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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.

Isabelle Schrauwen · Sankore

Isabelle Schrauwen

ORCID, self-asserted

ORCID 0000-0001-7310-6082

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

58

h-index

3

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

i10-index

2

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
Bi-Allelic MARVELD2 Variant Identified with Exome Sequencing in a Consanguineous Multiplex Ghanaian Family Segregating Non-Syndromic Hearing Loss
2025International Journal of Molecular SciencesJournalOpen access0 citations10.3390/ijms26073337
Variants of LRP2 , encoding a multifunctional cell‐surface endocytic receptor, associated with hearing loss and retinal dystrophy
2023Clinical GeneticsJournalOpen access23 citations10.1111/cge.14312
Exome sequencing of families from Ghana reveals known and candidate hearing impairment genes
2022Communications BiologyJournalOpen access21 citations10.1038/s42003-022-03326-8
A novel autosomal dominant GREB1L variant associated with non-syndromic hearing impairment in Ghana
2022BMC Medical GenomicsJournalOpen access5 citations10.1186/s12920-022-01391-w