Anna Richards

Mutations in Complement Factor I Predispose to Development of Atypical Hemolytic Uremic Syndrome

David Kavanagh, Elizabeth J. Kemp, Elizabeth Mayland et al. · Journal of the American Society of Nephrology · 2005 · 473 citations

C-terminal truncations in human 3′-5′ DNA exonuclease TREX1 cause autosomal dominant retinal vasculopathy with cerebral leukodystrophy

Anna Richards, Arn M. J. M. van den Maagdenberg, Joanna C. Jen et al. · Nature Genetics · 2007 · 444 citations

Ocular Disease, C-terminal Truncations, Retina +8

Mutations in human complement regulator, membrane cofactor protein (CD46), predispose to development of familial hemolytic uremic syndrome

Anna Richards, Elizabeth J. Kemp, M. Kathryn Liszewski et al. · Proceedings of the National Academy of Sciences · 2003 · 405 citations · Full text

Factor H Mutations in Hemolytic Uremic Syndrome Cluster in Exons 18–20, a Domain Important for Host Cell Recognition

Anna Richards, M. Buddles, Rosemary L. Donne et al. · The American Journal of Human Genetics · 2001 · 310 citations · Full text

Exons 18–20, Genetic Disorder, Factor H Mutations +9

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 et al. · Annals of Medicine · 2006 · 241 citations · Full text