SARA
ORTEGA CUBERO
Profesor Asociado
Publikationen (68) Publikationen von SARA ORTEGA CUBERO
2023
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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
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Seizure prophylaxis in meningiomas: A systematic review and meta-analysis
Neurologia, Vol. 38, Núm. 4, pp. 291-302
2022
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Viltolarsen y la Distrofia Muscular de Duchenne
MoleQla: revista de Ciencias de la Universidad Pablo de Olavide, Núm. 45
2021
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Exome-wide rare variant analysis in familial essential tremor
Parkinsonism and Related Disorders, Vol. 82, pp. 109-116
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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
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SLITRK2, an X-linked modifier of the age at onset in C9orf72 frontotemporal lobar degeneration
Brain, Vol. 144, Núm. 9, pp. 2798-2811
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Volumetric growth rate of incidental asymptomatic meningiomas: a single-center prospective cohort study
Acta Neurochirurgica, Vol. 163, Núm. 6, pp. 1665-1675
2020
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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
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Mendelian randomization implies no direct causal association between leukocyte telomere length and amyotrophic lateral sclerosis
Scientific Reports, Vol. 10, Núm. 1
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Vancomycin powder for the prevention of surgical site infection in posterior elective spinal surgery
Neurocirugia, Vol. 31, Núm. 2, pp. 64-75
2019
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Cauda equina syndrome due to disk herniation: Long-term functional prognosis
Neurocirugia, Vol. 30, Núm. 6, pp. 278-287
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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
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Globular glial tauopathy caused by MAPT P301T mutation: clinical and neuropathological findings
Journal of Neurology, Vol. 266, Núm. 10, pp. 2396-2405
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Identification of evolutionarily conserved gene networks mediating neurodegenerative dementia
Nature Medicine, Vol. 25, Núm. 1, pp. 152-164
2018
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A C6orf10/LOC101929163 locus is associated with age of onset in C9orf72 carriers
Brain, Vol. 141, Núm. 10, pp. 2895-2907
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CXCR4 involvement in neurodegenerative diseases
Translational Psychiatry, Vol. 8, Núm. 1
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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
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Heterozygous STUB1 mutation causes familial ataxia with cognitive affective syndrome (SCA48)
Neurology, Vol. 91, Núm. 21, pp. E1988-E1998
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Immune-related genetic enrichment in frontotemporal dementia: An analysis of genome-wide association studies
PLoS Medicine, Vol. 15, Núm. 1
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Papel de la cirugía en el tratamiento de las espondilodiscitis espontáneas: experiencia en 83 casos consecutivos
Neurocirugia, Vol. 29, Núm. 2, pp. 64-78