154 related articles for article (PubMed ID: 18246049)
1. Whole genome SNP arrays as a potential diagnostic tool for the detection of characteristic chromosomal aberrations in renal epithelial tumors.
Monzon FA; Hagenkord JM; Lyons-Weiler MA; Balani JP; Parwani AV; Sciulli CM; Li J; Chandran UR; Bastacky SI; Dhir R
Mod Pathol; 2008 May; 21(5):599-608. PubMed ID: 18246049
[TBL] [Abstract][Full Text] [Related]
2. Loss of heterozygosity and copy number abnormality in clear cell renal cell carcinoma discovered by high-density affymetrix 10K single nucleotide polymorphism mapping array.
Toma MI; Grosser M; Herr A; Aust DE; Meye A; Hoefling C; Fuessel S; Wuttig D; Wirth MP; Baretton GB
Neoplasia; 2008 Jul; 10(7):634-42. PubMed ID: 18592004
[TBL] [Abstract][Full Text] [Related]
3. Optimization of the Affymetrix GeneChip Mapping 10K 2.0 Assay for routine clinical use on formalin-fixed paraffin-embedded tissues.
Lyons-Weiler M; Hagenkord J; Sciulli C; Dhir R; Monzon FA
Diagn Mol Pathol; 2008 Mar; 17(1):3-13. PubMed ID: 18303412
[TBL] [Abstract][Full Text] [Related]
4. Detection of chromosomal aberrations in renal tumors: a comparative study of conventional cytogenetics and virtual karyotyping with single-nucleotide polymorphism microarrays.
Monzon FA; Alvarez K; Gatalica Z; Bridge JA; Nelson M; Kim HJ; Hagenkord JM
Arch Pathol Lab Med; 2009 Dec; 133(12):1917-22. PubMed ID: 19961245
[TBL] [Abstract][Full Text] [Related]
5. Genomic expression and single-nucleotide polymorphism profiling discriminates chromophobe renal cell carcinoma and oncocytoma.
Tan MH; Wong CF; Tan HL; Yang XJ; Ditlev J; Matsuda D; Khoo SK; Sugimura J; Fujioka T; Furge KA; Kort E; Giraud S; Ferlicot S; Vielh P; Amsellem-Ouazana D; Debré B; Flam T; Thiounn N; Zerbib M; Benoît G; Droupy S; Molinié V; Vieillefond A; Tan PH; Richard S; Teh BT
BMC Cancer; 2010 May; 10():196. PubMed ID: 20462447
[TBL] [Abstract][Full Text] [Related]
6. Genetic alterations in renal cell carcinoma with rhabdoid differentiation.
Perrino CM; Hucthagowder V; Evenson M; Kulkarni S; Humphrey PA
Hum Pathol; 2015 Jan; 46(1):9-16. PubMed ID: 25439741
[TBL] [Abstract][Full Text] [Related]
7. Genome-wide profiling of chromosomal alterations in renal cell carcinoma using high-density single nucleotide polymorphism arrays.
Chen M; Ye Y; Yang H; Tamboli P; Matin S; Tannir NM; Wood CG; Gu J; Wu X
Int J Cancer; 2009 Nov; 125(10):2342-8. PubMed ID: 19521957
[TBL] [Abstract][Full Text] [Related]
8. Virtual-karyotyping with SNP microarrays in morphologically challenging renal cell neoplasms: a practical and useful diagnostic modality.
Kim HJ; Shen SS; Ayala AG; Ro JY; Truong LD; Alvarez K; Bridge JA; Gatalica Z; Hagenkord JM; Gonzalez-Berjon JM; Monzon FA
Am J Surg Pathol; 2009 Sep; 33(9):1276-86. PubMed ID: 19461508
[TBL] [Abstract][Full Text] [Related]
9. Virtual karyotyping with SNP microarrays reduces uncertainty in the diagnosis of renal epithelial tumors.
Hagenkord JM; Parwani AV; Lyons-Weiler MA; Alvarez K; Amato R; Gatalica Z; Gonzalez-Berjon JM; Peterson L; Dhir R; Monzon FA
Diagn Pathol; 2008 Nov; 3():44. PubMed ID: 18990225
[TBL] [Abstract][Full Text] [Related]
10. High-resolution array copy number analyses for detection of deletion, gain, amplification and copy-neutral LOH in primary neuroblastoma tumors: four cases of homozygous deletions of the CDKN2A gene.
Carén H; Erichsen J; Olsson L; Enerbäck C; Sjöberg RM; Abrahamsson J; Kogner P; Martinsson T
BMC Genomics; 2008 Jul; 9():353. PubMed ID: 18664255
[TBL] [Abstract][Full Text] [Related]
11. Copy Number Alterations with Prognostic Potential in Clear Cell Renal Cell Carcinoma.
Maruschke M; Koczan D; Ziems B; Hakenberg OW
Urol Int; 2018; 101(4):417-424. PubMed ID: 30227442
[TBL] [Abstract][Full Text] [Related]
12. Single nucleotide polymorphism (SNP) chromosomal microarray as a diagnostic tool for mucinous tubular and spindle cell carcinoma: A validation study.
Nielson KJ; Rowsey R; Dasari S; Sukov WR; Kipp BR; Raghunathan A; Whaley RD; Ebare K; Stanton ML; Reynolds JP; Sharma V; Thompson RH; Boorjian SA; Leibovich BC; Hernandez LH; Jimenez RE; Cheville JC; Gupta S
Hum Pathol; 2024 Apr; 146():57-65. PubMed ID: 38615998
[TBL] [Abstract][Full Text] [Related]
13. Genome-wide analysis of DNA copy number changes and LOH in CLL using high-density SNP arrays.
Pfeifer D; Pantic M; Skatulla I; Rawluk J; Kreutz C; Martens UM; Fisch P; Timmer J; Veelken H
Blood; 2007 Feb; 109(3):1202-10. PubMed ID: 17053054
[TBL] [Abstract][Full Text] [Related]
14. Distinct Genomic Copy Number Alterations Distinguish Mucinous Tubular and Spindle Cell Carcinoma of the Kidney From Papillary Renal Cell Carcinoma With Overlapping Histologic Features.
Ren Q; Wang L; Al-Ahmadie HA; Fine SW; Gopalan A; Sirintrapun SJ; Tickoo SK; Reuter VE; Chen YB
Am J Surg Pathol; 2018 Jun; 42(6):767-777. PubMed ID: 29462091
[TBL] [Abstract][Full Text] [Related]
15. Characterization of chromosome arm 20q abnormalities in myeloid malignancies using genome-wide single nucleotide polymorphism array analysis.
Huh J; Tiu RV; Gondek LP; O'Keefe CL; Jasek M; Makishima H; Jankowska AM; Jiang Y; Verma A; Theil KS; McDevitt MA; Maciejewski JP
Genes Chromosomes Cancer; 2010 Apr; 49(4):390-9. PubMed ID: 20095039
[TBL] [Abstract][Full Text] [Related]
16. Clinical utilization of high-resolution single nucleotide polymorphism based oligonucleotide arrays in diagnostic studies of pediatric patients with solid tumors.
Dougherty MJ; Tooke LS; Sullivan LM; Hakonarson H; Wainwright LM; Biegel JA
Cancer Genet; 2012; 205(1-2):42-54. PubMed ID: 22429597
[TBL] [Abstract][Full Text] [Related]
17. High-resolution genomic profiling of chromosomal aberrations using Infinium whole-genome genotyping.
Peiffer DA; Le JM; Steemers FJ; Chang W; Jenniges T; Garcia F; Haden K; Li J; Shaw CA; Belmont J; Cheung SW; Shen RM; Barker DL; Gunderson KL
Genome Res; 2006 Sep; 16(9):1136-48. PubMed ID: 16899659
[TBL] [Abstract][Full Text] [Related]
18. SNP-based arrays complement classic cytogenetics in the detection of chromosomal aberrations in Wilms' tumor.
Zin R; Pham K; Ashleigh M; Ravine D; Waring P; Charles A
Cancer Genet; 2012 Mar; 205(3):80-93. PubMed ID: 22469507
[TBL] [Abstract][Full Text] [Related]
19. Genomewide scan for loss of heterozygosity and chromosomal amplification in breast carcinoma using single-nucleotide polymorphism arrays.
Argos M; Kibriya MG; Jasmine F; Olopade OI; Su T; Hibshoosh H; Ahsan H
Cancer Genet Cytogenet; 2008 Apr; 182(2):69-74. PubMed ID: 18406867
[TBL] [Abstract][Full Text] [Related]
20. Ploidy status and copy number aberrations in primary glioblastomas defined by integrated analysis of allelic ratios, signal ratios and loss of heterozygosity using 500K SNP Mapping Arrays.
Gardina PJ; Lo KC; Lee W; Cowell JK; Turpaz Y
BMC Genomics; 2008 Oct; 9():489. PubMed ID: 18928532
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
