| Issue Date | Title | Author(s) |
 | 2022 | Analysis of clinically relevant variants from ancestrally diverse Asian genomes | Chan, Sock Hoai; Bylstra, Yasmin; Teo, Jing Xian; Kuan, Jyn Ling; Bertin, Nicolas; Gonzalez-Porta, Mar; Hebrard, Maxime; Tirado-Magallanes, Roberto; Tan, Joanna Hui Juan; Jeyakani, Justin; Li, Zhihui; Chai, Jin Fang; Chong, Yap Seng; Davila, Sonia; Goh, Liuh Ling; Lee, Eng Sing; Wong, Eleanor; Wong, Tien Yin; Prabhakar, Shyam; Liu, Jianjun; Cheng, Ching-Yu; Eisenhaber, Birgit; Karnani, Neerja; Leong, Khai Pang; Sim, Xueling; Yeo, Khung Keong; Chambers, John Campbell; Tai, E-Shyong; Tan, Patrick; Jamuar, Saumya S.; Ngeow, Joanne; Lim, Weng Khong |
| 2022 | Automatic DNA replication tract measurement to assess replication and repair dynamics at the single-molecule level | Li, Longjie; Kolinjivadi, Arun Mouli; Ong, Kok Haur; Young, David M.; Marini, Gabriel Pik Liang; Chan, Sock Hoai; Chong, Siao Ting; Chew, Ee Ling; Lu, Haoda; Gole, Laurent; Yu, Weimiao; Ngeow, Joanne |
| | 2020 | Biallelic NF1 inactivation in high grade serous ovarian cancers from patients with neurofibromatosis type 1 | Courtney, Eliza; Chan, Sock Hoai; Li, Shao Tzu; Ishak, Diana; Merchant, Khurshid; Shaw, Tarryn; Chay, Wen Yee; Chin, Felicia Hui Xian; Wong, Wai Loong; Wong, Adele; Ngeow, Joanne |
| 2022 | Case report: olaparib use in metastatic lung adenocarcinoma with BRCA2 pathogenic variant | Soon, Jonathan Jian Hao; Chan, Sock Hoai; Tan, Daniel Shao Weng; Ngeow, Joanne; Chiang, Jianbang |
| 2018 | Clinical relevance of screening checklists for detecting cancer predisposition syndromes in Asian childhood tumours | Chan, Sock Hoai; Chew, Winston; Nur Diana Binte Ishak; Lim, Weng Khong; Li, Shao-Tzu; Tan, Sheng Hui; Teo, Jing Xian; Shaw, Tarryn; Chang, Kenneth; Chen, Yong; Iyer, Prasad; Tan, Enrica Ee Kar; Seng, Michaela Su-Fern; Chan, Mei Yoke; Tan, Ah Moy; Low, Sharon Yin Yee; Soh, Shui Yen; Loh, Amos Hong Pheng; Ngeow, Joanne |
| 2023 | COVID-19 vaccination uptake and safety profile among germline BRCA1 and BRCA2 pathogenic variant carriers in Singapore | Zhang, Zewen; Nur Diana Binte Ishak; Que, Frances Victoria Fajardo; Chua, Zi Yang; Chan, Sock Hoai; Chiang, Jianbang; Ngeow, Joanne |
| 2019 | Functional analysis of clinical BARD1 germline variants | Toh, Ming Ren; Chong, Siao Ting; Chan, Sock Hoai; Low, Chen Ee; Nur Diana Binte Ishak; Lim, Jing Quan; Courtney, Eliza; Ngeow, Joanne |
| | 2022 | Functional analysis of germline RAD51C missense variants highlight the role of RAD51C in replication fork protection | Kolinjivadi, Arun Mouli; Chong, Siao Ting; Choudhary, Ramveer; Sankar, Haresh; Chew, Ee Ling; Yeo, Claresta; Chan, Sock Hoai; Ngeow, Joanne |
| 2020 | Functional characterisation guides classification of novel BAP1 germline variants | Hong, Jing Han; Chong, Siao Ting; Lee, Po-Hsien; Tan, Jing; Heng, Hong Lee; Nur Diana Ishak; Chan, Sock Hoai; Teh, Bin Tean; Ngeow, Joanne |
| 2017 | Germline mutations in cancer predisposition genes are frequent in sporadic sarcomas | Chan, Sock Hoai; Lim, Weng Khong; Nur Diana Binte Ishak; Li, Shao-Tzu; Goh, Wei Lin; Tan, Gek San; Lim, Kiat Hon; Teo, Melissa; Ng, Cedric Chuan Young; Malik, Simeen; Tan, Mann Hong; Teh, Jonathan Yi Hui; Chin, Francis Kuok Choon; Kesavan, Sittampalam; Selvarajan, Sathiyamoorthy; Tan, Patrick; Teh, Bin Tean; Soo, Khee Chee; Mohamad Farid; Quek, Richard; Ngeow, Joanne |
| | 2021 | Impact of variant reclassification in cancer predisposition genes on clinical care | Chiang, Jianbang; Chia, Tze Hao; Yuen, Jeanette; Shaw, Tarryn; Li, Shao-Tzu; Nur Diana Binte Ishak; Chew, Ee Ling; Chong, Siao Ting; Chan, Sock Hoai; Ngeow, Joanne |
| | 2021 | Investigation into the origins of an ancient BRCA1 founder mutation identified among Chinese families in Singapore | Shaw, Tarryn; Chan, Sock Hoai; Teo, Jing Xian; Chong, Siao Ting; Li, Shao-Tzu; Courtney, Eliza; Ishak, Diana; Sankar, Haresh; Ang, Zoe Li Ting; Chiang, Jianbang; Loh, Marie; Zhou, Li; Lee, Soo Chin; Yeh, Hui-Yuan; Kolinjivadi, Arun Mouli; Lim, Weng Khong; Ngeow, Joanne |
| 2020 | Multiple neoplasia in a patient with Gitelman syndrome harboring germline monoallelic MUTYH mutation | Chan, Jason Yongsheng; Toh, Ming Ren; Chong, Siao Ting; Nur Diana Ishak; Kolinjivadi, Arun Mouli; Chan, Sock Hoai; Lee, Elizabeth; Boot, Arnoud; Shao-Tzu, Li; Chew, Min-Hoe; Ngeow, Joanne |
