Xiangyi Y. Jing

No. 9 Jinsui Road
Guangzhou, 510623, China

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 49 publications

Genetic architecture and prognostic significance of suspected fetal microcephaly: evidence from prenatal exome sequencing in a large prospective cohort.

Genetic architecture and prognostic significance of suspected fetal microcephaly: evidence from prenatal exome sequencing in a large prospective cohort.

Journal: Human genomics

Published: August 30, 2025

Prenatal diagnosis and perinatal outcomes of fetuses with congenital duodenal obstruction: A nine-year retrospective study from China.

Prenatal diagnosis and perinatal outcomes of fetuses with congenital duodenal obstruction: A nine-year retrospective study from China.

Journal: Acta obstetricia et gynecologica Scandinavica

Published: March 10, 2025

Prenatal Exome Sequencing for Fetal Macrocephaly: A Large Prospective Observational Cohort Study.

Prenatal Exome Sequencing for Fetal Macrocephaly: A Large Prospective Observational Cohort Study.

Journal: Prenatal diagnosis

Published: February 12, 2025

Prenatal diagnosis of 17q12 copy number variants in fetuses via chromosomal microarray analysis - A retrospective cohort study and literature review.

Prenatal diagnosis of 17q12 copy number variants in fetuses via chromosomal microarray analysis - A retrospective cohort study and literature review.

Journal: Heliyon

Published: April 14, 2024

PDIA2 variant associated with vitiligo.

PDIA2 variant associated with vitiligo.

Journal: Skin health and disease

Published: October 06, 2023

Prenatal diagnosis and outcomes in fetuses with duplex kidney.

Prenatal diagnosis and outcomes in fetuses with duplex kidney.

Journal: International journal of gynaecology and obstetrics: the official organ of the International Federation of Gynaecology and Obstetrics

Published: September 28, 2023

Prenatal diagnosis in fetal right aortic arch using chromosomal microarray analysis and whole exome sequencing: a Chinese single-center retrospective study.

Prenatal diagnosis in fetal right aortic arch using chromosomal microarray analysis and whole exome sequencing: a Chinese single-center retrospective study.

Journal: Molecular cytogenetics

Published: August 21, 2023

Prenatal diagnosis of polycystic renal diseases: diagnostic yield, novel disease-causing variants, and genotype-phenotype correlations.

Prenatal diagnosis of polycystic renal diseases: diagnostic yield, novel disease-causing variants, and genotype-phenotype correlations.

Journal: American journal of obstetrics & gynecology MFM

Published: August 06, 2023

Variant spectrum of F8 and F9 in hemophilia patients from southern China and 26 novel variants.

Variant spectrum of F8 and F9 in hemophilia patients from southern China and 26 novel variants.

Journal: Frontiers in genetics

Published: July 06, 2023

Association of prenatal thoracic ultrasound abnormalities with copy number variants at a single Chinese tertiary center.

Association of prenatal thoracic ultrasound abnormalities with copy number variants at a single Chinese tertiary center.

Journal: International journal of gynaecology and obstetrics: the official organ of the International Federation of Gynaecology and Obstetrics

Published: May 27, 2023

A Deep-Learning-Based Method Can Detect Both Common and Rare Genetic Disorders in Fetal Ultrasound.

A Deep-Learning-Based Method Can Detect Both Common and Rare Genetic Disorders in Fetal Ultrasound.

Journal: Biomedicines

Published: May 09, 2023

Prenatal diagnosis of ultrasound soft markers in a single medical center of mainland China.

Prenatal diagnosis of ultrasound soft markers in a single medical center of mainland China.

Journal: Molecular cytogenetics

Published: October 12, 2022

Showing 1-12 of 49

Last Updated: 09/26/2026