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Study of Inherited Retinal Diseases

Special Issue Information

Dear Colleagues,

Inherited retinal disease (IRD) is a major cause of bilateral visual decline and blindness worldwide. To date, there is no definitive treatment option for this condition. Recently, there have been advances in the field of genetic diagnosis and treatment methods, including gene therapy and genome editing. Since the approval of gene therapy for RPE65-related IRD, the future of treatment of IRD appears bright, and more patients with IRD may be saved from blindness as technology develops. To reach a better visual outcome for IRD patients, a greater understanding of IRD, including genetics, mechanism, clinical features, and preclinical and clinical trial results are needed for physicians, researchers, and patients, as well as pharmaceutical companies and governments.

In this Special Issue, we welcome reviews and original articles about the study of IRD. These include, but are not limited to, genetics and molecular mechanisms of IRD, diagnosis, clinical features and imaging of IRD cases, epidemiology, ethnic variability, preclinical research, and clinical trials of new treatments. We look forward to your contributions. Thank you.

Prof. Dr. Se Joon Woo
Guest Editor

Manuscript Submission Information

Manuscripts should be submitted online at www.mdpi.com by registering and logging in to this website. Once you are registered, click here to go to the submission form. Manuscripts can be submitted until the deadline. All submissions that pass pre-check are peer-reviewed. Accepted papers will be published continuously in the journal (as soon as accepted) and will be listed together on the special issue website. Research articles, review articles as well as short communications are invited. For planned papers, a title and short abstract (about 100 words) can be sent to the Editorial Office for announcement on this website.

Submitted manuscripts should not have been published previously, nor be under consideration for publication elsewhere (except conference proceedings papers). All manuscripts are thoroughly refereed through a single-blind peer-review process. A guide for authors and other relevant information for submission of manuscripts is available on the Instructions for Authors page. Genes is an international peer-reviewed open access monthly journal published by MDPI.

Please visit the Instructions for Authors page before submitting a manuscript. The Article Processing Charge (APC) for publication in this open access journal is 2600 CHF (Swiss Francs). Submitted papers should be well formatted and use good English. Authors may use MDPI's English editing service prior to publication or during author revisions.

Keywords

  • Inherited retinal diseases
  • Retinitis pigmentosa
  • Macular dystrophy
  • Cone dystrophy
  • Genotype
  • Gene therapy
  • Clinical trial
  • Imaging
  • Genetic mechanism
  • Genome editing
  • Phenotype

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Published Papers