Anita Y. Kan

Room 314, 3/F, 30 Hospital Road
Sai Ying Pun, HCW, Hong Kong Special Administrative Region

Last Updated: 09/26/2026

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Found 49 publications

Long-surviving Neu-Laxova syndrome confirmed by whole exome sequencing: a case report.

Long-surviving Neu-Laxova syndrome confirmed by whole exome sequencing: a case report.

Journal: Hong Kong medical journal = Xianggang yi xue za zhi

Published: May 29, 2024

Clinical and molecular characteristics of hemophilia A affected individuals and carriers: A 24 years experience from three centers.

Clinical and molecular characteristics of hemophilia A affected individuals and carriers: A 24 years experience from three centers.

Journal: American journal of medical genetics. Part A

Published: March 13, 2024

The incremental yield of prenatal exome sequencing over chromosome microarray for congenital heart abnormalities: A systematic review and meta-analysis.

The incremental yield of prenatal exome sequencing over chromosome microarray for congenital heart abnormalities: A systematic review and meta-analysis.

Journal: Prenatal diagnosis

Published: December 11, 2023

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

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

Journal: Science advances

Published: November 03, 2023

Prenatal diagnosis of Myhre syndrome with a heterozygous pathogenic variant in SMAD4 gene presented with thick nuchal translucency and cardiac abnormalities.

Prenatal diagnosis of Myhre syndrome with a heterozygous pathogenic variant in SMAD4 gene presented with thick nuchal translucency and cardiac abnormalities.

Journal: Prenatal diagnosis

Published: April 28, 2023

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

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

Journal: Human genomics

Published: February 02, 2023

Application of Prenatal Whole Exome Sequencing for Structural Congenital Anomalies-Experience from a Local Prenatal Diagnostic Laboratory.

Application of Prenatal Whole Exome Sequencing for Structural Congenital Anomalies-Experience from a Local Prenatal Diagnostic Laboratory.

Journal: Healthcare (Basel, Switzerland)

Published: October 27, 2022

Implementation of Public Funded Genome Sequencing in Evaluation of Fetal Structural Anomalies.

Implementation of Public Funded Genome Sequencing in Evaluation of Fetal Structural Anomalies.

Journal: Genes

Published: October 25, 2022

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

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

Journal: NPJ genomic medicine

Published: June 28, 2022

Analytical validity and clinical utility of whole-genome sequencing for cytogenetically balanced chromosomal abnormalities in prenatal diagnosis: abridged secondary publication.

Analytical validity and clinical utility of whole-genome sequencing for cytogenetically balanced chromosomal abnormalities in prenatal diagnosis: abridged secondary publication.

Journal: Hong Kong medical journal = Xianggang yi xue za zhi

Published: March 09, 2022

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

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

Journal: Clinical and translational medicine

Published: February 06, 2022

Aberrant phase separation and nucleolar dysfunction in rare genetic diseases.

Aberrant phase separation and nucleolar dysfunction in rare genetic diseases.

Journal: Nature

Published: November 09, 2021

Showing 1-12 of 49

Last Updated: 09/26/2026