Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Tat Hung, Koh"'
Autor:
Ishak D. Irwan, Jianjun Liu, Kyuyoung Song, E-Shyong Tai, Ho-Sung Ryu, Myunghee Hong, Herty Liany, Jimmy Lee, Tien Yin Wong, Louis C. Tan, Tat Hung Koh, Chiea Chuen Khor, Siow Ann Chong, Sun Ju Chung, Tin Aung, Jia Nee Foo, Wing Lok Au, Kumar M. Prakash, Ching-Yu Cheng, Eranga N. Vithana, Eng-King Tan
Publikováno v:
Movement Disorders. 31:484-487
Background Genome-wide association studies have identified several loci associated with Parkinson's disease (PD). Whole-exome sequencing detects rare coding variants, but their links with PD genome-wide association study loci are unknown. Our objecti
Autor:
Anne Y.Y. Chan, Wing Lok Au, Yusun Jung, Jimmy Lee, Jianjun Liu, Kyuyoung Song, Siow Ann Chong, Shen-Yang Lim, Azlina Ahmad-Annuar, Kumar M. Prakash, Jia Nee Foo, Eng-King Tan, Juyeon Kim, Yen Yek Ng, Tin Aung, Vincent Mok, Tat Hung Koh, Herty Liany, Sun Ju Chung, Louis C.S. Tan, Eranga N. Vithana, Chiea Chuen Khor, Tien Yin Wong, Ishak D. Irwan, E. Shyong Tai
Publikováno v:
Human Molecular Genetics. 23:3891-3897
To evaluate the contribution of non-synonymous-coding variants of known familial and genome-wide association studies (GWAS)-linked genes for Parkinson's disease (PD) to PD risk in the East Asian population, we sequenced all the coding exons of 39 PD-
Autor:
Degang Wu, Jinzhuang Dou, Xiaoran Chai, Claire Bellis, Andreas Wilm, Chih Chuan Shih, Wendy Wei Jia Soon, Nicolas Bertin, Clarabelle Bitong Lin, Chiea Chuen Khor, Michael DeGiorgio, Shanshan Cheng, Li Bao, Neerja Karnani, William Ying Khee Hwang, Sonia Davila, Patrick Tan, Asim Shabbir, Angela Moh, Eng-King Tan, Jia Nee Foo, Liuh Ling Goh, Khai Pang Leong, Roger S.Y. Foo, Carolyn Su Ping Lam, Arthur Mark Richards, Ching-Yu Cheng, Tin Aung, Tien Yin Wong, Huck Hui Ng, Jianjun Liu, Chaolong Wang, Matthew Andrew Ackers-Johnson, Edita Aliwarga, Kenneth Hon Kim Ban, Denis Bertrand, John C. Chambers, Dana Leng Hui Chan, Cheryl Xue Li Chan, Miao Li Chee, Miao Ling Chee, Pauline Chen, Yunxin Chen, Elaine Guo Yan Chew, Wen Jie Chew, Lynn Hui Yun Chiam, Jenny Pek Ching Chong, Ivan Chua, Stuart A. Cook, Wei Dai, Rajkumar Dorajoo, Chuan-Sheng Foo, Rick Siow Mong Goh, Axel M. Hillmer, Ishak D. Irwan, Fazlur Jaufeerally, Asif Javed, Justin Jeyakani, John Tat Hung Koh, Jia Yu Koh, Pavitra Krishnaswamy, Jyn Ling Kuan, Neelam Kumari, Ai Shan Lee, Seow Eng Lee, Sheldon Lee, Yen Ling Lee, See Ting Leong, Zheng Li, Peter Yiqing Li, Jun Xian Liew, Oi Wah Liew, Su Chi Lim, Weng Khong Lim, Chia Wei Lim, Tingsen Benson Lim, Choon Kiat Lim, Seet Yoong Loh, Au Wing Lok, Calvin W.L. Chin, Shivani Majithia, Sebastian Maurer-Stroh, Wee Yang Meah, Shi Qi Mok, Niranjan Nargarajan, Pauline Ng, Sarah B. Ng, Zhenyuan Ng, Jessica Yan Xia Ng, Ebonne Ng, Shi Ling Ng, Simon Nusinovici, Chin Thing Ong, Bangfen Pan, Vincent Pedergnana, Stanley Poh, Shyam Prabhakar, Kumar M. Prakash, Ivy Quek, Charumathi Sabanayagam, Wei Qiang See, Yee Yen Sia, Xueling Sim, Wey Cheng Sim, Jimmy So, Dinna K.N. Soon, E. Shyong Tai, Nicholas Y. Tan, Louis C.S. Tan, Hong Chang Tan, Wilson Lek Wen Tan, Moses Tandiono, Amanda Tay, Sahil Thakur, Yih Chung Tham, Zenia Tiang, Grace Li-Xian Toh, Pi Kuang Tsai, Lavanya Veeravalli, Chandra S. Verma, Ling Wang, Min Rui Wang, Wing-Cheong Wong, Zhicheng Xie, Khung Keong Yeo, Liang Zhang, Weiwei Zhai, Yi Zhao
Publikováno v:
Cell, 179(3), 736-749.e15. CELL PRESS
Underrepresentation of Asian genomes has hindered population and medical genetics research on Asians, leading to population disparities in precision medicine. By whole-genome sequencing of 4,810 Singapore Chinese, Malays, and Indians, we found 98.3 m
Autor:
Jia Nee, Foo, Sun Ju, Chung, Louis C, Tan, Herty, Liany, Ho-Sung, Ryu, Myunghee, Hong, Tat Hung, Koh, Ishak D, Irwan, Wing-Lok, Au, Kumar-M, Prakash, Tin, Aung, Ching-Yu, Cheng, Siow-Ann, Chong, Chiea Chuen, Khor, Jimmy, Lee, E-Shyong, Tai, Eranga N, Vithana, Tien-Yin, Wong, Kyuyoung, Song, Jianjun, Liu, Eng-King, Tan
Publikováno v:
Movement disorders : official journal of the Movement Disorder Society. 31(4)
Genome-wide association studies have identified several loci associated with Parkinson's disease (PD). Whole-exome sequencing detects rare coding variants, but their links with PD genome-wide association study loci are unknown. Our objective was to i