The genetic basis of major depression von Kendall, K. M., Van Assche, E., Andlauer, T. F. M., Choi, K. W., Luykx, J. J., Schulte, E. C., Lu, Y.

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Higher frequencies of HLA DQB105:01 and anti-glycosphingolipid antibodies in a cluster of severe Guillain–Barré syndrome von Schirmer, L., Worthington, V., Solloch, U., Loleit, V., Grummel, V., Lakdawala, N., Grant, D., Wassmuth, R., Schmidt, A. H., Gebhardt, F., Andlauer, T. F. M., Sauter, J., Berthele, A., Lunn, M. P., Hemmer, Bernhard

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Polygenic risk and hostile environments: Links to stable and dynamic antisocial behaviors across adolescence von Acland, E L, Pocuca, N, Paquin, S, Boivin, M, Ouellet-Morin, I, Andlauer, T F M, Gouin, J P, Côté, S M, Tremblay, R E, Geoffroy, M, Castellanos-Ryan, N

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Inner retinal layer thinning in radiologically isolated syndrome predicts conversion to multiple sclerosis von Aly, L., Havla, J., Lepennetier, G., Andlauer, T. F. M., Sie, C., Strauß, E.‐M., Hoshi, M.‐M., Kümpfel, T., Hiltensperger, M., Mitsdoerffer, M., Mühlau, M., Zimmer, C., Hemmer, B., Korn, T., Knier, B.

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MS susceptibility is not affected by single nucleotide polymorphisms in the MMP9 gene von Nischwitz, S, Wolf, C, Andlauer, T.F.M, Czamara, D, Zettl, U.K, Rieckmann, P, Buck, D, Ising, M, Bettecken, T, Mueller-Myhsok, B, Weber, F

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Genetic effects influencing risk for major depressive disorder in China and Europe von Bigdeli, T B, Ripke, S, Peterson, R E, Trzaskowski, M, Bacanu, S-A, Abdellaoui, A, Andlauer, T F M, Beekman, A T F, Berger, K, Blackwood, D H R, Boomsma, D I, Breen, G, Buttenschøn, H N, Byrne, E M, Cichon, S, Clarke, T-K, Couvy-Duchesne, B, Craddock, N, de Geus, E J C, Degenhardt, F, Dunn, E C, Edwards, A C, Fanous, A H, Forstner, A J, Frank, J, Gill, M, Gordon, S D, Grabe, H J, Hamilton, S P, Hardiman, O, Hayward, C, Heath, A C, Henders, A K, Herms, S, Hickie, I B, Hoffmann, P, Homuth, G, Hottenga, J-J, Ising, M, Jansen, R, Kloiber, S, Knowles, J A, Lang, M, Li, Q S, Lucae, S, MacIntyre, D J, Madden, P A F, Martin, N G, McGrath, P J, McGuffin, P, McIntosh, A M, Medland, S E, Mehta, D, Middeldorp, C M, Milaneschi, Y, Montgomery, G W, Mors, O, Müller-Myhsok, B, Nauck, M, Nyholt, D R, Nöthen, M M, Owen, M J, Penninx, B W J H, Pergadia, M L, Perlis, R H, Peyrot, W J, Porteous, D J, Potash, J B, Rice, J P, Rietschel, M, Riley, B P, Rivera, M, Schoevers, R, Schulze, T G, Shi, J, Shyn, S I, Smit, J H, Smoller, J W, Streit, F, Strohmaier, J, Teumer, A, Treutlein, J, Van der Auwera, S, van Grootheest, G, van Hemert, A M, Völzke, H, Webb, B T, Weissman, M M, Wellmann, J, Willemsen, G, Witt, S H, Levinson, D F, Lewis, C M, Wray, N R, Flint, J, Sullivan, P F, Kendler, K S

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Presynapses in Kenyon Cell Dendrites in the Mushroom Body Calyx of Drosophila von Christiansen, F., Zube, C., Andlauer, T. F. M., Wichmann, C., Fouquet, W., Owald, D., Mertel, S., Leiss, F., Tavosanis, G., Farca Luna, A. J., Fiala, A., Sigrist, S. J.

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A systems biology approach uncovers cell-specific gene regulatory effects of genetic associations in multiple sclerosis von Madireddy, Lohith, Patsopoulos, Nikolaos A., Cotsapas, Chris, Bos, Steffan D., Beecham, Ashley, McCauley, Jacob, Kim, Kicheol, Jia, Xiaoming, Santaniello, Adam, Caillier, Stacy J., Andlauer, Till F. M., Barcellos, Lisa F., Berge, Tone, Bernardinelli, Luisa, Martinelli-Boneschi, Filippo, Booth, David R., Briggs, Farren, Celius, Elisabeth G., Comabella, Manuel, Comi, Giancarlo, Cree, Bruce A. C., D’Alfonso, Sandra, Dedham, Katrina, Duquette, Pierre, Dardiotis, Efthimios, Esposito, Federica, Fontaine, Bertrand, Gasperi, Christiane, Goris, An, Dubois, Bénédicte, Gourraud, Pierre-Antoine, Hadjigeorgiou, Georgios, Haines, Jonathan, Hawkins, Clive, Hemmer, Bernhard, Hintzen, Rogier, Horakova, Dana, Isobe, Noriko, Kalra, Seema, Kira, Jun-ichi, Khalil, Michael, Kockum, Ingrid, Lill, Christina M., Lincoln, Matthew R., Luessi, Felix, Martin, Roland, Oturai, Annette, Palotie, Aarno, Pericak-Vance, Margaret A., Henry, Roland, Saarela, Janna, Ivinson, Adrian, Olsson, Tomas, Taylor, Bruce V., Stewart, Graeme J., Harbo, Hanne F., Compston, Alastair, Hauser, Stephen L., Hafler, David A., Zipp, Frauke, De Jager, Philip, Sawcer, Stephen, Oksenberg, Jorge R., Baranzini, Sergio E.

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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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Multiple sclerosis genomic map implicates peripheral immune cells and microglia in susceptibility von Patsopoulos, Nikolaos A., Baranzini, Sergio E., Santaniello, Adam, Shoostari, Parisa, Cotsapas, Chris, Wong, Garrett, Beecham, Ashley H., James, Tojo, Replogle, Joseph, Vlachos, Ioannis S., McCabe, Cristin, Pers, Tune H., Brandes, Aaron, White, Charles, Keenan, Brendan, Cimpean, Maria, Winn, Phoebe, Panteliadis, Ioannis-Pavlos, Robbins, Allison, Andlauer, Till F. M., Zarzycki, Onigiusz, Dubois, Bénédicte, Goris, An, Søndergaard, Helle Bach, Sellebjerg, Finn, Sorensen, Per Soelberg, Ullum, Henrik, Thørner, Lise Wegner, Saarela, Janna, Cournu-Rebeix, Isabelle, Damotte, Vincent, Fontaine, Bertrand, Guillot-Noel, Lena, Lathrop, Mark, Vukusic, Sandra, Berthele, Achim, Pongratz, Viola, Buck, Dorothea, Gasperi, Christiane, Graetz, Christiane, Grummel, Verena, Hemmer, Bernhard, Hoshi, Muni, Knier, Benjamin, Korn, Thomas, Lill, Christina M., Luessi, Felix, Mühlau, Mark, Zipp, Frauke, Dardiotis, Efthimios, Agliardi, Cristina, Amoroso, Antonio, Barizzone, Nadia, Benedetti, Maria D., Bernardinelli, Luisa, Cavalla, Paola, Clarelli, Ferdinando, Comi, Giancarlo, Cusi, Daniele, Esposito, Federica, Ferrè, Laura, Galimberti, Daniela, Guaschino, Clara, Leone, Maurizio A., Martinelli, Vittorio, Moiola, Lucia, Salvetti, Marco, Sorosina, Melissa, Vecchio, Domizia, Zauli, Andrea, Santoro, Silvia, Mancini, Nicasio, Zuccalà, Miriam, Mescheriakova, Julia, van Duijn, Cornelia, Bos, Steffan D., Celius, Elisabeth G., Spurkland, Anne, Comabella, Manuel, Montalban, Xavier, Alfredsson, Lars, Bomfim, Izaura L., Gomez-Cabrero, David, Hillert, Jan, Jagodic, Maja, Lindén, Magdalena, Piehl, Fredrik, Jelčić, Ilijas, Martin, Roland, Sospedra, Mirela, Baker, Amie, Ban, Maria, Hawkins, Clive, Hysi, Pirro, Kalra, Seema, Karpe, Fredrik, Khadake, Jyoti, Lachance, Genevieve, Molyneux, Paul, Neville, Matthew

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Dissecting the Shared Genetic Architecture of Suicide Attempt, Psychiatric Disorders, and Known Risk Factors von Mullins, Niamh, Campos, Adrian I., Shabalin, Andrey, Hafferty, Jonathan D., Okazaki, Satoshi, Bohus, Martin, Johnson, Craig, Li, Dong, Magistretti, Pierre J., Van der Auwera, Sandra, Byrne, Enda M., Casas, Miguel, Jonsson, Lina, O’Donovan, Michael C., Pato, Carlos, Ramos-Quiroga, Josep Antoni, Sánchez-Mora, Cristina, Smeland, Olav B., Shannon Weickert, Cynthia, Hauser, Elizabeth R., Andlauer, Till F.M., Colodro-Conde, Lucía, Craddock, Nick, Derks, Eske M., Escott-Price, Valentina, Gordon, Scott D., Wu, Yang, Xi, Hualin S., Esko, Tõnu, Kohane, Isaac S., McGrath, Patrick, McGuffin, Peter, Middeldorp, Christel M., Milaneschi, Yuri, Nauck, Matthias, Nyholt, Dale R., Nöthen, Markus M., Pedersen, Nancy L., Pedersen, Carsten Bøcker, Steinberg, Stacy, Potash, James B., Schaefer, Catherine, Smoller, Jordan W., Völzke, Henry, Drange, Ole Kristian, Ikeda, Masashi, Panagiotaropoulou, Georgia, Sloofman, Laura G., Casas, Miquel, Ferrier, I. Nicol, Guzman-Parra, José, Kogevinas, Manolis, Lee, Phil H., Magnusson, Sigurdur H., Mühleisen, Thomas W., Sirignano, Lea, Adolfsson, Rolf, Alda, Martin, Catts, Stanley, Corvin, Aiden, Craddock, Nicholas, Fullerton, Janice M., Iwata, Nakao, Mayoral, Fermin, Mowry, Bryan, McQuillin, Andrew, Bulik, Cynthia M., Courtet, Philippe, Dina, Christian, Fichter, Manfred M., Föcker, Manuel, Hinney, Anke, Hübel, Christopher, Purves, Kirstin L., Rujescu, Dan, Scherer, Stephen W., Slagboom, P. Eline, Steen, Vidar W., Karhunen, Leila, Kennedy, Martin A., Tsitsika, Artemis, Yao, Shuyang, Schwarze, Cornelia E., Bohus, Martin, Crivelli, Silvia, Muralidhar, Sumitra, Huang, Grant, Moser, Jennifer, Brewer, Jessica V., Connor, Todd, Humphries, Donald E., Hauser, Elizabeth, Whittle, Jeffrey, Hammer, Kimberly, Godschalk, Michael, Sriram, Peruvemba, Liangpunsakul, Suthat, Wallbom, Agnes, Esko, Tõnu, Martin, Nicholas G.

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Inner retinal layer thinning in radiologically isolated syndrome predicts conversion to multiple sclerosis von Aly, L, Havla, J, Lepennetier, G, Andlauer, T. F. M, Sie, C, Strauss, E.-M, Hoshi, M.-M, Kuempfel, T, Hiltensperger, M, Mitsdoerffer, M, Muehlau, M, Zimmer, C, Hemmer, B, Korn, T, Knier, B

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The Genetic Architecture of Depression in Individuals of East Asian Ancestry: A Genome-Wide Association Study von Giannakopoulou, Olga, Lin, Kuang, Meng, Xiangrui, Su, Mei-Hsin, Kuo, Po-Hsiu, Peterson, Roseann E, Awasthi, Swapnil, Moscati, Arden, Coleman, Jonathan R. I, Bass, Nick, Millwood, Iona Y, Chen, Yiping, Chen, Zhengming, Chen, Hsi-Chung, Lu, Mong-Liang, Huang, Ming-Chyi, Chen, Chun-Hsin, Stahl, Eli A, Loos, Ruth J. F, Mullins, Niamh, Ursano, Robert J, Kessler, Ronald C, Stein, Murray B, Sen, Srijan, Scott, Laura J, Burmeister, Margit, Fang, Yu, Tyrrell, Jess, Jiang, Yunxuan, Tian, Chao, McIntosh, Andrew M, Ripke, Stephan, Dunn, Erin C, Kendler, Kenneth S, Walters, Robin G, Lewis, Cathryn M, Kuchenbaecker, Karoline

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Genome-wide gene-environment analyses of major depressive disorder and reported lifetime traumatic experiences in UK Biobank von Coleman, Jonathan R. I., Peyrot, Wouter J., Purves, Kirstin L., Davis, Katrina A. S., Rayner, Christopher, Choi, Shing Wan, Hübel, Christopher, Gaspar, Héléna A., Kan, Carol, Van der Auwera, Sandra, Adams, Mark James, Lyall, Donald M., Choi, Karmel W., Dunn, Erin C., Vassos, Evangelos, Danese, Andrea, Maughan, Barbara, Grabe, Hans J., Lewis, Cathryn M., O’Reilly, Paul F., McIntosh, Andrew M., Smith, Daniel J., Wray, Naomi R., Hotopf, Matthew, Eley, Thalia C., Breen, Gerome

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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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Locus for severity implicates CNS resilience in progression of multiple sclerosis von Harroud, Adil, Stridh, Pernilla, McCauley, Jacob L., Saarela, Janna, van den Bosch, Aletta M. R., Engelenburg, Hendrik J., Beecham, Ashley H., Alfredsson, Lars, Alikhani, Katayoun, Amezcua, Lilyana, Andlauer, Till F. M., Ban, Maria, Barcellos, Lisa F., Barizzone, Nadia, Berge, Tone, Berthele, Achim, Bittner, Stefan, Bos, Steffan D., Briggs, Farren B. S., Caillier, Stacy J., Calabresi, Peter A., Caputo, Domenico, Carmona-Burgos, David X., Cavalla, Paola, Celius, Elisabeth G., Cerono, Gabriel, Chinea, Angel R., Chitnis, Tanuja, Clarelli, Ferdinando, Comabella, Manuel, Comi, Giancarlo, Cotsapas, Chris, Cree, Bruce C. A., D’Alfonso, Sandra, Dardiotis, Efthimios, De Jager, Philip L., Delgado, Silvia R., Dubois, Bénédicte, Engel, Sinah, Esposito, Federica, Fabis-Pedrini, Marzena J., Filippi, Massimo, Fitzgerald, Kathryn C., Gasperi, Christiane, Gomez, Lissette, Gomez, Refujia, Hadjigeorgiou, Georgios, Hamann, Jörg, Held, Friederike, Henry, Roland G., Hillert, Jan, Huang, Jesse, Huitinga, Inge, Islam, Talat, Isobe, Noriko, Jagodic, Maja, Kermode, Allan G., Khalil, Michael, Kilpatrick, Trevor J., Konidari, Ioanna, Kreft, Karim L., Lechner-Scott, Jeannette, Leone, Maurizio, Luessi, Felix, Malhotra, Sunny, Manouchehrinia, Ali, Manrique, Clara P., Martinelli-Boneschi, Filippo, Martinez, Andrea C., Martinez-Maldonado, Viviana, Mascia, Elisabetta, Metz, Luanne M., Midaglia, Luciana, Montalban, Xavier, Oksenberg, Jorge R., Olsson, Tomas, Oturai, Annette, Pääkkönen, Kimmo, Parnell, Grant P., Patsopoulos, Nikolaos A., Pericak-Vance, Margaret A., Piehl, Fredrik, Rubio, Justin P., Santaniello, Adam, Santoro, Silvia, Schaefer, Catherine, Sellebjerg, Finn, Shams, Hengameh, Shchetynsky, Klementy, Silva, Claudia, Siokas, Vasileios, Søndergaard, Helle B., Sorosina, Melissa, Taylor, Bruce, Vandebergh, Marijne, Vasileiou, Elena S., Vecchio, Domizia, Voortman, Margarete M., Weiner, Howard L., Wever, Dennis

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Discovery of 42 genome-wide significant loci associated with dyslexia von Doust, Catherine, Fontanillas, Pierre, Eising, Else, Gordon, Scott D., Wang, Zhengjun, Alagöz, Gökberk, Molz, Barbara, Pourcain, Beate St, Francks, Clyde, Marioni, Riccardo E., Zhao, Jingjing, Paracchini, Silvia, Talcott, Joel B., Monaco, Anthony P., Stein, John F., Gruen, Jeffrey R., Olson, Richard K., Willcutt, Erik G., DeFries, John C., Pennington, Bruce F., Smith, Shelley D., Wright, Margaret J., Martin, Nicholas G., Auton, Adam, Bates, Timothy C., Fisher, Simon E., Luciano, Michelle

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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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Integrated analysis of environmental and genetic influences on cord blood DNA methylation in new-borns von 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.

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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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