Genome-wide association study identifies 30 loci associated with bipolar disorder
EA Stahl, G Breen, AJ Forstner, A McQuillin, S Ripke, V Trubetskoy, M Mattheisen, Y Wang, JRI Coleman, HA Gaspar, CA de Leeuw, S Steinberg, JMW Pavlides, M Trzaskowski, EM Byrne, TH Pers, PA Holmans, AL Richards, L Abbott, E Agerbo, Huda Akil, D Albani, N Alliey-Rodriguez, TD Als, A Anjorin, V Antilla, S Awasthi, JA Badner, M Bækvad-Hansen, JD Barchas, N Bass, M Bauer, R Belliveau, . Bergen, . Pedersen, E Bøen, MP Boks, J Boocock, M Budde, W Bunney, Margit Burmeister, J Bybjerg-Grauholm, W Byerley, M Casas, F Cerrato, P Cervantes, K Chambert, AW Charney, D Chen, C Churchhouse, TK Clarke, W Coryell, DW Craig, C Cruceanu, D Curtis, PM Czerski, AM Dale, S de Jong, F Degenhardt, J Del-Favero, . DePaulo, S Djurovic, AL Dobbyn, A Dumont, T Elvsåshagen, V Escott-Price, CC Fan, SB Fischer, M Flickinger, TM Foroud, L Forty, J Frank, C Fraser, NB Freimer, L Frisén, K Gade, D Gage, J Garnham, C Giambartolomei, J Goldstein, SD Gordon, K Gordon-Smith, EK Green, MJ Green, TA Greenwood, J Grove, W Guan, J Guzman-Parra, ML Hamshere, M Hautzinger, U Heilbronner, S Herms, M Hipolito, P Hoffmann, D Holland, L Huckins, S Jamain, JS Johnson, A Juréus
Loss of the sphingolipid desaturase DEGS1 causes hypomyelinating leukodystrophy
DC Pant, I Dorboz, A Schluter, S Fourcade, N Launay, J Joya, S Aguilera-Albesa, ME Yoldi, C Casasnovas, MJ Willis, M Ruiz, D Ville, G Lesca, K Siquier-Pernet, I Desguerre, H Yan, J Wang, Margit Burmeister, L Brady, M Tarnopolsky, C Cornet, D Rubbini, J Terriente, KN James, D Musaev, . Zaki, MC Patterson, BC Lanpher, EW Klee, FP E Vairo, E Wohler, NLDM Sobreira, JS Cohen, R Maroofian, H Galehdari, N Mazaheri, G Shariati, L Colleaux, D Rodriguez, JG Gleeson, C Pujades, A Fatemi, O Boespflug-Tanguy, A Pujol
Bipolar multiplex families have an increased burden of common risk variants for psychiatric disorders
TFM Andlauer, J Guzman-Parra, F Streit, J Strohmaier, MJ González, S Gil Flores, FJ Cabaleiro Fabeiro, F del Río Noriega, FP Perez, J Haro González, G Orozco Diaz, Y de Diego-Otero, B Moreno-Küstner, G Auburger, F Degenhardt, S Heilmann-Heimbach, S Herms, P Hoffmann, J Frank, JC Foo, J Treutlein, SH Witt, S Cichon, M Kogevinas, EA Stahl, G Breen, AJ Forstner, A McQuillin, S Ripke, V Trubetskoy, M Mattheisen, Y Wang, JRI Coleman, HA Gaspar, CA de Leeuw, S Steinberg, JMW Pavlides, M Trzaskowski, TH Pers, PA Holmans, L Abbott, E Agerbo, Huda Akil, D Albani, N Alliey-Rodriguez, TD Als, A Anjorin, V Antilla, S Awasthi, JA Badner, M Bækvad-Hansen, JD Barchas, N Bass, M Bauer, R Belliveau, . Bergen, CB Pedersen, E Bøen, M Boks, J Boocock, M Budde, W Bunney, Margit Burmeister, J Bybjerg-Grauholm, W Byerley, M Casas, F Cerrato, P Cervantes, K Chambert, AW Charney, D Chen, C Churchhouse, TK Clarke, W Coryell, DW Craig, C Cruceanu, PM Czerski, AM Dale, S de Jong, J Del-Favero, . DePaulo, S Djurovic, AL Dobbyn, A Dumont, T Elvsåshagen, V Escott-Price, CC Fan, SB Fischer, M Flickinger, TM Foroud, L Forty, C Fraser, NB Freimer, L Frisén, K Gade, D Gage, J Garnham, C Giambartolomei
Extremely rare variants reveal patterns of germline mutation rate heterogeneity in humans
J Carlson, AE Locke, M Flickinger, Matthew Zawistowski, S Levy, RM Myers, Michael Boehnke, HM Kang, Laura Scott, Jun Li, S Zöllner, D Absher, Huda Akil, G Breen, Margit Burmeister, S Cohen-Woods, WG Iacono, JA Knowles, L Legrand, Q Lu, M McGue, Melvin McInnis, MT Pato, M Rivera, JL Sobell, JB Vincent, SJ Watson, Stanley Watson Jr, Sebastian Zoellner
Improving genetic prediction by leveraging genetic correlations among human diseases and traits
RM Maier, Z Zhu, SH Lee, M Trzaskowski, DM Ruderfer, EA Stahl, S Ripke, NR Wray, J Yang, PM Visscher, . Robinson, AJ Forstner, A Mcquillin, V Trubetskoy, W Wang, Y Wang, JRI Coleman, HA Gaspar, CA De Leeuw, JM Whitehead Pavlides, LM Olde Loohuis, TH Pers, PH Lee, AW Charney, AL Dobbyn, L Huckins, J Boocock, C Giambartolomei, P Roussos, N Mullins, S Awasthi, E Agerbo, TD Als, . Pedersen, J Grove, R Kupka, EJ Regeer, A Anjorin, M Casas, PB Mahon, J Allardyce, V Escott-Price, L Forty, C Fraser, M Kogevinas, J Frank, F Streit, J Strohmaier, J Treutlein, SH Witt, JL Kennedy, JS Strauss, J Garnham, C O'donovan, C Slaney, S Steinberg, TE Thorgeirsson, M Hautzinger, M Steffens, RH Perlis, C Sánchez-Mora, M Hipolito, WB Lawson, EA Nwulia, . Levy, TM Foroud, S Jamain, AH Young, JD Mckay, D Albani, P Zandi, JB Potash, P Zhang, J Raymond Depaulo, . Bergen, A Juréus, R Karlsson, R Kandaswamy, P Mcguffin, M Rivera, J Lissowska, C Cruceanu, S Lucae, P Cervantes, M Budde, K Gade, U Heilbronner, DW Morris, CS Weickert, TW Weickert, DJ Macintyre, J Lawrence, T Elvsåshagen, OB Smeland, S Djurovic, S Xi, EK Green, PM Czerski, J Hauser, Robert Thompson, Melvin McInnis, Stanley Watson Jr, Sebastian Zoellner, Fan Meng, Margit Burmeister
A correction for sample overlap in genome-wide association studies in a polygenic pleiotropy-informed framework
M LeBlanc, V Zuber, WK Thompson, OA Andreassen, A Frigessi, BK Andreassen, S Ripke, BM Neale, A Corvin, JTR Walters, KH Farh, P Lee, B Bulik-Sullivan, DA Collier, H Huang, TH Pers, I Agartz, E Agerbo, M Albus, M Alexander, F Amin, . Bacanu, M Begemann, RA Belliveau, J Bene, E Bevilacqua, TB Bigdeli, DW Black, R Bruggeman, NG Buccola, RL Buckner, W Cahn, G Cai, MJ Cairns, D Campion, RM Cantor, VJ Carr, N Carrera, SV Catts, KD Chambert, RCK Chan, EYH Chen, W Cheng, EFC Cheung, . Chong, CR Cloninger, N Cohen, P Cormican, N Craddock, B Crespo-Facorro, JJ Crowley, D Curtis, M Davidson, KL Davis, F Degenhardt, JD Favero, LE DeLisi, D Demontis, D Dikeos, T Dinan, G Donohoe, E Drapeau, J Duan, F Dudbridge, N Durmishi, P Eichhammer, J Eriksson, V Escott-Price, L Essioux, AH Fanous, . Farrell, J Frank, L Franke, R Freedman, NB Freimer, M Friedl, JI Friedman, M Fromer, G Genovese, L Georgieva, ES Gershon, I Giegling, P Giusti-Rodriguez, S Godard, JI Goldstein, V Golimbet, S Gopal, J Gratten, L de Haan, C Hammer, ML Hamshere, T Hansen, V Haroutunian, AM Hartmann, FA Henskens, S Herms, JN Hirschhorn, Michael Boehnke, Robert Thompson, Melvin McInnis, Stanley Watson Jr, Sebastian Zoellner, Margit Burmeister, Laura Scott, Fan Meng
Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 Subphenotypes
DM Ruderfer, S Ripke, A McQuillin, J Boocock, EA Stahl, JMW Pavlides, N Mullins, AW Charney, APS Ori, LMO Loohuis, E Domenici, A Di Florio, S Papiol, JL Kalman, V Trubetskoy, R Adolfsson, I Agartz, E Agerbo, Huda Akil, D Albani, M Albus, M Alda, M Alexander, N Alliey-Rodriguez, TD Als, F Amin, A Anjorin, MJ Arranz, S Awasthi, . Bacanu, JA Badner, M Baekvad-Hansen, S Bakker, G Band, JD Barchas, I Barroso, N Bass, M Bauer, BT Baune, M Begemann, C Bellenguez, RA Belliveau, F Bellivier, S Bender, J Bene, . Bergen, WH Berrettini, E Bevilacqua, JM Biernacka, TB Bigdeli, DW Black, H Blackburn, JM Blackwell, DHR Blackwood, CB Pedersen, Michael Boehnke, M Boks, AD Borglum, E Bramon, G Breen, MA Brown, R Bruggeman, NG Buccola, RL Buckner, M Budde, B Bulik-Sullivan, SJ Bumpstead, W Bunney, Margit Burmeister, JD Buxbaum, J Bybjerg-Grauholm, W Byerley, W Cahn, G Cai, MJ Cairns, D Campion, RM Cantor, VJ Carr, N Carrera, M Casas, SV Catts, P Cervantes, KD Chambert, RCK Chan, RYL Chen, W Cheng, EFC Cheung, . Chong, TK Clarke, CR Cloninger, N Cohen, JRI Coleman, DA Collier, P Cormican, W Coryell, N Craddock, DW Craig, Laura Scott, Melvin McInnis, Stanley Watson Jr, Sebastian Zoellner, Robert Thompson, Fan Meng
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