Anita Sik Yau Kan (Anita S Y Kan)

Publication Activity (10 Years)

Years Active: 2018-2024
Publications (10 Years): 15

Top Topics

Dna Methylation

Platelet Rich Plasma

Top Venues

NPJ genomic medicine

American journal of medical genetics. Part A

Healthcare (Basel, Switzerland)

Science advances

This page only lists publications with an associated author ORCID identifier.

Publications

Stephanie K L Ho, Samuel Y L Ng, Tsz-Kwai Yung, Myth T S Mok, Wing-Chung Yiu, Hiu Yee Heidi Cheng, Shirley S W Cheng, Ho-Ming Luk, Ivan F M Lo, Anita Sik Yau Kan
Clinical and molecular characteristics of hemophilia A affected individuals and carriers: A 24 years experience from three centers. American journal of medical genetics. Part A 194 (9) (2024)
Stephanie K L Ho, Samuel Y L Ng, Tsz-Kwai Yung, Myth T S Mok, Wing-Chung Yiu, Hiu Yee Heidi Cheng, Shirley S W Cheng, Ho-Ming Luk, Ivan F M Lo, Anita Sik Yau Kan
Clinical and molecular characteristics of hemophilia A affected individuals and carriers: A 24 years experience from three centers. American journal of medical genetics. Part A 194 (9) (2024)
Stephanie K L Ho, Samuel Y L Ng, Tsz-Kwai Yung, Myth T S Mok, Wing-Chung Yiu, Hiu Yee Heidi Cheng, Shirley S W Cheng, Ho-Ming Luk, Ivan F M Lo, Anita Sik Yau Kan
Clinical and molecular characteristics of hemophilia A affected individuals and carriers: A 24 years experience from three centers. American journal of medical genetics. Part A (2024)
Qingqing Zhang, Cheuk-Lun Lee, Tingyu Yang, Jianlin Li, Qunxiong Zeng, Xiaofeng Liu, Zhongzhen Liu, Degong Ruan, Zhuoxuan Li, Anita Sik Yau Kan, Ka-Wang Cheung, Annisa S L Mak, Vivian Wai-Yan Ng, Huashan Zhao, Xiujun Fan, Yong-Gang Duan, Liuying Zhong, Min Chen, Mei-Rong Du, Hang Wun Raymond Li, Pengtao Liu, Ernest Hung Yu Ng, William Shu Biu Yeung, Ya Gao, Yuanqing Yao, Philip C N Chiu
Adrenomedullin has a pivotal role in trophoblast differentiation: A promising nanotechnology-based therapeutic target for early-onset preeclampsia. Science advances 9 (44) (2023)
Mianne Lee, Anna K Y Kwong, Martin Man Chun Chui, Jeffrey F T Chau, Christopher Chun Yu Mak, Sandy L K Au, Hei Man Lo, Kelvin Y K Chan, Vicente A Yépez, Julien Gagneur, Anita Sik Yau Kan, Brian Hon-Yin Chung
Diagnostic potential of the amniotic fluid cells transcriptome in deciphering mendelian disease: a proof-of-concept. NPJ genomic medicine 7 (1) (2022)
Theodora Hei Tung Lai, Leung Kuen Sandy Au, Yuen Ting Eunice Lau, Hei Man Lo, Kelvin Yuen Kwong Chan, Ka Wang Cheung, Teresa Wei Ling Ma, Wing Cheong Leung, Choi Wah Kong, Wendy Shu, Po Lam So, Anna Ka Yee Kwong, Christopher Chun Yu Mak, Brian Hon-Yin Chung, Martin Man Chun Chui, Brian Hon Yin Chung, Anita Sik Yau Kan
Application of Prenatal Whole Exome Sequencing for Structural Congenital Anomalies-Experience from a Local Prenatal Diagnostic Laboratory. Healthcare (Basel, Switzerland) 10 (12) (2022)
Mianne Lee, Anna K Y Kwong, Martin Man Chun Chui, Jeffrey F T Chau, Christopher Chun Yu Mak, Sandy L K Au, Hei Man Lo, Kelvin Y K Chan, Vicente A Yépez, Julien Gagneur, Anita Sik Yau Kan, Brian Hon-Yin Chung
Diagnostic potential of the amniotic fluid cells transcriptome in deciphering mendelian disease: a proof-of-concept. NPJ genomic medicine 7 (1) (2022)
Pui Tak Yu, Wendy Shu, Sau-Lan Mok, Pui-Wah Hui, Lin-Wai Chan, Ka-Yin Kwok, Kelvin Yuen Kwong Chan, Tsz-Kin Lo, Brian Hon-Yin Chung, Ho-Ming Luk, Anita Sik Yau Kan
Prenatal presentation in two fetuses with features of Beckwith Wiedemann syndrome-An unexpected diagnosis of androgenetic chimera and its clinical implications. American journal of medical genetics. Part A 188 (5) (2022)
Jeffrey Fong Ting Chau, Mullin Ho Chung Yu, Martin Man Chun Chui, Cyrus Chun Wing Yeung, Aaron Wing Cheung Kwok, Xuehan Zhuang, Ryan Lee, Jasmine Lee Fong Fung, Mianne Lee, Christopher Chun Yu Mak, Nicole Ying Ting Ng, Claudia Ching Yan Chung, Marcus Chun Yin Chan, Mandy Ho Yin Tsang, Joshua Chun Ki Chan, Kelvin Yuen Kwong Chan, Anita Sik Yau Kan, Patrick Ho Yu Chung, Wanling Yang, So Lun Lee, Godfrey Chi Fung Chan, Paul Kwong Hang Tam, Yu Lung Lau, Kit San Yeung, Brian Hon-Yin Chung, Clara Sze Man Tang
Comprehensive analysis of recessive carrier status using exome and genome sequencing data in 1543 Southern Chinese. NPJ genomic medicine 7 (1) (2022)
Mianne Lee, Anna K Y Kwong, Martin Man Chun Chui, Jeffrey F T Chau, Christopher Chun Yu Mak, Sandy L K Au, Hei Man Lo, Kelvin Y K Chan, Vicente A Yépez, Julien Gagneur, Anita Sik Yau Kan, Brian Hon-Yin Chung
Diagnostic potential of the amniotic fluid cells transcriptome in deciphering mendelian disease: a proof-of-concept. NPJ genomic medicine 7 (1) (2022)
Theodora Hei Tung Lai, Leung Kuen Sandy Au, Yuen Ting Eunice Lau, Hei Man Lo, Kelvin Yuen Kwong Chan, Ka Wang Cheung, Teresa Wei Ling Ma, Wing Cheong Leung, Choi Wah Kong, Wendy Shu, Po Lam So, Anna Ka Yee Kwong, Christopher Chun Yu Mak, Brian Hon-Yin Chung, Martin Man Chun Chui, Brian Hon Yin Chung, Anita Sik Yau Kan
Application of Prenatal Whole Exome Sequencing for Structural Congenital Anomalies-Experience from a Local Prenatal Diagnostic Laboratory. Healthcare (Basel, Switzerland) 10 (12) (2022)
Wendy Shu, Shirley S W Cheng, Shuwen Xue, Lin Wai Chan, Sung Inda Soong, Anita Sik Yau Kan, Sunny Wai Hung Cheung, Kwong Wai Choy
First Case Report of Maternal Mosaic Tetrasomy 9p Incidentally Detected on Non-Invasive Prenatal Testing. Genes 12 (3) (2021)
Vivian Kwun Sin Ng, Tze Kin Lau, Anita Sik Yau Kan, Brian Hon Yin Chung, Ho Ming Luk, Wai Fu Ng, Mengmeng Shi, Kwong Wai Choy, Ye Cao, Wing Cheong Leung
A Fetus with Congenital Microcephaly, Microphthalmia and Cataract Was Detected with Biallelic Variants in the OCLN Gene: A Case Report. Diagnostics (Basel, Switzerland) 11 (9) (2021)
Florrie N Y Yu, Elizabeth Y Y Li, Meliza C W Kong, Teresa W L Ma, Kelvin Y K Chan, Elim Man, Brian Hon-Yin Chung, Anita Sik Yau Kan
Increasing prenatal diagnosis of chimeras with the use of noninvasive prenatal screening: Report of two cases. Prenatal diagnosis 41 (6) (2021)
Anita Sik Yau Kan, Elizabeth Tak Kwong Lau, Chun Hong So, Wan Pang Chan, Wing Cheuk Wong, Kam Cheong Lee, Mark D Pertile, Mary Hoi Yin Tang
A fetus coexisting with a complete hydatidiform mole with trisomy 9 of maternal origin. The journal of obstetrics and gynaecology research 44 (5) (2018)