| Role of secondary metabolites in plant defense against pathogens M Zaynab, M Fatima, S Abbas, Y Sharif, M Umair, MH Zafar, K Bahadar Microbial pathogenesis 124, 198-202, 2018 | 558 | 2018 |
| Global Burden of Cardiovascular Diseases and Risks, 1990-2022 GA Mensah, V Fuster, CJL Murray, GA Roth, YH Abate, M Abbasian, ... Journal of the American College of Cardiology 82 (25), 2350-2473, 2023 | 151 | 2023 |
| Global, regional, and national prevalence and mortality burden of sickle cell disease, 2000–2021: a systematic analysis from the Global Burden of Disease Study 2021 AM Thomson, TA McHugh, AP Oron, C Teply, N Lonberg, VV Tella, ... The Lancet Haematology, 2023 | 132 | 2023 |
| Clinical genetics of polydactyly: an updated review M Umair, F Ahmad, M Bilal, W Ahmad, M Alfadhel Frontiers in genetics 9, 447, 2018 | 108 | 2018 |
| Global, regional, and national burden of disorders affecting the nervous system, 1990–2021: a systematic analysis for the Global Burden of Disease Study 2021 JD Steinmetz, KM Seeher, N Schiess, E Nichols, B Cao, C Servili, ... The Lancet Neurology, 2024 | 63 | 2024 |
| A review on polysaccharides from Artemisia sphaerocephala Krasch seeds, their extraction, modification, structure, and applications MU Kakar, IU Kakar, MZ Mehboob, S Zada, H Soomro, M Umair, I Iqbal, ... Carbohydrate Polymers 252, 117113, 2021 | 60 | 2021 |
| Global age-sex-specific mortality, life expectancy, and population estimates in 204 countries and territories and 811 subnational locations, 1950–2021, and the impact of the … AE Schumacher, HH Kyu, A Aali, C Abbafati, J Abbas, ... The Lancet, 2024 | 57 | 2024 |
| Targeted SLC19A3 gene sequencing of 3000 Saudi newborn: a pilot study toward newborn screening M Alfadhel, M Umair, B Almuzzaini, S Alsaif, SA AlMohaimeed, ... Annals of Clinical and Translational Neurology 6 (10), 2097-2103, 2019 | 55 | 2019 |
| The use of fish and herptiles in traditional folk therapies in three districts of Chenab riverine area in Punjab, Pakistan M Altaf, AM Abbasi, M Umair, MS Amjad, K Irshad, AM Khan Journal of ethnobiology and ethnomedicine 16, 1-21, 2020 | 50 | 2020 |
| Exome sequencing revealed a splice site variant in the IQCE gene underlying post-axial polydactyly type A restricted to lower limb M Umair, K Shah, B Alhaddad, TB Haack, E Graf, TM Strom, T Meitinger, ... European Journal of Human Genetics 25 (8), 960-965, 2017 | 50 | 2017 |
| Anthropogenic impact on the distribution of the birds in the tropical thorn forest, Punjab, Pakistan M Altaf, A Javid, AM Khan, MSH Khan, M Umair, Z Ali Journal of Asia-Pacific Biodiversity 11 (2), 229-236, 2018 | 48 | 2018 |
| Next-generation sequencing-based pre-implantation genetic testing for aneuploidy (PGT-A): first report from Saudi arabia Y Alyafee, Q Alam, AA Tuwaijri, M Umair, S Haddad, M Alharbi, ... Genes 12 (4), 461, 2021 | 42 | 2021 |
| Genetic disorders associated with metal metabolism M Umair, M Alfadhel Cells 8 (12), 1598, 2019 | 39 | 2019 |
| 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 |
| Homozygous sequence variants in the FKBP10 gene underlie osteogenesis imperfecta in consanguineous families M Umair, A Hassan, A Jan, F Ahmad, M Imran, MI Samman, S Basit, ... Journal of human genetics 61 (3), 207-213, 2016 | 36 | 2016 |
| Outcomes of gynecologic cancer surgery during the COVID-19 pandemic: an international, multicenter, prospective CovidSurg-Gynecologic Oncology Cancer study C Fotopoulou, T Khan, J Bracinik, J Glasbey, N Abu-Rustum, L Chiva, ... American Journal of Obstetrics & Gynecology 227 (5), 735. e1-735. e25, 2022 | 34 | 2022 |
| Non-invasive prenatal testing for autosomal recessive disorders: A new promising approach Y Alyafee, A Al Tuwaijri, M Umair, M Alharbi, S Haddad, M Ballow, ... Frontiers in Genetics 13, 2022 | 34 | 2022 |
| Biallelic variants in four genes underlying recessive osteogenesis imperfecta A Hayat, S Hussain, M Bilal, M Kausar, B Almuzzaini, S Abbas, A Tanveer, ... European journal of medical genetics 63 (8), 103954, 2020 | 34 | 2020 |
| Next generation sequencing based non-invasive prenatal testing (NIPT): First report from Saudi Arabia Y Alyafee, A Al Tuwaijri, Q Alam, M Umair, S Haddad, M Alharbi, M Ballow, ... Frontiers in Genetics 12, 630787, 2021 | 33 | 2021 |
| A novel homozygous sequence variant in GLI1 underlies first case of autosomal recessive pre‐axial polydactyly A Ullah, M Umair, AI Majeed, A Jan, W Ahmad Clinical Genetics 95 (4), 540-541, 2019 | 33 | 2019 |
Dr. Safdar AbbasQuaid-i-Azam University Islamabad Pakistan在 bs.qau.edu.pk 的电子邮件经过验证
