FACULTAD DE CIENCIAS DE LA SALUD
Facultad/Centro de investigación
Columbia University
Nueva York, Estados UnidosPublicaciones en colaboración con investigadores/as de Columbia University (29)
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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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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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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Corrigendum to “Mortality and morbidity among hospitalized adult patients with neurological diseases in Cameroon” [J. Neurol. Sci. 381C (2017) 156–168] (S0022510X17337413) (10.1016/j.jns.2017.08.3245))
Journal of the Neurological Sciences
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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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Quality of Life in Huntington's Disease: Critique and Recommendations for Measures Assessing Patient Health-Related Quality of Life and Caregiver Quality of Life
Movement Disorders, Vol. 33, Núm. 5, pp. 742-749
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Rating Scales and Performance-based Measures for Assessment of Functional Ability in Huntington's Disease: Critique and Recommendations
Movement Disorders Clinical Practice, Vol. 5, Núm. 4, pp. 361-372
2017
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Mortality and morbidity among hospitalized adult patients with neurological diseases in Cameroon
Journal of the Neurological Sciences, Vol. 381, pp. 165-168
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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
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The Burden of Movement Disorders in Cameroon: A Rural and Urban-Based Inpatient/Outpatient Study
Movement Disorders Clinical Practice, Vol. 4, Núm. 4, pp. 568-573
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