Sophie Gié

Differential Impact of Complement Mutations on Clinical Characteristics in Atypical Hemolytic Uremic Syndrome

Anne‐Laure Sellier‐Leclerc, Véronique Frémeaux‐Bacchi, Marie‐Agnès Dragon‐Durey et al. · Journal of the American Society of Nephrology · 2007 · 427 citations

Mutations in complement C3 predispose to development of atypical hemolytic uremic syndrome

Véronique Frémeaux‐Bacchi, Elizabeth C. Miller, M. Kathryn Liszewski et al. · Blood · 2008 · 371 citations · Full text

Mutations of NPHP2 and NPHP3 in infantile nephronophthisis

Kálmán Tory, Caroline Rousset‐Rouvière, Marie-Claire Gübler et al. · Kidney International · 2009 · 117 citations

Biology, Genetic Disorder, Genetics +4

PKD2-Related Autosomal Dominant Polycystic Kidney Disease: Prevalence, Clinical Presentation, Mutation Spectrum, and Prognosis

Émilie Cornec-Le Gall, M.‐P. Audrézet, E. Renaudineau et al. · American Journal of Kidney Diseases · 2017 · 73 citations · Full text

The genetic landscape and clinical spectrum of nephronophthisis and related ciliopathies

Friederike Petzold, Katy Billot, Xiaoyi Chen et al. · Kidney International · 2023 · 44 citations · Full text