Dysregulation of the CD147 complex confers defective placental development: A pathogenesis of early‐onset preeclampsia
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.
Published in Clinical and translational medicine (01.06.2022)
Published in Clinical and translational medicine (01.06.2022)
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Under-recognition of 22q11.2 deletion in adult Chinese patients with conotruncal anomalies: Implications in transitional care
Liu, Anthony P.Y, Chow, Pak-Cheong, Lee, Pamela P.W, Mok, Gary T.K, Tang, Wing-Fai, Lau, Elizabeth T, Lam, Stephen T.S, Chan, Kelvin Y, Kan, Anita S.Y, Chau, Adolphus K.T, Cheung, Yiu-Fai, Lau, Yu-Lung, Chung, Brian H.Y
Published in European journal of medical genetics (01.05.2014)
Published in European journal of medical genetics (01.05.2014)
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A prenatal case of split-hand malformation associated with 17p13.3 triplication – A dilemma in genetic counseling
Luk, H.M, Wong, Vincent C.H, Lo, Ivan F.M, Chan, Kelvin Y.K, Lau, Elizabeth T, Kan, Anita S.Y, Tang, Mary H.Y, Tang, W.F, She, Wandy M.K, Chu, Yoyo W.Y, Sin, W.K, Chung, Brian H.Y
Published in European journal of medical genetics (01.02.2014)
Published in European journal of medical genetics (01.02.2014)
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Journal Article
Clinical and molecular characteristics of hemophilia A affected individuals and carriers: A 24 years experience from three centers
Ho, Stephanie K. L., Ng, Samuel Y. L., Yung, Tsz‐Kwai, Mok, Myth T. S., Yiu, Wing‐Chung, Cheng, Heidi H. Y., Cheng, Shirley S. W., Luk, Ho‐ming, Lo, Ivan F. M., Kan, Anita S. Y.
Published in American journal of medical genetics. Part A (01.09.2024)
Published in American journal of medical genetics. Part A (01.09.2024)
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Journal Article
Experience of chromosomal microarray applied in prenatal and postnatal settings in Hong Kong
Cheng, Shirley S. W., Chan, Kelvin Y. K., Leung, Kelphen K. P., Au, Patrick K. C., Tam, Wai‐Keung, Li, Samuel K. M., Luk, Ho‐Ming, Kan, Anita S. Y., Chung, Brian H. Y., Lo, Ivan F. M., Tang, Mary H. Y.
Published in American journal of medical genetics. Part C, Seminars in medical genetics (01.06.2019)
Published in American journal of medical genetics. Part C, Seminars in medical genetics (01.06.2019)
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Journal Article
Human placental exosomes induce maternal systemic immune tolerance by reprogramming circulating monocytes
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
Published in Journal of nanobiotechnology (18.02.2022)
Published in Journal of nanobiotechnology (18.02.2022)
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Optimal timing of hepatitis B virus DNA quantification and clinical predictors for higher viral load during pregnancy
Cheung, Ka W., Seto, Mimi T. Y., So, Po L., Wong, Daniel, Mak, Annisa S. L., Lau, Wai L., Wang, Weilan, Kan, Anita S. Y., Lee, Chin P., Ng, Ernest H. Y.
Published in Acta obstetricia et gynecologica Scandinavica (01.10.2019)
Published in Acta obstetricia et gynecologica Scandinavica (01.10.2019)
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Prenatal presentation in two fetuses with features of Beckwith Wiedemann syndrome—An unexpected diagnosis of androgenetic chimera and its clinical implications
Yu, Pui‐Tak, Shu, Wendy, Mok, Sau‐Lan, Hui, Pui‐Wah, Chan, Lin‐Wai, Kwok, Ka‐Yin, Chan, Kelvin Y. K., Lo, Tsz‐Kin, Chung, Brian H. Y., Luk, Ho‐Ming, Kan, Anita S. Y.
Published in American journal of medical genetics. Part A (01.05.2022)
Published in American journal of medical genetics. Part A (01.05.2022)
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Journal Article
Increasing prenatal diagnosis of chimeras with the use of noninvasive prenatal screening: Report of two cases
Yu, Florrie N. Y., Li, Elizabeth Y. Y., Kong, Meliza C. W., Ma, Teresa W. L., Chan, Kelvin Y. K., Man, Elim, Chung, Brian H. Y., Kan, Anita S. Y.
Published in Prenatal diagnosis (01.05.2021)
Published in Prenatal diagnosis (01.05.2021)
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Journal Article
Revealing parental mosaicism: the hidden answer to the recurrence of apparent de novo variants
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.
Published in Human genomics (05.10.2023)
Published in Human genomics (05.10.2023)
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Identifying the genetic causes for prenatally diagnosed structural congenital anomalies (SCAs) by whole-exome sequencing (WES)
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
Published in BMC medical genomics (25.10.2018)
Published in BMC medical genomics (25.10.2018)
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Journal Article
Whole-genome array CGH evaluation for replacing prenatal karyotyping in Hong Kong
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
Published in PloS one (05.02.2014)
Published in PloS one (05.02.2014)
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Adrenomedullin has a pivotal role in trophoblast differentiation: A promising nanotechnology-based therapeutic target for early-onset preeclampsia
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.
Published in Science advances (03.11.2023)
Published in Science advances (03.11.2023)
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Diagnostic potential of the amniotic fluid cells transcriptome in deciphering mendelian disease: a proof-of-concept
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
Published in Npj genomic medicine (28.12.2022)
Published in Npj genomic medicine (28.12.2022)
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The clinical impact of chromosomal microarray on paediatric care in Hong Kong
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
Published in PloS one (15.10.2014)
Published in PloS one (15.10.2014)
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Journal Article
The KLHL40 c.1516A>C is a Chinese‐specific founder mutation causing nemaline myopathy 8: Report of six patients with pre‐ and postnatal phenotypes
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.
Published in Molecular genetics & genomic medicine (01.07.2020)
Published in Molecular genetics & genomic medicine (01.07.2020)
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First Report of a Novel Deletion Due to εγδβ-Thalassemia in a Chinese Family
Hui, Annie S. Y., Au, Patrick K. C., Ting, Yuen-Ha, Kan, Anita S. Y., Cheng, Yvonne K. Y., Leung, Alex W. K., Chan, Kelvin Y. K., Li, Chi-Kong, Tang, Mary H. Y., Leung, Tak-Yeung
Published in Hemoglobin (04.05.2017)
Published in Hemoglobin (04.05.2017)
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An Unusual Hydrops Fetalis Associated with Compound Heterozygosity for Krüppel-like Factor 1 mutations
Lee, Helena H. L., Mak, Annisa S. L., Kou, K. O., Poon, C. F., Wong, W. S., Chiu, K. H., Au, Patrick K. C., Chan, Kelvin Y. K., Kan, Anita S. Y., Tang, Mary H. Y., Leung, K. Y.
Published in Hemoglobin (01.11.2016)
Published in Hemoglobin (01.11.2016)
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