| Rapamycin and rapalogs for tuberous sclerosis complex TH Sasongko, NFD Ismail, Z Zabidi‐Hussin Cochrane Database of Systematic Reviews, 2016 | 93* | 2016 |
| Combination of SMN2 copy number and NAIP deletion predicts disease severity in spinal muscular atrophy MS Watihayati, H Fatemeh, M Marini, AB Atif, WM Zahiruddin, ... Brain and Development 31 (1), 42-45, 2009 | 70 | 2009 |
| Combination of SMN2 copy number and NAIP deletion predicts disease severity in spinal muscular atrophy MS Watihayati, H Fatemeh, M Marini, AB Atif, WM Zahiruddin, ... Brain and Development 31 (1), 42-45, 2009 | 70 | 2009 |
| Histone deacetylase inhibitors as potential treatment for spinal muscular atrophy J Mohseni, Z Zabidi-Hussin, TH Sasongko Genetics and molecular biology 36 (3), 299-307, 2013 | 63 | 2013 |
| Angiotensin‐converting enzyme (ACE) inhibitors for proteinuria and microalbuminuria in people with sickle cell disease TH Sasongko, S Nagalla Cochrane Database of Systematic Reviews, 2021 | 50 | 2021 |
| A novel mutation at the N-terminal of SMN Tudor domain inhibits its interaction with target proteins T Kotani, R Sutomo, TH Sasongko, AH Sadewa, T Minato, E Fujii, S Endo, ... Journal of neurology 254 (5), 624, 2007 | 49 | 2007 |
| DNA methylation: an epigenetic insight into type 2 diabetes mellitus F Alam, A Islam, S Hua Gan, M Mohamed, T Haryo Sasongko Current pharmaceutical design 22 (28), 4398-4419, 2016 | 47 | 2016 |
| Analysis of sequence variations in low-density lipoprotein receptor gene among Malaysian patients with familial hypercholesterolemia A Al-Khateeb, MK Zahri, MS Mohamed, TH Sasongko, S Ibrahim, Z Yusof, ... BMC medical genetics 12, 1-11, 2011 | 42 | 2011 |
| SMN2 and NAIP gene dosages in Vietnamese patients with spinal muscular atrophy VK Tran, TH Sasongko, DD Hong, NT Hoan, VC Dung, MJ Lee, Gunadi, ... Pediatrics International 50 (3), 346-351, 2008 | 40 | 2008 |
| Germ‐line mutation of KCNQ2, p.R213W, in a Japanese family with benign familial neonatal convulsion AH Sadewa, TH Sasongko, Gunadi, MJ Lee, K Daikoku, A Yamamoto, ... Pediatrics International 50 (2), 167-171, 2008 | 31 | 2008 |
| In silico analyses and cytotoxicity study of asiaticoside and asiatic acid from malaysian plant as potential mTOR inhibitors NN Zulkipli, R Zakaria, I Long, SF Abdullah, EF Muhammad, HA Wahab, ... Molecules 25 (17), 3991, 2020 | 30 | 2020 |
| Natural products towards the discovery of potential future antithrombotic drugs MA Islam, F Alam, I Khalil, T Haryo Sasongko, S Hua Gan Current pharmaceutical design 22 (20), 2926-2946, 2016 | 30 | 2016 |
| Antiphospholipid antibody-mediated thrombotic mechanisms in antiphospholipid syndrome: towards pathophysiology-based treatment A Islam, F Alam, T Haryo Sasongko, S Hua Gan Current pharmaceutical design 22 (28), 4451-4469, 2016 | 28 | 2016 |
| ACE gene polymorphism in children with nephrotic syndrome in the Indonesian population TH Sasongko, AH Sadewa, PA Kusuma, MP Damanik, MJ Lee, H Ayaki, ... KOBE JOURNAL OF MEDICAL SCIENCES 51 (3/4), 41, 2005 | 28 | 2005 |
| Rapamycin and its analogues (rapalogs) for Tuberous Sclerosis Complex-associated tumors: a systematic review on non-randomized studies using meta-analysis TH Sasongko, NFD Ismail, NMA Nik Abdul Malik, Z Zabidi-Hussin Orphanet journal of rare diseases 10, 1-11, 2015 | 26 | 2015 |
| Antiphospholipid antibodies in epilepsy: A systematic review and meta-analysis MA Islam, F Alam, C Cavestro, C Calcii, TH Sasongko, RA Levy, SH Gan Autoimmunity reviews 17 (8), 755-767, 2018 | 25 | 2018 |
| Type 2 diabetes mellitus and Alzheimer’s disease: bridging the pathophysiology and management F Alam, M Asiful Islam, T Haryo Sasongko, S Hua Gan Current pharmaceutical design 22 (28), 4430-4442, 2016 | 24 | 2016 |
| ‘Non-criteria’neurologic manifestations of antiphospholipid syndrome: a hidden kingdom to be discovered A Islam, F Alam, M Amjad Kamal, K Keng Wong, T Haryo Sasongko, ... CNS & Neurological Disorders-Drug Targets (Formerly Current Drug Targets-CNS …, 2016 | 23 | 2016 |
| Permissibility of prenatal diagnosis and abortion for fetuses with severe genetic disorder: type 1 spinal muscular atrophy TH Sasongko, AR Salmi, BA Zilfalil, MA Albar, ZA Mohd Hussin Annals of Saudi medicine 30 (6), 427-431, 2010 | 20 | 2010 |
| Mutation Spectrum of Dystrophin Gene in Malaysian Patients with Duchenne/Becker Muscular Dystrophy AQ Rani, TH Sasongko, S Sulong, D Bunyan, AR Salmi, BA Zilfalil, ... Journal of Neurogenetics 27 (1-2), 11-15, 2013 | 19 | 2013 |
Zabidi-HussinProfessor of Paediatrics University of CyberjayaEmail yang diverifikasi di cyberjaya.edu.my
