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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 Mawuli Adadey · Sankore

University for Development Studies

Samuel Mawuli Adadey

ORCID, self-asserted

ORCID 0000-0002-1993-2786

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

Publications

30

Citations

202

h-index

8

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

i10-index

8

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.

University of Ghana18 works
West African Centre for Cell Biology of Infectious Pathogens16 works
University of Cape Town15 works
University for Development Studies10 works
University of Cape Coast1 works
Institute of Infectious Disease and Molecular Medicine1 works

Publications

27 works in the graph, newest first.

Burden and patterns of dyslipidaemia among adult Ghanaians: A systematic review
2026PLoS ONEJournalOpen accessCorresponding0 citations10.1371/journal.pone.0350185
Diagnostic utility of fasting versus non-fasting blood glucose: contextualising testing strategies-a narrative review
2026Diabetology & Metabolic SyndromeJournalOpen access0 citations10.1186/s13098-026-02213-0
Additional file 1 of Diagnostic utility of fasting versus non-fasting blood glucose: contextualising testing strategies-a narrative review
2026FigshareJournalOpen access0 citations10.6084/m9.figshare.33400850.v1
Additional file 1 of Diagnostic utility of fasting versus non-fasting blood glucose: contextualising testing strategies-a narrative review
2026FigshareJournalOpen access0 citations10.6084/m9.figshare.33400850

ABO blood groups and cardiovascular disease and its risk in continental Africans and people of African ancestry: A systematic review

2025PLoS ONEJournalOpen accessCorresponding2 citations10.1371/journal.pone.0333547

Mutational analysis of antibiotic resistance genes in Helicobacter pylori from Ghanaian dyspepsia patients: Implications for treatment strategies

2025Aspects of Molecular MedicineJournalOpen access1 citations10.1016/j.amolm.2025.100078

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

Early‐Onset Diabetes in Ghana's Upper East Region—Insights From Hospital Data

2025Endocrinology Diabetes & MetabolismJournalOpen accessSenior authorCorresponding0 citations10.1002/edm2.70079

Dysbetalipoproteinaemia in genetically predisposed Ghanaians

2025Lipids in Health and DiseaseJournalOpen access0 citations10.1186/s12944-025-02787-0

Knowledge, attitude and perception towards COVID-19 among representative educated sub-Saharan Africans: A cross-sectional study during the exponential phase of the pandemic

2024PLoS ONEJournalOpen access3 citations10.1371/journal.pone.0281342

A narrative review on trypanosomiasis and its effect on food production

2024Food Science TodayJournalOpen access0 citations10.58951/fstoday.2024.006

A Double Lysis Method for Animal Rotavirus RNA Extraction From Stool Samples

2024Current ProtocolsJournal0 citations10.1002/cpz1.70011

Prevalence and Impact of Cattle Infections in Ghana

2024Advanced Journal of Graduate ResearchJournalOpen access0 citations10.21467/ajgr.15.1.22-33

Variants of LRP2 , encoding a multifunctional cell‐surface endocytic receptor, associated with hearing loss and retinal dystrophy

2023Clinical GeneticsJournalOpen access23 citations10.1111/cge.14312

Global Distribution of Founder Variants Associated with Non-Syndromic Hearing Impairment

2023GenesJournalOpen access18 citations10.3390/genes14020399

Childhood Hearing Impairment in Senegal

2023GenesJournalOpen access5 citations10.3390/genes14030562

Early-onset diabetes in Africa: A mini-review of the current genetic profile

2023European Journal of Medical GeneticsJournalFirst authorCorresponding3 citations10.1016/j.ejmg.2023.104887

Advancing intercontinental collaboration in human genetics: success story of the African and European Young Investigator Forum

2023European Journal of Human GeneticsJournalOpen access0 citations10.1038/s41431-023-01487-6

Genetic Analysis of TB Susceptibility Variants in Ghana Reveals Candidate Protective Loci in SORBS2 and SCL11A1 Genes

2022Frontiers in GeneticsJournalOpen access46 citations10.3389/fgene.2021.729737

Exome sequencing of families from Ghana reveals known and candidate hearing impairment genes

2022Communications BiologyJournalOpen access21 citations10.1038/s42003-022-03326-8

The Role of Epstein-Barr Virus in Modulating Key Tumor Suppressor Genes in Associated Malignancies: Epigenetics, Transcriptional, and Post-Translational Modifications

2022BiomoleculesJournalOpen access19 citations10.3390/biom12010127

GJB2 Is a Major Cause of Non-Syndromic Hearing Impairment in Senegal

2022BiologyJournalOpen access14 citations10.3390/biology11050795

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

Age Estimate of GJB2-p.(Arg143Trp) Founder Variant in Hearing Impairment in Ghana, Suggests Multiple Independent Origins across Populations

2022BiologyJournalOpen access11 citations10.3390/biology11030476

Hearing Impairment in South Africa and the Lessons Learned for Planetary Health Genomics: A Systematic Review

2022OMICS A Journal of Integrative BiologyJournalOpen access8 citations10.1089/omi.2021.0181

A novel autosomal dominant GREB1L variant associated with non-syndromic hearing impairment in Ghana

2022BMC Medical GenomicsJournalOpen accessFirst author5 citations10.1186/s12920-022-01391-w

Cell-based analysis of CLIC5A and SLC12A2 variants associated with hearing impairment in two African families

2022Frontiers in GeneticsJournalOpen accessFirst author3 citations10.3389/fgene.2022.924904