Synaptic scaffold evolution generated components of vertebrate cognitive complexity
Nithianantharajah, Jess, Komiyama, Noboru H, McKechanie, Andrew, Johnstone, Mandy, Blackwood, Douglas H, St Clair, David, Emes, Richard D, van de Lagemaat, Louie N, Saksida, Lisa M, Bussey, Timothy J, Grant, Seth G N
Published in Nature neuroscience (01.01.2013)
Published in Nature neuroscience (01.01.2013)
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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)
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
Published in PloS one (16.11.2015)
Published in PloS one (16.11.2015)
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DISC1 and PDE4B Are Interacting Genetic Factors in Schizophrenia That Regulate cAMP Signaling
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.
Published in Science (American Association for the Advancement of Science) (18.11.2005)
Published in Science (American Association for the Advancement of Science) (18.11.2005)
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Effects of a Balanced Translocation between Chromosomes 1 and 11 Disrupting the DISC1 Locus on White Matter Integrity
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
Published in PloS one (23.06.2015)
Published in PloS one (23.06.2015)
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Transplanted t(1;11) patient-derived OPCs form shorter myelin internodes in the hypomyelinated shiverer mice
Vasistha, Navneet A, Johnstone, Mandy, Barton, Samantha K, Mayerl, Steffen E, Thangaraj Selvaraj, Bhuvaneish, Thomson, Pippa A, Dando, Owen
Published in Molecular psychiatry (01.11.2019)
Published in Molecular psychiatry (01.11.2019)
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Clustered coding variants in the glutamate receptor complexes of individuals with schizophrenia and bipolar disorder
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
Published in PloS one (29.04.2011)
Published in PloS one (29.04.2011)
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Disrupted in schizophrenia 1 and phosphodiesterase 4B: towards an understanding of psychiatric illness
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.
Published in The Journal of physiology (15.10.2007)
Published in The Journal of physiology (15.10.2007)
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DNA methylation in a Scottish family multiply affected by bipolar disorder and major depressive disorder
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
Published in Clinical epigenetics (20.01.2016)
Published in Clinical epigenetics (20.01.2016)
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GRIK4/KA1 protein expression in human brain and correlation with bipolar disorder risk variant status
Knight, Helen M., Walker, Robert, James, Rachel, Porteous, David J., Muir, Walter J., Blackwood, Douglas H.R., Pickard, Benjamin S.
Published in American journal of medical genetics. Part B, Neuropsychiatric genetics (01.01.2012)
Published in American journal of medical genetics. Part B, Neuropsychiatric genetics (01.01.2012)
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A Cytogenetic Abnormality and Rare Coding Variants Identify ABCA13 as a Candidate Gene in Schizophrenia, Bipolar Disorder, and Depression
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.
Published in American journal of human genetics (11.12.2009)
Published in American journal of human genetics (11.12.2009)
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Cognitive endophenotypes in a family with bipolar disorder with a risk locus on chromosome 4
Drysdale, Emma, Knight, Helen M, McIntosh, Andrew M, Blackwood, Douglas HR
Published in Bipolar disorders (01.03.2013)
Published in Bipolar disorders (01.03.2013)
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Association of GPR50, an X-linked orphan G protein-coupled receptor, and affective disorder in an independent sample of the Scottish population
MacIntyre, Donald J., McGhee, Kevin A., MacLean, Alan W., Afzal, Maryam, Briffa, Katy, Henry, Brian, Thomson, Pippa A., Muir, Walter J., Blackwood, Douglas H.R.
Published in Neuroscience letters (21.05.2010)
Published in Neuroscience letters (21.05.2010)
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Genome-wide association study reveals greater polygenic loading for schizophrenia in cases with a family history of illness
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.
Published in American journal of medical genetics. Part B, Neuropsychiatric genetics (01.03.2016)
Published in American journal of medical genetics. Part B, Neuropsychiatric genetics (01.03.2016)
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Identification of common genetic risk variants for autism spectrum disorder
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
Published in Nature genetics (01.03.2019)
Published in Nature genetics (01.03.2019)
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Genome-wide association study identifies 30 loci associated with bipolar disorder
Stahl, Eli A, Forstner, Andreas J, McQuillin, Andrew, Coleman, Jonathan R I, de Leeuw, Christiaan A, Steinberg, Stacy, Pavlides, Jennifer M Whitehead, Richards, Alexander L, Akil, Huda, Als, Thomas D, Awasthi, Swapnil, Barchas, Jack D, Boks, Marco P, Byerley, William, Casas, Miquel, Cerrato, Felecia, Craig, David W, Czerski, Piotr M, Dale, Anders M, de Jong, Simone, Degenhardt, Franziska, Djurovic, Srdjan, Fan, Chun Chieh, Forty, Liz, Frank, Josef, Fraser, Christine, Freimer, Nelson B, Gade, Katrin, Garnham, Julie, Goldstein, Jaqueline, Greenwood, Tiffany A, Hautzinger, Martin, Heilbronner, Urs, Herms, Stefan, Hoffmann, Per, Holland, Dominic, Huckins, Laura, Jamain, Stéphane, Johnson, Jessica S, Kandaswamy, Radhika, Lavebratt, Catharina, Levy, Shawn E, MacIntyre, Donald J, Martinsson, Lina, McInnis, Melvin G, McKay, James D, Montgomery, Grant W, Adolfsson, Annelie Nordin, Ori, Anil P S, Pfennig, Andrea, Regeer, Eline J, Reif, Andreas, Rivas, Fabio, Scheftner, William A, Shilling, Paul D, Slaney, Claire, Søholm Hansen, Christine, Spijker, Anne T, Streit, Fabian, Vedder, Helmut, Weickert, Thomas W, Xi, Simon, Xu, Wei, Zhang, Peng, Alda, Martin, Backlund, Lena, Baune, Bernhard T, Berrettini, Wade H, Blackwood, Douglas H R, Boehnke, Michael, Craddock, Nicholas, Esko, Tõnu, Etain, Bruno, Frye, Mark, Fullerton, Janice M, Gershon, Elliot S, Goes, Fernando, Hauser, Joanna, Hougaard, David M, Hultman, Christina M, Kahn, René S, Kirov, George, Leboyer, Marion, Mitchell, Philip B, Mors, Ole, Nöthen, Markus M, Oedegaard, Ketil J, Owen, Michael J, Paciga, Sara A, Pato, Carlos, Ramos-Quiroga, Josep Antoni, Schofield, Peter R, Serretti, Alessandro, Smoller, Jordan W, Vaaler, Arne E, Vieta, Eduard, Nurnberger, John I, Ophoff, Roel A, Andreassen, Ole A, Kelsoe, John
Published in Nature genetics (01.05.2019)
Published in Nature genetics (01.05.2019)
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Barriers to advance care planning with patients as perceived by nurses and other healthcare professionals: A systematic review
Blackwood, Douglas H., Walker, David, Mythen, Monty G., Taylor, Rachel M., Vindrola‐Padros, Cecilia
Published in Journal of clinical nursing (01.12.2019)
Published in Journal of clinical nursing (01.12.2019)
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A novel balanced chromosomal translocation found in subjects with schizophrenia and schizotypal personality disorder: Altered l-serine level associated with disruption of PSAT1 gene expression
Ozeki, Yuji, Pickard, Benjamin S., Kano, Shin-ichi, Malloy, Mary P., Zeledon, Mariela, Sun, Daniel Q., Fujii, Kumiko, Wakui, Keiko, Shirayama, Yukihiko, Fukushima, Yoshimitsu, Kunugi, Hiroshi, Hashimoto, Kenji, Muir, Walter J., Blackwood, Douglas H., Sawa, Akira
Published in Neuroscience research (01.02.2011)
Published in Neuroscience research (01.02.2011)
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A genome wide survey supports the involvement of large copy number variants in schizophrenia with and without intellectual disability
Derks, Eske M., Ayub, Muhammad, Chambert, Kimberly, Del Favero, Jurgen, Johnstone, Mandy, MacGregor, Stuart, Maclean, Alan, McKechanie, Andrew G., McRae, Allan F., Moran, Jennifer L., Pickard, Benjamin S., Purcell, Shaun, Sklar, Pamela, StCLair, David M., Wray, Naomi R., Visscher, Peter M., Blackwood, Douglas H. R.
Published in American journal of medical genetics. Part B, Neuropsychiatric genetics (01.12.2013)
Published in American journal of medical genetics. Part B, Neuropsychiatric genetics (01.12.2013)
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A mega-analysis of genome-wide association studies for major depressive disorder
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, 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, Kutalik, Zoltan, Teumer, Alexander, Viktorin, Alexander, Barnes, Michael R, Bettecken, Thomas, Binder, Elisabeth B, 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, Gallagher, Patience J, Gordon, Scott D, Goryachev, Sergey, Gross, Magdalena, Henders, Anjali K, Herms, Stefan, Hickie, Ian B, Hoefels, Susanne, Hoogendijk, Witte, Iosifescu, Dan V, Ising, Marcus, Jones, Ian, Jones, Lisa, Jung-Ying, Tzeng, Knowles, James A, Kohli, Martin A, Korszun, Ania, Landen, Mikael, Lawson, William B, Lewis, Glyn, Macintyre, Donald, Maier, Wolfgang, McIntosh, Andrew, McLean, Alan, Middeldorp, Christel M, Middleton, Lefkos, Montgomery, Grant M, Murphy, Shawn N, Nauck, Matthias, Nolen, Willem A, 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, Stefansson, Hreinn, Steffens, Michael, Thorgeirsson, Thorgeir, Treutlein, Jens, Uhr, Manfred, van den Oord, Edwin J C G, Van Grootheest, Gerard, Völzke, Henry, Weilburg, Jeffrey B, Willemsen, Gonneke, Daly, Mark, Levinson, Douglas F, Sullivan, Patrick F
Published in Molecular psychiatry (01.04.2013)
Published in Molecular psychiatry (01.04.2013)
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