Anita Sik-Yau Kan

11PUBLICATIONS
38CO-AUTHORS
NeonatologyHaematologyFoetal development and medicineGene expression (incl. microarray and other genome-wide approaches)Gene mapping
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Publications (11)

|Jul 12, 2025
Prenatal Phenotype in a Neonate with Prader-Willi Syndrome and Literature Review.

Libing Luo, Mary Hoi Yin Tang, Shengmou Lin

|May 15, 2024
Clinical and molecular characteristics of hemophilia A affected individuals and carriers: A 24 years experience from three centers.

Stephanie K L Ho, Samuel Y L Ng, Tsz-Kwai Yung

|Nov 03, 2023
Adrenomedullin has a pivotal role in trophoblast differentiation: A promising nanotechnology-based therapeutic target for early-onset preeclampsia.

Qingqing Zhang, Cheuk-Lun Lee, Tingyu Yang

|Dec 28, 2022
Diagnostic potential of the amniotic fluid cells transcriptome in deciphering mendelian disease: a proof-of-concept.

Mianne Lee, Anna K Y Kwong, Martin M C Chui

|Dec 23, 2022
Application of Prenatal Whole Exome Sequencing for Structural Congenital Anomalies-Experience from a Local Prenatal Diagnostic Laboratory.

Theodora Hei Tung Lai, Leung Kuen Sandy Au, Yuen Ting Eunice Lau

|Mar 22, 2022
Comprehensive analysis of recessive carrier status using exome and genome sequencing data in 1543 Southern Chinese.

Jeffrey Fong Ting Chau, Mullin Ho Chung Yu, Martin Man Chun Chui

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Frequent Collaborators

4 joint publications

Brian Hon Yin Chung

2 joint publications

Kelvin Yuen Kwong Chan

2 joint publications

Martin Man Chun Chui

2 joint publications

Christopher Chun Yu Mak