Françoise Janssen

CD81 gene defect in humans disrupts CD19 complex formation and leads to antibody deficiency

Menno C. van Zelm, Julie Smet, Brigitte Adams et al. · Journal of Clinical Investigation · 2010 · 385 citations · Full text

Immunodeficiencies, Immunology, Cd4 T Cell Responses +20

Role of truncating mutations in MME gene in fetomaternal alloimmunisation and antenatal glomerulopathies

Hanna Dêbiec, Jeroen Nauta, Florence Coulet et al. · The Lancet · 2004 · 212 citations

Fetomaternal Alloimmunisation, Glomerulonephritis, Genetics +6

Genotype–phenotype correlation in primary hyperoxaluria type 1: the p.Gly170Arg AGXT mutation is associated with a better outcome

Jérôme Harambat, Sonia Fargue, Cécile Acquaviva et al. · Kidney International · 2009 · 151 citations · Full text

Allelic Variant, Primary Hyperoxaluria, Genetic Disorder +10

Clinical characteristics and outcomes of children with stage 3–5 chronic kidney disease

Tran Thi Mong Hiep, Khalid Ismaïli, Frédéric Collart et al. · Pediatric Nephrology · 2010 · 111 citations

Glomerulonephritis, Hemodialysis, Renal Function +11

Ureteral Stenosis After Kidney Transplantation: True Incidence and Long-Term Followup After Surgical Correction

P Kinnaert, M. Hall, Françoise Janssen et al. · The Journal of Urology · 1985 · 88 citations