Ohcanbohtosat - Garcia-Barcelo, Maria-Mercè
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1
Role of RET and PHOX2B gene polymorphisms in risk of Hirschsprung's disease in Chinese population Dahkki Miao, Xiaoping, Garcia‐Barceló, Maria‐Mercè, So, Man‐ting, Yuk‐yu Leon, Thomas, Ko‐chun Lau, Danny, Liu, Ting‐Ting, Kin‐Wai Chan, Edwin, Chuen‐Leung Lan, Lawrence, Kak‐yuen Wong, Kenneth, Chi‐hang Lui, Vincent, Kwong‐hang Tam, Paul, Garcia‐Barceló, Maria‐Mercè, Kwong‐hang Tam, Paul
Almmustuhtton 2007Teaksta -
2
Cost effective assay choice for rare disease study designs Dahkki Campbell, Desmond D, Porsch, Robert M, Cherny, Stacey S, Capra, Valeria, Merello, Elisa, De Marco, Patrizia, Sham, Pak C, Garcia-Barceló, Maria-Mercè
Almmustuhtton 2015Teaksta -
3
AB113. The first genetic study on congenital choledochal dilatation (CCD) implicates extracellular matrix proteins Dahkki Garcia-Barceló, Maria-Mercè, Wong, John Kwong Leong, Ngo, Ngoc Diem, Tran, Ngoc Son, Nguyen, Thanh Liem, Nguyen, Liem, Sham, Pak, Cherny, Stacey, Tam, Paul
Almmustuhtton 2015Teaksta -
4
Depletion of the IKBKAP ortholog in zebrafish leads to hirschsprung disease-like phenotype Dahkki 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
Almmustuhtton 2015Teaksta -
5
Patient complexity and genotype-phenotype correlations in biliary atresia: a cross-sectional analysis Dahkki Cheng, Guo, Chung, Patrick Ho-Yu, Chan, Edwin Kin-Wai, So, Man-Ting, Sham, Pak-Chung, Cherny, Stacey S., Tam, Paul Kwong-Hang, Garcia-Barceló, Maria-Mercè
Almmustuhtton 2017Teaksta -
6
Gene Network Analysis of Candidate Loci for Human Anorectal Malformations Dahkki Wong, Emily H. M., Ng, Chun-Laam, Lui, Vincent Chi-Hang, So, Man-ting, Cherny, Stacey S., Sham, Pak-Chung, Tam, Paul Kwong-Hang, Garcia-Barceló, Maria-Mercè
Almmustuhtton 2013Teaksta -
7
Conditional deletion of platelet derived growth factor receptor alpha (Pdgfra) in urorectal mesenchyme causes mesenchyme apoptosis and urorectal developmental anomalies in mice Dahkki Qian, Chen, Wu, Zhongluan, Ng, Roy Chun-Laam, Garcia-Barceló, Maria-Mercè, Yuan, Zheng-Wei, Wong, Kenneth Kak Yuen, Tam, Paul Kwong Hang, Lui, Vincent Chi Hang
Almmustuhtton 2018Teaksta -
8
Genetic Analyses of a Three Generation Family Segregating Hirschsprung Disease and Iris Heterochromia Dahkki Cui, Long, Wong, Emily Hoi-Man, Cheng, Guo, Firmato de Almeida, Manoel, So, Man-Ting, Sham, Pak-Chung, Cherny, Stacey S., Tam, Paul Kwong-Hang, Garcia-Barceló, Maria-Mercè
Almmustuhtton 2013Teaksta -
9
Haplotype Analysis Reveals a Possible Founder Effect of RET Mutation R114H for Hirschsprung's Disease in the Chinese Population Dahkki 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
Almmustuhtton 2010Teaksta -
10
Sacral agenesis: a pilot whole exome sequencing and copy number study Dahkki Porsch, Robert M., Merello, Elisa, De Marco, Patrizia, Cheng, Guo, Rodriguez, Laura, So, Manting, Sham, Pak C., Tam, Paul K., Capra, Valeria, Cherny, Stacey S., Garcia-Barcelo, Maria-Mercè, Campbell, Desmond D.
Almmustuhtton 2016Teaksta -
11
A random forest-based framework for genotyping and accuracy assessment of copy number variations Dahkki 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
Almmustuhtton 2020Teaksta -
12
Uncovering the genetic lesions underlying the most severe form of Hirschsprung disease by whole-genome sequencing Dahkki 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
Almmustuhtton 2018Teaksta -
13
Cancer gene mutations in congenital pulmonary airway malformation patients Dahkki 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
Almmustuhtton 2019Teaksta -
14
Chinese family with diffuse oesophageal leiomyomatosis: a new COL4A5/COL4A6 deletion and a case of gonosomal mosaicism Dahkki 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
Almmustuhtton 2015Teaksta -
15
Genetic study of congenital bile-duct dilatation identifies de novo and inherited variants in functionally related genes Dahkki 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
Almmustuhtton 2016Teaksta -
16
Sequencing of a Chinese tetralogy of Fallot cohort reveals clustering mutations in myogenic heart progenitors Dahkki Tang, Clara Sze Man, Mononen, Mimmi, Lam, Wai-Yee, Jin, Sheng Chih, Zhuang, Xuehan, Garcia-Barcelo, Maria-Mercè, Lin, Qiongfen, Yang, Yujia, Sahara, Makoto, Eroglu, Elif, Chien, Kenneth R., Hong, Haifa, Tam, Paul Kwong Hang, Gruber, Peter J.
Almmustuhtton 2022Teaksta -
17
Whole-genome analysis of noncoding genetic variations identifies multiscale regulatory element perturbations associated with Hirschsprung disease Dahkki 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.
Almmustuhtton 2020Teaksta -
18
AB080. Genetic findings provide insight of biliary atresia patient complexity Dahkki Cheng, Guo, Garcia-Barceló, Maria-Mercè, Chung, Patrick Ho-Yu, Tang, Wai-Kiu, Man Wong, Emily Hoi, Chan, Edwin Kin-Wai, So, Man-Ting, Ngo, Diem Ngoc, Tran, Ngoc Son, Nguyen, Pham Anh Hoa, Sham, Pak-Chung, Cherny, Stacey S., Nicholls, John M., Tam, Paul Kwong-Hang
Almmustuhtton 2015Teaksta -
19
Hedgehog/Notch-induced premature gliogenesis represents a new disease mechanism for Hirschsprung disease in mice and humans Dahkki Ngan, Elly Sau-Wai, Garcia-Barceló, Maria-Mercè, Yip, Benjamin Hon-Kei, Poon, Hiu-Ching, Lau, Sin-Ting, Kwok, Carmen Ka-Man, Sat, Eric, Sham, Mai-Har, Wong, Kenneth Kak-Yuen, Wainwright, Brandon J., Cherny, Stacey S., Hui, Chi-Chung, Sham, Pak Chung, Lui, Vincent Chi-Hang, Tam, Paul Kwong-Hang
Almmustuhtton 2011Teaksta -
20
Functional polymorphisms in the promoter of BRCA1 influences transcription and are associated with decreased risk for breast cancer in Chinese women Dahkki Chan, Kelvin Yuen-Kwong, Liu, Wei, Long, Ji-Rong, Yip, Shea-Ping, Chan, Sum-Yin, Shu, Xiao-Ou, Chua, Daniel Tsin-Tien, Cheung, Annie Nga-Yin, Ching, Johannes Chi-Yun, Cai, Hui, Au, Gordon Kwok-Hung, Chan, Miranda, Foo, William, Ngan, Hextan Yuen-Sheung, Gao, Yu-Tang, Ngan, Elly Sau-Wai, Garcia-Barceló, Maria-Mercè, Zheng, Wei, Khoo, Ui-Soon
Almmustuhtton 2008Teaksta