Fang Yang
Guangdong Provincial Key Laboratory Of Single Cell And Extracellular Vesicles
Guangzhou, 510515, China
Guangzhou, 510515, China
Last Updated: 09/26/2026
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Found 27 publications
Molecular mechanism study of novel compound heterozygous EOGT mutations leading to Adams-Oliver syndrome type 4.
Journal: Global medical genetics
Published: January 20, 2026
Rapid Detection of Hemoglobinopathy Variants Using One-Step Library Preparation and Nanopore Sequencing.
Journal: Clinical chemistry
Published: December 22, 2025
Divergent Right Ventricular Adaptation in Fetal Growth Restriction Subtypes Revealed by Quantitative Cardiac Profiling.
Journal: Echocardiography (Mount Kisco, N.Y.)
Published: December 05, 2025
Identification and functional analysis of biallelic loss-of-function variants of WNT7B in a Chinese family affected with PDAC syndrome.
Journal: Gene
Published: November 28, 2025
Integrating imaging and genomics in prenatal Treacher Collins syndrome: evidence for practice and policy.
Journal: Orphanet journal of rare diseases
Published: May 23, 2025
Down-regulation of MYO1A inhibits trophoblast cell proliferation and migration through SMURF2/Hedgehog signaling pathway and leads to fetal growth restriction.
Journal: Placenta
Published: November 26, 2024
A De Novo Mutation (c.2423A>G) in SAMD9 Causing MIRAGE Syndrome With Intrauterine Growth Retardation and Renal Hypoplasia in a Chinese Family.
Journal: Human mutation
Published: October 21, 2024
Genome-wide nucleosome footprints of plasma cfDNA predict preterm birth: A case-control study.
Journal: PLoS medicine
Published: August 18, 2024
Transcriptomics-based identification of lysine crotonylation-related biomarkers in pre-eclampsia.
Journal: BMC pregnancy and childbirth
Published: July 02, 2024
Functional study of a rare L1CAM gene c.1759G>C variant prove its pathogenicity.
Journal: Cell biochemistry and function
Published: March 09, 2024
Last Updated: 09/26/2026