Rosa B Barkardottir


Ontology type: schema:Person     


Person Info

NAME

Rosa B

SURNAME

Barkardottir

Publications in SciGraph latest 50 shown

  • 2019-12 Shared heritability and functional enrichment across six solid cancers in NATURE COMMUNICATIONS
  • 2018-12 Genome-wide associations for benign prostatic hyperplasia reveal a genetic correlation with serum levels of PSA in NATURE COMMUNICATIONS
  • 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 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 An integrated genomics analysis of epigenetic subtypes in human breast tumors links DNA methylation patterns to chromatin states in normal mammary cells 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
  • 2016-09 Oestrogen receptor status, treatment and breast cancer prognosis in Icelandic BRCA2 mutation carriers in BRITISH JOURNAL OF CANCER
  • 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
  • 2015-02 Identification of six new susceptibility loci for invasive epithelial ovarian cancer in NATURE GENETICS
  • 2013-06 COMPLEXO: identifying the missing heritability of breast cancer via next generation collaboration in BREAST CANCER RESEARCH
  • 2012-12 The risk allele of SNP rs3803662 and the mRNA level of its closest genes TOX3 and LOC643714predict adverse outcome for breast cancer patients in BMC CANCER
  • 2012-12 A study based on whole-genome sequencing yields a rare variant at 8q24 associated with prostate cancer in NATURE GENETICS
  • 2012-06 Characterisation of amplification patterns and target genes at chromosome 11q13 in CCND1-amplified sporadic and familial breast tumours 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 A germline variant in the TP53 polyadenylation signal confers cancer susceptibility in NATURE GENETICS
  • 2011-11 Haplotype structure in Ashkenazi Jewish BRCA1 and BRCA2 mutation carriers in HUMAN GENETICS
  • 2011-10 High-resolution genomic profiling of male breast cancer reveals differences hidden behind the similarities with female breast cancer in BREAST CANCER RESEARCH AND TREATMENT
  • 2010-08 Genome-wide search for breast cancer linkage in large Icelandic non-BRCA1/2 families in BREAST CANCER RESEARCH
  • 2010-06 High-resolution genomic and expression analyses of copy number alterations in HER2-amplified breast cancer in BREAST CANCER RESEARCH
  • 2010-06 Genomic subtypes of breast cancer identified by array-comparative genomic hybridization display distinct molecular and clinical characteristics in BREAST CANCER RESEARCH
  • 2009-10 Genome-wide association and replication studies identify four variants associated with prostate cancer susceptibility in NATURE GENETICS
  • 2009-02 Sequence variants at the TERT-CLPTM1L locus associate with many cancer types in NATURE GENETICS
  • 2008-12 Evidence against PALB2 involvement in Icelandic breast cancer susceptibility in JOURNAL OF NEGATIVE RESULTS IN BIOMEDICINE
  • 2008-03 Common sequence variants on 2p15 and Xp11.22 confer susceptibility to prostate cancer in NATURE GENETICS
  • 2007-08 Two variants on chromosome 17 confer prostate cancer risk, and the one in TCF2 protects against type 2 diabetes in NATURE GENETICS
  • 2007-05 Genome-wide association study identifies a second prostate cancer susceptibility variant at 8q24 in NATURE GENETICS
  • 2006-06 A common variant associated with prostate cancer in European and African populations in NATURE GENETICS
  • 2002-06 Mutation analysis of the CHK2 gene in breast carcinoma and other cancers in BREAST CANCER RESEARCH
  • 2002-02 A genomic map of a 6-Mb region at 13q21-q22 implicated in cancer development: identification and characterization of candidate genes in HUMAN GENETICS
  • 2001-10 Haplotype analysis in Icelandic and Finnish BRCA2 999del5 breast cancer families in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2000-10 Analysis of HPC1, HPCX, and PCaP in Icelandic hereditary prostate cancer in HUMAN GENETICS
  • 1999-05 European multicenter study on LOH of APOC3 at 11q23 in 766 breast cancer patients: relation to clinical variables in BRITISH JOURNAL OF CANCER
  • 1998-01 High incidence of loss of heterozygosity at chromosome 17p13 in breast tumours from BRCA2 mutation carriers in ONCOGENE
  • 1998-01 Inherited BRCA2 mutation associated with high grade breast cancer in BREAST CANCER RESEARCH AND TREATMENT
  • 1995-10 Linkage analysis and allelic imbalance in human breast cancer kindreds using microsatellite markers from the short arm of chromosome 3 in HUMAN GENETICS
  • 1995-09 Loss of heterozygosity at chromosome 11 in breast cancer: association of prognostic factors with genetic alterations in BRITISH JOURNAL OF CANCER
  • 1987 Light Control and Developmental Regulation of Expression of Nuclear Genes in Young Barley Seedlings in PLANT MOLECULAR BIOLOGY
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