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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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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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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Chromosomal abnormalities and psychosis
Muir, Walter J., Pickard, Benjamin S., Blackwood, Douglas H. R.
Published in British journal of psychiatry (01.06.2006)
Published in British journal of psychiatry (01.06.2006)
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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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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
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.
Published in Nature genetics (01.05.2019)
Published in Nature genetics (01.05.2019)
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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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Verbal working memory and functional large-scale networks in schizophrenia
Dauvermann, Maria R., Moorhead, Thomas WJ, Watson, Andrew R., Duff, Barbara, Romaniuk, Liana, Hall, Jeremy, Roberts, Neil, Lee, Graham L., Hughes, Zoë A., Brandon, Nicholas J., Whitcher, Brandon, Blackwood, Douglas HR, McIntosh, Andrew M., Lawrie, Stephen M.
Published in Psychiatry research. Neuroimaging (30.12.2017)
Published in Psychiatry research. Neuroimaging (30.12.2017)
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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, 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
Published in Molecular psychiatry (01.04.2013)
Published in Molecular psychiatry (01.04.2013)
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Homozygosity mapping in a family presenting with schizophrenia, epilepsy and hearing impairment
KNIGHT, Helen M, MACLEAN, Alan, IRFAN, Muhammad, NAEEM, Farooq, CASS, Stephen, PICKARD, Benjamin S, MUIR, Walter J, BLACKWOOD, Douglas H. R, AYUB, Muhammad
Published in European journal of human genetics : EJHG (01.06.2008)
Published in European journal of human genetics : EJHG (01.06.2008)
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Genome-wide association study identifies five new schizophrenia loci
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
Published in Nature genetics (01.10.2011)
Published in Nature genetics (01.10.2011)
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Integrated analysis of environmental and genetic influences on cord blood DNA methylation in new-borns
Czamara, Darina, Eraslan, Gökçen, Page, Christian M., Lahti, Jari, Lahti-Pulkkinen, Marius, Hämäläinen, Esa, Kajantie, Eero, Laivuori, Hannele, Villa, Pia M., Reynolds, Rebecca M., Nystad, Wenche, Håberg, Siri E., London, Stephanie J., O’Donnell, Kieran J., Garg, Elika, Meaney, Michael J., Entringer, Sonja, Wadhwa, Pathik D., Buss, Claudia, Jones, Meaghan J., Lin, David T. S., MacIsaac, Julie L., Kobor, Michael S., Koen, Nastassja, Zar, Heather J., Koenen, Karestan C., Dalvie, Shareefa, Stein, Dan J., Kondofersky, Ivan, Müller, Nikola S., Theis, Fabian J., Räikkönen, Katri, Binder, Elisabeth B.
Published in Nature communications (11.06.2019)
Published in Nature communications (11.06.2019)
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Reversal of proliferation deficits caused by chromosome 16p13.11 microduplication through targeting NFκB signaling: an integrated study of patient-derived neuronal precursor cells, cerebral organoids and in vivo brain imaging
Johnstone, Mandy, Vasistha, Navneet A., Barbu, Miruna C., Dando, Owen, Burr, Karen, Christopher, Edward, Glen, Sophie, Robert, Christelle, Fetit, Rana, Macleod, Kenneth G., Livesey, Matthew R., Clair, David St, Blackwood, Douglas H. R., Millar, Kirsty, Carragher, Neil O., Hardingham, Giles E., Wyllie, David J. A., Johnstone, Eve C., Whalley, Heather C., McIntosh, Andrew M., Lawrie, Stephen M., Chandran, Siddharthan
Published in Molecular psychiatry (01.02.2019)
Published in Molecular psychiatry (01.02.2019)
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