Concepedia

Author

Martin Konrad

Philipps University of Marburg

Also Known As

Konrad, Martin, M Konrad, Martin Konrad

9

Publications

558

Citations

7

H-Index

16

Concepts

All Affiliations

Philipps University of MarburgHôpital Armand-TrousseauHeidelberg UniversityHôpital Necker-Enfants MaladesInserm
MK

About

Martin Konrad is an author at Philipps University of Marburg specializing in genetics, pathology, and urology.

Top Concepts

#ConceptH-IndexPublicationsCitations

1

Medicine

3

3

423

2

Pathology

3

3

423

3

Molecular Genetics

2

2

233

4

Nephrology

2

2

330

5

Biology

1

1

140

Martin Konrad

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6

Publications

549

Citations

6

H-Index

YearCitations

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,

Human Molecular Genetics

1997

190

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

Martin Konrad

Human Molecular Genetics

1996

140

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,

European Journal of Human Genetics

2000

93

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

Martin Konrad, Andreas Leonhardt, Peter Hensen,

PEDIATRICS

1999

57

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

Stephan C. Reinalter, Hermann-Josef Gröne, Martin Konrad,

The Journal of Pediatrics

2001

43

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

Martin Vollmer, Nikola Jeck, Henny H. Lemmink,

Nephrology Dialysis Transplantation

2000

26

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