| Lessons learned from large-scale, first-tier clinical exome sequencing in a highly consanguineous population D Monies, M Abouelhoda, M Assoum, N Moghrabi, R Rafiullah, ... The American Journal of Human Genetics 104 (6), 1182-1201, 2019 | 255 | 2019 |
| Whole exome sequencing reveals inherited and de novo variants in autism spectrum disorder: a trio study from Saudi families B Al-Mubarak, M Abouelhoda, A Omar, H AlDhalaan, M Aldosari, ... Scientific reports 7 (1), 5679, 2017 | 96 | 2017 |
| Recessive mutations in COL25A1 are a cause of congenital cranial dysinnervation disorder JMA Shinwari, A Khan, S Awad, Z Shinwari, A Alaiya, M Alanazi, A Tahir, ... The American Journal of Human Genetics 96 (1), 147-152, 2015 | 53 | 2015 |
| Association of the angiotensinogen gene polymorphism with atherosclerosis and its risk traits in the Saudi population M Al-Najai, P Muiya, AI Tahir, S Elhawari, D Gueco, E Andres, N Mazhar, ... BMC cardiovascular disorders 13, 1-12, 2013 | 40 | 2013 |
| A study of the role of GATA2 gene polymorphism in coronary artery disease risk traits NP Muiya, S Wakil, M Al-Najai, AI Tahir, B Baz, E Andres, O Al-Boudari, ... Gene 544 (2), 152-158, 2014 | 37 | 2014 |
| Genetic spectrum of Saudi Arabian patients with antenatal cystic kidney disease and ciliopathy phenotypes using a targeted renal gene panel MH Al-Hamed, W Kurdi, N Alsahan, Z Alabdullah, R Abudraz, M Tulbah, ... Journal of Medical Genetics 53 (5), 338-347, 2016 | 34 | 2016 |
| A new susceptibility locus for myocardial infarction, hypertension, type 2 diabetes mellitus, and dyslipidemia on chromosome 12q24 SM Wakil, NP Muiya, AI Tahir, M Al-Najai, B Baz, E Andres, N Mazhar, ... Disease markers 2014 (1), 291419, 2014 | 34 | 2014 |
| Parkinson’s disease in Saudi patients: a genetic study BR Al-Mubarak, SA Bohlega, TS Alkhairallah, AI Magrashi, MI AlTurki, ... PloS one 10 (8), e0135950, 2015 | 31 | 2015 |
| ILDR1: Novel mutation and a rare cause of congenital deafness in the Saudi Arabian population K Ramzan, K Taibah, AI Tahir, N Al-Tassan, A Berhan, AM Khater, ... European journal of medical genetics 57 (6), 253-258, 2014 | 24 | 2014 |
| Twenty novel mutations in BCKDHA, BCKDHB and DBT genes in a cohort of 52 Saudi Arabian patients with maple syrup urine disease F Imtiaz, A Al-Mostafa, R Allam, K Ramzan, N Al-Tassan, AI Tahir, ... Molecular Genetics and Metabolism Reports 11, 17-23, 2017 | 23 | 2017 |
| Clinical heterogeneity of PLA2G6-related Parkinsonism: analysis of two Saudi families SA Bohlega, BR Al-Mubarak, EA Alyemni, M Abouelhoda, D Monies, ... BMC research notes 9, 1-7, 2016 | 22 | 2016 |
| Expanding the phenotype and the genotype of Stromme syndrome: A novel variant of the CENPF gene and literature review A Malak, HA Waleed, J Dima, AN Ghada, T Asma, A Mohamed European Journal of Medical Genetics, 2020 | 16 | 2020 |
| Validation of Ion TorrentTM Inherited Disease Panel with the PGMTM Sequencing Platform for Rapid and Comprehensive Mutation Detection AE Mustafa, T Faquih, B Baz, R Kattan, A Al-Issa, AI Tahir, F Imtiaz, ... Genes 9 (5), 267, 2018 | 12 | 2018 |
| The 3′-UTR of the adiponectin Q gene harbours susceptibility loci for atherosclerosis and its metabolic risk traits N Muiya, M Al-Najai, AI Tahir, S Elhawari, D Gueco, E Andres, N Mazhar, ... BMC medical genetics 14, 1-9, 2013 | 11 | 2013 |
| A study of the role of GATA4 polymorphism in cardiovascular metabolic disorders NP Muiya, SM Wakil, AI Tahir, S Hagos, M Najai, D Gueco, N Al-Tassan, ... Human genomics 7, 1-11, 2013 | 10 | 2013 |
| The Affymetrix DMET Plus Platform Reveals Unique Distribution of ADME‐Related Variants in Ethnic Arabs SM Wakil, C Nguyen, NP Muiya, E Andres, A Lykowska-Tarnowska, B Baz, ... Disease Markers 2015 (1), 542543, 2015 | 8 | 2015 |
| Thymic Stromal Lymphopoietin (TSLP) gene variant rs1837253 is significantly associated with Asthma prevalence in Pakistani Pashtun women. S Afzal, K Ramzan, I Khan, A Ullah, AI Tahir, S Ramzan, S Ullah, A Jamal, ... Pakistan Journal of Pharmaceutical Sciences 33, 2020 | 5 | 2020 |
| Variable [beta]-globin haplotypes in Saudi [beta] thalassemia population J Shinwari, T Alshehri, AI Tahir, A Al Jefri, A AlMomen, D Bakheet, ... Open Journal of Genetics 3 (3), 171, 2013 | 2 | 2013 |
| Large-scale next generation sequencing based analysis of SLCO1B1 pharmacogenetics variants in the Saudi population E Goljan, M Abouelhoda, A Tahir, M ElKalioby, B Meyer, D Monies Human Genomics 18 (1), 30, 2024 | 1 | 2024 |
| Accomplishment of goal levels in multi team systems: Role of leadership skills and multicultural teams M Nawaz, A Tahir, RM Khan, GA Bhatti, A Namatullah International Journal of Management Excellence (ISSN: 2292-1648) 12 (2 …, 2019 | 1 | 2019 |
