Yanqiu Liu
Nanchang, China
Last Updated: 09/26/2026
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Found 48 publications
Chromosomal structural abnormalities and tissue-specific mosaicism: insights into false-negative noninvasive prenatal testing.
Journal: Frontiers in genetics
Published: April 02, 2026
Identification of EVC variants and the preimplantation genetic testing in a Chinese family.
Journal: Frontiers in medicine
Published: January 29, 2026
Integrating genome and RNA sequencing to enhance diagnostic precision in cerebral palsy.
Journal: BMC pediatrics
Published: January 23, 2026
A retrospective study for the diagnostic value of chromosomal microarray analysis in fetuses with high-risk prenatal indications.
Journal: Frontiers in genetics
Published: June 18, 2025
A novel splicing variant in TECTA associated with prelingual autosomal dominant nonsyndromic hearing loss via dominant-negative effect.
Journal: Human molecular genetics
Published: April 02, 2025
Molecular Characterization of Complex Thalassemia with Multiple Variants in β-Globin Gene Cluster and the Identification of a Novel Structural Rearrangement in γ-Globin Gene.
Journal: Hemoglobin
Published: March 27, 2025
Identification of novel COL4A5 variants and prenatal diagnosis in three large families.
Journal: Scientific reports
Published: January 16, 2025
Molecular Identification and the Hematological Findings of Four Novel Variants in Globin Genes in Jiangxi Province of Southern China.
Journal: Hemoglobin
Published: December 11, 2024
Clinical experience of the expanded carrier screening for recessive genetic diseases in a large cohort study in Southern central China.
Journal: Scientific reports
Published: December 11, 2024
Application of family whole-exome sequencing for prenatal diagnosis-an analysis of 357 cases.
Journal: Frontiers in medicine
Published: November 18, 2024
Exploring the correlation between homocysteine, red blood cell folate and MTHFRC677T genotypes with female infertility.
Journal: Biomarkers in medicine
Published: September 10, 2024
Clinical application of polar body-based preimplantation genetic testing for maternal mutations in women with a limited number of oocytes.
Journal: Orphanet journal of rare diseases
Published: April 18, 2024
Last Updated: 09/26/2026