Publications in collaboration with researchers from Hospital Universitario 12 de Octubre (28)

2023

  1. A second update on mapping the human genetic architecture of COVID-19

    Nature

  2. Epidemiology of ataxia and hereditary spastic paraplegia in Spain: a cross-sectional study

    Neurologia, Vol. 38, Núm. 6, pp. 379-386

  3. Rare predicted loss-of-function variants of type I IFN immunity genes are associated with life-threatening COVID-19

    Genome Medicine, Vol. 15, Núm. 1

2022

  1. Novel genes and sex differences in COVID-19 severity

    Human molecular genetics, Vol. 31, Núm. 22, pp. 3789-3806

2021

  1. Influence of Genetic Polymorphisms on the Response to Tramadol, Ibuprofen, and the Combination in Patients With Moderate to Severe Pain After Dental Surgery

    Clinical Therapeutics, Vol. 43, Núm. 5, pp. e86-e102

  2. SARS-CoV-2-related MIS-C: A key to the viral and genetic causes of Kawasaki disease?

    Journal of Experimental Medicine, Vol. 218, Núm. 6

2020

  1. Autoantibodies against type I IFNs in patients with life-threatening COVID-19

    Science, Vol. 370, Núm. 6515

  2. Inborn errors of type I IFN immunity in patients with life-threatening COVID-19

    Science, Vol. 370, Núm. 6515

  3. Pre-existing Hemagglutinin Stalk Antibodies Correlate with Protection of Lower Respiratory Symptoms in Flu-Infected Transplant Patients

    Cell Reports Medicine, Vol. 1, Núm. 8

2019

  1. Neurological disorders in central Spain, second survey: Feasibility pilot observational study

    Journal of Medical Internet Research, Vol. 21, Núm. 1

2018

  1. Improvement of impulse control disorders associated with levodopa–carbidopa intestinal gel treatment in advanced Parkinson’s disease

    Journal of Neurology, Vol. 265, Núm. 6, pp. 1279-1287

2017

  1. Parkinson's disease severity at 3 years can be predicted from non-motor symptoms at baseline

    Frontiers in Neurology, Vol. 8, Núm. OCT

2016

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

    Scientific Reports, Vol. 6

2015

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

    Brain

  2. 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

2014

  1. Characterization of the repeat expansion size in C9orf72 in amyotrophic lateral sclerosis and frontotemporal dementia

    Human Molecular Genetics, Vol. 23, Núm. 3, pp. 749-754

2012

  1. Clinical correlates of apathy in patients recently diagnosed with parkinson's disease: The ANIMO Study

    Neuroepidemiology, Vol. 38, Núm. 1, pp. 48-55

  2. Impact of apathy on health-related quality of life in recently diagnosed Parkinson's disease: The ANIMO study

    Movement Disorders, Vol. 27, Núm. 2, pp. 211-218

  3. School Performance in Tic Disorders. A Cross-Sectional Study of School Performance in 1,867 Children in Central Spain (IN10-1.001)

    Neurology, Vol. 78, Núm. 1 Supplement

2011

  1. Prevalence of tics in schoolchildren in central Spain: A population-based study

    Pediatric Neurology, Vol. 45, Núm. 2, pp. 100-108