Common and rare variants in patients with early onset drusen maculopathy-Reference-Cited by-同舟云学术

Common and rare variants in patients with early onset drusen maculopathy

Published:2022-09-13 Issue:5 Volume:102 Page:414-423
ISSN:0009-9163
Container-title:Clinical Genetics
language:en
Short-container-title:Clinical Genetics

Author:

de Breuk Anita¹^ORCID,Lechanteur Yara T. E.¹,Astuti Galuh²³,Galbany Jordi Corominas²,Klaver Caroline C. W.¹⁴⁵,Hoyng Carel B.¹,den Hollander Anneke I.¹^ORCID

Affiliation:

1. Department of Ophthalmology, Donders Institute for Brain, Cognition and Behaviour Radboud University Medical Center Nijmegen The Netherlands

2. Department of Human Genetics Radboud University Medical Center Nijmegen The Netherlands

3. Division of Human Genetics, Center for Biomedical Research, Faculty of Medicine Diponegoro University Semarang Indonesia

4. Department of Ophthalmology, Department of Epidemiology Erasmus Medical Center Rotterdam The Netherlands

5. Institute of Molecular and Clinical Ophthalmology Basel Switzerland

Funder

Nederlandse Organisatie voor Wetenschappelijk Onderzoek

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/cge.14212

Reference39 articles.

1. Global causes of blindness and distance vision impairment 1990–2020: a systematic review and meta-analysis

2. A large genome-wide association study of age-related macular degeneration highlights contributions of rare and common variants

3. Implications of genetic variation in the complement system in age-related macular degeneration

4. The complement system in age-related macular degeneration: A review of rare genetic variants and implications for personalized treatment

5. Rare variants in CFI, C3 and C9 are associated with high risk of advanced age-related macular degeneration