Cargando…

Genetic Variants Associated with Colorectal Adenoma Susceptibility

BACKGROUND: Common low-penetrance genetic variants have been consistently associated with colorectal cancer risk. AIM: To determine if these genetic variants are associated also with adenoma susceptibility and may improve selection of patients with increased risk for advanced adenomas and/or multipl...

Descripción completa

Detalles Bibliográficos
Autores principales:	Abulí, Anna, Castells, Antoni, Bujanda, Luis, Lozano, Juan José, Bessa, Xavier, Hernández, Cristina, Álvarez-Urturi, Cristina, Pellisé, Maria, Esteban-Jurado, Clara, Hijona, Elizabeth, Burón, Andrea, Macià, Francesc, Grau, Jaume, Guayta, Rafael, Castellví-Bel, Sergi, Andreu, Montserrat
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Public Library of Science 2016
Materias:	Research Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4831735/ https://www.ncbi.nlm.nih.gov/pubmed/27078840 http://dx.doi.org/10.1371/journal.pone.0153084

Ejemplares similares

Whole-exome sequencing identifies rare pathogenic variants in new predisposition genes for familial colorectal cancer
por: Esteban-Jurado, Clara, et al.
Publicado: (2015)

Multiple Sporadic Colorectal Cancers Display a Unique Methylation Phenotype
por: Gonzalo, Victoria, et al.
Publicado: (2014)

Single Nucleotide Polymorphisms in the Wnt and BMP Pathways and Colorectal Cancer Risk in a Spanish Cohort
por: Fernández-Rozadilla, Ceres, et al.
Publicado: (2010)

Identification of Lynch Syndrome Carriers among Patients with Small Bowel Adenocarcinoma
por: Sánchez, Ariadna, et al.
Publicado: (2021)

Accuracy of Colon Capsule Endoscopy in Detecting Colorectal Polyps in Individuals with Familial Colorectal Cancer: Could We Avoid Colonoscopies?
por: Alvarez-Urturi, Cristina, et al.
Publicado: (2017)

Aberrant Gene Promoter Methylation Associated with Sporadic Multiple Colorectal Cancer
por: Gonzalo, Victoria, et al.
Publicado: (2010)

Association between socioeconomic deprivation and colorectal cancer screening outcomes: Low uptake rates among the most and least deprived people
por: Buron, Andrea, et al.
Publicado: (2017)

A colorectal cancer genome-wide association study in a Spanish cohort identifies two variants associated with colorectal cancer risk at 1p33 and 8p12
por: Fernandez-Rozadilla, Ceres, et al.
Publicado: (2013)

Impact of comorbid conditions on participation in an organised colorectal cancer screening programme: a cross-sectional study
por: Guiriguet, Carolina, et al.
Publicado: (2017)

The MLH1 c.1852_1853delinsGC (p.K618A) Variant in Colorectal Cancer: Genetic Association Study in 18,723 Individuals
por: Abulí, Anna, et al.
Publicado: (2014)

Rectal Aberrant Crypt Foci in Humans Are Not Surrogate Markers for Colorectal Cancer Risk
por: Quintanilla, Isabel, et al.
Publicado: (2019)

Predictors of Metachronous Risk Polyps After Index Colonoscopy
por: Carot, Laura, et al.
Publicado: (2021)

The Fanconi anemia DNA damage repair pathway in the spotlight for germline predisposition to colorectal cancer
por: Esteban-Jurado, Clara, et al.
Publicado: (2016)

Analysis of A 6-Mirna Signature in Serum from Colorectal Cancer Screening Participants as Non-Invasive Biomarkers for Advanced Adenoma and Colorectal Cancer Detection
por: Marcuello, María, et al.
Publicado: (2019)

Evaluation of Alpha 1-Antitrypsin and the Levels of mRNA Expression of Matrix Metalloproteinase 7, Urokinase Type Plasminogen Activator Receptor and COX-2 for the Diagnosis of Colorectal Cancer
por: Bujanda, Luis, et al.
Publicado: (2013)

Integrated Analysis of Germline and Tumor DNA Identifies New Candidate Genes Involved in Familial Colorectal Cancer
por: Díaz-Gay, Marcos, et al.
Publicado: (2019)

Does digital mammography suppose an advance in early diagnosis? Trends in performance indicators 6 years after digitalization
por: Sala, Maria, et al.
Publicado: (2014)

A High Degree of LINE-1 Hypomethylation Is a Unique Feature of Early-Onset Colorectal Cancer
por: Antelo, Marina, et al.
Publicado: (2012)

Identification of New Genes Involved in Germline Predisposition to Early-Onset Gastric Cancer
por: Herrera-Pariente, Cristina, et al.
Publicado: (2021)

Molecular analysis of the APC and MUTYH genes in Galician and Catalonian FAP families: a different spectrum of mutations?
por: Gómez-Fernández, Nuria, et al.
Publicado: (2009)

Unraveling the impact of a germline heterozygous POLD1 frameshift variant in serrated polyposis syndrome
por: Bonjoch, Laia, et al.
Publicado: (2023)

Case-control study for colorectal cancer genetic susceptibility in EPICOLON: previously identified variants and mucins
por: Abulí, Anna, et al.
Publicado: (2011)

Inflammatory Mediators of Hepatic Steatosis
por: Hijona, Elizabeth, et al.
Publicado: (2010)

CNApp, a tool for the quantification of copy number alterations and integrative analysis revealing clinical implications
por: Franch-Expósito, Sebastià, et al.
Publicado: (2020)

Quantitative analysis of somatically acquired and constitutive uniparental disomy in gastrointestinal cancers
por: Torabi, Keyvan, et al.
Publicado: (2018)

Colorectal cancer after negative colonoscopy in fecal immunochemical test-positive participants from a colorectal cancer screening program
por: Rivero-Sánchez, Liseth, et al.
Publicado: (2018)

Effect of an information leaflet on breast cancer screening participation: A cluster randomized controlled trial
por: Montero-Moraga, Jose Maria, et al.
Publicado: (2021)

POLE and POLD1 screening in 155 patients with multiple polyps and early-onset colorectal cancer
por: Esteban-Jurado, Clara, et al.
Publicado: (2017)

Using linkage studies combined with whole‐exome sequencing to identify novel candidate genes for familial colorectal cancer
por: Toma, Claudio, et al.
Publicado: (2019)

Germline and Somatic Whole-Exome Sequencing Identifies New Candidate Genes Involved in Familial Predisposition to Serrated Polyposis Syndrome
por: Soares de Lima, Yasmin, et al.
Publicado: (2021)

Pharmacogenomics of CRC treatments: putting bricks on the path to personalized medicine
por: Fernández-Rozadilla, Ceres, et al.
Publicado: (2014)

Serum methylation of GALNT9, UPF3A, WARS, and LDB2 as noninvasive biomarkers for the early detection of colorectal cancer and advanced adenomas
por: Gallardo-Gómez, María, et al.
Publicado: (2023)

GeMSTONE: orchestrated prioritization of human germline mutations in the cloud
por: Chen, Siwei, et al.
Publicado: (2017)

A two-phase case–control study for colorectal cancer genetic susceptibility: candidate genes from chromosomal regions 9q22 and 3q22
por: Abulí, A, et al.
Publicado: (2011)

Colorectal cancer genetic variants are also associated with serrated polyposis syndrome susceptibility
por: Arnau-Collell, Coral, et al.
Publicado: (2020)

Differentially Deregulated MicroRNAs as Novel Biomarkers for Neoplastic Progression in Ulcerative Colitis
por: Quintanilla, Isabel, et al.
Publicado: (2022)

Lymph node pooling: a feasible and efficient method of lymph node molecular staging in colorectal carcinoma
por: Rakislova, Natalia, et al.
Publicado: (2017)

Long-Term Prediction of the Demand of Colonoscopies Generated by a Population-Based Colorectal Cancer Screening Program
por: Comas, Mercè, et al.
Publicado: (2016)

Identification of a Novel Candidate Gene for Serrated Polyposis Syndrome Germline Predisposition by Performing Linkage Analysis Combined With Whole-Exome Sequencing
por: Toma, Claudio, et al.
Publicado: (2019)

Hospital emergency department utilisation rates among the immigrant population in Barcelona, Spain
por: Buron, Andrea, et al.
Publicado: (2008)

Cannot write session to /tmp/vufind_sessions/sess_e6edei7r2ejuc3ghi99knst1he