tooney, Paul A., Wu, Jing Qin, Finucane, Hilary K., Bulik-Sullivan, Brendan K., Pollack, Samuela J., Schizophrenia Working Group of the Psychiatric Genomics Consortium,, de Candia, Teresa R., Lee, Sang Hong, Wray, Naomi R.. Nature Publishing; 2015. Contrasting genetic architectures of schizophrenia and other complex diseases using fast variance-components analysis.