Rita Guerreiro

Grand Rapids Community College — United States

Medicine · Health Sciences

80h-index41.7kcitations331works9.22yr avg
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Research Topics

Alzheimer's disease research and treatments(88), Parkinson's Disease Mechanisms and Treatments(51), Genomics and Rare Diseases(44), Neurological diseases and metabolism(42), Genetic Associations and Epidemiology(41)

Publications302 total

Domain mapping of disease mutations reveals pathogenic SORL1 variants in Alzheimer’s disease
Molecular Neurodegeneration·2025· 1 citedOpen Access
Changes in pediatric emergency department utilization and health literacy: a study of non-urgent visits before and after the COVID-19 pandemic
Portuguese Journal of Pediatrics·2025Open Access
Exome sequencing of a Portuguese cohort of early-onset Alzheimer’s disease implicates the X-linked lysosomal gene GLA
Scientific Reports·2025· 1 citedOpen Access
Genome‐wide association analysis identifies <i>APOE</i> as a mitophagy modifier in Lewy body disease
Alzheimer s & Dementia·2025· 5 citedOpen Access
Genome-wide association study of neuropathological features in Lewy body disease
Brain·2025· 2 cited
The Role of Salience and Emotional Resonance in Cultivating Conservation Caring Among Zoo Visitors
Anthrozoös·2025
<i>Ide</i> Copy Number Variant Does Not Influence Stroke Severity in 2 C57BL/6J Mouse Models nor in Humans: An Exploratory Study
Stroke·2025Open Access
Allocation Model for Workload Balance: A Case Study
Lecture notes in networks and systems·2025
Load Balancing in Parallel Machines: A Literature Review
Lecture notes in networks and systems·2025
Extremely rare CNVs contributing to Alzheimer disease risk: a case-control association analysis of exome sequencing data from 22,319 individuals
2024Open Access
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·2024· 3 citedOpen Access
Cerebral small vessel disease may not critically influence familial Parkinson’s disease
2024Open Access
<i>Ide</i> copy number variant does not influence lesion size and mortality in two C57BL/6J mouse models of cerebrovascular ischemia nor in human cerebrovascular disease. An exploratory study
2024Open Access
Whole‐exome sequencing of a Portuguese cohort of early‐onset Alzheimer’s disease implicates X‐linked lysosomal gene GLA
Alzheimer s & Dementia·2023Open Access
Genome-wide association study identifies <i>APOE</i> and <i>ZMIZ1</i> variants as mitophagy modifiers in Lewy body disease
2023· 5 citedOpen Access
Domain mapping of disease mutations supports genetic testing of specific <i>SORL1</i> variants in familial Alzheimer’s Disease
2023· 11 citedOpen Access
Online Scheduling: A Survey
2023· 5 citedOpen Access
Lysosomal polygenic risk is associated with the severity of neuropathology in Lewy body disease
Brain·2023· 26 citedOpen Access
Reply to: Genome-wide association studies of polygenic risk score-derived phenotypes may lead to inflated false positive rates
Scientific Reports·2023Open Access
Genetic forms of primary progressive aphasia within the GENetic Frontotemporal dementia Initiative (GENFI) cohort: comparison with sporadic primary progressive aphasia
Brain Communications·2023· 16 citedOpen Access
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Frequent Co-authors

José Brás(38), John Hardy(37), J. Raphael Gibbs(20), Javier Simón‐Sánchez(13), Andrew Singleton(13), Peter Heutink(11), Joshua Shulman(11), Huw R. Morris(10), Kevin Morgan(10), Sonja W. Scholz(9), Kristelle Brown(9), Nick C. Fox(9), Alison Goate(9), Peter Holmans(9), Nicholas Wood(9), Mark Cookson(9), María Martínez(9), Alexis Brice(9), Thomas Gasser(9), Mina Ryten(8)