Zimeng Ye

发表

Cutting edge approaches to detecting brain mosaicism associated with common focal epilepsies: implications for diagnosis and potential therapies

I. Scheffer, S. Berkovic, M. Bahlo, 2021, Expert review of neurotherapeutics.

Association of IGF1 and IGF1R gene polymorphisms with high myopia in a Han Chinese population

Xiaoqi Liu, B. Gong, Zhenglin Yang, 2017, Ophthalmic genetics.

Association of genetic variants at MYP10 and MYP15 with high myopia in a Han Chinese population

Lingxi Jiang, Rui Zheng, Xiaoqi Liu, 2019, Ophthalmic genetics.

Somatic GNAQ mutation in the forme fruste of Sturge-Weber syndrome

P. Lockhart, I. Scheffer, S. Berkovic, 2018, Neurology: Genetics.

Mutation screening in the FBN1 gene responsible for Marfan syndrome and related disorder in Chinese families

B. Gong, Zhenglin Yang, Yi Shi, 2019, Molecular genetics & genomic medicine.

Genetic association of COL1A1 polymorphisms with high myopia in Asian population: a Meta-analysis.

B. Gong, Yi Shi, Zimeng Ye, 2016, International journal of ophthalmology.

Association of catalase polymorphisms with primary open-angle glaucoma in a Chinese population

Xiaoqi Liu, B. Gong, Zhenglin Yang, 2018, Ophthalmic genetics.

Somatic mutation: The hidden genetics of brain malformations and focal epilepsies

I. Scheffer, H. Mefford, S. Berkovic, 2019, Epilepsy Research.

Evidence for a Dual-Pathway, 2-Hit Genetic Model for Focal Cortical Dysplasia and Epilepsy

I. Scheffer, J. Gécz, S. Berkovic, 2022, Neurology: Genetics.

Evaluation of genome-wide susceptibility loci for high myopia in a Han Chinese population

Ling Wan, Lingxi Jiang, B. Gong, 2017, Ophthalmic genetics.

Genetic landscape of FOXC2 mutations in lymphedema-distichiasis syndrome: Different mechanism of pathogenicity for mutations in different domains.

Lingxi Jiang, Chao Dai, Chunbao Xie, 2022, Experimental eye research.

Cerebrospinal fluid liquid biopsy for detecting somatic mosaicism in brain

P. Lockhart, I. Scheffer, R. Lister, 2021, Brain communications.

Novel Compound Heterozygous CBS Mutations Cause Homocystinuria in a Han Chinese Family

Xiaoqi Liu, B. Gong, Zhenglin Yang, 2015, Scientific Reports.

Evaluation of the Association Between Common Genetic Variants Near the ABCA1 Gene and Primary Angle Closure Glaucoma in a Han Chinese Population.

Xiaoqi Liu, B. Gong, Zhenglin Yang, 2015, Investigative ophthalmology & visual science.

Evaluation of the Association Between Common Genetic Variants Near the ABCA1 Gene and Primary Angle Closure Glaucoma in a Han Chinese Population.

Xiaoqi Liu, B. Gong, Zhenglin Yang, 2015, Investigative ophthalmology & visual science.

Improving Specificity of Cerebrospinal Fluid Liquid Biopsy for Genetic Testing

I. Scheffer, S. Berkovic, M. Hildebrand, 2021, Annals of neurology.

Association between SKIV2L polymorphism rs429608 and age-related macular degeneration: A meta-analysis

Xiaoqi Liu, B. Gong, Yi Shi, 2017, Ophthalmic genetics.

Associations of 6p21.3 Region with Age-related Macular Degeneration and Polypoidal Choroidal Vasculopathy

Xianjun Zhu, F. Wen, Lulin Huang, 2016, Scientific Reports.

Mosaicism in tuberous sclerosis complex: Lowering the threshold for clinical reporting

N. Brown, I. Scheffer, S. Berkovic, 2022, Human mutation.

Effects of dexamethasone and HA1077 on actin cytoskeleton and β-catenin in cultured human trabecular meshwork cells.

B. Gong, Chun-tao Lei, Zimeng Ye, 2016, International journal of ophthalmology.

Somatic IDH1 variant (p.R132C) in an adult male with Maffucci syndrome

N. Brown, C. Stutterd, S. Mandelstam, 2021, Cold Spring Harbor molecular case studies.

Evaluation of Four Genetic Variants in Han Chinese Subjects with High Myopia

B. Gong, Zhenglin Yang, Yi Shi, 2015, Journal of ophthalmology.

Contribution of Somatic Ras/Raf/Mitogen-Activated Protein Kinase Variants in the Hippocampus in Drug-Resistant Mesial Temporal Lobe Epilepsy

I. Scheffer, R. Richardson, Jidong Zhu, 2023, JAMA neurology.

Sporadic hypothalamic hamartoma is a ciliopathy with somatic and bi-allelic contributions.

P. Lockhart, I. Scheffer, J. Motelow, 2022, Human molecular genetics.

A novel APC mutation identified in a large Chinese family with familial adenomatous polyposis and a brief literature review

B. Gong, Zimeng Ye, Yijun Liu, 2018, Molecular medicine reports.

Genetic variants influencing lipid levels and risk of dyslipidemia in Chinese population

Ying Lin, Zimeng Ye, Huaichao Luo, 2017, Journal of Genetics.

Identification of a novel MYOC mutation in a Chinese family with primary open-angle glaucoma.

B. Gong, Zhenglin Yang, Yi Shi, 2015, Gene.

Somatic Mosaic Pathogenic Variant Gradient Detected in Trace Brain Tissue From Stereo-EEG Depth Electrodes

I. Scheffer, P. Kwan, S. Berkovic, 2022, Neurology.

A novel deleterious mutation in the COMP gene that causes pseudoachondroplasia

Zhenglin Yang, Yuanfeng Li, Ying Lin, 2016, Human Genome Variation.