Universität zu Köln

Collins, Ryan L., Glessner, Joseph T., Porcu, Eleonora, Lepamets, Maarja, Brandon, Rhonda, Lauricella, Christopher, Han, Lide, Morley, Theodore, Niestroj, Lisa-Marie, Ulirsch, Jacob ORCID: 0000-0002-7947-0827, Everett, Selin, Howrigan, Daniel P., Boone, Philip M., Fu, Jack ORCID: 0000-0003-4152-5471, Karczewski, Konrad J., Kellaris, Georgios, Lowther, Chelsea, Lucente, Diane, Mohajeri, Kiana, Noukas, Margit, Nuttle, Xander, Samocha, Kaitlin E., Trinh, Mi ORCID: 0000-0003-4185-0071, Ullah, Farid, Vosa, Urmo, Hurles, Matthew E., Aradhya, Swaroop, Davis, Erica E., Finucane, Hilary, Gusella, James F., Janze, Aura, Katsanis, Nicholas, Matyakhina, Ludmila, Neale, Benjamin M., Sanders, David, Warren, Stephanie, Hodge, Jennelle C., Lal, Dennis, Ruderfer, Douglas M., Meck, Jeanne, Magi, Reedik, Esko, Tonu, Reymond, Alexandre, Kutalik, Zoltan ORCID: 0000-0001-8285-7523, Hakonarson, Hakon, Sunyaev, Shamil, Brand, Harrison and Talkowski, Michael E. (2022). A cross-disorder dosage sensitivity map of the human genome. Cell, 185 (16). S. 3041 - 3082. CAMBRIDGE: CELL PRESS. ISSN 1097-4172

Demontis, Ditte ORCID: 0000-0001-9124-2766, Walters, Raymond K., Martin, Joanna ORCID: 0000-0002-8911-3479, Mattheisen, Manuel ORCID: 0000-0002-8442-493X, Als, Thomas D. ORCID: 0000-0002-2963-1928, Agerbo, Esben ORCID: 0000-0002-2849-524X, Baldursson, Gisli, Belliveau, Rich, Bybjerg-Grauholm, Jonas ORCID: 0000-0003-1705-4008, Baekvad-Hansen, Marie, Cerrato, Felecia, Chambert, Kimberly, Churchhouse, Claire, Dumont, Ashley, Eriksson, Nicholas, Gandal, Michael ORCID: 0000-0001-5800-5128, Goldstein, Jacqueline I., Grasby, Katrina L., Grove, Jakob ORCID: 0000-0003-2284-5744, Gudmundsson, Olafur O., Hansen, Christine S., Hauberg, Mads Engel, Hollegaard, Mads V., Howrigan, Daniel P., Huang, Hailiang, Maller, Julian B., Martin, Alicia R., Martin, Nicholas G., Moran, Jennifer ORCID: 0000-0002-5664-4716, Pallesen, Jonatan, Palmer, Duncan S., Pedersen, Carsten Bocker, Pedersen, Marianne Giortz, Poterba, Timothy, Poulsen, Jesper Buchhave, Ripke, Stephan, Robinson, Elise B., Satterstrom, F. Kyle, Stefansson, Hreinn, Stevens, Christine, Turley, Patrick, Walters, G. Bragi ORCID: 0000-0002-5415-6487, Won, Hyejung, Wright, Margaret J., Andreassen, Ole A., Asherson, Philip ORCID: 0000-0003-2667-2254, Burton, Christie L., Boomsma, Dorret I., Cormand, Bru ORCID: 0000-0001-5318-4382, Dalsgaard, Soren ORCID: 0000-0003-4659-0969, Franke, Barbara ORCID: 0000-0003-4375-6572, Gelernter, Joel, Geschwind, Daniel, Hakonarson, Hakon, Haavik, Jan, Kranzler, Henry R., Kuntsi, Jonna ORCID: 0000-0002-0113-8162, Langley, Kate, Lesch, Klaus-Peter ORCID: 0000-0001-8348-153X, Middeldorp, Christel ORCID: 0000-0002-6218-0428, Reif, Andreas, Rohde, Luis Augusto, Roussos, Panos, Schachar, Russell, Sklar, Pamela, Sonuga-Barke, Edmund J. S., Sullivan, Patrick F., Thapar, Anita ORCID: 0000-0002-3689-737X, Tung, Joyce Y., Waldman, Irwin D., Medland, Sarah E., Stefansson, Kari, Nordentoft, Merete ORCID: 0000-0003-4895-7023, Hougaard, David M., Werge, Thomas, Mors, Ole, Mortensen, Preben Bo, Daly, Mark J., Faraone, Stephen V., Borglum, Anders D., Neale, Benjamin M., Albayrak, Ozgur, Anney, Richard J. L., Arranz, Maria Jesus, Banaschewski, Tobias J., Bau, Claiton, Biederman, Joseph, Buitelaar, Jan K., Casas, Miguel, Charach, Alice, Crosbie, Jennifer, Dempfle, Astrid ORCID: 0000-0002-2618-3920, Doyle, Alysa E., Ebstein, Richard P., Elia, Josephine, Freitag, Christine, Focker, Manuel, Gill, Michael, Grevet, Eugenio ORCID: 0000-0002-6898-7126, Hawi, Ziarih ORCID: 0000-0002-0814-9112, Hebebrand, Johannes, Herpertz-Dahlmann, Beate, Hervas, Amaia, Hinney, Anke, Hohmann, Sarah, Holmans, Peter, Hutz, Mara, Ickowitz, Abel, Johansson, Stefan ORCID: 0000-0002-2298-7008, Kent, Lindsey, Kittel-Schneider, Sarah ORCID: 0000-0003-3057-6150, Lambregts-Rommelse, Nanda, Lehmkuhl, Gerd, Loo, Sandra K., McGough, James J., Meyer, Jobst, Mick, Eric, Middletion, Frank, Miranda, Ana, Mota, Nina Roth, Mulas, Fernando, Mulligan, Aisling, Nelson, Freimer, Nguyen, T. 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ORCID: 0000-0002-9105-2249, Krapohl, Eva, Murcia, Mario, Myhre, Ronny, Nolte, Ilja M., Nyholt, Dale R., Ormel, Johan, Ouwens, Klaasjan G., Pappa, Irene ORCID: 0000-0003-4936-5791, Pennell, Craig E., Plomin, Robert ORCID: 0000-0002-0756-3629, Ring, Susan, Standl, Marie ORCID: 0000-0002-5345-2049, Stergiakouli, Evie, St Pourcain, Beate ORCID: 0000-0002-4680-3517, Stoltenberg, Camilla, Sunyer, Jordi ORCID: 0000-0002-2602-4110, Thiering, Elisabeth ORCID: 0000-0002-5429-9584, Tiemeier, Henning ORCID: 0000-0002-4395-1397, Tiesler, Carla M. T., Timpson, Nicholas J., Trzaskowski, Maciej ORCID: 0000-0001-8559-6525, van der Most, Peter Johannes, Vilor-Tejedor, Natalia, Wang, Carol A., Whitehouse, Andrew J. O., Zhao, Huiying, Agee, Michelle, Alipanahi, Babak, Auton, Adam, Bell, Robert K., Bryc, Katarzyna, Elson, Sarah L., Fontanillas, Pierre, Furlotte, Nicholas A., Hinds, David A., Hromatka, Bethann S., Huber, Karen E., Kleinman, Aaron, Litterman, Nadia K., McIntyre, Matthew H., Mountain, Joanna L., Northover, Carrie A. M., Pitts, Steven J., Sathirapongsasuti, J. Fah, Sazonova, Olga V., Shelton, Janie F., Shringarpure, Suyash, Tian, Chao, Vacic, Vladimir and Wilson, Catherine H. (2019). Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder. Nature Genet., 51 (1). S. 63 - 79. NEW YORK: NATURE PUBLISHING GROUP. ISSN 1546-1718

Niestroj, Lisa-Marie, Perez-Palma, Eduardo ORCID: 0000-0003-0546-5141, Howrigan, Daniel P., Zhou, Yadi, Cheng, Feixiong, Saarentaus, Elmo ORCID: 0000-0002-8475-7187, Nuernberg, Peter, Stevelink, Remi, Daly, Mark J., Palotie, Aarno and Lal, Dennis (2020). Epilepsy subtype-specific copy number burden observed in a genome-wide study of 17 458 subjects. Brain, 143. S. 2106 - 2119. OXFORD: OXFORD UNIV PRESS. ISSN 1460-2156

Perez-Palma, Eduardo ORCID: 0000-0003-0546-5141, Helbig, Ingo ORCID: 0000-0001-8486-0558, Klein, Karl Martin ORCID: 0000-0002-6654-1665, Anttila, Verneri, Horn, Heiko, Reinthaler, Eva Maria, Gormley, Padhraig ORCID: 0000-0002-8908-6968, Ganna, Andrea ORCID: 0000-0002-8147-240X, Byrnes, Andrea, Pernhorst, Katharina, Toliat, Mohammad R., Saarentaus, Elmo ORCID: 0000-0002-8475-7187, Howrigan, Daniel P., Hoffman, Per, Miquel, Juan Francisco, De Ferrari, Giancarlo V., Nuernberg, Peter, Lerche, Holger, Zimprich, Fritz ORCID: 0000-0002-6998-5480, Neubauer, Bern A., Becker, Albert J., Rosenow, Felix, Perucca, Emilio, Zara, Federico ORCID: 0000-0001-9744-5222, Weber, Yvonne G. and Lal, Dennis (2017). Heterogeneous contribution of microdeletions in the development of common generalised and focal epilepsies. J. Med. Genet., 54 (9). S. 598 - 607. LONDON: BMJ PUBLISHING GROUP. ISSN 1468-6244

Taylor, Jacob L., Debost, Jean-Christophe P. G., Morton, Sarah U., Wigdor, Emilie M., Heyne, Henrike O., Lal, Dennis, Howrigan, Daniel P., Bloemendal, Alex, Larsen, Janne T., Kosmicki, Jack A., Weiner, Daniel J., Homsy, Jason, Seidman, Jonathan G., Seidman, Christine E., Agerbo, Esben ORCID: 0000-0002-2849-524X, McGrath, John J., Mortensen, Preben Bo, Petersen, Liselotte, Daly, Mark J. and Robinson, Elise B. (2019). Paternal-age-related de novo mutations and risk for five disorders. Nat. Commun., 10. LONDON: NATURE PUBLISHING GROUP. ISSN 2041-1723