Author

Esther Uwibambe

Observed names: E. Uwibambe, Uwibambe, Esther

Institution: University of Rwanda

Observed institutions: University of Cape Town, University of Rwanda, Rwanda Military Hospital, University of Global Health Equity

ORCID: 0009-0004-2046-9495

Observed ORCID: 0009-0004-2046-9495

OpenAlex ID: A5088557995

The Implementation of Laboratory Information Management System in Multi-Site Genetics Study in Africa: The Challenges and Up-Scaling Opportunities

2022 · Oluwafemi Gabriel Oluwole, Chandre Oosterwyk, et al. · Journal of Molecular Pathology · 11

The Vicious Worm education tool improves the knowledge of community health workers on Taenia solium cysticercosis in Rwanda

2024 · Esther Uwibambe, Anselme Shyaka, et al. · PLoS neglected tropical diseases · 2

The First Case of Kleefstra Syndrome in a Rwandan Patient with Global Developmental Delay

2026 · Norbert Dukuze, Janvier Hitayezu, et al. · Genes · 1

Exome sequencing revealed a novel homozygous variant in TRMT61 A in a multiplex family with atypical Cornelia de Lange Syndrome from Rwanda

2025 · Esther Uwibambe, Abdoulaye Yalcouyé, et al. · BMC Medical Genomics · 1

A Rare Homozygous AP4S1 Variant in Rwandan Siblings with Autosomal Recessive Hereditary Spastic Paraplegia Type 52 (SPG52)

2025 · Sylvine Niyoyita, Esther Uwibambe, et al. · Genes · 1

Etiologies of Early-Onset Hearing Impairment in Rwanda

2025 · Esther Uwibambe, Leon Mutesa, et al. · Genes · 1

A Novel Variant of ARID1B-Related CSS in a Rwandan patient: A Case Report

2026 · Adelaide Urugwiro Horanimpundu, Norbert Dukuze, et al. · Rwanda medical journal

A Novel Pathogenic Variant in EXT1 Causing Autosomal Dominant Multiple Hereditary Exostoses in a 5-Year-Old Rwandan Patient

2026 · Pierre Roger Kayumba, Hannah Umutoni Mugaragu, et al. · Rwanda medical journal

The First Genetically Confirmed Case of Ataxia with Oculomotor Apraxia Type 1 (AOA1) Due to an APTX Nonsense Variant in a Rwandan Patient: A Case Report

2026 · Hannah Umutoni Mugaragu, Charles Muhizi, et al. · Rwanda medical journal

Genetic and phenotypic presentation of Usher syndrome - a case report

2024 · N. Dukuze, E. Uwibambe, et al. · Rwanda medical journal

Works count: 12

Citation count: 17

H-index: 2

I10-index: 1