Federica Castelletti

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

Genetics of HUS: the impact of MCP, CFH, and IF mutations on clinical presentation, response to treatment, and outcome

Jessica Caprioli, Marina Noris, Simona Brioschi et al. · Blood · 2006 · 729 citations · Full text

Complement factor H mutations and gene polymorphisms in haemolytic uraemic syndrome: the C-257T, the A2089G and the G2881T polymorphisms are strongly associated with the disease

Jessica Caprioli, Federica Castelletti, Sara Bucchioni et al. · Human Molecular Genetics · 2003 · 306 citations

Hla, Histocompatibility, Hf1 Mutations +20

Mutations in <i>FN1</i> cause glomerulopathy with fibronectin deposits

Federica Castelletti, Roberta Donadelli, Federica Banterla et al. · Proceedings of the National Academy of Sciences · 2008 · 152 citations · Full text

Glomerular Disease, Fn1 Mutation, Genetics +17

Complement Factor H Mutation in Familial Thrombotic Thrombocytopenic Purpura with ADAMTS13 Deficiency and Renal Involvement

Marina Noris, Sara Bucchioni, Miriam Galbusera et al. · Journal of the American Society of Nephrology · 2005 · 136 citations

Glomerular Disease, Vasculitis, Genetics +21