Whole-Exome Sequencing Identifies Causative Mutations in Families with Congenital Anomalies of the Kidney and Urinary TractAmelie T. van der Ven, Simone Sanna‐Cherchi, Julian Schulz et al.|Journal of the American Society of Nephrology|2018Cited by 211
Exome Sequencing Discerns Syndromes in Patients from Consanguineous Families with Congenital Anomalies of the Kidneys and Urinary TractAsaf Vivante, Friedhelm Hildebrandt, Daw‐Yang Hwang et al.|Journal of the American Society of Nephrology|2016Cited by 98
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
Mutations of the SLIT2–ROBO2 pathway genes SLIT2 and SRGAP1 confer risk for congenital anomalies of the kidney and urinary tractDaw‐Yang Hwang, Friedhelm Hildebrandt, Stefan Kohl et al.|Human Genetics|2015Cited by 69