Ye Cao
Sar, China
Last Updated: 09/26/2026
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Found 18 publications
Prenatal-Onset Recessive Titinopathies: Clinical Spectrum, Genotype-Phenotype Correlations, and Outcomes.
Journal: Diagnostics (Basel, Switzerland)
Published: April 24, 2026
Genetic Investigation of X-Linked Defects with Optimized Targeted Long-Read Sequencing.
Journal: Clinical chemistry
Published: April 02, 2026
NONO-Related Syndromic X-Linked Developmental Disability 34: Further Clinical and Molecular Delineation in a Prenatal Cohort.
Journal: Prenatal diagnosis
Published: November 09, 2025
Underrecognized triploidy and genome-wide uniparental disomy in human blastocysts revealed by a concurrent preimplantation genetic testing approach.
Journal: Human reproduction open
Published: July 24, 2025
Correction: Genetic landscape of hypertrophic cardiomyopathy in Hong Kong Chinese population.
Journal: Frontiers in genetics
Published: June 05, 2025
Genetic landscape of hypertrophic cardiomyopathy in Hong Kong Chinese population.
Journal: Frontiers in genetics
Published: February 26, 2025
Prenatal diagnosis of polycystic kidney caused by biallelic hypomorphic variants in the PKD1 gene.
Journal: Prenatal diagnosis
Published: May 09, 2023
Single-cell analysis reveals specific neuronal transition during mouse corticogenesis.
Journal: Frontiers in cell and developmental biology
Published: April 20, 2023
Case Report: Prenatal Recurrent Microcephaly and Corpus Callosum Abnormalities in a Chinese Family with Novel Biallelic SASS6 Mutations.
Journal: Fetal diagnosis and therapy
Published: October 13, 2022
Case Report: Novel Biallelic Variants in the COL18A1 Gene in a Chinese Family With Knobloch Syndrome.
Journal: Frontiers in neurology
Published: January 13, 2022
Investigation of Chromosomal Structural Abnormalities in Patients With Undiagnosed Neurodevelopmental Disorders.
Journal: Frontiers in genetics
Published: October 27, 2021
Last Updated: 09/26/2026