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Risk of Cancer in Cases of Suspected Lynch Syndrome Without Germline Mutation

Gastroenterology (New York, N.Y. 1943), 2013-05, Vol.144 (5), p.926-932.e1

2013

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Mutational Signatures in Cancer (MuSiCa): a web application to implement mutational signatures analysis in cancer samples

BMC bioinformatics, 2018-06, Vol.19 (1), p.224-224, Article 224

2018

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Endoscopic surveillance for familial intestinal gastric cancer in low‐incidence areas: An effective strategy

International journal of cancer, 2024-01, Vol.154 (1), p.124-132

2024

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CNApp, a tool for the quantification of copy number alterations and integrative analysis revealing clinical implications

eLife, 2020-01, Vol.9

2020

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Prevalence of somatic mutl homolog 1 promoter hypermethylation in Lynch syndrome colorectal cancer

Cancer, 2015-05, Vol.121 (9), p.1395-1404

2015

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Using linkage studies combined with whole‐exome sequencing to identify novel candidate genes for familial colorectal cancer

International journal of cancer, 2020-03, Vol.146 (6), p.1568-1577

2020

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Concepts in Familial Colorectal Cancer: Where Do We Stand and What Is the Future?

Gastroenterology (New York, N.Y. 1943), 2009-08, Vol.137 (2), p.404-409

2009

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Data-Independent Acquisition Mass Spectrometry Analysis of FFPE Rectal Cancer Samples Offers In-Depth Proteomics Characterization of the Response to Neoadjuvant Chemoradiotherapy

International journal of molecular sciences, 2023-10, Vol.24 (20), p.15412

2023

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Quantitative analysis of somatically acquired and constitutive uniparental disomy in gastrointestinal cancers

International journal of cancer, 2019-02, Vol.144 (3), p.513-524

2019

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The simplest explanation does not have to be preferred: co-occurrence of pathogenic variants in cancer-predisposing genes

European journal of human genetics : EJHG, 2022-03, Vol.30 (3), p.260-261

Castellví-Bel, Sergi

2022

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Exploring novel genetic and hematological predictors of response to neoadjuvant chemoradiotherapy in locally advanced rectal cancer

Frontiers in genetics, 2023-08, Vol.14, p.1245594-1245594

2023

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Performance of Different Microsatellite Marker Panels for Detection of Mismatch Repair–Deficient Colorectal Tumors

JNCI : Journal of the National Cancer Institute, 2007-02, Vol.99 (3), p.244-252

2007

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Microbiome Profiling from Fecal Immunochemical Test Reveals Microbial Signatures with Potential for Colorectal Cancer Screening

Cancers, 2022-12, Vol.15 (1), p.120

2022

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Identification of New Genes Involved in Germline Predisposition to Early-Onset Gastric Cancer

International journal of molecular sciences, 2021-01, Vol.22 (3), p.1310

2021

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Comprehensive Genomic Characterization of Fifteen Early-Onset Lynch-Like Syndrome Colorectal Cancers

Cancers, 2021-03, Vol.13 (6), p.1259

2021

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Evidence for genetic association between chromosome 1q loci and predisposition to colorectal neoplasia

British journal of cancer, 2017-10, Vol.117 (6), p.1215-1223

2017

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Introduction to special issue – “New insights on the molecular aspects of colorectal cancer”

Molecular aspects of medicine, 2019-10, Vol.69, p.1-1

Castellví-Bel, Sergi

2019

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Pancreatic Cancer Surveillance in Carriers of a Germline Pathogenic Variant in CDKN2A

Cancers, 2023-03, Vol.15 (6), p.1690

2023

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Identification of MYH Mutation Carriers in Colorectal Cancer: A Multicenter, Case-Control, Population-Based Study

Clinical gastroenterology and hepatology, 2007-03, Vol.5 (3), p.379-387

2007

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Performance and Dimensionality of Pretreatment MRI Radiomics in Rectal Carcinoma Chemoradiotherapy Prediction

Journal of clinical medicine, 2024-01, Vol.13 (2), p.421

2024

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Molecular functions of MCM8 and MCM9 and their associated pathologies

iScience, 2023-06, Vol.26 (6), p.106737-106737, Article 106737

2023

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New genes emerging for colorectal cancer predisposition

World journal of gastroenterology : WJG, 2014-02, Vol.20 (8), p.1961-1971

2014

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Genetic Variants Associated with Colorectal Adenoma Susceptibility

PloS one, 2016-04, Vol.11 (4), p.e0153084-e0153084

2016

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Risk of Cancer in Cases of Suspected Lynch Syndrome Without Germline Mutation

Mutational Signatures in Cancer (MuSiCa): a web application to implement mutational signatures analysis in cancer samples

Endoscopic surveillance for familial intestinal gastric cancer in low‐incidence areas: An effective strategy

CNApp, a tool for the quantification of copy number alterations and integrative analysis revealing clinical implications

Prevalence of somatic mutl homolog 1 promoter hypermethylation in Lynch syndrome colorectal cancer

Using linkage studies combined with whole‐exome sequencing to identify novel candidate genes for familial colorectal cancer

Concepts in Familial Colorectal Cancer: Where Do We Stand and What Is the Future?

Data-Independent Acquisition Mass Spectrometry Analysis of FFPE Rectal Cancer Samples Offers In-Depth Proteomics Characterization of the Response to Neoadjuvant Chemoradiotherapy

Quantitative analysis of somatically acquired and constitutive uniparental disomy in gastrointestinal cancers

The simplest explanation does not have to be preferred: co-occurrence of pathogenic variants in cancer-predisposing genes

Exploring novel genetic and hematological predictors of response to neoadjuvant chemoradiotherapy in locally advanced rectal cancer

Performance of Different Microsatellite Marker Panels for Detection of Mismatch Repair–Deficient Colorectal Tumors

Germline and Somatic Whole-Exome Sequencing Identifies New Candidate Genes Involved in Familial Predisposition to Serrated Polyposis Syndrome

Microbiome Profiling from Fecal Immunochemical Test Reveals Microbial Signatures with Potential for Colorectal Cancer Screening

Identification of New Genes Involved in Germline Predisposition to Early-Onset Gastric Cancer

Comprehensive Genomic Characterization of Fifteen Early-Onset Lynch-Like Syndrome Colorectal Cancers

Evidence for genetic association between chromosome 1q loci and predisposition to colorectal neoplasia

Introduction to special issue – “New insights on the molecular aspects of colorectal cancer”

Pancreatic Cancer Surveillance in Carriers of a Germline Pathogenic Variant in CDKN2A

Identification of MYH Mutation Carriers in Colorectal Cancer: A Multicenter, Case-Control, Population-Based Study

Performance and Dimensionality of Pretreatment MRI Radiomics in Rectal Carcinoma Chemoradiotherapy Prediction

Molecular functions of MCM8 and MCM9 and their associated pathologies

Identification of Lynch Syndrome Carriers among Patients with Small Bowel Adenocarcinoma

New genes emerging for colorectal cancer predisposition

Genetic Variants Associated with Colorectal Adenoma Susceptibility

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