Winston Lee
Columbia University in the City of New York
H-index: 30
North America-United States
Top articles of Winston Lee
Towards Uncovering the Role of Incomplete Penetrance in Maculopathies through Sequencing of 105 Disease-Associated Genes
Biomolecules
2024/3/19
New trans-modifier genes in the most common monogenic eye disorder, ABCA4/Stargardt disease.
Investigative Ophthalmology & Visual Science
2023/6/1
Winston Lee
H-Index: 22
Genotype is a Significant Factor in Determining the Measurability of Atrophic Lesions in ABCA4 disease
Investigative Ophthalmology & Visual Science
2023/6/1
Winston Lee
H-Index: 22
CERT1 mutations perturb human development by disrupting sphingolipid homeostasis
The Journal of clinical investigation
2023/5/15
Monitoring Lesion Area Progression in Stargardt Disease: A Comparison of En Face Optical Coherence Tomography and Fundus Autofluorescence
Translational Vision Science & Technology
2023/5/1
Winston Lee
H-Index: 22
Insights Into PROM1-Macular Disease Using Multimodal Imaging
Investigative Ophthalmology & Visual Science
2023/4/3
Winston Lee
H-Index: 22
Alternative polyadenylation alters protein dosage by switching between intronic and 3′ UTR sites
Science advances
2023/2/17
Nicola De Prisco
H-Index: 4
Winston Lee
H-Index: 22
Marko Jovanovic
H-Index: 24
Hari Krishna Yalamanchili
H-Index: 15
The Monogenic Architecture of Retinal and Neurological Diseases
2023
Winston Lee
H-Index: 22
Determining the effects of loss of function mutations in human cell lines
STAR protocols
2022/6/17
Nicola De Prisco
H-Index: 4
Winston Lee
H-Index: 22
Protocol to assess the effect of disease-driving variants on mouse brain morphology and primary hippocampal neurons
STAR protocols
2022/6/17
Nicola De Prisco
H-Index: 4
Winston Lee
H-Index: 22
Clinical exome sequencing for inherited retinal degenerations at a tertiary care center
Scientific Reports
2022/6/7
A common haplotype in the PRPH2 gene modifies Stargardt/ABCA4 disease.
Investigative Ophthalmology & Visual Science
2022/6/1
Vitelliform foveomacular lesions in ABCA4 disease: A phenotypic expansion and longitudinal study
Investigative Ophthalmology & Visual Science
2022/6/1
Winston Lee
H-Index: 22
Identifying critical diagnostic features that distinguish ABCA4 disease from its Mendelian phenocopies
Investigative Ophthalmology & Visual Science
2022/6/1
Winston Lee
H-Index: 22
A homozygous in-frame duplication within the LRRCT consensus sequence of CFAP410 causes cone-rod dystrophy, macular staphyloma and short stature
Ophthalmic genetics
2022/5/4
Rare and common variants in ROM1 and PRPH2 genes trans-modify Stargardt/ABCA4 disease
PLoS Genetics
2022/3/30
Identifying patients and assessing variant pathogenicity for an autosomal dominant disease-driving gene
STAR protocols
2022/3/18
Winston Lee
H-Index: 22
Nicola De Prisco
H-Index: 4
A genotype-phenotype correlation matrix for ABCA4 disease based on long-term prognostic outcomes
JCI insight
2022/1/1
Winston Lee
H-Index: 22
A mutation in CRX causing pigmented paravenous retinochoroidal atrophy
European journal of ophthalmology
2022/1
Winston Lee
H-Index: 22
A pathogenic in-frame deletion-insertion variant in BEST1 phenocopies Stargardt disease
JCI insight
2022/12/12
Winston Lee
H-Index: 22
Tingting Yang
H-Index: 19
