Publicaciones en colaboración con investigadoras/es de Copenhagen University Hospital (11)

2024

  1. Severe steroid-related neuropsychiatric symptoms during paediatric acute lymphoblastic leukaemia therapy—An observational Ponte di Legno Toxicity Working Group Study

    British Journal of Haematology, Vol. 205, Núm. 4, pp. 1450-1459

2022

  1. Characteristics of white blood cell count in acute lymphoblastic leukemia: A COST LEGEND phenotype–genotype study

    Pediatric Blood and Cancer, Vol. 69, Núm. 6

  2. Hypersensitivity to Pegylated E.colia sparaginase as first-line treatment in contemporary paediatric acute lymphoblastic leukaemia protocols: a meta-analysis of the Ponte di Legno Toxicity working group

    European Journal of Cancer, Vol. 162, pp. 65-75

2021

  1. Pancreatitis-associated protein as an early marker of asparaginase-associated pancreatitis

    Leukemia and Lymphoma

  2. Severe toxicity free survival: physician-derived definitions of unacceptable long-term toxicities following acute lymphocytic leukaemia

    The Lancet Haematology, Vol. 8, Núm. 7, pp. e513-e523

  3. Systematic review of pharmacogenetic factors that influence high-dose methotrexate pharmacokinetics in pediatric malignancies

    Cancers, Vol. 13, Núm. 11

2015

  1. Exploring genetic factors involved in huntington disease age of onset: E2F2 as a new potential modifier gene

    PLoS ONE, Vol. 10, Núm. 7

  2. Imprinting disorders: a group of congenital disorders with overlapping patterns of molecular changes affecting imprinted loci

    Clinical Epigenetics, Vol. 7, Núm. 1

2008

  1. Refining genetic associations in multiple sclerosis

    The Lancet Neurology

2007

  1. Corrigendum to "Linkage disequilibrium screening for multiple sclerosis implicates JAG1 and POU2AF1 as susceptibility genes in Europeans" [J. Neuroimmunol. 179 (2006) 108-116] (DOI:10.1016/j.jneuroim.2006.06.003)

    Journal of Neuroimmunology

1998

  1. The Δccr5 mutation conferring protection against HIV-1 in Caucasian populations has a single and recent origin in Northeastern Europe

    Human Molecular Genetics, Vol. 7, Núm. 3, pp. 399-406