Shujin Li

发表

Associations of the PON1 rs854560 polymorphism with plasma lipid levels: a meta-analysis

Zhi-yang Luo, Shujin Li, I. Muhammad, 2018, Lipids in health and disease.

G Allele of the rs1801282 Polymorphism in PPARγ Gene Confers an Increased Risk of Obesity and Hypercholesterolemia, While T Allele of the rs3856806 Polymorphism Displays a Protective Role Against Dyslipidemia: A Systematic Review and Meta-Analysis

Shujin Li, Yongyan Song, Ruixia Wang, 2022, Frontiers in Endocrinology.

Novel truncating variants in CTNNB1 cause familial exudative vitreoretinopathy

Peiquan Zhao, Lulin Huang, Zhenglin Yang, 2022, Journal of Medical Genetics.

Exome sequencing revealed Notch ligand JAG1 as a novel candidate gene for familial exudative vitreoretinopathy

Peiquan Zhao, Xianjun Zhu, Lulin Huang, 2019, Genetics in Medicine.

Deep Sc-RNA sequencing decoding the molecular dynamic architecture of the human retina

Lulin Huang, Ling Zhong, Yi Shi, 2022, Science China Life Sciences.

CTNND1 variants cause familial exudative vitreoretinopathy through the Wnt/cadherin axis

Peiquan Zhao, Xianjun Zhu, Zhenglin Yang, 2022, JCI insight.

Whole-Exome Sequencing Reveals Novel NDP Variants in X-Linked Familial Exudative Vitreoretinopathy

Yunqi He, Shujin Li, Mu Yang, 2022, European journal of ophthalmology.

Whole Exome Sequencing Analysis Identifies Mutations in LRP5 in Indian Families with Familial Exudative Vitreoretinopathy.

R. Kim, Xianjun Zhu, Lulin Huang, 2016, Genetic testing and molecular biomarkers.

BBS7–SHH Signaling Activity Regulates Primary Cilia for Periodontal Homeostasis

Han-Sung Jung, Y. Choi, Hyun-Yi Kim, 2021, Frontiers in Cell and Developmental Biology.

Activation of Wnt signalling reduces the population of cancer stem cells in ameloblastoma

Han-Sung Jung, T. Muramatsu, Hyun-Yi Kim, 2021, Cell proliferation.

Catenin α 1 mutations cause familial exudative vitreoretinopathy by overactivating Norrin/β-catenin signaling

Peiquan Zhao, Xianjun Zhu, Lulin Huang, 2021 .

Runx3 regulates iron metabolism via modulation of BMP signalling

S. Bae, Han-Sung Jung, Hyun-Yi Kim, 2021, Cell proliferation.

Associations of the APOC 3 rs 2854116 and rs 2854117 polymorphisms with plasma APOC 3 and lipid levels : a meta-analysis

Min Zhou, Shujin Li, Yongyan Song, 2016 .

A comprehensive functional analysis on the pathogenesis of novel TSPAN12 and NDP variants in familial exudative vitreoretinopathy

Peiquan Zhao, Zhenglin Yang, Yunqi He, 2022, Clinical genetics.

Whole-Exome Sequencing Identified DLG1 as a Candidate Gene for Familial Exudative Vitreoretinopathy.

Peiquan Zhao, Xianjun Zhu, Lulin Huang, 2021, Genetic testing and molecular biomarkers.

Whole-exome Sequencing Analysis Identifies Mutations in the EYS Gene in Retinitis Pigmentosa in the Indian Population

R. Kim, Xianjun Zhu, Lulin Huang, 2016, Scientific Reports.

PPARγ Gene Polymorphisms, Metabolic Disorders, and Coronary Artery Disease

Shujin Li, Yongyan Song, Chuanxiong He, 2022, Frontiers in Cardiovascular Medicine.

Candidate Gene Analysis Identifies Mutations in CYP1B1 and LTBP2 in Indian Families with Primary Congenital Glaucoma.

Xianjun Zhu, Lin Zhang, Periasamy Sundaresan, 2017, Genetic testing and molecular biomarkers.

The ER membrane protein complex subunit Emc3 controls angiogenesis via the FZD4/WNT signaling axis

Huafu Chen, D. Yao, Xianjun Zhu, 2021, Science China Life Sciences.

CpG methylation patterns of human mitochondrial DNA

Chunling Ma, Shujin Li, C. Bin, 2016, Scientific Reports.

TMEM30A deficiency in endothelial cells impairs cell proliferation and angiogenesis

Xianjun Zhu, Lin Zhang, Shujin Li, 2019, Journal of Cell Science.

A splicing mutation in aryl hydrocarbon receptor associated with retinitis pigmentosa

Xianjun Zhu, K. Ramasamy, Lulin Huang, 2018, Human molecular genetics.

Targeted next-generation sequencing reveals that a compound heterozygous mutation in phosphodiesterase 6a gene leads to retinitis pigmentosa in a Chinese family

Xianjun Zhu, Zhenglin Yang, Lin Zhang, 2018, Ophthalmic genetics.

Disruption of Tmem30a results in cerebellar ataxia and degeneration of Purkinje cells

Xianjun Zhu, Zhilin Jiang, Lin Zhang, 2018, Cell Death & Disease.

Variants in the Wnt co-receptor LRP6 are associated with familial exudative vitreoretinopathy.

Peiquan Zhao, Xianjun Zhu, Lulin Huang, 2021, Journal of genetics and genomics = Yi chuan xue bao.

Loss of Tmem30a leads to photoreceptor degeneration

Xianjun Zhu, Xiong Zhu, Zhilin Jiang, 2017, Scientific Reports.

Exome sequencing revealed Notch ligand JAG1 as a novel candidate gene for familial exudative vitreoretinopathy

Peiquan Zhao, Xianjun Zhu, Lulin Huang, 2019, Genetics in Medicine.

Whole-Exome Sequencing Reveals Novel TSPAN12 Variants in Autosomal Dominant Familial Exudative Vitreoretinopathy.

Xianjun Zhu, Lulin Huang, Zhenglin Yang, 2021, Genetic testing and molecular biomarkers.

Targeted Next-Generation Sequencing Reveals Novel RP1 Mutations in Autosomal Recessive Retinitis Pigmentosa.

Xianjun Zhu, Zhenglin Yang, Lin Zhang, 2018, Genetic testing and molecular biomarkers.

Loss of Tmem30a leads to photoreceptor degeneration

Xianjun Zhu, Xiong Zhu, Zhilin Jiang, 2017, Scientific Reports.

Heterozygote loss‐of‐function variants in the LRP5 gene cause familial exudative vitreoretinopathy

Peiquan Zhao, Zhenglin Yang, Yunqi He, 2022, Clinical & experimental ophthalmology.

Defective EMC1 drives abnormal retinal angiogenesis via Wnt/β-catenin signaling and may be associated with the pathogenesis of familial exudative vitreoretinopathy

Peiquan Zhao, Xianjun Zhu, Zhenglin Yang, 2022, Genes & diseases.

Dynamic human retinal pigment epithelium (RPE) and choroid architecture based on single-cell transcriptomic landscape analysis

Lulin Huang, B. Gong, Zhenglin Yang, 2022, Genes & diseases.

Identification of Two Novel Variants in the LRP5 Gene that Cause Familial Exudative Vitreoretinopathy.

Yunqi He, Shujin Li, Yuze Wang, 2022, Genetic testing and molecular biomarkers.

A novel frameshift variant in the TSPAN12 gene causes autosomal dominant FEVR

Peiquan Zhao, Zhenglin Yang, Yunqi He, 2022, Molecular genetics & genomic medicine.

Catenin alpha 1 mutations cause familial exudative vitreoretinopathy by overactivating Norrin/beta-catenin signaling.

Peiquan Zhao, Xianjun Zhu, Lulin Huang, 2021, The Journal of clinical investigation.

Frameshift variants in the C-terminal of CTNNB1 cause familial exudative vitreoretinopathy by AXIN1-mediated ubiquitin-proteasome degradation condensation.

Yunqi He, Shujin Li, Mu Yang, 2023, International journal of biological macromolecules.

Dysfunction of Calcyphosine-Like gene impairs retinal angiogenesis through the MYC axis and is associated with familial exudative vitreoretinopathy

Lulin Huang, Shujin Li, Wenjing Liu, 2024, eLife.

Characterization of a novel heterozygous frameshift variant in NDP gene that causes familial exudative vitreoretinopathy in female patients.

Yunqi He, Shujin Li, Mu Yang, 2024, Molecular genetics and genomics : MGG.