Joachim Misselwitz

Mutations in<i>CYP24A1</i>and Idiopathic Infantile Hypercalcemia

Karl P. Schlingmann, Martin Kaufmann, Stefanie Weber et al. · New England Journal of Medicine · 2011 · 684 citations · Full text

Medicine, Pediatrics, Pharmacotherapy +17

Deletion of Complement Factor H–Related Genes CFHR1 and CFHR3 Is Associated with Atypical Hemolytic Uremic Syndrome

Peter F. Zipfel, Matthew Edey, Stefan Heinen et al. · PLoS Genetics · 2007 · 324 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Novel Paracellin-1 Mutations in 25 Families with Familial Hypomagnesemia with Hypercalciuria and Nephrocalcinosis

Stefanie Weber, Linda Schneider, Melanie Peters et al. · Journal of the American Society of Nephrology · 2001 · 271 citations

Medicine, Genetics, Nephrology +16

Mapping of the gene for autosomal recessive polycystic kidney disease (ARPKD) to chromosome 6p21–cen

Klaus Zerres, Gabi Mücher, L Bachner et al. · Nature Genetics · 1994 · 258 citations

Medicine, Genetics, Molecular Genetics +14

Day- and night-time blood pressure elevation in children with higher grades of renal scarring

Ludwig Patzer, Tomáš Seeman, Carmen Luck et al. · The Journal of Pediatrics · 2003 · 97 citations

Medicine, Nephrology, Pediatrics +16