Lewis TB - Search Results

1

Differentiating Ewing's sarcoma from other round blue cell tumors using a RT-PCR translocation panel on formalin-fixed paraffin-embedded tissues.

Lewis TB, Coffin CM, Bernard PS. Lewis TB, et al. Mod Pathol. 2007 Mar;20(3):397-404. doi: 10.1038/modpathol.3800755. Mod Pathol. 2007. PMID: 17334332 Free article.

2

Molecular classification of melanoma using real-time quantitative reverse transcriptase-polymerase chain reaction.

Lewis TB, Robison JE, Bastien R, Milash B, Boucher K, Samlowski WE, Leachman SA, Dirk Noyes R, Wittwer CT, Perreard L, Bernard PS. Lewis TB, et al. Cancer. 2005 Oct 15;104(8):1678-86. doi: 10.1002/cncr.21372. Cancer. 2005. PMID: 16116595 Free article.

3

High-throughput amplicon scanning of the TP53 gene in breast cancer using high-resolution fluorescent melting curve analyses and automatic mutation calling.

Bastien R, Lewis TB, Hawkes JE, Quackenbush JF, Robbins TC, Palazzo J, Perou CM, Bernard PS. Bastien R, et al. Among authors: lewis tb. Hum Mutat. 2008 May;29(5):757-64. doi: 10.1002/humu.20726. Hum Mutat. 2008. PMID: 18348286

4

Noncontinuously binding loop-out primers for avoiding problematic DNA sequences in PCR and sanger sequencing.

Sumner K, Swensen JJ, Procter M, Jama M, Wooderchak-Donahue W, Lewis T, Fong M, Hubley L, Schwarz M, Ha Y, Paul E, Brulotte B, Lyon E, Bayrak-Toydemir P, Mao R, Pont-Kingdon G, Best DH. Sumner K, et al. J Mol Diagn. 2014 Sep;16(5):477-480. doi: 10.1016/j.jmoldx.2014.04.005. Epub 2014 Jul 9. J Mol Diagn. 2014. PMID: 25017792 Free article.

5

Clinical utility of a next generation sequencing panel assay for Marfan and Marfan-like syndromes featuring aortopathy.

Wooderchak-Donahue W, VanSant-Webb C, Tvrdik T, Plant P, Lewis T, Stocks J, Raney JA, Meyers L, Berg A, Rope AF, Yetman AT, Bleyl SB, Mesley R, Bull DA, Collins RT, Ojeda MM, Roberts A, Lacro R, Woerner A, Stoler J, Bayrak-Toydemir P. Wooderchak-Donahue W, et al. Am J Med Genet A. 2015 Aug;167A(8):1747-57. doi: 10.1002/ajmg.a.37085. Epub 2015 May 5. Am J Med Genet A. 2015. PMID: 25944730

6

Processed Pseudogene Confounding Deletion/Duplication Assays for SMAD4.

Millson A, Lewis T, Pesaran T, Salvador D, Gillespie K, Gau CL, Pont-Kingdon G, Lyon E, Bayrak-Toydemir P. Millson A, et al. J Mol Diagn. 2015 Sep;17(5):576-82. doi: 10.1016/j.jmoldx.2015.05.005. Epub 2015 Jul 10. J Mol Diagn. 2015. PMID: 26165824 Free article.

7

Verification of multiplex ligation-dependent probe amplification probes in the absence of positive samples.

Wooderchak-Donahue W, Vaughn C, Chou LS, Lewis T, Sumner K, Procter M, Gedge F, Bayrak-Toydemir P, Lyon E, Pont-Kingdon G. Wooderchak-Donahue W, et al. Genet Test Mol Biomarkers. 2011 Nov;15(11):793-9. doi: 10.1089/gtmb.2011.0051. Epub 2011 Jun 20. Genet Test Mol Biomarkers. 2011. PMID: 21689003

8

Candidate locus analysis for PHACE syndrome.

Mitchell S, Siegel DH, Shieh JT, Stevenson DA, Grimmer JF, Lewis T, Metry D, Frieden I, Blei F, Kayserili H, Drolet BA, Bayrak-Toydemir P. Mitchell S, et al. Am J Med Genet A. 2012 Jun;158A(6):1363-7. doi: 10.1002/ajmg.a.35341. Epub 2012 Apr 27. Am J Med Genet A. 2012. PMID: 22544659 Free PMC article.

9

Hereditary hemorrhagic telangiectasia: two distinct ENG deletions in one family.

Wooderchak W, Gedge F, McDonald M, Krautscheid P, Wang X, Malkiewicz J, Bukjiok CJ, Lewis T, Bayrak-Toydemir P. Wooderchak W, et al. Clin Genet. 2010 Nov;78(5):484-9. doi: 10.1111/j.1399-0004.2010.01418.x. Clin Genet. 2010. PMID: 20412114

10

Characterization of large genomic deletions in the FBN1 gene using multiplex ligation-dependent probe amplification.

Furtado LV, Wooderchak-Donahue W, Rope AF, Yetman AT, Lewis T, Plant P, Bayrak-Toydemir P. Furtado LV, et al. BMC Med Genet. 2011 Sep 21;12:119. doi: 10.1186/1471-2350-12-119. BMC Med Genet. 2011. PMID: 21936929 Free PMC article.

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