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Hannsjörg W. Seyberth | doi.page

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Hannsjörg W. Seyberth

Publications by Year

Research Areas

Ion Transport and Channel Regulation, Inflammatory mediators and NSAID effects, Ion channel regulation and function, Pharmaceutical studies and practices, Electrolyte and hormonal disorders

Most-Cited Works

→ Hypomagnesemia with secondary hypocalcemia is caused by mutations in TRPM6, a new member of the TRPM gene family(2002)776 cited
→ Disruption of TRPM6/TRPM7 complex formation by a mutation in the TRPM6 gene causes hypomagnesemia with secondary hypocalcemia(2004)370 cited
→ Localization of cyclooxygenase-1 and -2 in adult and fetal human kidney: implication for renal function(1997)362 cited
→ Bartter's syndrome: A disorder characterized by high urinary prostaglandins and a dependence of hyperreninemia on prostaglandin synthesis(1976)324 cited
→ Salt Wasting and Deafness Resulting from Mutations in Two Chloride Channels(2004)280 cited
→ Novel Paracellin-1 Mutations in 25 Families with Familial Hypomagnesemia with Hypercalciuria and Nephrocalcinosis(2001)270 cited

→ Clinical presentation of genetically defined patients with hypokalemic salt-losing tubulopathies(2002)

261 cited

→ Mutations in the Chloride Channel Gene, CLCNKB, Leading to a Mixed Bartter-Gitelman Phenotype(2000)194 cited

→ 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](1997)190 cited

→ Polyhydramnios, Transient Antenatal Bartter’s Syndrome, andMAGED2Mutations(2016)182 cited