Publicaciones en colaboración con investigadores/as de Hospital Universitario Marqués de Valdecilla (8)

2021

  1. Author Correction: The utility of Next Generation Sequencing for molecular diagnostics in Rett syndrome (Scientific Reports, (2017), 7, 1, (12288), 10.1038/s41598-017-11620-3)

    Scientific Reports

2020

  1. Diagnostic delay and outcome in immunocompetent patients with primary central nervous system lymphoma in Spain: a multicentric study

    Journal of Neuro-Oncology, Vol. 148, Núm. 3, pp. 545-554

2019

  1. X chromosome inactivation does not necessarily determine the severity of the phenotype in Rett syndrome patients

    Scientific Reports, Vol. 9, Núm. 1

2017

  1. The utility of Next Generation Sequencing for molecular diagnostics in Rett syndrome

    Scientific Reports, Vol. 7, Núm. 1

2013

  1. Involvement of miRNAs in the Differentiation of Human Glioblastoma Multiforme Stem-Like Cells

    PLoS ONE, Vol. 8, Núm. 10

2008

  1. DRD3, but not COMT or DRD2, genotype affects executive functions in healthy and first-episode psychosis adolescents

    American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics, Vol. 147, Núm. 6, pp. 873-879

  2. The genetic contribution to first psychotic episodes in children and adolescents of the child and adolescent first-episode psychosis study

    Psychiatric Genetics, Vol. 18, Núm. 3, pp. 151-152

2007

  1. The child and adolescent first-episode psychosis study (CAFEPS): Design and baseline results

    Schizophrenia Research, Vol. 91, Núm. 1-3, pp. 226-237