FACULTAD DE CIENCIAS DE LA SALUD
Facultad/Centro de investigación
Washington University in St. Louis
San Luis, Estados UnidosPublications en collaboration avec des chercheurs de Washington University in St. Louis (16)
2024
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Multi-ancestry genome-wide association meta-analysis of Parkinson’s disease
Nature Genetics, Vol. 56, Núm. 1, pp. 27-36
2023
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Author Correction: Elucidating causative gene variants in hereditary Parkinson’s disease in the Global Parkinson’s Genetics Program (GP2) (npj Parkinson's Disease, (2023), 9, 1, (100), 10.1038/s41531-023-00526-9)
npj Parkinson's Disease
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Defining the causes of sporadic Parkinson’s disease in the global Parkinson’s genetics program (GP2)
npj Parkinson's Disease, Vol. 9, Núm. 1
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Rare predicted loss-of-function variants of type I IFN immunity genes are associated with life-threatening COVID-19
Genome Medicine, Vol. 15, Núm. 1
2021
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Age differences in emotion regulation during ongoing affective life: A naturalistic experience sampling study
Developmental psychology, Vol. 57, Núm. 1, pp. 126-138
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SARS-CoV-2-related MIS-C: A key to the viral and genetic causes of Kawasaki disease?
Journal of Experimental Medicine, Vol. 218, Núm. 6
2020
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Mendelian randomization implies no direct causal association between leukocyte telomere length and amyotrophic lateral sclerosis
Scientific Reports, Vol. 10, Núm. 1
2019
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Genetic variation across RNA metabolism and cell death gene networks is implicated in the semantic variant of primary progressive aphasia
Scientific Reports, Vol. 9, Núm. 1
2018
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CXCR4 involvement in neurodegenerative diseases
Translational Psychiatry, Vol. 8, Núm. 1
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Immune-related genetic enrichment in frontotemporal dementia: An analysis of genome-wide association studies
PLoS Medicine, Vol. 15, Núm. 1
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Pleiotropic effects of variants in dementia genes in Parkinson disease
Frontiers in Neuroscience, Vol. 12, Núm. APR
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Pooled-DNA target sequencing of Parkinson genes reveals novel phenotypic associations in Spanish population
Neurobiology of Aging, Vol. 70, pp. 325.e1-325.e5
2017
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Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease
Nature Genetics, Vol. 49, Núm. 9, pp. 1373-1384
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Susceptible genes and disease mechanisms identified in frontotemporal dementia and frontotemporal dementia with Amyotrophic Lateral Sclerosis by DNA-methylation and GWAS
Scientific Reports, Vol. 7, Núm. 1
2016
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Resequencing analysis of five Mendelian genes and the top genes from genome-wide association studies in Parkinson's Disease
Molecular Neurodegeneration, Vol. 11, Núm. 1
2014
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Frontotemporal dementia and its subtypes: A genome-wide association study
The Lancet Neurology, Vol. 13, Núm. 7, pp. 686-699