depressive disorder and herpes zoster oticus: a case report by Chebli, H., FARH, A., belbachir, S., ouanass, A.

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Schizophrenia risk from complex variation of complement component 4 by Sekar, Aswin, Bialas, Allison R., de Rivera, Heather, Davis, Avery, Hammond, Timothy R., Kamitaki, Nolan, Tooley, Katherine, Presumey, Jessy, Baum, Matthew, Van Doren, Vanessa, Genovese, Giulio, Rose, Samuel A., Handsaker, Robert E., Daly, Mark J., Carroll, Michael C., Stevens, Beth, McCarroll, Steven A.

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Integrative analysis of 111 reference human epigenomes by Kundaje, Anshul, Meuleman, Wouter, Ernst, Jason, Bilenky, Misha, Yen, Angela, Heravi-Moussavi, Alireza, Kheradpour, Pouya, Zhang, Zhizhuo, Wang, Jianrong, Ziller, Michael J., Amin, Viren, Whitaker, John W., Schultz, Matthew D., Ward, Lucas D., Sarkar, Abhishek, Quon, Gerald, Sandstrom, Richard S., Eaton, Matthew L., Wu, Yi-Chieh, Pfenning, Andreas R., Wang, Xinchen, Claussnitzer, Melina, Liu, Yaping, Coarfa, Cristian, Harris, R. Alan, Shoresh, Noam, Epstein, Charles B., Gjoneska, Elizabeta, Leung, Danny, Xie, Wei, Hawkins, R. David, Lister, Ryan, Hong, Chibo, Gascard, Philippe, Mungall, Andrew J., Moore, Richard, Chuah, Eric, Tam, Angela, Canfield, Theresa K., Hansen, R. Scott, Kaul, Rajinder, Sabo, Peter J., Bansal, Mukul S., Carles, Annaick, Dixon, Jesse R., Farh, Kai-How, Feizi, Soheil, Karlic, Rosa, Kim, Ah-Ram, Kulkarni, Ashwinikumar, Li, Daofeng, Lowdon, Rebecca, Elliott, GiNell, Mercer, Tim R., Neph, Shane J., Onuchic, Vitor, Polak, Paz, Rajagopal, Nisha, Ray, Pradipta, Sallari, Richard C., Siebenthall, Kyle T., Sinnott-Armstrong, Nicholas A., Stevens, Michael, Thurman, Robert E., Wu, Jie, Zhang, Bo, Zhou, Xin, Beaudet, Arthur E., Boyer, Laurie A., De Jager, Philip L., Farnham, Peggy J., Fisher, Susan J., Haussler, David, Jones, Steven J. M., Li, Wei, Marra, Marco A., McManus, Michael T., Sunyaev, Shamil, Thomson, James A., Tlsty, Thea D., Tsai, Li-Huei, Wang, Wei, Waterland, Robert A., Zhang, Michael Q., Chadwick, Lisa H., Bernstein, Bradley E., Costello, Joseph F., Ecker, Joseph R., Hirst, Martin, Meissner, Alexander, Milosavljevic, Aleksandar, Ren, Bing, Stamatoyannopoulos, John A., Wang, Ting, Kellis, Manolis

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Biological insights from 108 schizophrenia-associated genetic loci by Neale, Benjamin M, Pers, Tune H, Agartz, Ingrid, Agerbo, Esben, Amin, Farooq, Bergen, Sarah E, Bigdeli, Tim B, Buckner, Randy L, Cai, Guiqing, Catts, Stanley V, Chan, Raymond C. K, Chen, Eric Y. H, Cheng, Wei, Cheung, Eric F. C, Ann Chong, Siow, Robert Cloninger, C, Cohen, Nadine, Crowley, James J, Davidson, Michael, Davis, Kenneth L, Del Favero, Jurgen, Demontis, Ditte, Dinan, Timothy, Djurovic, Srdjan, Drapeau, Elodie, Eriksson, Johan, Escott-Price, Valentina, Friedl, Marion, Fromer, Menachem, Genovese, Giulio, Georgieva, Lyudmila, Giusti-Rodriguez, Paola, Gopal, Srihari, Gratten, Jacob, Hammer, Christian, Hofman, Andrea, Hougaard, David M, Julia, Antonio, Klovins, Janis, Ausrele Kucinskiene, Zita, Hong Lee, S, Lerer, Bernard, Limborska, Svetlana, Lubinski, Jan, Macek Jr, Milan, Magnusson, Patrik K. E, Mattheisen, Manuel, McDonald, Colm, Michie, Patricia T, Milanova, Vihra, Mokrab, Younes, Muller-Myhsok, Bertram, Nenadic, Igor, Nordin, Annelie, Van Os, Jim, Endophenotypes International Consortium, Psychosis, Parkhomenko, Elena, Pejovic-Milovancevic, Milica, Pimm, Jonathan, Price, Alkes, Purcell, Shaun M, Quested, Digby, Rasmussen, Henrik B, Roffman, Joshua L, Schubert, Christian R, Schwab, Sibylle G, Scott, Rodney J, Seidman, Larry J, Silverman, Jeremy M, Smoller, Jordan W, Steinberg, Stacy, Strengman, Eric, Strohmaier, Jana, Svrakic, Dragan M, Soderman, Erik, Thirumalai, Srinivas, Toncheva, Draga, Tosato, Sarah, Veijola, Juha, Walsh, Dermot, Weiser, Mark, Wolen, Aaron R, Zheng, Xuebin, Wray, Naomi R, Visscher, Peter M, Trust Case-Control Consortium, Wellcome, Andreassen, Ole A, Blackwood, Douglas H. R, Esko, Tonu, Gill, Michael, Jablensky, Assen V, McCarroll, Steven A, Mowry, Bryan J, Owen, Michael J, Pato, Carlos N, Posthuma, Danielle, Rujescu, Dan, Sham, Pak C, Sklar, Pamela, St Clair, David

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Modeling Linkage Disequilibrium Increases Accuracy of Polygenic Risk Scores by Gusev, Alexander, Ripke, Stephan, Walters, James T.R., Agartz, Ingrid, Albus, Margot, Bene, Judit, Bevilacqua, Elizabeth, Bigdeli, Tim B., Bruggeman, Richard, Buckner, Randy L., Carr, Vaughan J., Catts, Stanley V., Chan, Raymond C.K., Cheng, Wei, Cohen, Nadine, Curtis, David, Dikeos, Dimitris, Dinan, Timothy, Eriksson, Johan, Escott-Price, Valentina, Franke, Lude, Godard, Stephanie, Goldstein, Jacqueline I., de Haan, Lieuwe, Hartmann, Annette M., Hoffmann, Per, Hofman, Andrea, Hollegaard, Mads V., Hougaard, David M., Ikeda, Masashi, Kim, Yunjung, Kucinskas, Vaidutis, Laurent, Claudine, Limborska, Svetlana, Loughland, Carmel M., Macek, Milan, Marsal, Sara, Mattheisen, Manuel, Milanova, Vihra, Mors, Ole, Mortensen, Preben B., Olsen, Line, Parkhomenko, Elena, Paunio, Tiina, Pimm, Jonathan, Purcell, Shaun M., Reichenberg, Abraham, Reimers, Mark A., Richards, Alexander L., Roussos, Panos, Ruderfer, Douglas M., Sigurdsson, Engilbert, Silverman, Jeremy M., So, Hon-Cheong, Spencer, Chris C.A., Stefansson, Hreinn, Straub, Richard E., Strengman, Eric, Strohmaier, Jana, Svrakic, Dragan M., Tosato, Sarah, Veijola, Juha, Walsh, Dermot, Wang, Dai, Weiser, Mark, Wolen, Aaron R., Wong, Emily H.M., Stefansson, Kari, Andreassen, Ole A., Ehrenreich, Hannelore, Gill, Michael, Hultman, Christina M., Jablensky, Assen V., McQuillin, Andrew, Pato, Carlos N., Rietschel, Marcella, Sham, Pak C., Sklar, Pamela, Weinberger, Daniel R., Daly, Mark J., Crisponi, Laura, Figueroa, Jonine, Gaudet, Mia M., Hall, Per, Hein, Rebecca, Irwanto, Astrid, Johansson, Mattias, Lund, Eiliv, Peto, Julian, Rahman, Nazneen, Southey, Melissa C., Travis, Ruth, Waisfisz, Quinten, Pato, Carlos, Stahl, Eli, Belbin, Gillian, Kenny, Eimear E., Purcell, Shaun, Chasman, Daniel, Neale, Benjamin

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Complement genes contribute sex-biased vulnerability in diverse disorders by Kamitaki, Nolan, Sekar, Aswin, Handsaker, Robert E., de Rivera, Heather, Tooley, Katherine, Morris, David L., Taylor, Kimberly E., Whelan, Christopher W., Tombleson, Philip, Loohuis, Loes M. Olde, Boehnke, Michael, Kimberly, Robert P., Kaufman, Kenneth M., Harley, John B., Langefeld, Carl D., Seidman, Christine E., Pato, Michele T., Pato, Carlos N., Ophoff, Roel A., Graham, Robert R., Criswell, Lindsey A., Vyse, Timothy J., McCarroll, Steven A.

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A Comparison of Ten Polygenic Score Methods for Psychiatric Disorders Applied Across Multiple Cohorts by Ni, Guiyan, Wang, Ying, Ge, Tian, Smoller, Jordan W., Ripke, Stephan, Farh, Kai-How, Holmans, Peter A., Agartz, Ingrid, Belliveau, Richard A., Bigdeli, Tim B., Black, Donald W., Buckner, Randy L., Cheng, Wei, Degenhardt, Franziska, Dudbridge, Frank, Eichhammer, Peter, Farrell, Martilias S., Frank, Josef, Freedman, Robert, Friedl, Marion, Giegling, Ina, Giusti-Rodríguez, Paola, Gratten, Jacob, Hartmann, Annette M., Hollegaard, Mads V., Kahn, René S., Karachanak-Yankova, Sena, Kavanagh, David, Keller, Matthew C., Kennedy, James L., Knowles, James A., Kucinskiene, Zita Ausrele, Li, Tao, Loughland, Carmel M., Lubinski, Jan, Maier, Wolfgang, Mallet, Jacques, Michie, Patricia T., Myin-Germeys, Inez, Nertney, Deborah A., Nicodemus, Kristin K., Nikitina-Zake, Liene, O’Callaghan, Eadbhard, O’Dushlaine, Colm, Pejovic-Milovancevic, Milica, Pocklington, Andrew J., Powell, John, Pulver, Ann E., Ruderfer, Douglas M., Salomaa, Veikko, Shi, Jianxin, Sim, Kang, Slominsky, Petr, Spencer, Chris C.A., Stahl, Eli A., Steinberg, Stacy, Stogmann, Elisabeth, Suvisaari, Jaana, Williams, Nigel M., Witt, Stephanie H., Wormley, Brandon K., Blackwood, Douglas H.R., Bramon, Elvira, Buxbaum, Joseph D., Esko, Tõnu, Gurling, Hugh, Moran, Jennifer L., Mowry, Bryan J., Owen, Michael J., Petryshen, Tracey L., Weinberger, Daniel R., Byrne, Enda M., Abdellaoui, Abdel, Andlauer, Till F.M., Castelao, Enrique, Derks, Eske M., Foo, Jerome C., Forstner, Andreas J., Hall, Lynsey S., Homuth, Georg, Jansen, Rick, Jones, Ian, Jones, Lisa A., Kretzschmar, Warren W., McGuffin, Peter, Mihailov, Evelin, Mostafavi, Sara, Nivard, Michel G., O’Reilly, Paul F., Quiroz, Jorge A., Smith, Daniel J., Thompson, Wesley, Treutlein, Jens, Umbricht, Daniel, Wu, Yang, Zhang, Futao, Grabe, Hans J., Hayward, Caroline, Lewis, Glyn, Wray, Naomi R.

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Cerebral small vessel disease genomics and its implications across the lifespan by Sargurupremraj, Muralidharan, Suzuki, Hideaki, Jian, Xueqiu, Sarnowski, Chloé, Evans, Tavia E., Eiriksdottir, Gudny, Sakaue, Saori, Terzikhan, Natalie, Zhao, Wei, Armstrong, Nicola J., Yanek, Lisa R., Kumar, Rajan B., van den Akker, Erik B., McWhirter, Rebekah E., Trompet, Stella, Mishra, Aniket, Saba, Yasaman, Satizabal, Claudia L., Beaudet, Gregory, Petit, Laurent, Tsuchida, Ami, Schilling, Sabrina, Sigurdsson, Sigurdur, Lewis, Cora E., Lopez, Oscar L., Smith, Jennifer A., Valdés Hernández, Maria C., van der Grond, Jeroen, Wright, Margaret J., Knol, Maria J., Thomson, Russell J., Le Grand, Quentin, Duperron, Marie-Gabrielle, Smith, Albert V., Schreiner, Pamela J., Evans, Denis A., Rotter, Jerome I., Beiser, Alexa S., Maniega, Susana Muñoz, Beekman, Marian, Trollor, Julian, Stott, David J., Vernooij, Meike W., Wittfeld, Katharina, Niessen, Wiro J., Soumaré, Aicha, Sidney, Stephen, Turner, Stephen T., Davies, Gail, Thalamuthu, Anbupalam, Völker, Uwe, van Buchem, Mark A., Dupuis, Josée, Bastin, Mark E., Teumer, Alexander, Amouyel, Philippe, Kwok, John B., Bülow, Robin, Deary, Ian J., Schofield, Peter R., Brodaty, Henry, Jiang, Jiyang, Tabara, Yasuharu, Setoh, Kazuya, Miyamoto, Susumu, Yoshida, Kazumichi, Nagata, Manabu, Matsuda, Fumihiko, Psaty, Bruce M., Bennett, David A., De Jager, Philip L., Mosley, Thomas H., Sachdev, Perminder S., Schmidt, Reinhold, Evangelou, Evangelos, Trégouët, David-Alexandre, Ikram, Mohammad A., DeCarli, Charles, Srikanth, Velandai K., Jukema, J. Wouter, Slagboom, Eline P., Kardia, Sharon L. R., Okada, Yukinori, Mazoyer, Bernard, Wardlaw, Joanna M., Nyquist, Paul A., Mather, Karen A., Grabe, Hans J., Schmidt, Helena, Van Duijn, Cornelia M., Gudnason, Vilmundur, Longstreth, William T., Launer, Lenore J., Lathrop, Mark, Seshadri, Sudha, Tzourio, Christophe, Adams, Hieab H., Matthews, Paul M., Fornage, Myriam, Debette, Stéphanie

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Partitioning Heritability of Regulatory and Cell-Type-Specific Variants across 11 Common Diseases by Trynka, Gosia, Stahl, Eli, Neale, Benjamin M., Farh, Kai-How, Pers, Tune H., Albus, Margot, Cahn, Wiepke, Cai, Guiqing, Carr, Vaughan J., Carrera, Noa, Cheng, Wei, Cheung, Eric F.C., Cohen, David, Cormican, Paul, Craddock, Nick, Demontis, Ditte, Djurovic, Srdjan, Donohoe, Gary, Dudbridge, Frank, Durmishi, Naser, Eriksson, Johan, Farrell, Martilias S., Freimer, Nelson B., Fromer, Menachem, Godard, Stephanie, Goldstein, Jacqueline I., Grove, Jakob, Hartmann, Annette M., Henskens, Frans A., Herms, Stefan, Hirschhorn, Joel N., Hoffmann, Per, Hougaard, David M., Ikeda, Masashi, Julià, Antonio, Kelly, Brian J., Kennedy, James L., Kucinskas, Vaidutis, Kuzelova-Ptackova, Hana, Laurent, Claudine, Lee, S. Hong, Li, Tao, Lieberman, Jeffrey, Limborska, Svetlana, Loughland, Carmel M., Lnnqvist, Jouko, Marsal, Sara, McCarley, Robert W., Meijer, Carin J., Melegh, Bela, Melle, Ingrid, Milani, Lili, Mors, Ole, Myin-Germeys, Inez, Nikitina-Zake, Liene, O’Callaghan, Eadbhard, O’Dushlaine, Colm, O’Neill, F. Anthony, Oh, Sang-Yun, Pantelis, Christos, Parkhomenko, Elena, Perkins, Diana O., Powell, John, Quested, Digby, Salomaa, Veikko, Schubert, Christian R., Shi, Jianxin, Sigurdsson, Engilbert, Sim, Kang, Stogmann, Elisabeth, Strengman, Eric, Suvisaari, Jaana, Thirumalai, Srinivas, Veijola, Juha, Walsh, Dermot, Weiser, Mark, Witt, Stephanie H., Wong, Emily H.M., Wu, Jing Qin, Stefansson, Kari, Blackwood, Douglas H.R., Ehrenreich, Hannelore, Gurling, Hugh, Hultman, Christina M., Kirov, George, Malhotra, Anil K., McCarroll, Steven A., McQuillin, Andrew, Palotie, Aarno, Rietschel, Marcella, Sham, Pak C., O’Donovan, Michael C., Bergen, Sarah, Magnusson, Patrik K.E., Scolnick, Edward, Purcell, Shaun M., Pasaniuc, Bogdan, Sullivan, Patrick F., Raychaudhuri, Soumya, Price, Alkes L.

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Sex-Dependent Shared and Nonshared Genetic Architecture Across Mood and Psychotic Disorders by Alexander, Madeline, Amin, Farooq, Bacanu, Silviu A., Bergen, Sarah E., Cai, Guiqing, Chambert, Kimberly D., Chen, Eric Y.H., Cloninger, C. Robert, Cohen, David, Cormican, Paul, Djurovic, Srdjan, Drapeau, Elodie, Durmishi, Naser, Genovese, Giulio, Herms, Stefan, Hofman, Andrea, Kalaydjieva, Luba, Kim, Yunjung, Kuzelova-Ptackova, Hana, Liang, Kung-Yee, Lönnqvist, Jouko, Maher, Brion S., Meier, Sandra, Milanova, Vihra, Parkhomenko, Elena, Paunio, Tiina, Purcell, Shaun M., Quested, Digby, Rasmussen, Henrik B., Richards, Alexander L., Roussos, Panos, Sim, Kang, So, Hon-Cheong, Strengman, Eric, Strohmaier, Jana, Svrakic, Dragan M., Tosato, Sarah, Weiser, Mark, Zimprich, Fritz, Wray, Naomi R., Stefansson, Kari, Visscher, Peter M., Liu, Jianjun, McQuillin, Andrew, Rujescu, Dan, Sullivan, Patrick F., Barroso, Ines, Mathew, Christopher G., Trembath, Richard C., Su, Zhan, Bumpstead, Suzannah J., Gillman, Matthew, McCann, Owen T., Iyegbe, Conrad, Milani, Lili, Palotie, Aarno, Sanders, Alan R., Bramon, Elvira, Lee, Jimmy, Breen, Gerome, Whitehead Pavlides, Jennifer M., Pedersen, Carsten Bøcker, Bøen, Erlend, Coryell, William, Dobbyn, Amanda L., Garnham, Julie, Pedersen, Marianne Giørtz, Gordon-Smith, Katherine, Kupka, Ralph, Martinsson, Lina, McKay, James D., Meng, Fan, Mullins, Niamh, Rivera, Margarita, Shehktman, Tatyana, Spijker, Anne T., Streit, Fabian, Vedder, Helmut, Weickert, Thomas W., Zandi, Peter, Zöllner, Sebastian, Kogevinas, Manolis, Nöthen, Markus M., Smeland, Olav B., Andreassen, Ole A., Abdellaoui, Abdel, Andlauer, Till F.M., Eley, Thalia C., Lind, Penelope A., Mostafavi, Sara, Smith, Daniel J., Wellmann, Jürgen, Hayward, Caroline, Schaefer, Catherine, Boomsma, Dorret I., Willemsen, Gonneke, Teumer, Alexander, Van der Auwera, Sandra, Blokland, Gabriëlla A.M., Plath, Niels

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Estimation of Genetic Correlation via Linkage Disequilibrium Score Regression and Genomic Restricted Maximum Likelihood by Moser, Gerhard, Ripke, Stephan, Walters, James T.R., Farh, Kai-How, Bulik-Sullivan, Brendan, Collier, David A., Agartz, Ingrid, Amin, Farooq, Begemann, Martin, Buccola, Nancy G., Byerley, William, Carr, Vaughan J., Carrera, Noa, Catts, Stanley V., Chong, Siow Ann, Craddock, Nick, Crowley, James J., Curtis, David, Davidson, Michael, Davis, Kenneth L., Demontis, Ditte, Dinan, Timothy, Donohoe, Gary, Drapeau, Elodie, Essioux, Laurent, Fanous, Ayman H., Franke, Lude, Georgieva, Lyudmila, Godard, Stephanie, Hammer, Christian, Hansen, Mark, Hansen, Thomas, Henskens, Frans A., Hirschhorn, Joel N., Hollegaard, Mads V., Hougaard, David M., Ikeda, Masashi, Joa, Inge, Juliá, Antonio, Kahn, René S., Karachanak-Yankova, Sena, Karjalainen, Juha, Khrunin, Andrey, Li, Miaoxin, Lieberman, Jeffrey, Lönnqvist, Jouko, Mattheisen, Manuel, Mattingsda, Morten, McDonald, Colm, Melle, Ingrid, Milanova, Vihra, Mokrab, Younes, Murray, Robin M., Nenadic, Igor, O’Neill, F. Anthony, Van Os, Jim, Papio, Sergi, Parkhomenko, Elena, Perkins, Diana O., Pietiläinenl, Olli, Pulver, Ann E., Purcell, Shaun M., Rasmussen, Henrik B., Reichenberg, Abraham, Richards, Alexander L., Ruderfer, Douglas M., Salomaa, Veikko, Sanders, Alan R., Scott, Rodney J., Silverman, Jeremy M., Smoller, Jordan W., So, Hon-Cheong, Spencer, Chris C.A., Stefansson, Hreinn, Stogmann, Elisabeth, Strengman, Eric, Svrakic, Dragan M., Söderman, Erik, Toncheva, Draga, Veijola, Juha, Walsh, Dermot, Weiser, Mark, Wildenauer, Dieter B., Williams, Nigel M., Williams, Stephanie, Witt, Stephanie H., Wolen, Aaron R., Xi, Hualin Simon, Zai, Clement C., Stefansson, Kari, Blackwood, Douglas H.R., Buxbaum, Joseph D., Esko, Tõnu, Gill, Michael, McQuillin, Andrew, Moran, Jennifer L., Petryshen, Tracey L., Rietsche, Marcella, Sham, Pak C., Weinberger, Daniel R.

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Interaction Testing and Polygenic Risk Scoring to Estimate the Association of Common Genetic Variants with Treatment Resistance in Schizophrenia by Pardiñas, Antonio F, Smart, Sophie E, Willcocks, Isabella R, Holmans, Peter A, Dennison, Charlotte A, Lynham, Amy J, Legge, Sophie E, Baune, Bernhard T, Bigdeli, Tim B, Cairns, Murray J, Corvin, Aiden, Fanous, Ayman H, Frank, Josef, Kelly, Brian, McQuillin, Andrew, Melle, Ingrid, Mortensen, Preben B, Mowry, Bryan J, Pato, Carlos N, Periyasamy, Sathish, Rietschel, Marcella, Rujescu, Dan, Simonsen, Carmen Elisabeth, St Clair, David, Tooney, Paul, Wu, Jing Qin, Andreassen, Ole, Kowalec, Kaarina, Sullivan, Patrick F, Murray, Robin M, Owen, Michael J, MacCabe, James H, O'Donovan, Michael C, Walters, James T. R, Ajnakina, Olesya, Alameda, Luis, Barnes, Thomas R. E, Berardi, Domenico, Bonora, Elena, Camporesi, Sara, Cleusix, Martine, Conus, Philippe, Crespo-Facorro, Benedicto, D'Andrea, Giuseppe, Demjaha, Arsime, Do, Kim Q, Doody, Gillian A, Eap, Chin B, Ferchiou, Aziz, Di Forti, Marta, Guidi, Lorenzo, Homman, Lina, Jenni, Raoul, Joyce, Eileen M, Kassoumeri, Laura, Khadimallah, Inès, Lastrina, Ornella, Muratori, Roberto, Noyan, Handan, O'Neill, Francis A, Pignon, Baptiste, Restellini, Romeo, Richard, Jean-Romain, Schürhoff, Franck, Španiel, Filip, Szöke, Andrei, Tarricone, Ilaria, Tortelli, Andrea, Üçok, Alp, Vázquez-Bourgon, Javier

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A polygenic resilience score moderates the genetic risk for schizophrenia by Hess, Jonathan L., Tylee, Daniel S., Mattheisen, Manuel, Børglum, Anders D., Als, Thomas D., Grove, Jakob, Werge, Thomas, Mortensen, Preben Bo, Mors, Ole, Nordentoft, Merete, Hougaard, David M., Byberg-Grauholm, Jonas, Bækvad-Hansen, Marie, Greenwood, Tiffany A., Tsuang, Ming T., Curtis, David, Steinberg, Stacy, Sigurdsson, Engilbert, Stefánsson, Hreinn, Stefánsson, Kári, Edenberg, Howard J., Holmans, Peter, Faraone, Stephen V., Glatt, Stephen J.

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A genome-wide cross-phenotype meta-analysis of the association of blood pressure with migraine by Guo, Yanjun, Rist, Pamela M., Daghlas, Iyas, Giulianini, Franco, Kurth, Tobias, Chasman, Daniel I.

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Cross-trait analyses with migraine reveal widespread pleiotropy and suggest a vascular component to migraine headache by Siewert, Katherine M, Klarin, Derek, Damrauer, Scott M, Chang, Kyong-Mi, Tsao, Philip S, Assimes, Themistocles L, Davey Smith, George, Voight, Benjamin F

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Molecular genetic overlap between migraine and major depressive disorder by Yang, Yuanhao, Zhao, Huiying, Boomsma, Dorret I, Ligthart, Lannie, Belin, Andrea C, Smith, George Davey, Esko, Tonu, Freilinger, Tobias M, Hansen, Thomas Folkmann, Ikram, M Arfan, Kallela, Mikko, Kubisch, Christian, Paraskevi, Christofidou, Strachan, David P, Wessman, Maija, van den Maagdenberg, Arn M J M, Terwindt, Gisela M, Nyholt, Dale R

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Distinct genetic liability profiles define clinically relevant patient strata across common diseases by Trastulla, Lucia, Dolgalev, Georgii, Moser, Sylvain, Jiménez-Barrón, Laura T., Andlauer, Till F. M., von Scheidt, Moritz, Budde, Monika, Heilbronner, Urs, Papiol, Sergi, Teumer, Alexander, Homuth, Georg, Völzke, Henry, Dörr, Marcus, Falkai, Peter, Schulze, Thomas G., Gagneur, Julien, Iorio, Francesco, Müller-Myhsok, Bertram, Schunkert, Heribert, Ziller, Michael J.

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Migraine, inflammatory bowel disease and celiac disease: A Mendelian randomization study by Welander, Nike Zoe, Rask‐Andersen, Mathias, Harder, Aster V. E., Gormley, Padhraig, Anttila, Verneri, Palta, Priit, Esko, Tonu, Pers, Tune H., Cuenca‐Leon, Ester, Furlotte, Nicholas A., Kurth, Tobias, Ligthart, Lannie, Kallela, Mikko, Freilinger, Tobias M., Ran, Caroline, Gordon, Scott G., Stam, Anine H., Steinberg, Stacy, Borck, Guntram, Koiranen, Markku, Quaye, Lydia, Adams, Hieab H. H., Lehtimäki, Terho, Sarin, Antti‐Pekka, Hinds, David A., Buring, Julie E., Schürks, Markus, Hrafnsdottir, Maria Gudlaug, Hottenga, Jouke‐Jan, Penninx, Brenda W. J. H., Färkkilä, Markus, Artto, Ville, Kaunisto, Mari, Malik, Rainer, Heath, Andrew C., Martin, Nicholas G., Montgomery, Grant W., Kurki, Mitja, Kals, Mart, Mägi, Reedik, Pärn, Kalle, Hämäläinen, Eija, Huang, Hailiang, Byrnes, Andrea E., Franke, Lude, Huang, Jie, Lee, Phil H., Sandor, Cynthia, Webber, Caleb, Schreiber, Stefan, Eriksson, Johan G., Salomaa, Veikko, Heikkilä, Kauko, Loehrer, Elizabeth, Uitterlinden, Andre G., Hofman, Albert, Duijn, Cornelia M., Cherkas, Lynn, Stubhaug, Audun, Nielsen, Christopher S., Männikö, Minna, Mihailov, Evelin, Milani, Lili, Esserlind, Ann‐Louise, Werge, Thomas, Børte, Sigrid, Cormand, Bru, Eising, Else, Griffiths, Lyn, Hamalainen, Eija, Kajanne, Risto, Launer, Lenore, Lehtimaki, Terho, Lessel, Davor, Macaya, Alfons, Posthuma, Danielle, Pozo‐Rosich, Patricia, Pressman, Alice, Sintas, Celia, Zhao, Huiying, Kaprio, Jaakko, Aromaa, Arpo J., Ikram, M. Arfan, Spector, Tim, Järvelin, Marjo‐Riitta, Metspalu, Andres, Kubisch, Christian, Ferrari, Michel D., Dichgans, Martin, Wessman, Maija, Maagdenberg, Arn M. J. M., Boomsma, Dorret I., Smith, George Davey, Neale, Benjamin M., Olesen, Jes, Chasman, Daniel I., Nyholt, Dale R., Palotie, Aarno, Maagdenberg, Arn M. J. M., Schiöth, Helgi Birgir

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Age at first birth in women is genetically associated with increased risk of schizophrenia by Ni, Guiyan, Gratten, Jacob, Wray, Naomi R., Lee, Sang Hong

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Genome-wide association study reveals greater polygenic loading for schizophrenia in cases with a family history of illness by Bigdeli, Tim B., Ripke, Stephan, Bacanu, Silviu-Alin, Lee, Sang Hong, Wray, Naomi R., Gejman, Pablo V., Rietschel, Marcella, Cichon, Sven, St Clair, David, Corvin, Aiden, Kirov, George, McQuillin, Andrew, Gurling, Hugh, Rujescu, Dan, Andreassen, Ole A., Werge, Thomas, Blackwood, Douglas H. R., Pato, Carlos N., Pato, Michele T., Malhotra, Anil K., O'Donovan, Michael C., Kendler, Kenneth S., Fanous, Ayman H.

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