Search Page
Save citations to file
Email citations
Send citations to clipboard
Add to Collections
Add to My Bibliography
Create a file for external citation management software
Your saved search
Your RSS Feed
Search Results
7 results
Filters applied: . Clear all
Results are displayed in a computed author sort order.
The Results By Year timeline is not available.
Page 1
OncoKids: A Comprehensive Next-Generation Sequencing Panel for Pediatric Malignancies.
J Mol Diagn. 2018 Nov;20(6):765-776. doi: 10.1016/j.jmoldx.2018.06.009. Epub 2018 Aug 20.
J Mol Diagn. 2018.
PMID: 30138724
Free article.
Copy number alterations determined by single nucleotide polymorphism array testing in the clinical laboratory are indicative of gene fusions in pediatric cancer patients.
Busse TM, Roth JJ, Wilmoth D, Wainwright L, Tooke L, Biegel JA.
Busse TM, et al.
Genes Chromosomes Cancer. 2017 Oct;56(10):730-749. doi: 10.1002/gcc.22477. Epub 2017 Jul 1.
Genes Chromosomes Cancer. 2017.
PMID: 28597942
Item in Clipboard
Diagnostic application of high resolution single nucleotide polymorphism array analysis for children with brain tumors.
Roth JJ, Santi M, Rorke-Adams LB, Harding BN, Busse TM, Tooke LS, Biegel JA.
Roth JJ, et al. Among authors: busse tm.
Cancer Genet. 2014 Apr;207(4):111-23. doi: 10.1016/j.cancergen.2014.03.002. Epub 2014 Mar 15.
Cancer Genet. 2014.
PMID: 24767714
Free PMC article.
Item in Clipboard
SWI/SNF chromatin remodeling complexes and cancer.
Biegel JA, Busse TM, Weissman BE.
Biegel JA, et al. Among authors: busse tm.
Am J Med Genet C Semin Med Genet. 2014 Sep;166C(3):350-66. doi: 10.1002/ajmg.c.31410. Epub 2014 Aug 28.
Am J Med Genet C Semin Med Genet. 2014.
PMID: 25169151
Free PMC article.
Review.
Item in Clipboard
Clonal evolution and clinical significance of copy number neutral loss of heterozygosity of chromosome arm 6p in acquired aplastic anemia.
Betensky M, Babushok D, Roth JJ, Mason PJ, Biegel JA, Busse TM, Li Y, Lind C, Papazoglou A, Monos D, Podsakoff G, Bessler M, Olson TS.
Betensky M, et al. Among authors: busse tm.
Cancer Genet. 2016 Jan-Feb;209(1-2):1-10. doi: 10.1016/j.cancergen.2015.10.002. Epub 2015 Oct 30.
Cancer Genet. 2016.
PMID: 26702937
Free PMC article.
Item in Clipboard
Disrupting LIN28 in atypical teratoid rhabdoid tumors reveals the importance of the mitogen activated protein kinase pathway as a therapeutic target.
Weingart MF, Roth JJ, Hutt-Cabezas M, Busse TM, Kaur H, Price A, Maynard R, Rubens J, Taylor I, Mao XG, Xu J, Kuwahara Y, Allen SJ, Erdreich-Epstein A, Weissman BE, Orr BA, Eberhart CG, Biegel JA, Raabe EH.
Weingart MF, et al. Among authors: busse tm.
Oncotarget. 2015 Feb 20;6(5):3165-77. doi: 10.18632/oncotarget.3078.
Oncotarget. 2015.
PMID: 25638158
Free PMC article.
Item in Clipboard
High-Resolution genomic arrays identify CNVs that phenocopy the chromosome 22q11.2 deletion syndrome.
Busse T, Graham JM Jr, Feldman G, Perin J, Catherwood A, Knowlton R, Rappaport EF, Emanuel B, Driscoll DA, Saitta SC.
Busse T, et al.
Hum Mutat. 2011 Jan;32(1):91-7. doi: 10.1002/humu.21395.
Hum Mutat. 2011.
PMID: 21120947
Item in Clipboard
Cite
Cite