Anna Richards
Ecosystem Sciences(AU)
Publications by Year
Research Areas
Complement system in diseases, Hemoglobinopathies and Related Disorders, Blood groups and transfusion, Renal Diseases and Glomerulopathies, Erythrocyte Function and Pathophysiology
Most-Cited Works
- → Mutations in Complement Factor I Predispose to Development of Atypical Hemolytic Uremic Syndrome(2005)474 cited
- → C-terminal truncations in human 3′-5′ DNA exonuclease TREX1 cause autosomal dominant retinal vasculopathy with cerebral leukodystrophy(2007)447 cited
- → Mutations in human complement regulator, membrane cofactor protein (CD46), predispose to development of familial hemolytic uremic syndrome(2003)405 cited
- → Atypical Hemolytic Uremic Syndrome(2013)337 cited
- → Factor H Mutations in Hemolytic Uremic Syndrome Cluster in Exons 18–20, a Domain Important for Host Cell Recognition(2001)311 cited
- → Extended haplotypes in the complement factor H (CFH) and CFH‐related (CFHR) family of genes protect against age‐related macular degeneration: Characterization, ethnic distribution and evolutionary implications(2006)243 cited
- → Complement Regulatory Genes and Hemolytic Uremic Syndromes(2007)150 cited
- → Characterization of mutations in complement factor I (CFI) associated with hemolytic uremic syndrome(2007)148 cited
- → VEGF regulates local inhibitory complement proteins in the eye and kidney(2016)148 cited
- → Atypical haemolytic uraemic syndrome(2006)143 cited