Soller M - Search Results

1

A model for karyotypic evolution in testicular germ cell tumors.

Frigyesi A, Gisselsson D, Hansen GB, Soller M, Mitelman F, Höglund M. Frigyesi A, et al. Among authors: soller m. Genes Chromosomes Cancer. 2004 Jul;40(3):172-8. doi: 10.1002/gcc.20032. Genes Chromosomes Cancer. 2004. PMID: 15138997

2

Dissecting karyotypic patterns in renal cell carcinoma: an analysis of the accumulated cytogenetic data.

Höglund M, Gisselsson D, Soller M, Hansen GB, Elfving P, Mitelman F. Höglund M, et al. Among authors: soller m. Cancer Genet Cytogenet. 2004 Aug;153(1):1-9. doi: 10.1016/j.cancergencyto.2003.12.019. Cancer Genet Cytogenet. 2004. PMID: 15325087

3

The fetal thymus has a unique genomic copy number profile resulting from physiological T cell receptor gene rearrangement.

Valind A, Haikal C, Klasson ME, Johansson MC, Gullander J, Soller M, Baldetorp B, Gisselsson D. Valind A, et al. Among authors: soller m. Sci Rep. 2016 Mar 24;6:23500. doi: 10.1038/srep23500. Sci Rep. 2016. PMID: 27009469 Free PMC article.

4

Implementing precision medicine in a regionally organized healthcare system in Sweden.

Fioretos T, Wirta V, Cavelier L, Berglund E, Friedman M, Akhras M, Botling J, Ehrencrona H, Engstrand L, Helenius G, Fagerqvist T, Gisselsson D, Gruvberger-Saal S, Gyllensten U, Heidenblad M, Höglund K, Jacobsson B, Johansson M, Johansson Å, Soller MJ, Landström M, Larsson P, Levin LÅ, Lindstrand A, Lovmar L, Lyander A, Melin M, Nordgren A, Nordmark G, Mölling P, Palmqvist L, Palmqvist R, Repsilber D, Sikora P, Stenmark B, Söderkvist P, Stranneheim H, Strid T, Wheelock CE, Wadelius M, Wedell A, Edsjö A, Rosenquist R. Fioretos T, et al. Among authors: soller mj. Nat Med. 2022 Oct;28(10):1980-1982. doi: 10.1038/s41591-022-01963-4. Nat Med. 2022. PMID: 36123428 No abstract available.

5

Cytogenetic findings in pediatric renal cell carcinoma.

Soller MJ, Kullendorff CM, Békássy AN, Alumets J, Mertens F. Soller MJ, et al. Cancer Genet Cytogenet. 2007 Feb;173(1):75-80. doi: 10.1016/j.cancergencyto.2006.09.018. Cancer Genet Cytogenet. 2007. PMID: 17284375

6

Cytogenetic findings and clinical course in a consecutive series of Wilms tumors.

Kullendorff CM, Soller M, Wiebe T, Mertens F. Kullendorff CM, et al. Among authors: soller m. Cancer Genet Cytogenet. 2003 Jan 1;140(1):82-7. doi: 10.1016/s0165-4608(02)00635-0. Cancer Genet Cytogenet. 2003. PMID: 12550766

7

Array based characterization of a terminal deletion involving chromosome subband 15q26.2: an emerging syndrome associated with growth retardation, cardiac defects and developmental delay.

Davidsson J, Collin A, Björkhem G, Soller M. Davidsson J, et al. Among authors: soller m. BMC Med Genet. 2008 Jan 14;9:2. doi: 10.1186/1471-2350-9-2. BMC Med Genet. 2008. PMID: 18194513 Free PMC article.

8

Midline carcinoma with t(15;19) and BRD4-NUT fusion oncogene in a 30-year-old female with response to docetaxel and radiotherapy.

Engleson J, Soller M, Panagopoulos I, Dahlén A, Dictor M, Jerkeman M. Engleson J, et al. Among authors: soller m. BMC Cancer. 2006 Mar 16;6:69. doi: 10.1186/1471-2407-6-69. BMC Cancer. 2006. PMID: 16542442 Free PMC article.

9

dup(19)(q12q13.2): array-based genotype-phenotype correlation of a new possibly obesity-related syndrome.

Davidsson J, Jahnke K, Forsgren M, Collin A, Soller M. Davidsson J, et al. Among authors: soller m. Obesity (Silver Spring). 2010 Mar;18(3):580-7. doi: 10.1038/oby.2009.298. Epub 2009 Sep 17. Obesity (Silver Spring). 2010. PMID: 19763090 Free article.

10

Deletion of the SCN gene cluster on 2q24.4 is associated with severe epilepsy: an array-based genotype-phenotype correlation and a comprehensive review of previously published cases.

Davidsson J, Collin A, Olsson ME, Lundgren J, Soller M. Davidsson J, et al. Among authors: soller m. Epilepsy Res. 2008 Sep;81(1):69-79. doi: 10.1016/j.eplepsyres.2008.04.018. Epub 2008 Jun 9. Epilepsy Res. 2008. PMID: 18539002

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