Publicaciones en colaboración con investigadores/as de Medical Research Council (8)

2015

  1. Psychiatric genome-wide association study analyses implicate neuronal, immune and histone pathways

    Nature Neuroscience, Vol. 18, Núm. 2, pp. 199-209

2014

  1. Angiogenic, neurotrophic, and inflammatory system SNPs moderate the association between birth weight and ADHD symptom severity

    American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics, Vol. 165, Núm. 8, pp. 691-704

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

2009

  1. 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. 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

  2. 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

  3. 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

2006

  1. The analysis of 51 genes in DSM-IV combined type attention deficit hyperactivity disorder: Association signals in DRD4, DAT1 and 16 other genes

    Molecular Psychiatry, Vol. 11, Núm. 10, pp. 934-953