Jiansheng Zhu

Hefei, China

Last Updated: 09/26/2026

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Found 20 publications

Polydactyly and syndactyly in a Chinese family with Floating-Harbor syndrome: an expansion of the clinical phenotype.

Polydactyly and syndactyly in a Chinese family with Floating-Harbor syndrome: an expansion of the clinical phenotype.

Journal: Frontiers in genetics

Published: December 06, 2025

Application of chromosomal microarray analysis and trio whole-exome sequencing in first-trimester prenatal diagnosis for high-risk pregnancies.

Application of chromosomal microarray analysis and trio whole-exome sequencing in first-trimester prenatal diagnosis for high-risk pregnancies.

Journal: BMC pregnancy and childbirth

Published: August 18, 2025

Beyond carrier frequency: a preliminary multicenter study of simultaneous couple-based comprehensive carrier screening for common and rare genetic disorders.

Beyond carrier frequency: a preliminary multicenter study of simultaneous couple-based comprehensive carrier screening for common and rare genetic disorders.

Journal: Genome medicine

Published: July 31, 2025

Validation and depth evaluation of recurrent neural network-based ultra low-pass genome sequencing for the detection of absence of heterozygosity: A multi-centre study of 409 cases.

Validation and depth evaluation of recurrent neural network-based ultra low-pass genome sequencing for the detection of absence of heterozygosity: A multi-centre study of 409 cases.

Journal: Clinical and translational medicine

Published: May 10, 2024

Analysis of chromosomal aberrations in early pregnancy loss using high-throughput ligation-dependent probe amplification and single tandem repeats.

Analysis of chromosomal aberrations in early pregnancy loss using high-throughput ligation-dependent probe amplification and single tandem repeats.

Journal: Molecular cytogenetics

Published: November 19, 2023

Application of non-invasive prenatal testing to 91,280 spontaneous pregnancies and 3477 pregnancies conceived by in vitro fertilization.

Application of non-invasive prenatal testing to 91,280 spontaneous pregnancies and 3477 pregnancies conceived by in vitro fertilization.

Journal: Molecular cytogenetics

Published: March 28, 2023

Value of noninvasive prenatal testing in the detection of rare fetal autosomal abnormalities.

Value of noninvasive prenatal testing in the detection of rare fetal autosomal abnormalities.

Journal: European journal of obstetrics, gynecology, and reproductive biology

Published: August 12, 2022

Peripheral Blood Microbiome Analysis via Noninvasive Prenatal Testing Reveals the Complexity of Circulating Microbial Cell-Free DNA.

Peripheral Blood Microbiome Analysis via Noninvasive Prenatal Testing Reveals the Complexity of Circulating Microbial Cell-Free DNA.

Journal: Microbiology spectrum

Published: May 24, 2022

Chromosomal microarray analysis versus noninvasive prenatal testing in fetuses with increased nuchal translucency.

Chromosomal microarray analysis versus noninvasive prenatal testing in fetuses with increased nuchal translucency.

Journal: Journal of human genetics

Published: January 20, 2022

Clinical application value of expanded carrier screening in the population of childbearing age.

Clinical application value of expanded carrier screening in the population of childbearing age.

Journal: European journal of medical research

Published: January 19, 2022

Performance of non-invasive prenatal testing for foetal chromosomal abnormalities in 1048 twin pregnancies.

Performance of non-invasive prenatal testing for foetal chromosomal abnormalities in 1048 twin pregnancies.

Journal: Molecular cytogenetics

Published: April 05, 2021

Clinical application of noninvasive prenatal testing in the detection of fetal chromosomal diseases.

Clinical application of noninvasive prenatal testing in the detection of fetal chromosomal diseases.

Journal: Molecular cytogenetics

Published: March 17, 2021

Showing 1-12 of 20

Last Updated: 09/26/2026