Rare germline copy number variants in colorectal cancer predisposition characterized by exome sequencing analysis
- 1 January 2018
- journal article
- letter
- Published by Elsevier in Journal of Genetics and Genomics
- Vol. 45 (1) , 41-45
Abstract
No abstract availableFunding Information
- Ministerio de Economía y Competitividad (SAF2014-54453-R)
- Ministerio de Economía y Competitividad (GCB13131592CAST)
- Ministerio de Economía y Competitividad (SLT002/16/00398)
- Agència de Gestió d'Ajuts Universitaris i de Recerca (2014SGR135)
- Agència de Gestió d'Ajuts Universitaris i de Recerca (FI 2017 B00619)
- Agència de Gestió d'Ajuts Universitaris i de Recerca (2014SGR255)
- European Cooperation in Science and Technology (BM1206)
- Centro de Investigación Biomédica en Red de Enfermedades Hepáticas y Digestivas
- Society for Endocrinology
- Generalitat de Catalunya
- Federación Española de Enfermedades Raras (17/00878)
- Federación Española de Enfermedades Raras (14/00173)
- Federación Española de Enfermedades Raras (14/00230)
This publication has 19 references indexed in Scilit:
- Formation of new chromatin domains determines pathogenicity of genomic duplicationsNature, 2016
- The Fanconi anemia DNA damage repair pathway in the spotlight for germline predisposition to colorectal cancerEuropean Journal of Human Genetics, 2016
- Mechanisms underlying structural variant formation in genomic disordersNature Reviews Genetics, 2016
- miR-942 promotes cancer stem cell-like traits in esophageal squamous cell carcinoma through activation of Wnt/β-catenin signalling pathwayOncotarget, 2015
- Whole-exome sequencing identifies rare pathogenic variants in new predisposition genes for familial colorectal cancerGenetics in Medicine, 2015
- A colorectal cancer genome-wide association study in a Spanish cohort identifies two variants associated with colorectal cancer risk at 1p33 and 8p12BMC Genomics, 2013
- Hereditary mixed polyposis syndrome is caused by a 40-kb upstream duplication that leads to increased and ectopic expression of the BMP antagonist GREM1Nature Genetics, 2012
- TRIM proteins and cancerNature Reviews Cancer, 2011
- Evaluation of the 3p21.3 tumour-suppressor gene clusterOncogene, 2007
- RIS1, a gene with trinucleotide repeats, is a target in the mutator pathway of colorectal carcinogenesisCancer Genetics and Cytogenetics, 2006