M. Vollmer

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University of Groningen Novel molecular variants of the Na-K-2Cl cotransporter gene are responsible for antenatal Bartter syndrome Vargas-Poussou,

C. Antignac, F. Hildebrandt, L. Guay-Woodford, 2007 .

Molecular genetic identification of families with juvenile nephronophthisis type 1: rate of progression to renal failure. APN Study Group. Arbeitsgemeinschaft für Pädiatrische Nephrologie.

N. Gretz, F. Hildebrandt, H. Nothwang, 1997, Kidney international.

Antenatal Bartter syndrome with sensorineural deafness: refinement of the locus on chromosome 1p31.

C. Antignac, F. Hildebrandt, L. Guay-Woodford, 2000, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

Hypokalemic salt-losing tubulopathy with chronic renal failure and sensorineural deafness.

M. Konrad, K. Pasel, H. Seyberth, 2001, Pediatrics.

A Bartter’s Syndrome Mutation of ROMK1 Exerts Dominant Negative Effects on K+ Conductance

F. Hildebrandt, R. Schreiber, K. Kunzelmann, 2000, Cellular Physiology and Biochemistry.

Mutations in the chloride channel gene CLCNKB as a cause of classic Bartter syndrome.

C. Antignac, F. Hildebrandt, L. Guay-Woodford, 2000, Journal of the American Society of Nephrology : JASN.

Hereditary isolated renal magnesium loss maps to chromosome 11q23.

F. Hildebrandt, L. P. Van den Heuvel, A. Reis, 1999, American journal of human genetics.

Mutation of BSND causes Bartter syndrome with sensorineural deafness and kidney failure

H. Omran, R. Sudbrak, D. Milford, 2001, Nature Genetics.

Exclusion of the candidate genes ACE and Bcl-2 for six families with nephronophthisis not linked to the NPH1 locus.

H. Omran, G. Caridi, F. Hildebrandt, 1999, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

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

F. Hildebrandt, E. Otto, H. Nothwang, 1997, Nature Genetics.

Confirmation of the ATP6B1 gene as responsible for distal renal tubular acidosis

J. Weber, G. Rizzoni, C. Antignac, 2003, Pediatric Nephrology.

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.

A. Ziegler, K. Grzeschik, G. Rizzoni, 1997, Human molecular genetics.

Mutations in the gene encoding the inwardly-rectifying renal potassium channel, ROMK, cause the antenatal variant of Bartter syndrome: evidence for genetic heterogeneity

A. Ziegler, G. Rizzoni, C. Antignac, 2019 .

Two novel mutations of the gene for Kir 1.1 (ROMK) in neonatal Bartter syndrome

H. Omran, F. Hildebrandt, R. Topaloğlu, 1998, Pediatric Nephrology.

The gene for human fibronectin glomerulopathy maps to 1q32, in the region of the regulation of complement activation gene cluster.

T. Wienker, F. Hildebrandt, F. Rüschendorf, 1998, American journal of human genetics.

A common NKCC2 mutation in Costa Rican Bartter's syndrome patients: evidence for a founder effect.

M. Koch, L. Guay-Woodford, N. Knoers, 1997, Journal of the American Society of Nephrology : JASN.

mut0 methylmalonic acidemia: Eleven novel mutations of the methylmalonyl CoA mutase including a deletion‐insertion mutation

E. R. Baumgartner, F. Hildebrandt, A. Fuchshuber, 2000, Human mutation.

Novel molecular variants of the Na-K-2Cl cotransporter gene are responsible for antenatal Bartter syndrome.

C. Antignac, F. Hildebrandt, L. Guay-Woodford, 1998, American journal of human genetics.

Molecular cloning of the critical region for glomerulopathy with fibronectin deposits (GFND) and evaluation of candidate genes.

F. Hildebrandt, E. Otto, H. Nothwang, 2000, Genomics.

Autosomal dominant medullary cystic kidney disease: evidence of gene locus heterogeneity.

F. Hildebrandt, T. Feest, A. Pierides, 1998, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.