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

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Karolin Hansén Hallor

Department of Clinical Genetics

Lund University Hospital

Lund SE-221 85

Sweden

[email]@med.lu.se

Name/email consistency: high

 
 
 
 
 
 
 

Affiliation

  • Department of Clinical Genetics, Lund University Hospital, Lund SE-221 85, Sweden. 2005 - 2008

References

  1. Frequent deletion of the CDKN2A locus in chordoma: analysis of chromosomal imbalances using array comparative genomic hybridisation. Hallor, K.H., Staaf, J., Jönsson, G., Heidenblad, M., Vult von Steyern, F., Bauer, H.C., Ijszenga, M., Hogendoorn, P.C., Mandahl, N., Szuhai, K., Mertens, F. Br. J. Cancer (2008) [Pubmed]
  2. Heterogeneous genetic profiles in soft tissue myoepitheliomas. Hallor, K.H., Teixeira, M.R., Fletcher, C.D., Bizarro, S., Staaf, J., Domanski, H.A., von Steyern, F.V., Panagopoulos, I., Mandahl, N., Mertens, F. Mod. Pathol. (2008) [Pubmed]
  3. Tiling resolution array comparative genomic hybridization analysis of a fibrosarcoma of bone. Hallor, K.H., Heidenblad, M., Brosjö, O., Mandahl, N., Mertens, F. Cancer Genet. Cytogenet. (2007) [Pubmed]
  4. Fusion genes in angiomatoid fibrous histiocytoma. Hallor, K.H., Micci, F., Meis-Kindblom, J.M., Kindblom, L.G., Bacchini, P., Mandahl, N., Mertens, F., Panagopoulos, I. Cancer Lett. (2007) [Pubmed]
  5. Fusion of the EWSR1 and ATF1 genes without expression of the MITF-M transcript in angiomatoid fibrous histiocytoma. Hallor, K.H., Mertens, F., Jin, Y., Meis-Kindblom, J.M., Kindblom, L.G., Behrendtz, M., Kalén, A., Mandahl, N., Panagopoulos, I. Genes. Chromosomes. Cancer (2005) [Pubmed]
 
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