Publicaciones en las que colabora con P. Pastor (33)

2021

  1. Exome-wide rare variant analysis in familial essential tremor

    Parkinsonism and Related Disorders, Vol. 82, pp. 109-116

2020

  1. Mendelian randomization implies no direct causal association between leukocyte telomere length and amyotrophic lateral sclerosis

    Scientific Reports, Vol. 10, Núm. 1

2019

  1. Globular glial tauopathy caused by MAPT P301T mutation: clinical and neuropathological findings

    Journal of Neurology, Vol. 266, Núm. 10, pp. 2396-2405

2017

  1. Thr105Ile (rs11558538) polymorphism in the histamine-1-methyl-transferase (HNMT) gene and risk for restless legs syndrome

    Journal of Neural Transmission, Vol. 124, Núm. 3, pp. 285-291

2016

  1. A comprehensive study of the genetic impact of rare variants in SORL1 in European early-onset Alzheimer’s disease

    Acta Neuropathologica, Vol. 132, Núm. 2, pp. 213-224

  2. A family study of DRD3 rs6280, SLC1A2 rs3794087 and MAPT rs1052553 variants in essential tremor

    Neurological Research, Vol. 38, Núm. 10, pp. 880-887

  3. A novel Alzheimer disease locus located near the gene encoding tau protein

    Molecular Psychiatry, Vol. 21, Núm. 1, pp. 108-117

  4. Genome-wide analysis of genetic correlation in dementia with Lewy bodies, Parkinson's and Alzheimer's diseases

    Neurobiology of Aging, Vol. 38, pp. 214.e7-214.e10

  5. Heme Oxygenase-1 and 2 Common Genetic Variants and Risk for Multiple Sclerosis

    Scientific Reports, Vol. 6

  6. Neuroimaging Correlates of Frontotemporal Dementia Associated with SQSTM1 Mutations

    Journal of Alzheimer's Disease, Vol. 53, Núm. 1, pp. 303-313

  7. Resequencing analysis of five Mendelian genes and the top genes from genome-wide association studies in Parkinson's Disease

    Molecular Neurodegeneration, Vol. 11, Núm. 1

2015

  1. Analysis of the CHCHD10 gene in patients with frontotemporal dementia and amyotrophic lateral sclerosis from Spain

    Brain

  2. Association between Vitamin D receptor rs731236 (Taq1) polymorphism and risk for restless legs syndrome in the Spanish caucasian population

    Medicine (United States), Vol. 94, Núm. 47, pp. e2125

  3. Automated Neuromelanin Imaging as a Diagnostic Biomarker for Parkinson's Disease

    Movement Disorders, Vol. 30, Núm. 7, pp. 945-952

  4. Descripción de una serie de pacientes con diagnóstico de enfermedad priónica

    Neurologia, Vol. 30, Núm. 3, pp. 144-152

  5. Genetic variability in SQSTM1 and risk of early-onset Alzheimer dementia: A European early-onset dementia consortium study

    Neurobiology of Aging, Vol. 36, Núm. 5, pp. 2005.e15-2005.e22

  6. Heme Oxygenase 1 and 2 Common Genetic Variants and Risk for Essential Tremor

    Medicine, Vol. 94, Núm. 24, pp. e968

  7. Heme Oxygenase-1 and 2 Common Genetic Variants and Risk for Restless Legs Syndrome

    Medicine (United States), Vol. 94, Núm. 34, pp. e1448

  8. MAPT H1 haplotype is associated with late-onset Alzheimer's disease risk in APOE ε 4 noncarriers: Results from the dementia genetics Spanish consortium

    Journal of Alzheimer's Disease, Vol. 49, Núm. 2, pp. 343-352

  9. Missense mutations in TENM4, a regulator of axon guidance and central myelination, cause essential tremor

    Human Molecular Genetics, Vol. 24, Núm. 20, pp. 5677-5686