Ullmann R - Search Results

1

Gene amplification as double minutes or homogeneously staining regions in solid tumors: origin and structure.

Storlazzi CT, Lonoce A, Guastadisegni MC, Trombetta D, D'Addabbo P, Daniele G, L'Abbate A, Macchia G, Surace C, Kok K, Ullmann R, Purgato S, Palumbo O, Carella M, Ambros PF, Rocchi M. Storlazzi CT, et al. Among authors: ullmann r. Genome Res. 2010 Sep;20(9):1198-206. doi: 10.1101/gr.106252.110. Epub 2010 Jul 14. Genome Res. 2010. PMID: 20631050 Free PMC article.

2

Novel rearrangement of chromosome band 22q11.2 causing 22q11 microdeletion syndrome-like phenotype and rhabdoid tumor of the kidney.

Wieser R, Fritz B, Ullmann R, Müller I, Galhuber M, Storlazzi CT, Ramaswamy A, Christiansen H, Shimizu N, Rehder H. Wieser R, et al. Among authors: ullmann r. Hum Mutat. 2005 Aug;26(2):78-83. doi: 10.1002/humu.20195. Hum Mutat. 2005. PMID: 15957176

3

Impact of low copy repeats on the generation of balanced and unbalanced chromosomal aberrations in mental retardation.

Erdogan F, Chen W, Kirchhoff M, Kalscheuer VM, Hultschig C, Müller I, Schulz R, Menzel C, Bryndorf T, Ropers HH, Ullmann R. Erdogan F, et al. Among authors: ullmann r. Cytogenet Genome Res. 2006;115(3-4):247-53. doi: 10.1159/000095921. Cytogenet Genome Res. 2006. PMID: 17124407

4

Two independent chromosomal rearrangements, a very small (550 kb) duplication of the 7q subtelomeric region and an atypical 17q11.2 (NF1) microdeletion, in a girl with neurofibromatosis.

Bartsch O, Vlcková Z, Erdogan F, Ullmann R, Novotná D, Spiegel M, Beyer V, Haaf T, Zechner U, Seemanová E. Bartsch O, et al. Among authors: ullmann r. Cytogenet Genome Res. 2007;119(1-2):158-64. doi: 10.1159/000109634. Epub 2007 Dec 14. Cytogenet Genome Res. 2007. PMID: 18160797

5

AML/MDS with 11q/MLL amplification show characteristic gene expression signature and interplay of DNA copy number changes.

Zatkova A, Merk S, Wendehack M, Bilban M, Muzik EM, Muradyan A, Haferlach C, Haferlach T, Wimmer K, Fonatsch C, Ullmann R. Zatkova A, et al. Among authors: ullmann r. Genes Chromosomes Cancer. 2009 Jun;48(6):510-20. doi: 10.1002/gcc.20658. Genes Chromosomes Cancer. 2009. PMID: 19306356

6

Mapping translocation breakpoints by next-generation sequencing.

Chen W, Kalscheuer V, Tzschach A, Menzel C, Ullmann R, Schulz MH, Erdogan F, Li N, Kijas Z, Arkesteijn G, Pajares IL, Goetz-Sothmann M, Heinrich U, Rost I, Dufke A, Grasshoff U, Glaeser B, Vingron M, Ropers HH. Chen W, et al. Among authors: ullmann r. Genome Res. 2008 Jul;18(7):1143-9. doi: 10.1101/gr.076166.108. Epub 2008 Mar 7. Genome Res. 2008. PMID: 18326688 Free PMC article.

7

Characterization of a de novo complex chromosome rearrangement (CCR) involving chromosomes 2 and 12, associated with mental retardation and impaired speech development.

Schwarzbraun T, Ullmann R, Schubert M, Ledinegg M, Ofner L, Windpassinger C, Wagner K, Kroisel PM, Petek E. Schwarzbraun T, et al. Among authors: ullmann r. Cytogenet Genome Res. 2006;115(1):84-9. doi: 10.1159/000094804. Cytogenet Genome Res. 2006. PMID: 16974087

8

Genomic loss of the putative tumor suppressor gene E2A in human lymphoma.

Steininger A, Möbs M, Ullmann R, Köchert K, Kreher S, Lamprecht B, Anagnostopoulos I, Hummel M, Richter J, Beyer M, Janz M, Klemke CD, Stein H, Dörken B, Sterry W, Schrock E, Mathas S, Assaf C. Steininger A, et al. Among authors: ullmann r. J Exp Med. 2011 Aug 1;208(8):1585-93. doi: 10.1084/jem.20101785. Epub 2011 Jul 25. J Exp Med. 2011. PMID: 21788410 Free PMC article.

9

Positioning of necrotic lobular intraepithelial neoplasias (LIN, grade 3) within the sequence of breast carcinoma progression.

Boldt V, Stacher E, Halbwedl I, Popper H, Hultschig C, Moinfar F, Ullmann R, Tavassoli FA. Boldt V, et al. Among authors: ullmann r. Genes Chromosomes Cancer. 2010 May;49(5):463-70. doi: 10.1002/gcc.20756. Genes Chromosomes Cancer. 2010. PMID: 20155841

10

A cryptic unbalanced translocation t(2;9)(p25.2;q34.3) causes the phenotype of 9q subtelomeric deletion syndrome and additional exophthalmos and joint contractures.

Busche A, Klopocki E, Ullmann R, Mundlos S, Horn D. Busche A, et al. Among authors: ullmann r. Eur J Med Genet. 2008 Nov-Dec;51(6):615-21. doi: 10.1016/j.ejmg.2008.06.006. Epub 2008 Jul 12. Eur J Med Genet. 2008. PMID: 18674647

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