Martin Vollmer
University of Freiburg(DE)
Publications by Year
Research Areas
Ion Transport and Channel Regulation, Ion channel regulation and function, Magnesium in Health and Disease, Genetic and Kidney Cyst Diseases, Renal and related cancers
Most-Cited Works
- → Mutation of BSND causes Bartter syndrome with sensorineural deafness and kidney failure(2001)530 cited
- → A novel gene encoding an SH3 domain protein is mutated in nephronophthisis type 1(1997)351 cited
- → Mutations in the Chloride Channel Gene CLCNKB as a Cause of Classic Bartter Syndrome(2000)288 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
- → Novel Molecular Variants of the Na-K-2Cl Cotransporter Gene Are Responsible for Antenatal Bartter Syndrome(1998)155 cited
- → Hypokalemic Salt-Losing Tubulopathy With Chronic Renal Failure and Sensorineural Deafness(2001)116 cited
- → Molecular genetic identification of families with juvenile nephronophthisis type 1: Rate of progression to renal failure(1997)96 cited
- → A common NKCC2 mutation in Costa Rican Bartter's syndrome patients(1997)58 cited
- → Confirmation of the ATP6B1 gene as responsible for distal renal tubular acidosis(2002)55 cited
- → Hereditary Isolated Renal Magnesium Loss Maps to Chromosome 11q23(1999)50 cited