 | Up a level |
Chen, Faye H. and Hartman, Adam L. and Letinturier, Mary Catherine V. and Antoniadou, Victoria and Baynam, Gareth and Bloom, Lara and Crimi, Marco and Rocca, Maria G. Della and Didato, Giuseppe and Houge, Sofia Douzgou and Jonker, Anneliene and Kawome, Martina and Mueller, Friederike and O'Brien, James and Puri, Ratna Dua and Ryan, Nuala and Thong, Meow-Keong and Tumiene, Birute and Parisi, Melissa A. (2024) Telehealth for rare disease care, research, and education across the globe: A review of the literature by the IRDiRC telehealth task force. European Journal of Medical Genetics, 72. p. 104977. ISSN 1769-7212, DOI https://doi.org/10.1016/j.ejmg.2024.104977.
Halim-Fikri, Hashim and Zulkipli, Ninie Nadia and Alauddin, Hafiza and Bento, Celeste and Lederer, Carsten W. and Kountouris, Petros and Kleanthous, Marina and Hernaningsih, Yetti and Thong, Meow-Keong and Mahmood, Muhammad Hamdi and Yasin, Norafiza Mohd and Esa, Ezalia and Elion, Jacques and Coviello, Domenico and Raja-Sabudin, Raja-Zahratul-Azma and El-Kamah, Ghada and Burn, John and Yusoff, Narazah Mohd and Ramesar, Raj and Zilfalil, Bin Alwi and GGN, Global Globin Network (2024) Global Globin Network and adopting genomic variant database requirements for thalassemia. Database-the Journal of Biological Databases and Curation, 2024. baae080. ISSN 1758-0463, DOI https://doi.org/10.1093/database/baae080.
Wan, Puspa Melati and Ali, Affezah and Mognard, Elise and Jegathesan, Anasuya Jegathevi and Lee, Soon Li and Ganesan, Rajalakshmi and Noor, Mohd Ismail and Rochedy, Amandine and Valette, Marion and Tauber, Maithe and Thong, Meow-Keong and Poulain, Jean-Pierre (2024) Management of food socialization for children with Prader-Willi Syndrome: An exploration study in Malaysia. PLoS ONE, 19 (8). e0307874. ISSN 1932-6203, DOI https://doi.org/10.1371/journal.pone.0307874.
Ho, Weang-Kee and Hassan, Nur Tiara and Yoon, Sook-Yee and Yang, Xin and Lim, Joanna M. C. and Ishak, Nur Diana Binte and Ho, Peh Joo and Wijaya, Eldarina A. and Ng, Patsy Pei-Sze and Luccarini, Craig and Allen, Jamie and Tai, Mei-Chee and Chiang, Jianbang and Zhang, Zewen and See, Mee-Hoong and Thong, Meow-Keong and Woo, Yin-Ling and Dunning, Alison M. and Hartman, Mikael and Yip, Cheng-Har and Taib, Nur Aishah Mohd and Easton, Douglas F. and Li, Jingme and Ngeow, Joanne and Antoniou, Antonis C. and Teo, Soo-Hwang (2024) Age-specific breast and ovarian cancer risks associated with germline BRCA1 or BRCA2 pathogenic variants - an Asian study of 572 families. Lancet Regional Health-Western Pacific, 44. p. 101017. ISSN 2666-6065, DOI https://doi.org/10.1016/j.lanwpc.2024.101017.
Tae, Sok-Kun and Ra, Mazlan and Thong, Meow-Keong (2024) Case report: The evolving phenotype of ESCO2 spectrum disorder in a 15-year-old Malaysian child. FRONTIERS IN GENETICS, 14. ISSN 1664-8021, DOI https://doi.org/10.3389/fgene.2023.1286489.
Ho, Weang-Kee and Hassan, Nur Tiara and Yoon, Sook-Yee and Yang, Xin and Lim, Joanna M.C. and Binte Ishak, Nur Diana and Ho, Peh Joo and Wijaya, Eldarina A. and Ng, Patsy Pei-Sze and Luccarini, Craig and Allen, Jamie and Tai, Mei-Chee and Chiang, Jianbang and Zhang, Zewen and See, Mee-Hoong and Thong, Meow-Keong and Woo, Yin-Ling and Dunning, Alison M. and Hartman, Mikael and Yip, Cheng-Har and Mohd Taib, Nur Aishah and Easton, Douglas F. and Li, Jingmei and Ngeow, Joanne and Antoniou, Antonis C. and Teo, Soo-Hwang (2024) Age-specific breast and ovarian cancer risks associated with germline BRCA1 or BRCA2 pathogenic variants – an Asian study of 572 families. Lancet Regional Health-Western Pacific, 44. p. 101017. ISSN 2666-6065, DOI https://doi.org/10.1016/j.lanwpc.2024.101017.
Kumuthini, Judit and Zick, Brittany and Balasopoulou, Angeliki and Chalikiopoulou, Constantina and Dandara, Collet and El-Kamah, Ghada and Findley, Laura and Katsila, Theodora and Li, Rongling and Bon Maceda, Ebner and Monye, Henrietta and Rada, Gabriel and Thong, Meow-Keong and Wanigasekera, Thilina and Kennel, Hannah and Marimuthu, Veeramani and Williams, Marc S. and Al-Mulla, Fahd and Abramowicz, Marc and Investigators, G2MC Evidence (2022) The clinical utility of polygenic risk scores in genomic medicine practices: A systematic review. Human Genetics, 141 (11). pp. 1697-1704. ISSN 0340-6717, DOI https://doi.org/10.1007/s00439-022-02452-x.
Lee, Yong-Quan and Yoon, Sook-Yee and Hassan, Tiara and Padmanabhan, Heamanthaa and Yip, Cheng-Har and Keng, Wee-Teik and Thong, Meow-Keong and Annuar, Muhammad Azrif Ahmad and Taib, Nur Aishah Mohd and Teo, Soo-Hwang (2022) Attitudes and training needs of oncologists and surgeons in mainstreaming breast cancer genetic counseling in a low-to-middle income Asian country. Journal of Genetic Counseling, 31 (5). pp. 1080-1089. ISSN 1059-7700, DOI https://doi.org/10.1002/jgc4.1579.
Mohd-Zin, Siti Waheeda and Tan, Amelia Cheng Wei and Atroosh, Wahib Mohammed Mohsin and Thong, Meow-Keong and Azizi, Abu Bakar and Greene, Nicholas D. E. and Abdul-Aziz, Noraishah Mydin (2022) Eph and ephrin variants in Malaysian neural tube defect families. Genes, 13 (6). ISSN 2073-4425, DOI https://doi.org/10.3390/genes13060952.
Yoon, Sook-Yee and Wong, Siu Wan and Lim, Joanna and Ahmad, Syuhada and Mariapun, Shivaani and Padmanabhan, Heamanthaa and Hassan, Nur Tiara and Lau, Shao Yan and Ch'ng, Gaik-Siew and Haniffa, Muzhirah and Ong, Winnie P. and Rethanavelu, Kavitha and Moey, Lip Hen and Keng, Wee Teik and Omar, Jamil and Mohd Abas, Mohd Norazam and Yong, Chee Meng and Ramasamy, Vickneswaren and Md Noor, Mohd Rushdan and Aliyas, Ismail and Lim, Michael C. K. and Suberamaniam, Anuradha and Mat Adenan, Noor Azmi and Ahmad, Zatul Akmar and Ho, Gwo Fuang and Abdul Malik, Rozita and Subramaniam, Suguna and Khoo, Boom Ping and Raja, Arivendran and Chin, Yeung Sing and Sim, Wee Wee and Teh, Beng Hock and Kho, Swee Kiong and Ong, Eunice S. E. and Voon, Pei Jye and Ismail, Ghazali and Lee, Chui Ling and Abdullah, Badrul Zaman and Loo, Kwong Sheng and Lim, Chun Sen and Lee, Saw Joo and Lim, Keng Joo Lim and Shafiee, Mohamad Nasir and Ismail, Fuad and Latiff, Zarina Abdul and Ismail, Mohd Pazudin and Mohamed Jamli, Mohamad Faiz and Kumarasamy, Suresh and Leong, Kin Wah and Low, John and Md Yusof, Mastura and Ahmad Mustafa, Ahmad Muzamir and Mat Ali, Nor Huda and Makanjang, Mary and Tayib, Shahila and Cheah, Nellie and Lim, Boon Kiong and Fong, Chee Kin and Foo, Yoke Ching and Mellor Abdullah, Matin and Tan, Teck Sin and Chow, Doris S. Y. and Ho, Kean Fatt and Raman, Rakesh and Radzi, Ahmad and Deniel, Azura and Teoh, Daren C. Y. and Ang, Soo Fan and Joseph, Joseph K. and Ng, Paul Hock Oon and Tho, Lye-Mun and Ahmad, Azura Rozila and Muin, Ileena and Bleiker, Eveline and George, Angela and Thong, Meow-Keong and Woo, Yin Ling and Teo, Soo Hwang (2022) Oncologist-led BRCA counselling improves access to cancer genetic testing in middle-income Asian country, with no significant impact on psychosocial outcomes. Journal of Medical Genetics, 59 (3). pp. 220-229. ISSN 0022-2593, DOI https://doi.org/10.1136/jmedgenet-2020-107416.
Padmanabhan, Heamanthaa and Hassan, Nur Tiara and Wong, Siu-Wan and Lee, Yong-Quan and Lim, Joanna and Hasan, Siti Norhidayu and Yip, Cheng-Har and Teo, Soo-Hwang and Thong, Meow-Keong and Mohd Taib, Nur Aishah and Yoon, Sook-Yee (2022) Psychosocial outcome and health behaviour intent of breast cancer patients with BRCA1/2 and PALB2 pathogenic variants unselected by a priori risk. PLoS ONE, 17 (2). ISSN 1932-6203, DOI https://doi.org/10.1371/journal.pone.0263675.
Lee, Daphne S. -C. and Meiser, Bettina and Mariapun, Shivaani and Hassan, Tiara and Yip, Cheng-Har and Mohd Taib, Nur Aishah and Teo, Soo-Hwang and Thong, Meow-Keong and Yoon, Sook-Yee (2021) Communication about positive BRCA1 and BRCA2 genetic test results and uptake of testing in relatives in a diverse Asian setting. Journal of Genetic Counseling, 30 (3). pp. 720-729. ISSN 1059-7700, DOI https://doi.org/10.1002/jgc4.1360.
Tay, Chee Geap and Fong, Choong Yi and Li, Limin and Ganesan, Vigneswari and Teh, Chee Ming and Gan, Chin Seng and Thong, Meow-Keong (2020) Congenital myasthenic syndrome with novel pathogenic variants in the COLQ gene associated with the presence of antibodies to acetylcholine receptors. Journal of Clinical Neuroscience, 72. pp. 468-471. ISSN 0967-5868, DOI https://doi.org/10.1016/j.jocn.2019.12.007.
