Weiqin Tang
Publications by Year
Research Areas
Prenatal Screening and Diagnostics, Genomic variations and chromosomal abnormalities, RNA modifications and cancer, Neurogenetic and Muscular Disorders Research, Hearing, Cochlea, Tinnitus, Genetics
Most-Cited Works
- → Haplotype-Based Noninvasive Prenatal Diagnosis of 21 Families With Duchenne Muscular Dystrophy: Real-World Clinical Data in China(2021)18 cited
- → Exploring factors impacting haplotype‐based noninvasive prenatal diagnosis for single‐gene recessive disorders(2023)8 cited
- → Noninvasive prenatal testing of Duchenne muscular dystrophy in a twin gestation(2022)7 cited
- → Haplotype‐based noninvasive prenatal diagnosis of methylmalonic acidemia and the discovery of a recurrent pathogenic haplotype associated with c.609G>A(2023)3 cited
- → High‐Resolution Haplotyping of the PAH Gene Enables Early Gestation Noninvasive Prenatal Diagnosis of Phenylketonuria and Evolution Analysis of Recurrent Pathogenic Variations(2024)2 cited
- → The promise of carrier screening: noninvasive prenatal diagnoses without proband for spinal muscular atrophy in early gestation age(2024)1 cited
- → Noninvasive prenatal diagnosis (NIPD) of non-syndromic hearing loss (NSHL) for singleton and twin pregnancies in the first trimester(2024)
- → PRS9 HOW CLINICAL TRIALS INCORPORATED OUTCOMES RELEVANT FOR HEALTH ECONOMIC EVALUATION: AN EVIDENCE GAP ANALYSIS BASED ON SYSTEMATIC REVIEW OF CLINICAL TRIALS FOR MODERATE-TO-SEVERE ASTHMA IN JAPAN(2019)
- → MLDP-AS: an optimized next-generation sequencing assay for enhanced detection of technically challenging variants in expanded carrier screening(2026)