Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)

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M. Födinger

Department of Laboratory Medicine

University of Vienna

Austria

[email]@akh-wien.ac.at

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Affiliations

Department of Laboratory Medicine, University of Vienna, Austria. 1997 - 2001
Department of Medicine III, Division of Nephrology and Dialysis, University of Vienna, Austria. 2001

References

Recent insights into the molecular genetics of the homocysteine metabolism. Födinger, M., Wagner, O.F., Hörl, W.H., Sunder-Plassmann, G. Kidney Int. Suppl. (2001) [Pubmed]
Association of two MTHFR polymorphisms with total homocysteine plasma levels in dialysis patients. Födinger, M., Buchmayer, H., Heinz, G., Papagiannopoulos, M., Kletzmayr, J., Perschl, A., Vychytil, A., Hörl, W.H., Sunder-Plassmann, G. Am. J. Kidney Dis. (2001) [Pubmed]
Molecular biology of 5,10-methylenetetrahydrofolate reductase. Födinger, M., Hörl, W.H., Sunder-Plassmann, G. J. Nephrol. (2000) [Pubmed]
Erythropoietin-inducible immediate-early genes in human vascular endothelial cells. Födinger, M., Fritsche-Polanz, R., Buchmayer, H., Skoupy, S., Sengoelge, G., Hörl, W.H., Sunder-Plassmann, G. J. Investig. Med. (2000) [Pubmed]
Inherited disorders of iron metabolism. Födinger, M., Sunder-Plassmann, G. Kidney Int. Suppl. (1999) [Pubmed]
Molecular analysis of the carboxy terminus of the beta and gamma subunits of the epithelial sodium channel in patients with end-stage renal disease. Födinger, M., Schedler, D., Fritsche-Polanz, R., Hörl, W.H., Sunder-Plassmann, G. Nephron (1999) [Pubmed]
Molecular genetics of homocysteine metabolism. Födinger, M., Buchmayer, H., Sunder-Plassmann, G. Miner. Electrolyte. Metab (1999) [Pubmed]
Mutations in the carboxy terminus of the beta and gamma subunits of the epithelial sodium channel are not present in patients with hypertensive crisis. Födinger, M., Hirschl, M.M., Schedler, D., Herkner, H., Bur, A., Laggner, A.N., Hörl, W.H., Sunder-Plassmann, G. Eur. J. Clin. Invest. (1998) [Pubmed]
Mutation (677 C to T) in the methylenetetrahydrofolate reductase gene aggravates hyperhomocysteinemia in hemodialysis patients. Födinger, M., Mannhalter, C., Wölfl, G., Pabinger, I., Müller, E., Schmid, R., Hörl, W.H., Sunder-Plassmann, G. Kidney Int. (1997) [Pubmed]

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