List of works - Karolin H Nord

A benign vascular tumor with a new fusion gene: EWSR1-NFATC1 in hemangioma of the bone.

scientific article

A novel GTF2I/NCOA2 fusion gene emphasizes the role of NCOA2 in soft tissue angiofibroma development

scientific article published on 10 December 2012

Assessment of the clinical and molecular impact of different cytogenetic subgroups in a series of 272 lipomas with abnormal karyotype

scientific article published in June 2007

Biphasic, hyperdiploid breast tumors in children: a distinct entity?

scientific article published in January 2013

Clonal evolution through loss of chromosomes and subsequent polyploidization in chondrosarcoma

scientific article

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

scientific article

Concomitant deletions of tumor suppressor genes MEN1 and AIP are essential for the pathogenesis of the brown fat tumor hibernoma

scientific article

Cytogenetic and single nucleotide polymorphism array findings in soft tissue tumors in infants

scientific article

FOSL1 as a candidate target gene for 11q12 rearrangements in desmoplastic fibroblastoma

scientific article published on 12 March 2012

Frequent deletion of the CDKN2A locus in chordoma: analysis of chromosomal imbalances using array comparative genomic hybridisation

scientific article

Fusion genes in angiomatoid fibrous histiocytoma.

scientific article

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

scientific article published on 15 February 2012

Fusion of the EWSR1 and ATF1 genes without expression of the MITF-M transcript in angiomatoid fibrous histiocytoma

scientific article

Genetic profiling of a chondroblastoma-like osteosarcoma/malignant phosphaturic mesenchymal tumor of bone reveals a homozygous deletion of CDKN2A, intragenic deletion of DMD, and a targetable FN1-FGFR1 gene fusion

scientific article published on 15 May 2019

Integrative genome and transcriptome analyses reveal two distinct types of ring chromosome in soft tissue sarcomas

scientific article published on 26 September 2013

Loss of NF2 defines a genetic subgroup of non-FOS-rearranged osteoblastoma

scientific article published on 16 June 2020

Loss of chromosomes is the primary event in near-haploid and low-hypodiploid acute lymphoblastic leukemia

scientific article published on 14 August 2012

Loss of the tumour suppressor gene AIP mediates the browning of human brown fat tumours

scientific article

NTRK fusions in osteosarcoma are rare and non-functional events

scientific article published on 05 February 2020

Rearrangements of chromosome bands 15q12-q21 are secondary to HMGA2 deregulation in conventional lipoma

scientific article published on 2 December 2013

Recurrent chromosome 22 deletions in osteoblastoma affect inhibitors of the Wnt/beta-catenin signaling pathway

scientific article

Recurrent rearrangement of the PHF1 gene in ossifying fibromyxoid tumors

scientific article

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

scientific article

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

scientific article

List of works by Karolin H Nord

A benign vascular tumor with a new fusion gene: EWSR1-NFATC1 in hemangioma of the bone.

A novel GTF2I/NCOA2 fusion gene emphasizes the role of NCOA2 in soft tissue angiofibroma development

Assessment of the clinical and molecular impact of different cytogenetic subgroups in a series of 272 lipomas with abnormal karyotype

Biphasic, hyperdiploid breast tumors in children: a distinct entity?

Clonal evolution through loss of chromosomes and subsequent polyploidization in chondrosarcoma

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

Concomitant deletions of tumor suppressor genes MEN1 and AIP are essential for the pathogenesis of the brown fat tumor hibernoma

Cytogenetic and single nucleotide polymorphism array findings in soft tissue tumors in infants

FOSL1 as a candidate target gene for 11q12 rearrangements in desmoplastic fibroblastoma

Frequent deletion of the CDKN2A locus in chordoma: analysis of chromosomal imbalances using array comparative genomic hybridisation

Fusion genes in angiomatoid fibrous histiocytoma.

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

Fusion of the EWSR1 and ATF1 genes without expression of the MITF-M transcript in angiomatoid fibrous histiocytoma

Genetic profiling of a chondroblastoma-like osteosarcoma/malignant phosphaturic mesenchymal tumor of bone reveals a homozygous deletion of CDKN2A, intragenic deletion of DMD, and a targetable FN1-FGFR1 gene fusion

Integrative genome and transcriptome analyses reveal two distinct types of ring chromosome in soft tissue sarcomas

Loss of NF2 defines a genetic subgroup of non-FOS-rearranged osteoblastoma

Loss of chromosomes is the primary event in near-haploid and low-hypodiploid acute lymphoblastic leukemia

Loss of the tumour suppressor gene AIP mediates the browning of human brown fat tumours

NTRK fusions in osteosarcoma are rare and non-functional events

Rearrangements of chromosome bands 15q12-q21 are secondary to HMGA2 deregulation in conventional lipoma

Recurrent chromosome 22 deletions in osteoblastoma affect inhibitors of the Wnt/beta-catenin signaling pathway

Recurrent rearrangement of the PHF1 gene in ossifying fibromyxoid tumors

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

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