Xiuqing Ji
Nanjing, China
Last Updated: 09/26/2026
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Found 20 publications
Integrating Optical Genome Mapping With Conventional Methods in Families Seeking Genetic Counseling.
Integrating Optical Genome Mapping With Conventional Methods in Families Seeking Genetic Counseling.
Journal: Prenatal diagnosis
Published: September 02, 2025
From iPSCs to myotubes: Identifying potential biomarkers for human FSHD by single-cell transcriptomics.
Journal: Clinical and translational medicine
Published: April 07, 2025
Optical Genome Mapping for Prenatal Diagnosis in Fetuses With Structural Anomalies.
Journal: Prenatal diagnosis
Published: January 17, 2025
Long read Nanopore sequencing identifies precise breakpoints of a de novo paracentric inversion that disrupt the MEIS2 gene in a Chinese girl with syndromic developmental delay.
Journal: BMC pediatrics
Published: August 23, 2024
Optical Genome Mapping for Chromosomal Aberrations Detection-False-Negative Results and Contributing Factors.
Journal: Diagnostics (Basel, Switzerland)
Published: December 06, 2023
Prenatal diagnosis of chromosomal abnormalities using optical genome mapping vs chromosomal microarray.
Journal: American journal of obstetrics and gynecology
Published: August 17, 2023
Optical genome mapping for detection of chromosomal aberrations in prenatal diagnosis.
Journal: Acta obstetricia et gynecologica Scandinavica
Published: March 28, 2023
11q13.3q13.4 deletion plus 9q21.13q21.33 duplication in an affected girl arising from a familial four-way balanced chromosomal translocation.
Journal: Molecular genetics & genomic medicine
Published: January 17, 2023
Current attitudes and preconceptions towards expanded carrier screening in the Eastern Chinese reproductive-aged population.
Journal: Journal of assisted reproduction and genetics
Published: September 03, 2020
Prenatal Diagnosis of Recurrent Distal 1q21.1 Duplication in Three Fetuses With Ultrasound Anomalies.
Journal: Frontiers in genetics
Published: April 20, 2018
Prenatal diagnosis of sex chromosome mosaicism with two marker chromosomes in three cell lines and a review of the literature.
Journal: Molecular medicine reports
Published: March 31, 2018
Perinatal outcomes following cell-free DNA screening in >32 000 women: Clinical follow-up data from a single tertiary center.
Journal: Prenatal diagnosis
Published: March 14, 2018
Last Updated: 09/26/2026