Publicaciones en colaboración con investigadores/as de Hospital General Universitario Gregorio Marañón (9)

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

  2. The paediatric cancer clinical research landscape in Spain: a 13-year multicentre experience of the new agents group of the Spanish Society of Paediatric Haematology and Oncology (SEHOP)

    Clinical and Translational Oncology, Vol. 23, Núm. 12, pp. 2489-2496

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

2015

  1. Correlation of myelodysplastic syndromes with i(17)(q10) and TP53 and SETBP1 mutations

    British Journal of Haematology

  2. Recommendations for somatic and germline genetic testing of single pheochromocytoma and paraganglioma based on findings from a series of 329 patients

    Journal of Medical Genetics, Vol. 52, Núm. 10, pp. 647-656

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