Juan Carlos
Martínez Castrillo
Profesor/a Asociado/a en CC. de la Salud
![Foto de Juan Carlos](/img/nophoto.png)
![Foto de Hospital Universitario Virgen de las Nieves](/img/noimage_org.png)
Hospital Universitario Virgen de las Nieves
Granada, EspañaPublicacións en colaboración con investigadores/as de Hospital Universitario Virgen de las Nieves (17)
2024
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Concerns with the new biological research criteria for synucleinopathy
The Lancet Neurology
2023
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Staging Parkinson's Disease According to the MNCD (Motor/Non-motor/Cognition/Dependency) Classification Correlates with Disease Severity and Quality of Life
Journal of Parkinson's disease, Vol. 13, Núm. 3, pp. 379-402
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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Management of Parkinson's disease and other movement disorders in woman of childbearing age: Part 1
Neurologia, Vol. 36, Núm. 2, pp. 149-158
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Management of Parkinson's disease and other movement disorders in women of childbearing age: Part 2
Neurologia, Vol. 36, Núm. 2, pp. 159-168
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Mutational spectrum of GNAL, THAP1 and TOR1A genes in isolated dystonia: study in a population from Spain and systematic literature review
European Journal of Neurology, Vol. 28, Núm. 4, pp. 1188-1197
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Opicapone for the treatment of Parkinson’s disease: real-life data in Spain
Revista de Neurologia, Vol. 73, pp. S1-S14
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Present and future of parkinson’s disease in Spain: Parkinson-2030 delphi project
Brain Sciences, Vol. 11, Núm. 8
2020
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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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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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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
2014
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BDNF Val66Met polymorphism in primary adult-onset dystonia: A case-control study and meta-analysis
Movement Disorders, Vol. 29, Núm. 8, pp. 1083-1086
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Lack of validation of variants associated with cervical dystonia risk: A GWAS replication study
Movement Disorders, Vol. 29, Núm. 14, pp. 1825-1828
2006
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A longitudinal study of patients with Parkinson's disease (ELEP): Aims and methodology
Revista de Neurologia, Vol. 42, Núm. 6, pp. 360-365
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Creación y protocolo de seguimiento longitudinal de una cohorte multipropósito de pacientes con enfermedad de Parkinson de reciente diagnóstico: Proyecto VIP
Revista de Neurologia, Vol. 43, Núm. 6, pp. 366-373