Kevin Kum Esoh
14PUBLICATIONS
57CO-AUTHORS
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Publications (14)
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|Mar 02, 2025
FLT1 and other candidate fetal haemoglobin modifying loci in sickle cell disease in African ancestries.Ambroise Wonkam, Kevin Esoh, Rachel M Levine
|Aug 26, 2024
Mapping Epigenetic Gene Variant Dynamics: Comparative Analysis of Frequency, Functional Impact and Trait Associations in African and European Populations.Musalula Sinkala, Gaone Retshabile, Phelelani T Mpangase
|Feb 08, 2023
Genome-wide association study identifies novel candidate malaria resistance genes in Cameroon.Kevin K Esoh, Tobias O Apinjoh, Alfred Amambua-Ngwa
|Apr 20, 2022
Exome sequencing of families from Ghana reveals known and candidate hearing impairment genes.Ambroise Wonkam, Samuel Mawuli Adadey, Isabelle Schrauwen
|Mar 26, 2022
Age Estimate of <i>GJB2</i>-p.(Arg143Trp) Founder Variant in Hearing Impairment in Ghana, Suggests Multiple Independent Origins across Populations.Elvis Twumasi Aboagye, Samuel Mawuli Adadey, Kevin Esoh
|Nov 27, 2021
A Monoallelic Variant in <i>REST</i> Is Associated with Non-Syndromic Autosomal Dominant Hearing Impairment in a South African Family.Noluthando Manyisa, Isabelle Schrauwen, Leonardo Alves de Souza Rios
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Frequent Collaborators
10 joint publications
Ambroise Wonkam
4 joint publications
Abdul Nasir
3 joint publications
Jacob Souopgui
3 joint publications
Samuel Mawuli Adadey
3 joint publications
Liz M Nouel-Saied
2 joint publications
Stephen Mbigha Ghogomu
2 joint publications
Osbourne Quaye
2 joint publications
Rose Njemini
2 joint publications
Isabelle Schrauwen
2 joint publications
Shaheen Mowla
