Xueting Yang

Peking Union Medical College Hospital, Chinese Academy Of Medical Sciences & Peking Union Medical College
Beijing, 100730, China

Last Updated: 09/26/2026

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Found 24 publications

The Asymmetric Threat of Maternal Cell Contamination in Prenatal Single-Gene Testing.

The Asymmetric Threat of Maternal Cell Contamination in Prenatal Single-Gene Testing.

Journal: Diagnostics (Basel, Switzerland)

Published: June 08, 2026

Cell-free DNA screening for sex chromosome aneuploidy in 67,099 pregnancies: A retrospective analysis.

Cell-free DNA screening for sex chromosome aneuploidy in 67,099 pregnancies: A retrospective analysis.

Journal: Journal of medical screening

Published: March 18, 2026

Prenatal diagnosis and estimated penetrance of 15q11.2 BP1-BP2 microdeletion syndrome in a Chinese cohort: a retrospective study and literature review.

Prenatal diagnosis and estimated penetrance of 15q11.2 BP1-BP2 microdeletion syndrome in a Chinese cohort: a retrospective study and literature review.

Journal: Human genomics

Published: March 11, 2026

Development of a High-Throughput Microarray Platform for Rapid, Low-Cost Expanded Carrier Screening.

Development of a High-Throughput Microarray Platform for Rapid, Low-Cost Expanded Carrier Screening.

Journal: Prenatal diagnosis

Published: January 08, 2026

Xq28 duplication not F8 inversion: integrated genetic reanalysis redefines prenatal carrier diagnosis.

Xq28 duplication not F8 inversion: integrated genetic reanalysis redefines prenatal carrier diagnosis.

Journal: Scientific reports

Published: November 17, 2025

A methodological study on the process of prenatal optical genome mapping: focusing on cell culture and quality control.

A methodological study on the process of prenatal optical genome mapping: focusing on cell culture and quality control.

Journal: Molecular cytogenetics

Published: June 24, 2025

Incidental Identification of Potentially Affected Individuals Through Expanded Carrier Screening During Preconception or Early Pregnancy.

Incidental Identification of Potentially Affected Individuals Through Expanded Carrier Screening During Preconception or Early Pregnancy.

Journal: Prenatal diagnosis

Published: April 30, 2025

The clinical utility of systematic reporting of secondary findings in prenatal diagnosis.

The clinical utility of systematic reporting of secondary findings in prenatal diagnosis.

Journal: Genetics in medicine : official journal of the American College of Medical Genetics

Published: April 02, 2025

Complete defect in PA-PLA1α secretion function leading to autosomal recessive woolly hair and hypotrichosis: insights from a novel compound heterozygous LIPH variant study in a Chinese pedigree.

Complete defect in PA-PLA1α secretion function leading to autosomal recessive woolly hair and hypotrichosis: insights from a novel compound heterozygous LIPH variant study in a Chinese pedigree.

Journal: Frontiers in genetics

Published: March 11, 2025

Evaluation of the efficacy of optical genome mapping in prenatal diagnosis: a retrospective cohort study.

Evaluation of the efficacy of optical genome mapping in prenatal diagnosis: a retrospective cohort study.

Journal: Journal of translational medicine

Published: February 10, 2025

The distribution of D4Z4 repeats in China and direct prenatal diagnosis of FSHD by optical genome mapping.

The distribution of D4Z4 repeats in China and direct prenatal diagnosis of FSHD by optical genome mapping.

Journal: Orphanet journal of rare diseases

Published: December 23, 2024

Genetic Diagnosis and Clinical Features of Fetuses With Congenital Diaphragmatic Hernia.

Genetic Diagnosis and Clinical Features of Fetuses With Congenital Diaphragmatic Hernia.

Journal: Prenatal diagnosis

Published: July 22, 2024

Showing 1-12 of 24

Last Updated: 09/26/2026