A common haplotype in the complement regulatory gene factor H ( <i>HF1/CFH</i> ) predisposes individuals to age-related macular degeneration

Gregory S. Hageman, Don H. Anderson, Lincoln V. Johnson, +24

Proceedings of the National Academy of Sciences

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

Lars G. Fritsche, Wilmar Igl, Jessica N. Cooke Bailey, +158

Nature Genetics

Genome-wide Association StudyOcular DiseaseOphthalmologyGeneticsAge-related Diseases +4

Variation in factor B (BF) and complement component 2 (C2) genes is associated with age-related macular degeneration

Bert Gold, Joanna E. Merriam, Jana Zernant, +11

Nature Genetics

Complement SystemComplement Component 2Ocular DiseaseOphthalmologyGenetics +8

Seven new loci associated with age-related macular degeneration

Lars G. Fritsche, Wei Chen, Matthew Schu, +150

Nature Genetics

Ocular DiseaseOphthalmologyAge-related DiseasesPathologyNew Loci +1

Genome-wide association study of advanced age-related macular degeneration identifies a role of the hepatic lipase gene ( <i>LIPC</i> )

Benjamin M. Neale, Jesen Fagerness, Robyn Reynolds, +23

Proceedings of the National Academy of Sciences

Ocular DiseaseGeneticsGenetic EpidemiologyHuman PolymorphismHyperlipidemia +16

Extended haplotypes in the complement factor H (<i>CFH</i>) and CFH‐related (<i>CFHR</i>) family of genes protect against age‐related macular degeneration: Characterization, ethnic distribution and evolutionary implications

Gregory S. Hageman, Lisa S. Hancox, Andrew J. Taiber, +14

Annals of Medicine

Cadherin 5 is Regulated by Corticosteroids and Associated with Central Serous Chorioretinopathy

Carl Schubert, Anders Pryds, Shemin Zeng, +17

Human Mutation

Vascular DiseaseOcular DiseaseImmunologyPathologyCellular Physiology +16

Three Major Loci Involved in Age-Related Macular Degeneration Are Also Associated with Polypoidal Choroidal Vasculopathy

Luiz H. Lima, Carl Schubert, Daniela Ferrara, +6

Ophthalmology

Ocular DiseaseOphthalmologyAge-related DiseasesPathologyGlaucoma +4

Mutations in NR2E3 can cause dominant or recessive retinal degenerations in the same family

Pascal Escher, Peter Gouras, Raphaël Roduit, +12

Human Mutation

Ocular DiseaseMolecular RegulationGeneticsMolecular BiologyMolecular Genetics +18

Rare and common variants in extracellular matrix gene Fibrillin 2 (FBN2) are associated with macular degeneration

Rinki Ratnapriya, Xiaowei Zhan, Robert N. Fariss, +62

Human Molecular Genetics