Revealing parental mosaicism: the hidden answer to the recurrence of apparent de novo variants

por Lee, Mianne, Lui, Adrian C. Y., Chan, Joshua C. K., Doong, Phoenix H. L., Kwong, Anna K. Y., Mak, Christopher C. Y., Li, Raymond H. W., Kan, Anita S. Y., Chung, Brian H. Y.
Publicado 2023

Human placental exosomes induce maternal systemic immune tolerance by reprogramming circulating monocytes

por Bai, Kunfeng, Lee, Cheuk-Lun, Liu, Xiaofeng, Li, Jianlin, Cao, Dandan, Zhang, Li, Hu, Duanlin, Li, Hong, Hou, Yanqing, Xu, Yue, Kan, Anita S. Y., Cheung, Ka-Wang, Ng, Ernest H. Y., Yeung, William S. B., Chiu, Philip C. N.
Publicado 2022

Whole-Genome Array CGH Evaluation for Replacing Prenatal Karyotyping in Hong Kong

por Kan, Anita S. Y., Lau, Elizabeth T., Tang, W. F., Chan, Sario S. Y., Ding, Simon C. K., Chan, Kelvin Y. K., Lee, C. P., Hui, Pui Wah, Chung, Brian H. Y., Leung, K. Y., Ma, Teresa, Leung, Wing C., Tang, Mary H. Y.
Publicado 2014

Diagnostic potential of the amniotic fluid cells transcriptome in deciphering mendelian disease: a proof-of-concept

por Lee, Mianne, Kwong, Anna K. Y., Chui, Martin M. C., Chau, Jeffrey F. T., Mak, Christopher C. Y., Au, Sandy L. K., Lo, Hei Man, Chan, Kelvin Y. K., Yépez, Vicente A., Gagneur, Julien, Kan, Anita S. Y., Chung, Brian H. Y.
Publicado 2022

The Clinical Impact of Chromosomal Microarray on Paediatric Care in Hong Kong

por Tao, Victoria Q., Chan, Kelvin Y. K., Chu, Yoyo W. Y., Mok, Gary T. K., Tan, Tiong Y., Yang, Wanling, Lee, So Lun, Tang, Wing Fai, Tso, Winnie W. Y., Lau, Elizabeth T., Kan, Anita S. Y., Tang, Mary H., Lau, Yu-lung, Chung, Brian H. Y.
Publicado 2014

Dysregulation of the CD147 complex confers defective placental development: A pathogenesis of early‐onset preeclampsia

por Lee, Cheuk‐Lun, Chen, Zhilong, Zhang, Qingqing, Guo, Yue, Ng, Vivian W.Y., Zhang, Baozhen, Bai, Kunfeng, Ruan, Degong, Kan, Anita S.Y., Cheung, Ka‐Wang, Mak, Annisa S.L., Yeung, William S.B., Su, Rui, Yang, Qing, Chen, Min, Du, Mei‐Rong, Jian, Zhang, Fan, Xiujun, Chiu, Philip C.N.
Publicado 2022

Identifying the genetic causes for prenatally diagnosed structural congenital anomalies (SCAs) by whole-exome sequencing (WES)

por Leung, Gordon K C, Mak, Christopher C Y, Fung, Jasmine L F, Wong, Wilfred H S, Tsang, Mandy H Y, Yu, Mullin H C, Pei, Steven L C, Yeung, K S, Mok, Gary T K, Lee, C P, Hui, Amelia P W, Tang, Mary H Y, Chan, Kelvin Y K, Liu, Anthony P Y, Yang, Wanling, Sham, P C, Kan, Anita S Y, Chung, Brian H Y
Publicado 2018

The KLHL40 c.1516A>C is a Chinese‐specific founder mutation causing nemaline myopathy 8: Report of six patients with pre‐ and postnatal phenotypes

por Yeung, Kit San, Yu, Florrie N. Y., Fung, Cheuk Wing, Wong, Sheila, Lee, Hencher H. C., Fung, Sharon T. H., Fung, Genevieve P. G., Leung, Kwok Yin, Chung, Wai Hang, Lee, Yun Ting, Ng, Vivian K. S., Yu, Mullin H. C., Fung, Jasmine L. F., Tsang, Mandy H. Y., Chan, Kelvin Y. K., Chan, Sophelia H. S., Kan, Anita S. Y., Chung, Brian H. Y.
Publicado 2020

Adrenomedullin has a pivotal role in trophoblast differentiation: A promising nanotechnology-based therapeutic target for early-onset preeclampsia

por Zhang, Qingqing, Lee, Cheuk-Lun, Yang, Tingyu, Li, Jianlin, Zeng, Qunxiong, Liu, Xiaofeng, Liu, Zhongzhen, Ruan, Degong, Li, Zhuoxuan, Kan, Anita S. Y., Cheung, Ka-Wang, Mak, Annisa S. L., Ng, Vivian W. Y., Zhao, Huashan, Fan, Xiujun, Duan, Yong-Gang, Zhong, Liuying, Chen, Min, Du, Meirong, Li, Raymond H. W., Liu, Pengtao, Ng, Ernest H. Y., Yeung, William S. B., Gao, Ya, Yao, Yuanqing, Chiu, Philip C. N.
Publicado 2023