CIENCIAS DE LA SALUD
Departamento
University College London
Londres, Reino UnidoPublicaciones en colaboración con investigadores/as de University College London (24)
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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A second update on mapping the human genetic architecture of COVID-19
Nature
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Addressing leadership competency gaps and gender disparities in India's medical workforce: a call to action
LANCET REGIONAL HEALTH - SOUTHEAST ASIA
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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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GWAS and meta-analysis identifies 49 genetic variants underlying critical COVID-19
Nature, Vol. 617, Núm. 7962, pp. 764-768
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Use of aequorin-based indicators for monitoring Ca2+ in acidic organelles
Biochimica et Biophysica Acta - Molecular Cell Research, Vol. 1870, Núm. 6
2021
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SLITRK2, an X-linked modifier of the age at onset in C9orf72 frontotemporal lobar degeneration
Brain, Vol. 144, Núm. 9, pp. 2798-2811
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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Identification of evolutionarily conserved gene networks mediating neurodegenerative dementia
Nature Medicine, Vol. 25, Núm. 1, pp. 152-164
2018
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A C6orf10/LOC101929163 locus is associated with age of onset in C9orf72 carriers
Brain, Vol. 141, Núm. 10, pp. 2895-2907
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Collaborative hierarchy maintains cooperation in asymmetric games
Scientific Reports, 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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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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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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Identification of genetic variants associated with Huntington's disease progression: a genome-wide association study
The Lancet Neurology, Vol. 16, Núm. 9, pp. 701-711
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