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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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ORCID — researcher identity
Crossref — publisher confirmation

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Coverage is partial and says so. A country appears with its research output only once its works have been swept; until then the portal shows whatever the graph happens to hold for it and labels it as exactly that.

Noluthando Manyisa · Sankore

University of Cape Town

Noluthando Manyisa

ORCID, self-asserted

ORCID 0000-0003-0518-338X

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

Publications

7

Citations

53

h-index

4

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

i10-index

2

Read this before using these figures

The graph holds no coverage record for this country.

Affiliations

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

University of Cape Town5 works
Institute of Infectious Disease and Molecular Medicine1 works

Publications

5 works in the graph, newest first.

The Diverse Genetic Landscape of Hearing Impairment in South African Families
2025Clinical GeneticsJournalOpen access3 citations10.1111/cge.14765
Exome sequencing of families from Ghana reveals known and candidate hearing impairment genes
2022Communications BiologyJournalOpen access21 citations10.1038/s42003-022-03326-8
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
Hearing Impairment in South Africa and the Lessons Learned for Planetary Health Genomics: A Systematic Review
2022OMICS A Journal of Integrative BiologyJournalOpen accessFirst author8 citations10.1089/omi.2021.0181

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