Zhengwen Jiang
218 Xinghu St
Suzhou, China
Suzhou, China
Last Updated: 09/26/2026
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Found 26 publications
Novel rapid molecular diagnosis methods for comprehensive genetic analysis of 21-hydroxylase deficiency.
Journal: Orphanet journal of rare diseases
Published: February 01, 2024
The implication of chromosomal abnormalities in the surgical outcomes of Chinese pediatric patients with congenital heart disease.
Journal: Frontiers in cardiovascular medicine
Published: February 13, 2023
Publisher Correction: A capillary electrophoresis-based multiplex PCR assay for expanded carrier screening in the eastern Han Chinese population.
Journal: NPJ genomic medicine
Published: February 22, 2022
Noninvasive fetal genotyping of single nucleotide variants and linkage analysis for prenatal diagnosis of monogenic disorders.
Journal: Human genomics
Published: December 22, 2021
A capillary electrophoresis-based variant hotspot genotyping method for rapid and reliable analysis of the phenylalanine hydroxylase gene in the Chinese Han population.
Journal: Clinica chimica acta; international journal of clinical chemistry
Published: August 24, 2021
HER2 copy number quantification in primary tumor and cell-free DNA provides additional prognostic information in HER2 positive early breast cancer.
Journal: Breast (Edinburgh, Scotland)
Published: April 23, 2021
A capillary electrophoresis-based multiplex PCR assay for expanded carrier screening in the eastern Han Chinese population.
Journal: NPJ genomic medicine
Published: March 09, 2021
Comprehensive copy number analysis of Y chromosome-linked loci for detection of structural variations and diagnosis of male infertility.
Journal: Journal of human genetics
Published: December 11, 2020
Identification of Chromosomal Abnormalities in Early Pregnancy Loss Using a High-Throughput Ligation-Dependent Probe Amplification-Based Assay.
Journal: The Journal of molecular diagnostics : JMD
Published: June 08, 2020
High-throughput sequencing-based microsatellite genotyping for polyploids to resolve allele dosage uncertainty and improve analyses of genetic diversity, structure and differentiation: A case study of the hexaploid Camellia oleifera.
Journal: Molecular ecology resources
Published: March 03, 2020
Intronic (TTTGA)n insertion in SAMD12 also causes familial cortical myoclonic tremor with epilepsy.
Journal: Movement disorders : official journal of the Movement Disorder Society
Published: February 22, 2019
Genetic Study on Small Insertions and Deletions in Psoriasis Reveals a Role in Complex Human Diseases.
Journal: The Journal of investigative dermatology
Published: October 25, 2018
Last Updated: 09/26/2026