DISC1 and PDE4B Are Interacting Genetic Factors in Schizophrenia That Regulate cAMP Signaling von Millar, J. Kirsty, Pickard, Benjamin S., Mackie, Shaun, James, Rachel, Christie, Sheila, Buchanan, Sebastienne R., Malloy, M. Pat, Chubb, Jennifer E., Huston, Elaine, Baillie, George S., Thomson, Pippa A., Hill, Elaine V., Brandon, Nicholas J., Rain, Jean-Christophe, Camargo, L. Miguel, Whiting, Paul J., Houslay, Miles D., Douglas H. R. Blackwood, Muir, Walter J., Porteous, David J.

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Epidemiology and Heritability of Major Depressive Disorder, Stratified by Age of Onset, Sex, and Illness Course in Generation Scotland: Scottish Family Health Study (GS:SFHS) von Fernandez-Pujals, Ana Maria, Adams, Mark James, Thomson, Pippa, McKechanie, Andrew G, Blackwood, Douglas H R, Smith, Blair H, Dominiczak, Anna F, Morris, Andrew D, Matthews, Keith, Campbell, Archie, Linksted, Pamela, Haley, Chris S, Deary, Ian J, Porteous, David J, MacIntyre, Donald J, McIntosh, Andrew M

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Synaptic scaffold evolution generated components of vertebrate cognitive complexity von Nithianantharajah, Jess, Komiyama, Noboru H, McKechanie, Andrew, Johnstone, Mandy, Blackwood, Douglas H, Clair, David St, Emes, Richard D, van de Lagemaat, Louie N, Saksida, Lisa M, Bussey, Timothy J, Grant, Seth G N

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Human brain imaging studies of DISC1 in schizophrenia, bipolar disorder and depression: A systematic review von Duff, Barbara J, Macritchie, Karine A.N, Moorhead, Thomas W.J, Lawrie, Stephen M, Blackwood, Douglas H.R

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Effects of a Balanced Translocation between Chromosomes 1 and 11 Disrupting the DISC1 Locus on White Matter Integrity von Whalley, Heather C, Dimitrova, Rali, Sprooten, Emma, Dauvermann, Maria R, Romaniuk, Liana, Duff, Barbara, Watson, Andrew R, Moorhead, Bill, Bastin, Mark, Semple, Scott I, Giles, Stephen, Hall, Jeremy, Thomson, Pippa, Roberts, Neil, Hughes, Zoe A, Brandon, Nick J, Dunlop, John, Whitcher, Brandon, Blackwood, Douglas H R, McIntosh, Andrew M, Lawrie, Stephen M

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Genome-wide association study identifies 30 loci associated with bipolar disorder von Forstner, Andreas J., Wang, Yunpeng, Steinberg, Stacy, Trzaskowski, Maciej, Byrne, Enda M., Abbott, Liam, Akil, Huda, Anjorin, Adebayo, Antilla, Verneri, Barchas, Jack D., Belliveau, Richard, Pedersen, Carsten Bøcker, Bøen, Erlend, Budde, Monika, Bunney, William, Churchhouse, Claire, Clarke, Toni-Kim, Craig, David W., Cruceanu, Cristiana, Czerski, Piotr M., de Jong, Simone, Dumont, Ashley, Fischer, Sascha B., Frisén, Louise, Garnham, Julie, Giambartolomei, Claudia, Pedersen, Marianne Giørtz, Goldstein, Jaqueline, Gordon, Scott D., Green, Melissa J., Grove, Jakob, Heilbronner, Urs, Herms, Stefan, Huckins, Laura, Johnson, Jessica S., Juréus, Anders, Kandaswamy, Radhika, Knowles, James A., Lavebratt, Catharina, Lawrence, Jacob, Lee, Phil H., Levy, Shawn E., Li, Jun Z., Lucae, Susanne, Maaser, Anna, Maier, Wolfgang, McCarroll, Steve, McKay, James D., Meng, Fan, Montgomery, Grant W., Mühleisen, Thomas W., Nguyen, Hoang, Nievergelt, Caroline M., O’Donovan, Claire, Loohuis, Loes M. Olde, Ori, Anil P. S., Ösby, Urban, Perlis, Roy H., Pfennig, Andrea, Potash, James B., Reif, Andreas, Reinbold, Céline S., Rivera, Margarita, Roussos, Panos, Ryu, Euijung, Sánchez-Mora, Cristina, Slaney, Claire, Steffens, Michael, Strauss, John S., Zhang, Peng, Adolfsson, Rolf, Agartz, Ingrid, Alda, Martin, Baune, Bernhard T., Berrettini, Wade H., Biernacka, Joanna M., Blackwood, Douglas H. R., Børglum, Anders D., Corvin, Aiden, Hauser, Joanna, Kahn, René S., Lewis, Cathryn M., Li, Qingqin S., Melle, Ingrid, Morken, Gunnar, O’Donovan, Michael C., Paciga, Sara A., Pato, Carlos, Ramos-Quiroga, Josep Antoni, Ribasés, Marta, Rouleau, Guy A., Schulze, Thomas G., Sullivan, Patrick F., Vaaler, Arne E., Vincent, John B., Nurnberger, John I., Wray, Naomi R., Cichon, Sven, Scott, Laura J., Andreassen, Ole A.

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Transplanted t(1;11) patient-derived OPCs form shorter myelin internodes in the hypomyelinated shiverer mice von Vasistha, Navneet A., Johnstone, Mandy, Barton, Samantha K., Mayerl, Steffen E., Thangaraj Selvaraj, Bhuvaneish, Thomson, Pippa A., Dando, Owen, Grünewald, Ellen, Alloza, Clara, Bastin, Mark E., Livesey, Matthew R., Economides, Kyriakos, Magnani, Dario, Makedonopolou, Paraskevi, Burr, Karen, Story, David J., Blackwood, Douglas H. R., Wyllie, David J. A., McIntosh, Andrew M., Millar, J. Kirsty, ffrench-Constant, Charles, Hardingham, Giles E., Lawrie, Stephen M., Chandran, Siddharthan

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Identification of common genetic risk variants for autism spectrum disorder von Grove, Jakob, Ripke, Stephan, Als, Thomas D., Mattheisen, Manuel, Walters, Raymond K., Won, Hyejung, Pallesen, Jonatan, Agerbo, Esben, Andreassen, Ole A., Anney, Richard, Awashti, Swapnil, Belliveau, Rich, Bettella, Francesco, Buxbaum, Joseph D., Bybjerg-Grauholm, Jonas, Bækvad-Hansen, Marie, Cerrato, Felecia, Chambert, Kimberly, Christensen, Jane H., Churchhouse, Claire, Dellenvall, Karin, Demontis, Ditte, De Rubeis, Silvia, Devlin, Bernie, Djurovic, Srdjan, Dumont, Ashley L., Goldstein, Jacqueline I., Hansen, Christine S., Hauberg, Mads Engel, Hollegaard, Mads V., Hope, Sigrun, Howrigan, Daniel P., Huang, Hailiang, Hultman, Christina M., Klei, Lambertus, Maller, Julian, Martin, Joanna, Martin, Alicia R., Moran, Jennifer L., Nyegaard, Mette, Nærland, Terje, Palmer, Duncan S., Palotie, Aarno, Pedersen, Carsten Bøcker, Pedersen, Marianne Giørtz, dPoterba, Timothy, Poulsen, Jesper Buchhave, Pourcain, Beate St, Qvist, Per, Rehnström, Karola, Reichenberg, Abraham, Reichert, Jennifer, Robinson, Elise B., Roeder, Kathryn, Roussos, Panos, Saemundsen, Evald, Sandin, Sven, Satterstrom, F. Kyle, Davey Smith, George, Stefansson, Hreinn, Steinberg, Stacy, Stevens, Christine R., Sullivan, Patrick F., Turley, Patrick, Walters, G. Bragi, Xu, Xinyi, Stefansson, Kari, Geschwind, Daniel H., Nordentoft, Merete, Hougaard, David M., Werge, Thomas, Mors, Ole, Mortensen, Preben Bo, Neale, Benjamin M., Daly, Mark J., Børglum, Anders D.

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A Cytogenetic Abnormality and Rare Coding Variants Identify ABCA13 as a Candidate Gene in Schizophrenia, Bipolar Disorder, and Depression von Knight, Helen M., Pickard, Benjamin S., Maclean, Alan, Malloy, Mary P., Soares, Dinesh C., McRae, Allan F., Condie, Alison, White, Angela, Hawkins, William, McGhee, Kevin, van Beck, Margaret, MacIntyre, Donald J., Starr, John M., Deary, Ian J., Visscher, Peter M., Porteous, David J., Cannon, Ronald E., St Clair, David, Muir, Walter J., Blackwood, Douglas H.R.

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Clustered coding variants in the glutamate receptor complexes of individuals with schizophrenia and bipolar disorder von Frank, René A W, McRae, Allan F, Pocklington, Andrew J, van de Lagemaat, Louie N, Navarro, Pau, Croning, Mike D R, Komiyama, Noboru H, Bradley, Sophie J, Challiss, R A John, Armstrong, J Douglas, Finn, Robert D, Malloy, Mary P, MacLean, Alan W, Harris, Sarah E, Starr, John M, Bhaskar, Sanjeev S, Howard, Eleanor K, Hunt, Sarah E, Coffey, Alison J, Ranganath, Venkatesh, Deloukas, Panos, Rogers, Jane, Muir, Walter J, Deary, Ian J, Blackwood, Douglas H, Visscher, Peter M, Grant, Seth G N

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Genome-wide association study reveals greater polygenic loading for schizophrenia in cases with a family history of illness von 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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Genome-wide association study identifies five new schizophrenia loci von Ripke, Stephan, Sanders, Alan R, Kendler, Kenneth S, Levinson, Douglas F, Sklar, Pamela, Holmans, Peter A, Lin, Dan-Yu, Duan, Jubao, Ophoff, Roel A, Andreassen, Ole A, Scolnick, Edward, Cichon, Sven, St Clair, David, Corvin, Aiden, Gurling, Hugh, Werge, Thomas, Rujescu, Dan, Blackwood, Douglas H R, Pato, Carlos N, Malhotra, Anil K, Purcell, Shaun, Dudbridge, Frank, Neale, Benjamin M, Rossin, Lizzy, Visscher, Peter M, Posthuma, Danielle, Ruderfer, Douglas M, Fanous, Ayman, Stefansson, Hreinn, Steinberg, Stacy, Mowry, Bryan J, Golimbet, Vera, De Hert, Marc, Jonsson, Erik G, Bitter, Istvan, Pietilaeinen, Olli P H, Collier, David A, Tosato, Sarah, Agartz, Ingrid, Albus, Margot, Alexander, Madeline, Amdur, Richard L, Amin, Farooq, Bass, Nicholas, Bergen, Sarah E, Black, Donald W, Boerglum, Anders D, Brown, Matthew A, Bruggeman, Richard, Buccola, Nancy G

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GRIK4/KA1 protein expression in human brain and correlation with bipolar disorder risk variant status von Knight, Helen M., Walker, Robert, James, Rachel, Porteous, David J., Muir, Walter J., Blackwood, Douglas H.R., Pickard, Benjamin S.

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Barriers to advance care planning with patients as perceived by nurses and other healthcare professionals: A systematic review von Blackwood, Douglas H., Walker, David, Mythen, Monty G., Taylor, Rachel M., Vindrola‐Padros, Cecilia

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DNA methylation in a Scottish family multiply affected by bipolar disorder and major depressive disorder von Walker, Rosie May, Christoforou, Andrea Nikie, McCartney, Daniel L, Morris, Stewart W, Kennedy, Nicholas A, Morten, Peter, Anderson, Susan Maguire, Torrance, Helen Scott, Macdonald, Alix, Sussmann, Jessika Elizabeth, Whalley, Heather Clare, Blackwood, Douglas H R, McIntosh, Andrew Mark, Porteous, David John, Evans, Kathryn Louise

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Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects von Merico, Daniele, Antaki, Danny, Shetty, Aniket, Gujral, Madhusudan, Brandler, William M, Malhotra, Dheeraj, Alexander, Madeline, Belliveau, Richard A, Bergen, Sarah E, Bertalan, Marcelo, Bevilacqua, Elizabeth, Cantor, Rita M, Carrera, Noa, Cormican, Paul, Crespo-Facorro, Benedicto, Curtis, David, Davidson, Michael, Degenhardt, Franziska, Del Favero, Jurgen, DeLisi, Lynn E, Dudbridge, Frank, Eichhammer, Peter, Eriksson, Johan, Essioux, Laurent, Farrell, Martilias S, Freedman, Robert, Freimer, Nelson B, Georgieva, Lyudmila, Gershon, Elliot S, Giegling, Ina, Godard, Stephanie, Goldstein, Jacqueline I, Hamshere, Marian L, Hartmann, Annette M, Hofman, Andrea, Kähler, Anna K, Kalaydjieva, Luba, Kelly, Brian J, Lee, S Hong, Legge, Sophie E, Lerer, Bernard, Levy, Deborah L, Maher, Brion S, Mattingsdal, Morten, McDonald, Colm, Metspalu, Andres, Milanova, Vihra, Morris, Derek W, Murray, Robin M, Nestadt, Gerald, Nicodemus, Kristin K, Nordin, Annelie, Oh, Sang-Yun, Olsen, Line, Van Os, Jim, Pantelis, Christos, Pers, Tune H, Powell, John, Price, Alkes, Pulver, Ann E, Purcell, Shaun M, Rasmussen, Henrik B, Richards, Alexander L, Roussos, Panos, Schall, Ulrich, Schwab, Sibylle G, Smoller, Jordan W, Spencer, Chris C A, Stahl, Eli A, Stroup, T Scott, Suvisaari, Jaana, Svrakic, Dragan M, Szatkiewicz, Jin P, Veijola, Juha, Waddington, John, Webb, Bradley T, Williams, Nigel M, Williams, Stephanie, Wolen, Aaron R, Adolfsson, Rolf, Blackwood, Douglas H R, Bramon, Elvira, Buxbaum, Joseph D, Collier, David A, Daly, Mark J, Darvasi, Ariel, Domenici, Enrico, Gill, Michael, Iwata, Nakao, Jablensky, Assen V, Jönsson, Erik G, Kirov, George, Knight, Jo, Levinson, Douglas F, Ophoff, Roel A, Owen, Michael J, Rietschel, Marcella, Rujescu, Dan, O'Donovan, Michael C, Neale, Benjamin M

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Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs von Lee, S Hong, Ripke, Stephan, Neale, Benjamin M, Faraone, Stephen V, Purcell, Shaun M, Perlis, Roy H, Mowry, Bryan J, Thapar, Anita, Goddard, Michael E, Witte, John S, Absher, Devin, Agartz, Ingrid, Akil, Huda, Amin, Farooq, Andreassen, Ole A, Anjorin, Adebayo, Anney, Richard, Anttila, Verneri, Arking, Dan E, Asherson, Philip, Azevedo, Maria H, Backlund, Lena, Badner, Judith A, Bailey, Anthony J, Banaschewski, Tobias, Barchas, Jack D, Barnes, Michael R, Barrett, Thomas B, Bass, Nicholas, Battaglia, Agatino, Bauer, Michael, Bayés, Mònica, Bellivier, Frank, Bergen, Sarah E, Berrettini, Wade, Betancur, Catalina, Bettecken, Thomas, Biederman, Joseph, Binder, Elisabeth B, Black, Donald W, Blackwood, Douglas H R, Bloss, Cinnamon S, Boehnke, Michael, Boomsma, Dorret I, Breen, Gerome, Breuer, René, Bruggeman, Richard, Cormican, Paul, Buccola, Nancy G, Buitelaar, Jan K, Bunney, William E, Buxbaum, Joseph D, Byerley, William F, Byrne, Enda M, Caesar, Sian, Cahn, Wiepke, Cantor, Rita M, Casas, Miguel, Chakravarti, Aravinda, Chambert, Kimberly, Choudhury, Khalid, Cichon, Sven, Cloninger, C Robert, Collier, David A, Cook, Edwin H, Coon, Hilary, Cormand, Bru, Corvin, Aiden, Coryell, William H, Craig, David W, Craig, Ian W, Crosbie, Jennifer, Cuccaro, Michael L, Curtis, David, Czamara, Darina, Datta, Susmita, Dawson, Geraldine, Day, Richard, De Geus, Eco J, Degenhardt, Franziska, Djurovic, Srdjan, Donohoe, Gary J, Doyle, Alysa E, Duan, Jubao, Dudbridge, Frank, Duketis, Eftichia, Ebstein, Richard P, Edenberg, Howard J, Elia, Josephine, Ennis, Sean, Etain, Bruno, Fanous, Ayman, Farmer, Anne E, Ferrier, I Nicol, Flickinger, Matthew, Fombonne, Eric, Foroud, Tatiana, Frank, Josef, Franke, Barbara, Fraser, Christine

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Disrupted in schizophrenia 1 and phosphodiesterase 4B: towards an understanding of psychiatric illness von Millar, J. Kirsty, Mackie, Shaun, Clapcote, Steven J., Murdoch, Hannah, Pickard, Ben S., Christie, Sheila, Muir, Walter J., Blackwood, Douglas H., Roder, John C., Houslay, Miles D., Porteous, David J.

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A mega-analysis of genome-wide association studies for major depressive disorder von Ripke, Stephan, Wray, Naomi R, Lewis, Cathryn M, Hamilton, Steven P, Weissman, Myrna M, Breen, Gerome, Byrne, Enda M, Blackwood, Douglas H R, Boomsma, Dorret I, Cichon, Sven, Heath, Andrew C, Holsboer, Florian, Lucae, Susanne, Madden, Pamela A F, Martin, Nicholas G, McGuffin, Peter, Muglia, Pierandrea, Noethen, Markus M, Penninx, Brenda P, Pergadia, Michele L, Potash, James B, Rietschel, Marcella, Lin, Danyu, Müller-Myhsok, Bertram, Shi, Jianxin, Steinberg, Stacy, Grabe, Hans J, Lichtenstein, Paul, Magnusson, Patrik, Perlis, Roy H, Preisig, Martin, Smoller, Jordan W, Stefansson, Kari, Uher, Rudolf, Kutalik, Zoltan, Tansey, Katherine E, Teumer, Alexander, Viktorin, Alexander, Barnes, Michael R, Bettecken, Thomas, Binder, Elisabeth B, Breuer, René, Castro, Victor M, Churchill, Susanne E, Coryell, William H, Craddock, Nick, Craig, Ian W, Czamara, Darina, De Geus, Eco J, Degenhardt, Franziska, Farmer, Anne E, Fava, Maurizio, Frank, Josef, Gainer, Vivian S, Gallagher, Patience J, Gordon, Scott D, Goryachev, Sergey, Gross, Magdalena, Guipponi, Michel, Henders, Anjali K, Herms, Stefan, Hickie, Ian B, Hoefels, Susanne, Hoogendijk, Witte, Hottenga, Jouke Jan, Iosifescu, Dan V, Ising, Marcus, Jones, Ian, Jones, Lisa, Jung-Ying, Tzeng, Knowles, James A, Kohane, Isaac S, Kohli, Martin A, Korszun, Ania, Landen, Mikael, Lawson, William B, Lewis, Glyn, Macintyre, Donald, Maier, Wolfgang, Mattheisen, Manuel, McGrath, Patrick J, McIntosh, Andrew, McLean, Alan, Middeldorp, Christel M, Middleton, Lefkos, Montgomery, Grant M, Murphy, Shawn N, Nauck, Matthias, Nolen, Willem A, Nyholt, Dale R, O'Donovan, Michael, Oskarsson, Högni, Pedersen, Nancy, Scheftner, William A, Schulz, Andrea, Schulze, Thomas G, Shyn, Stanley I, Sigurdsson, Engilbert, Slager, Susan L, Smit, Johannes H

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Cognitive endophenotypes in a family with bipolar disorder with a risk locus on chromosome 4 von Drysdale, Emma, Knight, Helen M, McIntosh, Andrew M, Blackwood, Douglas HR

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