Staaf J - Search Results

1

Genomic profiling of malignant melanoma using tiling-resolution arrayCGH.

Jönsson G, Dahl C, Staaf J, Sandberg T, Bendahl PO, Ringnér M, Guldberg P, Borg A. Jönsson G, et al. Among authors: staaf j. Oncogene. 2007 Jul 12;26(32):4738-48. doi: 10.1038/sj.onc.1210252. Epub 2007 Jan 29. Oncogene. 2007. PMID: 17260012

2

ACID: a database for microarray clone information.

Ringnér M, Veerla S, Andersson S, Staaf J, Häkkinen J. Ringnér M, et al. Among authors: staaf j. Bioinformatics. 2004 Sep 22;20(14):2305-6. doi: 10.1093/bioinformatics/bth089. Epub 2004 Feb 12. Bioinformatics. 2004. PMID: 14962935

3

Distinct genomic profiles in hereditary breast tumors identified by array-based comparative genomic hybridization.

Jönsson G, Naylor TL, Vallon-Christersson J, Staaf J, Huang J, Ward MR, Greshock JD, Luts L, Olsson H, Rahman N, Stratton M, Ringnér M, Borg A, Weber BL. Jönsson G, et al. Among authors: staaf j. Cancer Res. 2005 Sep 1;65(17):7612-21. doi: 10.1158/0008-5472.CAN-05-0570. Cancer Res. 2005. PMID: 16140926

4

Mapping of a novel ocular and cutaneous malignant melanoma susceptibility locus to chromosome 9q21.32.

Jönsson G, Bendahl PO, Sandberg T, Kurbasic A, Staaf J, Sunde L, Crüger DG, Ingvar C, Olsson H, Borg A. Jönsson G, et al. Among authors: staaf j. J Natl Cancer Inst. 2005 Sep 21;97(18):1377-82. doi: 10.1093/jnci/dji280. J Natl Cancer Inst. 2005. PMID: 16174859

5

Detection and delineation of an unusual 17p11.2 deletion by array-CGH and refinement of the Smith-Magenis syndrome minimum deletion to approximately 650 kb.

Schoumans J, Staaf J, Jönsson G, Rantala J, Zimmer KS, Borg A, Nordenskjöld M, Anderlid BM. Schoumans J, et al. Among authors: staaf j. Eur J Med Genet. 2005 Jul-Sep;48(3):290-300. doi: 10.1016/j.ejmg.2005.05.004. Eur J Med Genet. 2005. PMID: 16179224

6

High-resolution genome-wide array-based comparative genome hybridization reveals cryptic chromosome changes in AML and MDS cases with trisomy 8 as the sole cytogenetic aberration.

Paulsson K, Heidenblad M, Strömbeck B, Staaf J, Jönsson G, Borg A, Fioretos T, Johansson B. Paulsson K, et al. Among authors: staaf j. Leukemia. 2006 May;20(5):840-6. doi: 10.1038/sj.leu.2404145. Leukemia. 2006. PMID: 16498392

7

Hemizygosity for chromosome 2q14.2-q22.1 spanning the GLI2 and PROC genes associated with growth hormone deficiency, polydactyly, deep vein thrombosis and urogenital abnormalities.

Gustavsson P, Schoumans J, Staaf J, Jönsson G, Carlsson F, Kristoffersson U, Borg A, Nordenskjöld M, Dahl N. Gustavsson P, et al. Among authors: staaf j. Clin Genet. 2006 May;69(5):441-3. doi: 10.1111/j.1399-0004.2006.00601.x. Clin Genet. 2006. PMID: 16650085 No abstract available.

8

Genomic profiling of bone and soft tissue tumors with supernumerary ring chromosomes using tiling resolution bacterial artificial chromosome microarrays.

Heidenblad M, Hallor KH, Staaf J, Jönsson G, Borg A, Höglund M, Mertens F, Mandahl N. Heidenblad M, et al. Among authors: staaf j. Oncogene. 2006 Nov 9;25(53):7106-16. doi: 10.1038/sj.onc.1209693. Epub 2006 May 29. Oncogene. 2006. PMID: 16732325

9

Characterisation of dic(9;20)(p11-13;q11) in childhood B-cell precursor acute lymphoblastic leukaemia by tiling resolution array-based comparative genomic hybridisation reveals clustered breakpoints at 9p13.2 and 20q11.2.

Schoumans J, Johansson B, Corcoran M, Kuchinskaya E, Golovleva I, Grandér D, Forestier E, Staaf J, Borg A, Gustafsson B, Blennow E, Nordgren A. Schoumans J, et al. Among authors: staaf j. Br J Haematol. 2006 Nov;135(4):492-9. doi: 10.1111/j.1365-2141.2006.06328.x. Epub 2006 Sep 26. Br J Haematol. 2006. PMID: 16999846 Free article.

10

Comprehensive mutational analysis of a cohort of Swedish Cornelia de Lange syndrome patients.

Schoumans J, Wincent J, Barbaro M, Djureinovic T, Maguire P, Forsberg L, Staaf J, Thuresson AC, Borg A, Nordgren A, Malm G, Anderlid BM. Schoumans J, et al. Among authors: staaf j. Eur J Hum Genet. 2007 Feb;15(2):143-9. doi: 10.1038/sj.ejhg.5201737. Epub 2006 Nov 15. Eur J Hum Genet. 2007. PMID: 17106445

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