Publicaciones en colaboración con investigadoras/es de Hospital de Cruces (29)

2021

  1. Drug compatibility in neonatal intensive care units: gaps in knowledge and discordances

    European Journal of Pediatrics, Vol. 180, Núm. 7, pp. 2305-2313

  2. Physical compatibility of alprostadil with selected drugs commonly used in the neonatal intensive care units

    European Journal of Pediatrics, Vol. 180, Núm. 4, pp. 1169-1176

2020

  1. BRAF V600E mutational load as a prognosis biomarker in malignant melanoma

    PLoS ONE, Vol. 15, Núm. 3

2014

  1. Coregulation and modulation of NFκB-related genes in celiac disease: Uncovered aspects of gut mucosal inflammation

    Human Molecular Genetics, Vol. 23, Núm. 5

2013

  1. A novel form of human disease

    Prion Biology: Research and Advances (Apple Academic Press), pp. 179-210

  2. Simultaneous purifying selection on the Ancestral MC1R allele and positive selection on the melanoma-risk Allele V60L in South Europeans

    Molecular Biology and Evolution, Vol. 30, Núm. 12, pp. 2654-2665

2012

  1. UBQ-8i polymorphism is not an independent risk factor for mild cognitive impairment and Alzheimer's disease in APOE-4 carriers

    Current Alzheimer Research, Vol. 9, Núm. 4, pp. 467-472

2011

  1. Progression from amnesic mild cognitive impairment to alzheimer's disease: ESR1 and ESR2 polymorphisms and APOE gene

    Dementia and Geriatric Cognitive Disorders, Vol. 32, Núm. 5, pp. 332-341

2010

  1. Cardiac sympathetic denervation precedes nigrostriatal loss in the E46K mutation of the α-synuclein gene (SNCA)

    Clinical Autonomic Research, Vol. 20, Núm. 4, pp. 267-269

  2. The diversity profile of TP53 is influenced by positive selection on the immediately upstream locus WDR79

    Human Heredity, Vol. 69, Núm. 1, pp. 34-44

2009

  1. Lrrk2 R1441G-related Parkinson's disease: Evidence of a common founding event in the seventh century in Northern Spain

    Neurogenetics, Vol. 10, Núm. 4, pp. 347-353

  2. The COMT Val158 met polymorphism as an associated risk factor for Alzheimer disease and mild cognitive impairment in APOE 4 carriers

    BMC Neuroscience, Vol. 10, pp. 125

2008

  1. Complex signatures of selection for the melanogenic loci TYR, TYRP1 and DCT in humans

    BMC Evolutionary Biology, Vol. 8, Núm. 1

  2. Molecular evidence of founder effects of fatal familial insomnia through SNP haplotypes around the D178N mutation

    Neurogenetics, Vol. 9, Núm. 2, pp. 109-118

2007

  1. Lrrk2-associated parkinsonism is a major cause of disease in Northern Spain

    Parkinsonism and Related Disorders, Vol. 13, Núm. 8, pp. 509-515

2006

  1. Fetal sex determination from maternal plasma by nested PCR of the amelogenin gene

    International Congress Series, Vol. 1288, pp. 691-693

  2. Polymorphism in the cholesterol 24S-hydroxylase gene (CYP46A1) associated with the APOEε3 allele increases the risk of Alzheimer's disease and of mild cognitive impairment progressing to Alzheimer's disease

    Dementia and Geriatric Cognitive Disorders, Vol. 21, Núm. 2, pp. 81-87

2005

  1. A novel mutation (K317M) in the MAPT gene causes FTDP and motor neuron disease

    Neurology, Vol. 64, Núm. 9, pp. 1578-1585

  2. Ancestral origins of the prion protein gene D178N mutation in the Basque Country

    Human Genetics, Vol. 117, Núm. 1, pp. 61-69

2004

  1. High levels of p53 protein expression do not correlate with p53 mutations in hepatocellular carcinoma

    Journal of Viral Hepatitis, Vol. 11, Núm. 6, pp. 502-510