Zirui N. Dong
Shenzhen, China
Last Updated: 09/26/2026
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Found 36 publications
Characterization of rare genomic structural variants across 2,981 genomes reveals significant involvements in recessive conditions.
Journal: Science China. Life sciences
Published: January 15, 2026
TEDD 2.0: an advanced temporal gene expression database enabled by in-silico functional analyses for developmental mechanism investigation.
Journal: Science China. Life sciences
Published: July 26, 2025
Clinical validation of artificial intelligence-assisted karyotyping on peripheral blood in a cytogenetic diagnostic laboratory.
Journal: Human genetics
Published: June 21, 2025
3D visualization of uterus and ovary: tissue clearing techniques and biomedical applications.
Journal: Frontiers in bioengineering and biotechnology
Published: April 12, 2025
Detection of genomic variants by genome sequencing in foetuses with central nervous system abnormalities.
Journal: Annals of medicine
Published: September 06, 2024
Genome sequencing in the prenatal diagnosis of structural malformations in the fetus.
Journal: Best practice & research. Clinical obstetrics & gynaecology
Published: June 05, 2024
Contribution of Genomic Imbalance in Prenatal Congenital Anomalies of the Kidney and Urinary Tract: A Multi-Center Cohort Study.
Journal: Prenatal diagnosis
Published: September 29, 2023
Identification of cryptic balanced translocations in couples with unexplained recurrent pregnancy loss based upon embryonic PGT-A results.
Journal: Journal of assisted reproduction and genetics
Published: September 11, 2023
Incremental yield of whole-genome sequencing over chromosomal microarray analysis and exome sequencing for congenital anomalies in prenatal period and infancy: systematic review and meta-analysis.
Journal: Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology
Published: June 30, 2023
Low-Pass Genome Sequencing-Based Detection of Paternity: Validation in Clinical Cytogenetics.
Journal: Genes
Published: May 12, 2023
A pilot investigation of low-pass genome sequencing identifying site-specific variation in chromosomal mosaicisms by a multiple site sampling approach in first-trimester miscarriages.
Journal: Human reproduction (Oxford, England)
Published: February 02, 2023
Last Updated: 09/26/2026