Heim S - Search Results

1

Whole-transcriptome sequencing identifies novel IRF2BP2-CDX1 fusion gene brought about by translocation t(1;5)(q42;q32) in mesenchymal chondrosarcoma.

Nyquist KB, Panagopoulos I, Thorsen J, Haugom L, Gorunova L, Bjerkehagen B, Fosså A, Guriby M, Nome T, Lothe RA, Skotheim RI, Heim S, Micci F. Nyquist KB, et al. Among authors: heim s. PLoS One. 2012;7(11):e49705. doi: 10.1371/journal.pone.0049705. Epub 2012 Nov 21. PLoS One. 2012. PMID: 23185413 Free PMC article.

2

Cytogenetic heterogeneity in a clear cell hidradenoma of the skin.

Gorunova L, Mertens F, Mandahl N, Jonsson N, Persson B, Heim S, Mitelman F. Gorunova L, et al. Among authors: heim s. Cancer Genet Cytogenet. 1994 Oct;77(1):26-32. doi: 10.1016/0165-4608(94)90144-9. Cancer Genet Cytogenet. 1994. PMID: 7923079

3

Deletion of 1p loci and microsatellite instability in colorectal polyps.

Lothe RA, Andersen SN, Hofstad B, Meling GI, Peltomäki P, Heim S, Brøgger A, Vatn M, Rognum TO, Børresen AL. Lothe RA, et al. Among authors: heim s. Genes Chromosomes Cancer. 1995 Nov;14(3):182-8. doi: 10.1002/gcc.2870140305. Genes Chromosomes Cancer. 1995. PMID: 8589034

4

Gain of 17q24-qter detected by comparative genomic hybridization in malignant tumors from patients with von Recklinghausen's neurofibromatosis.

Lothe RA, Karhu R, Mandahl N, Mertens F, Saeter G, Heim S, Borresen-Dale AL, Kallioniemi OP. Lothe RA, et al. Among authors: heim s. Cancer Res. 1996 Oct 15;56(20):4778-81. Cancer Res. 1996. PMID: 8840998

5

Allelic imbalance and cytogenetic deletion of 1p in colorectal adenomas: a target region identified between DIS199 and DIS234.

Bomme L, Heim S, Bardi G, Fenger C, Kronborg O, Brøgger A, Lothe RA. Bomme L, et al. Among authors: heim s. Genes Chromosomes Cancer. 1998 Mar;21(3):185-94. doi: 10.1002/(sici)1098-2264(199803)21:3<185::aid-gcc2>3.0.co;2-w. Genes Chromosomes Cancer. 1998. PMID: 9523193

6

Chromosome abnormalities in squamous cell carcinoma of the urethra.

Fadl-Elmula I, Gorunova L, Mandahl N, Elfving P, Heim S. Fadl-Elmula I, et al. Among authors: heim s. Genes Chromosomes Cancer. 1998 Sep;23(1):72-3. Genes Chromosomes Cancer. 1998. PMID: 9714000

7

Combined RxFISH/G-banding allows refined karyotyping of solid tumors.

Micci F, Teixeira MR, Dietrich CU, Saeter G, Bjerkehagen B, Heim S. Micci F, et al. Among authors: heim s. Hum Genet. 1999 May;104(5):370-5. doi: 10.1007/s004390050970. Hum Genet. 1999. PMID: 10394927

8

Cross-species color banding characterization of chromosomal rearrangements in leukemias with incomplete G-band karyotypes.

Teixeira MR, Micci F, Dietrich CU, Heim S. Teixeira MR, et al. Among authors: heim s. Genes Chromosomes Cancer. 1999 Sep;26(1):13-9. Genes Chromosomes Cancer. 1999. PMID: 10441000

9

Extraskeletal myxoid chondrosarcoma: multimodal diagnosis and identification of a new cytogenetic subgroup characterized by t(9;17)(q22;q11).

Bjerkehagen B, Dietrich C, Reed W, Micci F, Saeter G, Berner A, Nesland JM, Heim S. Bjerkehagen B, et al. Among authors: heim s. Virchows Arch. 1999 Nov;435(5):524-30. doi: 10.1007/s004280050437. Virchows Arch. 1999. PMID: 10592057

10

Fusion of the RBP56 and CHN genes in extraskeletal myxoid chondrosarcomas with translocation t(9;17)(q22;q11).

Panagopoulos I, Mencinger M, Dietrich CU, Bjerkehagen B, Saeter G, Mertens F, Mandahl N, Heim S. Panagopoulos I, et al. Among authors: heim s. Oncogene. 1999 Dec 9;18(52):7594-8. doi: 10.1038/sj.onc.1203155. Oncogene. 1999. PMID: 10602519

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