Shixiu J. Liao
No. 7 Weiwu Road
Zhengzhou, 450003, China
Zhengzhou, 450003, China
Last Updated: 09/26/2026
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Found 131 publications
Gestational age-associated differences in amniotic fluid extracellular vesicle-enriched preparations during mid-pregnancy: an exploratory proteomic study.
Journal: Journal of proteomics
Published: May 29, 2026
A novel SERPING1 splice-site variant (c.1029 + 2T > A) causing hereditary angioedema type I: functional characterization and clinical analysis.
Journal: Orphanet journal of rare diseases
Published: April 25, 2026
Genomic Profiling of Anophthalmia/Microphthalmia-Associated CNVs Reveals Complex Genotype-Phenotype Correlations and Incomplete Penetrance.
Journal: Molecular genetics & genomic medicine
Published: March 30, 2026
Revisiting down syndrome through the lens of interferonopathy and innate immune dysregulation.
Journal: Frontiers in immunology
Published: March 23, 2026
Identification and functional analysis of a novel variant of CHD23 gene in a Chinese pedigree affected with Non-syndromic autosomal recessive deafness 12
Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: March 11, 2026
Stepwise genetic testing strategy identified pathogenic variants in 10 Chinese duchenne muscular dystrophy patients.
Journal: Frontiers in genetics
Published: February 06, 2026
Integrated multiomics profiling of amniotic fluid exosomes reveals dysregulated lipid and protein signatures in fetal 22q11.2 deletion syndrome.
Journal: Human genomics
Published: January 24, 2026
Phenotypic spectrum of 11p15.5 duplications: parent-of-origin and copy number variant size shape outcomes from Silver-Russell to Beckwith-Wiedemann syndromes.
Journal: Human genomics
Published: December 09, 2025
The D826V point mutation in IREB2 causes early-onset neurodegeneration in mice.
Journal: Acta biochimica et biophysica Sinica
Published: November 14, 2025
CCN5 overexpression suppresses trophoblast HTR-8/SVneo cell proliferation, migration, invasion, and epithelial-mesenchymal transition.
Journal: European journal of pharmacology
Published: November 12, 2025
The D826V point mutation in IREB2 induces lipogenesis in adipose tissues.
Journal: Frontiers in cell and developmental biology
Published: October 14, 2025
A study on the conversion between SMN1 and SMN2 genes
Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: October 10, 2025
Last Updated: 09/26/2026