| Epidemiology of cancer in Saudi Arabia thru 2010–2019: a systematic review with constrained meta-analysis WS Alqahtani, NA Almufareh, DM Domiaty, G Albasher, MA Alduwish, ... AIMS public health 7 (3), 679, 2020 | 182 | 2020 |
| β‐Actin‐dependent global chromatin organization and gene expression programs control cellular identity X Xie, B Almuzzaini, N Drou, S Kremb, A Yousif, AKÖ Farrants, ... The FASEB Journal 32 (3), 1296-1314, 2018 | 70 | 2018 |
| Nuclear myosin 1 contributes to a chromatin landscape compatible with RNA polymerase II transcription activation B Almuzzaini, AA Sarshad, AKÖ Farrants, P Percipalle BMC biology 13, 1-15, 2015 | 66 | 2015 |
| Interferon-induced transmembrane protein-3 genetic variant rs12252 is associated with COVID-19 mortality J Alghamdi, M Alaamery, T Barhoumi, M Rashid, H Alajmi, N Aljasser, ... Genomics 113 (4), 1733-1741, 2021 | 60 | 2021 |
| 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 | 58 | 2019 |
| In β‐actin knockouts, epigenetic reprogramming and rDNA transcription inactivation lead to growth and proliferation defects B Almuzzaini, AA Sarshad, AS Rahmanto, ML Hansson, A Von Euler, ... The FASEB Journal 30 (8), 2860-2873, 2016 | 44 | 2016 |
| 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 | 37 | 2020 |
| Biallelic variant in DACH1, encoding Dachshund Homolog 1, defines a novel candidate locus for recessive postaxial polydactyly type A M Umair, O Palander, M Bilal, B Almuzzaini, Q Alam, F Ahmad, M Younus, ... Genomics 113 (4), 2495-2502, 2021 | 28 | 2021 |
| Nuclear Wiskott–Aldrich syndrome protein co-regulates T cell factor 1-mediated transcription in T cells NV Kuznetsov, B Almuzzaini, JS Kritikou, MAP Baptista, MMS Oliveira, ... Genome Medicine 9, 1-18, 2017 | 27 | 2017 |
| Mutated RAP1GDS1 causes a new syndrome of dysmorphic feature, intellectual disability & speech delay A Asiri, E Aloyouni, M Umair, Y Alyafee, A Al Tuwaijri, KM Alhamoudi, ... Annals of Clinical and Translational Neurology 7 (6), 956-964, 2020 | 20 | 2020 |
| The effect of the VKORC1 promoter variant on warfarin responsiveness in the Saudi WArfarin Pharmacogenetic (SWAP) cohort M Al Ammari, M AlBalwi, K Sultana, IB Alabdulkareem, B Almuzzaini, ... Scientific Reports 10 (1), 11613, 2020 | 18 | 2020 |
| Identification of the TTC26 splice variant in a novel complex ciliopathy syndrome with biliary, renal, neurological, and skeletal manifestations M Alfadhel, M Umair, B Almuzzaini, A Asiri, A Al Tuwaijri, K Alhamoudi, ... Molecular Syndromology 12 (3), 133-140, 2021 | 13 | 2021 |
| Pancytopenia, Recurrent Infection, Poor Wound Healing, Heterotopia of the Brain Probably Associated with A Candidate Novel de Novo CDC42 Gene Defect … A Asiri, D Alwadaani, M Umair, KM Alhamoudi, MH Almuhanna, A Nasir, ... Genes 12 (2), 294, 2021 | 11 | 2021 |
| Blockade of p38 MAPK overcomes AML stem cell line KG1a resistance to 5-Fluorouridine and the impact on miRNA profiling S Matou-Nasri, M Najdi, NA AlSaud, Y Alhaidan, H Al-Eidi, G Alatar, ... PLoS One 17 (5), e0267855, 2022 | 9 | 2022 |
| A classification system for split-hand/foot malformation (SHFM): a proposal based on 3 pedigrees with WNT10B mutations MA Al Ghamdi, MM Al-Qattan, A Hadadi, A Alabdulrahman, B Almuzzaini, ... European Journal of Medical Genetics 63 (3), 103738, 2020 | 8 | 2020 |
| Identification of novel mutations in colorectal cancer patients using AmpliSeq comprehensive cancer panel B Almuzzaini, J Alghamdi, A Alomani, S AlGhamdi, AA Alsharm, ... Journal of Personalized Medicine 11 (6), 535, 2021 | 7 | 2021 |
| Blood pressure–lowering activity of statins: a systematic literature review and meta-analysis of placebo-randomized controlled trials J Alghamdi, A Alqadi, A Alharf, B Almuzzaini, A Mahmud, T Barhoumi, ... European Journal of Clinical Pharmacology 76, 1745-1754, 2020 | 7 | 2020 |
| A novel interstitial deletion of chromosome 2q21. 1‐q23. 3: case report and literature review B Almuzzaini, NS Alatwi, S Alsaif, MA Al Balwi Molecular Genetics & Genomic Medicine 8 (4), e1135, 2020 | 7 | 2020 |
| Population pharmacokinetics of busulfan in Saudi pediatric patients undergoing hematopoietic stem cell transplantation A Alsultan, AA Albassam, A Alturki, A Alsultan, M Essa, B Almuzzaini, ... International Journal of Clinical Pharmacy 42, 703-712, 2020 | 7 | 2020 |
| Can first-dose therapeutic drug monitoring predict the steady state area under the blood concentration-time curve of busulfan in pediatric patients undergoing hematopoietic … A Alsultan, AA Albassam, A Alturki, A Alsultan, M Essa, B Almuzzaini, ... Frontiers in Pediatrics 10, 834773, 2022 | 6 | 2022 |
