FACULTAD DE CIENCIAS DE LA SALUD
Facultad/Centro de investigación
University of Oxford
Oxford, Reino UnidoUniversity of Oxford-ko ikertzaileekin lankidetzan egindako argitalpenak (16)
2023
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A second update on mapping the human genetic architecture of COVID-19
Nature
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GWAS and meta-analysis identifies 49 genetic variants underlying critical COVID-19
Nature, Vol. 617, Núm. 7962, pp. 764-768
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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
2022
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Six Action Steps to Address Global Disparities in Parkinson Disease: A World Health Organization Priority
JAMA Neurology, Vol. 79, Núm. 9, pp. 929-936
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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Clinical and genetic characteristics of late-onset Huntington's disease
Parkinsonism and Related Disorders, Vol. 61, pp. 101-105
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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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Immune-related genetic enrichment in frontotemporal dementia: An analysis of genome-wide association studies
PLoS Medicine, Vol. 15, Núm. 1
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Reduced Cancer Incidence in Huntington's Disease: Analysis in the Registry Study
Journal of Huntington's Disease, Vol. 7, Núm. 3, pp. 209-222
2017
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Cognitive decline in Huntington's disease expansion gene carriers
Cortex, Vol. 95, pp. 51-62
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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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Interaction between the ADAMTS-12 metalloprotease and fibulin-2 induces tumor-suppressive effects in breast cancer cells
Oncotarget, Vol. 5, Núm. 5, pp. 1253-1264
2013
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Suicidal ideation in a European Huntington's disease population
Journal of Affective Disorders, Vol. 151, Núm. 1, pp. 248-258
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The V471A Polymorphism in Autophagy-Related Gene ATG7 Modifies Age at Onset Specifically in Italian Huntington Disease Patients
PLoS ONE, Vol. 8, Núm. 7