| Synthesis, molecular docking and α-glucosidase inhibition of 5-aryl-2-(6′-nitrobenzofuran-2′-yl)-1, 3, 4-oxadiazoles M Taha, NH Ismail, S Imran, A Wadood, F Rahim, SM Saad, KM Khan, ... Bioorganic chemistry 66, 117-123, 2016 | 81 | 2016 |
| Benzenesulfonamide derivatives containing imine and amine groups: Inhibition on human paraoxonase and molecular docking studies M Işık, Ş Beydemir, Y Demir, M Durgun, C Türkeş, A Nasır, A Necip, ... International journal of biological macromolecules 146, 1111-1123, 2020 | 68 | 2020 |
| Nanotechnology, a tool for diagnostics and treatment of cancer A Nasir, A Khan, J Li, M Naeem, AAK Khalil, K Khan, M Qasim Current topics in medicinal chemistry 21 (15), 1360-1376, 2021 | 46 | 2021 |
| Identification of CACNA1D variants associated with sinoatrial node dysfunction and deafness in additional Pakistani families reveals a clinical significance K Liaqat, I Schrauwen, SI Raza, K Lee, S Hussain, I Chakchouk, A Nasir, ... Journal of human genetics 64 (2), 153-160, 2019 | 39 | 2019 |
| Novel homozygous sequence variants in the GDF5 gene underlie acromesomelic dysplasia type‐grebe in consanguineous families M Umair, A Rafique, A Ullah, F Ahmad, RH Ali, A Nasir, M Ansar, ... Congenital Anomalies 57 (2), 45-51, 2017 | 32 | 2017 |
| Autosomal dominantly inherited GREB1L variants in individuals with profound sensorineural hearing impairment I Schrauwen, K Liaqat, I Schatteman, T Bharadwaj, A Nasir, A Acharya, ... Genes 11 (6), 687, 2020 | 30 | 2020 |
| Exome sequencing revealed a novel biallelic deletion in the DCAF17 gene underlying Woodhouse Sakati syndrome RH Ali, K Shah, A Nasir, W Steyaert, PJ Coucke, W Ahmad Clinical genetics 90 (3), 263-269, 2016 | 28 | 2016 |
| Potential Nutraceutical Benefits of In Vivo Grown Saffron (Crocus sativus L.) As Analgesic, Anti-inflammatory, Anticoagulant, and Antidepressant in Mice A Khan, NA Muhamad, H Ismail, A Nasir, AAK Khalil, Y Anwar, Z Khan, ... Plants 9 (11), 1414, 2020 | 27 | 2020 |
| Engineering an aldehyde dehydrogenase toward its substrates, 3-hydroxypropanal and NAD+, for enhancing the production of 3-hydroxypropionic acid YS Park, UJ Choi, NH Nam, SJ Choi, A Nasir, SG Lee, KJ Kim, GY Jung, ... Scientific Reports 7 (1), 17155, 2017 | 26 | 2017 |
| Mechanism of zinc ejection by disulfiram in nonstructural protein 5A AU Rehman, G Zhen, B Zhong, D Ni, J Li, A Nasir, MT Gabr, H Rafiq, ... Physical Chemistry Chemical Physics 23 (21), 12204-12215, 2021 | 25 | 2021 |
| A novel missense variant in the PNPLA1 gene underlies congenital ichthyosis in three consanguineous families F Ahmad, M Ansar, S Mehmood, A Izoduwa, K Lee, A Nasir, M Abrar, ... Journal of the European Academy of Dermatology and Venereology: JEADV 30 (12 …, 2016 | 23 | 2016 |
| Variants affecting diverse domains of MEPE are associated with two distinct bone disorders, a craniofacial bone defect and otosclerosis I Schrauwen, H Valgaeren, L Tomas-Roca, M Sommen, U Altunoglu, ... Genetics in Medicine 21 (5), 1199-1208, 2019 | 20 | 2019 |
| A homozygous potentially pathogenic variant in the PAXBP1 gene in a large family with global developmental delay and myopathic hypotonia E Alharby, AM Albalawi, A Nasir, SA Alhijji, A Mahmood, K Ramzan, ... Clinical Genetics 92 (6), 579-586, 2017 | 20 | 2017 |
| Evaluation of the Hypoglycemic Activity of Morchella conica by Targeting Protein Tyrosine Phosphatase 1B N Begum, A Nasir, Z Parveen, T Muhammad, A Ahmed, S Farman, ... Frontiers in pharmacology 12, 661803, 2021 | 19 | 2021 |
| A variant in LMX1A causes autosomal recessive severe-to-profound hearing impairment I Schrauwen, I Chakchouk, K Liaqat, A Jan, A Nasir, S Hussain, ... Human genetics 137, 471-478, 2018 | 19 | 2018 |
| A novel mutation in homeobox DNA binding domain of HOXC13 gene underlies pure hair and nail ectodermal dysplasia (ECTD9) in a Pakistani family AK Khan, N Muhammad, A Aziz, SA Khan, K Shah, A Nasir, MA Khan, ... BMC Medical Genetics 18, 1-5, 2017 | 16 | 2017 |
| Hearing impairment locus heterogeneity and identification of PLS1 as a new autosomal dominant gene in Hungarian Roma I Schrauwen, BI Melegh, I Chakchouk, A Acharya, A Nasir, A Poston, ... European Journal of Human Genetics 27 (6), 869-878, 2019 | 14 | 2019 |
| Identification of novel L2HGDH mutation in a large consanguineous Pakistani family- a case report MI Ullah, A Nasir, A Ahmad, GV Harlalka, W Ahmad, MJ Hassan, ... BMC medical genetics 19, 1-5, 2018 | 14 | 2018 |
| 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 |
| Synthesis of novel disulfide and sulfone hybrid scaffolds as potent β-glucuronidase inhibitor M Taha, NH Ismail, S Imran, A Wadood, F Rahim, LMR Al Muqarrabin, ... Bioorganic Chemistry 68, 15-22, 2016 | 13 | 2016 |
Anushree AcharyaColumbia University在 cumc.columbia.edu 的电子邮件经过验证
