Katharina Hohenfellner

Role of the Angiotensin Type 2 Receptor Gene in Congenital Anomalies of the Kidney and Urinary Tract, CAKUT, of Mice and Men

Hideki Nishimura, Elizabeth B. Yerkes, Katharina Hohenfellner et al. · Molecular Cell · 1999 · 363 citations · Full text

Medicine, Genetics, Molecular Genetics +14

One Year of Newborn Screening for SMA – Results of a German Pilot Project

Katharina Vill, Heike Kölbel, Oliver Schwartz et al. · Journal of Neuromuscular Diseases · 2019 · 189 citations · Full text

Medicine, Neurology, Pediatrics +17

Controversies and research agenda in nephropathic cystinosis: conclusions from a “Kidney Disease: Improving Global Outcomes” (KDIGO) Controversies Conference

Craig B. Langman, Bruce A. Barshop, Georges Deschênes et al. · Kidney International · 2016 · 83 citations

Medicine, Nephrology, Pathology +13

ACE I/D gene polymorphism predicts renal damage in congenital uropathies

Katharina Hohenfellner, Tracy E. Hunley, R. Brezinska et al. · Pediatric Nephrology · 1999 · 77 citations

Medicine, Genetics, Molecular Genetics +11

An international cohort study spanning five decades assessed outcomes of nephropathic cystinosis

Francesco Emma, William van’t Hoff, Katharina Hohenfellner et al. · Kidney International · 2021 · 71 citations · Full text

Medicine, Nephrology, Pathology +6