| Single point mutations in pediatric differentiated thyroid cancer AS Alzahrani, AK Murugan, E Qasem, M Alswailem, H Al-Hindi, Y Shi Thyroid 27 (2), 189-196, 2017 | 67 | 2017 |
| TERT promoter mutations in thyroid cancer: a report from a Middle Eastern population E Qasem, AK Murugan, H Al-Hindi, M Xing, M Almohanna, M Alswailem, ... Endocrine-related cancer 22 (6), 901-908, 2015 | 62 | 2015 |
| Genetic alterations in pediatric thyroid cancer using a comprehensive childhood cancer gene panel AS Alzahrani, M Alswailem, AA Alswailem, H Al-Hindi, E Goljan, ... The Journal of Clinical Endocrinology & Metabolism 105 (10), 3324-3334, 2020 | 49 | 2020 |
| Uncommon TERT Promoter Mutations in Pediatric Thyroid Cancer AS Alzahrani, E Qasem, AK Murugan, HN Al-Hindi, D AlKhafaji, ... Thyroid 26 (2), 235-241, 2016 | 44 | 2016 |
| Lung metastasis in pediatric thyroid cancer: radiological pattern, molecular genetics, response to therapy, and outcome AS Alzahrani, M Alswailem, Y Moria, R Almutairi, M Alotaibi, AK Murugan, ... The Journal of Clinical Endocrinology & Metabolism 104 (1), 103-110, 2019 | 42 | 2019 |
| PAC exhibits potent anti‐colon cancer properties through targeting cyclin D1 and suppressing epithelial‐to‐mesenchymal transition A Al‐Qasem, HA Al‐Howail, M Al‐Swailem, A Al‐Mazrou, B Al‐Otaibi, ... Molecular carcinogenesis 55 (3), 233-244, 2016 | 26 | 2016 |
| Mutational profile and genotype/phenotype correlation of non-familial pheochromocytoma and paraganglioma S Albattal, M Alswailem, Y Moria, H Al-Hindi, M Dasouki, M Abouelhoda, ... Oncotarget 10 (57), 5919, 2019 | 22 | 2019 |
| Absence of EIF1AX, PPM1D, and CHEK2 mutations reported in Thyroid Cancer Genome Atlas (TCGA) in a large series of thyroid cancer AS Alzahrani, AK Murugan, E Qasem, MM Alswailem, B AlGhamdi, ... Endocrine 63, 94-100, 2019 | 21 | 2019 |
| Mutational analysis of rare subtypes of congenital adrenal hyperplasia in a highly inbred population MM Alswailem, OS Alzahrani, DS Alhomaidah, R Alasmari, E Qasem, ... Molecular and Cellular Endocrinology 461, 105-111, 2018 | 18 | 2018 |
| A novel claudin-10 mutation with a unique mechanism in two unrelated families with HELIX syndrome AS Alzahrani, M Hussein, M Alswailem, A Mouna, L Albalawi, Y Moria, ... Kidney International 100 (2), 415-429, 2021 | 17 | 2021 |
| Molecular genetics and phenotype/genotype correlation of 5-α reductase deficiency in a highly consanguineous population MM Alswailem, OS Alzahrani, L Alghofaili, E Qasem, M Almohanaa, ... Endocrine 63, 361-368, 2019 | 16 | 2019 |
| A unique genotype of pseudohypoaldosteronism type 1b in a highly consanguineous population AS Alzahrani, M Alswailem, BB Abbas, E Qasem, A Alsagheir, ... Journal of the Endocrine Society 5 (8), bvab095, 2021 | 8 | 2021 |
| Molecular genetics of diffuse sclerosing papillary thyroid cancer M Alswailem, B Alghamdi, A Alotaibi, A Aljomiah, H Al-Hindi, AK Murugan, ... The Journal of Clinical Endocrinology & Metabolism 108 (9), e704-e711, 2023 | 6 | 2023 |
| Fumarate hydratase is a novel gene for familial non-medullary thyroid cancer AS Alzahrani, M Alswailem, B Alghamdi, H Al-Hindi The Journal of Clinical Endocrinology & Metabolism 107 (9), 2539-2544, 2022 | 6 | 2022 |
| Molecular genetics of disorders of sex development in a highly consanguineous population M Alswailem, A Alsagheir, BB Abbas, O Alzahrani, AS Alzahrani The Journal of Steroid Biochemistry and Molecular Biology 208, 105736, 2021 | 6 | 2021 |
| A high rate of novel CYP11B1 mutations in Saudi Arabia AS Alzahrani, MM Alswailem, AK Murugan, DS Alhomaidah, CP Capper, ... The Journal of Steroid Biochemistry and Molecular Biology 174, 217-224, 2017 | 6 | 2017 |
| Papillary Thyroid Cancer and a TERT Promotor Mutation-positive Paraganglioma in a Patient With a Germline SDHB Mutation AS Alzahrani, M Alswailem, AK Murugan, B Alghamdi, H Al-Hindi Journal of the Endocrine Society 6 (7), bvac076, 2022 | 4 | 2022 |
| Case Report: Severe Gonadal Dysgenesis Causing 46,XY Disorder of Sex Development Due to a Novel NR5A1 Variant KM Alhamoudi, B Alghamdi, A Aljomaiah, M Alswailem, H Al-Hindi, ... Frontiers in Genetics 13, 885589, 2022 | 3 | 2022 |
| EPAS1-related pheochromocytoma/paraganglioma AS Alzahrani, M Alswailem, A Buffet, B Alghamdi, L Alobaid, O Alsagheir, ... Endocrine-Related Cancer 31 (8), 2024 | 2 | 2024 |
| How do BRAFV600E and TERT promoter mutations interact with the ATA and TNM staging systems in thyroid cancer? N Mukhtar, K Alhamoudi, M Alswailem, H Alhindi, AK Murugan, ... Frontiers in Endocrinology 14, 1270796, 2023 | 2 | 2023 |
Ali AlzahraniConsultant Endocrinologist, King Faisal Specialist Hospital 在 kfshrc.edu.sa 的电子邮件经过验证
