340 related articles for article (PubMed ID: 23695279)
1. Combined array CGH plus SNP genome analyses in a single assay for optimized clinical testing.
Wiszniewska J; Bi W; Shaw C; Stankiewicz P; Kang SH; Pursley AN; Lalani S; Hixson P; Gambin T; Tsai CH; Bock HG; Descartes M; Probst FJ; Scaglia F; Beaudet AL; Lupski JR; Eng C; Cheung SW; Bacino C; Patel A
Eur J Hum Genet; 2014 Jan; 22(1):79-87. PubMed ID: 23695279
[TBL] [Abstract][Full Text] [Related]
2. Novel applications of array comparative genomic hybridization in molecular diagnostics.
Cheung SW; Bi W
Expert Rev Mol Diagn; 2018 Jun; 18(6):531-542. PubMed ID: 29848116
[TBL] [Abstract][Full Text] [Related]
3. Evaluation of copy number variation detection for a SNP array platform.
Zhang X; Du R; Li S; Zhang F; Jin L; Wang H
BMC Bioinformatics; 2014 Feb; 15():50. PubMed ID: 24555668
[TBL] [Abstract][Full Text] [Related]
4. SNP arrays: comparing diagnostic yields for four platforms in children with developmental delay.
D'Amours G; Langlois M; Mathonnet G; Fetni R; Nizard S; Srour M; Tihy F; Phillips MS; Michaud JL; Lemyre E
BMC Med Genomics; 2014 Dec; 7():70. PubMed ID: 25539807
[TBL] [Abstract][Full Text] [Related]
5. Identification of De Novo and Rare Inherited Copy Number Variants in Children with Syndromic Congenital Heart Defects.
Hussein IR; Bader RS; Chaudhary AG; Bassiouni R; Alquaiti M; Ashgan F; Schulten HJ; Al Qahtani MH
Pediatr Cardiol; 2018 Jun; 39(5):924-940. PubMed ID: 29541814
[TBL] [Abstract][Full Text] [Related]
6. Clinical significance of previously cryptic copy number alterations and loss of heterozygosity in pediatric acute myeloid leukemia and myelodysplastic syndrome determined using combined array comparative genomic hybridization plus single-nucleotide polymorphism microarray analyses.
Koh KN; Lee JO; Seo EJ; Lee SW; Suh JK; Im HJ; Seo JJ
J Korean Med Sci; 2014 Jul; 29(7):926-33. PubMed ID: 25045224
[TBL] [Abstract][Full Text] [Related]
7. Global assessment of genomic variation in cattle by genome resequencing and high-throughput genotyping.
Zhan B; Fadista J; Thomsen B; Hedegaard J; Panitz F; Bendixen C
BMC Genomics; 2011 Nov; 12():557. PubMed ID: 22082336
[TBL] [Abstract][Full Text] [Related]
8. A discovery resource of rare copy number variations in individuals with autism spectrum disorder.
Prasad A; Merico D; Thiruvahindrapuram B; Wei J; Lionel AC; Sato D; Rickaby J; Lu C; Szatmari P; Roberts W; Fernandez BA; Marshall CR; Hatchwell E; Eis PS; Scherer SW
G3 (Bethesda); 2012 Dec; 2(12):1665-85. PubMed ID: 23275889
[TBL] [Abstract][Full Text] [Related]
9. Application of Nexus copy number software for CNV detection and analysis.
Darvishi K
Curr Protoc Hum Genet; 2010 Apr; Chapter 4():Unit 4.14.1-28. PubMed ID: 20373515
[TBL] [Abstract][Full Text] [Related]
10. Density matters: comparison of array platforms for detection of copy-number variation and copy-neutral abnormalities.
Mason-Suares H; Kim W; Grimmett L; Williams ES; Horner VL; Kunig D; Goldlust IS; Wu BL; Shen Y; Miller DT; Martin CL; Rudd MK
Genet Med; 2013 Sep; 15(9):706-12. PubMed ID: 23558256
[TBL] [Abstract][Full Text] [Related]
11. Detection of clinically relevant exonic copy-number changes by array CGH.
Boone PM; Bacino CA; Shaw CA; Eng PA; Hixson PM; Pursley AN; Kang SH; Yang Y; Wiszniewska J; Nowakowska BA; del Gaudio D; Xia Z; Simpson-Patel G; Immken LL; Gibson JB; Tsai AC; Bowers JA; Reimschisel TE; Schaaf CP; Potocki L; Scaglia F; Gambin T; Sykulski M; Bartnik M; Derwinska K; Wisniowiecka-Kowalnik B; Lalani SR; Probst FJ; Bi W; Beaudet AL; Patel A; Lupski JR; Cheung SW; Stankiewicz P
Hum Mutat; 2010 Dec; 31(12):1326-42. PubMed ID: 20848651
[TBL] [Abstract][Full Text] [Related]
12. Combined array-comparative genomic hybridization and single-nucleotide polymorphism-loss of heterozygosity analysis reveals complex genetic alterations in cervical cancer.
Kloth JN; Oosting J; van Wezel T; Szuhai K; Knijnenburg J; Gorter A; Kenter GG; Fleuren GJ; Jordanova ES
BMC Genomics; 2007 Feb; 8():53. PubMed ID: 17311676
[TBL] [Abstract][Full Text] [Related]
13. The use of ultra-dense array CGH analysis for the discovery of micro-copy number alterations and gene fusions in the cancer genome.
Przybytkowski E; Ferrario C; Basik M
BMC Med Genomics; 2011 Jan; 4():16. PubMed ID: 21272361
[TBL] [Abstract][Full Text] [Related]
14. Copy number variations and stroke.
Colaianni V; Mazzei R; Cavallaro S
Neurol Sci; 2016 Dec; 37(12):1895-1904. PubMed ID: 27393281
[TBL] [Abstract][Full Text] [Related]
15. The clinical benefit of array-based comparative genomic hybridization for detection of copy number variants in Czech children with intellectual disability and developmental delay.
Wayhelova M; Smetana J; Vallova V; Hladilkova E; Filkova H; Hanakova M; Vilemova M; Nikolova P; Gromesova B; Gaillyova R; Kuglik P
BMC Med Genomics; 2019 Jul; 12(1):111. PubMed ID: 31337399
[TBL] [Abstract][Full Text] [Related]
16. Semiconductor Sequencing Analysis of Chromosomal Copy Number Variations in Spontaneous Miscarriage.
Wang MZ; Lin FQ; Li M; He D; Yu QH; Yang XX; Wu YS
Med Sci Monit; 2017 Nov; 23():5550-5557. PubMed ID: 29162795
[TBL] [Abstract][Full Text] [Related]
17. Comprehensive performance comparison of high-resolution array platforms for genome-wide Copy Number Variation (CNV) analysis in humans.
Haraksingh RR; Abyzov A; Urban AE
BMC Genomics; 2017 Apr; 18(1):321. PubMed ID: 28438122
[TBL] [Abstract][Full Text] [Related]
18. Reference-unbiased copy number variant analysis using CGH microarrays.
Ju YS; Hong D; Kim S; Park SS; Kim S; Lee S; Park H; Kim JI; Seo JS
Nucleic Acids Res; 2010 Nov; 38(20):e190. PubMed ID: 20802225
[TBL] [Abstract][Full Text] [Related]
19. Genome-wide mapping of copy number variation in humans: comparative analysis of high resolution array platforms.
Haraksingh RR; Abyzov A; Gerstein M; Urban AE; Snyder M
PLoS One; 2011; 6(11):e27859. PubMed ID: 22140474
[TBL] [Abstract][Full Text] [Related]
20. Identification of copy number variants from exome sequence data.
Samarakoon PS; Sorte HS; Kristiansen BE; Skodje T; Sheng Y; Tjønnfjord GE; Stadheim B; Stray-Pedersen A; Rødningen OK; Lyle R
BMC Genomics; 2014 Aug; 15(1):661. PubMed ID: 25102989
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]