Karolin H. Nord

Somatic mosaic IDH1 and IDH2 mutations are associated with enchondroma and spindle cell hemangioma in Ollier disease and Maffucci syndrome

Twinkal C. Pansuriya, Ronald van Eijk, Pio D’Adamo et al. · Nature Genetics · 2011 · 546 citations · Full text

Developmental Biology, Somatic Variant, Genetic Disorder +8

Comprehensive genetic analysis identifies a pathognomonic <i>NAB2/STAT6</i> fusion gene, nonrandom secondary genomic imbalances, and a characteristic gene expression profile in solitary fibrous tumor

Arezoo Mohajeri, Johnbosco Tayebwa, Anna Collin et al. · Genes Chromosomes and Cancer · 2013 · 273 citations

A novel <i><scp>SERPINE1–FOSB</scp></i> fusion gene results in transcriptional up‐regulation of <i><scp>FOSB</scp></i> in pseudomyogenic haemangioendothelioma

Charles Walther, Johnbosco Tayebwa, Henrik Lilljebjörn et al. · The Journal of Pathology · 2013 · 197 citations

Recurrent EWSR1-CREB3L1 Gene Fusions in Sclerosing Epithelioid Fibrosarcoma

Elsa Arbajian, Florian Puls, Linda Magnusson et al. · The American Journal of Surgical Pathology · 2014 · 154 citations

Tumoral Pathology, Sclerosing Epithelioid Fibrosarcoma, Tumor Heterogeneity +11

Two genetic pathways, t(1;10) and amplification of 3p11–12, in myxoinflammatory fibroblastic sarcoma, haemosiderotic fibrolipomatous tumour, and morphologically similar lesions

Karolin H. Nord, Raf Sciot, Johan Staaf et al. · The Journal of Pathology · 2009 · 152 citations