CIENCIAS DE LA SALUD
Departamento
Washington University in St. Louis School of Medicine
San Luis, Estados UnidosPublicacións en colaboración con investigadores/as de Washington University in St. Louis School of Medicine (15)
2021
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Exome-wide rare variant analysis in familial essential tremor
Parkinsonism and Related Disorders, Vol. 82, pp. 109-116
2020
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Autoantibodies against type I IFNs in patients with life-threatening COVID-19
Science, Vol. 370, Núm. 6515
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Inborn errors of type I IFN immunity in patients with life-threatening COVID-19
Science, Vol. 370, Núm. 6515
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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
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Identification of evolutionarily conserved gene networks mediating neurodegenerative dementia
Nature Medicine, Vol. 25, Núm. 1, pp. 152-164
2018
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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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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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Genetic architecture of sporadic frontotemporal dementia and overlap with Alzheimer's and Parkinson's diseases
Journal of Neurology, Neurosurgery and Psychiatry, Vol. 88, Núm. 2, pp. 152-164
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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
2016
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A novel Alzheimer disease locus located near the gene encoding tau protein
Molecular Psychiatry, Vol. 21, Núm. 1, pp. 108-117
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Genome-wide analysis of genetic correlation in dementia with Lewy bodies, Parkinson's and Alzheimer's diseases
Neurobiology of Aging, Vol. 38, pp. 214.e7-214.e10
2014
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Frontobasal gray matter loss is associated with the TREM2 p.R47H variant
Neurobiology of Aging, Vol. 35, Núm. 12, pp. 2681-2690
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Frontotemporal dementia and its subtypes: A genome-wide association study
The Lancet Neurology, Vol. 13, Núm. 7, pp. 686-699