Gabriel Capellá
Researcher Next ID · RN-035413
Researcher · Biochemistry, Genetics and Molecular Biology
Department of Natural and Environmental Resources
San Juan, Spain
- Works count
- 707
- Citation count
- 28,224
- H-index
- 81
- i10-index
- 319
Research interests
Publications
Variation in the risk of colorectal cancer in families with Lynch syndrome: a retrospective cohort study
The Lancet Oncology · 2021 · https://doi.org/10.1016/s1470-2045(21)00189-3
Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome Database
Genetics in Medicine · 2019 · https://doi.org/10.1038/s41436-019-0596-9
Cancer Risks for PMS2 -Associated Lynch Syndrome
Journal of Clinical Oncology · 2018 · https://doi.org/10.1200/jco.2018.78.4777
Cancer risk and survival in path_MMR carriers by gene and gender up to 75 years of age: a report from the Prospective Lynch Syndrome Database
Gut · 2017 · https://doi.org/10.1136/gutjnl-2017-314057
POLE and POLD1 mutations in 529 kindred with familial colorectal cancer and/or polyposis: review of reported cases and recommendations for genetic testing and surveillance
Genetics in Medicine · 2015 · 10.1038/gim.2015.75
Cancer incidence and survival in Lynch syndrome patients receiving colonoscopic and gynaecological surveillance: first report from the prospective Lynch syndrome database
Gut · 2015 · https://doi.org/10.1136/gutjnl-2015-309675
Application of a 5-tiered scheme for standardized classification of 2,360 unique mismatch repair gene variants in the InSiGHT locus-specific database
Nature Genetics · 2013 · https://doi.org/10.1038/ng.2854
Revised guidelines for the clinical management of Lynch syndrome (HNPCC): recommendations by a group of European experts
Gut · 2013 · https://doi.org/10.1136/gutjnl-2012-304356
Colorectal cancer intrinsic subtypes predict chemotherapy benefit, deficient mismatch repair and epithelial‐to‐mesenchymal transition
International Journal of Cancer · 2013 · https://doi.org/10.1002/ijc.28387
A DNA methylation fingerprint of 1628 human samples
Genome Research · 2011 · https://doi.org/10.1101/gr.119867.110
Peutz–Jeghers syndrome: a systematic review and recommendations for management
Gut · 2010 · https://doi.org/10.1136/gut.2009.198499
Gene Expression Signature to Improve Prognosis Prediction of Stage II and III Colorectal Cancer
Journal of Clinical Oncology · 2010 · https://doi.org/10.1200/jco.2010.30.1077
Jagged1 is the pathological link between Wnt and Notch pathways in colorectal cancer
Proceedings of the National Academy of Sciences · 2009 · 10.1073/pnas.0813221106
The dynamic DNA methylomes of double-stranded DNA viruses associated with human cancer
Genome Research · 2009 · https://doi.org/10.1101/gr.083550.108
A TARBP2 mutation in human cancer impairs microRNA processing and DICER1 function
Nature Genetics · 2009 · 10.1038/ng.317
Recent Advances in Cancer Therapy: An Overview
Current Pharmaceutical Design · 2009 · https://doi.org/10.2174/138161210789941847
Genome-wide association scan identifies a colorectal cancer susceptibility locus on 11q23 and replicates risk loci at 8q24 and 18q21
Nature Genetics · 2008 · https://doi.org/10.1038/ng.133
Guidelines for the clinical management of familial adenomatous polyposis (FAP)
Gut · 2008 · https://doi.org/10.1136/gut.2007.136127
Guidelines for the clinical management of Lynch syndrome (hereditary non-polyposis cancer)
Journal of Medical Genetics · 2007 · https://doi.org/10.1136/jmg.2007.048991
Polymorphisms in Genes of Nucleotide and Base Excision Repair: Risk and Prognosis of Colorectal Cancer
Clinical Cancer Research · 2006 · 10.1158/1078-0432.ccr-05-1363
Chromosomal Instability Correlates with Genome-wide DNA Demethylation in Human Primary Colorectal Cancers
Cancer Research · 2006 · 10.1158/0008-5472.can-06-0293
Association of common polymorphisms in inflammatory genes interleukin (IL)6, IL8, tumor necrosis factor alpha, NFKB1, and peroxisome proliferator-activated receptor gamma with colorectal cancer.
PubMed · 2003
Genetic susceptibility and gastric cancer risk
International Journal of Cancer · 2002 · 10.1002/ijc.10466
Promoter hypermethylation of the DNA repair gene O(6)-methylguanine-DNA methyltransferase is associated with the presence of G:C to A:T transition mutations in p53 in human colorectal tumorigenesis.
PubMed · 2001
Hypermethylation-associated inactivation of p14(ARF) is independent of p16(INK4a) methylation and p53 mutational status.
PubMed · 2000
Inactivation of the DNA repair gene O6-methylguanine-DNA methyltransferase by promoter hypermethylation is associated with G to A mutations in K-ras in colorectal tumorigenesis.
PubMed · 2000
Analysis of adenomatous polyposis coli promoter hypermethylation in human cancer.
PubMed · 2000
K-ras Mutations in DNA Extracted From the Plasma of Patients With Pancreatic Carcinoma: Diagnostic Utility and Prognostic Significance
Journal of Clinical Oncology · 1999 · https://doi.org/10.1200/jco.1999.17.2.578
Current projects
No projects listed.