| Global, regional, and national burden of stroke and its risk factors, 1990–2019: a systematic analysis for the Global Burden of Disease Study 2019 VL Feigin, BA Stark, CO Johnson, GA Roth, C Bisignano, GG Abady, ... The Lancet Neurology 20 (10), 795-820, 2021 | 3006 | 2021 |
| Global, regional, and national burden of diabetes from 1990 to 2021, with projections of prevalence to 2050: a systematic analysis for the Global Burden of Disease Study 2021 KL Ong, LK Stafford, SA McLaughlin, EJ Boyko, SE Vollset, AE Smith, ... The Lancet, 2023 | 482 | 2023 |
| The global burden of cancer attributable to risk factors, 2010–19: a systematic analysis for the Global Burden of Disease Study 2019 KB Tran, JJ Lang, K Compton, R Xu, AR Acheson, HJ Henrikson, ... The Lancet 400 (10352), 563-591, 2022 | 397 | 2022 |
| Global burden of cardiovascular diseases and risks, 1990-2022 GA Mensah, V Fuster, CJL Murray, GA Roth Journal of the American College of Cardiology 82 (25), 2350-2473, 2023 | 57 | 2023 |
| Evidence of trem2 variant associated with triple risk of Alzheimer’s disease Z Abduljaleel, FA Al-Allaf, W Khan, M Athar, N Shahzad, MM Taher, ... PloS one 9 (3), e92648, 2014 | 45 | 2014 |
| Next generation sequencing to identify novel genetic variants causative of autosomal dominant familial hypercholesterolemia associated with increased risk of coronary heart disease FA Al-Allaf, M Athar, Z Abduljaleel, MM Taher, W Khan, FA Ba-Hammam, ... Gene 565 (1), 76-84, 2015 | 43 | 2015 |
| Next-generation sequencing for molecular diagnosis of autosomal recessive polycystic kidney disease BM Edrees, M Athar, FA Al-Allaf, MM Taher, W Khan, A Bouazzaoui, ... Gene 591 (1), 214-226, 2016 | 24 | 2016 |
| Modifying inter-cistronic sequence significantly enhances IRES dependent second gene expression in bicistronic vector: Construction of optimised cassette for gene therapy of … FA Al-Allaf, Z Abduljaleel, M Athar, MM Taher, W Khan, H Mehmet, ... Non-coding RNA research 4 (1), 1-14, 2019 | 22 | 2019 |
| The spectrum of familial hypercholesterolemia (FH) in Saudi Arabia: prime time for patient FH registry F Alallaf, FAH Nazar, M Alnefaie, A Almaymuni, OM Rashidi, K Alhabib, ... The open cardiovascular medicine journal 11, 66, 2017 | 22 | 2017 |
| Identification of a novel nonsense variant c. 1332dup, p.(D445*) in the LDLR gene that causes familial hypercholesterolemia FA Al-Allaf, M Athar, Z Abduljaleel, A Bouazzaoui, MM Taher, R Own, ... Human genome variation 1 (1), 1-3, 2014 | 22 | 2014 |
| Compound heterozygous LDLR variant in severely affected familial hypercholesterolemia patient. FA Al-Allaf, A Alashwal, Z Abduljaleel, MM Taher, A Bouazzaoui, ... Acta Biochimica Polonica 64 (1), 75-79, 2017 | 20 | 2017 |
| Identification of a recurrent frameshift mutation at the LDLR exon 14 (c. 2027delG, p.(G676Afs* 33)) causing familial hypercholesterolemia in Saudi Arab homozygous children FA Al-Allaf, A Alashwal, Z Abduljaleel, MM Taher, SS Siddiqui, ... Genomics 107 (1), 24-32, 2016 | 20 | 2016 |
| Novel combined variants of LDLR and LDLRAP1 genes causing severe familial hypercholesterolemia F Alnouri, M Athar, FA Al-Allaf, Z Abduljaleel, MM Taher, A Bouazzaoui, ... Atherosclerosis 277, 425-433, 2018 | 18 | 2018 |
| Next generation DNA sequencing of atypical choroid plexus papilloma of brain: Identification of novel mutations in a female patient by Ion Proton FAAA Mohiuddin M. Taher, Amal Ali Hassan, Muhammad Saeed, Raid A. Jastania ... Oncology Letters, 2019 | 17 | 2019 |
| Variations in the Yamuna River water quality during the COVID-19 lockdowns BP Singh, P Rana, N Mittal, S Kumar, M Athar, Z Abduljaleel, S Rahman Frontiers in Environmental Science 10, 940640, 2022 | 16 | 2022 |
| Substantial Changes in Selected Volatile Organic Compounds (VOCs) and Associations with Health Risk Assessments in Industrial Areas during the COVID-19 Pandemic BP Singh, SS Sohrab, M Athar, TA Alandijany, S Kumari, A Nair, S Kumari, ... Toxics 11 (2), 165, 2023 | 15 | 2023 |
| Abstracts from the 3rd International Genomic Medicine Conference (3rd IGMC 2015) Jeddah, Kingdom of Saudi Arabia. 30 November-3 December 2015 JW Shay, N Homma, R Zhou, MI Naseer, AG Chaudhary, M Al-Qahtani, ... BMC genomics 17, 1-78, 2016 | 15 | 2016 |
| Hoechst 33342 induces radiosensitization in malignant glioma cells via increase in mitochondrial reactive oxygen species M Athar, NK Chaudhury, ME Hussain, R Varshney Free radical research 44 (8), 936-949, 2010 | 15 | 2010 |
| Xanthomas Can Be Misdiagnosed and Mistreated in Homozygous Familial Hypercholesterolemia Patients: A Call for Increased Awareness Among Dermatologists and Health Care Practitioners F Alnouri, FA Al-Allaf, M Athar, Z Abduljaleel, M Alabdullah, D Alammari, ... Global Heart 15 (1), 2020 | 12 | 2020 |
| Molecular Analysis of Factor VIII and Factor IX Genes in Hemophilia Patients: Identification of Novel Mutations and Molecular Dynamics Studies FA Al-Allaf, MM Taher, Z Abduljaleel, A Bouazzaoui, M Athar, NM Bogari, ... Journal of clinical medicine research 9 (4), 317, 2017 | 12 | 2017 |
Faisal AL-ALLAFUmm Al-Qura University, Faculty of Medicine, Department of Medical Genetics, Associate Professor ofVerified email at uqu.edu.sa
