Trinidad Caldés


Ontology type: schema:Person     


Person Info

NAME

Trinidad

SURNAME

Caldés

Publications in SciGraph latest 50 shown

  • 2019-12 Shared heritability and functional enrichment across six solid cancers in NATURE COMMUNICATIONS
  • 2019-01 Correction: Evaluation of copy-number variants as modifiers of breast and ovarian cancer risk for BRCA1 pathogenic variant carriers in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2018-12 Differential distribution and enrichment of non-coding RNAs in exosomes from normal and Cancer-associated fibroblasts in colorectal cancer in MOLECULAR CANCER
  • 2018-07 A transcriptome-wide association study of 229,000 women identifies new candidate susceptibility genes for breast cancer in NATURE GENETICS
  • 2017-12 Tumor burden monitoring using cell-free tumor DNA could be limited by tumor heterogeneity in advanced breast cancer and should be evaluated together with radiographic imaging in BMC CANCER
  • 2017-12 Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer in NATURE GENETICS
  • 2017-11 Association analysis identifies 65 new breast cancer risk loci in NATURE
  • 2017-10 A novel TP53 germline inframe deletion identified in a Spanish series of Li-fraumeni syndrome suspected families in FAMILIAL CANCER
  • 2017-09-26 Characterisation of the novel deleterious RAD51C p.Arg312Trp variant and prioritisation criteria for functional analysis of RAD51C missense changes in BRITISH JOURNAL OF CANCER
  • 2017-05 Identification of 12 new susceptibility loci for different histotypes of epithelial ovarian cancer in NATURE GENETICS
  • 2017-04 Evaluation of copy-number variants as modifiers of breast and ovarian cancer risk for BRCA1 pathogenic variant carriers in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2017-02 Almost 2% of Spanish breast cancer families are associated to germline pathogenic mutations in the ATM gene in BREAST CANCER RESEARCH AND TREATMENT
  • 2016-12 Inheritance of deleterious mutations at both BRCA1 and BRCA2 in an international sample of 32,295 women in BREAST CANCER RESEARCH
  • 2016-12 Male breast cancer in BRCA1 and BRCA2 mutation carriers: pathology data from the Consortium of Investigators of Modifiers of BRCA1/2 in BREAST CANCER RESEARCH
  • 2016-12 Identification of independent association signals and putative functional variants for breast cancer risk through fine-scale mapping of the 12p11 locus in BREAST CANCER RESEARCH
  • 2016-10 The Fanconi anemia DNA damage repair pathway in the spotlight for germline predisposition to colorectal cancer in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2016-09-07 Functional mechanisms underlying pleiotropic risk alleles at the 19p13.1 breast–ovarian cancer susceptibility locus in NATURE COMMUNICATIONS
  • 2016-04-27 Identification of four novel susceptibility loci for oestrogen receptor negative breast cancer in NATURE COMMUNICATIONS
  • 2016-04 Breast cancer risk variants at 6q25 display different phenotype associations and regulate ESR1, RMND1 and CCDC170 in NATURE GENETICS
  • 2015-12 Prognostic Value of BRAF, PI3K, PTEN, EGFR Copy Number, Amphiregulin and Epiregulin Status in Patients with KRAS Codon 12 Wild-Type Metastatic Colorectal Cancer Receiving First-Line Chemotherapy with Anti-EGFR Therapy in MOLECULAR DIAGNOSIS & THERAPY
  • 2015-12 An original phylogenetic approach identified mitochondrial haplogroup T1a1 as inversely associated with breast cancer risk in BRCA2 mutation carriers in BREAST CANCER RESEARCH
  • 2015-12 BRCA1 Alternative splicing landscape in breast tissue samples in BMC CANCER
  • 2015-12 BRCA1 and BRCA2 mutations in males with familial breast and ovarian cancer syndrome. Results of a Spanish multicenter study in FAMILIAL CANCER
  • 2015-02 Whole-exome sequencing identifies rare pathogenic variants in new predisposition genes for familial colorectal cancer in GENETICS IN MEDICINE
  • 2015-02 Identification of six new susceptibility loci for invasive epithelial ovarian cancer in NATURE GENETICS
  • 2014-12 Refined histopathological predictors of BRCA1 and BRCA2mutation status: a large-scale analysis of breast cancer characteristics from the BCAC, CIMBA, and ENIGMA consortia in BREAST CANCER RESEARCH
  • 2014-12 Associations of common breast cancer susceptibility alleles with risk of breast cancer subtypes in BRCA1 and BRCA2 mutation carriers in BREAST CANCER RESEARCH
  • 2014-11 Limited family structure and triple-negative breast cancer (TNBC) subtype as predictors of BRCA mutations in a genetic counseling cohort of early-onset sporadic breast cancers in BREAST CANCER RESEARCH AND TREATMENT
  • 2014-03 Cancer risk and overall survival in mismatch repair proficient hereditary non-polyposis colorectal cancer, Lynch syndrome and sporadic colorectal cancer in FAMILIAL CANCER
  • 2013-08 Low prevalence of SLX4 loss-of-function mutations in non-BRCA1/2 breast and/or ovarian cancer families in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2013-04 Multiple independent variants at the TERT locus are associated with telomere length and risks of breast and ovarian cancer in NATURE GENETICS
  • 2012-12 Association of tamoxifen use and reduced risk of contralateral breast cancer for BRCA1 and BRCA2 mutation carriers in HEREDITARY CANCER IN CLINICAL PRACTICE
  • 2012-12 Study of KRAS new predictive marker in a clinical laboratory in CLINICAL AND TRANSLATIONAL ONCOLOGY
  • 2012-12 Colon cancer molecular subtypes identified by expression profiling and associatedto stroma, mucinous type and different clinical behavior in BMC CANCER
  • 2012-05 Changes in the expression of plasma proteins associated with thrombosis in BRCA1 mutation carriers in JOURNAL OF CANCER RESEARCH AND CLINICAL ONCOLOGY
  • 2012-05 Characterization of four novel BRCA2 large genomic rearrangements in Spanish breast/ovarian cancer families: review of the literature, and reevaluation of the genetic mechanisms involved in their origin in BREAST CANCER RESEARCH AND TREATMENT
  • 2012-03 Topoisomerase 2 alpha: a real predictor of anthracycline efficacy? in CLINICAL AND TRANSLATIONAL ONCOLOGY
  • 2012-02 Detection of a large rearrangement in PALB2 in Spanish breast cancer families with male breast cancer in BREAST CANCER RESEARCH AND TREATMENT
  • 2012-02 Common variants at 12p11, 12q24, 9p21, 9q31.2 and in ZNF365 are associated with breast cancer risk for BRCA1 and/or BRCA2mutation carriers in BREAST CANCER RESEARCH
  • 2011-12 Common breast cancer susceptibility alleles are associated with tumour subtypes in BRCA1 and BRCA2 mutation carriers: results from the Consortium of Investigators of Modifiers of BRCA1/2 in BREAST CANCER RESEARCH
  • 2011-11 Haplotype structure in Ashkenazi Jewish BRCA1 and BRCA2 mutation carriers in HUMAN GENETICS
  • 2011-10 Evidence for a link between TNFRSF11A and risk of breast cancer in BREAST CANCER RESEARCH AND TREATMENT
  • 2011-10 A HRM-based screening method detects RAD51C germ-line deleterious mutations in Spanish breast and ovarian cancer families in BREAST CANCER RESEARCH AND TREATMENT
  • 2011-07 Genomic predictors of response to doxorubicin versus docetaxel in primary breast cancer in BREAST CANCER RESEARCH AND TREATMENT
  • 2011-06 International distribution and age estimation of the Portuguese BRCA2 c.156_157insAlu founder mutation in BREAST CANCER RESEARCH AND TREATMENT
  • 2011-04 Exploring the link between MORF4L1 and risk of breast cancer in BREAST CANCER RESEARCH
  • 2010-10 Reassessing the TARBP2 mutation rate in hereditary nonpolyposis colorectal cancer in NATURE GENETICS
  • 2010-10 A locus on 19p13 modifies risk of breast cancer in BRCA1 mutation carriers and is associated with hormone receptor–negative breast cancer in the general population in NATURE GENETICS
  • 2010-01 Parity and the risk of breast and ovarian cancer in BRCA1 and BRCA2 mutation carriers in BREAST CANCER RESEARCH AND TREATMENT
  • 2009-12 Association of MUTYH and MSH6 germline mutations in colorectal cancer patients in FAMILIAL CANCER
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