Whole-Exome Sequencing Identifies Causative Mutations in Families with Congenital Anomalies of the Kidney and Urinary TractAmelie T. van der Ven, Simone Sanna‐Cherchi, Tilman Jobst‐Schwan et al.|Journal of the American Society of Nephrology|2018Cited by 211
Whole-Exome Sequencing Enables a Precision Medicine Approach for Kidney Transplant RecipientsNina Mann, Friedhelm Hildebrandt, Daniela A. Braun et al.|Journal of the American Society of Nephrology|2019Cited by 156
Mutations in multiple components of the nuclear pore complex cause nephrotic syndromeDaniela A. Braun, Fowzan S. Alkuraya, Friedhelm Hildebrandt et al.|Journal of Clinical Investigation|2018Cited by 146
Mutations in <i>WDR4</i> as a new cause of Galloway–Mowat syndromeDaniela A. Braun, Friedhelm Hildebrandt, Shirlee Shril et al.|American Journal of Medical Genetics Part A|2018Cited by 101
ADCK4 Deficiency Destabilizes the Coenzyme Q Complex, Which Is Rescued by 2,4-Dihydroxybenzoic Acid TreatmentEugen Widmeier, Heon Yung Gee, Seyoung Yu et al.|Journal of the American Society of Nephrology|2020Cited by 63