EDITORIAL
Published on 24 Dec 2021
Editorial: Genetic Mutations Associated With Ocular Diseases
doi 10.3389/fcell.2021.815522
- 2,136 views
- 1 citation
- Frontiers in Cell and Developmental Biology
- Molecular and Cellular Pathology
- Research Topics
- Genetic Mutations Associated with Ocular Diseases
Genetic Mutations Associated with Ocular Diseases
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Articles
ORIGINAL RESEARCH
Published on 20 Aug 2021
Discovery of Novel Genetic Risk Loci for Acute Central Serous Chorioretinopathy and Genetic Pleiotropic Effect With Age-Related Macular Degeneration
doi 10.3389/fcell.2021.696885
- 1,483 views
- 2 citations
ORIGINAL RESEARCH
Published on 17 Aug 2021
A Novel ARL3 Gene Mutation Associated With Autosomal Dominant Retinal Degeneration
doi 10.3389/fcell.2021.720782
- 5,599 views
- 15 citations
ORIGINAL RESEARCH
Published on 13 Jul 2021
Updating the Genetic Landscape of Inherited Retinal Dystrophies
doi 10.3389/fcell.2021.645600
- 7,581 views
- 23 citations
BRIEF RESEARCH REPORT
Published on 25 Jun 2021
An Early Diagnostic Clue for COL18A1- and LAMA1-Associated Diseases: High Myopia With Alopecia Areata in the Cranial Midline
doi 10.3389/fcell.2021.644947
- 2,816 views
- 5 citations
ORIGINAL RESEARCH
Published on 18 Jun 2021
Whole-Exome Sequencing in a Cohort of High Myopia Patients in Northwest China
doi 10.3389/fcell.2021.645501
- 3,191 views
- 9 citations
ORIGINAL RESEARCH
Published on 11 Jun 2021
Genotype Profile of Global EYS-Associated Inherited Retinal Dystrophy and Clinical Findings in a Large Chinese Cohort
doi 10.3389/fcell.2021.634220
- 3,152 views
- 3 citations
ORIGINAL RESEARCH
Published on 31 May 2021
Genetic Screening Revealed Latent Keratoconus in Asymptomatic Individuals
doi 10.3389/fcell.2021.650344
- 3,113 views
- 14 citations
ORIGINAL RESEARCH
Published on 21 Apr 2021
Long-Read Sequencing to Unravel Complex Structural Variants of CEP78 Leading to Cone-Rod Dystrophy and Hearing Loss
doi 10.3389/fcell.2021.664317
- 4,971 views
- 18 citations
ORIGINAL RESEARCH
Published on 18 Mar 2021
Evaluation of the Genetic Variation Spectrum Related to Corneal Dystrophy in a Large Cohort
doi 10.3389/fcell.2021.632946
- 3,461 views
- 4 citations
ORIGINAL RESEARCH
Published on 11 Mar 2021
Ocular Characteristics of Patients With Bardet–Biedl Syndrome Caused by Pathogenic BBS Gene Variation in a Chinese Cohort
doi 10.3389/fcell.2021.635216
- 7,996 views
- 18 citations
ORIGINAL RESEARCH
Published on 05 Mar 2021
Absence of Cytochrome P450-1b1 Increases Susceptibility of Pressure-Induced Axonopathy in the Murine Retinal Projection
doi 10.3389/fcell.2021.636321
- 2,253 views
- 8 citations
Published in
Frontiers in Cell and Developmental Biology
- Molecular and Cellular Pathology
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- 87kTopic views
- 62kArticle views
- 22kArticle downloads