David Kavanagh
Newcastle University(GB)
Publications by Year
Research Areas
Complement system in diseases, Renal Diseases and Glomerulopathies, Blood groups and transfusion, Retinal Diseases and Treatments, Adenosine and Purinergic Signaling
Most-Cited Works
- → Biological insights from 108 schizophrenia-associated genetic loci(2014)8,017 cited
- → The ExAC browser: displaying reference data information from over 60 000 exomes(2016)819 cited
- → Genetics of HUS: the impact of MCP, CFH, and IF mutations on clinical presentation, response to treatment, and outcome(2006)729 cited
- → Atypical hemolytic uremic syndrome and C3 glomerulopathy: conclusions from a “Kidney Disease: Improving Global Outcomes” (KDIGO) Controversies Conference(2016)680 cited
- → 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
- → C3 glomerulopathy — understanding a rare complement-driven renal disease(2019)380 cited
- → Thrombotic Microangiopathy and the Kidney(2017)354 cited
- → Rare variants in CFI, C3 and C9 are associated with high risk of advanced age-related macular degeneration(2013)353 cited
- → Association of factor H autoantibodies with deletions of CFHR1, CFHR3, CFHR4, and with mutations in CFH, CFI, CD46, and C3 in patients with atypical hemolytic uremic syndrome(2009)353 cited