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Mesaki Kenneth Ndugga-Kabuye

Observed names: MK Ndugga-Kabuye, Mesaki K. Ndugga-Kabuye
ORCID: 0000-0002-8310-5697
Observed ORCID: 0000-0002-8310-5697
OpenAlex ID: A5031075803
Inequities in multi-gene hereditary cancer testing: lower diagnostic yield and higher VUS rate in individuals who identify as Hispanic, African or Asian and Pacific Islander as compared to European
2019 · Mesaki K. Ndugga-Kabuye, Rachel B. Issaka · Familial Cancer · 108
The Impact of Rapid Exome Sequencing on Medical Management of Critically Ill Children
2020 · Amanda S. Freed, Sarah V. Clowes Candadai, et al. · The Journal of Pediatrics · 63
Complications of the Low Phenylalanine Diet for Patients with Phenylketonuria and the Benefits of Increased Natural Protein
2022 · Nicole McWhorter, Mesaki K. Ndugga-Kabuye, et al. · Nutrients · 36
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Heterozygous STUB1 missense variants cause ataxia, cognitive decline, and STUB1 mislocalization
2020 · Dong-Hui Chen, Caitlin Latimer, et al. · Neurology Genetics · 30
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Glycogen storage disease type IV: dilated cardiomyopathy as the isolated initial presentation in an adult patient
2019 · Mesaki Kenneth Ndugga-Kabuye, Joseph Maleszewski, et al. · BMJ Case Reports · 9
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Proof-of-Concept Study of Oxalate-Consuming Synthetic Biotic Medicine SYNB8802 in Enteric Hyperoxaluria after Roux-en-Y Surgery
2021 · Marja Puurunen, William Denney, et al. · Journal of the American Society of Nephrology · 1
Dietary management outcomes during SynPheny-1, a Phase 2 clinical trial of a live biotherapeutic, SYNB1618, for the management of phenylketonuria
2022 · N McWhorter, M Puurunen, et al. · Molecular Genetics and Metabolism
Dietary protein intake and perceptions in patients with PKU: survey results from patients and caregivers
2022 · MK Ndugga-Kabuye, N McWhorter, et al. · Molecular Genetics and Metabolism
Works count: 8
Citation count: 247
H-index: 5
I10-index: 4
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