| Connexin genes variants associated with non-syndromic hearing impairment: a systematic review of the global burden SM Adadey, E Wonkam-Tingang, E Twumasi Aboagye, DW Nayo-Gyan, ... Life 10 (11), 258, 2020 | 27 | 2020 |
| A cross-sectional comparative study of perceived stigma between patients with epilepsy and patients living with HIV/AIDS in Accra, Ghana P Adjei, K Nkromah, A Akpalu, R Laryea, FO Poku, S Ohene, P Puplampu, ... Epilepsy & Behavior 89, 1-7, 2018 | 15 | 2018 |
| Hearing loss in Africa: current genetic profile SM Adadey, E Wonkam-Tingang, ET Aboagye, O Quaye, GA Awandare, ... Human genetics, 1-13, 2022 | 14 | 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 | 13 | 2022 |
| Association between eNOS gene polymorphism (T786C and VNTR) and sickle cell disease patients in Ghana C Antwi-Boasiako, B Dzudzor, W Kudzi, A Doku, CA Dale, F Sey, KH Otu, ... Diseases 6 (4), 90, 2018 | 13 | 2018 |
| GJB2 Is a Major Cause of Non-Syndromic Hearing Impairment in Senegal Y Dia, SM Adadey, JPD Diop, ET Aboagye, SA Ba, C De Kock, CAT Ly, ... Biology 11 (5), 795, 2022 | 12 | 2022 |
| Clinical and therapeutic outcomes of COVID-19 intensive care units (ICU) patients: a retrospective study in Ghana J Afriyie-Mensah, ET Aboagye, VJ Ganu, S Bondzi, D Tetteh, E Kwarteng, ... Pan African Medical Journal 38 (1), 2021 | 11 | 2021 |
| 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 | 9 | 2021 |
| Global distribution of founder variants associated with non-syndromic hearing impairment ET Aboagye, SM Adadey, E Wonkam-Tingang, L Amenga-Etego, ... Genes 14 (2), 399, 2023 | 8 | 2023 |
| 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 | 8 | 2022 |
| Catheter-related bloodstream infections among patients on maintenance haemodialysis: a cross-sectional study at a tertiary hospital in Ghana B Opoku-Asare, V Boima, VJ Ganu, E Aboagye, O Asafu-Adjaye, ... BMC Infectious Diseases 23 (1), 664, 2023 | 6 | 2023 |
| The implementation of laboratory information management system in multi-site genetics study in Africa: the challenges and up-scaling opportunities OG Oluwole, C Oosterwyk, D Anderson, SM Adadey, K Mnika, N Manyisa, ... Journal of Molecular Pathology 3 (4), 262-272, 2022 | 6 | 2022 |
| Enhancing Genetic Medicine: Rapid and Cost-Effective Molecular Diagnosis for a GJB2 Founder Mutation for Hearing Impairment in Ghana S M. Adadey, E Tingang Wonkam, E Twumasi Aboagye, D Quansah, ... Genes 11 (2), 132, 2020 | 6 | 2020 |
| Variants of LRP2, encoding a multifunctional cell‐surface endocytic receptor, associated with hearing loss and retinal dystrophy R Faridi, R Yousaf, S Gu, S Inagaki, AE Turriff, K Pelstring, B Guan, A Naik, ... Clinical genetics 103 (6), 699-703, 2023 | 5 | 2023 |
| A novel autosomal dominant GREB1L variant associated with non-syndromic hearing impairment in Ghana SM Adadey, ET Aboagye, K Esoh, A Acharya, T Bharadwaj, NS Lin, ... BMC Medical Genomics 15 (1), 237, 2022 | 4 | 2022 |
| Risk factors of nevirapine hypersensitivity reaction among human immunodeficiency virus-1 infected treatment naïve patients at Korle-Bu Teaching Hospital W Kudzi, E Aboagye, B Dzudzor, E Nartey, D Achel Journal of AIDS and Clinical Research 8 (1), 2017 | 2 | 2017 |
| Childhood Hearing Impairment in Senegal Y Dia, B Loum, YJKB Dieng, JPD Diop, SM Adadey, ET Aboagye, SA Ba, ... Genes 14 (3), 562, 2023 | 1 | 2023 |
| Cell-based analysis of CLIC5A and SLC12A2 variants associated with hearing impairment in two African families SM Adadey, E Wonkam-Tingang, L Alves de Souza Rios, ET Aboagye, ... Frontiers in Genetics 13, 924904, 2022 | 1 | 2022 |
| Cyp2b6 and Sult1a1 Single Nucleotide Polymorphism: Implication for Nevirapine-based Hiv Therapy Among Ghanaians IE Prah, IJ Asiedu-Gyekye, ET Nartey, ET Aboagye, W Kudzi | | 2023 |
| Childhood Hearing Impairment in Senegal. Genes 2023, 14, 562 Y Dia, B Loum, Y Dieng, JPD Diop, SM Adadey, ET Aboagye, SA BA, ... | | 2023 |
