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| Issue Date | Title | Author(s) |
|---|---|---|
| 10-Jun-2012 | Genome-wide association analysis identifies susceptibility loci for migraine without aura | Cormand Rifà, Bru; Sintas Vives, Cèlia |
| 2020 | Genomic analysis of the natural history of attention-deficit/hyperactivity disorder using Neanderthal and ancient Homo sapiens samples | Esteller-Cucala, Paula; Maceda, Iago; Børglum, Anders D.; Demontis, Ditte; Faraone, Stephen V.; Cormand Rifà, Bru; Lao, Oscar |
| 5-Sep-2018 | Live fast, die young? A review on the developmental trajectories of ADHD across the lifespan | Franke, Barbara; Michelini, Giorgia; Asherson, Philip; Banaschewski, Tobias; Bilbow, Andrea; Buitelaar, Jan K.; Cormand Rifà, Bru; Faraone, Stephen V.; Ginsberg, Yiva; Haavik, Jan; Kuntsi, Jonna; Larsson, Henrik; Lesch, Klaus-Peter; Ramos-Quiroga, J. Antoni; Réthelyi, János M.; Ribasés Haro, Marta; Reif, Andreas |
| Jan-2015 | Frustrated expected reward induces differential transcriptional changes in the mouse brain | Martín-García, E.; Fernàndez Castillo, Noèlia; Burokas, A.; Gutiérrez-Cuesta, J.; Sánchez Mora, Cristina; Casas, M.; Ribasés Haro, Marta; Cormand Rifà, Bru; Maldonado, Rafael, 1961- |
| 24-Nov-2020 | Variants of the aggression-related RBFOX1 gene in a population representative birth cohort study: aggressiveness, personality and alcohol use disorder | Vaht, Mariliis; Laas, Kariina; Fernàndez Castillo, Noèlia; Kurrikoff, Triin; Kanarik, Margus; Faraone, Stephen V.; Tooding, Liina-Mai; Veidebaum, Toomas; Franke, Barbara; Reif, Andreas; Cormand Rifà, Bru; Harro, Jaanus |
| 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 |
| 31-May-2017 | Mutation spectrum in the CACNA1A gene in 49 patients with episodic ataxia | Sintas Vives, Cèlia; Carreño, Oriel; Fernàndez Castillo, Noèlia; Corominas Castiñeira, Roser; Vila Pueyo, Marta; Toma, Claudio; Cuenca León, Ester; Barroeta, Isabel; Roig i Arnall, Carles; Volpini Bertrán, Víctor; Macaya Ruiz, Alfons; Cormand Rifà, Bru |
| 10-Mar-2017 | A de novo nonsense mutation in MAGEL2 in a patient initially diagnosed as Opitz-C: Similarities between Schaaf-Yang and Opitz-C syndromes | Urreizti, Roser; Cueto Gonzalez, Anna Maria; Franco Valls, Héctor; Mort Farre, Sílvia; Roca Ayats, Neus; Ponomarenko, Julia; Cozzuto, Luca; Company, Carlos; Bosio, Mattia; Ossowski, Stephan; Montfort Roca, Magda; Hecht, Jochen; Tizzano Ferrari, Eduardo; Cormand Rifà, Bru; Vilageliu i Arqués, Lluïsa; Opitz, John M.; Neri, Giovanni; Grinberg Vaisman, Daniel Raúl; Balcells Comas, Susana |
| 1999 | Patologia molecular de la malaltia de Gaucher | Grinberg Vaisman, Daniel Raúl; Cormand Rifà, Bru; Gort i Mas, Laura; Montfort Roca, Magda; Chabás Bergón, Amparo; Vilageliu i Arqués, Lluïsa |
| 21-Feb-2013 | Chiari malformation type I: a case-control association study of 58 developmental genes | Urbizu Serrano, Aintzane; Toma, Claudio; Poca Pastor, María Antonia; Sahuquillo, Juan; Cuenca León, Ester; Cormand Rifà, Bru; Macaya Ruiz, Alfons |
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