Yani Liu
Wuhan, China
Last Updated: 09/26/2026
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Found 20 publications
Ultra-large stokes shift probe enables SIM super-resolution tracking of lysosomal acidification impairment in Aβ trafficking dysregulation during Alzheimer's disease.
Journal: Biosensors & bioelectronics
Published: May 27, 2025
Identifying microglia-derived NFKBIA as a potential contributor to the pathogenesis of Alzheimer's disease and age-related macular degeneration.
Journal: Journal of Alzheimer's disease : JAD
Published: March 19, 2025
Identifying blood mitochondrial DNA copy number as a biomarker for development of neurodegenerative diseases: Evidence from Mendelian randomization analysis.
Journal: Neuroscience
Published: December 08, 2024
The important role of cuproptosis and cuproptosis-related genes in the development of thyroid carcinoma revealed by transcriptomic analysis and experiments.
Journal: Brazilian journal of otorhinolaryngology
Published: July 30, 2024
Identifying the important involvement of cuproptosis in the pathophysiology of age-related macular degeneration.
Journal: European journal of medical research
Published: July 28, 2024
The impact of stoma management education on the self-care abilities of individuals with an intestinal stoma.
Journal: British journal of nursing (Mark Allen Publishing)
Published: March 23, 2023
Distinct mutations with different inheritance mode caused similar retinal dystrophies in one family: a demonstration of the importance of genetic annotations in complicated pedigrees.
Journal: Journal of translational medicine
Published: November 27, 2017
CEP78 is mutated in a distinct type of Usher syndrome.
Journal: Journal of medical genetics
Published: July 15, 2016
GUCA1A mutation causes maculopathy in a five-generation family with a wide spectrum of severity.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: July 06, 2016
CCT2 Mutations Evoke Leber Congenital Amaurosis due to Chaperone Complex Instability.
Journal: Scientific reports
Published: March 17, 2016
Whole exome sequencing confirms the clinical diagnosis of Marfan syndrome combined with X-linked hypophosphatemia.
Journal: Journal of translational medicine
Published: February 07, 2015
Targeted next-generation sequencing reveals novel EYS mutations in Chinese families with autosomal recessive retinitis pigmentosa.
Journal: Scientific reports
Published: October 23, 2014
Last Updated: 09/26/2026