Kevin Kum Esoh (Kevin K Esoh, Kevin K Esoh, Kevin Esoh)

Scopus Author ID ORCID

Publication Activity (10 Years)

Years Active: 2019-2024
Publications (10 Years): 13

Top Venues

Experimental biology and medicine (Maywood, N.J.)

Genes

Pathogens (Basel, Switzerland)

Scientific reports

University of Cape Town (PHD)

This page only lists publications with an associated author ORCID identifier.

Education History

University of Cape Town Apr 01 2020

South Africa

PHD :: Pathology

Publications

Musalula Sinkala, Gaone Retshabile, Phelelani Thokozani Mpangase, Salia Bamba, Modibo K Goita, Victoria Nembaware, Samar S M Elsheikh, Jeannine M Heckmann, Kevin Kum Esoh, Mogomotsi Matshaba, Clement A Adebamowo, Sally N Adebamowo, Ofon E Amih, Ambroise Wonkam, Michelle Ramsay, Nicola M Mulder
Mapping Epigenetic Gene Variant Dynamics: Comparative Analysis of Frequency, Functional Impact and Trait Associations in African and European Populations. medRxiv : the preprint server for health sciences (2024)
Kevin Kum Esoh, Tobias O Apinjoh, Alfred Amambua-Ngwa, Steven G Nyanjom, Emile R Chimusa, Lucas Amenga-Etego, Ambroise Wonkam, Eric A Achidi
Genome-wide association study identifies novel candidate malaria resistance genes in Cameroon. Human molecular genetics (2023)
Elvis Twumasi Aboagye, Samuel Mawuli Adadey, Kevin Kum Esoh, Mario Jonas, Carmen de Kock, Lucas Amenga-Etego, Gordon A Awandare, Ambroise Wonkam
Age Estimate of GJB2 -p.(Arg143Trp) Founder Variant in Hearing Impairment in Ghana, Suggests Multiple Independent Origins across Populations. Biology 11 (3) (2022)
Ambroise Wonkam, Samuel Mawuli Adadey, Isabelle Schrauwen, Elvis Twumasi Aboagye, Edmond Wonkam-Tingang, Kevin Kum Esoh, Kalinka Popel, Noluthando Manyisa, Mario Jonas, Carmen deKock, Victoria Nembaware, Diana M Cornejo Sanchez, Thashi Bharadwaj, Abdul Nasir, Jenna L Everard, Magda K Kadlubowska, Liz M Nouel-Saied, Anushree Acharya, Osbourne Quaye, Geoffrey K Amedofu, Gordon Akanzuwine Awandare, Suzanne M Leal
Exome sequencing of families from Ghana reveals known and candidate hearing impairment genes. Communications biology 5 (1) (2022)
Robert Adamu Shey, Stephen Mbigha Ghogomu, Cabirou Mounchili Shintouo, Francis Nongley Nkemngo, Derrick Neba Nebangwa, Kevin Kum Esoh, Ntang Emmaculate Yaah, Muyanui Manka'aFri, Joel Ebai Nguve, Roland Akwelle Ngwese, Ferdinand Ngale Njume, Fru Asa Bertha, Lawrence Ayong, Rose Njemini, Luc Vanhamme, Jacob Souopgui
Computational Design and Preliminary Serological Analysis of a Novel Multi-Epitope Vaccine Candidate against Onchocerciasis and Related Filarial Diseases. Pathogens (Basel, Switzerland) 10 (2) (2021)
Samuel M Adadey, Isabelle Schrauwen, Elvis Twumasi Aboagye, Thashi Bharadwaj, Kevin Kum Esoh, Sulman Basit, Anushree Acharya, Liz M Nouel-Saied, Khurram Liaqat, Edmond Wonkam-Tingang, Shaheen Mowla, Gordon A Awandare, Wasim Ahmad, Regie Lyn P Santos-Cortez, Ambroise Wonkam
Further confirmation of the association of SLC12A2 with non-syndromic autosomal-dominant hearing impairment. Journal of human genetics 66 (12) (2021)
Edmond Wonkam-Tingang, Isabelle Schrauwen, Kevin Kum Esoh, Thashi Bharadwaj, Liz M Nouel Saied, Anushree Acharya, Abdul Nasir, Suzanne M Leal, Ambroise Wonkam
A novel variant in DMXL2 gene is associated with autosomal dominant non-syndromic hearing impairment (DFNA71) in a Cameroonian family. Experimental biology and medicine (Maywood, N.J.) 246 (13) (2021)
Noluthando Manyisa, Isabelle Schrauwen, Leonardo Alves de Souza Rios, Shaheen Mowla, Cedrik Tekendo-Ngongang, Kalinka Popel, Kevin Kum Esoh, Thashi Bharadwaj, Liz M Nouel Saied, Anushree Acharya, Abdul Nasir, Edmond Wonkam-Tingang, Carmen de Kock, Collet Dandara, Suzanne M Leal, Ambroise Wonkam
A Monoallelic Variant in REST Is Associated with Non-Syndromic Autosomal Dominant Hearing Impairment in a South African Family. Genes 12 (11) (2021)
Edmond Wonkam-Tingang, Isabelle Schrauwen, Kevin Kum Esoh, Thashi Bharadwaj, Liz M Nouel Saied, Anushree Acharya, Abdul Nasir, Samuel Mawuli Adadey, Shaheen Mowla, Suzanne M Leal, Ambroise Wonkam
Bi-Allelic Novel Variants in CLIC5 Identified in a Cameroonian Multiplex Family with Non-Syndromic Hearing Impairment. Genes 11 (11) (2020)
Oluwafemi Gabriel Oluwole, Kevin Kum Esoh, Edmond Wonkam-Tingang, Noluthando Manyisa, Jean Jacques Noubiap, Emile R Chimusa, Ambroise Wonkam
Whole exome sequencing identifies rare coding variants in novel human-mouse ortholog genes in African individuals diagnosed with non-syndromic hearing impairment. Experimental biology and medicine (Maywood, N.J.) 246 (2) (2020)
Samuel M Adadey, Kevin Kum Esoh, Osbourne Quaye, Geoffrey K Amedofu, Gordon A Awandare, Ambroise Wonkam
GJB4 and GJC3 variants in non-syndromic hearing impairment in Ghana. Experimental biology and medicine (Maywood, N.J.) 245 (15) (2020)
Cabirou Mounchili Shintouo, Robert Adamu Shey, Derrick Neba Nebangwa, Kevin Kum Esoh, Nkemngo Francis Nongley, Joel Ebai Nguve, Philippe Giron, Léon Mutesa, Luc Vanhamme, Jacob Souopgui, Stephen Mbigha Ghogomu, Rose Njemini
In Silico Design and Validation of OvMANE1, a Chimeric Antigen for Human Onchocerciasis Diagnosis. Pathogens (Basel, Switzerland) 9 (6) (2020)
Robert Adamu Shey, Stephen Mbigha Ghogomu, Kevin Kum Esoh, Neba Derrick Nebangwa, Cabirou Mounchili Shintouo, Nkemngo Francis Nongley, Bertha Fru Asa, Ferdinand Njume Ngale, Luc Vanhamme, Jacob Souopgui
In-silico design of a multi-epitope vaccine candidate against onchocerciasis and related filarial diseases. Scientific reports 9 (1) (2019)

Kevin Kum Esoh.css-eqlu8i{font-size:small;padding-left:4px;} (Kevin K Esoh, Kevin K Esoh, Kevin Esoh)

Publication Activity (10 Years)

Top Topics

Top Venues

Kevin Kum Esoh (Kevin K Esoh, Kevin K Esoh, Kevin Esoh)