MANUEL
MENENDEZ GONZALEZ
Profesor Titular de Universidad
Centro de Investigación Biomédica en Red sobre Enfermedades Neurodegenerativas
Madrid, EspañaPublikationen in Zusammenarbeit mit Forschern von 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