Jessica Caprioli

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

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 · 730 citations · Full text

Life Sciences, Genetics, Molecular Genetics +12

Combined Complement Gene Mutations in Atypical Hemolytic Uremic Syndrome Influence Clinical Phenotype

Elena Bresin, Erica Rurali, Jessica Caprioli et al. · Journal of the American Society of Nephrology · 2013 · 350 citations

Life Sciences, Genetics, Molecular Genetics +17

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

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 · 308 citations

Life Sciences, Genetics, Molecular Genetics +12