Raphael Schild

SIX2 and BMP4 Mutations Associate With Anomalous Kidney Development

Stefanie Weber, Jaclyn C. Taylor, Paul J.D. Winyard et al. · Journal of the American Society of Nephrology · 2008 · 214 citations · Full text

Life Sciences, Developmental Biology, Genetics +17

Phenotypic Spectrum of Children with Nephronophthisis and Related Ciliopathies

Jens König, Birgitta Kranz, Sabine König et al. · Clinical Journal of the American Society of Nephrology · 2017 · 107 citations · Full text

Medicine, Genetics, Pediatrics +16

Refining genotype–phenotype correlations in 304 patients with autosomal recessive polycystic kidney disease and PKHD1 gene variants

Kathrin Burgmaier, Leonie Violetta Brinker, Florian Erger et al. · Kidney International · 2021 · 87 citations · Full text

Medicine, Genetics, Molecular Genetics +16

HNF1B nephropathy has a slow-progressive phenotype in childhood—with the exception of very early onset cases: results of the German Multicenter HNF1B Childhood Registry

Christine Okorn, Anne Goertz, Udo Vester et al. · Pediatric Nephrology · 2019 · 68 citations · Full text

Medicine, Genetics, Pediatrics +17

Risk Factors for Early Dialysis Dependency in Autosomal Recessive Polycystic Kidney Disease

Kathrin Burgmaier, Kevin Kunzmann, Gema Ariceta et al. · The Journal of Pediatrics · 2018 · 61 citations · Full text

Medicine, Nephrology, Dialysis +13