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Ceah, Fook Choe and Thong, Meow Keong and Zulkifli, Ismail and Zilfalil, Alwi and Amir Hamzah, Abdul Latiff and Chan, Patrick Wai Kiong and Khoo, Erwin Jiayuan and Noran Naqiah, Hairi (2022) COVID-19 vaccination for children in Malaysia- A position statement by the College of Paediatrics, Academy of Medicine of Malaysia. Malaysian Journal of Pathology, 44 (2). pp. 177-185. ISSN 0126-8635, DOI https://doi.org/10.1520/malay.124.
Torpey, Kwasi and Shafie, Asrul Akmal and Supian, Azuwana and Ahmad Hassali, Mohamed Azmi and Ngu, Lock Hock and Thong, Meow Keong and Ayob, Hatijah and Chaiyakunapruk, Nathorn (2020) Rare disease in Malaysia: Challenges and solutions. PLoS ONE, 15 (4). e0230850. ISSN 1932-6203, DOI https://doi.org/10.1371/journal.pone.0230850.
Wasant, Pornswan and Padilla, Carmencita and Lam, Stephen and Thong, Meow Keong and Lai, Poh San (2019) Asia Pacific Society of Human Genetics (APSHG) from conception to 2019: 13 years of collaboration to tackle congenital malformation and genetic disorders in Asia. American Journal of Medical Genetics Part C: Seminars in Medical Genetics, 181 (2). pp. 155-165. ISSN 1552-4868, DOI https://doi.org/10.1002/ajmg.c.31701.
Zahari, Norazah and Mat Bah, Mohd Nizam and A. Razak, Hasliza and Thong, Meow Keong (2019) Ten-year trend in prevalence and outcome of Down syndrome with congenital heart disease in a middle-income country. European Journal of Pediatrics, 178 (8). pp. 1267-1274. ISSN 0340-6199, DOI https://doi.org/10.1007/s00431-019-03403-x.
Qian, Emily and Thong, Meow Keong and Flodman, Pamela and Gargus, Jay (2019) A comparative study of patients’ perceptions of genetic and genomic medicine services in California and Malaysia. Journal of Community Genetics, 10 (3). pp. 351-361. ISSN 1868-310X, DOI https://doi.org/10.1007/s12687-018-0399-8.
Abdullah, Nor Linda and Gunasekaran, Renuka and Mohd-Zin, Siti Waheeda and Lim, Bee Hui and Maniam, Pramila and Mohd-Salleh, Anis Shuhada and Thong, Meow Keong and Chik, Zamri and Nordin, Noreena and Omar, Zaliha and Engkasan, Julia Patrick and Ganesan, Dharmendra and Aiezzah, Zakaria Nurul and Ahmad-Annuar, Azlina and Abdul-Aziz, Noraishah Mydin (2018) Cranial neural tube defect after trimethoprim exposure. BMC Research Notes, 11 (1). p. 475. ISSN 1756-0500, DOI https://doi.org/10.1186/s13104-018-3593-1.
Maddirevula, Sateesh and AlZahrani, Fatema and Anazi, Shams and Almureikhi, Mariam and Ben-Omran, Tawfeg and Abdel-Salam, Ghada M.H. and Hashem, Mais and Ibrahim, Niema and Abdulwahab, Firdous M. and Meriki, Neama and Bashiri, Fahad A. and Thong, Meow Keong and Muthukumarasamy, Premala and Mazlan, Rifhan Azwani and Shaheen, Ranad and Alkuraya, Fowzan S. (2018) GWAS signals revisited using human knockouts. Genetics in Medicine, 20 (1). pp. 64-68. ISSN 1098-3600, DOI https://doi.org/10.1038/gim.2017.78.
Lim, Ka Keat and Yoon, Sook Yee and Mohd Taib, Nur Aishah and Shabaruddin, Fatiha Hana and Dahlui, Maznah and Woo, Yin Ling and Thong, Meow Keong and Teo, Soo Hwang and Chaiyakunapruk, Nathorn (2018) Is BRCA Mutation Testing Cost Effective for Early Stage Breast Cancer Patients Compared to Routine Clinical Surveillance? The Case of an Upper Middle-Income Country in Asia. Applied Health Economics and Health Policy, 16 (3). pp. 395-406. ISSN 1175-5652, DOI https://doi.org/10.1007/s40258-018-0384-8.
Laurino, Mercy Y. and Leppig, Kathleen A. and Abad, Peter James and Cham, Breana and Chu, Yoyo Wing Yiu and Kejriwal, Saahil and Lee, Juliana M. H. and Sternen, Darci L. and Thompson, Jennifer K. and Burgess, Matthew J. and Chien, Shu and Elackatt, Niby and Lim, Jiin Ying and Sura, Thanyachai and Faradz, Sultana and Padilla, Carmencita and Paz, Eva Cutiongco de-la and Nauphar, Donny and Nguyen, Khanh Ngoc and Zayts, Olya and Vu, Dung Chi and Thong, Meow Keong (2018) A Report on Ten Asia Pacific Countries on Current Status and Future Directions of the Genetic Counseling Profession: The Establishment of the Professional Society of Genetic Counselors in Asia. Journal of Genetic Counseling, 27 (1). pp. 21-32. ISSN 1059-7700, DOI https://doi.org/10.1007/s10897-017-0115-6.
Kruszka, Paul and Porras, Antonio R. and de Souza, Deise Helena and Moresco, Angélica and Huckstadt, Victoria and Gill, Ashleigh D. and Boyle, Alec P. and Hu, Tommy and Addissie, Yonit A. and Mok, Gary T. K. and Tekendo-Ngongang, Cedrik and Fieggen, Karen and Prijoles, Eloise J. and Tanpaiboon, Pranoot and Honey, Engela and Luk, Ho-Ming and Lo, Ivan F. M. and Thong, Meow Keong and Muthukumarasamy, Premala and Jones, Kelly L. and Belhassan, Khadija and Ouldim, Karim and El Bouchikhi, Ihssane and Bouguenouch, Laila and Shukla, Anju and Girisha, Katta M. and Sirisena, Nirmala D. and Dissanayake, Vajira H. W. and Paththinige, C. Sampath and Mishra, Rupesh and Kisling, Monisha S. and Ferreira, Carlos R. and de Herreros, María Beatriz and Lee, Ni-Chung and Jamuar, Saumya S. and Lai, Angeline and Tan, Ee Shien and Ying Lim, Jiin and Wen-Min, Cham Breana and Gupta, Neerja and Lotz-Esquivel, Stephanie and Badilla-Porras, Ramsés and Hussen, Dalia Farouk and El Ruby, Mona O. and Ashaat, Engy A. and Patil, Siddaramappa J. and Dowsett, Leah and Eaton, Alison and Innes, A. Micheil and Shotelersuk, Vorasuk and Badoe, Ëben and Wonkam, Ambroise and Obregon, María Gabriela and Chung, Brian H. Y. and Trubnykova, Milana and La Serna, Jorge and Gallardo Jugo, Bertha Elena and Chávez Pastor, Miguel and Abarca Barriga, Hugo Hernán and Megarbane, Andre and Kozel, Beth A. and van Haelst, Mieke M. and Stevenson, Roger E. and Summar, Marshall and Adeyemo, A. Adebowale and Morris, Colleen A. and Moretti-Ferreira, Danilo and Linguraru, Marius George and Muenke, Maximilian (2018) Williams-Beuren syndrome in diverse populations. American Journal of Medical Genetics Part A, 176 (5). pp. 1128-1136. ISSN 1552-4825, DOI https://doi.org/10.1002/ajmg.a.38672.
Goh, Liang Chye and Azman, Ali and Konting, Siti Hufaidah and Khoo, Wee Vien and Muthukumarasamy, Premala and Thong, Meow Keong and Zulkiflee, Abu Bakar and Manuel, Anura Michelle (2018) An audiological evaluation of syndromic and non-syndromic craniosynostosis in pre-school going children. International Journal of Pediatric Otorhinolaryngology, 109. pp. 50-53. ISSN 0165-5876, DOI https://doi.org/10.1016/j.ijporl.2018.03.010.
Tan, Min Min and Ho, Weang Kee and Yoon, Sook Yee and Mariapun, Shivaani and Hasan, Siti Norhidayu and Lee, Daphne Shin Chi and Hassan, Tiara and Lee, Sheau Yee and Phuah, Sze Yee and Sivanandan, Kavitta and Ng, Patsy Pei Sze and Rajaram, Nadia and Jaganathan, Maheswari and Jamaris, Suniza and Islam, Tania and Rahmat, Kartini and Fadzli, Farhana and Vijayananthan, Anushya and Rajadurai, Pathmanathan and See, Mee Hong and Thong, Meow Keong and Mohd Taib, Nur Aishah and Yip, Cheng Har and Teo, Soo Hwang (2018) A case-control study of breast cancer risk factors in 7,663 women in Malaysia. PLoS ONE, 13 (9). e0203469. ISSN 1932-6203, DOI https://doi.org/10.1371/journal.pone.0203469.
Luk, Anderson Dik Wai and Lee, Pamela P. and Mao, Huawei and Chan, Koon Wing and Chen, Xiang Yuan and Chen, Tong Xin and He, Jian Xin and Kechout, Nadia and Suri, Deepti and Tao, Yin Bo and Xu, Yong Bin and Jiang, Li Ping and Liew, Woei Kang and Jirapongsananuruk, Orathai and Daengsuwan, Tassalapa and Gupta, Anju and Singh, Surjit and Rawat, Amit and Abdul Latiff, Amir Hamzah and Lee, Anselm Chi Wai and Shek, Lynette P. and Nguyen, Thi Van Anh and Chin, Tek Jee and Chien, Yin Hsiu and Latiff, Zarina Abdul and Le, Thi Minh Huong and Le, Nguyen Ngoc Quynh and Lee, Bee Wah and Li, Qiang and Raj, Dinesh and Barbouche, Mohamed-Ridha and Thong, Meow Keong and Ang, Maria Carmen D. and Wang, Xiao Chuan and Xu, Chen Guang and Yu, Hai Guo and Yu, Hsin Hui and Lee, Tsz Leung and Yau, Felix Yat Sun and Wong, Wilfred Hing Sang and Tu, Wenwei and Yang, Wangling and Chong, Patrick Chun Yin and Ho, Marco Hok Kung and Lau, Yu Lung (2017) Family History of Early Infant Death Correlates with Earlier Age at Diagnosis But Not Shorter Time to Diagnosis for Severe Combined Immunodeficiency. Frontiers in Immunology, 8. p. 808. ISSN 1664-3224, DOI https://doi.org/10.3389/fimmu.2017.00808.
Yang, W. and Lee, P.P.W. and Thong, Meow Keong and Ramanujam, T.M. and Shanmugam, A. and Koh, M.T. and Chan, K.W. and Ying, D. and Wang, Y. and Shen, J.J. and Yang, J. and Lau, Y.L. (2015) Compound heterozygous mutations in TTC7A cause familial multiple intestinal atresias and severe combined immunodeficiency. Clinical Genetics, 88 (6). pp. 542-549. ISSN 0009-9163, DOI https://doi.org/10.1111/cge.12553.
Yoon, Sook Yee and Thong, Meow Keong and Mohd Taib, Nur Aishah and Yip, Cheng Har and Teo, Soo Hwang (2011) Genetic counseling for patients and families with hereditary breast and ovarian cancer in a developing Asian country: An observational descriptive study. Familial Cancer, 10 (2). pp. 199-205. ISSN 1389-9600, DOI https://doi.org/10.1007/s10689-011-9420-7.
Sim, Si Mui and Lian, Lay Hoong and Kanthimathi, M.S. and Thong, Meow Keong and Tan, Nget Hong (2011) Students perception and acceptance of problem-based learning (PBL) in a hybrid traditional-PBL curriculum. Journal of Medical Education, 15 (4). pp. 361-371. ISSN 1028-2424,
