| Centers for Mendelian Genomics: A decade of facilitating gene discovery SM Baxter, JE Posey, NJ Lake, N Sobreira, JX Chong, S Buyske, EE Blue, ... Genetics in Medicine 24 (4), 784-797, 2022 | 53 | 2022 |
| Beyond the exome: what’s next in diagnostic testing for Mendelian conditions MH Wojcik, CM Reuter, S Marwaha, M Mahmoud, MH Duyzend, ... The American Journal of Human Genetics 110 (8), 1229-1248, 2023 | 42 | 2023 |
| Genotoxicity of cisplatin and carboplatin in cultured human lymphocytes: a comparative study B Azab, A Alassaf, A Abu-Humdan, Z Dardas, H Almousa, M Alsalem, ... Interdisciplinary Toxicology 12 (2), 93-97, 2019 | 20 | 2019 |
| Novel CERKL variant in consanguineous Jordanian pedigrees with inherited retinal dystrophies B Azab, R Barham, D Ali, Z Dardas, L Rashdan, M Bijawi, R Maswadi, ... Canadian Journal of Ophthalmology 54 (1), 51-59, 2019 | 11 | 2019 |
| Long read sequencing and expression studies of AHDC1 deletions in Xia‐Gibbs syndrome reveal a novel genetic regulatory mechanism V Chander, M Mahmoud, J Hu, Z Dardas, CM Grochowski, M Dawood, ... Human mutation 43 (12), 2033-2053, 2022 | 7 | 2022 |
| Enteric anendocrinosis attributable to a novel Neurogenin-3 variant B Azab, Z Dardas, O Rabab'h, L Srour, H Telfah, MH Ma'mon, L Mustafa, ... European Journal of Medical Genetics 63 (9), 103981, 2020 | 7 | 2020 |
| Clinical heterogeneity in retinitis pigmentosa caused by variants in RP1 and RLBP1 in five extended consanguineous pedigrees M Al-Bdour, S Pauleck, Z Dardas, R Barham, D Ali, S Amr, L Mustafa, ... Molecular Vision 26, 445, 2020 | 7 | 2020 |
| TBX5 variant with the novel phenotype of mixed-type total anomalous pulmonary venous return in Holt-Oram Syndrome and variable intrafamilial heart defects B Azab, D Aburizeg, W Ji, L Jeffries, NJ Isbeih, AS Al-Akily, H Mohammad, ... Molecular Medicine Reports 25 (6), 210, 2022 | 6 | 2022 |
| Unique variant spectrum in a Jordanian cohort with inherited retinal dystrophies B Azab, Z Dardas, D Aburizeg, M Al-Bdour, M Abu-Ameerh, T Saleh, ... Genes 12 (4), 593, 2021 | 6 | 2021 |
| The impact of exome sequencing on the diagnostic yield of muscular dystrophies in consanguineous families Z Dardas, S Swedan, AAS Qassem, B Azab European Journal of Medical Genetics 63 (4), 103845, 2020 | 6 | 2020 |
| Extending the spectrum of CLRN1‐ and ABCA4‐associated inherited retinal dystrophies caused by novel and recurrent variants using exome sequencing M Abu‐Ameerh, H Mohammad, Z Dardas, R Barham, D Ali, M Bijawi, ... Molecular Genetics & Genomic Medicine 8 (3), e1123, 2020 | 5 | 2020 |
| Novel frameshift variant in the IDUA gene underlies Mucopolysaccharidoses type I in a consanguineous Yemeni pedigree B Azab, Z Dardas, M Hamarsheh, M Alsalem, Z Kilani, F Kilani, A Awidi, ... Molecular Genetics and Metabolism Reports 12, 76-79, 2017 | 5 | 2017 |
| NODAL variants are associated with a continuum of laterality defects from simple D-transposition of the great arteries to heterotaxy Z Dardas, JM Fatih, A Jolly, M Dawood, H Du, CM Grochowski, EG Jones, ... Genome Medicine 16 (1), 53, 2024 | 3 | 2024 |
| HMZDupFinder: a robust computational approach for detecting intragenic homozygous duplications from exome sequencing data H Du, Z Dardas, A Jolly, CM Grochowski, SN Jhangiani, H Li, D Muzny, ... Nucleic Acids Research 52 (4), e18-e18, 2024 | 3 | 2024 |
| SLC26A4 Phenotypic Variability Influences Intra- and Inter-Familial Diagnosis and Management M Tawalbeh, D Aburizeg, BO Abu Alragheb, WS Alaqrabawi, Z Dardas, ... Genes 13 (12), 2192, 2022 | 3 | 2022 |
| Potential Composite Digenic Contribution of NPC1 and NOD2 Leading to Atypical Lethal Niemann-Pick Type C with Initial Crohn’s Disease-like Presentation … B Azab, O Rabab’h, D Aburizeg, H Mohammad, Z Dardas, L Mustafa, ... Genes 13 (6), 973, 2022 | 3 | 2022 |
| Effect of genetic testing on diagnosing gastrointestinal pediatric patients with previously undiagnosed diseases E Altamimi, M Khanfar, O Rabab’h, Z Dardas, L Srour, L Mustafa, B Azab The application of clinical genetics, 221-231, 2020 | 3 | 2020 |
| Considerations for reporting variants in novel candidate genes identified during clinical genomic testing JX Chong, SI Berger, S Baxter, E Smith, C Xiao, DG Calame, MH Hawley, ... Genetics in Medicine 26 (10), 101199, 2024 | 1 | 2024 |
| Investigating the genetic profile of familial atypical cystic fibrosis patients (DeltaF508-CFTR) with neonatal biliary atresia E Altamimi, O Rabab’h, D Aburizeg, L Akasheh, Z Dardas, L Srour, ... Journal of Applied Genetics 64 (1), 71-80, 2023 | 1 | 2023 |
| Genotoxicity assessment in autism spectrum disorder patients using sister chromatid exchange and chromosomal aberration assays B Azab, Z Dardas, L Alzghoul, A Masri, D Hasan, T Saleh, M Alsalem Int J Clin Exp Med 12 (9), 11476-11482, 2019 | 1 | 2019 |
