Rita Joao Guerreiro, PhD
Affiliations: | Molecular Neuroscience | University College London, London, United Kingdom |
Area:
NeurogeneticsGoogle:
"Rita Guerreiro"Parents
Sign in to add mentorCatarina Resende de Oliveira | grad student | UCL | |
John Hardy | grad student | UCL | |
Andrew Singleton | grad student | UCL |
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Publications
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Valentino RR, Koga S, Soto-Beasley AI, et al. (2025) Genome-wide association study of neuropathological features in Lewy body disease. Brain : a Journal of Neurology |
Tábuas-Pereira M, Bernardes C, Durães J, et al. (2024) Exploring first-degree family history in a cohort of Portuguese Alzheimer's disease patients: population evidence for X-chromosome linked and recessive inheritance of risk factors. Journal of Neurology |
Hou X, Heckman MG, Fiesel FC, et al. (2023) Genome-wide association study identifies and variants as mitophagy modifiers in Lewy body disease. Medrxiv : the Preprint Server For Health Sciences |
Tunold JA, Tan MMX, Koga S, et al. (2023) Lysosomal polygenic risk is associated with the severity of neuropathology in Lewy body disease. Brain : a Journal of Neurology |
Sousa JA, Bernardes C, Bernardo-Castro S, et al. (2023) Reconsidering the role of blood-brain barrier in Alzheimer's disease: From delivery to target. Frontiers in Aging Neuroscience. 15: 1102809 |
Foddis M, Blumenau S, Holtgrewe M, et al. (2022) TREX1 p.A129fs and p.Y305C variants in a large multi-ethnic cohort of CADASIL-like unrelated patients. Neurobiology of Aging. 123: 208-215 |
Holstege H, Hulsman M, Charbonnier C, et al. (2022) Exome sequencing identifies rare damaging variants in ATP8B4 and ABCA1 as risk factors for Alzheimer's disease. Nature Genetics |
Khani M, Gibbons E, Bras J, et al. (2022) Correction: Challenge accepted: Uncovering the role of rare genetic variants in Alzheimer's disease. Molecular Neurodegeneration. 17: 70 |
Tábuas-Pereira M, Guerreiro R, Kun-Rodrigues C, et al. (2022) Whole-exome sequencing reveals PSEN1 and ATP7B combined variants as a possible cause of early-onset Lewy body dementia: a case study of genotype-phenotype correlation. Neurogenetics |
Gouveia C, Gibbons E, Dehghani N, et al. (2022) Genome-wide association of polygenic risk extremes for Alzheimer's disease in the UK Biobank. Scientific Reports. 12: 8404 |