| Genetics of human Bardet–Biedl syndrome, an updates SA Khan, N Muhammad, MA Khan, A Kamal, ZU Rehman, S Khan Clinical genetics 90 (1), 3-15, 2016 | 176 | 2016 |
| High frequency of methicillin-resistant Staphylococcus aureus in Peshawar Region of Pakistan A Ullah, M Qasim, H Rahman, J Khan, M Haroon, N Muhammad, A Khan, ... Springerplus 5, 1-6, 2016 | 89 | 2016 |
| Genetic studies of autosomal recessive primary microcephaly in 33 Pakistani families: novel sequence variants in ASPM gene A Gul, MJ Hassan, S Mahmood, W Chen, S Rahmani, MI Naseer, ... Neurogenetics 7, 105-110, 2006 | 75 | 2006 |
| Engineering of the E. coli Outer Membrane Protein FhuA to overcome the Hydrophobic Mismatch in Thick Polymeric Membranes N Muhammad, T Dworeck, M Fioroni, U Schwaneberg Journal of nanobiotechnology 9, 1-9, 2011 | 74 | 2011 |
| Chlorophyll derivatives can be an efficient weapon in the fight against dengue A Azizullah, ZU Rehman, I Ali, W Murad, N Muhammad, W Ullah, ... Parasitology research 113, 4321-4326, 2014 | 65 | 2014 |
| Chemical Characterization, Analgesic, Antioxidant, and Anticholinesterase Potentials of Essential Oils From Isodon rugosus Wall. ex. Benth A Sadiq, A Zeb, F Ullah, S Ahmad, M Ayaz, U Rashid, N Muhammad Frontiers in pharmacology 9, 623, 2018 | 61 | 2018 |
| Punica granatum peel extracts: HPLC fractionation and LC MS analysis to quest compounds having activity against multidrug resistant bacteria I Khan, H Rahman, NM Abd El-Salam, A Tawab, A Hussain, TA Khan, ... BMC complementary and alternative medicine 17, 1-6, 2017 | 57 | 2017 |
| Polymersome surface decoration by an EGFP fusion protein employing Cecropin A as peptide “anchor” M Noor, T Dworeck, A Schenk, P Shinde, M Fioroni, U Schwaneberg Journal of biotechnology 157 (1), 31-37, 2012 | 52 | 2012 |
| Alleviation of lead-induced physiological, metabolic, and ultramorphological changes in leaves of upland cotton through glutathione M Khan, MK Daud, A Basharat, MJ Khan, A Azizullah, N Muhammad, ... Environmental Science and Pollution Research 23, 8431-8440, 2016 | 51 | 2016 |
| Novel mutations in natriuretic peptide receptor-2 gene underlie acromesomelic dysplasia, type maroteaux S Khan, RH Ali, S Abbasi, M Nawaz, N Muhammad, W Ahmad BMC medical genetics 13, 1-8, 2012 | 45 | 2012 |
| Chlorpyrifos and lambda cyhalothrin-induced oxidative stress in human erythrocytes: in vitro studies F Deeba, I Raza, N Muhammad, H Rahman, Z ur Rehman, A Azizullah, ... Toxicology and industrial health 33 (4), 297-307, 2017 | 36 | 2017 |
| Beta-lactamase-producingPseudomonas aeruginosa: Phenotypic characteristics and molecular identification of virulence genes W Ullah, M Qasim, H Rahman, Y Jie, N Muhammad Journal of the Chinese Medical Association 80 (3), 173-177, 2017 | 35 | 2017 |
| Multi drug resistant Pseudomonas aeruginosa: pathogen burden and associated antibiogram in a tertiary care hospital of Pakistan W Ullah, M Qasim, H Rahman, F Bari, S Khan, ZU Rehman, Z Khan, ... Microbial pathogenesis 97, 209-212, 2016 | 34 | 2016 |
| Pakistan genetic mutation database (PGMD); a centralized Pakistani mutome data source I Qasim, B Ahmad, MA Khan, N Khan, N Muhammad, S Basit, S Khan European journal of medical genetics 61 (4), 204-208, 2018 | 32 | 2018 |
| Novel homozygous mutations in the WNT10B gene underlying autosomal recessive split hand/foot malformation in three consanguineous families A Aziz, S Khan, FK Zimri, N Muhammad, S Rashid, W Ahmad Gene 534 (2), 265-271, 2014 | 28 | 2014 |
| Genetics of human isolated hereditary nail disorders S Khan, S Basit, R Habib, A Kamal, N Muhammad, W Ahmad British Journal of Dermatology 173 (4), 922-929, 2015 | 25 | 2015 |
| Deleterious Variants in WNT10A, EDAR, and EDA Causing Isolated and Syndromic Tooth Agenesis: A Structural Perspective from Molecular Dynamics Simulations A Parveen, SA Khan, MU Mirza, H Bashir, F Arshad, M Iqbal, W Ahmad, ... International Journal of Molecular Sciences 20 (21), 5282, 2019 | 24 | 2019 |
| CTX-M-15 and OXA-10 beta lactamases in multi drug resistant Pseudomonas aeruginosa: first report from Pakistan W Ullah, M Qasim, H Rahman, S Khan, Z ur Rehman, N Ali, N Muhammad Microbial pathogenesis 105, 240-244, 2017 | 22 | 2017 |
| Genetics of human isolated acromesomelic dysplasia S Khan, S Basit, MA Khan, N Muhammad, W Ahmad European Journal of Medical Genetics 59 (4), 198-203, 2016 | 22 | 2016 |
| Novel mutations in ALDH1A3 associated with autosomal recessive anophthalmia/microphthalmia, and review of the literature S Lin, GV Harlalka, A Hameed, HM Reham, M Yasin, N Muhammad, ... BMC medical genetics 19, 1-8, 2018 | 19 | 2018 |
Saad Ullah KhanAssociate Prof. Kohat Uni of Science & Technology Kohat,在 kust.edu.pk 的电子邮件经过验证
