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

Hildegard Kehrer-Sawatzki

Abteilung Humangenetik

Universität Ulm

Albert-Einstein-Allee 11




Name/email consistency: high



  • Abteilung Humangenetik, Universität Ulm, Albert-Einstein-Allee 11, 89081, Germany. 1998 - 2005
  • Department of Human Genetics, University of Ulm, Germany. 2000 - 2005
  • Abteilung Humangenetik, Germany. 1997


  1. Breakpoint analysis of the pericentric inversion between chimpanzee chromosome 10 and the homologous chromosome 12 in humans. Kehrer-Sawatzki, H., Sandig, C.A., Goidts, V., Hameister, H. Cytogenet. Genome Res. (2005) [Pubmed]
  2. Breakpoint analysis of the pericentric inversion distinguishing human chromosome 4 from the homologous chromosome in the chimpanzee (Pan troglodytes). Kehrer-Sawatzki, H., Sandig, C., Chuzhanova, N., Goidts, V., Szamalek, J.M., Tänzer, S., Müller, S., Platzer, M., Cooper, D.N., Hameister, H. Hum. Mutat. (2005) [Pubmed]
  3. Extensively high load of internal tumors determined by whole body MRI scanning in a patient with neurofibromatosis type 1 and a non-LCR-mediated 2-Mb deletion in 17q11.2. Kehrer-Sawatzki, H., Kluwe, L., Fünsterer, C., Mautner, V.F. Hum. Genet. (2005) [Pubmed]
  4. Molecular characterization of the pericentric inversion of chimpanzee chromosome 11 homologous to human chromosome 9. Kehrer-Sawatzki, H., Szamalek, J.M., Tänzer, S., Platzer, M., Hameister, H. Genomics (2005) [Pubmed]
  5. Interstitial deletion del(10)(q25.2q25.3 approximately 26.11)--case report and review of the literature. Kehrer-Sawatzki, H., Daumiller, E., Müller-Navia, J., Kendziorra, H., Rossier, E., du Bois, G., Barbi, G. Prenat. Diagn. (2005) [Pubmed]
  6. High frequency of mosaicism among patients with neurofibromatosis type 1 (NF1) with microdeletions caused by somatic recombination of the JJAZ1 gene. Kehrer-Sawatzki, H., Kluwe, L., Sandig, C., Kohn, M., Wimmer, K., Krammer, U., Peyrl, A., Jenne, D.E., Hansmann, I., Mautner, V.F. Am. J. Hum. Genet. (2004) [Pubmed]
  7. Molecular characterization of the pericentric inversion that causes differences between chimpanzee chromosome 19 and human chromosome 17. Kehrer-Sawatzki, H., Schreiner, B., Tänzer, S., Platzer, M., Müller, S., Hameister, H. Am. J. Hum. Genet. (2002) [Pubmed]
  8. Mutation and expression analysis of the KRIT1 gene associated with cerebral cavernous malformations (CCM1). Kehrer-Sawatzki, H., Wilda, M., Braun, V.M., Richter, H.P., Hameister, H. Acta Neuropathol. (2002) [Pubmed]
  9. Characterization of the Fugu rubripes NLK and FN5 genes flanking the NF1 (Neurofibromatosis type 1) gene in the 5' direction and mapping of the human counterparts. Kehrer-Sawatzki, H., Moschgath, E., Maier, C., Legius, E., Elgar, G., Krone, W. Gene (2000) [Pubmed]
  10. Characterization of three genes, AKAP84, BAW and WSB1, located 3' to the neurofibromatosis type 1 locus in Fugu rubripes. Kehrer-Sawatzki, H., Maier, C., Moschgath, E., Elgar, G., Krone, W. Gene (1999) [Pubmed]
  11. Genomic characterization of the Neurofibromatosis Type 1 gene of Fugu rubripes. Kehrer-Sawatzki, H., Maier, C., Moschgath, E., Elgar, G., Krone, W. Gene (1998) [Pubmed]
  12. Mutational analysis and expression studies of the neurofibromatosis type 2 (NF2) gene in a patient with a ring chromosome 22 and NF2. Kehrer-Sawatzki, H., Udart, M., Krone, W., Baden, R., Fahsold, R., Thomas, G., Schmucker, B., Assum, G. Hum. Genet. (1997) [Pubmed]
  13. A third neurofibromatosis type 1 (NF1) pseudogene at chromosome 15q11.2. Kehrer-Sawatzki, H., Schwickardt, T., Assum, G., Rocchi, M., Krone, W. Hum. Genet. (1997) [Pubmed]
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