| Novel loss-of-function mutations in COCH cause autosomal recessive nonsyndromic hearing loss KT Booth, A Ghaffar, M Rashid, LT Hovey, M Hussain, K Frees, ... Human genetics 139, 1565-1574, 2020 | 18 | 2020 |
| Biallelic in-frame deletion of SOX4 is associated with developmental delay, hypotonia and intellectual disability A Ghaffar, F Rasheed, M Rashid, H van Bokhoven, ZM Ahmed, ... European Journal of Human Genetics 30 (2), 243-247, 2022 | 6 | 2022 |
| Syntaxin 4 is essential for hearing in human and zebrafish I Schrauwen, A Ghaffar, T Bharadwaj, K Shah, S Rehman, A Acharya, ... Human Molecular Genetics 32 (7), 1184-1192, 2023 | 1 | 2023 |
| Parkinson’s Disease Treatment and the Role of Genetic Polymorphisms in the Efficacy and Adverse Effects H Usman, T Khalid, A Ghaffar Precision Medicine Communications 1 (01), 25-47, 2021 | | 2021 |
| Alzheimer’s Disease Therapy, and the Effects of Genetic Polymorphisms on Its Efficacy and Safety H Usman, A Ghaffar Molecular Medicine Communications 1 (1), 57-77, 2021 | | 2021 |
| Molecular Medicine Communications H Usman, A Ghaffar | | 2021 |
