Adaptive Evolution Hotspots at the GC-Extremes of the Human Genome: Evidence for Two Functionally Distinct Pathways of Positive Selection

Por Tang, Clara S. M., Epstein, Richard J.
Publicado em 2010

A Structural Split in the Human Genome

Por Tang, Clara S.M., Epstein, Richard J.
Publicado em 2007

Persistent barrage firing in cortical interneurons can be induced in vivo and may be important for the suppression of epileptiform activity

Por Suzuki, Norimitsu, Tang, Clara S.-M., Bekkers, John M.
Publicado em 2014

Coverage and diagnostic yield of Whole Exome Sequencing for the Evaluation of Cases with Dilated and Hypertrophic Cardiomyopathy

Por Mak, Timothy Shin Heng, Lee, Yee-Ki, Tang, Clara S., Hai, JoJo S. H., Ran, Xinru, Sham, Pak-Chung, Tse, Hung-Fat
Publicado no Sci Rep (2018)

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 Genome-Wide Linkage and Association Scan Reveals Novel Loci for Hypertension and Blood Pressure Traits

Por Guo, Youling, Tomlinson, Brian, Chu, Tanya, Fang, Yu Jing, Gui, Hongsheng, Tang, Clara S., Yip, Benjamin H., Cherny, Stacey S., Hur, Yoon-Mi, Sham, Pak Chung, Lam, Tai Hing, Thomas, Neil G.
Publicado em 2012

Correction: A Genome-Wide Linkage and Association Scan Reveals Novel Loci for Hypertension and Blood Pressure Traits

Por Guo, Youling, Tomlinson, Brian, Chu, Tanya, Fang, Yu Jing, Gui, Hongsheng, Tang, Clara S., Yip, Benjamin H., Cherny, Stacey S., Hur, Yoon-Mi, Sham, Pak Chung, Lam, Tai Hing, Thomas, Neil G.
Publicado em 2012

Haplotype Analysis Reveals a Possible Founder Effect of RET Mutation R114H for Hirschsprung's Disease in the Chinese Population

Por Cornes, Belinda K., Tang, Clara S., Leon, Thomas Y. Y., Hui, Kenneth J. W. S., So, Man-Ting, Miao, Xiaoping, Cherny, Stacey S., Sham, Pak C., Tam, Paul K. H., Garcia-Barcelo, Maria-Merce
Publicado em 2010

Uncovering the genetic lesions underlying the most severe form of Hirschsprung disease by whole-genome sequencing

Por 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
Publicado no Eur J Hum Genet (2018)

Cancer gene mutations in congenital pulmonary airway malformation patients

Por Hsu, Jacob Shujui, Zhang, Ruizhong, Yeung, Fanny, Tang, Clara S.M., Wong, John K.L., So, Man-Ting, Xia, Huimin, Sham, Pak, Tam, Paul K., Li, Miaoxin, Wong, Kenneth K.Y., Garcia-Barcelo, Maria-Mercè
Publicado no ERJ Open Res (2019)

Chinese family with diffuse oesophageal leiomyomatosis: a new COL4A5/COL4A6 deletion and a case of gonosomal mosaicism

Por Liu, Wei, Wong, John KL, He, Qiuming, Wong, Emily HM, Tang, Clara SM, Zhang, Ruizhong, So, Man-ting, Wong, Kenneth KY, Nicholls, John, Cherny, Stacey S, Sham, Pak C, Tam, Paul K, Garcia-Barcelo, Maria-Mercè, Xia, Huimin
Publicado no BMC Med Genet (2015)

High-sensitivity troponin I and B-type natriuretic peptide biomarkers for prediction of cardiovascular events in patients with coronary artery disease with and without diabetes mel...

Por Wong, Yuen-Kwun, Cheung, Chloe Y. Y., Tang, Clara S., Hai, JoJo S. H., Lee, Chi-Ho, Lau, Kui-Kai, Au, Ka-Wing, Cheung, Bernard M. Y., Sham, Pak-Chung, Xu, Aimin, Lam, Karen S. L., Tse, Hung-Fat
Publicado no Cardiovasc Diabetol (2019)

Genetic study of congenital bile-duct dilatation identifies de novo and inherited variants in functionally related genes

Por Wong, John K. L., Campbell, Desmond, Ngo, Ngoc Diem, Yeung, Fanny, Cheng, Guo, Tang, Clara S. M., Chung, Patrick H. Y., Tran, Ngoc Son, So, Man-ting, Cherny, Stacey S., Sham, Pak C., Tam, Paul K., Garcia-Barcelo, Maria-Mercè
Publicado no BMC Med Genomics (2016)

Exome sequencing reveals a high genetic heterogeneity on familial Hirschsprung disease

Por Luzón-Toro, Berta, Gui, Hongsheng, Ruiz-Ferrer, Macarena, Sze-Man Tang, Clara, Fernández, Raquel M., Sham, Pak-Chung, Torroglosa, Ana, Kwong-Hang Tam, Paul, Espino-Paisán, Laura, Cherny, Stacey S., Bleda, Marta, Enguix-Riego, María del Valle, Dopazo, Joaquín, Antiñolo, Guillermo, García-Barceló, María-Mercé, Borrego, Salud
Publicado no Sci Rep (2015)

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