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2024
Female carrier of RPGR mutation presenting with high myopia
Ophthalmic Genetics
2024
Genetic background of high myopia in children
PLOS ONE
2023
Rare variant analyses across multiethnic cohorts identify novel genes for refractive error
Communications Biology
2023
Identification of Rare Variants Involved in High Myopia Unraveled by Whole Genome Sequencing
Ophthalmology Science
2023
Screening of genes interacting with high myopia and neuropsychiatric disorders
Scientific Reports
2023
Whole-Exome Sequencing of 21 Families: Candidate Genes for Early-Onset High Myopia
International Journal of Molecular Sciences
2022
Whole exome sequencing of known eye genes reveals genetic causes for high myopia
Human Molecular Genetics
2022
Predominance of hyperopia in autosomal dominant Best vitelliform macular dystrophy
British Journal of Ophthalmology
2022
Next-Generation Sequencing Screening of 43 Families with Non-Syndromic Early-Onset High Myopia: A Clinical and Genetic Study
International Journal of Molecular Sciences
2021
SLC39A5 dysfunction impairs extracellular matrix synthesis in high myopia pathogenesis
Journal of Cellular and Molecular Medicine
2021
Variants in FLRT3 and SLC35E2B identified using exome sequencing in seven high myopia families from Central Europe
Advances in Medical Sciences
2021
A Bibliometric and Citation Network Analysis of Myopia Genetics
Genes
2021
Whole-Exome Sequencing in a Cohort of High Myopia Patients in Northwest China
Frontiers in Cell and Developmental Biology
2020
Application of targeted exome and whole‐exome sequencing for Chinese families with Stargardt disease
Annals of Human Genetics
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