| In Search of Genetic Markers for Nonsyndromic Deafness in Africa: A Study in Cameroonians and Black South Africans with the GJB6 and GJA1 Candidate Genes J Bosch, K Lebeko, JJN Nziale, C Dandara, N Makubalo, A Wonkam Omics: a journal of integrative biology 18 (7), 481-485, 2014 | 41 | 2014 |
| Targeted genomic enrichment and massively parallel sequencing identifies novel nonsyndromic hearing impairment pathogenic variants in Cameroonian families K Lebeko, CM Sloan-Heggen, JJN Noubiap, C Dandara, DL Kolbe, ... Clinical genetics 90 (3), 288, 2016 | 38 | 2016 |
| Genetics of hearing loss in Africans: use of next generation sequencing is the best way forward K Lebeko, J Bosch, JJN Noubiap, C Dandara, A Wonkam The Pan African Medical Journal 20, 2015 | 38 | 2015 |
| No evidence for clinical utility in investigating the connexin genes GJB2, GJB6 and GJA1 in non-syndromic hearing loss in black Africans : forum - genetics in … A Wonkam, J Bosch, JJN Noubiap, K Lebeko, N Makubalo, C Dandara South African Medical Journal 105 (1), 23-26, 2015 | 32 | 2015 |
| A genomic and protein–protein interaction analyses of nonsyndromic hearing impairment in Cameroon using targeted genomic enrichment and massively parallel sequencing K Lebeko, N Manyisa, ER Chimusa, N Mulder, C Dandara, A Wonkam OMICS: A Journal of Integrative Biology 21 (2), 90-99, 2017 | 17 | 2017 |
| Whole exome sequencing reveals a biallelic frameshift mutation in GRXCR2 in hearing impairment in Cameroon A Wonkam, K Lebeko, S Mowla, JJ Noubiap, M Chong, G Pare Molecular Genetics & Genomic Medicine 9 (3), e1609, 2021 | 7 | 2021 |
| Genetic aetiology of autosomal recessive non-syndromic hearing loss in sub-Saharan African patients: evaluation using targeted and whole exome sequencing K Lebeko | 1 | 2019 |
