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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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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nextnano: General Purpose 3-D Simulations by Birner, S., Zibold, T., Andlauer, T., Kubis, T., Sabathil, M., Trellakis, A., Vogl, P.

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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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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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Isotope effect on electron paramagnetic resonance of boron acceptors in silicon by Stegner, A. R., Tezuka, H., Andlauer, T., Stutzmann, M., Thewalt, M. L. W., Brandt, M. S., Itoh, K. M.

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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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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, 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 by 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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Locus for severity implicates CNS resilience in progression of multiple sclerosis by 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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Dielectric screening versus quantum confinement of phosphorus donors in silicon nanocrystals investigated by magnetic resonance by Pereira, R. N., Stegner, A. R., Andlauer, T., Klein, K., Wiggers, H., Brandt, M. S., Stutzmann, 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 by 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 gene-environment analyses of major depressive disorder and reported lifetime traumatic experiences in UK Biobank by 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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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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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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Integrated analysis of environmental and genetic influences on cord blood DNA methylation in new-borns by 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 by 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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Association of polygenic score for major depression with response to lithium in patients with bipolar disorder by Amare, Azmeraw T., Schubert, Klaus Oliver, Clark, Scott R., Papiol, Sergi, Cearns, Micah, Heilbronner, Urs, Degenhardt, Franziska, Tekola-Ayele, Fasil, Hsu, Yi-Hsiang, Shekhtman, Tatyana, Adli, Mazda, Akula, Nirmala, Akiyama, Kazufumi, Ardau, Raffaella, Arias, Bárbara, Aubry, Jean-Michel, Backlund, Lena, Bhattacharjee, Abesh Kumar, Bellivier, Frank, Bengesser, Susanne, Biernacka, Joanna M., Birner, Armin, Brichant-Petitjean, Clara, Cervantes, Pablo, Chen, Hsi-Chung, Chillotti, Caterina, Cichon, Sven, Cruceanu, Cristiana, Czerski, Piotr M., Dalkner, Nina, Del Zompo, Maria, DePaulo, J. Raymond, Étain, Bruno, Jamain, Stephane, Falkai, Peter, Forstner, Andreas J., Frisen, Louise, Frye, Mark A., Fullerton, Janice M., Gard, Sébastien, Garnham, Julie S., Goes, Fernando S., Grof, Paul, Hashimoto, Ryota, Hauser, Joanna, Herms, Stefan, Hoffmann, Per, Hofmann, Andrea, Jiménez, Esther, Kahn, Jean-Pierre, Kassem, Layla, Kuo, Po-Hsiu, Kato, Tadafumi, Kelsoe, John R., Kliwicki, Sebastian, König, Barbara, Landén, Mikael, Lavebratt, Catharina, Leboyer, Marion, Leckband, Susan G., Tortorella, Alfonso, Martinsson, Lina, McCarthy, Michael J., McElroy, Susan L., Colom, Francesc, Mitjans, Marina, Mondimore, Francis M., Monteleone, Palmiero, Nievergelt, Caroline M., Nöthen, Markus M., Novák, Tomas, Ozaki, Norio, Pfennig, Andrea, Potash, James B., Reif, Andreas, Reininghaus, Eva, Rybakowski, Janusz K., Schofield, Peter R., Schweizer, Barbara W., Severino, Giovanni, Shilling, Paul D., Shimoda, Katzutaka, Simhandl, Christian, Slaney, Claire M., Squassina, Alessio, Stamm, Thomas, Stopkova, Pavla, Maj, Mario, Turecki, Gustavo, Vieta, Eduard, Veeh, Julia, Witt, Stephanie H., Wright, Adam, Zandi, Peter P., Mitchell, Philip B., Bauer, Michael, Alda, Martin, Rietschel, Marcella, Schulze, Thomas G., Baune, Bernhard T.

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Does Childhood Trauma Moderate Polygenic Risk for Depression? A Meta-analysis of 5765 Subjects From the Psychiatric Genomics Consortium by Peyrot, Wouter J., Milaneschi, Yuri, Madden, Pamela A.F., Ripke, Stephan, Mullins, Niamh, Heat, Andrew C., Fisher, Helen L., Byrne, Enda M., Air, Tracy A., Wray, Naomi R., Trzaskowski, Maciej, Byrne, Enda M., Abdellaoui, Abdel, Air, Tracy M., Blackwood, Douglas H.R., Bryois, Julien, Bybjerg-Grauholm, Jonas, Cai, Na, Clarke, Toni-Kim, Crawford, Gregory E., Dolan, Conor V., Escott-Price, Valentina, Farnush, Kiadeh, Farhadi Hassan, Finucane, Hilary K., Forstner, Andreas J., Frank, Josef, Hansen, Thomas F., Herms, Stefan, Hicki, Ian B., Hoffmann, Per, Homuth, Georg, Horn, Carsten, Hottenga, Jouke-Jan, Hougaard, David M., Ising, Marcus, Jansen, Rick, Jorgenson, Eric, Kohane, Isaac S., Kretzschmar, Warren W., Li, Yihan, MacKinnon, Dean F., Maier, Wolfgang, Marchini, Jonathan, Mbarek, Hamdi, McGuffin, Peter, Medland, Sarah E., Mehta, Divya, Middeldorp, Christel M., Mihailov, Evelin, Mondimore, Francis M., Mullins, Niamh, Nauck, Matthias, Nyholt, Dale R., Oskarsson, Hogni, Painter, Jodie N., Pedersen, Marianne Giørtz, Peterson, Roseann E., Pistis, Giorgio, Qvist, Per, Rice, John P., Rivera, Margarita, Shen, Ling, Shi, Jianxin, Smit, Johannes H., Steinberg, Stacy, Strohmaier, Jana, Teumer, Alexander, Thorgeirsson, Thorgeir E., Trubetskoy, Vassily, Uitterlinden, André G., van Hemert, Albert M., Wang, Yunpeng, Webb, Bradley T., Weinsheimer, Shantel Marie, Wu, Yang, Xi, Hualin S., Yang, Jian, Arolt, Volker, de Geus, E.J.C., Hamilton, Steven P., Hayward, Caroline, Kendler, Kenneth S., Madden, Pamela A.F., Magnusson, Patrik K., Metspalu, Andres, Nöthen, Markus M., Penninx, Brenda W.J.H., Schaefer, Catherine, Schulze, Thomas G., Uher, Rudolf, Werge, Thomas, Lewis, Cathryn M., Levinson, Douglas F., Breen, Gerome, Børglum, Anders D., Sullivan, Patrick F., Breen, Gerome, Martin, Nick G., Grabe, Hans J.

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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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