| In-silico design of a multi-epitope vaccine candidate against onchocerciasis and related filarial diseases RA Shey, SM Ghogomu, KK Esoh, ND Nebangwa, CM Shintouo, ... Scientific reports 9 (1), 4409, 2019 | 279 | 2019 |
| Evolutionary history of sickle-cell mutation: implications for global genetic medicine K Esoh, A Wonkam Human molecular genetics 30 (R1), R119-R128, 2021 | 51 | 2021 |
| Sickle cell disease in sub-Saharan Africa: transferable strategies for prevention and care K Esoh, E Wonkam-Tingang, A Wonkam The Lancet Haematology 8 (10), e744-e755, 2021 | 28 | 2021 |
| Open science in Kenya: Where are we? KW Mwangi, N Mainye, DO Ouso, K Esoh, AW Muraya, CK Mwangi, ... Frontiers in research metrics and analytics 6, 669675, 2021 | 15 | 2021 |
| Computational design and preliminary serological analysis of a novel multi-epitope vaccine candidate against onchocerciasis and related filarial diseases RA Shey, SM Ghogomu, CM Shintouo, FN Nkemngo, DN Nebangwa, ... Pathogens 10 (2), 99, 2021 | 14 | 2021 |
| Five priorities of African genomics research: the next frontier A Wonkam, NS Munung, C Dandara, KK Esoh, NA Hanchard, G Landoure Annual Review of Genomics and Human Genetics 23, 499-521, 2022 | 13 | 2022 |
| Exome sequencing of families from Ghana reveals known and candidate hearing impairment genes A Wonkam, SM Adadey, I Schrauwen, ET Aboagye, E Wonkam-Tingang, ... Communications biology 5 (1), 369, 2022 | 11 | 2022 |
| A novel variant in DMXL2 gene is associated with autosomal dominant non-syndromic hearing impairment (DFNA71) in a Cameroonian family E Wonkam-Tingang, I Schrauwen, KK Esoh, T Bharadwaj, ... Experimental Biology and Medicine 246 (13), 1524-1532, 2021 | 11 | 2021 |
| Bi-Allelic Novel Variants in CLIC5 Identified in a Cameroonian Multiplex Family with Non-Syndromic Hearing Impairment E Wonkam-Tingang, I Schrauwen, KK Esoh, T Bharadwaj, ... Genes 11 (11), 1249, 2020 | 11 | 2020 |
| In silico design and validation of ovmane1, a chimeric antigen for human onchocerciasis diagnosis CM Shintouo, RA Shey, DN Nebangwa, K K. Esoh, NF Nongley, ... Pathogens 9 (6), 495, 2020 | 10 | 2020 |
| Further confirmation of the association of SLC12A2 with non-syndromic autosomal-dominant hearing impairment SM Adadey, I Schrauwen, ET Aboagye, T Bharadwaj, KK Esoh, S Basit, ... Journal of human genetics 66 (12), 1169-1175, 2021 | 8 | 2021 |
| Whole exome sequencing identifies rare coding variants in novel human-mouse ortholog genes in African individuals diagnosed with non-syndromic hearing impairment OG Oluwole, KK Esoh, E Wonkam-Tingang, N Manyisa, JJ Noubiap, ... Experimental Biology and Medicine 246 (2), 197-206, 2021 | 7 | 2021 |
| Current profile of Charcot‐Marie‐Tooth disease in Africa: A systematic review A Yalcouyé, K Esoh, L Guida, A Wonkam Journal of the Peripheral Nervous System 27 (2), 100-112, 2022 | 6 | 2022 |
| Age Estimate of GJB2-p.(Arg143Trp) Founder Variant in Hearing Impairment in Ghana, Suggests Multiple Independent Origins across Populations ET Aboagye, SM Adadey, K Esoh, M Jonas, C de Kock, L Amenga-Etego, ... Biology 11 (3), 476, 2022 | 6 | 2022 |
| The sickle cell disease ontology: enabling collaborative research and co-designing of new planetary health applications V Nembaware, GK Mazandu, J Hotchkiss, JM Safari Serufuri, J Kent, ... OMICS: A Journal of Integrative Biology 24 (10), 559-567, 2020 | 6 | 2020 |
| In-silico design of a multi-epitope vaccine candidate against onchocerciasis and related filarial diseases. Sci Rep. 2019; 9 RA Shey, SM Ghogomu, KK Esoh, ND Nebangwa, CM Shintouo, ... | 6 | |
| Genetic analysis of TB susceptibility variants in Ghana reveals candidate protective loci in SORBS2 and SCL11A1 genes A Asante-Poku, P Morgan, S Osei-Wusu, SY Aboagye, P Asare, ... Frontiers in Genetics 12, 729737, 2022 | 5 | 2022 |
| Fine scale human genetic structure in three regions of Cameroon reveals episodic diversifying selection KK Esoh, TO Apinjoh, SG Nyanjom, A Wonkam, ER Chimusa, ... Scientific reports 11 (1), 1039, 2021 | 5 | 2021 |
| In-silico design of a multi-epitope vaccine candidate against onchocerciasis and related filarial diseases, Sci. Rep. 9 (2019) 4409 RA Shey, SM Ghogomu, KK Esoh, ND Nebangwa, CM Shintouo, ... | 5 | |
| A Monoallelic Variant in REST Is Associated with Non-Syndromic Autosomal Dominant Hearing Impairment in a South African Family N Manyisa, I Schrauwen, LA de Souza Rios, S Mowla, ... Genes 12 (11), 1765, 2021 | 4 | 2021 |
