Gefei Xiao
Zhuhai, China
Last Updated: 09/26/2026
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Found 11 publications
A Hereditary Pulmonary Alveolar Proteinosis Caused by a Novel Hemizygous Variation of the CSF2RA Gene Case Report and Literature Review.
Journal: Molecular genetics & genomic medicine
Published: May 24, 2025
Early prediction of preeclampsia from clinical, multi-omics and laboratory data using random forest model.
Journal: BMC pregnancy and childbirth
Published: January 14, 2025
Predicting preeclampsia in early pregnancy using clinical and laboratory data via machine learning model.
Journal: BMC medical informatics and decision making
Published: January 06, 2025
Cell-free DNA fragmentomics for preeclampsia risk assessment.
Journal: Nature communications
Published: January 21, 2024
Application of various genetic analysis techniques for detecting two rare cases of 9p duplication mosaicism during prenatal diagnosis.
Journal: Molecular genetics & genomic medicine
Published: September 15, 2022
Prenatal diagnosis of a 4.5-Mb deletion at chromosome 4q35.1q35.2: Case report and literature review.
Journal: Molecular cytogenetics
Published: October 21, 2021
Health economic evaluation of noninvasive prenatal testing and serum screening for down syndrome.
Journal: PloS one
Published: April 05, 2021
Application of various genetic techniques for the diagnosis of Prader-Willi syndrome
Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: August 08, 2020
Genetic analysis of a fetus with partial 18p tetraploidy syndrome
Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: October 10, 2018
Association of GPER gene polymorphism with social function of children with attention deficit hyperactivity disorder
Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: August 12, 2018
Showing 1-11 of 11
Last Updated: 09/26/2026