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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.

Gareth Baynam · Sankore

Gareth Baynam

ORCID, self-asserted

ORCID 0000-0003-4920-9553

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

Publications

11

Citations

591

h-index

8

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

i10-index

7

Publications

7 works in the graph, newest first.

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 accessFirst authorCorresponding59 citations10.1016/s2214-109x(24)00134-7
Pushing the boundaries of rare disease diagnostics with the help of the first Undiagnosed Hackathon
2024Nature GeneticsJournalOpen access9 citations10.1038/s41588-024-01941-1
The Human Phenotype Ontology in 2024: phenotypes around the world
2023Nucleic Acids ResearchJournalOpen access407 citations10.1093/nar/gkad1005
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 accessCorresponding14 citations10.1186/s13023-022-02328-3