检索结果 - Bru Cormand

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  1. 1
    Aggressive behavior in humans: Genes and pathways identified through association studies

    Aggressive behavior in humans: Genes and pathways identified through association studies 由 Noèlia Fernàndez‐Castillo, Bru Cormand

    出版 2016
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  2. 2
    Genome-wide association meta-analysis of cocaine dependence: Shared genetics with comorbid conditions

    Genome-wide association meta-analysis of cocaine dependence: Shared genetics with comorbid conditions 由 Judit Cabana‐Domínguez, Anu Shivalikanjli, Noèlia Fernàndez‐Castillo, Bru Cormand

    出版 2019
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  3. 3
    Molecular genetics of cocaine use disorders in humans

    Molecular genetics of cocaine use disorders in humans 由 Noèlia Fernàndez‐Castillo, Judit Cabana‐Domínguez, Roser Corominas, Bru Cormand

    出版 2021
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  4. 4
    Comprehensive exploration of the genetic contribution of the dopaminergic and serotonergic pathways to psychiatric disorders

    Comprehensive exploration of the genetic contribution of the dopaminergic and serotonergic pathways to psychiatric disorders 由 Judit Cabana‐Domínguez, Bàrbara Torrico, Andreas Reif, Noèlia Fernàndez‐Castillo, Bru Cormand

    出版 2022
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  5. 5
    Chiari Malformation Type I: A Case-Control Association Study of 58 Developmental Genes

    Chiari Malformation Type I: A Case-Control Association Study of 58 Developmental Genes 由 Aintzane Urbizu, Claudio Toma, María A. Poca, Juan Sahuquillo, Ester Cuenca-León, Bru Cormand, Alfons Macaya

    出版 2013
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  6. 6
    An integrated analysis of genes and functional pathways for aggression in human and rodent models

    An integrated analysis of genes and functional pathways for aggression in human and rodent models 由 Yanli Zhang‐James, Noèlia Fernàndez‐Castillo, Jonathan Hess, Karim Malki, Stephen J. Glatt, Bru Cormand, Stephen V. Faraone

    出版 2018
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  7. 7
    Assignment of the Muscle-Eye-Brain Disease Gene to 1p32-p34 by Linkage Analysis and Homozygosity Mapping

    Assignment of the Muscle-Eye-Brain Disease Gene to 1p32-p34 by Linkage Analysis and Homozygosity Mapping 由 Bru Cormand, Kristiina Avela, Helena Pihko, Pirkko Santavuori, Beril Talim, Haluk Topaloğlu, Albert de la Chapelle, Anna‐Elina Lehesjoki

    出版 1999
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  8. 8
    Genetic Analysis of 27 Spanish Patients with Hemiplegic Migraine, Basilar-Type Migraine and Childhood Periodic Syndromes

    Genetic Analysis of 27 Spanish Patients with Hemiplegic Migraine, Basilar-Type Migraine and Childhood Periodic Syndromes 由 Ester Cuenca-León, Roser Corominas, Noèlia Fernàndez‐Castillo, V. Volpini, Mireia del Toro, Manuel G. Roig, Alfons Macaya, Bru Cormand

    出版 2008
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  9. 9
    Unusual expression of Gaucher's disease: cardiovascular calcifications in three sibs homozygous for the D409H mutation.

    Unusual expression of Gaucher's disease: cardiovascular calcifications in three sibs homozygous for the D409H mutation. 由 Amparo Chabás, Bru Cormand, Daniel Grinberg, José M. Burguera, Susana Balcells, José Luís Merino, I Maté, José A. Sobrino, Roser Gonzàlez‐Duarte, Lluı̈sa Vilageliu

    出版 1995
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  10. 10
    New suggestive genetic loci and biological pathways for attention function in adult attention‐deficit/hyperactivity disorder

    New suggestive genetic loci and biological pathways for attention function in adult attention‐deficit/hyperactivity disorder 由 Silvia Alemany, Marta Ribasés, Natàlia Vilor‐Tejedor, Mariona Bustamante, Cristina Sánchez‐Mora, Rosa Bosch, Vanesa Richarte, Bru Cormand, Miguel Casas, Josep Antoni Ramos‐Quiroga, Jordi Sunyer

    出版 2015
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  11. 11
    Exome sequencing in multiplex autism families suggests a major role for heterozygous truncating mutations

    Exome sequencing in multiplex autism families suggests a major role for heterozygous truncating mutations 由 Claudio Toma, Bàrbara Torrico, Amaia Hervás, Rafael Valdés‐Mas, Alba Tristán‐Noguero, Vanesa Padillo, Marta Maristany, Marta Morgade Salgado, C. Arenas, Xosé S. Puente, Mónica Bayés, Bru Cormand

    出版 2013
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  12. 12
    Mutation Spectrum in the CACNA1A Gene in 49 Patients with Episodic Ataxia

    Mutation Spectrum in the CACNA1A Gene in 49 Patients with Episodic Ataxia 由 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

    出版 2017
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  13. 13
    RBFOX1, encoding a splicing regulator, is a candidate gene for aggressive behavior

    RBFOX1, encoding a splicing regulator, is a candidate gene for aggressive behavior 由 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

    出版 2017
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  14. 14
    Cerebral Folate Deficiency Syndromes in Childhood

    Cerebral Folate Deficiency Syndromes in Childhood 由 Belén Pérez‐Dueñas, Aída Ormazábal, Claudio Toma, Bàrbara Torrico, Bru Cormand, Mercedes Serrano, Cristina Sierra, Elisa De Grandis, Mercè Pineda Marfà, Àngels García‐Cazorla, Jaime Campistol, Juan M. Pascual, Rafael Artuch

    出版 2011
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  15. 15
    Genetic architecture of ADHD and overlap with other psychiatric disorders and cognition-related phenotypes

    Genetic architecture of ADHD and overlap with other psychiatric disorders and cognition-related phenotypes 由 Marta Ribasés, Marina Mitjans, C.A. Hartman, María Soler Artigas, Ditte Demontis, Henrik Larsson, Josep Antoni Ramos‐Quiroga, Jonna Kuntsi, Stephen V. Faraone, Børglum Ad, Andreas Reif, Barbara Franke, Bru Cormand

    出版 2023
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  16. 16
    Contribution of LPHN3 to the genetic susceptibility to ADHD in adulthood: a replication study

    Contribution of LPHN3 to the genetic susceptibility to ADHD in adulthood: a replication study 由 Marta Ribasés, Josep Antoni Ramos‐Quiroga, Cristina Sánchez‐Mora, Rosa Bosch, Vanesa Richarte, Glòria Palomar, Xavier Gastaminza, Anna Bielsa, Mauricio Arcos‐Burgos, Maximilian Muenke, F. Xavier Castellanos, Bru Cormand, Mónica Bayés, Miguel Casas

    出版 2010
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  17. 17
    The genetics of attention deficit/hyperactivity disorder in adults, a review

    The genetics of attention deficit/hyperactivity disorder in adults, a review 由 Barbara Franke, Stephen V. Faraone, Philip Asherson, Jan K. Buitelaar, Claiton Henrique Dotto Bau, Josep Antoni Ramos‐Quiroga, Eric Mick, Eugênio H. Grevet, Stefan Johansson, Jan Haavik, Klaus‐Peter Lesch, Bru Cormand, Andreas Reif

    出版 2011
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  18. 18
    A homozygous nonsense mutation in the Fukutin gene causes a Walker-Warburg syndrome phenotype

    A homozygous nonsense mutation in the Fukutin gene causes a Walker-Warburg syndrome phenotype 由 Daniel Beltrán Valero de Bernabé, Hans van Bokhoven, Ellen van Beusekom, Willem M.R. van den Akker, Sarina G. Kant, William B. Dobyns, Bru Cormand, Sophie Currier, Ben C.J. Hamel, Beril Talim, Haluk Topaloğlu, Han G. Brunner

    出版 2003
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  19. 19
    Live fast, die young? A review on the developmental trajectories of ADHD across the lifespan

    Live fast, die young? A review on the developmental trajectories of ADHD across the lifespan 由 Barbara Franke, Giorgia Michelini, Philip Asherson, Tobias Banaschewski, Andrea Bilbow, Jan K. Buitelaar, Bru Cormand, Stephen V. Faraone, Ylva Ginsberg, Jan Haavik, Jonna Kuntsi, Henrik Larsson, Klaus‐Peter Lesch, Josep Antoni Ramos‐Quiroga, János Réthelyi, Marta Ribasés, Andreas Reif

    出版 2018
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  20. 20
    Novel Candidate Genes and a Wide Spectrum of Structural and Point Mutations Responsible for Inherited Retinal Dystrophies Revealed by Exome Sequencing

    Novel Candidate Genes and a Wide Spectrum of Structural and Point Mutations Responsible for Inherited Retinal Dystrophies Revealed by Exome Sequencing 由 Marta de Castro‐Miró, Raúl Tonda, Paula Escudero-Ferruz, Rosa Andrés, Andrés Mayor-Lorenzo, J Albuquerque e Castro, Marcela Ciccioli, Daniel A. Hidalgo, Juan José Rodríguez-Ezcurra, Jorge Farrando, Juan J. Pérez-Santonja, Bru Cormand, Gemma Marfany, Roser Gonzàlez‐Duarte

    出版 2016
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