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9 Jun 2026 BMRC Bioinformatics Institute Genomic landscape of drug binding and pharmacogenetic variation across diverse populations using SNPdrug3D (Pending publish) Ashar J. Malik, Dimitar Kenanov, Cheng-Shoong Chong, Mert Burak Ozturk, Qiqi Wang, Hong-Yun Chang, Maxime Hebrard, Ying Swan Ho, Zhenxun Wang, Vachiranee Limviphuvadh, Jhoann M. T. Miyajima, Srinivasaraghavan Kannan, Roberto Tirado Magallanes, Xueling Sim, Jin Fang Chai, Sonia Davila, Khung Keong Yeo, Khai Pang Leong, Liuh Ling Goh, Neerja Karnani, Johan Gunnar Eriksson, Ching-Yu Cheng, Tien Yin Wong, Marie Loh, Rinkoo Dalan, Chiea Chuen Khor, Guo-Liang Chew, Weng Khong Lim, Joanne Ngeow, John C. Chambers, E. Shyong Tai, Nicolas Bertin, Chris Soon Heng Tan, Judice Koh, Patrick Tan, , Tin Aung, Claire Bellis, Miao Ling Chee, Paul Chung Pui Cheng, Wen Jie Chew, Calvin Woon Loong Chin, Yap Seng Chong, Stuart Alexander Cook, Paul Eillot, Johan G. Eriksson, Peter D. Gluckman, Pritesh Rajesh Jain, Saumya S. Jamuar, Justin Jeyakani, Rodrigo Toro Jimenez, Tat Hung Koh, Eng Sing Lee, Jimmy Lee, Yung Seng Lee, Hengtong Li, Zhihui Li, Chia Wei Lim, Tock Han Lim, Bitong Clarabelle Alexandrine Lin, Jianjun Liu, Dorrain Low, Roberto-Tirado Magallanes, Theresia Mina, Shiqi Mok, Hong Kiat Ng, Jack Ling Ow, Qingsheng Peng, Shyam Prabhakar, Chee Jian Pua, Elio Riboli, Charumathi Sabanayagam, Nilanjana Sadhu, Yee Yen Sia, Wey Ching Sim, Joanna Hui Juan Tan, Erwin Tantoso, Darwin Tay, Yik Ying Teo, Yih Chung Tham, Li-xian Grace Toh, Pi Kuang Tsai, Rob M. van Dam, Chandra Verma, Xiaoyan Wang, Can Can Xue, Chengxi Yang, Fabian Yap, Chandra S. Verma, Sebastian Maurer-Stroh Nature Communications
26 Dec 2025 Others Diagnostics Development Hub Expanding carrier screening: beyond the genes, to include underrepresented ancestries Yasmin Bylstra, Pua Chee Jian, Sui Lin, Jeannette Goh, Christina Choi, Jing Xian Teo, Sandy Lim, Jan Hodgson, Melody Menezes, Ruifen Weng, David J. Amor, Weng Khong Lim, Saumya S. Jamuar npj Genomic Medicine
30 Jan 2020 BMRC Institute of Molecular and Cell Biology Loss-of-function mutations in UDP-Glucose 6-Dehydrogenase cause recessive developmental epileptic encephalopathy Monica Yau, Nader Handal, Werner Deigendesch, Reinhard Keimer, Hiyam M. Marzouqa, Holger Hengel, Célia Bosso-Lefèvre, George Grady, Emmanuelle Szenker-Ravi, Hankun Li, Sarah Pierce, Élise Lebigot, Thong-Teck Tan, Michelle Y. Eio, Gunaseelan Narayanan, Kagistia Hana Utami, Meral Gunay-Aygun, Michael J. Muriello, Helene Verhelst, Sarah Weckhuysen, Sonal Mahida, Sakkubai Naidu, Terrence G. Thomas, Jiin Ying Lim, Ee Shien Tan, Damien Haye, Michèl A. A. P. Willemsen, Renske Oegema, Wendy G. Mitchell, Tyler Mark Pierson, Marisa V. Andrews, Marcia C. Willing, Lance H. Rodan, Tahsin Stefan Barakat, Marjon van Slegtenhorst, Ralitza H. Gavrilova, Diego Martinelli, Tal Gilboa, Abdullah M. Tamim, Mais O. Hashem, Moeenaldeen D. AlSayed, Maha M. Abdulrahim, Mohammed Al-Owain, Ali Awaji, Adel A. H. Mahmoud, Eissa A. Faqeih, Ali Al Asmari, Sulwan M. Algain, Lamyaa A. Jad, Hesham M. Aldhalaan, Ingo Helbig, David A. Koolen, Angelika Riess, Ingeborg Kraegeloh-Mann, Peter Bauer, Suleyman Gulsuner, Hannah Stamberger, Alvin Yu Jin Ng, Sha Tang, Sumanty Tohari, Boris Keren, Laura E. Schultz-Rogers, Eric W. Klee, Sabina Barresi, Marco Tartaglia, Hagar Mor-Shaked, Sateesh Maddirevula, Amber Begtrup, Aida Telegrafi, Rolph Pfundt, Rebecca Schüle, Brian Ciruna, Carine Bonnard, Mahmoud A. Pouladi, James C. Stewart, Adam Claridge-Chang, Dirk J. Lefeber, Fowzan S. Alkuraya, Bruno Reversade, Ajay S. Mathuru, Byrappa Venkatesh, Joseph J. Barycki, Melanie A. Simpson, Saumya S. Jamuar, Ludger Schöls Nature Communications