- Facultat de Medicina
Centre
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Universidad de Málaga
Málaga, EspañaPublicacions en col·laboració amb investigadors/es de Universidad de Málaga (34)
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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Design and baseline characteristics of SALT-HF trial: hypertonic saline therapy in ambulatory heart failure
ESC Heart Failure, Vol. 11, Núm. 3, pp. 1767-1776
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Genetic Association Studies in Host-Pathogen Interaction Analysis
Methods in molecular biology (Clifton, N.J.), Vol. 2751, pp. 19-30
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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Genetic Associations between Modifiable Risk Factors and Alzheimer Disease
JAMA Network Open, Vol. 6, Núm. 5
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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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Multiancestry analysis of the HLA locus in Alzheimer's and Parkinson's diseases uncovers a shared adaptive immune response mediated by HLA-DRB1*04 subtypes
Proceedings of the National Academy of Sciences of the United States of America, Vol. 120, Núm. 36
2022
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Association of Rare APOE Missense Variants V236E and R251G with Risk of Alzheimer Disease
JAMA Neurology, Vol. 79, Núm. 7, pp. 652-663
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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
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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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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Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition)1
Autophagy, Vol. 17, Núm. 1, pp. 1-382
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Long runs of homozygosity are associated with Alzheimer’s disease
Translational Psychiatry, Vol. 11, Núm. 1
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Straightforward protocol for allele-specific chromatin conformation capture
Gene, Vol. 767
2020
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ADHD Symptoms, Academic and Social Difficulties in Parents of Children with ADHD
Psychiatry (New York), Vol. 83, Núm. 3, pp. 231-243
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De novo assembly of the Brown trout (Salmo trutta m. fario) brain and muscle transcriptome: transcript annotation, tissue differential expression profile and SNP discovery
BMC Research Notes, Vol. 13, Núm. 1
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Toll-Like Receptor 2 Promoter -196 to -174 Deletion Affects CD4 Levels Along Human Immunodeficiency Virus Infection Progression
The Journal of infectious diseases, Vol. 222, Núm. 12, pp. 2007-2011
2018
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A common copy-number variant within SIRPB1 correlates with human out-of-Africa migration after genetic drift correction
PLoS ONE, Vol. 13, Núm. 3
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The rs2108622 polymorphism is related to the early risk of ischemic stroke in non-valvular atrial fibrillation subjects under oral anticoagulation
Pharmacogenomics Journal, Vol. 18, Núm. 5, pp. 652-656
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Vitamin D Receptor polymorphisms and risk of enveloped virus infection: A meta-analysis
Gene, Vol. 678, pp. 384-394