195 related articles for article (PubMed ID: 34181357)
1. Copy Number Variants Captured by the Array Comparative Genomic Hybridization in a Cohort of Patients Affected with Hereditary Colorectal Cancer in Sri Lanka: The First CNV Analysis Study of the Hereditary Colorectal Cancer in the Sri Lankan Population.
Wijesiriwardhana P; Wettasinghe K; Dissanayeke VHW
Asian Pac J Cancer Prev; 2021 Jun; 22(6):1957-1966. PubMed ID: 34181357
[TBL] [Abstract][Full Text] [Related]
2. Continuing difficulties in interpreting CNV data: lessons from a genome-wide CNV association study of Australian HNPCC/lynch syndrome patients.
Talseth-Palmer BA; Holliday EG; Evans TJ; McEvoy M; Attia J; Grice DM; Masson AL; Meldrum C; Spigelman A; Scott RJ
BMC Med Genomics; 2013 Mar; 6():10. PubMed ID: 23531357
[TBL] [Abstract][Full Text] [Related]
3. DNA copy number profiling in microsatellite-stable and microsatellite-unstable hereditary non-polyposis colorectal cancers by targeted CNV array.
Chen W; Ding J; Jiang L; Liu Z; Zhou X; Shi D
Funct Integr Genomics; 2017 Jan; 17(1):85-96. PubMed ID: 27896456
[TBL] [Abstract][Full Text] [Related]
4. Copy number variation analysis and targeted NGS in 77 families with suspected Lynch syndrome reveals novel potential causative genes.
Kayser K; Degenhardt F; Holzapfel S; Horpaopan S; Peters S; Spier I; Morak M; Vangala D; Rahner N; von Knebel-Doeberitz M; Schackert HK; Engel C; Büttner R; Wijnen J; Doerks T; Bork P; Moebus S; Herms S; Fischer S; Hoffmann P; Aretz S; Steinke-Lange V
Int J Cancer; 2018 Dec; 143(11):2800-2813. PubMed ID: 29987844
[TBL] [Abstract][Full Text] [Related]
5. RB1 screening of retinoblastoma patients in Sri Lanka using targeted next generation sequencing (NGS) and gene ratio analysis copy enumeration PCR (GRACE-PCR).
Kugalingam N; De Silva D; Abeysekera H; Nanayakkara S; Tirimanne S; Ranaweera D; Suravajhala P; Chandrasekharan V
BMC Med Genomics; 2023 Nov; 16(1):279. PubMed ID: 37932687
[TBL] [Abstract][Full Text] [Related]
6. Identification of chromosomal copy number variations and novel candidate loci in hereditary nonpolyposis colorectal cancer with mismatch repair proficiency.
Chen W; Yuan L; Cai Y; Chen X; Chi Y; Wei P; Zhou X; Shi D
Genomics; 2013 Jul; 102(1):27-34. PubMed ID: 23434627
[TBL] [Abstract][Full Text] [Related]
7. Contribution of rare germline copy number variations and common susceptibility loci in Lynch syndrome patients negative for mutations in the mismatch repair genes.
Villacis RA; Miranda PM; Gomy I; Santos EM; Carraro DM; Achatz MI; Rossi BM; Rogatto SR
Int J Cancer; 2016 Apr; 138(8):1928-35. PubMed ID: 26620301
[TBL] [Abstract][Full Text] [Related]
8. Germline DNA copy number variation in familial and early-onset breast cancer.
Krepischi AC; Achatz MI; Santos EM; Costa SS; Lisboa BC; Brentani H; Santos TM; Gonçalves A; Nóbrega AF; Pearson PL; Vianna-Morgante AM; Carraro DM; Brentani RR; Rosenberg C
Breast Cancer Res; 2012 Feb; 14(1):R24. PubMed ID: 22314128
[TBL] [Abstract][Full Text] [Related]
9. Hereditary nonpolyposis colorectal cancer: diagnostic strategies and their implications.
Bonis PA; Trikalinos TA; Chung M; Chew P; Ip S; DeVine DA; Lau J
Evid Rep Technol Assess (Full Rep); 2007 May; (150):1-180. PubMed ID: 17764220
[TBL] [Abstract][Full Text] [Related]
10. Rare germline alterations in cancer-related genes associated with the risk of multiple primary tumor development.
Villacis RAR; Basso TR; Canto LM; Pinheiro M; Santiago KM; Giacomazzi J; de Paula CAA; Carraro DM; Ashton-Prolla P; Achatz MI; Rogatto SR
J Mol Med (Berl); 2017 May; 95(5):523-533. PubMed ID: 28093616
[TBL] [Abstract][Full Text] [Related]
11. Genetic Testing for Hereditary Nonpolyposis Colorectal Cancer (HNPCC).
Nallamilli BRR; Hegde M
Curr Protoc Hum Genet; 2017 Jul; 94():10.12.1-10.12.23. PubMed ID: 28696559
[TBL] [Abstract][Full Text] [Related]
12. Prevalence of CNV-neutral structural genomic rearrangements in MLH1, MSH2, and PMS2 not detectable in routine NGS diagnostics.
Morak M; Steinke-Lange V; Massdorf T; Benet-Pages A; Locher M; Laner A; Kayser K; Aretz S; Holinski-Feder E
Fam Cancer; 2020 Apr; 19(2):161-167. PubMed ID: 32002723
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. Copy Number Variations (CNVs) Account for 10.8% of Pathogenic Variants in Patients Referred for Hereditary Cancer Testing.
Agiannitopoulos K; Pepe G; Tsaousis GN; Potska K; Bouzarelou D; Katseli A; Ntogka C; Meintani A; Tsoulos N; Giassas S; Venizelos V; Markopoulos C; Iosifidou R; Karageorgopoulou S; Christodoulou C; Natsiopoulos I; Papazisis K; Vasilaki-Antonatou M; Kabletsas E; Psyrri A; Ziogas D; Lalla E; Koumarianou A; Anastasakou K; Papadimitriou C; Ozmen V; Tansan S; Kaban K; Ozatli T; Eniu DT; Chiorean A; Blidaru A; Rinsma M; Papadopoulou E; Nasioulas G
Cancer Genomics Proteomics; 2023; 20(5):448-455. PubMed ID: 37643779
[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. Integrative analysis of hereditary nonpolyposis colorectal cancer: the contribution of allele-specific expression and other assays to diagnostic algorithms.
De Lellis L; Aceto GM; Curia MC; Catalano T; Mammarella S; Veschi S; Fantini F; Battista P; Stigliano V; Messerini L; Mareni C; Sala P; Bertario L; Radice P; Cama A
PLoS One; 2013; 8(11):e81194. PubMed ID: 24278394
[TBL] [Abstract][Full Text] [Related]
17. Genetic profiles distinguish different types of hereditary ovarian cancer.
Domanska K; Malander S; Staaf J; Karlsson A; Borg A; Jönsson G; Nilbert M
Oncol Rep; 2010 Oct; 24(4):885-95. PubMed ID: 20811668
[TBL] [Abstract][Full Text] [Related]
18. Genome-wide CNV analysis in 221 unrelated patients and targeted high-throughput sequencing reveal novel causative candidate genes for colorectal adenomatous polyposis.
Horpaopan S; Spier I; Zink AM; Altmüller J; Holzapfel S; Laner A; Vogt S; Uhlhaas S; Heilmann S; Stienen D; Pasternack SM; Keppler K; Adam R; Kayser K; Moebus S; Draaken M; Degenhardt F; Engels H; Hofmann A; Nöthen MM; Steinke V; Perez-Bouza A; Herms S; Holinski-Feder E; Fröhlich H; Thiele H; Hoffmann P; Aretz S
Int J Cancer; 2015 Mar; 136(6):E578-89. PubMed ID: 25219767
[TBL] [Abstract][Full Text] [Related]
19. Genotype-phenotype associations in children with copy number variants associated with high neuropsychiatric risk in the UK (IMAGINE-ID): a case-control cohort study.
Chawner SJRA; Owen MJ; Holmans P; Raymond FL; Skuse D; Hall J; van den Bree MBM
Lancet Psychiatry; 2019 Jun; 6(6):493-505. PubMed ID: 31056457
[TBL] [Abstract][Full Text] [Related]
20. High-resolution array-CGH analysis on 46,XX patients affected by early onset primary ovarian insufficiency discloses new genes involved in ovarian function.
Bestetti I; Castronovo C; Sironi A; Caslini C; Sala C; Rossetti R; Crippa M; Ferrari I; Pistocchi A; Toniolo D; Persani L; Marozzi A; Finelli P
Hum Reprod; 2019 Mar; 34(3):574-583. PubMed ID: 30689869
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]