Publicaciones en colaboración con investigadores/as de Trinity College Dublin (22)

2024

  1. Circulating myeloid-derived MMP8 in stress susceptibility and depression

    Nature, Vol. 626, Núm. 8001, pp. 1108-1115

  2. Smartphone-based serious games for mental health: a scoping review

    Multimedia Tools and Applications

2022

  1. An aphasia research agenda–a consensus statement from the collaboration of aphasia trialists

    Aphasiology, Vol. 36, Núm. 4, pp. 555-574

2021

  1. Internet-Based Cognitive Behavioral Therapy for Depression: A Systematic Review and Individual Patient Data Network Meta-analysis

    JAMA Psychiatry, Vol. 78, Núm. 4, pp. 361-371

2020

  1. How and for whom does a positive affect intervention work in fibromyalgia: An analysis of mediators and moderators

    European Journal of Pain (United Kingdom), Vol. 24, Núm. 1, pp. 248-262

2019

  1. Effects of the Best Possible Self intervention: A systematic review and meta-analysis

    PLoS ONE, Vol. 14, Núm. 9

2018

  1. Exploring the incorporation of a positive psychology component in a cognitive behavioral internet-based program for depressive symptoms. Results throughout the intervention process

    Frontiers in Psychology, Vol. 9, Núm. NOV

2016

  1. Mild cognitive decline. A position statement of the Cognitive Decline Group of the European Innovation Partnership for Active and Healthy Ageing (EIPAHA)

    Maturitas, Vol. 83, pp. 83-93

2013

  1. Humane Orientation as a New Cultural Dimension of the GLOBE Project: A Validation Study of the GLOBE Scale and Out-Group Humane Orientation in 25 Countries

    Journal of Cross-Cultural Psychology, Vol. 44, Núm. 4, pp. 535-551

2011

  1. A functional variant of the serotonin transporter gene ((SLC6A4) moderates impulsive choice in attention-deficit/hyperactivity disorder boys and siblings

    Biological Psychiatry, Vol. 70, Núm. 3, pp. 230-236

2010

  1. Performance variability, impulsivity errors and the impact of incentives as gender-independent endophenotypes for ADHD

    Journal of Child Psychology and Psychiatry and Allied Disciplines, Vol. 51, Núm. 2, pp. 210-218

2009

  1. Autism symptoms in attention-deficit/hyperactivity disorder: A familial trait which correlates with conduct, oppositional defiant, language and motor disorders

    Journal of Autism and Developmental Disorders, Vol. 39, Núm. 2, pp. 197-209

  2. Autism symptoms in attention-deficit/hyperactivity disorder: A familial trait which correlates with conduct, oppositional defiant, language and motor disorders (Journal of Autism and Developmental Disorders DOI: 10.1007/s10803-008-0621-3)

    Journal of Autism and Developmental Disorders

  3. Delay and Reward Choice in ADHD: An Experimental Test of the Role of Delay Aversion

    Neuropsychology, Vol. 23, Núm. 3, pp. 367-380

  4. No association between two polymorphisms of the serotonin transporter gene and combined type attention deficit hyperactivity disorder (American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics (2008) 147B, (1306-1309))

    American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics

2008

  1. A high-density SNP linkage scan with 142 combined subtype ADHD sib pairs identifies linkage regions on chromosomes 9 and 16

    Molecular Psychiatry, Vol. 13, Núm. 5, pp. 514-521

  2. Co-transmission of conduct problems with attention-deficit/hyperactivity disorder: Familial evidence for a distinct disorder

    Journal of Neural Transmission, Vol. 115, Núm. 2, pp. 163-175

  3. DSM-IV combined type ADHD shows familial association with sibling trait scores: A sampling strategy for QTL linkage

    American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics, Vol. 147, Núm. 8, pp. 1450-1460

  4. Linkage to Chromosome 1p36 for Attention-Deficit/Hyperactivity Disorder Traits in School and Home Settings

    Biological Psychiatry, Vol. 64, Núm. 7, pp. 571-576

  5. No association between two polymorphisms of the serotonin transporter gene and combined type attention deficit hyperactivity disorder

    American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics, Vol. 147, Núm. 7, pp. 1306-1309