Deletion of Complement Factor H–Related Genes CFHR1 and CFHR3 Is Associated with Atypical Hemolytic Uremic SyndromePeter F. Zipfel, Christine Skerka, Bernd Höppe et al.|PLoS Genetics|2007Cited by 324
Primary, Nonsyndromic Vesicoureteric Reflux and Its Nephropathy Is Genetically Heterogeneous, with a Locus on Chromosome 1Sally Feather, Judith A. Goodship, Sue Malcolm et al.|The American Journal of Human Genetics|2000Cited by 132
Mutations in TBX18 Cause Dominant Urinary Tract Malformations via Transcriptional Dysregulation of Ureter DevelopmentAsaf Vivante, Friedhelm Hildebrandt, Marc‐Jens Kleppa et al.|The American Journal of Human Genetics|2015Cited by 93