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Sankore

Named after the University of Sankore in Timbuktu — one of the world’s oldest centres of learning. Every figure here is computed from work-level records in our own graph, never copied from a source’s summary count.

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Elvis Twumasi Aboagye · Sankore

University of Ghana

Elvis Twumasi Aboagye

ORCID, self-asserted

ORCID 0000-0002-2994-3761

This profile carries an ORCID the researcher published on their own record — the strongest evidence available short of a human confirming it.

Publications

16

Citations

139

h-index

7

Computed over the works the graph holds, so it is a floor rather than a career figure.

i10-index

7

Works published 2022 onward have been swept for this country. Figures are complete within that window, to the extent the open indexes are.

Affiliations

Every institution this scholar has appeared with on a work, by how many.

University of Ghana13 works
West African Centre for Cell Biology of Infectious Pathogens12 works
University of Cape Town10 works

Publications

13 works in the graph, newest first.

The Diverse Genetic Landscape of Hearing Impairment in South African Families
2025Clinical GeneticsJournalOpen access3 citations10.1111/cge.14765
Bi-Allelic MARVELD2 Variant Identified with Exome Sequencing in a Consanguineous Multiplex Ghanaian Family Segregating Non-Syndromic Hearing Loss
2025International Journal of Molecular SciencesJournalOpen accessFirst author0 citations10.3390/ijms26073337
Genetics of Waardenburg Syndrome in Africa: A Systematic Review
2025International Journal of Molecular SciencesJournalOpen accessFirst author0 citations10.3390/ijms27010127
Variants of LRP2 , encoding a multifunctional cell‐surface endocytic receptor, associated with hearing loss and retinal dystrophy
2023Clinical GeneticsJournalOpen access23 citations10.1111/cge.14312

Catheter-Related Bloodstream Infections among patients on maintenance haemodialysis: a cross-sectional study at a tertiary hospital in Ghana

2023BMC Infectious DiseasesJournalOpen access21 citations10.1186/s12879-023-08581-6

Global Distribution of Founder Variants Associated with Non-Syndromic Hearing Impairment

2023GenesJournalOpen accessFirst author18 citations10.3390/genes14020399

Childhood Hearing Impairment in Senegal

2023GenesJournalOpen access5 citations10.3390/genes14030562

Exome sequencing of families from Ghana reveals known and candidate hearing impairment genes

2022Communications BiologyJournalOpen access21 citations10.1038/s42003-022-03326-8

GJB2 Is a Major Cause of Non-Syndromic Hearing Impairment in Senegal

2022BiologyJournalOpen access14 citations10.3390/biology11050795

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

2022Journal of Molecular PathologyJournalOpen access12 citations10.3390/jmp3040022

Age Estimate of GJB2-p.(Arg143Trp) Founder Variant in Hearing Impairment in Ghana, Suggests Multiple Independent Origins across Populations

2022BiologyJournalOpen accessFirst author11 citations10.3390/biology11030476

A novel autosomal dominant GREB1L variant associated with non-syndromic hearing impairment in Ghana

2022BMC Medical GenomicsJournalOpen access5 citations10.1186/s12920-022-01391-w

Cell-based analysis of CLIC5A and SLC12A2 variants associated with hearing impairment in two African families

2022Frontiers in GeneticsJournalOpen access3 citations10.3389/fgene.2022.924904