Effects of digital game-based learning on elementary science learning: A systematic review MH Hussein, SH Ow, LS Cheong, MK Thong, NA Ebrahim IEEE Access 7, 62465-62478, 2019 | 171 | 2019 |
Ten novel FBN2 mutations in congenital contractural arachnodactyly: Delineation of the molecular pathogenesis and clinical phenotype PA Gupta, EA Putnam, SG Carmical, I Kaitila, B Steinmann, A Child, ... Human mutation 19 (1), 39-48, 2002 | 168 | 2002 |
Effects of MECP2 mutation type, location and X‐inactivation in modulating Rett syndrome phenotype LS Weaving, SL Williamson, B Bennetts, M Davis, CJ Ellaway, H Leonard, ... American Journal of Medical Genetics Part A 118 (2), 103-114, 2003 | 158 | 2003 |
Undescended testes: incidence in 1,002 consecutive male infants and outcome at 1 year of age MK Thong, CT Lim, H Fatimah Pediatric surgery international 13, 37-41, 1998 | 152 | 1998 |
22q11. 2 deletion syndrome in diverse populations P Kruszka, YA Addissie, DE McGinn, AR Porras, E Biggs, M Share, ... American Journal of Medical Genetics Part A 173 (4), 879-888, 2017 | 145 | 2017 |
Down syndrome in diverse populations P Kruszka, AR Porras, AK Sobering, FA Ikolo, S La Qua, V Shotelersuk, ... American Journal of Medical Genetics Part A 173 (1), 42-53, 2017 | 106 | 2017 |
A case-control study of breast cancer risk factors in 7,663 women in Malaysia MM Tan, WK Ho, SY Yoon, S Mariapun, SN Hasan, DSC Lee, T Hassan, ... PloS one 13 (9), e0203469, 2018 | 104 | 2018 |
Evaluation of BRCA1 and BRCA2 mutations and risk-prediction models in a typical Asian country (Malaysia) with a relatively low incidence of breast cancer E Thirthagiri, SY Lee, P Kang, DS Lee, GT Toh, S Selamat, SY Yoon, ... Breast Cancer Research 10, 1-12, 2008 | 96 | 2008 |
Comparable frequency of BRCA1, BRCA2 and TP53 germline mutations in a multi-ethnic Asian cohort suggests TP53 screening should be offered together with … DSC Lee, SY Yoon, LM Looi, P Kang, IN Kang, K Sivanandan, H Ariffin, ... Breast Cancer Research 14, 1-8, 2012 | 93 | 2012 |
Dengue-associated adult respiratory distress syndrome LCS Lum, MK Thong, YK Cheah, SK Lam Annals of tropical paediatrics 15 (4), 335-339, 1995 | 93 | 1995 |
Beyond critical congenital heart disease: newborn screening using pulse oximetry for neonatal sepsis and respiratory diseases in a middle-income country V Jawin, HL Ang, A Omar, MK Thong PloS one 10 (9), e0137580, 2015 | 92 | 2015 |
Noonan syndrome in diverse populations P Kruszka, AR Porras, YA Addissie, A Moresco, S Medrano, GTK Mok, ... American Journal of Medical Genetics Part A 173 (9), 2323-2334, 2017 | 91 | 2017 |
International perspectives on the implementation of reproductive carrier screening MB Delatycki, F Alkuraya, A Archibald, C Castellani, M Cornel, WW Grody, ... Prenatal diagnosis 40 (3), 301-310, 2020 | 83 | 2020 |
Williams–Beuren syndrome in diverse populations P Kruszka, AR Porras, DH De Souza, A Moresco, V Huckstadt, AD Gill, ... American Journal of Medical Genetics Part A 176 (5), 1128-1136, 2018 | 80 | 2018 |
A digital game-based learning method to improve students’ critical thinking skills in elementary science MH Hussein, SH Ow, LS Cheong, MK Thong Ieee Access 7, 96309-96318, 2019 | 75 | 2019 |
A population-based study of birth defects in Malaysia MK Thong, JJ Ho, NN Khatijah Annals of Human Biology 32 (2), 180-187, 2005 | 66 | 2005 |
Genetic polymorphisms in LDLR, APOB, PCSK9 and other lipid related genes associated with familial hypercholesterolemia in Malaysia SH Lye, JK Chahil, P Bagali, L Alex, J Vadivelu, WAW Ahmad, SP Chan, ... PloS one 8 (4), e60729, 2013 | 61 | 2013 |
Tropical distal renal tubular acidosis: clinical and epidemiological studies in 78 patients S Khositseth, LJ Bruce, SB Walsh, WM Bawazir, GD Ogle, RJ Unwin, ... QJM: An International Journal of Medicine 105 (9), 861-877, 2012 | 58 | 2012 |
Large BRCA1 and BRCA2 genomic rearrangements in Malaysian high risk breast-ovarian cancer families P Kang, S Mariapun, SY Phuah, LS Lim, J Liu, SY Yoon, MK Thong, ... Breast cancer research and treatment 124, 579-584, 2010 | 53 | 2010 |
Genetic counseling for patients and families with hereditary breast and ovarian cancer in a developing Asian country: an observational descriptive study SY Yoon, MK Thong, NAM Taib, CH Yip, SH Teo Familial cancer 10, 199-205, 2011 | 52 | 2011 |