Publicaciones (68) Publicaciones de SARA ORTEGA CUBERO

2023

  1. Prioritization of Drug Targets for Neurodegenerative Diseases by Integrating Genetic and Proteomic Data From Brain and Blood

    Biological Psychiatry, Vol. 93, Núm. 9, pp. 770-779

  2. Seizure prophylaxis in meningiomas: A systematic review and meta-analysis

    Neurologia, Vol. 38, Núm. 4, pp. 291-302

2022

  1. Viltolarsen y la Distrofia Muscular de Duchenne

    MoleQla: revista de Ciencias de la Universidad Pablo de Olavide, Núm. 45

2021

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

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

  2. Gene Expression Imputation Across Multiple Tissue Types Provides Insight Into the Genetic Architecture of Frontotemporal Dementia and Its Clinical Subtypes

    Biological Psychiatry, Vol. 89, Núm. 8, pp. 825-835

  3. SLITRK2, an X-linked modifier of the age at onset in C9orf72 frontotemporal lobar degeneration

    Brain, Vol. 144, Núm. 9, pp. 2798-2811

  4. Volumetric growth rate of incidental asymptomatic meningiomas: a single-center prospective cohort study

    Acta Neurochirurgica, Vol. 163, Núm. 6, pp. 1665-1675

2020

  1. Correction to: A nonsynonymous mutation in PLCG2 reduces the risk of Alzheimer’s disease, dementia with Lewy bodies and frontotemporal dementia, and increases the likelihood of longevity (Acta Neuropathologica, (2019), 138, 2, (237-250), 10.1007/s00401-019-02026-8)

    Acta Neuropathologica

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

    Scientific Reports, Vol. 10, Núm. 1

  3. Vancomycin powder for the prevention of surgical site infection in posterior elective spinal surgery

    Neurocirugia, Vol. 31, Núm. 2, pp. 64-75

2019

  1. Cauda equina syndrome due to disk herniation: Long-term functional prognosis

    Neurocirugia, Vol. 30, Núm. 6, pp. 278-287

  2. Genetic variation across RNA metabolism and cell death gene networks is implicated in the semantic variant of primary progressive aphasia

    Scientific Reports, Vol. 9, Núm. 1

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

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

  4. Identification of evolutionarily conserved gene networks mediating neurodegenerative dementia

    Nature Medicine, Vol. 25, Núm. 1, pp. 152-164

2018

  1. A C6orf10/LOC101929163 locus is associated with age of onset in C9orf72 carriers

    Brain, Vol. 141, Núm. 10, pp. 2895-2907

  2. CXCR4 involvement in neurodegenerative diseases

    Translational Psychiatry, Vol. 8, Núm. 1

  3. Genetically elevated high-density lipoprotein cholesterol through the cholesteryl ester transfer protein gene does not associate with risk of Alzheimer's disease

    Alzheimer's and Dementia: Diagnosis, Assessment and Disease Monitoring, Vol. 10, pp. 595-598

  4. Heterozygous STUB1 mutation causes familial ataxia with cognitive affective syndrome (SCA48)

    Neurology, Vol. 91, Núm. 21, pp. E1988-E1998

  5. Immune-related genetic enrichment in frontotemporal dementia: An analysis of genome-wide association studies

    PLoS Medicine, Vol. 15, Núm. 1

  6. Papel de la cirugía en el tratamiento de las espondilodiscitis espontáneas: experiencia en 83 casos consecutivos

    Neurocirugia, Vol. 29, Núm. 2, pp. 64-78