Browse by Author "Ruiz Ponte, Clara"

A candidate gene study of capecitabine-related toxicity in colorectal cancer identifies new toxicity variants at DPYD and a putative role for ENOSF1 rather than TYMS

2015- Carracedo Álvarez, Ángel; Ruiz Ponte, Clara

A colorectal cancer genome-wide association study in a Spanish cohort identifies two variants associated with colorectal cancer risk at 1p33 and 8p12

2013- Fernandez-Rozadilla, Ceres; Cazier, Jean-Baptiste; Tomlinson, Ian P; Carvajal-Carmona, Luis G; Palles, Claire; [et al.]

A colorectal cancer susceptibility new variant at 4q26 in the Spanish population identified by genome-wide association analysis

2014- Real, Luis M; Ruiz, Agustín; Gayán, Javier; González-Pérez, A; Sáez, ME; [et al.]

A genome-wide association study on copy-number variation identifies a 11q11 loss as a candidate susceptibility variant for colorectal cancer

2014- Carracedo Álvarez, Ángel; Fernández Rozadilla, Ceres; Ruiz Ponte, Clara; Lamas Díaz, María Jesús; Clofent Villaplana, Juan [et al.]

A two-phase case-control study for colorectal cancer genetic susceptibility: Candidate genes from chromosomal regions 9q22 and 3q22

2011- Carracedo Álvarez, Ángel; Fernández Rozadilla, Ceres; Ruiz Ponte, Clara

Association between CASP8 -652 6N del polymorphism (rs3834129) and colorectal cancer risk: results from a multi-centric study

2014- Carracedo Álvarez, Ángel; Ruiz Ponte, Clara

BMP2/BMP4 colorectal cancer susceptibility loci in northern and southern european populations

2013- Brea Fernández, Alejandro; Carracedo Álvarez, Ángel; Fernández Rozadilla, Ceres; Ruiz Ponte, Clara; Lamas Díaz, María Jesús; [et al.]

BMPR1A mutations in early-onset colorectal cancer with mismatch repair proficiency

2013- Brea Fernández, Alejandro; Carracedo Álvarez, Ángel; Fernández Rozadilla, Ceres; Ruiz Ponte, Clara

Colorectal cancer eqtls as susceptibility loci Candidates

2012- Ruiz Ponte, Clara; Carracedo Álvarez, Ángel

Comparison between universal molecular screening for Lynch syndrome and revised Bethesda guidelines in a large population-based cohort of patients with colorectal cancer

2012- Brea Fernández, Alejandro; Carracedo Álvarez, Ángel; Ruiz Ponte, Clara; De Castro Parga, María Luisa

Correction: Association between CASP8 -652 6N del polymorphism (rs3834129) and colorectal cancer risk: Results from a multi-centric study (PLoS ONE)

2014- Carracedo Álvarez, Ángel; Ruiz Ponte, Clara

Cumulative impact of common genetic variants and other risk factors on colorectal cancer risk in 42 103 individuals

2013- Ruiz Ponte, Clara

Diagnosis of Constitutional Mismatch Repair-Deficiency Syndrome Based on Microsatellite Instability and Lymphocyte Tolerance to Methylating Agents

2015- Ruiz Ponte, Clara

Diagnostic criteria for constitutional mismatch repair deficiency syndrome: suggestions of the European consortium 'care for CMMRD' (C4CMMRD)

2014- Ruiz Ponte, Clara

Evidence for classification of c.1852_1853AA>GC in MLH1 as a neutral variant for Lynch syndrome

2011- Castillejo, A; Guarinos, C; Martínez-Canto, A; Barbera VM; Egoavil C; [et al.]

Genetic Associations in the Vitamin D Receptor and Colorectal Cancer in African Americans and Caucasians.

2011- Ruiz Ponte, Clara; Carracedo Álvarez, Ángel

Genetic susceptibility variants associated with colorectal cancer prognosis

2013- Cubiella Fernández, Joaquín; Carracedo Álvarez, Ángel; Fernández Rozadilla, Ceres; Ruiz Ponte, Clara; Clofent Villaplana, Juan [et al.]

High incidence of large deletions in the PMS2 gene in Spanish Lynch syndrome families

2014- Cameselle Teijeiro, Jose Manuel; Cubiella Fernández, Joaquín; Brea Fernández, Alejandro; Anido Herranz, Urbano; Carracedo Álvarez, Ángel; [et al.]

Implication of the 3'UTR region of TGFbetaR1 with MSS HNPCC and sporadic colorectal cancer

2013- Carracedo Álvarez, Ángel; Ruiz Ponte, Clara

Meta-Analysis of Mismatch Repair Polymorphisms within the Cogent Consortium for Colorectal Cancer Susceptibility

2013- Cubiella Fernández, Joaquín; Carracedo Álvarez, Ángel; Fernández Rozadilla, Ceres; Ruiz Ponte, Clara; Sánchez Hernández, Eloy; [et al.]

RUNA digital repository

Browse by Author "Ruiz Ponte, Clara"

A candidate gene study of capecitabine-related toxicity in colorectal cancer identifies new toxicity variants at DPYD and a putative role for ENOSF1 rather than TYMS ﻿

A colorectal cancer genome-wide association study in a Spanish cohort identifies two variants associated with colorectal cancer risk at 1p33 and 8p12 ﻿

A colorectal cancer susceptibility new variant at 4q26 in the Spanish population identified by genome-wide association analysis ﻿

A genome-wide association study on copy-number variation identifies a 11q11 loss as a candidate susceptibility variant for colorectal cancer ﻿

A two-phase case-control study for colorectal cancer genetic susceptibility: Candidate genes from chromosomal regions 9q22 and 3q22 ﻿

Association between CASP8 -652 6N del polymorphism (rs3834129) and colorectal cancer risk: results from a multi-centric study ﻿

BMP2/BMP4 colorectal cancer susceptibility loci in northern and southern european populations ﻿

BMPR1A mutations in early-onset colorectal cancer with mismatch repair proficiency ﻿

Colorectal cancer eqtls as susceptibility loci Candidates ﻿

Comparison between universal molecular screening for Lynch syndrome and revised Bethesda guidelines in a large population-based cohort of patients with colorectal cancer ﻿

Correction: Association between CASP8 -652 6N del polymorphism (rs3834129) and colorectal cancer risk: Results from a multi-centric study (PLoS ONE) ﻿

Cumulative impact of common genetic variants and other risk factors on colorectal cancer risk in 42 103 individuals ﻿

Diagnosis of Constitutional Mismatch Repair-Deficiency Syndrome Based on Microsatellite Instability and Lymphocyte Tolerance to Methylating Agents ﻿

Diagnostic criteria for constitutional mismatch repair deficiency syndrome: suggestions of the European consortium 'care for CMMRD' (C4CMMRD) ﻿

Evidence for classification of c.1852_1853AA>GC in MLH1 as a neutral variant for Lynch syndrome ﻿

Genetic Associations in the Vitamin D Receptor and Colorectal Cancer in African Americans and Caucasians. ﻿

Genetic susceptibility variants associated with colorectal cancer prognosis ﻿

High incidence of large deletions in the PMS2 gene in Spanish Lynch syndrome families ﻿

Implication of the 3'UTR region of TGFbetaR1 with MSS HNPCC and sporadic colorectal cancer ﻿

Meta-Analysis of Mismatch Repair Polymorphisms within the Cogent Consortium for Colorectal Cancer Susceptibility ﻿

A candidate gene study of capecitabine-related toxicity in colorectal cancer identifies new toxicity variants at DPYD and a putative role for ENOSF1 rather than TYMS

A colorectal cancer genome-wide association study in a Spanish cohort identifies two variants associated with colorectal cancer risk at 1p33 and 8p12

A colorectal cancer susceptibility new variant at 4q26 in the Spanish population identified by genome-wide association analysis

A genome-wide association study on copy-number variation identifies a 11q11 loss as a candidate susceptibility variant for colorectal cancer

A two-phase case-control study for colorectal cancer genetic susceptibility: Candidate genes from chromosomal regions 9q22 and 3q22

Association between CASP8 -652 6N del polymorphism (rs3834129) and colorectal cancer risk: results from a multi-centric study

BMP2/BMP4 colorectal cancer susceptibility loci in northern and southern european populations

BMPR1A mutations in early-onset colorectal cancer with mismatch repair proficiency

Colorectal cancer eqtls as susceptibility loci Candidates

Comparison between universal molecular screening for Lynch syndrome and revised Bethesda guidelines in a large population-based cohort of patients with colorectal cancer

Correction: Association between CASP8 -652 6N del polymorphism (rs3834129) and colorectal cancer risk: Results from a multi-centric study (PLoS ONE)

Cumulative impact of common genetic variants and other risk factors on colorectal cancer risk in 42 103 individuals

Diagnosis of Constitutional Mismatch Repair-Deficiency Syndrome Based on Microsatellite Instability and Lymphocyte Tolerance to Methylating Agents

Diagnostic criteria for constitutional mismatch repair deficiency syndrome: suggestions of the European consortium 'care for CMMRD' (C4CMMRD)

Evidence for classification of c.1852_1853AA>GC in MLH1 as a neutral variant for Lynch syndrome

Genetic Associations in the Vitamin D Receptor and Colorectal Cancer in African Americans and Caucasians.

Genetic susceptibility variants associated with colorectal cancer prognosis

High incidence of large deletions in the PMS2 gene in Spanish Lynch syndrome families

Implication of the 3'UTR region of TGFbetaR1 with MSS HNPCC and sporadic colorectal cancer

Meta-Analysis of Mismatch Repair Polymorphisms within the Cogent Consortium for Colorectal Cancer Susceptibility