Grant Dorsey

The paper characterizes the population structure and drug resistance of Plasmodium falciparum in Uganda and neighboring countries using whole-genome data, identifying key resistance-associated haplotypes.

The paper examines how exposure to P. falciparum and common cold viruses influences vaccine responses in Ugandan infants, finding positive associations between microbial exposure and antibody levels.

The paper identifies CXCR6⁺ CD127⁻ Tr1 cells as key regulators in Plasmodium falciparum infection, showing they balance immunity and parasite persistence.

This study uses genomic data to analyze evolutionary dynamics of Anopheles gambiae under different insecticidal tools, revealing distinct resistance mechanisms and allele frequency shifts.

The paper examines how maternal malaria and early-life infections affect P. falciparum-specific antibody responses in infants, finding no protective association between maternal antibodies or early infections and clinical malaria.

The paper shows congenital CMV infection leads to oligoclonal expansion of cytotoxic γδ T cells with fetal-like TCR features in neonates.

The paper examines inhibitory NK receptors on γδ T cells in Ugandan children, finding that some enhance and others reduce antimalarial responses to repeated infections.

In Tororo, Uganda, An. funestus tolerated clothianidin-sprayed walls better than An. gambiae yet was killed on pirimiphos-methyl walls up to 7 months post-spray, implicating it in the malaria resurgence.

This paper uses genomic surveillance in a cluster randomized trial to detect insecticide resistance variants in Ugandan Anopheles funestus and An. gambiae s.l., showing differential population responses to pyrethroid and PBO interventions.

The paper compares methylation profiles of placentas with non-malarial and PM-associated FGR, finding distinct differentially methylated CpGs and a shared hypomethylated site in BMP4.

The paper compares transcriptional profiles of maternal and fetal placental macrophages in term pregnancies, finding distinct gene expression patterns linked to gravidity.