Neurociencias
Departamento
Javier
Pagonabarraga Mora
Publicaciones en las que colabora con Javier Pagonabarraga Mora (26)
2023
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Cognitive impairment and dementia in young onset Parkinson’s disease
Journal of Neurology, Vol. 270, Núm. 12, pp. 5793-5812
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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Predictors of clinically significant quality of life impairment in Parkinson’s disease
npj Parkinson's Disease, Vol. 7, Núm. 1
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Sleep Problems Are Related to a Worse Quality of Life and a Greater Non-Motor Symptoms Burden in Parkinson’s Disease
Journal of Geriatric Psychiatry and Neurology, Vol. 34, Núm. 6, pp. 642-658
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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Effects of Motor Symptom Laterality on Clinical Manifestations and Quality of Life in Parkinson's Disease
Journal of Parkinson's Disease, Vol. 10, Núm. 4, pp. 1611-1620
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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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Non-motor symptom burden in patients with Parkinson’s disease with impulse control disorders and compulsive behaviours: results from the COPPADIS cohort
Scientific Reports, Vol. 10, Núm. 1
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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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The impact of freezing of gait on functional dependency in Parkinson’s disease with regard to motor phenotype
Neurological Sciences, Vol. 41, Núm. 10, pp. 2883-2892
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Transcriptomic differences in MSA clinical variants
Scientific Reports, Vol. 10, Núm. 1
2019
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COPPADIS-2015 (COhort of Patients with PArkinson's DIsease in Spain, 2015): an ongoing global Parkinson's disease project about disease progression with more than 1000 subjects included. Results from the baseline evaluation
European Journal of Neurology, Vol. 26, Núm. 11, pp. 1399-1407
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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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Clinical and genetic characteristics of late-onset Huntington's disease
Parkinsonism and Related Disorders, Vol. 61, pp. 101-105
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High ultrasensitive serum C-reactive protein may be related to freezing of gait in Parkinson’s disease patients
Journal of Neural Transmission, Vol. 126, Núm. 12, pp. 1599-1608
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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