Katja Harbst

31 – 36 of 36

show: 10
|
sort: year (new to old)

News feed Embed this list Save this search Mark all Export

Cancel

Embed this list

copy and paste the html snippet below into your own page:

<iframe src="https://lup.lub.lu.se/search/person/med-kbn?embed=1&amp;hide_pagination=1&amp;hide_info=1&amp;hide_options=1"
  width="100%"
  height="400"
  allowtransparency="true"
  frameborder="0">
</iframe>

« previous
1
2
3
4
next »

2010
Mark A locus on 19p13 modifies risk of breast cancer in BRCA1 mutation carriers and is associated with hormone receptor-negative breast cancer in the general population
Antoniou, Antonis C. ; Wang, Xianshu ; Fredericksen, Zachary S. ; McGuffog, Lesley ; Tarrell, Robert ; Sinilnikova, Olga M. ; Healey, Sue ; Morrison, Jonathan ; Kartsonaki, Christiana and Lesnick, Timothy , et al. (2010) In Nature Genetics 42(10). p.885-892
- Contribution to journal › Article
Mark Swedish CDKN2A mutation carriers do not present the atypical mole syndrome phenotype.
Nielsen, Kari ^LU ; Harbst, Katja ^LU ; Måsbäck, Anna ^LU ; Jönsson, Göran B ^LU ; Borg, Åke ^LU ; Olsson, Håkan ^LU and Ingvar, Christian ^LU (2010) In Melanoma Research Jul 1. p.266-272
- Contribution to journal › Article
Mark Multiple metastases from cutaneous malignant melanoma patients may display heterogeneous genomic and epigenomic patterns.
Harbst, Katja ^LU ; Staaf, Johan ^LU ; Måsbäck, Anna ^LU ; Olsson, Håkan ^LU ; Ingvar, Christian ^LU ; Vallon-Christersson, Johan ^LU ; Ringnér, Markus ^LU ; Borg, Åke ^LU and Jönsson, Göran B ^LU (2010) In Melanoma Research 20(5). p.381-391
- Contribution to journal › Article
2009
Mark Common variants in LSP1, 2q35 and 8q24 and breast cancer risk for BRCA1 and BRCA2 mutation carriers
Antoniou, Antonis C. ; Sinilnikova, Olga M. ; McGuffog, Lesley ; Healey, Sue ; Nevanlinna, Heli ; Heikkinen, Tuomas ; Simard, Jacques ; Spurdle, Amanda B. ; Beesley, Jonathan and Chen, Xiaoqing , et al. (2009) In Human Molecular Genetics 18(22). p.4442-4456
- Contribution to journal › Article
2007
Mark AURKA F31I polymorphism and breast cancer risk in BRCA1 and BRCA2 mutation carriers: A consortium of investigators of modifiers of BRCA1/2 study
Couch, Fergus J. ; Sinilnikova, Olga ; Vierkant, Robert A. ; Pankratz, V. Shane ; Fredericksen, Zachary S. ; Stoppa-Lyonnet, Dominique ; Coupier, Isabelle ; Hughes, David ; Hardouin, Agnes and Berthet, Pascaline , et al. (2007) In Cancer Epidemiology Biomarkers & Prevention 16(7). p.1416-1421
- Contribution to journal › Article
2006
Mark Nordic collaborative study of the BARD1 Cys557Ser allele in 3956 patients with cancer: enrichment in familial BRCA1/BRCA2 mutation-negative breast cancer but not in other malignancies
Karppinen, S. -M. ; Barkardottir, R. B. ; Harbst, Katja ^LU ; Sydenham, T. ; Syrjakoski, K. ; Schleutker, J. ; Ikonen, T. ; Pylkas, K. ; Rapakko, K. and Erkko, H. , et al. (2006) In Journal of Medical Genetics 43(11). p.856-862
- Contribution to journal › Article

« previous
1
2
3
4
next »