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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.

Carmen J. Buxó · Sankore

Carmen J. Buxó

ORCID, self-asserted

ORCID 0000-0002-8819-1643

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

Publications

8

Citations

48

h-index

4

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

i10-index

2

Publications

6 works in the graph, newest first.

Rare variants in PRKCI cause Van der Woude syndrome and other features of peridermopathy
2025The American Journal of Human GeneticsJournalOpen access4 citations10.1016/j.ajhg.2025.08.008
Distinguishing syndromic and nonsyndromic cleft palate through analysis of protein-altering de novo variants in 818 trios
2025The American Journal of Human GeneticsJournalOpen access3 citations10.1016/j.ajhg.2025.09.009
Variants in CALD1, ESRP1, and RBFOX1 are associated with orofacial cleft risk
2025PLoS GeneticsJournalOpen access2 citations10.1371/journal.pgen.1011581
Genome-wide study of gene-by-sex interactions identifies risks for cleft palate
2024Human GeneticsJournalOpen access5 citations10.1007/s00439-024-02704-y
Trio-based GWAS identifies novel associations and subtype-specific risk factors for cleft palate
2023Human Genetics and Genomics AdvancesJournalOpen access14 citations10.1016/j.xhgg.2023.100234
Clinically actionable secondary findings in 130 triads from sub‐Saharan African families with non‐syndromic orofacial clefts
2023Molecular Genetics & Genomic MedicineJournalOpen access5 citations10.1002/mgg3.2237