Javier
Pagonabarraga Mora
Publicacions en què col·labora amb Javier Pagonabarraga Mora (15)
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
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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Regulatory sites for splicing in human basal ganglia are enriched for disease-relevant information
Nature Communications, Vol. 11, Núm. 1
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Transcriptomic differences in MSA clinical variants
Scientific Reports, Vol. 10, 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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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
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The Genetic Architecture of Parkinson Disease in Spain: Characterizing Population-Specific Risk, Differential Haplotype Structures, and Providing Etiologic Insight
Movement Disorders, Vol. 34, Núm. 12, pp. 1851-1863
2018
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Cerebrospinal fluid levels of coenzyme Q10 are reduced in multiple system atrophy
Parkinsonism and Related Disorders, Vol. 46, pp. 16-23
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LRP10 in α-synucleinopathies
The Lancet Neurology