| Silicon Carbide Whisker-Mediated Embryogenic Callus Transformation of Cotton (Gossypium hirsutum L.) and Regeneration of Salt Tolerant Plants S Asad, Z Mukhtar, F Nazir, JA Hashmi, S Mansoor, Y Zafar, M Arshad Molecular biotechnology 40, 161-169, 2008 | 77 | 2008 |
| Engineering cotton (Gossypium hirsutum L.) for resistance to cotton leaf curl disease using viral truncated AC1 DNA sequences JA Hashmi, Y Zafar, M Arshad, S Mansoor, S Asad Virus Genes 42, 286-296, 2011 | 65 | 2011 |
| Characterization of cellular and molecular heterogeneity of bone marrow stromal cells M Elsafadi, M Manikandan, M Atteya, JA Hashmi, Z Iqbal, A Aldahmash, ... Stem cells international 2016, 2016 | 63 | 2016 |
| TGFβ1-induced differentiation of human bone marrow-derived MSCs is mediated by changes to the actin cytoskeleton M Elsafadi, M Manikandan, S Almalki, M Mobarak, M Atteya, Z Iqbal, ... Stem Cells International 2018, 2018 | 36 | 2018 |
| High-resolution SNP genotyping platform identified recurrent and novel CNVs in autism multiplex families LY AlAyadhi, JA Hashmi, M Iqbal, AM Albalawi, MI Samman, NE Elamin, ... Neuroscience 339, 561-570, 2016 | 32 | 2016 |
| A novel splice-site mutation in the ASPM gene underlies autosomal recessive primary microcephaly JA Hashmi, KM Al-Harbi, K Ramzan, AM Albalawi, A Mehmood, ... Annals of Saudi Medicine 36 (6), 391-396, 2016 | 29 | 2016 |
| NR2F1 mediated down-regulation of osteoblast differentiation was rescued by bone morphogenetic protein-2 (BMP-2) in human MSC M Manikandan, S Abuelreich, M Elsafadi, H Alsalman, H Almalak, A Siyal, ... Differentiation 104, 36-41, 2018 | 19 | 2018 |
| Novel homozygous loss-of-function mutations in RP1 and RP1L1 genes in retinitis pigmentosa patients MA Albarry, JA Hashmi, AQ Alreheli, AM Albalawi, B Khan, K Ramzan, ... Ophthalmic Genetics 40 (6), 507-513, 2019 | 15 | 2019 |
| Biallelic loss of function variant in the unfolded protein response gene PDIA6 is associated with asphyxiating thoracic dystrophy and neonatal‐onset diabetes FM Al‐Fadhli, M Afqi, MH Sairafi, M Almuntashri, E Alharby, G Alharbi, ... Clinical Genetics 99 (5), 694-703, 2021 | 13 | 2021 |
| Whole exome sequencing identified a novel single base pair insertion mutation in the EYS gene in a six generation family with retinitis pigmentosa JA Hashmi, MA Albarry, AM Almatrafi, AM Albalawi, A Mahmood, S Basit Congenital anomalies 58 (1), 10-15, 2018 | 13 | 2018 |
| Whole exome sequencing identification of a novel insertion mutation in the phospholipase C ε‑1 gene in a family with steroid resistant inherited nephrotic syndrome JA Hashmi, RA Safar, S Afzal, AM Albalawi, F Abdu‑Samad, Z Iqbal, ... Molecular Medicine Reports 18 (6), 5095-5100, 2018 | 11 | 2018 |
| An 18 bps in-frame deletion mutation in RUNX2 gene is a population polymorphism rather than a pathogenic variant JA Hashmi, A Almatrafi, M Latif, A Nasir, S Basit European Journal of Medical Genetics 62 (2), 124-128, 2019 | 10 | 2019 |
| Homozygosity mapping and whole exome sequencing provide exact diagnosis of Cohen syndrome in a Saudi family JA Hashmi, F Fadhli, A Almatrafi, S Afzal, K Ramzan, H Thiele, ... Brain and Development 42 (8), 587-593, 2020 | 8 | 2020 |
| Centromere protein I (CENPI) is a candidate gene for X-linked steroid sensitive nephrotic syndrome S Basit, HM Al-Edressi, MH Sairafi, JA Hashmi, E Alharby, R Safar, ... Journal of Nephrology 33, 763-769, 2020 | 7 | 2020 |
| A Heterozygous mutation in the triple helical region of the Alpha 1 (II) chain of the COL2A1 protein causes non-lethal spondyloepiphyseal dysplasia congenita A Almatrafi, F Alfadhli, YN Khan, S Afzal, JA Hashmi, A Ullah, AM Albalawi, ... Genetic testing and molecular biomarkers 23 (5), 310-315, 2019 | 7 | 2019 |
| A homozygous missense variant in the homeobox domain of the NKX6‐2 results in progressive spastic ataxia type 8 associated with lower limb weakness and … A Almatrafi, M Umair, A Eldardear, M Al‐Luqmani, JA Hashmi, ... The Journal of Gene Medicine 22 (8), e3196, 2020 | 6 | 2020 |
| Biallelic variants in HECT E3 paralogs, HECTD4 and UBE3C, encoding ubiquitin ligases cause neurodevelopmental disorders that overlap Angelman syndrome EA EA Faqeih, MA Alghamdi, MA Almahroos Genetics in Medicine 25 (2), 100323, 2022 | 5* | 2022 |
| A novel frameshift mutation in the ITGB3 gene leading to Glanzmann's thrombasthenia in a Saudi Arabian family A Alharbi, JA Hashmi, E Alharby, AM Albalawi, K Ramzan, S Basit Hematology/Oncology and Stem Cell Therapy, 2021 | 5 | 2021 |
| Missense mutations in the CTSC gene in Saudi families segregating Papillon-Lefèvre syndrome AM Albalawi, JA Hashmi, F Alfadhli, A Almatrafi, K Ramzan, S Basit Annals of Dermatology 32 (1), 77, 2020 | 5 | 2020 |
| High frequency and poor prognosis of late childhood BCR-ABL-positive and MLL-AF4-positive ALL define the need for advanced molecular diagnostics and improved therapeutic … Z Iqbal, T Akhtar, T Awan, A Aleem, N Sabir, M Rasool, M Absar, ... Molecular diagnosis & therapy 19, 277-287, 2015 | 5 | 2015 |
