Whole Exome Sequencing in Patients with the Cuticular Drusen Subtype of Age-Related Macular Degeneration

Whole-exome sequencing identifies rare, functional CFH variants in families with macular degeneration

(2014) Yi Yu et al.   HUMAN MOLECULAR GENETICS

Analysis of Rare Variants in the C3 Gene in Patients with Age-Related Macular Degeneration

(2014) Maheswara R. Duvvari et al.   PLoS One

Age-related macular degeneration and changes in the extracellular matrix

(2014) Wanda Romaniuk   MEDICAL SCIENCE MONITOR

Global prevalence of age-related macular degeneration and disease burden projection for 2020 and 2040: a systematic review and meta-analysis

(2014) Wan Ling Wong et al.   Lancet Global Health

A functional variant in the CFI gene confers a high risk of age-related macular degeneration

(2013) Johannes P H van de Ven et al.   NATURE GENETICS

Seven new loci associated with age-related macular degeneration

(2013) Lars G Fritsche et al.   NATURE GENETICS

Cuticular drusen: Stars in the sky

(2013) Camiel J.F. Boon et al.   PROGRESS IN RETINAL AND EYE RESEARCH

Short-Term Changes of Basal Laminar Drusen on Spectral-Domain Optical Coherence Tomography

(2012) Johannes P.H. van de Ven et al.   AMERICAN JOURNAL OF OPHTHALMOLOGY

A rare penetrant mutation in CFH confers high risk of age-related macular degeneration

(2011) Soumya Raychaudhuri et al.   NATURE GENETICS

The extracellular matrix at a glance

(2010) C. Frantz et al.   JOURNAL OF CELL SCIENCE

Unraveling a Multifactorial Late-Onset Disease: From Genetic Susceptibility to Disease Mechanisms for Age-Related Macular Degeneration

(2009) Anand Swaroop et al.   Annual Review of Genomics and Human Genetics

Targeted capture and massively parallel sequencing of 12 human exomes

(2009) Sarah B. Ng et al.   NATURE

Genetic diagnosis by whole exome capture and massively parallel DNA sequencing

(2009) Murim Choi et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Basal Laminar Drusen Caused by Compound Heterozygous Variants in the CFH Gene

(2008) Camiel J.F. Boon et al.   AMERICAN JOURNAL OF HUMAN GENETICS