Zhenhua D. Zhao
Zhengzhou, China
Last Updated: 09/26/2026
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Found 44 publications
Proband-independent noninvasive prenatal diagnosis for spinal muscular atrophy: early detection paving the way for early prenatal treatment.
Journal: Annals of medicine
Published: January 05, 2026
MLDP-AS: an optimized next-generation sequencing assay for enhanced detection of technically challenging variants in expanded carrier screening.
Journal: Journal of translational medicine
Published: June 16, 2025
Has the Era of Individualized Intrauterine Treatment for Congenital Adrenal Hyperplasia Arrived?
Journal: Prenatal diagnosis
Published: July 29, 2024
Unraveling the genetic mysteries of spinal muscular atrophy in Chinese families.
Journal: Orphanet journal of rare diseases
Published: July 20, 2024
High-Resolution Haplotyping of the PAH Gene Enables Early Gestation Noninvasive Prenatal Diagnosis of Phenylketonuria and Evolution Analysis of Recurrent Pathogenic Variations.
Journal: Prenatal diagnosis
Published: March 13, 2024
Noninvasive prenatal diagnosis (NIPD) of non-syndromic hearing loss (NSHL) for singleton and twin pregnancies in the first trimester.
Journal: Orphanet journal of rare diseases
Published: March 11, 2024
Accurate prenatal diagnosis of facioscapulohumeral muscular dystrophy 1 using nanopore sequencing.
Journal: Journal of medical genetics
Published: December 20, 2023
First-trimester noninvasive prenatal diagnosis of seven facioscapulohumeral muscular dystrophy type 1 families using SNP-based amplicon sequencing: An earlier, rapid and safer way.
Journal: American journal of medical genetics. Part A
Published: November 18, 2023
Haplotype-based noninvasive prenatal diagnosis of methylmalonic acidemia and the discovery of a recurrent pathogenic haplotype associated with c.609G>A.
Journal: Prenatal diagnosis
Published: July 31, 2023
Noninvasive twin genotyping for recessive monogenic disorders by relative haplotype dosage.
Journal: Prenatal diagnosis
Published: July 05, 2023
Application of low-depth whole genome sequencing for copy number variation analysis in children with disorders of sex development
Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: January 29, 2023
Last Updated: 09/26/2026