Sheila Pinto

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

Human C3 mutation reveals a mechanism of dense deposit disease pathogenesis and provides insights into complement activation and regulation

Rubén Martínez-Barricarte, Meike Heurich, Francisco Valdés-Cañedo et al. · Journal of Clinical Investigation · 2010 · 222 citations · Full text

Medicine, Genetics, Pathobiology +17

Statistical Validation of Rare Complement Variants Provides Insights into the Molecular Basis of Atypical Hemolytic Uremic Syndrome and C3 Glomerulopathy

Amy J. Osborne, Matteo Breno, Nicolò Ghiringhelli Borsa et al. · The Journal of Immunology · 2018 · 168 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Elevated factor H–related protein 1 and factor H pathogenic variants decrease complement regulation in IgA nephropathy

Agustín Tortajada, Eduardo Gutiérrez, Elena Goicoechea de Jorge et al. · Kidney International · 2017 · 119 citations · Full text

Medicine, Nephrology, Pathology +17

Complement Mutations in Diacylglycerol Kinase-ε–Associated Atypical Hemolytic Uremic Syndrome

Daniel Sánchez Chinchilla, Sheila Pinto, Bernd Höppe et al. · Clinical Journal of the American Society of Nephrology · 2014 · 69 citations

Medicine, Hematology, Molecular Genetics +17