Kevin Esoh
Overview
Explore the profile of Kevin Esoh including associated specialties, affiliations and a list of published articles.
Author names and details appear as published. Due to indexing inconsistencies, multiple individuals may share a name, and a single author may have variations. MedLuna displays this data as publicly available, without modification or verification
Snapshot
Snapshot
Articles
16
Citations
81
Followers
0
Related Specialties
Top 10 Co-Authors
Top 10 Co-Authors
Published In
Affiliations
Affiliations
Soon will be listed here.
Recent Articles
1.
Wonkam A, Esoh K, Levine R, Ngo Bitoungui V, Mnika K, Nimmagadda N, et al.
Nat Commun
. 2025 Mar;
16(1):2092.
PMID: 40025045
Known fetal haemoglobin (HbF)-modulating loci explain 10-24% variation of HbF level in Africans with Sickle Cell Disease (SCD), compared to 50% among Europeans. Here, we report fourteen candidate loci from...
2.
Yalcouye A, Schrauwen I, Traore O, Bamba S, Aboagye E, Acharya A, et al.
HGG Adv
. 2024 Dec;
6(1):100391.
PMID: 39663698
Hearing impairment (HI) is the most common neurosensory disorder globally and is reported to be more prevalent in low-income countries. In high-income countries, up to 50% of congenital childhood HI...
3.
Nnodu O, Munung N, Chirande L, Chunda-Liyoka C, Kiguli S, Sarfo F, et al.
BMJ Open
. 2024 Nov;
14(11):e089056.
PMID: 39515852
Background: Sickle cell disease (SCD) is a prevalent inherited blood disorder. Globally, approximately 515 000 babies are born with SCD annually, with 75% of these births occurring in Africa. Integrating...
4.
Sinkala M, Retshabile G, Mpangase P, Bamba S, Goita M, Nembaware V, et al.
medRxiv
. 2024 Aug;
PMID: 39185519
Epigenetic modifications influence gene expression levels, impact organismal traits, and play a role in the development of diseases. Therefore, variants in genes involved in epigenetic processes are likely to be...
5.
Yalcouye A, Rebelo A, Cisse L, Rives L, Bamba S, Cogan J, et al.
Brain Commun
. 2023 Dec;
5(5):fcad227.
PMID: 38074074
has been recently reported causing a rare axonal Charcot-Marie-Tooth disease in three independent Caucasian families carrying a recurrent change. We describe the first alternative causative mutation in in a family...
6.
Adadey S, Aboagye E, Esoh K, Acharya A, Bharadwaj T, Lin N, et al.
BMC Med Genomics
. 2022 Nov;
15(1):237.
PMID: 36357908
Background: Childhood hearing impairment (HI) is genetically heterogeneous with many implicated genes, however, only a few of these genes are reported in African populations. Methods: This study used exome and...
7.
Adadey S, Wonkam-Tingang E, Alves de Souza Rios L, Aboagye E, Esoh K, Manyisa N, et al.
Front Genet
. 2022 Aug;
13:924904.
PMID: 36035115
We have previously reported and variants in two families from Cameroon and Ghana, segregating non-syndromic hearing impairment (NSHI). In this study, biological assays were performed to further functionally investigate the...
8.
Yalcouye A, Traore O, Diarra S, Schrauwen I, Esoh K, Kadlubowska M, et al.
Mol Genet Genomic Med
. 2022 Jun;
10(7):e1995.
PMID: 35698919
Background: Branchio-otic syndrome (BO) is one of the most common types of syndromic hearing impairment (HI) with an incidence of 1/40,000 globally. It is an autosomal dominant disorder typically characterized...
9.
Wonkam A, Adadey S, Schrauwen I, Aboagye E, Wonkam-Tingang E, Esoh K, et al.
Commun Biol
. 2022 Apr;
5(1):369.
PMID: 35440622
We investigated hearing impairment (HI) in 51 families from Ghana with at least two affected members that were negative for GJB2 pathogenic variants. DNA samples from 184 family members underwent...
10.
Yalcouye A, Esoh K, Guida L, Wonkam A
J Peripher Nerv Syst
. 2022 Apr;
27(2):100-112.
PMID: 35383421
Background And Aims: Charcot-Marie-Tooth disease (CMT) is the most common inherited peripheral neuropathy characterised by a high clinical and genetic heterogeneity. While most cases were described in populations with Caucasian...