Karolin H. Nord
Lund University(SE)PCI Biotech (Norway)(NO)
Publications by Year
Research Areas
Sarcoma Diagnosis and Treatment, Bone Tumor Diagnosis and Treatments, Cancer Genomics and Diagnostics, Tumors and Oncological Cases, Soft tissue tumor case studies
Most-Cited Works
- → Somatic mosaic IDH1 and IDH2 mutations are associated with enchondroma and spindle cell hemangioma in Ollier disease and Maffucci syndrome(2011)547 cited
- → Comprehensive genetic analysis identifies a pathognomonic NAB2/STAT6 fusion gene, nonrandom secondary genomic imbalances, and a characteristic gene expression profile in solitary fibrous tumor(2013)273 cited
- → A novel SERPINE1–FOSB fusion gene results in transcriptional up‐regulation of FOSB in pseudomyogenic haemangioendothelioma(2013)201 cited
- → Fusion of theEWSR1andATF1genes without expression of theMITF‐Mtranscript in angiomatoid fibrous histiocytoma(2005)154 cited
- → Recurrent EWSR1-CREB3L1 Gene Fusions in Sclerosing Epithelioid Fibrosarcoma(2014)154 cited
- → Two genetic pathways, t(1;10) and amplification of 3p11–12, in myxoinflammatory fibroblastic sarcoma, haemosiderotic fibrolipomatous tumour, and morphologically similar lesions(2009)152 cited
- → Fusion of the AHRR and NCOA2 genes through a recurrent translocation t(5;8)(p15;q13) in soft tissue angiofibroma results in upregulation of aryl hydrocarbon receptor target genes(2012)149 cited
- → Recurrent Rearrangement of the PHF1 Gene in Ossifying Fibromyxoid Tumors(2012)147 cited
- → Frequent deletion of the CDKN2A locus in chordoma: analysis of chromosomal imbalances using array comparative genomic hybridisation(2007)107 cited
- → GRM1 is upregulated through gene fusion and promoter swapping in chondromyxoid fibroma(2014)97 cited