Dongyi Yu
Jinan, China
Last Updated: 09/26/2026
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Found 23 publications
Identification of the Novel HLA-A*24:671 Allele by Next-Generation Sequencing.
Journal: HLA
Published: January 21, 2026
Prenatal Diagnosis of a Fetus With Congenital Malformations Caused by Compound Heterozygous Mutations in FANCA: A Case Report and Literature Review.
Journal: Molecular genetics & genomic medicine
Published: December 21, 2025
Application of trio-based whole-exome sequencing in fetal ultrasound anomalies: a single-center retrospective study of 454 cases.
Journal: Frontiers in genetics
Published: July 09, 2025
Genetic analysis of two fetuses with Mosaic variegated aneuploidy syndrome caused by compound heterozygous variants in BUB1B and its upstream regulatory elements and a literature Review
Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: June 24, 2025
Paternal Obesity-Induced H3K27me3 Elevation Leads to MANF-Mediated Transgenerational Metabolic Dysfunction in Female Offspring.
Journal: Advanced science (Weinheim, Baden-Wurttemberg, Germany)
Published: November 29, 2024
Application of Chromosomal Microarray Analysis in Genetic Reasons of Miscarriage Tissues.
Journal: The application of clinical genetics
Published: January 27, 2024
GR/P300 Regulates MKP1 Signaling Pathway and Mediates Depression-like Behavior in Prenatally Stressed Offspring.
Journal: Molecular neurobiology
Published: October 13, 2023
Analysis of a fetus with multiple malformations due to a hemizygous variant of FANCB gene
Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: September 20, 2023
Slow flow HD and traditional CDFI technologies in identifying pulmonary veins in the first trimester.
Journal: Archives of gynecology and obstetrics
Published: July 20, 2023
Comprehensive Analysis of Hemophilia A (CAHEA): Towards Full Characterization of the F8 Gene Variants by Long-Read Sequencing.
Journal: Thrombosis and haemostasis
Published: June 07, 2023
Detection of complex chromosome rearrangements using optical genome mapping.
Journal: Gene
Published: May 20, 2023
Development of CRISPR Cas9, spin-off technologies and their application in model construction and potential therapeutic methods of Parkinson's disease.
Journal: Frontiers in neuroscience
Published: May 16, 2023
Last Updated: 09/26/2026