The genetic basis of major depression by 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 by 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 by 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 by 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 by 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 by 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 by 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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Multiple sclerosis genomic map implicates peripheral immune cells and microglia in susceptibility by Patsopoulos, Nikolaos A., Baranzini, Sergio E., Santaniello, Adam, Shoostari, Parisa, Cotsapas, Chris, Vlachos, Ioannis S., Pers, Tune H., Brandes, Aaron, White, Charles, Panteliadis, Ioannis-Pavlos, Robbins, Allison, Andlauer, Till F. M., Zarzycki, Onigiusz, Dubois, Bénédicte, Søndergaard, Helle Bach, Sellebjerg, Finn, Ullum, Henrik, Saarela, Janna, Cournu-Rebeix, Isabelle, Damotte, Vincent, Fontaine, Bertrand, Guillot-Noel, Lena, Lathrop, Mark, Vukusic, Sandra, Berthele, Achim, Pongratz, Viola, Buck, Dorothea, Knier, Benjamin, Lill, Christina M., Zipp, Frauke, Amoroso, Antonio, Barizzone, Nadia, Cavalla, Paola, Comi, Giancarlo, Cusi, Daniele, Esposito, Federica, Ferrè, Laura, Galimberti, Daniela, Guaschino, Clara, Martinelli, Vittorio, Moiola, Lucia, Salvetti, Marco, Vecchio, Domizia, Zauli, Andrea, Santoro, Silvia, Zuccalà, Miriam, Mescheriakova, Julia, van Duijn, Cornelia, Celius, Elisabeth G., Spurkland, Anne, Comabella, Manuel, Montalban, Xavier, Alfredsson, Lars, Hillert, Jan, Jagodic, Maja, Lindén, Magdalena, Piehl, Fredrik, Martin, Roland, Sospedra, Mirela, Baker, Amie, Ban, Maria, Hawkins, Clive, Kalra, Seema, Khadake, Jyoti, Molyneux, Paul, Neville, Matthew, Thorpe, John, Bradshaw, Elizabeth, Caillier, Stacy J., Cree, Bruce A. C., Davis, Mary, de Bakker, Paul W. I., Delgado, Silvia, Dembele, Marieme, Edwards, Keith, Gourraud, Pierre-Antoine, Haines, Jonathan L, Kimbrough, Dorlan, Isobe, Noriko, Lathi, Ellen, Lee, Michelle H., An, David, Zimmer, Andrew, Manrique, Clara P., Mitrovic, Mitja, Piccio, Laura, Weiner, Howard, Compston, Alastair, Harbo, Hanne F., Hauser, Stephen L., Stewart, Graeme, Hadjigeorgiou, Georgios, Taylor, Bruce, Booth, David, Kockum, Ingrid, Oksenberg, Jorge R., Sawcer, Stephen, Ivinson, Adrian J., Olsson, Tomas, De Jager, Philip L.

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Locus for severity implicates CNS resilience in progression of multiple sclerosis by Stridh, Pernilla, McCauley, Jacob L., Saarela, Janna, van den Bosch, Aletta M. R., 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., Chinea, Angel R., Chitnis, Tanuja, Clarelli, Ferdinando, Comabella, Manuel, Comi, Giancarlo, Cotsapas, Chris, Cree, Bruce C. A., De Jager, Philip L., Delgado, Silvia R., Engel, Sinah, Esposito, Federica, Fabis-Pedrini, Marzena J., Fitzgerald, Kathryn C., Gasperi, Christiane, Gomez, Lissette, Gomez, Refujia, Hadjigeorgiou, Georgios, Held, Friederike, Henry, Roland G., Hillert, Jan, Huang, Jesse, Huitinga, Inge, Islam, Talat, Isobe, Noriko, Jagodic, Maja, Kermode, Allan G., Kilpatrick, Trevor J., Konidari, Ioanna, Kreft, Karim L., Lechner-Scott, Jeannette, Leone, Maurizio, Luessi, Felix, Manouchehrinia, Ali, Manrique, Clara P., Martinez, Andrea C., Martinez-Maldonado, Viviana, Mascia, Elisabetta, Metz, Luanne M., Midaglia, Luciana, Montalban, Xavier, Oksenberg, Jorge R., Oturai, Annette, Parnell, Grant P., Pericak-Vance, Margaret A., Piehl, Fredrik, Santaniello, Adam, Santoro, Silvia, Schaefer, Catherine, Sellebjerg, Finn, Shams, Hengameh, Shchetynsky, Klementy, Siokas, Vasileios, Søndergaard, Helle B., Sorosina, Melissa, Taylor, Bruce, Vandebergh, Marijne, Vecchio, Domizia, Wever, Dennis, Yong, V. Wee, Stewart, Graeme J., Compston, Alastair, Zipp, Frauke, Harbo, Hanne F., Hemmer, Bernhard, Goris, An, Smolders, Joost, Hauser, Stephen L., Kockum, Ingrid, Sawcer, Stephen J., Baranzini, Sergio E., Harroud, Adil, Blanco, Yolanda, Llufriu, Sara, Madireddy, Lohith, Saiz, Albert, Villoslada, Pablo, Stefánsson, Kári

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Low-Frequency and Rare-Coding Variation Contributes to Multiple Sclerosis Risk by Patsopoulos, Nikolaos A., Beecham, Ashley H., Goris, An, Dubois, Bénédicte, D’hooghe, Marie B., Van Damme, Philip, Søndergaard, Helle Bach, Sellebjerg, Finn, Ullum, Henrik, Thørner, Lise W., Werge, Thomas, Damotte, Vincent, Fontaine, Bertrand, Lathrop, Mark, Gourraud, Pierre-Antoine, Pongratz, Viola, Gasperi, Christiane, Bayas, Antonios, Heesen, Christoph, Linker, Ralf, Paul, Friedemann, Stangel, Martin, Tackenberg, Björn, Bergh, Florian Then, Wildemann, Brigitte, Tumani, Hayrettin, Gold, Ralf, Grummel, Verena, Knier, Benjamin, Lill, Christina M., Dardiotis, Efthimios, Agliardi, Cristina, Barizzone, Nadia, Mascia, Elisabetta, Bernardinelli, Luisa, Cusi, Daniele, Ferrè, Laura, Comi, Cristoforo, Galimberti, Daniela, Leone, Maurizio A., Mescheriakova, Julia, Hintzen, Rogier, van Duijn, Cornelia, Teunissen, Charlotte E., Bos, Steffan D., Myhr, Kjell-Morten, Celius, Elisabeth G., Lie, Benedicte A., Comabella, Manuel, Montalban, Xavier, Alfredsson, Lars, Stridh, Pernilla, Hillert, Jan, Piehl, Fredrik, Jelčić, Ilijas, Martin, Roland, Sospedra, Mireia, Hawkins, Clive, Hysi, Pirro, Karpe, Fredrik, Khadake, Jyoti, Lachance, Genevieve, Neville, Matthew, Santaniello, Adam, Caillier, Stacy J., Calabresi, Peter A., Cross, Anne, Davis, Mary F., de Bakker, Paul I.W., Delgado, Silvia, Dembele, Marieme, Edwards, Keith, Fitzgerald, Kathryn C., Hakonarson, Hakon, Konidari, Ioanna, Lathi, Ellen, Manrique, Clara P., Pericak-Vance, Margaret A., Piccio, Laura, Schaefer, Cathy, McCabe, Cristin, Hadjigeorgiou, Georgios, Taylor, Bruce, Tajouri, Lotti, Charlesworth, Jac, Booth, David R., Harbo, Hanne F., Ivinson, Adrian J., Hauser, Stephen L., Compston, Alastair, Stewart, Graeme, Zipp, Frauke, Barcellos, Lisa F., Baranzini, Sergio E., Martinelli-Boneschi, Filippo, Ziegler, Andreas, McCauley, Jacob L., Sawcer, Stephen J., De Jager, Philip L., Kockum, Ingrid

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A systems biology approach uncovers cell-specific gene regulatory effects of genetic associations in multiple sclerosis by 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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Author Correction: A systems biology approach uncovers cell-specific gene regulatory effects of genetic associations in multiple sclerosis by 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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Hypothesis-driven genome-wide association studies provide novel insights into genetics of reading disabilities by Price, Kaitlyn M, Wigg, Karen G, Eising, Else, Feng, Yu, Blokland, Kirsten, Wilkinson, Margaret, Kerr, Elizabeth N, Guger, Sharon L, Fisher, Simon E, Lovett, Maureen W, Strug, Lisa J, Barr, Cathy L

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Low-Frequency and Rare-Coding Variation Contributes to Multiple Sclerosis Risk by Patsopoulos, Nikolaos A., Beecham, Ashley H., Goris, An, Dubois, Bénédicte, D’hooghe, Marie B., Van Damme, Philip, Søndergaard, Helle Bach, Sellebjerg, Finn, Ullum, Henrik, Thørner, Lise W., Werge, Thomas, Damotte, Vincent, Fontaine, Bertrand, Lathrop, Mark, Gourraud, Pierre-Antoine, Pongratz, Viola, Gasperi, Christiane, Bayas, Antonios, Heesen, Christoph, Linker, Ralf, Paul, Friedemann, Stangel, Martin, Tackenberg, Björn, Bergh, Florian Then, Wildemann, Brigitte, Tumani, Hayrettin, Gold, Ralf, Grummel, Verena, Knier, Benjamin, Lill, Christina M., Dardiotis, Efthimios, Agliardi, Cristina, Barizzone, Nadia, Mascia, Elisabetta, Bernardinelli, Luisa, Cusi, Daniele, Ferrè, Laura, Comi, Cristoforo, Galimberti, Daniela, Leone, Maurizio A., Mescheriakova, Julia, Hintzen, Rogier, van Duijn, Cornelia, Teunissen, Charlotte E., Bos, Steffan D., Myhr, Kjell-Morten, Celius, Elisabeth G., Lie, Benedicte A., Comabella, Manuel, Montalban, Xavier, Alfredsson, Lars, Stridh, Pernilla, Hillert, Jan, Piehl, Fredrik, Jelčić, Ilijas, Martin, Roland, Sospedra, Mireia, Hawkins, Clive, Hysi, Pirro, Karpe, Fredrik, Khadake, Jyoti, Lachance, Genevieve, Neville, Matthew, Santaniello, Adam, Caillier, Stacy J., Calabresi, Peter A., Cross, Anne, Davis, Mary F., de Bakker, Paul I.W., Delgado, Silvia, Dembele, Marieme, Edwards, Keith, Fitzgerald, Kathryn C., Hakonarson, Hakon, Konidari, Ioanna, Lathi, Ellen, Manrique, Clara P., Pericak-Vance, Margaret A., Piccio, Laura, Schaefer, Cathy, McCabe, Cristin, Hadjigeorgiou, Georgios, Taylor, Bruce, Tajouri, Lotti, Charlesworth, Jac, Booth, David R., Harbo, Hanne F., Ivinson, Adrian J., Hauser, Stephen L., Compston, Alastair, Stewart, Graeme, Zipp, Frauke, Barcellos, Lisa F., Baranzini, Sergio E., Martinelli-Boneschi, Filippo, Ziegler, Andreas, McCauley, Jacob L., Sawcer, Stephen J., De Jager, Philip L., Kockum, Ingrid

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Low-Frequency and Rare-Coding Variation Contributes to Multiple Sclerosis Risk by Patsopoulos, Nikolaos A., Beecham, Ashley H., Goris, An, Dubois, Bénédicte, D’hooghe, Marie B., Van Damme, Philip, Søndergaard, Helle Bach, Sellebjerg, Finn, Ullum, Henrik, Thørner, Lise W., Werge, Thomas, Damotte, Vincent, Fontaine, Bertrand, Lathrop, Mark, Gourraud, Pierre-Antoine, Pongratz, Viola, Gasperi, Christiane, Bayas, Antonios, Heesen, Christoph, Linker, Ralf, Paul, Friedemann, Stangel, Martin, Tackenberg, Björn, Bergh, Florian Then, Wildemann, Brigitte, Tumani, Hayrettin, Gold, Ralf, Grummel, Verena, Knier, Benjamin, Lill, Christina M., Dardiotis, Efthimios, Agliardi, Cristina, Barizzone, Nadia, Mascia, Elisabetta, Bernardinelli, Luisa, Cusi, Daniele, Ferrè, Laura, Comi, Cristoforo, Galimberti, Daniela, Leone, Maurizio A., Mescheriakova, Julia, Hintzen, Rogier, van Duijn, Cornelia, Teunissen, Charlotte E., Bos, Steffan D., Myhr, Kjell-Morten, Celius, Elisabeth G., Lie, Benedicte A., Comabella, Manuel, Montalban, Xavier, Alfredsson, Lars, Stridh, Pernilla, Hillert, Jan, Piehl, Fredrik, Jelčić, Ilijas, Martin, Roland, Sospedra, Mireia, Hawkins, Clive, Hysi, Pirro, Karpe, Fredrik, Khadake, Jyoti, Lachance, Genevieve, Neville, Matthew, Santaniello, Adam, Caillier, Stacy J., Calabresi, Peter A., Cross, Anne, Davis, Mary F., de Bakker, Paul I.W., Delgado, Silvia, Dembele, Marieme, Edwards, Keith, Fitzgerald, Kathryn C., Hakonarson, Hakon, Konidari, Ioanna, Lathi, Ellen, Manrique, Clara P., Pericak-Vance, Margaret A., Piccio, Laura, Schaefer, Cathy, McCabe, Cristin, Hadjigeorgiou, Georgios, Taylor, Bruce, Tajouri, Lotti, Charlesworth, Jac, Booth, David R., Harbo, Hanne F., Ivinson, Adrian J., Hauser, Stephen L., Compston, Alastair, Stewart, Graeme, Zipp, Frauke, Barcellos, Lisa F., Baranzini, Sergio E., Martinelli-Boneschi, Filippo, Ziegler, Andreas, McCauley, Jacob L., Sawcer, Stephen J., De Jager, Philip L., Kockum, Ingrid

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Spermidine Suppresses Age-Associated Memory Impairment by Preventing Adverse Increase of Presynaptic Active Zone Size and Release by Gupta, Varun K, Pech, Ulrike, Bhukel, Anuradha, Fulterer, Andreas, Ender, Anatoli, Mauermann, Stephan F, Andlauer, Till F M, Antwi-Adjei, Emmanuel, Beuschel, Christine, Thriene, Kerstin, Maglione, Marta, Quentin, Christine, Bushow, René, Schwärzel, Martin, Mielke, Thorsten, Madeo, Frank, Dengjel, Joern, Fiala, André, Sigrist, Stephan J

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Genome-wide association study reveals new insights into the heritability and genetic correlates of developmental dyslexia by Gialluisi, Alessandro, Andlauer, Till F M, Mirza-Schreiber, Nazanin, Moll, Kristina, Becker, Jessica, Hoffmann, Per, Ludwig, Kerstin U, Czamara, Darina, Pourcain, Beate St, Honbolygó, Ferenc, Tóth, Dénes, Csépe, Valéria, Huguet, Guillaume, Chaix, Yves, Iannuzzi, Stephanie, Demonet, Jean-Francois, Morris, Andrew P, Hulslander, Jacqueline, Willcutt, Erik G, DeFries, John C, Olson, Richard K, Smith, Shelley D, Pennington, Bruce F, Vaessen, Anniek, Maurer, Urs, Lyytinen, Heikki, Peyrard-Janvid, Myriam, Leppänen, Paavo H T, Brandeis, Daniel, Bonte, Milene, Stein, John F, Talcott, Joel B, Fauchereau, Fabien, Wilcke, Arndt, Kirsten, Holger, Müller, Bent, Francks, Clyde, Bourgeron, Thomas, Monaco, Anthony P, Ramus, Franck, Landerl, Karin, Kere, Juha, Scerri, Thomas S, Paracchini, Silvia, Fisher, Simon E, Schumacher, Johannes, Nöthen, Markus M, Müller-Myhsok, Bertram, Schulte-Körne, Gerd

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DeepWAS: Multivariate genotype-phenotype associations by directly integrating regulatory information using deep learning by Arloth, Janine, Eraslan, Gökcen, Andlauer, Till F M, Martins, Jade, Iurato, Stella, Kühnel, Brigitte, Waldenberger, Melanie, Frank, Josef, Gold, Ralf, Hemmer, Bernhard, Luessi, Felix, Nischwitz, Sandra, Paul, Friedemann, Wiendl, Heinz, Gieger, Christian, Heilmann-Heimbach, Stefanie, Kacprowski, Tim, Laudes, Matthias, Meitinger, Thomas, Peters, Annette, Rawal, Rajesh, Strauch, Konstantin, Lucae, Susanne, Müller-Myhsok, Bertram, Rietschel, Marcella, Theis, Fabian J, Binder, Elisabeth B, Mueller, Nikola S

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Fatigue, depression, and pain in multiple sclerosis: How neuroinflammation translates into dysfunctional reward processing and anhedonic symptoms by Heitmann, Henrik, Andlauer, Till F M, Korn, Thomas, Mühlau, Mark, Henningsen, Peter, Hemmer, Bernhard, Ploner, Markus

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Adolescent anxiety and pain problems: A joint, genome-wide investigation and pathway-based analysis by Mascheretti, Sara, Forni, Diego, Lampis, Valentina, Fumagalli, Luca, Paquin, Stéphane, Andlauer, Till F M, Wang, Wei, Dionne, Ginette, Brendgen, Mara R, Vitaro, Frank, Ouellet-Morin, Isabelle, Rouleau, Guy, Gouin, Jean-Philippe, Côté, Sylvana, Tremblay, Richard E, Turecki, Gustavo, Garon-Carrier, Gabrielle, Boivin, Michel, Battaglia, Marco

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