| Efficacy of phototherapy for neonatal jaundice is increased by the use of low-cost white reflecting curtains S Djokomuljanto, BS Quah, Y Surini, R Noraida, NZN Ismail, ... Archives of Disease in Childhood-Fetal and Neonatal Edition 91 (6), F439-F442, 2006 | 67 | 2006 |
| Increase in tumour-infiltrating lymphocytes with regulatory T cell immunophenotypes and reduced ζ-chain expression in nasopharyngeal carcinoma patients WK Yip, MA Abdullah, SM Yusoff, HF Seow Clinical & Experimental Immunology 155 (3), 412-422, 2009 | 50 | 2009 |
| Frequencies of A(TA)7TAA, G71R, and G493R Mutations of the UGT1A1 Gene in the Malaysian Population S Yusoff, H Van Rostenberghe, NM Yusoff, NA Talib, N Ramli, ... Neonatology 89 (3), 171-176, 2006 | 50 | 2006 |
| Valproic acid increases SMN2 expression and modulates SF2/ASF and hnRNPA1 expression in SMA fibroblast cell lines ISK Harahap, T Saito, LP San, N Sasaki, DKP Nurputra, S Yusoff, ... Brain and Development 34 (3), 213-222, 2012 | 44 | 2012 |
| Generalized epilepsy with febrile seizures plus (GEFS+) spectrum: clinical manifestations and SCN1A mutations in Indonesian patients ES Herini, ISK Harahap, S Yusoff, S Morikawa, SY Patria, N Nishimura, ... Epilepsy research 90 (1-2), 132-139, 2010 | 37 | 2010 |
| A polymorphic mutation, c.-3279T> G, in the UGT1A1 promoter is a risk factor for neonatal jaundice in the Malay population S Yusoff, A Takeuchi, C Ashi, M Tsukada, NH Ma'Amor, BA Zilfalil, ... Pediatric research 67 (4), 401-406, 2010 | 36 | 2010 |
| The first Malay database toward the ethnic-specific target molecular variation H Halim-Fikri, A Etemad, AZA Latif, AF Merican, AA Baig, AA Annuar, ... BMC research notes 8, 1-6, 2015 | 27 | 2015 |
| Guidelines for nucleic acid detection and analysis in hematological disorders F Rosline Hassan MMED, SG Dip, SK Cheong The Malaysian journal of pathology 37 (2), 165, 2015 | 25 | 2015 |
| Multiplex amplification refractory mutation system (MARMS) for the detection of β-globin gene mutations among the transfusion-dependent β-thalassemia Malay patients in Kelantan … S Hanafi, R Hassan, R Bahar, WZ Abdullah, MF Johan, ND Rashid, ... American journal of blood research 4 (1), 33, 2014 | 20 | 2014 |
| 3-D conjugate heat transfer analysis of PLCC packages mounted in-line on a Printed Circuit Board S Yusoff, M Mohamed, KA Ahmad, MZ Abdullah, MA Mujeebu, ZM Ali, ... International Communications in Heat and Mass Transfer 36 (8), 813-819, 2009 | 18 | 2009 |
| The influence of angiotensin-converting enzyme gene ID polymorphism on human physical fitness performance in European and other populations X Li, FK Ooi, BA Zilfalil, S Yusoff Sport Sciences for Health 13, 495-506, 2017 | 13 | 2017 |
| Practice of iron chelation therapy for transfusion-dependent thalassemia in Southeast Asia NF Azman, WZ Abdullah, N Mohamad, R Bahar, MF Johan, R Diana, ... Asian Biomedicine 10 (6), 537-547, 2016 | 13 | 2016 |
| Novel SCN1A mutations in Indonesian patients with severe myoclonic epilepsy in infancy ES Herini, Gunadi, MJA Van Kempen, S Yusoff, Sutaryo, Sunartini, ... Pediatrics International 52 (2), 234-239, 2010 | 12 | 2010 |
| A homozygous mutation in UGT1A1 exon 5 may be responsible for persistent hyperbilirubinemia in a Japanese girl with Gilbert's syndrome T Nakagawa, T Mure, S Yusoff, E Ono, IS Kusuma Harahap, S Morikawa, ... Kobe J Med Sci 57 (1), e26-e31, 2011 | 11 | 2011 |
| High allele frequency of CYP2C9*3 (rs1057910) in a Negrito’s subtribe population in Malaysia; Aboriginal people of Jahai RA Rosdi, N Mohd Yusoff, R Ismail, T Soo Choon, M Saleem, N Musa, ... Annals of human biology 43 (5), 445-450, 2016 | 10 | 2016 |
| Herbal medicine containing licorice may be contraindicated for a patient with an HSD11B2 mutation ISK Harahap, N Sasaki, S Yusoff, MJ Lee, S Morikawa, N Nishimura, ... Evidence-Based Complementary and Alternative Medicine 2011, 2011 | 10 | 2011 |
| Genetic disorders associated with neonatal jaundice I Morioka, S Morikawa, S Yusoff, ISK Harahap, N Nishimura, N Yokoyama, ... Eastern Journal of Medicine 15 (4), 155, 2010 | 10 | 2010 |
| Hypomutability at the Polyadenine Tract in SMN Intron 3 Shows the Invariability of the a‐SMN Protein Structure Gunadi, TH Sasongko, S Yusoff, MJ Lee, E Nishioka, M Matsuo, H Nishio Annals of Human Genetics 72 (2), 288-291, 2008 | 10 | 2008 |
| Evaluation of mutation effects on UGT1A1 activity toward 17β-estradiol using liquid chromatography–tandem mass spectrometry K Wada, A Takeuchi, K Saiki, R Sutomo, H Van Rostenberghe, NM Yusoff, ... Journal of Chromatography B 838 (1), 9-14, 2006 | 10 | 2006 |
| High resolution melting analysis of the NR1I3 genetic variants: Is there an association with neonatal hyperbilirubinemia? TP Cheung, H Van Rostenberghe, R Ismail, NN Nawawi, NA Abdullah, ... Gene 573 (2), 198-204, 2015 | 7 | 2015 |
