Antonis C Antoniou


Ontology type: schema:Person     


Person Info

NAME

Antonis C

SURNAME

Antoniou

Publications in SciGraph latest 50 shown

  • 2019-12 Shared heritability and functional enrichment across six solid cancers in NATURE COMMUNICATIONS
  • 2019-01-15 BOADICEA: a comprehensive breast cancer risk prediction model incorporating genetic and nongenetic risk factors in GENETICS IN MEDICINE
  • 2019-01-07 Meta-analysis of up to 622,409 individuals identifies 40 novel smoking behaviour associated genetic loci in MOLECULAR PSYCHIATRY
  • 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
  • 2019-01 Clinicians’ use of breast cancer risk assessment tools according to their perceived importance of breast cancer risk factors: an international survey in JOURNAL OF COMMUNITY GENETICS
  • 2018-12 Risks of breast or ovarian cancer in BRCA1 or BRCA2 predictive test negatives: findings from the EMBRACE study in GENETICS IN MEDICINE
  • 2018-12 Age-specific breast cancer risk by body mass index and familial risk: prospective family study cohort (ProF-SC) in BREAST CANCER RESEARCH
  • 2018-07 Corrections to: Use of the BOADICEA Web Application in clinical practice: appraisals by clinicians from various countries in FAMILIAL CANCER
  • 2018-01 Use of the BOADICEA Web Application in clinical practice: appraisals by clinicians from various countries in FAMILIAL 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
  • 2017-05 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
  • 2017-01 Association of breast cancer risk in BRCA1 and BRCA2 mutation carriers with genetic variants showing differential allelic expression: identification of a modifier of breast cancer risk at locus 11q22.3 in BREAST CANCER RESEARCH AND TREATMENT
  • 2017-01 Breast cancer risk prediction using a polygenic risk score in the familial setting: a prospective study from the Breast Cancer Family Registry and kConFab in GENETICS IN MEDICINE
  • 2016-12 Incorporating truncating variants in PALB2, CHEK2, and ATM into the BOADICEA breast cancer risk model in GENETICS IN MEDICINE
  • 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
  • 2016-09-07 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
  • 2016-02 iPrevent®: a tailored, web-based, decision support tool for breast cancer risk assessment and management in BREAST CANCER RESEARCH AND TREATMENT
  • 2015-12 Corrigendum: Rare coding variants and X-linked loci associated with age at menarche 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
  • 2015-12 Rare coding variants and X-linked loci associated with age at menarche in NATURE COMMUNICATIONS
  • 2015-11 Large-scale genomic analyses link reproductive aging to hypothalamic signaling, breast cancer susceptibility and BRCA1-mediated DNA repair in NATURE GENETICS
  • 2015-02 Identification of six new susceptibility loci for invasive epithelial ovarian cancer in NATURE GENETICS
  • 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
  • 2014-12 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
  • 2014-11 Attenuated familial adenomatous polyposis manifests as autosomal dominant late-onset colorectal cancer in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2014-03 Frequent germline deleterious mutations in DNA repair genes in familial prostate cancer cases are associated with advanced disease in BRITISH JOURNAL OF CANCER
  • 2014-01 BOADICEA breast cancer risk prediction model: updates to cancer incidences, tumour pathology and web interface in BRITISH JOURNAL OF CANCER
  • 2013-12 Identification and molecular characterization of a new ovarian cancer susceptibility locus at 17q21.31 in NATURE COMMUNICATIONS
  • 2013-09 Prospective validation of the breast cancer risk prediction model BOADICEA and a batch-mode version BOADICEACentre in BRITISH JOURNAL OF CANCER
  • 2013-06 Estimating single nucleotide polymorphism associations using pedigree data: applications to breast cancer in BRITISH JOURNAL OF CANCER
  • 2013-04 Identification of 23 new prostate cancer susceptibility loci using the iCOGS custom genotyping array in NATURE 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
  • 2012-12-16 Mosaic PPM1D mutations are associated with predisposition to breast and ovarian cancer in NATURE
  • 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 Clinical software development for the Web: lessons learned from the BOADICEA project in BMC MEDICAL INFORMATICS AND DECISION MAKING
  • 2012-12 A multi-center study to evaluate the impact of germline BRCA1 and BRCA2 mutations on ovarian cancer survival in HEREDITARY CANCER IN CLINICAL PRACTICE
  • 2012-11 Evaluation of chromosome 6p22 as a breast cancer risk modifier locus in a follow-up study of BRCA2 mutation carriers in BREAST CANCER RESEARCH AND TREATMENT
  • 2012-06 Association of PHB 1630 C>T and MTHFR 677 C>T polymorphisms with breast and ovarian cancer risk in BRCA1/2 mutation carriers: results from a multicenter study in BRITISH JOURNAL OF CANCER
  • 2012-05 Germline RAD51C mutations confer susceptibility to ovarian cancer in NATURE GENETICS
  • 2012-04 The KL-VS sequence variant of Klotho and cancer risk in BRCA1 and BRCA2 mutation carriers in BREAST CANCER RESEARCH AND TREATMENT
  • 2012-04 Effects of BRCA2 cis-regulation in normal breast and cancer risk amongst BRCA2 mutation carriers in BREAST CANCER RESEARCH
  • 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
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