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Navegar por autor "Ruiz Ponte, Clara"

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

      2013- Ruiz Ponte, Clara
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      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.]
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      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.]
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      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.]
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      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.]
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      Genetic Associations in the Vitamin D Receptor and Colorectal Cancer in African Americans and Caucasians. 

      2011- Ruiz Ponte, Clara; Carracedo Álvarez, Ángel
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      Multiple sporadic colorectal cancers display a unique methylation phenotype 

      2014- Carracedo Álvarez, Ángel; Ruiz Ponte, Clara
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      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
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      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
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      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.]
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      Susceptibility genetic variants associated with early-onset colorectal cancer 

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