Rezultaty - Man-Ting, SO
- Rezultaty 1 - 12 Rezultaty od 12
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Genetic Analyses of a Three Generation Family Segregating Hirschsprung Disease and Iris Heterochromia od Long Cui, Emily Hoi-Man Wong, Guo Cheng, Manoel Firmato de Almeida, Man-ting So, Pak C. Sham, Stacey S. Cherny, Paul Kwong-Hang Tam, Maria‐Mercè Garcia‐Barceló
Wydane 2013Artigo -
3
Uncovering the genetic lesions underlying the most severe form of Hirschsprung disease by whole-genome sequencing od Tang, Clara SM, Zhuang, Xuehan, Lam, Wai-Yee, Ngan, Elly Sau-Wai, Hsu, Jacob Shujui, Michelle, YU, Man-Ting, SO, Cherny, Stacey S, Ngo, Ngoc Diem, Sham, Pak C, Tam, Paul KH, Garcia-Barcelo, Maria-Mercè
Wydane 2018Text -
4
A Germline Mutation (A339V) in Thyroid Transcription Factor-1 (TITF-1/NKX2.1) in Patients With Multinodular Goiter and Papillary Thyroid Carcinoma od Esw Ngan, Brian Hung‐Hin Lang, Tingting Liu, Cathy K.Y. Shum, Man-Ting So, Danny Ko‐chun Lau, Thomas Y.Y. Leon, Stacey S. Cherny, Sophia Y. Tsai, Chung‐Yau Lo, US Khoo, Paul Tam, Maria‐Mercè Garcia‐Barceló
Wydane 2009Artigo -
5
Common Variants on Xq28 Conferring Risk of Schizophrenia in Han Chinese od Emily H. M. Wong, Hon‐Cheong So, Miaoxin Li, Quang Wang, Amy W. Butler, Paul Basil, Hei-Man Wu, Tomy C.K. Hui, Siu-chung Choi, Man‐Ting So, María-Mercé García-Barceló, Gráinne McAlonan, Eric Chen, Eric F.C. Cheung, Raymond C. K. Chan, Shaun Purcell, Stacey S. Cherny, Ronald R.L. Chen, Tao Li, Pak C. Sham
Wydane 2013Artigo -
6
Identification of a wide spectrum of ciliary gene mutations in nonsyndromic biliary atresia patients implicates ciliary dysfunction as a novel disease mechanism od Wai-Yee Lam, Clara Sze-Man Tang, Man‐Ting So, Haibing Yue, Jacob Shujui Hsu, Bhy Chung, John Nicholls, Fanny Yeung, Chun-Wai Davy Lee, Diem Ngoc Ngo, Pham Anh Nguyen, Hannah M. Mitchison, Dagan Jenkins, Christopher O’Callaghan, María-Mercé García-Barceló, So Lun Lee, Pak C. Sham, Vincent Chi‐Hang Lui, Paul Kwong‐Hang Tam
Wydane 2021Artigo -
7
Genome-Wide Copy Number Analysis Uncovers a New HSCR Gene: NRG3 od Clara Sze-Man Tang, Guo Cheng, Man‐Ting So, Benjamin Hon Kei Yip, Xiaoping Miao, Emily Hoi-Man Wong, Esw Ngan, Vincent Chi‐Hang Lui, You‐Qiang Song, Danny Chan, Kmc Cheung, Zhenwei Yuan, Lei Liu, Bhy Chung, Xuelai Liu, Kenneth Kak‐Yuen Wong, Christian R. Marshall, Stephen W. Scherer, Stacey S. Cherny, Pak-Chung Sham, Paul Kwong‐Hang Tam, María-Mercé García-Barceló
Wydane 2012Artigo -
8
Fine Mapping of the NRG1 Hirschsprung's Disease Locus od Clara Sze-Man Tang, Wai-Kiu Tang, Man-Ting So, Xiaoping Miao, Brian Man-Chun Leung, Benjamin Hon Kei Yip, Thomas Yuk-Yu Leon, Esw Ngan, Vincent Chi‐Hang Lui, Yan Chen, Ivy Hau-Yee Chan, Bhy Chung, Xue-Lai Liu, Xuan-Zhao Wu, Kenneth Kak-Yuen Wong, Pak C. Sham, Stacey S. Cherny, Paul Kwong-Hang Tam, Maria‐Mercè Garcia‐Barceló
Wydane 2011Artigo -
9
Genome-wide association study identifies <i>NRG1</i> as a susceptibility locus for Hirschsprung's disease od María-Mercé García-Barceló, Clara Sze-Man Tang, Esw Ngan, Vincent Chi‐Hang Lui, Yan Chen, Man‐Ting So, Thomas Yuk-Yu Leon, Xiaoping Miao, Cathy K.Y. Shum, Fengqin Liu, Ming-Yiu Yeung, Zhenwei Yuan, Weihong Guo, Lei Liu, Xiao‐bing Sun, Liuming Huang, Jinfa Tou, You‐Qiang Song, Danny Chan, Kmc Cheung, Kenneth Kak‐Yuen Wong, Stacey S. Cherny, Pak C. Sham, Paul Kwong‐Hang Tam
Wydane 2009Artigo -
10
Genome-wide association study identifies a susceptibility locus for biliary atresia on 10q24.2 od María-Mercé García-Barceló, Ming-Yiu Yeung, Xiaoping Miao, Clara Sze-Man Tang, Chen Guo, Man‐Ting So, Esw Ngan, Vincent Chi‐Hang Lui, Yan Chen, Xuelai Liu, Kenneth-Jeremy W. S. Hui, Long Li, Weihong Guo, Xiaobin Sun, Jinfa Tou, KW Chan, Xuan-Zhao Wu, You‐Qiang Song, Danny Chan, Kmc Cheung, Bhy Chung, Kenneth Kak‐Yuen Wong, Pak C. Sham, Stacey S. Cherny, Paul Kwong‐Hang Tam
Wydane 2010Artigo -
11
<i>Trans</i>-ethnic meta-analysis of genome-wide association studies for Hirschsprung disease od Clara Sze-Man Tang, Hongsheng Gui, Ashish Kapoor, Jeong‐Hyun Kim, Berta Luzón‐Toro, Anna Pelet, Grzegorz Burzynski, Francesca Lantieri, Man-Ting So, Courtney Berrios, Hyoung Doo Shin, Raquel M. Fernández, Thuy-Linh Le, Joanne Verheij, Ivana Matera, Stacey S. Cherny, Priyanka Nandakumar, Hyun Sub Cheong, Guillermo Antiñolo, Jeanne Amiel, Jeong-Meen Seo, Dae Yeon Kim, Jung-Tak Oh, Stanislas Lyonnet, Salud Borrego, Isabella Ceccherini, Robert M.W. Hofstra, Aravinda Chakravarti, Hyun‐Young Kim, Pak C. Sham, Paul Tam, Maria‐Mercè Garcia‐Barceló
Wydane 2016Revisão -
12
Whole exome sequencing coupled with unbiased functional analysis reveals new Hirschsprung disease genes od Hongsheng Gui, Duco Schriemer, William Cheng, Rajendra Chauhan, Guillermo Antiñolo, Courtney Berrios, Marta Bleda, Alice S. Brooks, Rutger W. W. Brouwer, Alan J. Burns, Stacey S. Cherny, Joaquı́n Dopazo, Bart J. L. Eggen, Paola Griseri, Binta Jalloh, Thuy-Linh Le, Vincent Chi Hang Lui, Berta Luzón‐Toro, Ivana Matera, Esw Ngan, Anna Pelet, Macarena Ruiz‐Ferrer, Pak C. Sham, Iain T. Shepherd, Man-Ting So, Yunia Sribudiani, Clara Sze-Man Tang, Mirjam C. G. N. van den Hout, Herma C. van der Linde, Tjakko J. van Ham, Wilfred F. J. van IJcken, Joanne Verheij, Jeanne Amiel, Salud Borrego, Isabella Ceccherini, Aravinda Chakravarti, Stanislas Lyonnet, Paul Kwong Hang Tam, Maria‐Mercè Garcia‐Barceló, Robert M.W. Hofstra
Wydane 2017Artigo
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