Martin Konrad

Hypomagnesemia with secondary hypocalcemia is caused by mutations in TRPM6, a new member of the TRPM gene family

Karl P. Schlingmann, Stefanie Weber, Melanie Peters et al. · Nature Genetics · 2002 · 784 citations

Life Sciences, Genetics, Molecular Genetics +11

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

Mutation of BSND causes Bartter syndrome with sensorineural deafness and kidney failure

Ralf Birkenhäger, Edgar A. Otto, Maria J. Schürmann et al. · Nature Genetics · 2001 · 538 citations

Medicine, Nephrology, Neurology +9

Mutations in the Tight-Junction Gene Claudin 19 (CLDN19) Are Associated with Renal Magnesium Wasting, Renal Failure, and Severe Ocular Involvement

Martin Konrad, André Schaller, Dominik Seelow et al. · The American Journal of Human Genetics · 2006 · 522 citations · Full text

Medicine, Genetics, Molecular Genetics +15

Disruption of TRPM6/TRPM7 complex formation by a mutation in the <i>TRPM6</i> gene causes hypomagnesemia with secondary hypocalcemia

Vladimir Chubanov, Siegfried Waldegger, Michael Mederos y Schnitzler et al. · Proceedings of the National Academy of Sciences · 2004 · 372 citations · Full text

Life Sciences, Cell Biology, Molecular Biology +17