Navegar por autor "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.]

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- Fernández Rozadilla, Ceres; Palles, C.; Carvajal-Carmona, L.; Peterlongo, P.; Nici, C.; [et al.]

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

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- Bodo, S.; Colas, C.; Buhard, O.; Collura, A.; Tinat, J.; [et al.]

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

2014- Wimmer, K.; Kratz, C. P.; Vasen, H. F.; Caron, O.; Colas, C.; [et al.]

Early Colorectal Cancers Provide New Evidence for a Lynch Syndrome-to-CMMRD Phenotypic Continuum

2019- Fernández Rozadilla, Ceres; Alvarez-Barona, M.; Schamschula, E.; Bodo, S.; López Novo, Anael; [et al.]

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

Multiple sporadic colorectal cancers display a unique methylation phenotype

2014- Carracedo Álvarez, Ángel; Ruiz Ponte, Clara

Prevalence of MLH1 constitutional epimutations as a cause of Lynch syndrome in unselected versus selected consecutive series of patients with colorectal cancer

2015- Brea Fernández, Alejandro; Carracedo Álvarez, Ángel; Ruiz Ponte, Clara

Refinement of the associations between risk of colorectal cancer and polymorphisms on chromosomes 1q41 and 12q13.13

2012- Carracedo Álvarez, Ángel; Fernández Rozadilla, Ceres; Ruiz Ponte, Clara

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

2013- Rodríguez-Soler, María; Pérez-Carbonell, Lucía; Guarinos, Carla; Zapater, Pedro; Castillejo, Adela; [et al.]

Susceptibility genetic variants associated with early-onset colorectal cancer

2012- Carracedo Álvarez, Ángel; Fernández Rozadilla, Ceres; Ruiz Ponte, Clara

Systematic meta-analyses, field synopsis and global assessment of the evidence of genetic association studies in colorectal cancer

2020- Montazeri, Z; Li, X; Nyiraneza, C; Ma, XY; Timofeeva, M; [et al.]

The MLH1 c.1852_1853delinsGC (p.K618A) variant in colorectal cancer: genetic association study in 18,723 individuals

2014- Carracedo Álvarez, Ángel; Ruiz Ponte, Clara

Thyroid cancer GWAS identifies 10q26.12 and 6q14.1 as novel susceptibility loci and reveals genetic heterogeneity among populations

2015- Mancikova, V.; Cruz Guerrero, Raquel; Inglada-Perez, L.; Fernández Rozadilla, Ceres; Landa, I.; [et al.]

Repositorio digital RUNA

Navegar por autor "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 ﻿

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 ﻿

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

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) ﻿

Early Colorectal Cancers Provide New Evidence for a Lynch Syndrome-to-CMMRD Phenotypic Continuum ﻿

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. ﻿

Multiple sporadic colorectal cancers display a unique methylation phenotype ﻿

Prevalence of MLH1 constitutional epimutations as a cause of Lynch syndrome in unselected versus selected consecutive series of patients with colorectal cancer ﻿

Refinement of the associations between risk of colorectal cancer and polymorphisms on chromosomes 1q41 and 12q13.13 ﻿

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

Susceptibility genetic variants associated with early-onset colorectal cancer ﻿

Systematic meta-analyses, field synopsis and global assessment of the evidence of genetic association studies in colorectal cancer ﻿

The MLH1 c.1852_1853delinsGC (p.K618A) variant in colorectal cancer: genetic association study in 18,723 individuals ﻿

Thyroid cancer GWAS identifies 10q26.12 and 6q14.1 as novel susceptibility loci and reveals genetic heterogeneity among populations ﻿

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

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

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

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)

Early Colorectal Cancers Provide New Evidence for a Lynch Syndrome-to-CMMRD Phenotypic Continuum

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.

Multiple sporadic colorectal cancers display a unique methylation phenotype

Prevalence of MLH1 constitutional epimutations as a cause of Lynch syndrome in unselected versus selected consecutive series of patients with colorectal cancer

Refinement of the associations between risk of colorectal cancer and polymorphisms on chromosomes 1q41 and 12q13.13

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

Susceptibility genetic variants associated with early-onset colorectal cancer

Systematic meta-analyses, field synopsis and global assessment of the evidence of genetic association studies in colorectal cancer

The MLH1 c.1852_1853delinsGC (p.K618A) variant in colorectal cancer: genetic association study in 18,723 individuals

Thyroid cancer GWAS identifies 10q26.12 and 6q14.1 as novel susceptibility loci and reveals genetic heterogeneity among populations