Drakoulis Yannoukakos

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Publications in SciGraph latest 50 shown

  • 2019-12 Shared heritability and functional enrichment across six solid cancers in NATURE COMMUNICATIONS
  • 2018-11 Contribution of RAD51D germline mutations in breast and ovarian cancer in Greece in JOURNAL OF HUMAN GENETICS
  • 2018-08 Characterization and prevalence of two novel CHEK2 large deletions in Greek breast cancer patients in JOURNAL OF HUMAN GENETICS
  • 2018-05 Germline deleterious mutations in genes other than BRCA2 are infrequent in male breast cancer in BREAST CANCER RESEARCH AND TREATMENT
  • 2018-04-10 Publisher Correction: Evidence that breast cancer risk at the 2q35 locus is mediated through IGFBP5 regulation in NATURE COMMUNICATIONS
  • 2017-12 Mutational analysis of TSC1 and TSC2 genes in Tuberous Sclerosis Complex patients from Greece in SCIENTIFIC REPORTS
  • 2017-12 Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer in NATURE GENETICS
  • 2017-05 Identification of 12 new susceptibility loci for different histotypes of epithelial ovarian cancer in NATURE GENETICS
  • 2016-12 rs2735383, located at a microRNA binding site in the 3’UTR of NBS1, is not associated with breast cancer risk in SCIENTIFIC REPORTS
  • 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
  • 2016-09-07 Functional mechanisms underlying pleiotropic risk alleles at the 19p13.1 breast–ovarian cancer susceptibility locus in NATURE COMMUNICATIONS
  • 2016-05 Genes associated with histopathologic features of triple negative breast tumors predict molecular subtypes in BREAST CANCER RESEARCH AND TREATMENT
  • 2016-04-27 Identification of four novel susceptibility loci for oestrogen receptor negative breast cancer in NATURE COMMUNICATIONS
  • 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
  • 2015-11 Large-scale genomic analyses link reproductive aging to hypothalamic signaling, breast cancer susceptibility and BRCA1-mediated DNA repair in NATURE GENETICS
  • 2015-04 Genome-wide association analysis of more than 120,000 individuals identifies 15 new susceptibility loci for breast cancer in NATURE GENETICS
  • 2014-12 Evidence that breast cancer risk at the 2q35 locus is mediated through IGFBP5 regulation in NATURE COMMUNICATIONS
  • 2014-06 Genetic variation at CYP3A is associated with age at menarche and breast cancer risk: a case-control study in BREAST CANCER RESEARCH
  • 2014-02 FGF receptor genes and breast cancer susceptibility: results from the Breast Cancer Association Consortium in BRITISH JOURNAL OF CANCER
  • 2013-04 Multiple independent variants at the TERT locus are associated with telomere length and risks of breast and ovarian cancer in NATURE GENETICS
  • 2012-07 Prevalence of BRCA1 mutations among 403 women with triple-negative breast cancer: implications for genetic screening selection criteria: a Hellenic Cooperative Oncology Group Study in BREAST CANCER RESEARCH AND TREATMENT
  • 2011-12 A common variant at the TERT-CLPTM1L locus is associated with estrogen receptor–negative breast cancer in NATURE GENETICS
  • 2011-06 International distribution and age estimation of the Portuguese BRCA2 c.156_157insAlu founder mutation in BREAST CANCER RESEARCH AND TREATMENT
  • 2011-03 On the origin and diffusion of BRCA1 c.5266dupC (5382insC) in European populations in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2010-12 Mutational spectrum of APC and genotype-phenotype correlations in Greek FAP patients in BMC CANCER
  • 2010-12 Screening of the DNA mismatch repair genes MLH1, MSH2 and MSH6in a Greek cohort of Lynch syndrome suspected families in BMC CANCER
  • 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
  • 2010-09 A distinct mutation on the alternative splice site of APC exon 9 results in attenuated familial adenomatous polyposis phenotype in FAMILIAL CANCER
  • 2010-08 Collaborative genomics for human health and cooperation in the Mediterranean region in NATURE GENETICS
  • 2009-12 Evaluation of a candidate breast cancer associated SNP in ERCC4 as a risk modifier in BRCA1 and BRCA2 mutation carriers. Results from the Consortium of Investigators of Modifiers of BRCA1/BRCA2 (CIMBA) in BRITISH JOURNAL OF CANCER
  • 2009-07 Contribution of <i>BRCA1</i> germ-line mutations to breast cancer in Greece: a hospital-based study of 987 unselected breast cancer cases in BRITISH JOURNAL OF CANCER
  • 2008-07 G1738R is a BRCA1 founder mutation in Greek breast/ovarian cancer patients: evaluation of its pathogenicity and inferences on its genealogical history in BREAST CANCER RESEARCH AND TREATMENT
  • 2008-02 Greek BRCA1 and BRCA2 mutation spectrum: two BRCA1 mutations account for half the carriers found among high-risk breast/ovarian cancer patients in BREAST CANCER RESEARCH AND TREATMENT
  • 2007-04-15 A newly detected mutation of the RET protooncogene in exon 8 as a cause of multiple endocrine neoplasia type 2A. in HORMONES
  • 2004-12 Characterization of a novel large deletion and single point mutations in the BRCA1gene in a Greek cohort of families with suspected hereditary breast cancer in BMC CANCER
  • 2000-03 BRCA1mutation analysis in breast and ovarian cancer families from Greece in BREAST CANCER RESEARCH
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