Françoise Broux

KLHL3 mutations cause familial hyperkalemic hypertension by impairing ion transport in the distal nephron

Hélène Louis-Dit-Picard, Julien Barc, Daniel Trujillano et al. · Nature Genetics · 2012 · 337 citations · Full text

Medicine, Genetics, Nephrology +17

Phenotype–genotype correlation in antenatal and neonatal variants of Bartter syndrome

Karine Brochard, Olivia Boyer, Anne Blanchard et al. · Nephrology Dialysis Transplantation · 2008 · 165 citations

Medicine, Genetics, Pediatrics +17

Low incidence of SARS-CoV-2, risk factors of mortality and the course of illness in the French national cohort of dialysis patients

Cécile Couchoud, Florian Bayer, Carole Ayav et al. · Kidney International · 2020 · 150 citations · Full text

Medicine, Infectious Diseases, Internal Medicine +6

Familial Hypocalciuric Hypercalcemia Types 1 and 3 and Primary Hyperparathyroidism: Similarities and Differences

Rosa Vargas‐Poussou, Lamisse Mansour‐Hendili, Stéphanie Baron et al. · The Journal of Clinical Endocrinology & Metabolism · 2016 · 120 citations · Full text

Medicine, Endocrinology, Genetics +17

Comprehensive PKD1 and PKD2 Mutation Analysis in Prenatal Autosomal Dominant Polycystic Kidney Disease

Marie‐Pierre Audrézet, Christine Corbiere, Saïd Lebbah et al. · Journal of the American Society of Nephrology · 2015 · 85 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17