MANUEL
MENENDEZ GONZALEZ
Profesor Titular de Universidad
Centro de Investigación Biomédica en Red sobre Enfermedades Neurodegenerativas
Madrid, EspañaPublicaciones en colaboración con investigadores/as de Centro de Investigación Biomédica en Red sobre Enfermedades Neurodegenerativas (24)
2024
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An Insertion Within SIRPβ1 Shows a Dual Effect Over Alzheimer's Disease Cognitive Decline Altering the Microglial Response
Journal of Alzheimer's Disease, Vol. 98, Núm. 2, pp. 601-618
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Huntingtin CAG repeats in neuropathologically confirmed tauopathies: Novel insights
Brain Pathology
2023
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Erratum: Author Correction: Common variants in Alzheimer's disease and risk stratification by polygenic risk scores (Nature communications (2021) 12 1 (3417))
Nature communications
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Mendelian Randomisation Confirms the Role of Y-Chromosome Loss in Alzheimer’s Disease Aetiopathogenesis in Men
International Journal of Molecular Sciences, Vol. 24, Núm. 2
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Sex Differences in Motor and Non-Motor Symptoms among Spanish Patients with Parkinson’s Disease
Journal of Clinical Medicine, Vol. 12, Núm. 4
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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
2022
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Intermediate and Expanded HTT Alleles and the Risk for α-Synucleinopathies
Movement Disorders, Vol. 37, Núm. 9, pp. 1841-1849
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New insights into the genetic etiology of Alzheimer's disease and related dementias
Nature genetics, Vol. 54, Núm. 4, pp. 412-436
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New, Fully Implantable Device for Selective Clearance of CSF-Target Molecules: Proof of Concept in a Murine Model of Alzheimer's Disease
International journal of molecular sciences, Vol. 23, Núm. 16
2021
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Common variants in Alzheimer's disease and risk stratification by polygenic risk scores
Nature communications, Vol. 12, Núm. 1, pp. 3417
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Genetic variation in APOE, GRN, and TP53 are phenotype modifiers in frontotemporal dementia
Neurobiology of Aging, Vol. 99, pp. 99.e15-99.e22
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Genomic characterization of host factors related to SARS-CoV-2 infection in people with dementia and control populations: The GR@ACE/DEGESCO study
Journal of Personalized Medicine, Vol. 11, Núm. 12
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Long runs of homozygosity are associated with Alzheimer’s disease
Translational Psychiatry, Vol. 11, Núm. 1
2020
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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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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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Role for ATXN1, ATXN2, and HTT intermediate repeats in frontotemporal dementia and Alzheimer's disease
Neurobiology of Aging, Vol. 87, pp. 139.e1-139.e7
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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
2019
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Genome-wide association analysis of dementia and its clinical endophenotypes reveal novel loci associated with Alzheimer's disease and three causality networks: The GR@ACE project
Alzheimer's and Dementia, Vol. 15, Núm. 10, pp. 1333-1347
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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