Betz BL - Search Results

1

Genomic analyses reveal recurrent mutations in epigenetic modifiers and the JAK-STAT pathway in Sézary syndrome.

Kiel MJ, Sahasrabuddhe AA, Rolland DCM, Velusamy T, Chung F, Schaller M, Bailey NG, Betz BL, Miranda RN, Porcu P, Byrd JC, Medeiros LJ, Kunkel SL, Bahler DW, Lim MS, Elenitoba-Johnson KSJ. Kiel MJ, et al. Among authors: betz bl. Nat Commun. 2015 Sep 29;6:8470. doi: 10.1038/ncomms9470. Nat Commun. 2015. PMID: 26415585 Free PMC article.

2

Whole-genome sequencing identifies recurrent somatic NOTCH2 mutations in splenic marginal zone lymphoma.

Kiel MJ, Velusamy T, Betz BL, Zhao L, Weigelin HG, Chiang MY, Huebner-Chan DR, Bailey NG, Yang DT, Bhagat G, Miranda RN, Bahler DW, Medeiros LJ, Lim MS, Elenitoba-Johnson KS. Kiel MJ, et al. Among authors: betz bl. J Exp Med. 2012 Aug 27;209(9):1553-65. doi: 10.1084/jem.20120910. Epub 2012 Aug 13. J Exp Med. 2012. PMID: 22891276 Free PMC article.

3

A multiplexed fragment analysis-based assay for detection of JAK2 exon 12 mutations.

Furtado LV, Weigelin HC, Elenitoba-Johnson KS, Betz BL. Furtado LV, et al. Among authors: betz bl. J Mol Diagn. 2013 Sep;15(5):592-9. doi: 10.1016/j.jmoldx.2013.04.006. Epub 2013 Jun 28. J Mol Diagn. 2013. PMID: 23810504 Free article.

4

Detection of MPL mutations by a novel allele-specific PCR-based strategy.

Furtado LV, Weigelin HC, Elenitoba-Johnson KS, Betz BL. Furtado LV, et al. Among authors: betz bl. J Mol Diagn. 2013 Nov;15(6):810-8. doi: 10.1016/j.jmoldx.2013.07.006. Epub 2013 Aug 28. J Mol Diagn. 2013. PMID: 23994117 Free article.

5

Requisite analytic and diagnostic performance characteristics for the clinical detection of BRAF V600E in hairy cell leukemia: a comparison of 2 allele-specific PCR assays.

Brown NA, Weigelin HC, Bailey N, Laliberte J, Elenitoba-Johnson KS, Lim MS, Betz BL. Brown NA, et al. Among authors: betz bl. Appl Immunohistochem Mol Morphol. 2015 Sep;23(8):590-600. doi: 10.1097/PAI.0000000000000024. Appl Immunohistochem Mol Morphol. 2015. PMID: 24503706

6

Integrated genomic sequencing reveals mutational landscape of T-cell prolymphocytic leukemia.

Kiel MJ, Velusamy T, Rolland D, Sahasrabuddhe AA, Chung F, Bailey NG, Schrader A, Li B, Li JZ, Ozel AB, Betz BL, Miranda RN, Medeiros LJ, Zhao L, Herling M, Lim MS, Elenitoba-Johnson KS. Kiel MJ, et al. Among authors: betz bl. Blood. 2014 Aug 28;124(9):1460-72. doi: 10.1182/blood-2014-03-559542. Epub 2014 May 13. Blood. 2014. PMID: 24825865 Free PMC article.

7

High prevalence of somatic MAP2K1 mutations in BRAF V600E-negative Langerhans cell histiocytosis.

Brown NA, Furtado LV, Betz BL, Kiel MJ, Weigelin HC, Lim MS, Elenitoba-Johnson KS. Brown NA, et al. Among authors: betz bl. Blood. 2014 Sep 4;124(10):1655-8. doi: 10.1182/blood-2014-05-577361. Epub 2014 Jun 30. Blood. 2014. PMID: 24982505 Free article.

8

Activating FGFR2-RAS-BRAF mutations in ameloblastoma.

Brown NA, Rolland D, McHugh JB, Weigelin HC, Zhao L, Lim MS, Elenitoba-Johnson KS, Betz BL. Brown NA, et al. Among authors: betz bl. Clin Cancer Res. 2014 Nov 1;20(21):5517-26. doi: 10.1158/1078-0432.CCR-14-1069. Epub 2014 Jul 3. Clin Cancer Res. 2014. PMID: 24993163

9

A novel recurrent NPM1-TYK2 gene fusion in cutaneous CD30-positive lymphoproliferative disorders.

Velusamy T, Kiel MJ, Sahasrabuddhe AA, Rolland D, Dixon CA, Bailey NG, Betz BL, Brown NA, Hristov AC, Wilcox RA, Miranda RN, Medeiros LJ, Jeon YK, Inamdar KV, Lim MS, Elenitoba-Johnson KS. Velusamy T, et al. Among authors: betz bl. Blood. 2014 Dec 11;124(25):3768-71. doi: 10.1182/blood-2014-07-588434. Epub 2014 Oct 27. Blood. 2014. PMID: 25349176 Free article.

10

A clinical grade sequencing-based assay for CEBPA mutation testing: report of a large series of myeloid neoplasms.

Behdad A, Weigelin HC, Elenitoba-Johnson KS, Betz BL. Behdad A, et al. Among authors: betz bl. J Mol Diagn. 2015 Jan;17(1):76-84. doi: 10.1016/j.jmoldx.2014.09.007. Epub 2014 Nov 6. J Mol Diagn. 2015. PMID: 25468431 Free article.

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