Depletion of the IKBKAP ortholog in zebrafish leads to hirschsprung disease-like phenotype

Por Cheng, William Wai-Chun, Tang, Clara Sze-Man, Gui, Hong-Sheng, So, Man-Ting, Lui, Vincent Chi-Hang, Tam, Paul Kwong-Hang, Garcia-Barcelo, Maria-Mercè
Publicado no World J Gastroenterol (2015)

A random forest-based framework for genotyping and accuracy assessment of copy number variations

Por Zhuang, Xuehan, Ye, Rui, So, Man-Ting, Lam, Wai-Yee, Karim, Anwarul, Yu, Michelle, Ngo, Ngoc Diem, Cherny, Stacey S, Tam, Paul Kwong-Hang, Garcia-Barcelo, Maria-Mercè, Tang, Clara Sze-man, Sham, Pak Chung
Publicado no NAR Genom Bioinform (2020)

Whole-genome analysis of noncoding genetic variations identifies multiscale regulatory element perturbations associated with Hirschsprung disease

Por Fu, Alexander Xi, Lui, Kathy Nga-Chu, Tang, Clara Sze-Man, Ng, Ray Kit, Lai, Frank Pui-Ling, Lau, Sin-Ting, Li, Zhixin, Garcia-Barcelo, Maria-Mercè, Sham, Pak-Chung, Tam, Paul Kwong-Hang, Ngan, Elly Sau-Wai, Yip, Kevin Y.
Publicado no Genome Res (2020)

Fine Mapping of the NRG1 Hirschsprung's Disease Locus

Por Tang, Clara Sze-Man, Tang, Wai-Kiu, So, Man-Ting, Miao, Xiao-Ping, Leung, Brian Man-Chun, Yip, Benjamin Hon-Kei, Leon, Thomas Yuk-Yu, Ngan, Elly Sau-Wai, Lui, Vincent Chi-Hang, Chen, Yan, Chan, Ivy Hau-Yee, Chung, Patrick Ho-Yu, Liu, Xue-Lai, Wu, Xuan-Zhao, Wong, Kenneth Kak-Yuen, Sham, Pak-Chung, Cherny, Stacey S., Tam, Paul Kwong-Hang, Garcia-Barceló, Maria-Mercè
Publicado em 2011

Genome-Wide Copy Number Analysis Uncovers a New HSCR Gene: NRG3

Por Tang, Clara Sze-Man, Cheng, Guo, So, Man-Ting, Yip, Benjamin Hon-Kei, Miao, Xiao-Ping, Wong, Emily Hoi-Man, Ngan, Elly Sau-Wai, Lui, Vincent Chi-Hang, Song, You-Qiang, Chan, Danny, Cheung, Kenneth, Yuan, Zhen-Wei, Lei, Liu, Chung, Patrick Ho-Yu, Liu, Xue-Lai, Wong, Kenneth Kak-Yuen, Marshall, Christian R., Scherer, Steve, Cherny, Stacey S., Sham, Pak-Chung, Tam, Paul Kwong-Hang, Garcia-Barceló, Maria-Mercè
Publicado em 2012

Correction: Genome-Wide Copy Number Analysis Uncovers a New HSCR Gene: NRG3

Por Tang, Clara Sze-Man, Cheng, Guo, So, Man-Ting, Yip, Benjamin Hon-Kei, Miao, Xiao-Ping, Wong, Emily Hoi-Man, Ngan, Elly Sau-Wai, Lui, Vincent Chi-Hang, Song, You-Qiang, Chan, Danny, Cheung, Kenneth, Yuan, Zhen-Wei, Lei, Liu, Chung, Patrick Ho-Yu, Liu, Xue-Lai, Wong, Kenneth Kak-Yuen, Marshall, Christian R., Scherer, Stephen, Cherny, Stacey S., Sham, Pak-Chung, Tam, Paul Kwong-Hang, Garcia-Barceló, Maria-Mercè
Publicado em 2012

Genome-wide association study identifies NRG1 as a susceptibility locus for Hirschsprung's disease

Por Garcia-Barcelo, Maria-Mercè, Tang, Clara Sze-man, Ngan, Elly Sau-wai, Lui, Vincent Chi-hang, Chen, Yan, So, Man-ting, Leon, Thomas Yuk-yu, Miao, Xiao-ping, Shum, Cathy Ka-yee, Liu, Feng-qin, Yeung, Ming-yiu, Yuan, Zhen-wei, Guo, Wei-hong, Liu, Lei, Sun, Xiao-bing, Huang, Liu-ming, Tou, Jin-fa, Song, You-qiang, Chan, Danny, Cheung, Kenneth M. C., Wong, Kenneth Kak-yuen, Cherny, Stacey S., Sham, Pak-chung, Tam, Paul Kwong-hang
Publicado em 2009

Genome-wide association study identifies a susceptibility locus for biliary atresia on 10q24.2

Por Garcia-Barceló, Maria-Mercè, Yeung, Ming-Yiu, Miao, Xiao-Ping, Tang, Clara Sze-Man, Chen, Guo, So, Man-Ting, Ngan, Elly Sau-Wai, Lui, Vincent Chi-Hang, Chen, Yan, Liu, Xue-Lai, Hui, Kenneth-Jeremy W.S., Li, Long, Guo, Wei-Hong, Sun, Xiao-Bin, Tou, Jin-Fa, Chan, Kin-Wai, Wu, Xuan-Zhao, Song, You-Qiang, Chan, Danny, Cheung, Kenneth, Chung, Patrick Ho-Yu, Wong, Kenneth Kak-Yuen, Sham, Pak-Chung, Cherny, Stacey S., Tam, Paul Kwong-Hang
Publicado em 2010

Genome-wide association study identifies a susceptibility locus for biliary atresia on 10q24.2

Por Garcia-Barceló, Maria-Mercè, Yeung, Ming-Yiu, Miao, Xiao-Ping, Tang, Clara Sze-Man, Cheng, Guo, So, Man-Ting, Ngan, EllySau-Wai, Lui, Vincent Chi-Hang, Chen, Yan, Liu, Xue-Lai, Hui, Kenneth-Jeremy W.S., Li, Long, Guo, Wei-Hong, Sun, Xiao-Bin, Tou, Jin-Fa, Chan, Kin-Wai, Wu, Xuan-Zhao, Song, You-Qiang, Chan, Danny, Cheung, Kenneth, Chung, Patrick Ho-Yu, Wong, Kenneth Kak-Yuen, Sham, Pak-Chung, Cherny, Stacey S., Tam, Paul Kwong-Hang
Publicado em 2011

Whole-exome sequencing identifies MST1R as a genetic susceptibility gene in nasopharyngeal carcinoma

Por Dai, Wei, Zheng, Hong, Cheung, Arthur Kwok Leung, Tang, Clara Sze-man, Ko, Josephine Mun Yee, Wong, Bonnie Wing Yan, Leong, Merrin Man Long, Sham, Pak Chung, Cheung, Florence, Kwong, Dora Lai-Wan, Ngan, Roger Kai Cheong, Ng, Wai Tong, Yau, Chun Chung, Pan, Jianji, Peng, Xun, Tung, Stewart, Zhang, Zengfeng, Ji, Mingfang, Chiang, Alan Kwok-Shing, Lee, Anne Wing-Mui, Lee, Victor Ho-fun, Lam, Ka-On, Au, Kwok Hung, Cheng, Hoi Ching, Yiu, Harry Ho-Yin, Lung, Maria Li
Publicado no Proc Natl Acad Sci U S A (2016)

Actionable pharmacogenetic variants in Hong Kong Chinese exome sequencing data and projected prescription impact in the Hong Kong population

Por Yu, Mullin Ho Chung, Chan, Marcus Chun Yin, Chung, Claudia Ching Yan, Li, Andrew Wang Tat, Yip, Chara Yin Wa, Mak, Christopher Chun Yu, Chau, Jeffrey Fong Ting, Lee, Mianne, Fung, Jasmine Lee Fong, Tsang, Mandy Ho Yin, Chan, Joshua Chun Ki, Wong, Wilfred Hing Sang, Yang, Jing, Chui, William Chun Ming, Chung, Patrick Ho Yu, Yang, Wanling, Lee, So Lun, Chan, Godfrey Chi Fung, Tam, Paul Kwong Hang, Lau, Yu Lung, Tang, Clara Sze Man, Yeung, Kit San, Chung, Brian Hon Yin
Publicado no PLoS Genet (2021)

RET Mutational Spectrum in Hirschsprung Disease: Evaluation of 601 Chinese Patients

Por So, Man-Ting, Leon, Thomas Yuk-Yu, Cheng, Guo, Tang, Clara Sze-Man, Miao, Xiao-Ping, Cornes, Belinda K., Ngo, Diem Ngoc, Cui, Long, Ngan, Elly Sau-Wai, Lui, Vincent Chai-Hang, Wu, Xuan-Zhao, Wang, Bin, Wang, Hualong, Yuan, Zheng-Wei, Huang, Liu-Ming, Li, Long, Xia, Huimin, Zhu, Deli, Liu, Juncheng, Nguyen, Thanh Liem, Chan, Ivy Hau-Yee, Chung, Patrick Ho-Yu, Liu, Xue-Lai, Zhang, Ruizhong, Wong, Kenneth Kak-Yuen, Sham, Pak-Chung, Cherny, Stacey S., Tam, Paul Kwong-Hang, Garcia-Barcelo, Maria-Mercè
Publicado em 2011

Trans-ethnic meta-analysis of genome-wide association studies for Hirschsprung disease

Por Tang, Clara Sze-man, Gui, Hongsheng, Kapoor, Ashish, Kim, Jeong-Hyun, Luzón-Toro, Berta, Pelet, Anna, Burzynski, Grzegorz, Lantieri, Francesca, So, Man-ting, Berrios, Courtney, Shin, Hyoung Doo, Fernández, Raquel M., Le, Thuy-Linh, Verheij, Joke B.G.M., Matera, Ivana, Cherny, Stacey S., Nandakumar, Priyanka, Cheong, Hyun Sub, Antiñolo, Guillermo, Amiel, Jeanne, Seo, Jeong-Meen, Kim, Dae-Yeon, Oh, Jung-Tak, Lyonnet, Stanislas, Borrego, Salud, Ceccherini, Isabella, Hofstra, Robert M.W., Chakravarti, Aravinda, Kim, Hyun-Young, Sham, Pak Chung, Tam, Paul K.H., Garcia-Barceló, Maria-Mercè
Publicado no Hum Mol Genet (2016)

Exome chip meta-analysis identifies novel loci and East Asian-specific coding variants contributing to lipid levels and coronary artery disease

Por Lu, Xiangfeng, Peloso, Gina M, Liu, Dajiang J., Wu, Ying, Zhang, He, Zhou, Wei, Li, Jun, Tang, Clara Sze-man, Dorajoo, Rajkumar, Li, Huaixing, Long, Jirong, Guo, Xiuqing, Xu, Ming, Spracklen, Cassandra N., Chen, Yang, Liu, Xuezhen, Zhang, Yan, Khor, Chiea Chuen, Liu, Jianjun, Sun, Liang, Wang, Laiyuan, Gao, Yu-Tang, Hu, Yao, Yu, Kuai, Wang, Yiqin, Cheung, Chloe Yu Yan, Wang, Feijie, Huang, Jianfeng, Fan, Qiao, Cai, Qiuyin, Chen, Shufeng, Shi, Jinxiu, Yang, Xueli, Zhao, Wanting, Sheu, Wayne H.-H., Cherny, Stacey Shawn, He, Meian, Feranil, Alan B., Adair, Linda S., Gordon-Larsen, Penny, Du, Shufa, Varma, Rohit, da Chen, Yii-Der I, Shu, XiaoOu, Lam, Karen Siu Ling, Wong, Tien Yin, Ganesh, Santhi K., Mo, Zengnan, Hveem, Kristian, Fritsche, Lars, Nielsen, Jonas Bille, Tse, Hung-fat, Huo, Yong, Cheng, Ching-Yu, Chen, Y. Eugene, Zheng, Wei, Tai, E Shyong, Gao, Wei, Lin, Xu, Huang, Wei, Abecasis, Goncalo, Consortium, GLGC, Kathiresan, Sekar, Mohlke, Karen L., Wu, Tangchun, Sham, Pak Chung, Gu, Dongfeng, Willer, Cristen J
Publicado no Nat Genet (2017)