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Issue Date	Title	Author(s)
29-Jan-2019	ADGRL3 (LPHN3) variants predict substance use disorder	Arcos Burgos, Mauricio; Ribasés Haro, Marta; Martínez, Ariel F.; Ramos Quiroga, Josep Antoni; Sánchez Mora, Cristina; Richarte, Vanesa; Roncero, Carlos; Cormand Rifà, Bru; Fernàndez Castillo, Noèlia; Casas, Miguel; Vélez, Jorge I.; Lopera, Francisco; Pineda, David A.; Palacio, Juan D.; Molina, Brooke S. G.; Boden, Margaret T.; Wallis, Deeann; Lidbury, Brett; Patel, Hardip; Newman, Saul; Easteal, Simon; Swanson, James; Mastronardi, Claudio A.; Volkow, Nora D., 1956-; Acosta, Maria T.; Castellanos, Francisco X.; Leon, José de; Muenke, Maximillian; Acosta López, Johan E.; MTA Cooperative Group; Cervantes Henriquez, Martha L.; Sánchez Rojas, Manuel G.; Puentes Rozo, Pedro J.; Molina, Brooke S. G.
9-Sep-2019	Biallelic mutations in neurofascin cause neurodevelopmental impairment and peripheral demyelination	Efthymiou, S.; Salpietro, V.; Malintan,N.; Poncelet, M.; Kriouile, Y.; Fortuna, S.; De Zorzi, R.; Payne, K.; Henderson, L.B.; Cortese, A.; Maddirevula, S.; Alhashmi, N.; Wiethoff, S.; Ryten, M.; Botia, J.A.; Provitera, V.; Schuelke, M.; Vandrovcova, J.; SYNAPS Study Group; Walsh, L.; Torti, E.; Iodice, V.; Najafi, M.; Karimiani, E.G.; Maroofian, R.; Siquier-Pernet, K.; Boddaert, N.; De Lonlay, P.; Cantagrel, V.; Aguennouz, M.; El Khorassani, M.; Schmidts, M.; Alkuraya, F.S.; Edvardson, S.; Nolano, M.; Devaux, J.; Houlden, H.; Cormand Rifà, Bru
16-May-2019	Truncating variant burden in high functioning autism and pleiotropic effects of lrp1 across psychiatric phenotypes	Torrico Avilés, Bàrbara; Shaw, Alex D.; Mosca, Roberto; Vivó-Luque, Norma; Hervás, A.; Fernàndez Castillo, Noèlia; Aloy, Patrick, 1972-; Bayés Colomer, Mònica; Fullerton, J.M.; Cormand Rifà, Bru; Toma, Claudio
3-Oct-2019	Exploring genetic variation that influences brain methylation in attention-deficit/hyperactivity disorder	Pineda Cirera, Laura; Shivalikanjli, Anu; Cabana Domínguez, Judit; Demontis, Ditte; Rajagopal, Veera M.; Børglum, Anders D.; Faraone, Stephen V.; Cormand Rifà, Bru; Fernàndez Castillo, Noèlia
15-Jun-2019	Genome-wide association meta-analysis of cocaine dependence: shared genetics with comorbid conditions	Cabana Domínguez, Judit; Shivalikanjli, Anu; Fernàndez Castillo, Noèlia; Cormand Rifà, Bru
Jan-2019	Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder	Demontis, Ditte; Walters, Raymond K.; Martin, Joanna; Mattheisen, Manuel; Als, Thomas D.; Agerbo, Esben; Baldursson, Gísli; Belliveau, Rich; Bybjerg-Grauholm, Jonas; Bækvad-Hansen, Marie; Cerrato, Felicia; Chambert, Kimberly; Churchhouse, Claire; Dumont, Ashley; Eriksson, Nicholas; Gandal, Michael; Goldstein, Jacqueline I.; Grasby, Katrina L.; Grove, Jakob; 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; Pallesen, Jonatan; Palmer, Duncan S.; Pedersen, Carsten Bøcker; Pedersen, Marianne Giørtz; Poterba, Timothy; Poulsen, Jesper Buchhave; Ripke, Stephan; Robinson, Elise B.; Satterstrom, F. Kyle; Stefansson, Hreinn; Stevens, Christine; Turley, Patrick; Walters, G. Bragi; Won, Hyejung; Wright, Margaret J.; ADHD Working Group of the Psychiatric Genomics Consortium (PGC); Early Lifecourse & Genetic Epidemiology (EAGLE) Consortium; 23andMe Research Team; Andreassen, Ole A.; Asherson, Philip; Burton, Christie L.; Boomsma, Dorret I.; Cormand Rifà, Bru; Dalsgaard, Søren; Franke, Barbara; Gelernter, Joel; Geschwind, Daniel; Hakonarson, Hakon; Haavik, Jan; Kranzler, Henry R.; Kuntsi, Joanna; Langley, Kate; Lesch, Klaus-Peter; Middeldorp, Christel; Reif, Andreas; Rhode, Luis Augusto; Roussos, Panos; Schachar, Russell; Sklar, Pamela; Sonuga-Barke, Edmund J. S; Sullivan, Patrick F.; Thapar, Anita; Tung, Joyce Y.; Waldman, Irwin D.; Medland, Sarah E.; Stefansson, Kari; Nordentoft, Merete; Hougaard, David M.; Werge, Thomas; Mors, Ole; Mortensen, Preben Bo; Daly, Mark J.; Faraone, Stephen V.; Børglum, Anders D.; Neale, Benjamin M.