Peter F. Zipfel

Relative Role of Genetic Complement Abnormalities in Sporadic and Familial aHUS and Their Impact on Clinical Phenotype

Marina Noris, Jessica Caprioli, Elena Bresin et al. · Clinical Journal of the American Society of Nephrology · 2010 · 1K citations · Full text

Life Sciences, Genetics, Human Genetics +13

Atypical hemolytic uremic syndrome and C3 glomerulopathy: conclusions from a “Kidney Disease: Improving Global Outcomes” (KDIGO) Controversies Conference

Timothy H.J. Goodship, H. Terence Cook, Fádi Fakhouri et al. · Kidney International · 2016 · 695 citations · Full text

Medicine, Nephrology, Pathology +17

Complement factor H binds malondialdehyde epitopes and protects from oxidative stress

David Weismann, Karsten Hartvigsen, Nadine Lauer et al. · Nature · 2011 · 525 citations

Life Sciences, Immunology, Molecular Biology +16

Factor H autoantibodies in atypical hemolytic uremic syndrome correlate with CFHR1/CFHR3 deficiency

Mihály Józsi, Christoph Licht, Svante Zipfel et al. · Blood · 2007 · 356 citations

Life Sciences, Hematology, Immunology +13

Mutations in factor H reduce binding affinity to C3b and heparin and surface attachment to endothelial cells in hemolytic uremic syndrome

Tamara Manuelian, Jens Hellwage, Seppo Meri et al. · Journal of Clinical Investigation · 2003 · 342 citations · Full text

Medicine, Genetics, Molecular Genetics +15