Concepedia

Martin Vollmer

MV

15

Publications

1.8K

Citations

13

H-Index

1997

Active since

Affiliations

University Medical Center Freiburg(Current)

Radboud University Nijmegen

Philipps University of Marburg

University of Freiburg

University of Alabama at Birmingham

Martin Vollmer is an author at University Medical Center Freiburg specializing in medicine, genetics, and nephrology.

Top concepts

Publications per year

1997–2002

15

Publications

15

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 · 529 citations

, , +6

A novel gene encoding an SH3 domain protein is mutated in nephronophthisis type 1

Friedhelm Hildebrandt, Edgar A. Otto, Hans Gerd Nothwang et al. · Nature Genetics · 1997 · 350 citations

, , +10

Mutations in the Chloride Channel Gene CLCNKB as a Cause of Classic Bartter Syndrome

Martin Konrad, Martin Vollmer, Henny H. Lemmink et al. · Journal of the American Society of Nephrology · 2000 · 288 citations

Novel Molecular Variants of the Na-K-2Cl Cotransporter Gene Are Responsible for Antenatal Bartter Syndrome

Rosa Vargas‐Poussou, Delphine Feldmann, Martin Vollmer et al. · The American Journal of Human Genetics · 1998 · 155 citations · Full text

, , +6

Hypokalemic Salt-Losing Tubulopathy With Chronic Renal Failure and Sensorineural Deafness

Nikola Jeck, Stephan C. Reinalter, Thomas Henne et al. · PEDIATRICS · 2001 · 116 citations

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