A modified version of the interlocking finger test as a bedside screening test for visuospatial deficits and dementia in Parkinson's disease von Schmidt, Nele, Strohmaier, Tim, Witt, Karsten

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Dysphagia in Patients with Acute Ischemic Stroke: Early Dysphagia Screening May Reduce Stroke-Related Pneumonia and Improve Stroke Outcomes von Al-Khaled, Mohamed, Matthis, Christine, Binder, Andreas, Mudter, Jonas, Schattschneider, Joern, Pulkowski, Ulrich, Strohmaier, Tim, Niehoff, Torsten, Zybur, Roland, Eggers, Juergen, Valdueza, Jose M., Royl, Georg

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Derœ Interlocking Finger Test als Screening-Instrument zur Detektion visuell-räumlicher Defizite und einer dementiellen Entwicklung bei Patienten mit Morbus Parkinson : eine Pilots... von Strohmaier, Tim Michael

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Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection von Pardiñas, Antonio F., Holmans, Peter, Pocklington, Andrew J., Escott-Price, Valentina, Ripke, Stephan, Carrera, Noa, Legge, Sophie E., Bishop, Sophie, Cameron, Darren, Hamshere, Marian L., Han, Jun, Hubbard, Leon, Lynham, Amy, Mantripragada, Kiran, Rees, Elliott, MacCabe, James H., McCarroll, Steven A., Baune, Bernhard T., Breen, Gerome, Byrne, Enda M., Dannlowski, Udo, Eley, Thalia C., Hayward, Caroline, Martin, Nicholas G., McIntosh, Andrew M., Plomin, Robert, Porteous, David J., Wray, Naomi R., Caballero, Armando, Geschwind, Daniel H., Huckins, Laura M., Ruderfer, Douglas M., Santiago, Enrique, Sklar, Pamela, Stahl, Eli A., Won, Hyejung, Agerbo, Esben, Als, Thomas D., Andreassen, Ole A., Bækvad-Hansen, Marie, Mortensen, Preben Bo, Pedersen, Carsten Bøcker, Børglum, Anders D., Bybjerg-Grauholm, Jonas, Djurovic, Srdjan, Durmishi, Naser, Pedersen, Marianne Giørtz, Golimbet, Vera, Grove, Jakob, Hougaard, David M., Mattheisen, Manuel, Molden, Espen, Mors, Ole, Nordentoft, Merete, Pejovic-Milovancevic, Milica, Sigurdsson, Engilbert, Silagadze, Teimuraz, Hansen, Christine Søholm, Stefansson, Kari, Stefansson, Hreinn, Steinberg, Stacy, Tosato, Sarah, Werge, Thomas, Collier, David A., Rujescu, Dan, Kirov, George, Owen, Michael J., O’Donovan, Michael C., Walters, James T. R.

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Targeted High-Throughput Sequencing Identifies Mutations in atlastin-1 as a Cause of Hereditary Sensory Neuropathy Type I von Guelly, Christian, Zhu, Peng-Peng, Leonardis, Lea, Papić, Lea, Zidar, Janez, Schabhüttl, Maria, Strohmaier, Heimo, Weis, Joachim, Strom, Tim M., Baets, Jonathan, Willems, Jan, De Jonghe, Peter, Reilly, Mary M., Fröhlich, Eleonore, Hatz, Martina, Trajanoski, Slave, Pieber, Thomas R., Janecke, Andreas R., Blackstone, Craig, Auer-Grumbach, Michaela

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The protocadherin 17 gene affects cognition, personality, amygdala structure and function, synapse development and risk of major mood disorders von Chang, H, Hoshina, N, Zhang, C, Ma, Y, Cao, H, Wang, Y, Wu, D-d, Bergen, S E, Landén, M, Hultman, C M, Preisig, M, Kutalik, Z, Castelao, E, Grigoroiu-Serbanescu, M, Forstner, A J, Strohmaier, J, Hecker, J, Schulze, T G, Müller-Myhsok, B, Reif, A, Mitchell, P B, Martin, N G, Schofield, P R, Cichon, S, Nöthen, M M, Walter, H, Erk, S, Heinz, A, Amin, N, van Duijn, C M, Meyer-Lindenberg, A, Tost, H, Xiao, X, Yamamoto, T, Rietschel, M, Li, M

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The Genetics of the Mood Disorder Spectrum: Genome-wide Association Analyses of More Than 185,000 Cases and 439,000 Controls von de Leeuw, Christiaan A., McQuillin, Andrew, Ripke, Stephan, Trzaskowski, Maciej, Agerbo, Esben, Alliey-Rodriguez, Ney, Andlauer, Till F.M., Awasthi, Swapnil, Badner, Judith A., Bækvad-Hansen, Marie, Bøen, Erlend, Castelao, Enrique, Cerrato, Felecia, Cervantes, Pablo, Colodro-Conde, Lucía, Davies, Gail, Del-Favero, Jurgen, Dumont, Ashley, Fischer, Sascha B., Foo, Jerome C., Forty, Liz, Gordon, Scott D., Green, Melissa J., Grove, Jakob, Hansen, Christine Søholm, Hansen, Thomas F., Heilbronner, Urs, van Hemert, Albert M., Hipolito, Maria, Hoffmann, Per, Holland, Dominic, Jamain, Stéphane, Jansen, Rick, Johnson, Jessica S., de Jong, Simone, Hassan Kiadeh, Farnush Farhadi, Kraft, Julia, Krogh, Jesper, Lawson, William B., Li, Yihan, Maaser, Anna, MacKinnon, Dean F., Mahon, Pamela B., Maier, Robert M., Medland, Sarah E., Mehta, Divya, Mihailov, Evelin, Montgomery, Grant W., Mullins, Niamh, Nyholt, Dale R., Ösby, Urban, Peterson, Roseann E., Pistis, Giorgio, Reinbold, Céline S., Ryu, Euijung, Schoevers, Robert, Schork, Nicholas J., Schulte, Eva C., Shehktman, Tatyana, Streit, Fabian, Thompson, Robert C., Traylor, Matthew, Vedder, Helmut, Viktorin, Alexander, Visscher, Peter M., Watson, Stanley J., Weinsheimer, Shantel Marie, Wu, Yang, Zhang, Peng, Agartz, Ingrid, Backlund, Lena, Bellivier, Frank, Blackwood, Douglas H.R., Domenici, Enrico, Fullerton, Janice M., Goes, Fernando, Hayward, Caroline, Hultman, Christina M., Jones, Ian, Kahn, René S., Kloiber, Stefan, Leboyer, Marion, Li, Qingqin S., Lucae, Susanne, Madden, Pamela A.F., Magnusson, Patrik K., Martin, Nicholas G., Mortensen, Preben Bo, Neale, Benjamin M., Nordentoft, Merete, O'Donovan, Michael C., Pato, Carlos, Pato, Michele T., Penninx, Brenda W.J. H., Posthuma, Danielle, Stefansson, Kari, Vieta, Eduard, Di Florio, Arianna, Ophoff, Roel A., Wray, Naomi R.

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Genome-wide Association for Major Depression Through Age at Onset Stratification: Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium von Power, Robert A, Tansey, Katherine E, Buttenschøn, Henriette Nørmølle, Cohen-Woods, Sarah, Bigdeli, Tim, Hall, Lynsey S, Kutalik, Zoltán, Lee, S. Hong, Ripke, Stephan, Steinberg, Stacy, Teumer, Alexander, Viktorin, Alexander, Wray, Naomi R, Arolt, Volker, Baune, Bernard T, Boomsma, Dorret I, Børglum, Anders D, Byrne, Enda M, Castelao, Enrique, Craddock, Nick, Craig, Ian W, Dannlowski, Udo, Deary, Ian J, Degenhardt, Franziska, Forstner, Andreas J, Gordon, Scott D, Grabe, Hans J, Grove, Jakob, Hamilton, Steven P, Hayward, Caroline, Heath, Andrew C, Hocking, Lynne J, Homuth, Georg, Hottenga, Jouke J, Kloiber, Stefan, Krogh, Jesper, Landén, Mikael, Lang, Maren, Levinson, Douglas F, Lichtenstein, Paul, Lucae, Susanne, MacIntyre, Donald J, Madden, Pamela, Magnusson, Patrik K.E, Martin, Nicholas G, McIntosh, Andrew M, Middeldorp, Christel M, Milaneschi, Yuri, Montgomery, Grant W, Mors, Ole, Müller-Myhsok, Bertram, Nyholt, Dale R, Oskarsson, Hogni, Owen, Michael J, Padmanabhan, Sandosh, Penninx, Brenda W.J.H, Pergadia, Michele L, Porteous, David J, Potash, James B, Preisig, Martin, Rivera, Margarita, Shi, Jianxin, Shyn, Stanley I, Sigurdsson, Engilbert, Smit, Johannes H, Smith, Blair H, Stefansson, Hreinn, Stefansson, Kari, Strohmaier, Jana, Sullivan, Patrick F, Thomson, Pippa, Thorgeirsson, Thorgeir E, Van der Auwera, Sandra, Weissman, Myrna M, Breen, Gerome, Lewis, Cathryn M

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Genetic Association of Major Depression With Atypical Features and Obesity-Related Immunometabolic Dysregulations von Milaneschi, Yuri, Lamers, Femke, Peyrot, Wouter J, Baune, Bernhard T, Breen, Gerome, Dehghan, Abbas, Forstner, Andreas J, Grabe, Hans J, Homuth, Georg, Kan, Carol, Lewis, Cathryn, Mullins, Niamh, Nauck, Matthias, Pistis, Giorgio, Preisig, Martin, Rivera, Margarita, Rietschel, Marcella, Streit, Fabian, Strohmaier, Jana, Teumer, Alexander, Van der Auwera, Sandra, Wray, Naomi R, Boomsma, Dorret I, Penninx, Brenda W. J. H

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A large-scale genome-wide association study meta-analysis of cannabis use disorder von Johnson, Emma C, Demontis, Ditte, Thorgeirsson, Thorgeir E, Walters, Raymond K, Polimanti, Renato, Hatoum, Alexander S, Clarke, Toni-Kim, Baranger, David A A, Wedow, Robbee, Bacanu, Silviu-Alin, Brown, Sandra A, Degenhardt, Louisa, Goate, Alison M, Gordon, Scott D, Lind, Penelope A, McQueen, Matthew B, Pearson, John F, Peterson, Roseann E, Reynolds, Maureen D, Saccone, Nancy L, Sherva, Richard, Tyrfingsson, Thorarinn, Wall, Tamara L, Werge, Thomas, Wetherill, Leah, Wright, Margaret J, Zellers, Stephanie, Boardman, Jason D, Copeland, William E, Gillespie, Nathan A, Grucza, Richard A, Kendler, Kenneth S, Maes, Hermine H, McIntosh, Andrew M, Porjesz, Bernice, Vanyukov, Michael M, Vrieze, Scott, Walters, Raymond, Polimanti, Renato, Johnson, Emma, He, June, Adkins, Amy, Biernacka, Joanna, Bigdeli, Tim, Chen, Li-Shiun, Docherty, Anna, Edwards, Alexis, Gordon, Scott, Hartmann, Annette, Hartz, Sarah, Hodgkinson, Colin, Hottenga, Jouke, Lahti-Pulkkinen, Marius, Ligthart, Lannie, Maher, Brion, McQueen, Matthew, Meyers, Jacquelyn, Milaneschi, Yuri, Palviainen, Teemu, Pearson, John, Ripatti, Samuli, Saccone, Nancy, Sherva, Richard, Thomas, Nathaniel, Wang, Jen-Chyong, Wedow, Robbee, Choi, Doo-Sup, Culverhouse, Robert, Dahmen, Norbert, Degenhardt, Louisa, Domingue, Benjamin, Frye, Mark, Gäbel, Wolfgang, Mann, Karl, Nurnberger, John, Reynolds, Maureen, Schuckit, Marc, Soyka, Michael, Wodarz, Norbert, Zill, Peter, Boomsma, Dorret, Bierut, Laura, Bucholz, Kathleen, Cichon, Sven, Costello, E. Jane, Diazgranados, Nancy, Dick, Danielle, Goldman, David, Heath, Andrew, Hesselbrock, Victor, Hewitt, John, Hopfer, Christian, Kendler, Kenneth, Madden, Pamela, Magnusson, Patrik, Medland, Sarah, Rietschel, Marcella, Riley, Brien, Silberg, Judy, Stefansson, Kari

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A phenome-wide association and Mendelian Randomisation study of polygenic risk for depression in UK Biobank von Shen, Xueyi, Howard, David M., Adams, Mark J., Hill, W. David, Clarke, Toni-Kim, Deary, Ian J., Whalley, Heather C., McIntosh, Andrew M.

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Identifying the Common Genetic Basis of Antidepressant Response von Pain, Oliver, Adams, Mark J., Byrne, Enda M., Cattaneo, Annamaria, Als, Thomas D., Hayward, Caroline, Henigsberg, Neven, Lewis, Glyn, Martin, Nicholas G., Mors, Ole, Rentería, Miguel E., Reynolds, Charles F., Rietschel, Marcella, Uher, Rudolf, Wigmore, Eleanor M., Baune, Bernhard T., Domschke, Katharina, Li, Qingqin S., Serretti, Alessandro, Turecki, Gustavo, Weinshilboum, Richard, Montgomery, Stuart, Mendlewicz, Julien, Wray, Naomi R., Ripke, Stephan, Trzaskowski, Maciej, Abdellaoui, Abdel, Agerbo, Esben, Andlauer, Till F.M., Bybjerg-Grauholm, Jonas, Clarke, Toni-Kim, Deary, Ian J., Derks, Eske M., Direk, Nese, Dolan, Conor V., Dunn, Erin C., Escott-Price, Valentina, Hassan Kiadeh, Farnush Farhadi, Gordon, Scott D., Hickie, Ian B., Horn, Carsten, Hottenga, Jouke-Jan, Howard, David M., Ising, Marcus, Jansen, Rick, Jones, Lisa A., Jorgenson, Eric, Kraft, Julia, Kretzschmar, Warren W., Maier, Wolfgang, Marchini, Jonathan, McGrath, Patrick, Mehta, Divya, Mondimore, Francis M., Mostafavi, Sara, Mullins, Niamh, Nyholt, Dale R., O’Reilly, Paul F., Oskarsson, Hogni, Owen, Michael J., Pedersen, Carsten Bøcker, Pedersen, Marianne Giørtz, Peyrot, Wouter J., Pistis, Giorgio, Mirza, Saira Saeed, Schoevers, Robert, Shi, Jianxin, Sigurdsson, Engilbert, Steinberg, Stacy, Streit, Fabian, Strohmaier, Jana, Teumer, Alexander, Thompson, Wesley, Thorgeirsson, Thorgeir E., Treutlein, Jens, Trubetskoy, Vassily, Van der Auwera, Sandra, van Hemert, Albert M., Visscher, Peter M., Wang, Yunpeng, Webb, Bradley T., Weinsheimer, Shantel Marie, Zhang, Futao, Berger, Klaus, Boomsma, Dorret I., Domenici, Enrico, Grabe, Hans J., Hayward, Caroline, Kloiber, Stefan, Lewis, Glyn, Magnusson, Patrik K., Martin, Nicholas G., Mors, Ole, Mortensen, Preben Bo, Paciga, Sara A., Porteous, David J., Stefansson, Kari, Werge, Thomas, Lewis, Cathryn M., Levinson, Douglas F.

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Dissection of phenotype reveals possible association between schizophrenia and Glutamate Receptor Delta 1 ( GRID1 ) gene promoter von Treutlein, Jens, Mühleisen, Thomas W, Frank, Josef, Mattheisen, Manuel, Herms, Stefan, Ludwig, Kerstin U, Treutlein, Tsendsesmee, Schmael, Christine, Strohmaier, Jana, Böβhenz, Katja Veronika, Breuer, René, Paul, Torsten, Witt, Stephanie H, Schulze, Thomas G, Schlösser, Ralf G.M, Nenadic, Igor, Sauer, Heinrich, Becker, Tim, Maier, Wolfgang, Cichon, Sven, Nöthen, Markus M, Rietschel, Marcella

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No Reliable Association between Runs of Homozygosity and Schizophrenia in a Well-Powered Replication Study von Johnson, Emma C, Bjelland, Douglas W, Howrigan, Daniel P, Abdellaoui, Abdel, Breen, Gerome, Borglum, Anders, Cichon, Sven, Degenhardt, Franziska, Forstner, Andreas J, Frank, Josef, Genovese, Giulio, Heilmann-Heimbach, Stefanie, Herms, Stefan, Hoffman, Per, Maier, Wolfgang, Mattheisen, Manuel, Morris, Derek, Mowry, Bryan, Müller-Mhysok, Betram, Neale, Benjamin, Nenadic, Igor, Nöthen, Markus M, O'Dushlaine, Colm, Rietschel, Marcella, Ruderfer, Douglas M, Rujescu, Dan, Schulze, Thomas G, Simonson, Matthew A, Stahl, Eli, Strohmaier, Jana, Witt, Stephanie H, Sullivan, Patrick F, Keller, Matthew C

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Publisher Correction: Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection von Pardiñas, Antonio F., Holmans, Peter, Pocklington, Andrew J., Escott-Price, Valentina, Ripke, Stephan, Carrera, Noa, Legge, Sophie E., Bishop, Sophie, Cameron, Darren, Hamshere, Marian L., Han, Jun, Hubbard, Leon, Lynham, Amy, Mantripragada, Kiran, Rees, Elliott, MacCabe, James H., McCarroll, Steven A., Baune, Bernhard T., Breen, Gerome, Byrne, Enda M., Dannlowski, Udo, Eley, Thalia C., Hayward, Caroline, Martin, Nicholas G., McIntosh, Andrew M., Plomin, Robert, Porteous, David J., Wray, Naomi R., Caballero, Armando, Geschwind, Daniel H., Huckins, Laura M., Ruderfer, Douglas M., Santiago, Enrique, Sklar, Pamela, Stahl, Eli A., Won, Hyejung, Agerbo, Esben, Als, Thomas D., Andreassen, Ole A., Bækvad-Hansen, Marie, Mortensen, Preben Bo, Pedersen, Carsten Bøcker, Børglum, Anders D., Bybjerg-Grauholm, Jonas, Djurovic, Srdjan, Durmishi, Naser, Pedersen, Marianne Giørtz, Golimbet, Vera, Grove, Jakob, Hougaard, David M., Mattheisen, Manuel, Molden, Espen, Mors, Ole, Nordentoft, Merete, Pejovic-Milovancevic, Milica, Sigurdsson, Engilbert, Silagadze, Teimuraz, Hansen, Christine Søholm, Stefansson, Kari, Stefansson, Hreinn, Steinberg, Stacy, Tosato, Sarah, Werge, Thomas, Collier, David A., Rujescu, Dan, Kirov, George, Owen, Michael J., O’Donovan, Michael C., Walters, James T. R.

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Genome-wide association study of suicide attempt in psychiatric disorders identifies association with major depression polygenic risk scores von Mullins, Niamh, Bigdeli, Tim B., Børglum, Anders D, Coleman, Jonathan R I, Demontis, Ditte, Fanous, Ayman H., Mehta, Divya, Power, Robert A., Ripke, Stephan, Stahl, Eli A, Starnawska, Anna, Anjorin, Adebayo, Corvin, Aiden, Sanders, Alan R, Forstner, Andreas J, Reif, Andreas, Koller, Anna C, Świątkowska, Beata, Baune, Bernhard T, Müller-Myhsok, Bertram, Konte, Bettina, Penninx, Brenda WJH, Pato, Carlos, Zai, Clement, Rujescu, Dan, Hougaard, David M, Quested, Digby, Levinson, Douglas F, Binder, Elisabeth B, Byrne, Enda M, Agerbo, Esben, Streit, Fabian, Mayoral, Fermin, Bellivier, Frank, Degenhardt, Franziska, Breen, Gerome, Morken, Gunnar, Turecki, Gustavo, Rouleau, Guy A, Grabe, Hans J, Völzke, Henry, Jones, Ian, Giegling, Ina, Agartz, Ingrid, Melle, Ingrid, Lawrence, Jacob, Potash, James B, Walters, James TR, Strohmaier, Jana, Shi, Jianxin, Hauser, Joanna, Biernacka, Joanna M, Vincent, John B, Kelsoe, John, Strauss, John S, Lissowska, Jolanta, Pimm, Jonathan, Smoller, Jordan W, Guzman Parra, José, Berger, Klaus, Scott, Laura J, Jones, Lisa A, Azevedo, M. Helena, Trzaskowski, Maciej, Kogevinas, Manolis, Rietschel, Marcella, Boks, Marco, Ising, Marcus, Grigoroiu-Serbanescu, Maria, Hamshere, Marian L, Leboyer, Marion, Frye, Mark, Nöthen, Markus M, Alda, Martin, Preisig, Martin, Nordentoft, Merete, Boehnke, Michael, O’Donovan, Michael C, Owen, Michael J, Pato, Michele T, Renteria, Miguel, Budde, Monika, Weissman, Myrna M, Wray, Naomi R, Bass, Nicholas, Craddock, Nicholas, Smeland, Olav B, Andreassen, Ole A, Mors, Ole, Gejman, Pablo V, Sklar, Pamela, McGrath, Patrick, Hoffmann, Per, McGuffin, Peter, Lee, Phil H, Mortensen, Preben Bo, Kahn, René S, Ophoff, Roel A, Adolfsson, Rolf, Van der Auwera, Sandra

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Trans-ancestral GWAS of alcohol dependence reveals common genetic underpinnings with psychiatric disorders von Walters, Raymond K., Polimanti, Renato, Johnson, Emma C., McClintick, Jeanette N., Adams, Mark J., Adkins, Amy E., Aliev, Fazil, Bacanu, Silviu-Alin, Batzler, Anthony, Bertelsen, Sarah, Biernacka, Joanna M., Bigdeli, Tim B., Chen, Li-Shiun, Clarke, Toni-Kim, Chou, Yi-Ling, Degenhardt, Franziska, Docherty, Anna R., Edwards, Alexis C., Fontanillas, Pierre, Foo, Jerome C., Fox, Louis, Frank, Josef, Giegling, Ina, Gordon, Scott, Hack, Laura M., Hartmann, Annette M., Hartz, Sarah M., Heilmann-Heimbach, Stefanie, Herms, Stefan, Hodgkinson, Colin, Hoffmann, Per, Hottenga, Jouke Jan, Kennedy, Martin A., Alanne-Kinnunen, Mervi, Konte, Bettina, Lahti, Jari, Lahti-Pulkkinen, Marius, Lai, Dongbing, Ligthart, Lannie, Loukola, Anu, Maher, Brion S., Mbarek, Hamdi, McIntosh, Andrew M., McQueen, Matthew B., Meyers, Jacquelyn L., Milaneschi, Yuri, Palviainen, Teemu, Pearson, John F., Peterson, Roseann E., Ripatti, Samuli, Ryu, Euijung, Saccone, Nancy L., Salvatore, Jessica E., Sanchez-Roige, Sandra, Schwandt, Melanie, Sherva, Richard, Streit, Fabian, Strohmaier, Jana, Thomas, Nathaniel, Wang, Jen-Chyong, Webb, Bradley T., Wedow, Robbee, Wetherill, Leah, Wills, Amanda G., Boardman, Jason D., Chen, Danfeng, Choi, Doo-Sup, Copeland, William E., Culverhouse, Robert C., Dahmen, Norbert, Degenhardt, Louisa, Domingue, Benjamin W., Elson, Sarah L., Frye, Mark A., Gäbel, Wolfgang, Hayward, Caroline, Ising, Marcus, Keyes, Margaret, Kiefer, Falk, Kramer, John, Kuperman, Samuel, Lucae, Susanne, Lynskey, Michael T., Maier, Wolfgang, Mann, Karl, Männistö, Satu, Müller-Myhsok, Bertram, Murray, Alison D., Nurnberger, John I., Palotie, Aarno, Preuss, Ulrich, Räikkönen, Katri, Reynolds, Maureen D., Ridinger, Monika, Scherbaum, Norbert, Schuckit, Marc A., Soyka, Michael, Treutlein, Jens, Witt, Stephanie

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Identification of a Bipolar Disorder Vulnerable Gene CHDH at 3p21.1 von Chang, Hong, Li, Lingyi, Peng, Tao, Grigoroiu-Serbanescu, Maria, Bergen, Sarah E., Landén, Mikael, Hultman, Christina M., Forstner, Andreas J., Strohmaier, Jana, Hecker, Julian, Schulze, Thomas G., Müller-Myhsok, Bertram, Reif, Andreas, Mitchell, Philip B., Martin, Nicholas G., Cichon, Sven, Nöthen, Markus M., Jamain, Stéphane, Leboyer, Marion, Bellivier, Frank, Etain, Bruno, Kahn, Jean-Pierre, Henry, Chantal, Rietschel, Marcella, Xiao, Xiao, Li, Ming

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Identification of shared risk loci and pathways for bipolar disorder and schizophrenia von Forstner, Andreas J, Hecker, Julian, Hofmann, Andrea, Reinbold, Celine S, Mühleisen, Thomas W, Leber, Markus, Strohmaier, Jana, Degenhardt, Franziska, Treutlein, Jens, Mattheisen, Manuel, Schumacher, Johannes, Streit, Fabian, Meier, Sandra, Herms, Stefan, Hoffmann, Per, Lacour, André, Witt, Stephanie H, Maaser, Anna, Reif, Andreas, Müller-Myhsok, Bertram, Lucae, Susanne, Maier, Wolfgang, Schwarz, Markus, Vedder, Helmut, Kammerer-Ciernioch, Jutta, Pfennig, Andrea, Bauer, Michael, Hautzinger, Martin, Moebus, Susanne, Schenk, Lorena M, Fischer, Sascha B, Sivalingam, Sugirthan, Czerski, Piotr M, Hauser, Joanna, Lissowska, Jolanta, Szeszenia-Dabrowska, Neonila, Brennan, Paul, McKay, James D, Wright, Adam, Mitchell, Philip B, Fullerton, Janice M, Schofield, Peter R, Montgomery, Grant W, Medland, Sarah E, Gordon, Scott D, Martin, Nicholas G, Krasnov, Valery, Chuchalin, Alexander, Babadjanova, Gulja, Pantelejeva, Galina, Abramova, Lilia I, Tiganov, Alexander S, Polonikov, Alexey, Khusnutdinova, Elza, Alda, Martin, Cruceanu, Cristiana, Rouleau, Guy A, Turecki, Gustavo, Laprise, Catherine, Rivas, Fabio, Mayoral, Fermin, Kogevinas, Manolis, Grigoroiu-Serbanescu, Maria, Becker, Tim, Schulze, Thomas G, Rietschel, Manolis, Cichon, Sven, Fier, Heide, Nöthen, Markus M

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TR Discover: A Natural Language Interface for Querying and Analyzing Interlinked Datasets von Song, Dezhao, Schilder, Frank, Smiley, Charese, Brew, Chris, Zielund, Tom, Bretz, Hiroko, Martin, Robert, Dale, Chris, Duprey, John, Miller, Tim, Harrison, Johanna

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