Shanshan Zhang
Sichuan Provincial Key Laboratory For Human Disease Gene Study And The Center For Medical Genetics
Chengdu, 610075, China
Chengdu, 610075, China
Last Updated: 09/26/2026
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Found 15 publications
Exploring the role of VAV2 rare variants in primary open-angle glaucoma: genetic insights and pathophysiological mechanisms.
Journal: Science China. Life sciences
Published: November 07, 2024
Unilateral upper cervical cord infarction in Opalski's syndrome caused by spontaneous vertebral artery dissection.
Journal: Clinical medicine (London, England)
Published: July 31, 2023
Deep Sc-RNA sequencing decoding the molecular dynamic architecture of the human retina.
Journal: Science China. Life sciences
Published: November 21, 2021
Whole-Exome Sequencing Identified DLG1 as a Candidate Gene for Familial Exudative Vitreoretinopathy.
Whole-Exome Sequencing Identified DLG1 as a Candidate Gene for Familial Exudative Vitreoretinopathy.
Journal: Genetic testing and molecular biomarkers
Published: May 04, 2021
A new hand-held holder optimizes the parameters of the laser-induced choroidal neovascularization model in mice.
Journal: Experimental eye research
Published: July 26, 2020
Catenin α 1 mutations cause familial exudative vitreoretinopathy by overactivating Norrin/β-catenin signaling.
Journal: The Journal of clinical investigation
Published: May 04, 2020
Deletion of the Impg2 gene causes the degeneration of rod and cone cells in mice.
Journal: Human molecular genetics
Published: February 11, 2020
Whole-Exome Sequencing Analysis Identified Novel Mutations in the TSPAN12 Gene in Chinese Families with Familial Exudative Vitreoretinopathy.
Journal: Genetic testing and molecular biomarkers
Published: September 13, 2019
Identification of novel variants in the FZD4 gene associated with familial exudative vitreoretinopathy in Chinese families.
Journal: Clinical & experimental ophthalmology
Published: June 17, 2019
Exome sequencing revealed Notch ligand JAG1 as a novel candidate gene for familial exudative vitreoretinopathy.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: February 14, 2019
TMEM30A deficiency in endothelial cells impairs cell proliferation and angiogenesis.
Journal: Journal of cell science
Published: September 10, 2018
Mutant RAMP2 causes primary open-angle glaucoma via the CRLR-cAMP axis.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: August 07, 2018
Last Updated: 09/26/2026