Yunan Wang
Guangzhou, 511430, China
Last Updated: 09/26/2026
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Found 18 publications
Repeated oral exposure to polyethylene microplastics induces thyroid toxicity in rats: Evidence from in vivo toxicokinetics and multi-omics analyses.
Journal: Environment international
Published: January 14, 2026
Clinical utility of exome sequencing in hearing loss: a retrospective cohort study.
Journal: Frontiers in genetics
Published: June 09, 2025
OSGEP-associated Galloway-Mowat syndrome: a longitudinal genotype-phenotype correlation from prenatal imaging markers to lifespan neurologic-renal trajectories.
Journal: QJM : monthly journal of the Association of Physicians
Published: May 06, 2025
Pityriasis versicolor in the paediatric age group: a descriptive observational study of 415 children.
Journal: Archives of dermatological research
Published: April 07, 2025
Decoding the hypoxia-exosome-immune triad in OSA: PRCP/UCHL1/BTG2-driven metabolic dysregulation revealed by interpretable machine learning.
Journal: Frontiers in immunology
Published: March 05, 2025
ALG8-CDG: advances in molecular and prenatal phenotyping facilitate prenatal diagnosis and genetic counseling.
Journal: QJM : monthly journal of the Association of Physicians
Published: November 20, 2024
Teratogenic effect evaluation of Monascus red oral exposure to pregnant rats and their gut microbiota.
Journal: Reproductive toxicology (Elmsford, N.Y.)
Published: October 30, 2024
Exome sequencing for nonimmune hydrops fetalis and clinical utility of data reanalysis.
Journal: QJM : monthly journal of the Association of Physicians
Published: August 06, 2024
Epigenetic phenotype of plasma cell-free DNA in the prediction of early-onset preeclampsia.
Journal: Journal of obstetrics and gynaecology : the journal of the Institute of Obstetrics and Gynaecology
Published: December 01, 2023
Prenatal phenotype features and genetic etiology of the Williams-Beuren syndrome and literature review.
Journal: Frontiers in pediatrics
Published: January 10, 2023
Intrauterine phenotype features of fetuses with 7q11.23 microduplication syndrome.
Journal: Orphanet journal of rare diseases
Published: November 03, 2022
Last Updated: 09/26/2026