Publikationen in Zusammenarbeit mit Forschern von Universitat Autònoma de Barcelona (22)

2024

  1. DRD4 gene polymorphism and impulse control disorder induced by dopamine agonists in Parkinson's disease

    Annals of Clinical and Translational Neurology, Vol. 11, Núm. 8, pp. 2222-2229

2023

  1. Midbrain and pons MRI shape analysis and its clinical and CSF correlates in degenerative parkinsonisms: a pilot study

    European Radiology, Vol. 33, Núm. 7, pp. 4540-4551

2022

  1. Cannabinoid signaling modulation through JZL184 restores key phenotypes of a mouse model for Williams-Beuren syndrome

    eLife, Vol. 11

  2. Handling and novel object recognition modulate fear response and endocannabinoid signaling in nucleus basalis magnocellularis

    European Journal of Neuroscience, Vol. 55, Núm. 6, pp. 1532-1546

2021

  1. Finding genetically-supported drug targets for Parkinson’s disease using Mendelian randomization of the druggable genome

    Nature Communications, Vol. 12, Núm. 1

  2. Human-lineage-specific genomic elements are associated with neurodegenerative disease and APOE transcript usage

    Nature Communications, Vol. 12, Núm. 1

  3. Modulation of neurolipid signaling and specific lipid species in the triple transgenic mouse model of alzheimer’s disease

    International Journal of Molecular Sciences, Vol. 22, Núm. 22

  4. Serum metabolic biomarkers for synucleinopathy conversion in isolated REM sleep behavior disorder

    npj Parkinson's Disease, Vol. 7, Núm. 1

2020

  1. Regulatory sites for splicing in human basal ganglia are enriched for disease-relevant information

    Nature Communications, Vol. 11, Núm. 1

2019

  1. Cerebrospinal fluid cytokines in multiple system atrophy: A cross-sectional Catalan MSA registry study

    Parkinsonism and Related Disorders, Vol. 65, pp. 3-12

  2. Mitochondria function associated genes contribute to Parkinson’s Disease risk and later age at onset

    npj Parkinson's Disease, Vol. 5, Núm. 1

  3. Moving beyond neurons: the role of cell type-specific gene regulation in Parkinson’s disease heritability

    npj Parkinson's Disease, Vol. 5, Núm. 1

  4. 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

  5. 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

  1. Cerebrospinal fluid levels of coenzyme Q10 are reduced in multiple system atrophy

    Parkinsonism and Related Disorders, Vol. 46, pp. 16-23

  2. α-synuclein (SNCA) but not dynamin 3 (DNM3) influences age at onset of leucine-rich repeat kinase 2 (LRRK2) Parkinson's disease in Spain

    Movement Disorders, Vol. 33, Núm. 4, pp. 637-641

2017

  1. Cross-sectional and longitudinal cognitive correlates of FDDNP PET and CSF amyloid-β and tau in Parkinson's disease

    Journal of Alzheimer's Disease, Vol. 55, Núm. 3, pp. 1261-1272

2016

  1. Knowledge and Attitudes of Nurses in Spain about Inhaled Therapy: Results of a National Survey

    Journal of Aerosol Medicine and Pulmonary Drug Delivery, Vol. 29, Núm. 1, pp. 86-93

2015

  1. A Native Ternary Complex Trapped in a Crystal Reveals the Catalytic Mechanism of a Retaining Glycosyltransferase

    Angewandte Chemie - International Edition, Vol. 54, Núm. 34, pp. 9898-9902

2014

  1. Diagnostic validity of the alzheimer's disease functional assessment and change scale in mild cognitive impairment and mild to moderate alzheimer's disease

    Dementia and Geriatric Cognitive Disorders, Vol. 37, Núm. 5-6, pp. 366-375