The transmission blocking activity of artemisinin-combination, non-artemisinin, and 8-aminoquinoline antimalarial therapies: a pooled analysis of individual participant data. www.medrxiv.org/content/10.1101/2024.09.27.24314479v1
Background Interrupting human-to-mosquito transmission is important for malaria elimination strategi
Predicting Mobile Health Clinic Utilization for COVID-19 Vaccination in South Carolina: A Statistical Framework for Strategic Resource Allocation www.medrxiv.org/content/10.1101/2024.09.27.24314475v1
Background: Mobile health clinics (MHCs) are effective tools for providing health services to disadv
PP mediated the relationship between METS-IR and AIS in non-diabetic patients www.medrxiv.org/content/10.1101/2024.09.26.24314461v1
Background: The correlation between metabolic score for insulin resistance (METS-IR) and high insuli
A Southern African Map of Blood Regulatory Variation Enables GWAS Interpretation www.medrxiv.org/content/10.1101/2024.09.27.24314510v1
Functional genomics resources are critical for interpreting human genetic studies, however they are
Cognitively healthy young adults with APOEe4 gene show disrupted functional connectivity of graph properties in multiple resting-state networks www.medrxiv.org/content/10.1101/2024.09.27.24314481v1
The apolipoprotein (APOE) e4 allele is associated with brain changes in healthy carriers that are si
Outcome of Graves' Disease and Associated Genetic Predisposition: A Systematic Review of Literature www.medrxiv.org/content/10.1101/2024.09.27.24314519v1
Background: Graves' disease (GD) is an autoimmune hyperthyroidism that primarily affects the thyroid
Evaluating large language model workflows in clinical decision support: referral, triage, and diagnosis www.medrxiv.org/content/10.1101/2024.09.27.24314505v1
Accurate medical decision-making is critical for both patients and clinicians. Patients often strugg
Resolution of SLC6A1 variable expressivity in a multi-generational family using deep clinical phenotyping and Drosophila models www.medrxiv.org/content/10.1101/2024.09.27.24314092v1
Variants of uncertain significance pose a difficult diagnostic and therapeutic problem, even when th
Genetic Interplay Between White Matter Hyperintensities and Alzheimer Disease: A Brain-Body Perspective www.medrxiv.org/content/10.1101/2024.09.27.24314431v1
MRI-detected white matter hyperintensities (WMH) are often recognized as markers of cerebrovascular
Identification of genetic variants and their causal association underlying autism spectrum disorder www.medrxiv.org/content/10.1101/2024.09.27.24314463v1
Abstract Background: Autism spectrum disorder (ASD) is an early-onset neurodevelopmental disorder wi