Exome sequencing reveals MCM8 mutation underlies ovarian failure and chromosomal instability S AlAsiri, S Basit, MA Wood-Trageser, SA Yatsenko, EP Jeffries, U Surti, ... The Journal of clinical investigation 125 (1), 258-262, 2015 | 224 | 2015 |
Comparison of periodontal and peri-implant inflammatory parameters among patients with prediabetes, type 2 diabetes mellitus and non-diabetic controls T Abduljabbar, F Al-Sahaly, M Al-Kathami, S Afzal, F Vohra Acta Odontologica Scandinavica 75 (5), 319-324, 2017 | 77 | 2017 |
MR imaging and targeting of a specific alveolar macrophage subpopulation in LPS-induced COPD animal model using antibody-conjugated magnetic nanoparticles A Al Faraj, AS Shaik, S Afzal, B Al Sayed, R Halwani International journal of nanomedicine, 1491-1503, 2014 | 70 | 2014 |
A novel anti-IL4Rα nanoparticle efficiently controls lung inflammation during asthma R Halwani, A Sultana Shaik, E Ratemi, S Afzal, R Kenana, S Al-Muhsen, ... Experimental & Molecular Medicine 48 (10), e262-e262, 2016 | 43 | 2016 |
PCA (Principal Component Analysis) Approach towards Identifying the Factors Determining the Medication Behavior of Indian Patients: An Empirical Study SM Roland G., Kumaraperumal S., Kumar S., Gupta A.D., Afzal S. Tobacco Regulatory Science 7 (6-1), 7391-7401., 2022 | 28* | 2022 |
Impact of Patients Approach towards Healthcare Costs on their perception towards Health: An Empirical Study D Kakti A., Kumar S., John N.K., Ratna V.V., Afzal S., Gupta A Tobacco Regulatory Science 7 (6-1), 7380-7390, 2022 | 24* | 2022 |
Association of vitamin D receptor gene polymorphisms with prostate cancer risk in the Pakistani population N Yousaf, S Afzal, T Hayat, J Shah, N Ahmad, R Abbasi, K Ramzan, R Jan, ... Asian Pacific Journal of Cancer Prevention 15 (22), 10009-10013, 2014 | 22 | 2014 |
Rosuvastatin Attenuates Rheumatoid Arthritis-Associated Manifestations via Modulation of the Pro- and Anti-inflammatory Cytokine Network: A Combination of In Vitro and … S Qasim, Alamgeer, S Kalsoom, M Shahzad, IA Bukhari, F Vohra, S Afzal ACS omega 6 (3), 2074-2084, 2021 | 20 | 2021 |
Alterations in the RB1 gene in Pakistani patients with retinoblastoma using direct sequencing analysis S Kalsoom, M Wasim, S Afzal, MS Shahzad, S Ramzan, AR Awan, ... Molecular vision 21, 1085, 2015 | 20 | 2015 |
Specific targeting and noninvasive magnetic resonance imaging of an asthma biomarker in the lung using polyethylene glycol functionalized magnetic nanocarriers A Al Faraj, AS Shaik, S Afzal, S Al‐Muhsen, R Halwani Contrast media & molecular imaging 11 (3), 172-183, 2016 | 17 | 2016 |
Integrated genomic analysis identifies ankrd36 gene as a novel and common biomarker of disease progression in chronic myeloid leukemia Z Iqbal, M Absar, T Akhtar, A Aleem, A Jameel, S Basit, A Ullah, S Afzal, ... Biology 10 (11), 1182, 2021 | 16 | 2021 |
Appraisal of disease-modifying potential of amlodipine as an anti-arthritic agent: new indication for an old drug S Qasim, Alamgeer, S Kalsoom, M Shahzad, HM Irfan, MS Zafar, ... Inflammopharmacology 28, 1121-1136, 2020 | 16 | 2020 |
Identification of TMC1 as a relatively common cause for nonsyndromic hearing loss in the Saudi population K Ramzan, M Al‐Owain, NS Al‐Numair, S Afzal, S Al‐Ageel, S Al‐Amer, ... American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 183 …, 2020 | 16 | 2020 |
Sequence analysis of four vitamin D family genes (VDR, CYP24A1, CYP27B1 and CYP2R1) in Vogt-Koyanagi-Harada (VKH) patients: identification of a potentially … MA Al-Barry, AM Albalawi, MA Sayf, A Badawi, S Afzal, M Latif, ... BMC ophthalmology 16, 1-8, 2016 | 14 | 2016 |
XPC gene mutations in families with xeroderma pigmentosum from Pakistan; prevalent founder effect A Ijaz, S Basit, A Gul, L Batool, A Hussain, S Afzal, K Ramzan, J Ahmad, ... Congenital anomalies 59 (1), 18-21, 2019 | 13 | 2019 |
Whole exome sequencing identification of a novel insertion mutation in the phospholipase C ε‑1 gene in a family with steroid resistant inherited nephrotic syndrome JA Hashmi, RA Safar, S Afzal, AM Albalawi, F Abdu‑Samad, Z Iqbal, ... Molecular Medicine Reports 18 (6), 5095-5100, 2018 | 13 | 2018 |
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 |
A novel mutation in the HPGD gene causing primary hypertrophic osteoarthropathy with digital clubbing in a Pakistani family AK Khan, N Muhammad, SA Khan, W Ullah, A Nasir, S Afzal, K Ramzan, ... Annals of Human Genetics 82 (3), 171-176, 2018 | 12 | 2018 |
Association of the STAT-6 rs324011 (C2892T) variant but not rs324015 (G2964A), with atopic asthma in a Saudi Arabian population S Al-Muhsen, A Vazquez-Tello, A Jamhawi, H Al-Jahdali, A Bahammam, ... Human immunology 75 (8), 791-795, 2014 | 11 | 2014 |
Homozygosity mapping and whole exome sequencing provide exact diagnosis of Cohen syndrome in a Saudi family JA Hashmi, F Fadhli, A Almatrafi, S Afzal, K Ramzan, H Thiele, ... Brain and Development 42 (8), 587-593, 2020 | 10 | 2020 |