Browsing by Author Cormand Rifà, Bru
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| Issue Date | Title | Author(s) |
|---|---|---|
| 23-Jul-2020 | Early-infantile onset epilepsy and developmental delay caused by bi-allelic GAD1 variants | Neuray, Caroline; Maroofian, Reza; Scala, Marcello; Sultan, Tipu; Pai, Gurpur S.; Mojarrad, Majid; El Khashab, Heba; deHoll, Leigh; Yue, Wyatt; Alsaif, Hessa S.; Zanetti, Maria N.; Bello, Oscar; Person, Richard; Eslahi, Atieh; Khazaei, Zaynab; Feizabadi, Masoumeh H; Efthymiou, Stephanie; SYNaPS Study Group; El Bassyouni, Hala T.; Soliman, Doaa R.; Tekes, Selahattin; Ozer, Leyla; Baltaci, Volkan; Khan, Suliman; Beetz, Christian; Amr, Khalda S.; Salpietro, Vicenzo; Jamshidi, Yalda; Alkuraya, Fowzan S.; Houlden, Henry; Cormand Rifà, Bru |
| 19-Aug-2015 | Evaluation of aminoglycoside and non-aminoglycoside compounds for stop-codon readthrough therapy in four lysosomal storage diseases | Gómez Grau, Marta; Garrido Fernández, Elena; Cozar, Mónica; Rodríguez Sureda, Víctor; Domínguez, Carmen; Arenas Solà, Concepción; Gatti, Richard A; Cormand Rifà, Bru; Grinberg Vaisman, Daniel Raúl; Vilageliu i Arqués, Lluïsa |
| 18-Oct-2016 | Exome chip analyses in adult attention deficit hyperactivity disorder | Zayats, T.; Jacobsen, K. K.; Kleppe, R.; Jacob, C. P.; Kittel-Schneider, S.; Ribasés Haro, Marta; Ramos Quiroga, Josep Antoni; Richarte, Vanesa; Casas, M.; Mota, N. R.; Grevet, Eugenio Horacio; Klein, M.; Corominas, J.; Bralten, J.; Galesloot, T.; Vasquez, A. A.; Herms, Stefan; Forstner, Andreas J.; Larsson, H.; Breen, G.; Asherson, P.; Gross-Lesch, S.; Lesch, Klaus-Peter; Cichon, Sven; Gabrielsen, M. B.; Holmen, O. L.; Bau, Claiton Henrique Dotto; Buitelaar, Jan K.; Kiemeney, Lambertus A. L. M.; Faraone, Stephen V.; Cormand Rifà, Bru; Franke, B.; Reif, Andreas; Haavik, J.; Johansson, S. |
| 2020 | Exploring allele specific methylation in drug dependence susceptibility | Pineda-Cirera, Laura; Cabana Domínguez, Judit; Grau-López, Laura; Daigree, Constanza; Sánchez-Mora, Cristina; Palma-Álvarez, Raul Felipe; Ramos-Quiroga, Josep Antoni; Ribasés Haro, Marta; Cormand Rifà, Bru; Fernàndez Castillo, Noèlia |
| 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 |
| 30-Dec-2021 | Exploring the contribution to ADHD of genes involved in Mendelian Disorders presenting with hyperactivity and/or inattention | Fernàndez Castillo, Noèlia; Cabana Domínguez, Judit; Kappel, Djenifer B.; Torrico Avilés, Bàrbara; Weber, Heike; Lesch, Klaus-Peter; Lao, Oscar; Reif, Andreas; Cormand Rifà, Bru |
| 23-Jun-2011 | Factors genètics de susceptibilitat al Transtorn per dèficit d'atenció amb hiperactivitat (TDAH) | Sánchez Mora, Cristina |
| 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- |
| 2000 | Fusion of the human gene for the polyubiquitination coeffector UEV1 with Kua, a newly identified gene | Thomson, Timothy M.; Lozano, Juan José; Loukili, Noureddine; Carrió, Roberto; Serras Rigalt, Florenci; Cormand Rifà, Bru; Valeri, Marta; Díaz, Víctor M.; Abril Ferrando, Josep Francesc, 1970-; Burset Albareda, Moisès; Merino, Jesús; Macaya, Alfons; Corominas, Montserrat (Corominas Guiu); Guigó, Roderic |
| 14-Jul-2017 | Gene-wide Association Study Reveals RNF122 Ubiquitin Ligase as a Novel Susceptibility Gene for Attention Deficit Hyperactivity Disorder | García Martínez, Iris; Sánchez Mora, Cristina; Soler Artigas, María; Rovira, Paula; Pagerols Teixidó, Mireia; Corrales, Montserrat; Calvo Sánchez, Eva; Richarte, Vanesa; Bustamante Pineda, Mariona; Sunyer Deu, Jordi; Cormand Rifà, Bru; Casas, Miquel; Ramos Quiroga, Josep Antoni; Ribasés Haro, Marta |
| Oct-2023 | Genetic Architecture of ADHD and Overlap With Other Psychiatric Disorders And Cognition-Related Phenotypes | Ribasés Haro, Marta; Mitjans Niubó, Marina; Hartman, C.A.; Soler Artigas, María; Demontis, D.; Larsson, H.; Ramos-Quiroga, Josep Antoni; Kuntsi, J.; Faraone, S.V.; Børglum, A.D.; Reif, A.; Franke, B.; Cormand Rifà, Bru |
| 2003 | Genetic evidence of heterogeneity in intrahepatic cholestasis of pregnancy | Savander, M.; Ropponen, A.; Avela, K.; Weerasekera, N.; Cormand Rifà, Bru; Hirvioja, M. L.; Riikonen, S.; Ylikorkala, O.; Lehesjoki, A. E.; Williamson, C.; Aittomäki, Kristiina |
| 6-Apr-2021 | Genetics and epigenetics of attention-deficit/hyperactivity disorder and comorbid conditions | Shivalikanjli, Anu |
| 5-Oct-2018 | Genètica i dependència de cocaïna: Estudis d'associació, transcriptòmica i models animals | Cabana Domínguez, Judit |
| 27-May-2011 | Genètica i drogues psicoestimulants: dependència de cocaïna i consum d’èxtasi | Fernàndez Castillo, Noèlia |
| 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 |