Clara Ruiz-Ponte


Ontology type: schema:Person     


Person Info

NAME

Clara

SURNAME

Ruiz-Ponte

Publications in SciGraph latest 50 shown

  • 2021-05-27 Exome sequencing of early-onset patients supports genetic heterogeneity in colorectal cancer in SCIENTIFIC REPORTS
  • 2020-07-02 Report of the fifth meeting of the European Consortium 'Care for CMMRD' (C4CMMRD), Leiden, The Netherlands, July 6th 2019 in FAMILIAL CANCER
  • 2019-02-01 Patterns of genetic differentiation and the footprints of historical migrations in the Iberian Peninsula in NATURE COMMUNICATIONS
  • 2017-10-12 Evidence for genetic association between chromosome 1q loci and predisposition to colorectal neoplasia in BRITISH JOURNAL OF CANCER
  • 2017-07-25 Evidence for genetic association between chromosome 1q loci and predisposition to colorectal neoplasia in BRITISH JOURNAL OF CANCER
  • 2016-11-25 Candidate predisposing germline copy number variants in early onset colorectal cancer patients in CLINICAL AND TRANSLATIONAL ONCOLOGY
  • 2016-05-11 The Fanconi anemia DNA damage repair pathway in the spotlight for germline predisposition to colorectal cancer in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2016-03-10 Correspondence: SEMA4A variation and risk of colorectal cancer in NATURE COMMUNICATIONS
  • 2015-11-10 Recurrent Coding Sequence Variation Explains Only A Small Fraction of the Genetic Architecture of Colorectal Cancer in SCIENTIFIC REPORTS
  • 2014-07-24 Whole-exome sequencing identifies rare pathogenic variants in new predisposition genes for familial colorectal cancer in GENETICS IN MEDICINE
  • 2014-04-02 Pharmacogenomics of CRC treatments: putting bricks on the path to personalized medicine in BMC GENOMICS
  • 2013-11-12 A genome-wide association study on copy-number variation identifies a 11q11 loss as a candidate susceptibility variant for colorectal cancer in HUMAN GENETICS
  • 2013-01-26 A colorectal cancer genome-wide association study in a Spanish cohort identifies two variants associated with colorectal cancer risk at 1p33 and 8p12 in BMC GENOMICS
  • 2012-02-07 Pharmacogenomics in colorectal cancer: a genome-wide association study to predict toxicity after 5-fluorouracil or FOLFOX administration in THE PHARMACOGENOMICS JOURNAL
  • 2011-08-05 Case-control study for colorectal cancer genetic susceptibility in EPICOLON: previously identified variants and mucins in BMC CANCER
  • 2011-08-02 A two-phase case–control study for colorectal cancer genetic susceptibility: candidate genes from chromosomal regions 9q22 and 3q22 in BRITISH JOURNAL OF CANCER
  • 2011-01-19 Evidence for classification of c.1852_1853AA>GC in MLH1 as a neutral variant for Lynch syndrome in BMC MEDICAL GENETICS
  • 2010-01-19 COGENT (COlorectal cancer GENeTics): an international consortium to study the role of polymorphic variation on the risk of colorectal cancer in BRITISH JOURNAL OF CANCER
  • 2010-01-10 Common variants at 2q37.3, 8q24.21, 15q21.3, and 16q24.1 influence chronic lymphocytic leukemia risk in NATURE GENETICS
  • 2009-11-17 COGENT (COlorectal cancer GENeTics): an international consortium to study the role of polymorphic variation on the risk of colorectal cancer in BRITISH JOURNAL OF CANCER
  • 2009-08-15 Association of MUTYH and MSH6 germline mutations in colorectal cancer patients in FAMILIAL CANCER
  • 2009-06-16 Molecular analysis of the APC and MUTYH genes in Galician and Catalonian FAP families: a different spectrum of mutations? in BMC MEDICAL GENETICS
  • 2008-03-30 A genome-wide association study identifies colorectal cancer susceptibility loci on chromosomes 10p14 and 8q23.3 in NATURE GENETICS
  • 2007-08-15 Ligneous conjunctivitis: a clinicopathological, immunohistochemical, and genetic study including the treatment of two sisters with multiorgan involvement in VIRCHOWS ARCHIV
  • 2007-06-29 Multiplex SNaPshot for detection of BRCA1/2 common mutations in Spanish and Spanish related breast/ovarian cancer families in BMC MEDICAL GENETICS
  • 2005-06-17 Large-scale single nucleotide polymorphism analysis of candidates for low-penetrance breast cancer genes in BREAST CANCER RESEARCH
  • 2004-12-01 Genotyping SNPs With the LightCycler in FORENSIC DNA TYPING PROTOCOLS
  • 2004 Rapid Detection of Gene Duplications in Charcot-Marie-Tooth 1A Disease by SNP Genotyping Using Real-Time PCR in RAPID CYCLE REAL-TIME PCR — METHODS AND APPLICATIONS
  • 2000-03-12 HRAS1 minisatellite alleles and breast cancer in Spanish women under age forty years in BREAST CANCER RESEARCH
  • 1999-01-01 The Benefit of a Roseobacter Species on the Survival of Scallop Larvae in MARINE BIOTECHNOLOGY
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