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

S.M. Baumgartner-Parzer

Department of Internal Medicine III

Division of Endocrinology and Metabolism

Waehringer Guertel 18-20

A-1090 Vienna



Name/email consistency: high



  • Department of Internal Medicine III, Division of Endocrinology and Metabolism, Waehringer Guertel 18-20, A-1090 Vienna, Austria. 2005 - 2007
  • Department of Internal Medicine III, Medical University of Vienna, A-1090 Vienna, Austria. 2005


  1. Predisposition for de novo gene aberrations in the offspring of mothers with a duplicated CYP21A2 gene. Baumgartner-Parzer, S.M., Fischer, G., Vierhapper, H. J. Clin. Endocrinol. Metab. (2007) [Pubmed]
  2. Carrier frequency of congenital adrenal hyperplasia (21-hydroxylase deficiency) in a middle European population. Baumgartner-Parzer, S.M., Nowotny, P., Heinze, G., Waldhäusl, W., Vierhapper, H. J. Clin. Endocrinol. Metab. (2005) [Pubmed]
  3. Polymorphisms in exon 13 and intron 14 of the RET protooncogene: genetic modifiers of medullary thyroid carcinoma?. Baumgartner-Parzer, S.M., Lang, R., Wagner, L., Heinze, G., Niederle, B., Kaserer, K., Waldhäusl, W., Vierhapper, H. J. Clin. Endocrinol. Metab. (2005) [Pubmed]
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