A. Lehnhardt

Mutations in TBX18 Cause Dominant Urinary Tract Malformations via Transcriptional Dysregulation of Ureter Development

Asaf Vivante, Marc‐Jens Kleppa, Julian Schulz et al. · The American Journal of Human Genetics · 2015 · 92 citations · Full text

Medicine, Genetics, Molecular Genetics +13

Secondary Nephrogenic Diabetes Insipidus as a Complication of Inherited Renal Diseases

Detlef Böckenhauer, William van’t Hoff, Mehul Dattani et al. · Nephron Physiology · 2010 · 78 citations

Medicine, Endocrinology, Nephrology +17

Fibroblast growth factor 23 and bone metabolism in children with chronic kidney disease

Michael van Husen, Ann‐Katrin Fischer, A. Lehnhardt et al. · Kidney International · 2010 · 76 citations

Medicine, Nephrology, Pediatrics +14

Clinical and Molecular Characterization of Patients with Heterozygous Mutations in Wilms Tumor Suppressor Gene 1

A. Lehnhardt, Claartje Karnatz, Thurid Ahlenstiel-Grunow et al. · Clinical Journal of the American Society of Nephrology · 2015 · 75 citations · Full text

Medicine, Genetics, Nephrology +15

Long-term Clinical Relevance of De Novo Donor-Specific Antibodies After Pediatric Liver Transplantation

Enke Grabhorn, Thomas M. C. Binder, Denise Obrecht et al. · Transplantation · 2015 · 65 citations

Medicine, Immunology, Pediatrics +17