Alpha 2.0
Login Register
» Authors » Kevin Esoh

Kevin Esoh

Explore the profile of Kevin Esoh including associated specialties, affiliations and a list of published articles. Areas
Snapshot
Articles 16
Citations 81
Followers 0
Related Specialties
Genetics
Biology
Neurology
Top 10 Co-Authors
Ambroise Wonkam
Samuel Mawuli Adadey
Suzanne M Leal
Thashi Bharadwaj
Elvis Twumasi Aboagye
Isabelle Schrauwen
Mario Jonas
Abdoulaye Yalcouye
Gordon A Awandare
Edmond Wonkam-Tingang
Published In
Front Genet
Hum Mol Genet
Lancet Haematol
Biology (Basel)
Mol Genet Genomic Med
Affiliations
Soon will be listed here.
Recent Articles
11.
Age Estimate of -p.(Arg143Trp) Founder Variant in Hearing Impairment in Ghana, Suggests Multiple Independent Origins across Populations
Aboagye E, Adadey S, Esoh K, Jonas M, de Kock C, Amenga-Etego L, et al.
Biology (Basel) . 2022 Mar; 11(3). PMID: 35336849
Gap junction protein beta 2 () (connexin 26) variants are commonly implicated in non-syndromic hearing impairment (NSHI). In Ghana, the variant p.(Arg143Trp) is the largest contributor to NSHI and has...
12.
Genetic Analysis of TB Susceptibility Variants in Ghana Reveals Candidate Protective Loci in and Genes
Asante-Poku A, Morgan P, Osei-Wusu S, Aboagye S, Asare P, Otchere I, et al.
Front Genet . 2022 Mar; 12():729737. PMID: 35242163
Despite advancements made toward diagnostics, caused by (Maf) and (Mtbss) remains a major public health issue. Human host factors are key players in (TB) outcomes and treatment. Research is required...
13.
A Monoallelic Variant in Is Associated with Non-Syndromic Autosomal Dominant Hearing Impairment in a South African Family
Manyisa N, Schrauwen I, Alves de Souza Rios L, Mowla S, Tekendo-Ngongang C, Popel K, et al.
Genes (Basel) . 2021 Nov; 12(11). PMID: 34828371
Hearing impairment (HI) is a sensory disorder with a prevalence of 0.0055 live births in South Africa. DNA samples from a South African family presenting with progressive, autosomal dominant non-syndromic...
14.
Sickle cell disease in sub-Saharan Africa: transferable strategies for prevention and care
Esoh K, Wonkam-Tingang E, Wonkam A
Lancet Haematol . 2021 Sep; 8(10):e744-e755. PMID: 34481550
Sickle cell disease can be life-threatening or chronically debilitating for both children and adults. Worldwide, more than 300 000 children are born with sickle cell disease every year, over 75%...
15.
Open Science in Kenya: Where Are We?
Mwangi K, Mainye N, Ouso D, Esoh K, Muraya A, Mwangi C, et al.
Front Res Metr Anal . 2021 May; 6:669675. PMID: 34056516
According to the United Nations Educational, Scientific, and Cultural Organization (UNESCO), Open Science is the movement to make scientific research and data accessible to all. It has great potential for...
16.
Computational Design and Preliminary Serological Analysis of a Novel Multi-Epitope Vaccine Candidate against Onchocerciasis and Related Filarial Diseases
Shey R, Ghogomu S, Shintouo C, Nongley Nkemngo F, Nebangwa D, Esoh K, et al.
Pathogens . 2021 Jan; 10(2). PMID: 33494344
Onchocerciasis is a skin and eye disease that exerts a heavy socio-economic burden, particularly in sub-Saharan Africa, a region which harbours greater than 96% of either infected or at-risk populations....
17.
Evolutionary history of sickle-cell mutation: implications for global genetic medicine
Esoh K, Wonkam A
Hum Mol Genet . 2021 Jan; 30(R1):R119-R128. PMID: 33461216
Resistance afforded by the sickle-cell trait against severe malaria has led to high frequencies of the sickle-cell mutation [HBB; c.20T>A, p.Glu6Val; OMIM: 141900 (HBB-βS)] in most parts of Africa. High-coverage...