Karl P. Schlingmann

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 · 775 citations

Trpm Gene Family, Natural Sciences, Genetics +8

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

Karl P. Schlingmann, Martin Kaufmann, Stefanie Weber et al. · New England Journal of Medicine · 2011 · 663 citations · Full text

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 · 511 citations · Full text

Urology, Ophthalmology, Medicine +7

SLC39A8 Deficiency: A Disorder of Manganese Transport and Glycosylation

Julien H. Park, Max Hogrebe, Marianne Grüneberg et al. · The American Journal of Human Genetics · 2015 · 303 citations · Full text

Slc39a8 Deficiency, Biochemistry, Natural Sciences +3

Salt Wasting and Deafness Resulting from Mutations in Two Chloride Channels

Karl P. Schlingmann, Martin Konrad, Nikola Jeck et al. · New England Journal of Medicine · 2004 · 280 citations · Full text

Biology, Chloride Transporters, Deafness Resulting +11