Case report: The evolving phenotype of ESCO2 spectrum disorder in a 15-year-old Malaysian child

by Tae, Sok-Kun, Ra, Mazlan, Thong, Meow-Keong
Published 2024

A comparative study of patients’ perceptions of genetic and genomic medicine services in California and Malaysia

by Qian, Emily, Thong, Meow Keong, Flodman, Pamela, Gargus, Jay
Published 2019

Medical genetics in developing countries in the Asia-Pacific region: challenges and opportunities

by Thong, Meow Keong, See-Toh, Yiling, Hassan, Jamiyah, Syed Mohamed Ali, Jaffar
Published 2018

Ten-year trend in prevalence and outcome of Down syndrome with congenital heart disease in a middle-income country

by Zahari, Norazah, Mat Bah, Mohd Nizam, A. Razak, Hasliza, Thong, Meow Keong
Published 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

by Wasant, Pornswan, Padilla, Carmencita, Lam, Stephen, Thong, Meow Keong, Lai, Poh San
Published 2019

Students perception and acceptance of problem-based learning (PBL) in a hybrid traditional-PBL curriculum

by Sim, Si Mui, Lian, Lay Hoong, Kanthimathi, M.S., Thong, Meow Keong, Tan, Nget Hong
Published 2011

Genetic counseling for patients and families with hereditary breast and ovarian cancer in a developing Asian country: An observational descriptive study

by Yoon, Sook Yee, Thong, Meow Keong, Mohd Taib, Nur Aishah, Yip, Cheng Har, Teo, Soo Hwang
Published 2011

Congenital myasthenic syndrome with novel pathogenic variants in the COLQ gene associated with the presence of antibodies to acetylcholine receptors

by Tay, Chee Geap, Fong, Choong Yi, Li, Limin, Ganesan, Vigneswari, Teh, Chee Ming, Gan, Chin Seng, Thong, Meow-Keong
Published 2020

An audiological evaluation of syndromic and non-syndromic craniosynostosis in pre-school going children

by Goh, Liang Chye, Azman, Ali, Konting, Siti Hufaidah, Khoo, Wee Vien, Muthukumarasamy, Premala, Thong, Meow Keong, Zulkiflee, Abu Bakar, Manuel, Anura Michelle
Published 2018

COVID-19 vaccination for children in Malaysia- A position statement by the College of Paediatrics, Academy of Medicine of Malaysia

by Ceah, Fook Choe, Thong, Meow Keong, Zulkifli, Ismail, Zilfalil, Alwi, Amir Hamzah, Abdul Latiff, Chan, Patrick Wai Kiong, Khoo, Erwin Jiayuan, Noran Naqiah, Hairi
Published 2022

Communication about positive BRCA1 and BRCA2 genetic test results and uptake of testing in relatives in a diverse Asian setting

by Lee, Daphne S. -C., Meiser, Bettina, Mariapun, Shivaani, Hassan, Tiara, Yip, Cheng-Har, Mohd Taib, Nur Aishah, Teo, Soo-Hwang, Thong, Meow-Keong, Yoon, Sook-Yee
Published 2021

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

by Lim, Ka Keat, Yoon, Sook Yee, Mohd Taib, Nur Aishah, Shabaruddin, Fatiha Hana, Dahlui, Maznah, Woo, Yin Ling, Thong, Meow Keong, Teo, Soo Hwang, Chaiyakunapruk, Nathorn
Published 2018

Eph and ephrin variants in Malaysian neural tube defect families

by Mohd-Zin, Siti Waheeda, Tan, Amelia Cheng Wei, Atroosh, Wahib Mohammed Mohsin, Thong, Meow-Keong, Azizi, Abu Bakar, Greene, Nicholas D. E., Abdul-Aziz, Noraishah Mydin
Published 2022

Attitudes and training needs of oncologists and surgeons in mainstreaming breast cancer genetic counseling in a low-to-middle income Asian country

by Lee, Yong-Quan, Yoon, Sook-Yee, Hassan, Tiara, Padmanabhan, Heamanthaa, Yip, Cheng-Har, Keng, Wee-Teik, Thong, Meow-Keong, Annuar, Muhammad Azrif Ahmad, Taib, Nur Aishah Mohd, Teo, Soo-Hwang
Published 2022

Compound heterozygous mutations in TTC7A cause familial multiple intestinal atresias and severe combined immunodeficiency

by Yang, W., Lee, P.P.W., Thong, Meow Keong, Ramanujam, T.M., Shanmugam, A., Koh, M.T., Chan, K.W., Ying, D., Wang, Y., Shen, J.J., Yang, J., Lau, Y.L.
Published 2015

Psychosocial outcome and health behaviour intent of breast cancer patients with BRCA1/2 and PALB2 pathogenic variants unselected by a priori risk

by Padmanabhan, Heamanthaa, Hassan, Nur Tiara, Wong, Siu-Wan, Lee, Yong-Quan, Lim, Joanna, Hasan, Siti Norhidayu, Yip, Cheng-Har, Teo, Soo-Hwang, Thong, Meow-Keong, Mohd Taib, Nur Aishah, Yoon, Sook-Yee
Published 2022

GWAS signals revisited using human knockouts

by Maddirevula, Sateesh, AlZahrani, Fatema, Anazi, Shams, Almureikhi, Mariam, Ben-Omran, Tawfeg, Abdel-Salam, Ghada M.H., Hashem, Mais, Ibrahim, Niema, Abdulwahab, Firdous M., Meriki, Neama, Bashiri, Fahad A., Thong, Meow Keong, Muthukumarasamy, Premala, Mazlan, Rifhan Azwani, Shaheen, Ranad, Alkuraya, Fowzan S.
Published 2018

Cranial neural tube defect after trimethoprim exposure

by Abdullah, Nor Linda, Gunasekaran, Renuka, Mohd-Zin, Siti Waheeda, Lim, Bee Hui, Maniam, Pramila, Mohd-Salleh, Anis Shuhada, Thong, Meow Keong, Chik, Zamri, Nordin, Noreena, Omar, Zaliha, Engkasan, Julia Patrick, Ganesan, Dharmendra, Aiezzah, Zakaria Nurul, Ahmad-Annuar, Azlina, Abdul-Aziz, Noraishah Mydin
Published 2018

The clinical utility of polygenic risk scores in genomic medicine practices: A systematic review

by Kumuthini, Judit, Zick, Brittany, Balasopoulou, Angeliki, Chalikiopoulou, Constantina, Dandara, Collet, El-Kamah, Ghada, Findley, Laura, Katsila, Theodora, Li, Rongling, Bon Maceda, Ebner, Monye, Henrietta, Rada, Gabriel, Thong, Meow-Keong, Wanigasekera, Thilina, Kennel, Hannah, Marimuthu, Veeramani, Williams, Marc S., Al-Mulla, Fahd, Abramowicz, Marc, Investigators, G2MC Evidence
Published 2022

Global Globin Network and adopting genomic variant database requirements for thalassemia

by Hashim, Halim-Fikri, Ninie Nadia, Zulkiplii, Hafza, Alauddin, Celestea, Bento, Carsten, W Lederer, Petros, Kountouris, Marina, Kleanthous, Yetti, Hernaningsih, Thong, Meow Keong, Muhammad Hamdi, Mahmood, Norafiza, Mohd Yasin, Ezalia, Esa, Jacques, Elion, Domenico, Coviello, Raja Zahratul Azma, Raja Sabudin, Ghada, El-Kamah, John, Burn, Narazah, Mohd Yusoff, Raj, Ramesar, Zilfalil, Alwi
Published 2024