| Wnt signaling: a potential therapeutic target in head and neck squamous cell carcinoma Z Javed, HM Farooq, M Ullah, MZ Iqbal, Q Raza, H Sadia, R Pezzani, ... Asian Pacific journal of cancer prevention: APJCP 20 (4), 995, 2019 | 24 | 2019 |
| LncRNAs as potential therapeutic targets in thyroid cancer Z Javed, FA Shah, S Rajabi, Q Raza, Z Iqbal, M Ullah, T Ahmad, B Salehi, ... Asian Pacific journal of cancer prevention: APJCP 21 (2), 281, 2020 | 22 | 2020 |
| Role of MicroRNA in endometrial carcinoma Z Javed, M Ullah, HA Ashfaq, AH Shah, M Shahzad, M Bilal, A Sumrin, ... Advancements in life sciences 4 (1), 08-13, 2016 | 7 | 2016 |
| Phytochemical analysis and anti-microbial activities of Rosa indica collected from Kohat Pakistan R Saeed, S Ali, H Ullah, M Ullah, S Hassan, S Ahmed, S Akhwan Am J Phytomed Clin Ther 2, 1370-77, 2014 | 7 | 2014 |
| Chromatin remodeling and cardiac differentiation of stem cells M Ullah, H Iqbal, K Haneef, I Khan, A Salim Stem cells: from potential to promise, 251-272, 2021 | 6 | 2021 |
| Unravelling the genetic basis of retinal dystrophies in Pakistani consanguineous families M Marwan, M Dawood, M Ullah, IU Shah, N Khan, MT Hassan, M Karam, ... BMC ophthalmology 23 (1), 205, 2023 | 1 | 2023 |
| A novel homozygous missense substitution p.Thr313Ile in the PDE6B gene underlies autosomal recessive retinitis pigmentosa in a consanguineous Pakistani family N Aziz, M Ullah, A Rashid, Z Hussain, K Shah, A Awan, M Khan, I Ullah, ... BMC ophthalmology 23 (1), 116, 2023 | 1 | 2023 |
| Genetic causes of congenital cataract in consanguineous pedigrees from Pakistan M Ullah, S Irshad, HMA Baig, N Saba, S Gulzar, S Parveen, JH Han, ... Investigative Ophthalmology & Visual Science 63 (7), 486–A0063-486–A0063, 2022 | 1 | 2022 |
| Mutational analysis of exons 5-9 of TP53 gene in breast cancer patients of Punjabi ethnicity H Sadia, M Ullah, A Irshad, K Malik, W Ahmad, R Ahmed, MU Khan, ... Advancements in Life Sciences 9 (1), 18-23, 2022 | 1 | 2022 |
| Substitution of a single non-coding nucleotide upstream of TMEM216 causes non-syndromic retinitis pigmentosa and is associated with reduced TMEM216 expression S Malka, P Biswas, AM Berry, R Sangermano, M Ullah, S Lin, M D’Antonio, ... The American Journal of Human Genetics 111 (9), 2012-2030, 2024 | | 2024 |
| Identification of novel candidate genes for inherited retinal disorders in consanguineous families from Pakistan and Iran HN Frederiksen, A Munir, I Anwar, S Oreshkov, A Zafar, R Choung, ... Investigative Ophthalmology & Visual Science 65 (7), 1520-1520, 2024 | | 2024 |
| Identification and evaluation of a non-coding variant located in the 5'-UTR of TMEM216 as an underlying cause of non-syndromic recessive retinal degeneration (RD) in Pakistani … AM Berry, P Biswas, G Arno, M Quinodoz, R Sangermano, J Xiaodong, ... Investigative Ophthalmology & Visual Science 65 (7), 5287-5287, 2024 | | 2024 |
| A missense mutation in SLC6A6 impairs taurine transport and results in Leber congenital amaurosis with short cardiac atrioventricular conduction time M Ullah, M Quinodoz, AU Rehman, M Shetty, R Grijalva, G Calzetti, ... Investigative Ophthalmology & Visual Science 64 (8), 4529-4529, 2023 | | 2023 |
| A novel intronic deletion in PDE6B causes autosomal recessive retinitis pigmentosa by interfering with RNA splicing M Ullah, AU Rehman, M Folcher, A Ullah, F Usman, A Rashid, B Khan, ... Ophthalmic Research 66 (1), 866-872, 2023 | | 2023 |
| A new nonsense mutation in HMX1 in two siblings with oculoauricular syndrome M Ansar, S Javed, HMA Baig, M Quinodoz, M Ullah, JH Han, MU Rahim, ... Ophthalmic Genetics 43 (5), 720-723, 2022 | | 2022 |
Carlo RivoltaIOB and Dept. of Ophthalmology, University of Basel, Basel, Switzerland在 iob.ch 的电子邮件经过验证
