Gaia Pianetti

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

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

Membrane cofactor protein mutations in atypical hemolytic uremic syndrome (aHUS), fatal Stx-HUS, C3 glomerulonephritis, and the HELLP syndrome

Celia J. Fang, Véronique Frémeaux‐Bacchi, M. Kathryn Liszewski et al. · Blood · 2007 · 147 citations · Full text

Medicine, Hematology, Nephrology +14

The Complement Factor H R1210C Mutation Is Associated With Atypical Hemolytic Uremic Syndrome

Rubén Martínez-Barricarte, Gaia Pianetti, Ruxandra Gautard et al. · Journal of the American Society of Nephrology · 2008 · 86 citations

Life Sciences, Genetics, Hematology +14