Bilaketaren emaitzak - Noèlia Fernàndez‐Castillo
- Erakusten 1 - 13 emaitzak -- 13
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Molecular genetics of cocaine use disorders in humans nork Noèlia Fernàndez‐Castillo, Judit Cabana‐Domínguez, Roser Corominas, Bru Cormand
Argitaratua 2021Revisão -
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Genetic Analysis of 27 Spanish Patients with Hemiplegic Migraine, Basilar-Type Migraine and Childhood Periodic Syndromes nork Ester Cuenca-León, Roser Corominas, Noèlia Fernàndez‐Castillo, V. Volpini, Mireia del Toro, Manuel G. Roig, Alfons Macaya, Bru Cormand
Argitaratua 2008Artigo -
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Mutation Spectrum in the CACNA1A Gene in 49 Patients with Episodic Ataxia nork Cèlia Sintas, Oriel Carreño, Noèlia Fernàndez‐Castillo, Roser Corominas, Marta Vila‐Pueyo, Claudio Toma, Ester Cuenca-León, Isabel Barroeta, Carles Roig, Vı́ctor Volpini, Alfons Macaya, Bru Cormand
Argitaratua 2017Artigo -
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RBFOX1, encoding a splicing regulator, is a candidate gene for aggressive behavior nork Noèlia Fernàndez‐Castillo, Gabriela Gan, Marjolein M. J. van Donkelaar, Mariliis Vaht, Heike Weber, Wolfgang Retz, Andreas Meyer‐Lindenberg, Barbara Franke, Jaanus Harro, Andreas Reif, Stephen V. Faraone, Bru Cormand
Argitaratua 2017Revisão -
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Three‐Photon Infrared Stimulation of Endogenous Neuroreceptors in Vivo nork Rosalba Sortino, Marina Cunquero, Gustavo Castro‐Olvera, Ricard Gelabert, Miquel Moreno, Fabio Riefolo, Carlo Matera, Noèlia Fernàndez‐Castillo, Luca Agnetta, Michael Decker, José M. Lluch, Jordi Hernando, Pablo Loza‐Álvarez, Pau Gorostiza
Argitaratua 2023Artigo -
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Gut microbiota signatures of vulnerability to food addiction in mice and humans nork S. Samulenaite, Alejandra García‐Blanco, Jordi Mayneris‐Perxachs, Laura Domingo‐Rodriguez, Judit Cabana‐Domínguez, Noèlia Fernàndez‐Castillo, Edurne Gago-García, Laura Pineda-Cirera, Aurelijus Burokas, Jose Espinosa‐Carrasco, Silvia Arboleya, Jèssica Latorre, Catherine Stanton, Koji Hosomi, Jun Kunisawa, Bru Cormand, José Manuel Fernández‐Real, Rafaël Maldonado, Elena Martín‐García
Argitaratua 2024Artigo -
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ADGRL3 (LPHN3) variants predict substance use disorder nork Mauricio Arcos‐Burgos, Jorge I. Vélez, Ariel F. Martinez, Marta Ribasés, Josep Antoni Ramos‐Quiroga, Cristina Sánchez‐Mora, Vanesa Richarte, Carlos Roncero, Bru Cormand, Noèlia Fernàndez‐Castillo, Miguel Casas, Francisco Lopera, David Pineda, Juan David Palacio, Johan E. Acosta-López, Martha L. Cervantes-Henríquez, Manuel Sánchez-Rojas, Pedro Puentes Rozo, Brooke S. G. Molina, Margaret T. Boden, Deeann Wallis, Brett A. Lidbury, Saul Newman, Simon Easteal, James M. Swanson, Hardip R. Patel, Nora D. Volkow, Maria T. Acosta, F. Xavier Castellanos, José de León, Claudio A. Mastronardi, Maximilian Muenke
Argitaratua 2019Artigo -
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Multicenter Analysis of the SLC6A3/DAT1 VNTR Haplotype in Persistent ADHD Suggests Differential Involvement of the Gene in Childhood and Persistent ADHD nork Barbara Franke, Alejandro Arias Vásquez, Stefan Johansson, Martine Hoogman, Jasmin Romanos, Andrea Boreatti‐Hümmer, Monika Heine, Christian Jacob, Klaus‐Peter Lesch, Miguel Casas, Marta Ribasés, Rosa Bosch, Cristina Sánchez‐Mora, Núria Gómez-Barros, Noèlia Fernàndez‐Castillo, Mónica Bayés, Anne Halmøy, Helene Barone Halleland, Elisabeth Toverud Landaas, Ole Bernt Fasmer, Per M. Knappskog, Angelien J.G.A.M. Heister, Lambertus A. Kiemeney, J. J. Sandra Kooij, Albert Boonstra, Cees C Kan, Philip Asherson, Stephen V. Faraone, Jan K. Buitelaar, Jan Haavik, Bru Cormand, Josep Antoni Ramos‐Quiroga, Andreas Reif
Argitaratua 2009Revisão -
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Behavioural and functional evidence revealing the role of RBFOX1 variation in multiple psychiatric disorders and traits nork Aet O’Leary, Noèlia Fernàndez‐Castillo, Gabriela Gan, Yunbo Yang, A.Y. Yotova, Thorsten M. Kranz, Lena Grünewald, Florian Freudenberg, Ester Antón-Galindo, Judit Cabana‐Domínguez, Anais Harneit, Janina I. Schweiger, Kristina Schwarz, Ren Ma, Junfang Chen, Emanuel Schwarz, Marcella Rietschel, Heike Tost, Andreas Meyer‐Lindenberg, Christiane A. Pané‐Farré, Tilo Kircher, Alfons O. Hamm, Demián Burguera, Nina Roth Mota, Barbara Franke, Susann Schweiger, Jennifer Winter, Andreas Heinz, Susanne Erk, Nina Romanczuk‐Seiferth, Henrik Walter, Andreas Ströhle, Lydia Fehm, Thomas Fydrich, Ulrike Lueken, Heike Weber, Thomas Lang�, Alexander L. Gerlach, Markus M. Nöthen, Georg W. Alpers, Volker Arolt, Stephanie H. Witt, Jan Richter, Benjamin Straube, Bru Cormand, David A. Slattery, Andreas Reif
Argitaratua 2022Artigo
Bilaketa egiteko lanabesak:
Antzeko gaiak
Biology
Genetics
Gene
Genotype
Neuroscience
Psychiatry
Psychology
Medicine
Single-nucleotide polymorphism
Genome-wide association study
Genetic association
Phenotype
Schizophrenia (object-oriented programming)
Internal medicine
Addiction
Attention deficit hyperactivity disorder
Candidate gene
Clinical psychology
Cognition
Comorbidity
Heritability
Receptor
Serotonergic
Serotonin
Substance abuse
16S ribosomal RNA
Aggression
Ataxia
Aura
Autism