Carel B. Hoyng

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 et al. · Nature Genetics · 2015 · 1.6K citations · Full text

Genome-wide Association Study, Ocular Disease, Ophthalmology +6

A saturated map of common genetic variants associated with human height

Loïc Yengo, Sailaja Vedantam, Eirini Marouli et al. · Nature · 2022 · 827 citations · Full text

Consensus Definition for Atrophy Associated with Age-Related Macular Degeneration on OCT

Srinivas R. Sadda, Robyn H. Guymer, Frank G. Holz et al. · Ophthalmology · 2017 · 796 citations · Full text

Ocular Disease, Aging, Ophthalmology +8

Mutations in the CEP290 (NPHP6) Gene Are a Frequent Cause of Leber Congenital Amaurosis

Anneke I. den Hollander, Robert K. Koenekoop, Suzanne Yzer et al. · The American Journal of Human Genetics · 2006 · 670 citations · Full text

Developmental Biology, Genetic Disorder, Genetics +7

Rare and low-frequency coding variants alter human adult height

Eirini Marouli, Mariaelisa Graff, Carolina Medina‐Gómez et al. · Nature · 2017 · 647 citations · Full text

Allelic Variant, Genetics, Statistical Genetics +2