Organización Sanitaria Integrada Ezkerraldea-Enkarterri-Cruces
Organización de Osakidetza
Eduardo
Tolosa Sarró
Publikationen, an denen er mitarbeitet Eduardo Tolosa Sarró (39)
2024
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Magnetic Resonance Imaging Measures to Track Atrophy Progression in Progressive Supranuclear Palsy in Clinical Trials
Movement Disorders, Vol. 39, Núm. 8, pp. 1329-1342
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Mitochondrial DNA deletions in the cerebrospinal fluid of patients with idiopathic REM sleep behaviour disorder
eBioMedicine, Vol. 102
2022
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Cell-free mitochondrial DNA deletions in idiopathic, but not LRRK2, Parkinson's disease
Neurobiology of Disease, Vol. 174
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Differential Phospho-Signatures in Blood Cells Identify LRRK2 G2019S Carriers in Parkinson's Disease
Movement Disorders, Vol. 37, Núm. 5, pp. 1004-1015
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Increased Phospho-AKT in Blood Cells from LRRK2 G2019S Mutation Carriers
Annals of Neurology, Vol. 92, Núm. 5, pp. 888-894
2021
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Finding genetically-supported drug targets for Parkinson’s disease using Mendelian randomization of the druggable genome
Nature Communications, Vol. 12, Núm. 1
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Human-lineage-specific genomic elements are associated with neurodegenerative disease and APOE transcript usage
Nature Communications, Vol. 12, Núm. 1
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Identification of sixteen novel candidate genes for late onset Parkinson’s disease
Molecular Neurodegeneration, Vol. 16, Núm. 1
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Investigation of Autosomal Genetic Sex Differences in Parkinson's Disease
Annals of Neurology, Vol. 90, Núm. 1, pp. 35-42
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Serum metabolic biomarkers for synucleinopathy conversion in isolated REM sleep behavior disorder
npj Parkinson's Disease, Vol. 7, Núm. 1
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Transcriptome analysis in LRRK2 and idiopathic Parkinson’s disease at different glucose levels
npj Parkinson's Disease, Vol. 7, Núm. 1
2020
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Dystonia genes functionally converge in specific neurons and share neurobiology with psychiatric disorders
Brain, Vol. 143, Núm. 9, pp. 2771-2787
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MicroRNA Deregulation in Blood Serum Identifies Multiple System Atrophy Altered Pathways
Movement Disorders, Vol. 35, Núm. 10, pp. 1873-1879
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Nonsteroidal Anti-inflammatory Use and LRRK2 Parkinson's Disease Penetrance
Movement Disorders, Vol. 35, Núm. 10, pp. 1755-1764
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Regulatory sites for splicing in human basal ganglia are enriched for disease-relevant information
Nature Communications, Vol. 11, Núm. 1
2019
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Cerebrospinal fluid cytokines in multiple system atrophy: A cross-sectional Catalan MSA registry study
Parkinsonism and Related Disorders, Vol. 65, pp. 3-12
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Identification of novel risk loci, causal insights, and heritable risk for Parkinson's disease: a meta-analysis of genome-wide association studies
The Lancet Neurology, Vol. 18, Núm. 12, pp. 1091-1102
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Mitochondria function associated genes contribute to Parkinson’s Disease risk and later age at onset
npj Parkinson's Disease, Vol. 5, Núm. 1
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Moving beyond neurons: the role of cell type-specific gene regulation in Parkinson’s disease heritability
npj Parkinson's Disease, Vol. 5, Núm. 1
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SNCA and mTOR Pathway Single Nucleotide Polymorphisms Interact to Modulate the Age at Onset of Parkinson's Disease
Movement Disorders, Vol. 34, Núm. 9, pp. 1333-1344