| The genetic and molecular mechanisms of congenital hyperinsulinism S Galcheva, H Demirbilek, S Al-Khawaga, K Hussain Frontiers in endocrinology 10, 111, 2019 | 119 | 2019 |
| Potential application of mesenchymal stem cells and their exosomes in lung injury: an emerging therapeutic option for COVID-19 patients S Al-Khawaga, EM Abdelalim Stem cell research & therapy 11, 1-33, 2020 | 76 | 2020 |
| Enhanced differentiation of human pluripotent stem cells into pancreatic progenitors co-expressing PDX1 and NKX6. 1 B Memon, M Karam, S Al-Khawaga, EM Abdelalim Stem cell research & therapy 9, 1-15, 2018 | 74 | 2018 |
| Neuroimmune communication regulating pruritus in atopic dermatitis M Steinhoff, F Ahmad, A Pandey, A Datsi, A AlHammadi, S Al-Khawaga, ... Journal of Allergy and Clinical Immunology 149 (6), 1875-1898, 2022 | 73 | 2022 |
| Diagnosis and management of hyperinsulinaemic hypoglycaemia S Galcheva, S Al-Khawaga, K Hussain Best Practice & Research Clinical Endocrinology & Metabolism 32 (4), 551-573, 2018 | 50 | 2018 |
| Pathways governing development of stem cell‐derived pancreatic β cells: lessons from embryogenesis S Al‐Khawaga, B Memon, AE Butler, S Taheri, AB Abou‐Samra, ... Biological Reviews 93 (1), 364-389, 2018 | 48 | 2018 |
| Ion transporters, channelopathies, and glucose disorders H Demirbilek, S Galcheva, D Vuralli, S Al-Khawaga, K Hussain International journal of molecular sciences 20 (10), 2590, 2019 | 34 | 2019 |
| A systematic review of childhood diabetes research in the Middle East region S Saraswathi, S Al-Khawaga, N Elkum, K Hussain Frontiers in endocrinology 10, 805, 2019 | 32 | 2019 |
| The clinical and genetic characteristics of permanent neonatal diabetes (PNDM) in the state of Qatar S Al‐Khawaga, I Mohammed, S Saraswathi, B Haris, R Hasnah, A Saeed, ... Molecular genetics & genomic medicine 7 (10), e00753, 2019 | 28 | 2019 |
| Clinical features, epidemiology, autoantibody status, HLA haplotypes and genetic mechanisms of type 1 diabetes mellitus among children in Qatar B Haris, I Ahmed, N Syed, H Almabrazi, S Saraswathi, S Al-Khawaga, ... Scientific reports 11 (1), 18887, 2021 | 16 | 2021 |
| Clinical Characteristics and Long-term Follow-up of Patients with Diabetes Due To PTF1A Enhancer Mutations H Demirbilek, A Cayir, SE Flanagan, R Yıldırım, Y Kor, F Gurbuz, ... The Journal of Clinical Endocrinology & Metabolism 105 (12), e4351-e4359, 2020 | 13 | 2020 |
| A SLC16A1 mutation in an infant with ketoacidosis and neuroimaging assessment: expanding the clinical spectrum of MCT1 deficiency S Al-Khawaga, J AlRayahi, F Khan, S Saraswathi, R Hasnah, B Haris, ... Frontiers in Pediatrics 7, 299, 2019 | 13 | 2019 |
| Epidemiology, genetic landscape and classification of childhood diabetes mellitus in the State of Qatar B Haris, S Saraswathi, S Al‐Khawaga, R Hasnah, A Saeed, ... Journal of Diabetes Investigation 12 (12), 2141-2148, 2021 | 10 | 2021 |
| Epigenetic control of inflammation in Atopic Dermatitis S Akhtar, RKME Alsayed, F Ahmad, A AlHammadi, S Al-Khawaga, ... Seminars in Cell & Developmental Biology 154, 199-207, 2024 | 9 | 2024 |
| Generation of two human iPSC lines from patients with maturity-onset diabetes of the young type 2 (MODY2) and permanent neonatal diabetes due to mutations in the GCK gene YWA Aqel, G Ali, AK Elsayed, S Al-Khawaga, K Hussain, EM Abdelalim Stem Cell Research 48, 101991, 2020 | 7 | 2020 |
| Derivation of a human induced pluripotent stem cell line (QBRIi007-A) from a patient carrying a homozygous intronic mutation (c. 613-7T> G) in the SLC2A2 gene AK Elsayed, M Aghadi, S Al-Khawaga, K Hussain, EM Abdelalim Stem Cell Research 44, 101736, 2020 | 7 | 2020 |
| Diabetes mellitus in a patient with Lafora disease: possible links with pancreatic β-cell dysfunction and insulin resistance RC Nicolescu, S Al-Khawaga, BA Minassian, K Hussain Frontiers in Pediatrics 6, 424, 2019 | 7 | 2019 |
| Emerging role of the IL-36/IL-36R Axis in multiple inflammatory skin diseases F Ahmad, MA Alam, AW Ansari, A Jochebeth, R Leo, MN Al-Abdulla, ... Journal of Investigative Dermatology, 2024 | 6 | 2024 |
| Haploinsufficiency of the FOXA2 associated with a complex clinical phenotype I Mohammed, S Al‐Khawaga, D Bohanna, A Shabani, F Khan, DR Love, ... Molecular Genetics & Genomic Medicine 8 (6), e1086, 2020 | 5 | 2020 |
| Generation of a human induced pluripotent stem cell line (QBRIi009-A) from a patient with a heterozygous deletion of FOXA2 AK Elsayed, M Aghadi, G Ali, S Al-Khawaga, K Hussain, EM Abdelalim Stem Cell Research 42, 101705, 2020 | 5 | 2020 |
