Papenhausen PR - Search Results

1

Increased genomic instability may contribute to the development of kinase domain mutations in chronic myeloid leukemia.

Sweet K, Al Ali NH, Dalia SM, Komrokji RS, Crescentini RM, Tinsley S, Lancet JE, Papenhausen PR, Zhang L, Pinilla-Ibarz J. Sweet K, et al. Among authors: papenhausen pr. Int J Hematol. 2014 Dec;100(6):567-74. doi: 10.1007/s12185-014-1685-9. Epub 2014 Oct 4. Int J Hematol. 2014. PMID: 25281405

2

Concurrence of B-lymphoblastic leukemia and myeloproliferative neoplasm with copy neutral loss of heterozygosity at chromosome 1p harboring a MPL W515S mutation.

Tao J, Zhang X, Lancet J, Bennett JM, Cai L, Papenhausen P, Moscinski L, Zhang L. Tao J, et al. Cancer Genet. 2014 Oct-Dec;207(10-12):489-94. doi: 10.1016/j.cancergen.2014.10.001. Epub 2014 Oct 13. Cancer Genet. 2014. PMID: 25453399

3

Transformed aggressive γδ-variant T-cell large granular lymphocytic leukemia with acquired copy neutral loss of heterozygosity at 17q11.2q25.3 and additional aberrations.

Zhang L, Ramchandren R, Papenhausen P, Loughran TP, Sokol L. Zhang L, et al. Eur J Haematol. 2014 Sep;93(3):260-4. doi: 10.1111/ejh.12313. Epub 2014 Apr 7. Eur J Haematol. 2014. PMID: 24635703

4

Burkitt lymphoma arising from lymphoplasmacytic lymphoma following acquisition of MYC translocation and loss of the ETV6 tumor suppressor gene.

Peker D, Quigley B, Qin D, Papenhausen P, Zhang L. Peker D, et al. Arch Pathol Lab Med. 2013 Jan;137(1):130-3. doi: 10.5858/arpa.2011-0429-CR. Arch Pathol Lab Med. 2013. PMID: 23276184 Free article.

5

Double-hit mantle cell lymphoma with MYC gene rearrangement or amplification: a report of four cases and review of the literature.

Setoodeh R, Schwartz S, Papenhausen P, Zhang L, Sagatys EM, Moscinski LC, Shao H. Setoodeh R, et al. Int J Clin Exp Pathol. 2013;6(2):155-67. Epub 2013 Jan 15. Int J Clin Exp Pathol. 2013. PMID: 23330001 Free PMC article. Review.

6

Zhou J, Papenhausen P, Shao H. Zhou J, et al. Int J Clin Exp Pathol. 2015 May 1;8(5):5812-20. eCollection 2015. Int J Clin Exp Pathol. 2015. PMID: 26191303 Free PMC article. Review.

7

Multidisciplinary analysis of pediatric T-ALL: 9q34 gene fusions.

Papenhausen P, Kelly CA, Zhang Z, Tepperberg J, Burnside RD, Schwartz S. Papenhausen P, et al. Cancer Genet. 2019 Feb;231-232:1-13. doi: 10.1016/j.cancergen.2018.12.002. Epub 2018 Dec 12. Cancer Genet. 2019. PMID: 30803551

8

Microarray, gene sequencing, and reverse transcriptase-polymerase chain reaction analyses of a cryptic PML-RARA translocation.

Koshy J, Qian YW, Bhagwath G, Willis M, Kelley TW, Papenhausen P. Koshy J, et al. Cancer Genet. 2012 Oct;205(10):537-40. doi: 10.1016/j.cancergen.2012.07.017. Epub 2012 Sep 13. Cancer Genet. 2012. PMID: 22982005

9

MYC amplification in multiple marker chromosomes and EZH2 microdeletion in a man with acute myeloid leukemia.

Xiang Z, Abdallah AO, Govindarajan R, Mehta P, Emanuel PD, Papenhausen P, Schichman SA. Xiang Z, et al. Cancer Genet. 2015 Mar;208(3):96-100. doi: 10.1016/j.cancergen.2015.01.010. Epub 2015 Feb 7. Cancer Genet. 2015. PMID: 25800664

10

Unusual concurrence of T-cell large granular lymphocytic leukemia with Franklin disease (gamma heavy chain disease) manifested with massive splenomegaly.

Zhang L, Sotomayor EM, Papenhausen PR, Shao H, Moscinski LC, Sandin RL, Caceres G, Valenica H, Malafa M, List AF, Sokol L. Zhang L, et al. Among authors: papenhausen pr. Leuk Lymphoma. 2013 Jan;54(1):205-8. doi: 10.3109/10428194.2012.697561. Epub 2012 Jul 9. Leuk Lymphoma. 2013. PMID: 22694793 No abstract available.

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