Browsing by Author Cormand Rifà, Bru
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| Issue Date | Title | Author(s) |
|---|---|---|
| 22-Sep-2020 | Genètica i epigenètica de les addiccions i trastorns comòrbids | Pineda i Cirera, Laura |
| 17-Jul-2015 | Genètica molecular de l'autisme: recerca de variants de susceptibilitat i estudis funcionals | Torrico Avilés, Bàrbara |
| 10-Jun-2012 | Genome-wide association analysis identifies susceptibility loci for migraine without aura | Cormand Rifà, Bru; Sintas Vives, Cèlia |
| 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 |
| 9-Feb-2023 | Genome-wide DNA methylation analysis in an antimigraine-treated preclinical model of cortical spreading depolarization | Vila-Pueyo, Marta; Cuenca León, Ester; Queirós, Ana C.; Kulis, Marta; Sintas Vives, Cèlia; Cormand Rifà, Bru; Martín-Subero, José Ignacio; Pozo-Rosich, Patricia; Fernàndez Castillo, Noèlia; Macaya Ruiz, Alfons |
| 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 |
| 11-May-2021 | Genomics and epigenomics of substance use disorders: An introduction | Cormand Rifà, Bru; Cabana Domínguez, Judit; Forero, Diego A.; Fernàndez Castillo, Noèlia |
| 15-Jul-2015 | Gens i migranya. Anàlisi mutacional i estudis d'associació en pacients | Sintas Vives, Cèlia |
| 16-Aug-2018 | Identification of ADHD risk genes in extended pedigrees by combining linkage analysis and whole-exome sequencing | Corominas, Jordi; Klein, Marieke; Zayats, Tetyana; Rivero, Olga; Ziegler, Georg C.; Pauper, Marc; Neveling, Kornelia; Poelmans, Geert; Jansch, Charline; Svirin, Evgeniy; Geissler, Julia; Weber, Heike; Reif, Andreas; Arias Vasquez, Alejandro; Galesloot, Tessel E.; Kiemeney, Lambertus A. L. M.; Buitelaar, Jan K.; Ramos Quiroga, Josep Antoni; Cormand Rifà, Bru; Ribasés Haro, Marta; Hveem, Kristian; Gabrielsen, Maiken Elvestad; Hoffmann, Per; Jacob, Christian P.; Romanos, Marcel; Franke, Barbara; Lesch, Klaus-Peter |
| 8-Mar-2022 | Identification of genetic variants influencing methylation in brain with pleiotropic effects on psychiatric disorders. | Pineda-Cirera, Laura; Cabana Domínguez, Judit; Lee, Phil H.; Fernàndez Castillo, Noèlia; Cormand Rifà, Bru |
| 26-Sep-2022 | Identification of shared and differentiating genetic risk for autism spectrum disorder, attention deficit hyperactivity disorder and case subgroups | Mattheisen, Manuel; Grove, Jakob; Als, Thomas D.; Martin, Joanna; Voloudakis, Georgios; Meier, Sandra; Demontis, Ditte; Bendl, Jaroslav; Walters, Raymond; Carrey, Caitlin E.; Rosengren, Anders; Strom, Nora I.; Hauberg, Mads Engel; Zeng, Biao; Hoffman, Gabriel; Bybjerg-Grauholm, J.; Bækvad-Hansen, M.; Agerbo, Esben; Cormand Rifà, Bru; Nordentoft, Merete; Werge, Thomas; Mors, Ole; Hougaard, David M.; Buxbaum, Joseph D.; Faraone, Stephen V.; Franke, Barbara; Dalsgaard, Søren; Mortensen, Preben B.; Robinson, Elise B.; Roussos, Panos; Neale, Benjamin M.; Daly, Mark J.; Børglum, Anders D. |
| 1-Sep-2020 | Improved diagnosis of rare disease patients through systematic detection of runs of homozygosity | Matalonga Borrel, Lesley; Laurie, Steven; Papakonstantinou, Anastasios; Piscia, Davide; Mereu, Elisabetta; Bullich, Gemma; Thompson, Rachel; Horvath, Rita; Pérez Jurado, Luis; Riess, Olaf; Gut, Ivo; van Ommen, Gert Jan; Lochmüller, Hanns; Beltrán, Sergi; RD-Connect Genome-Phenome Analysis Platform and UR; Cormand Rifà, Bru; Balcells Comas, Susana; Grinberg Vaisman, Daniel Raúl; Urreizti, Roser; Garrabou Tornos, Glòria |
| 10-Nov-2020 | Inhibition of G-protein signalling in cardiac dysfunction of intellectual developmental disorder with cardiac arrhythmia (IDDCA) syndrome | De Nittis, Pasquelena; Efthymiou. Sephanie; Sarre, Alexandre; Guex, Nicolas; Chrast, Jacqueline; Putoux, Audrey; Sultan, Tipu; Raza Alvi, Javeria; Ur Rahman, Zia; Zafar, Faisal; Rana, Nuzhat; Rahman, Fatima; Anwar, Najwa; Maqbool, Shazia; Zaki, Maha S.; Gleeson, Joseph G; Murphy, David; Galehdari, Hamid; Shariati, Gholamreza; Mazaheri, Neda; Sedaghat, Alireza; Lesca, Gaetan; Chatron, Nicolas; Salpietro, Vincenzo; Christoforou, Marilena; Houlden, Henry; Simonds, William F; Pedrazzini, Thierry; Maroofian, Reza; Reymond, Alexandre; Cormand Rifà, Bru; SYNAPS Study Group |
| 30-Jan-2018 | Integrative genomic analysis of methylphenidate response in attention-deficit/hyperactivity disorder | Pagerols Teixidó, Mireia; Richarte, Vanesa; Sánchez Mora, Cristina; Rovira, Paula; Soler Artigas, María; Garcia-Martínez, Iris; Calvo-Sánchez, Eva; Corrales, Montserrat; Santos da Silva, Bruna; Roth-Mota, Nina; Victor, Marcelo Moraes; Rohde, Luis Augusto; Grevet, Eugenio Horacio; Bau, Claiton Henrique Dotto; Cormand Rifà, Bru; Casas, Miquel; Ramos Quiroga, Josep Antoni; Ribasés Haro, Marta |
| 13-Jun-2020 | Involvement of the 14-3-3 gene family in autism spectrum disorder and schizophrenia: Genetics, transcriptomics and functional analyses | Torrico Avilés, Bàrbara; Antón Galindo, Ester; Fernàndez Castillo, Noèlia; Rojo Francàs, Eva; Ghorbani, Sadaf; Pineda Cirera, Laura; Hervás, Amaia; Rueda, Isabel; Moreno Guillén, Estefanía; Fullerton, Janice M.; Casadó, Vicent; Buitelaar, Jan K.; Rommelse, Nanda; Franke, Barbara; Reif, Andreas; Chiocchetti, Andreas G.; Freitag, Christine; Kleppe, Rune; Haavik, Jan; Toma, Claudio; Cormand Rifà, Bru |
| 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 |
| Aug-2016 | Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine | International Headache Genetics Consortium; Cormand Rifà, Bru; Sintas Vives, Cèlia |
| 13-Sep-2017 | Metodologies d'alt rendiment per a la identificació de noves mutacions i gens causants de distròfies de retina: estudi funcional de nous candidats | Castro Miró, Marta de |
| 28-Mar-2022 | MicroRNA signatures associated with vulnerability to food addiction in mice and humans | García-Blanco, Alejandra; Domingo-Rodriguez, Laura; Cabana Domínguez, Judit; Fernàndez Castillo, Noèlia; Pineda-Cirera, Laura; Mayneris-Perxachs, Jordi; Burokas, Aurelijus; Espinosa-Carrasco, Jose; Arboleya, Silvia A; Latorre, Jessica; Stanton, Catherine; Cormand Rifà, Bru; Fernández-Real, Jose-Manuel; Martín-García, Elena; Maldonado, Rafael |
| 27-Jan-2023 | Migraine, inflammatory bowel disease and celiac disease: A Mendelian randomization study | Welander, Nike Zoe; Rukh, Gull; Rask-Andersen, Mathias; Harder, Aster V.E.; The International Headache Genetics Consortium; van den Maagdenberg, Arn M.J.M.; Schiöth, Helgi Birgir; Mwinyi, Jessica; Cormand Rifà, Bru |