Mutations in 12 known dominant disease-causing genes clarify many congenital anomalies of the kidney and urinary tractDaw‐Yang Hwang, Friedhelm Hildebrandt, Gabriel C. Dworschak et al.|Kidney International|2014Cited by 263
Whole-exome resequencing reveals recessive mutations in TRAP1 in individuals with CAKUT and VACTERL associationPawaree Saisawat, Friedhelm Hildebrandt, S. Natarajan et al.|Kidney International|2013Cited by 128
Mild Recessive Mutations in Six Fraser Syndrome–Related Genes Cause Isolated Congenital Anomalies of the Kidney and Urinary TractStefan Kohl, Friedhelm Hildebrandt, Daw‐Yang Hwang et al.|Journal of the American Society of Nephrology|2014Cited by 115
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
Targeted Resequencing of 29 Candidate Genes and Mouse Expression Studies Implicate<i>ZIC3</i>and<i>FOXF1</i>in Human VATER/VACTERL AssociationAlina C. Hilger, Friedhelm Hildebrandt, Jan Halbritter et al.|Human Mutation|2015Cited by 56