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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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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.

Samuel Agyei Wiafe · Sankore

University of Health and Allied Sciences

Samuel Agyei Wiafe

ORCID, self-asserted

ORCID 0000-0003-2125-2285

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

Publications

10

Citations

157

h-index

6

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

i10-index

5

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.

Ghana Health Service13 works
University of Health and Allied Sciences3 works

Publications

10 works in the graph, newest first.

Biallelic variants in RNU2-2 cause a remarkably frequent developmental and epileptic encephalopathy
2026Nature GeneticsJournalOpen access1 citations10.1038/s41588-026-02551-9
Phenotypic and transcriptomic characterization of biallelic RNU2‐2 developmental and epileptic encephalopathy
2026EpilepsiaJournalOpen access0 citations10.1002/epi.70473
Multiple molecular diagnoses identified through genome sequencing in individuals with suspected rare disease
2025Human Genetics and Genomics AdvancesJournalOpen access6 citations10.1016/j.xhgg.2025.100430
A global survey about undiagnosed rare diseases: perspectives, challenges, and solutions
2025Frontiers in Public HealthJournalOpen access5 citations10.3389/fpubh.2025.1510818
Global health for rare diseases through primary care

2024The Lancet Global HealthJournalOpen access59 citations10.1016/s2214-109x(24)00134-7

The impact of clinical genome sequencing in a global population with suspected rare genetic disease

2024The American Journal of Human GeneticsJournalOpen access21 citations10.1016/j.ajhg.2024.05.006

Pushing the boundaries of rare disease diagnostics with the help of the first Undiagnosed Hackathon

2024Nature GeneticsJournalOpen access9 citations10.1038/s41588-024-01941-1

Undiagnosed diseases: Needs and opportunities in 20 countries participating in the Undiagnosed Diseases Network International

2023Frontiers in Public HealthJournalOpen access24 citations10.3389/fpubh.2023.1079601

Unmet needs in countries participating in the undiagnosed diseases network international: an international survey considering national health care and economic indicators

2023Frontiers in Public HealthJournalOpen access18 citations10.3389/fpubh.2023.1248260

Unlocking sociocultural and community factors for the global adoption of genomic medicine

2022Orphanet Journal of Rare DiseasesJournalOpen access14 citations10.1186/s13023-022-02328-3