Znoyko I - Search Results

1

Whole-Genome Single Nucleotide Polymorphism Microarray for Copy Number and Loss of Heterozygosity Analysis in Tumors.

Rowsey R, Znoyko I, Wolff DJ. Rowsey R, et al. Among authors: znoyko i. Methods Mol Biol. 2019;1908:89-111. doi: 10.1007/978-1-4939-9004-7_7. Methods Mol Biol. 2019. PMID: 30649723

2

Tetraploidy and 5q deletion in myelodysplastic syndrome: a case report.

Znoyko I, Stuart RK, Ellingham T, Winters J, Wolff DJ, Quigley DI. Znoyko I, et al. Cancer Genet Cytogenet. 2008 May;183(1):64-8. doi: 10.1016/j.cancergencyto.2008.01.022. Cancer Genet Cytogenet. 2008. PMID: 18474300

3

Clonal diversity analysis using SNP microarray: a new prognostic tool for chronic lymphocytic leukemia.

Zhang L, Znoyko I, Costa LJ, Conlin LK, Daber RD, Self SE, Wolff DJ. Zhang L, et al. Among authors: znoyko i. Cancer Genet. 2011 Dec;204(12):654-65. doi: 10.1016/j.cancergen.2011.10.012. Cancer Genet. 2011. PMID: 22285017

4

A multicenter, cross-platform clinical validation study of cancer cytogenomic arrays.

Li MM, Monzon FA, Biegel JA, Jobanputra V, Laffin JJ, Levy B, Leon A, Miron P, Rossi MR, Toruner G, Alvarez K, Doho G, Dougherty MJ, Hu X, Kash S, Streck D, Znoyko I, Hagenkord JM, Wolff DJ. Li MM, et al. Among authors: znoyko i. Cancer Genet. 2015 Nov;208(11):525-36. doi: 10.1016/j.cancergen.2015.08.002. Epub 2015 Aug 28. Cancer Genet. 2015. PMID: 26454669

5

Chromothripsis in Two Patients With Renal Cell Carcinoma: A Case Series.

Gullett JC, Znoyko IY, Wolff DJ, Schandl CA. Gullett JC, et al. Clin Genitourin Cancer. 2017 Feb;15(1):e137-e143. doi: 10.1016/j.clgc.2016.06.005. Epub 2016 Jun 23. Clin Genitourin Cancer. 2017. PMID: 27426636 No abstract available.

6

First Report of Prenatal Ascertainment of a Fetus With Homozygous Loss of the SOX10 Gene and Phenotypic Correlation by Autopsy Examination.

LeBel DP 2nd, Wolff DJ, Batalis NI, Ellingham T, Matics N, Patwardhan SC, Znoyko IY, Schandl CA. LeBel DP 2nd, et al. Among authors: znoyko iy. Pediatr Dev Pathol. 2018 Nov-Dec;21(6):561-567. doi: 10.1177/1093526617744714. Epub 2017 Dec 7. Pediatr Dev Pathol. 2018. PMID: 29216801

7

Expression of renal cell markers and detection of 3p loss links endolymphatic sac tumor to renal cell carcinoma and warrants careful evaluation to avoid diagnostic pitfalls.

Jester R, Znoyko I, Garnovskaya M, Rozier JN, Kegl R, Patel S, Tran T, Abedalthagafi M, Horbinski CM, Richardson M, Wolff DJ, Lapadat R, Moore W, Rodriguez FJ, Mull J, Olar A. Jester R, et al. Among authors: znoyko i. Acta Neuropathol Commun. 2018 Oct 19;6(1):107. doi: 10.1186/s40478-018-0607-0. Acta Neuropathol Commun. 2018. PMID: 30340515 Free PMC article.

8

A high prevalence of biallelic RPE65 mutations in Costa Rican children with Leber congenital amaurosis and early-onset retinal dystrophy.

Glen WB Jr, Peterseim MMW, Badilla R, Znoyko I, Bourg A, Wilson R, Hardiman G, Wolff D, Martinez J. Glen WB Jr, et al. Among authors: znoyko i. Ophthalmic Genet. 2019 Apr;40(2):110-117. doi: 10.1080/13816810.2019.1582069. Epub 2019 Mar 14. Ophthalmic Genet. 2019. PMID: 30870047

9

Cryptic and atypical KMT2A-USP2 and KMT2A-USP8 rearrangements identified by mate pair sequencing in infant and childhood leukemia.

Blackburn PR, Smadbeck JB, Znoyko I, Webley MR, Pitel BA, Vasmatzis G, Xu X, Greipp PT, Hoppman NL, Ketterling RP, Baughn LB, Lindsey KG, Schandl CA, Wolff DJ, Peterson JF. Blackburn PR, et al. Among authors: znoyko i. Genes Chromosomes Cancer. 2020 Jul;59(7):422-427. doi: 10.1002/gcc.22842. Epub 2020 Mar 26. Genes Chromosomes Cancer. 2020. PMID: 32196814

10

Integrated genomic analysis using chromosomal microarray, fluorescence in situ hybridization and mate pair analyses: Characterization of a cryptic t(9;22)(p24.1;q11.2)/BCR-JAK2 in myeloid/lymphoid neoplasm with eosinophilia.

Snider JS, Znoyko I, Lindsey KG, Morse J, Baughn LB, Hoppman NL, Pitel BA, Pearce KE, Schandl CA, Wolff DJ. Snider JS, et al. Among authors: znoyko i. Cancer Genet. 2020 Aug;246-247:44-47. doi: 10.1016/j.cancergen.2020.08.004. Epub 2020 Aug 7. Cancer Genet. 2020. PMID: 32827877

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