Gene panel sequencing identifies a likely monogenic cause in 7% of 235 Pakistani families with nephrolithiasis A Amar, AJ Majmundar, I Ullah, A Afzal, DA Braun, S Shril, A Daga, ... Human genetics 138, 211-219, 2019 | 41 | 2019 |
Recessive NOS1AP variants impair actin remodeling and cause glomerulopathy in humans and mice AJ Majmundar, F Buerger, TA Forbes, V Klämbt, R Schneider, K Deutsch, ... Science advances 7 (1), eabe1386, 2021 | 31 | 2021 |
Direct sequencing of FAH gene in Pakistani tyrosinemia type 1 families reveals a novel mutation S Ijaz, MY Zahoor, M Imran, S Afzal, MA Bhinder, I Ullah, HA Cheema, ... Journal of Pediatric Endocrinology and Metabolism 29 (3), 327-332, 2016 | 13 | 2016 |
An in vitro antiviral activity of iodine complexes against SARS-CoV-2 I Altaf, MF Nadeem, N Hussain, M Nawaz, S Raza, MA Shabbir, ... Archives of Microbiology 203 (7), 4743-4749, 2021 | 9 | 2021 |
Association study of CLDN14 variations in patients with kidney stones I Ullah, K Murtaza, H Ammara, Misbah, MA Bhinder, A Riaz, W Shehzad, ... Open Life Sciences 17 (1), 81-90, 2022 | 6 | 2022 |
Vitamin E boosted the protective potential of Aloe vera in CCl4-treated rats R Fatima, MS Yasin, H Anwar, I Ullah, W Shehzad, I Murtaza, T Ali Biologia, 1-8, 2021 | 5 | 2021 |
Mitochondrial DNA diversity and maternal origins of Pakistani donkey S Earnist, S Nawaz, I Ullah, MA Bhinder, M Imran, MA Rasheed, ... Brazilian Journal of Biology 84, e256942, 2022 | 3 | 2022 |
OXGR1 is a candidate disease gene for human calcium oxalate nephrolithiasis AJ Majmundar, E Widmeier, JF Heneghan, A Daga, CHW Wu, F Buerger, ... Genetics in Medicine 25 (3), 100351, 2023 | 1 | 2023 |
Sequencing the CaSR locus in Pakistani stone formers reveals a novel loss-of-function variant atypically associated with nephrolithiasis I Ullah, I Ottlewski, W Shehzad, A Riaz, S Ijaz, A Tufail, H Ammara, ... BMC Medical Genomics 14, 1-7, 2021 | 1 | 2021 |