Martin Konrad

Mutations in the gene encoding the inwardly-rectifying renal potassium channel, ROMK, cause the antenatal variant of Bartter syndrome: evidence for genetic heterogeneity. International Collaborative Study Group for Bartter-like Syndromes [published erratum appears in Hum Mol Genet 1997 Apr;6(4):650]

Lothar Károlyi, Martin Konrad, Arnold Köckerling et al. · Human Molecular Genetics · 1997 · 190 citations · Full text

Electrolyte Disorder, Genetics, Renal Pathology +19

Large homozygous deletions of the 2q13 region are a major cause of juvenile nephronophthisis

Martin Konrad · Human Molecular Genetics · 1996 · 140 citations · Full text

Genetics, Juvenile Nephronophthisis, Pathology +16

Familial hypomagnesaemia with hypercalciuria and nephrocalcinosis maps to chromosome 3q27 and is associated with mutations in the PCLN-1 gene

Stefanie Weber, Katrin Hoffmann, Nikola Jeck et al. · European Journal of Human Genetics · 2000 · 93 citations · Full text

Mendelian Disorder, Genetic Disorder, Genetics +9

Prenatal and Postnatal Management of Hyperprostaglandin E Syndrome After Genetic Diagnosis From Amniocytes

Martin Konrad, Andreas Leonhardt, Peter Hensen et al. · PEDIATRICS · 1999 · 57 citations

Evaluation of long-term treatment with indomethacin in hereditary hypokalemic salt-losing tubulopathies

Stephan C. Reinalter, Hermann-Josef Gröne, Martin Konrad et al. · The Journal of Pediatrics · 2001 · 43 citations

Urology, Long-term Treatment