| Combination of SMN2 copy number and NAIP deletion predicts disease severity in spinal muscular atrophy ZBA Watihayati MS, Fatemeh H, Marini M, Atif AB, Zahiruddin WM, Sasongko TH ... Brain Dev 31 (1), 42-5, 2009 | 66 | 2009 |
| Two Novel Gross Deletions of TSC2 in Malaysian Patients with Tuberous Sclerosis Complex and TSC2/PKD1 Contiguous Deletion Syndrome STH Ismail NF1, Nik Abdul Malik NM, Mohseni J, Rani AM, Hayati F, Salmi AR ... Jpn J Clin Oncol 44 ((5)), 506-11, 2014 | 17* | 2014 |
| Allele-specific PCR for a cost-effective & time-efficient diagnostic screening of spinal muscular atrophy HN M. Marini, T.H. Sasongko, M.S. Watihayati, A.B. Atif, F. Hayati, Gunadi4 ... Indian J Med Res 135 (1), 31-5, 2012 | 15 | 2012 |
| Novel Complex Re-Arrangement of ARG1 commonly shared by unrelated patients with Hyperargininemia STH Mohseni J1, Boon Hock C, Abdul Razak C, Othman SN, Hayati F, Peitee WO ... Gene 533 (1), 240-5, 2014 | 10 | 2014 |
| Efficacy and safety of sitagliptin as a third therapeutic agent in the treatment of type 2 diabetes mellitus NSYWMWB Fatemeh Hayati , Amjed Hazim , Teguh Haryo Sasongko , Gan Siew Hua ... Journal of Diabetes Research & Clinical Metabolism 3 (10), 2014 | 5 | 2014 |
| Screening of the LIX1 gene in Japanese and Malaysian patients with SMA and/or SMA-like disorder BAZ Teguh Haryo Sasongko, Gunadi, Surini Yusoff , Amin Baig Atif , Hayati ... Brain & Development 32 (2010), 385-389, 2010 | 2 | 2010 |
| DEVELOPMENT OF ALLELE SPECIFIC PCR FOR THE DETECTION OF HOMOZYGOUS DELETION OF THE SMN1 GENE IN SPINAL MUSCULAR ATROPHY (SMA) PATIENTS IN MALAYSIA M M, W M. S., A A. B., F H., Ravichandranm, Z B. A. Malaysian Journal of Medical Sciences 15 (1), 36, 2008 | | 2008 |
| The USM Human Genome Centre Experience on Molecular Diagnostic Testing of SMA Cases ZBA Fatemeh Hayati, Watihayati Mohd shamshudin, Marini Marzuki, Nur ... Malaysian Journal of Pediatrics and Child Health 15, 24-27, 2007 | | 2007 |
