Anna Jakubowska


Ontology type: schema:Person     


Person Info

NAME

Anna

SURNAME

Jakubowska

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 Frequency of BRCA1 and BRCA2 causative founder variants in ovarian cancer patients in South-East Poland in HEREDITARY CANCER IN CLINICAL PRACTICE
  • 2018-07 A transcriptome-wide association study of 229,000 women identifies new candidate susceptibility genes for breast cancer in NATURE GENETICS
  • 2018-01 Serum selenium levels predict survival after breast cancer in BREAST CANCER RESEARCH AND TREATMENT
  • 2017-12 Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer in NATURE GENETICS
  • 2017-12 Meeting abstracts from the Annual Conference on Hereditary Cancers 2016 in HEREDITARY CANCER IN CLINICAL PRACTICE
  • 2017-11 Unraveling genetic predisposition to familial or early onset gastric cancer using germline whole-exome sequencing in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2017-11 Association analysis identifies 65 new breast cancer risk loci in NATURE
  • 2017-10 Meeting abstracts from the Annual Conference on Hereditary Cancers 2015 in HEREDITARY CANCER IN CLINICAL PRACTICE
  • 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
  • 2016-12 BRCA1 founder mutations do not contribute to increased risk of gastric cancer in the Polish population in HEREDITARY CANCER IN CLINICAL PRACTICE
  • 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 Patient survival and tumor characteristics associated with CHEK2:p.I157T – findings from the Breast Cancer Association Consortium 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 Genetic predisposition to ductal carcinoma in situ of the breast in BREAST CANCER RESEARCH
  • 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 A novel deleterious c.2656G>T MSH2 germline mutation in a Pakistani family with a phenotypic overlap of hereditary breast and ovarian cancer and Lynch syndrome in HEREDITARY CANCER IN CLINICAL PRACTICE
  • 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 Fine scale mapping of the 17q22 breast cancer locus using dense SNPs, genotyped within the Collaborative Oncological Gene-Environment Study (COGs) in SCIENTIFIC REPORTS
  • 2016-09-07 Functional mechanisms underlying pleiotropic risk alleles at the 19p13.1 breast–ovarian cancer susceptibility locus in NATURE COMMUNICATIONS
  • 2016-07 Assessing the genetic architecture of epithelial ovarian cancer histological subtypes in HUMAN GENETICS
  • 2016-06 An international survey of surveillance schemes for unaffected BRCA1 and BRCA2 mutation carriers in BREAST CANCER RESEARCH AND TREATMENT
  • 2016-05 Association of genetic susceptibility variants for type 2 diabetes with breast cancer risk in women of European ancestry in CANCER CAUSES & CONTROL
  • 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
  • 2016-01 Genetic variation in the immunosuppression pathway genes and breast cancer susceptibility: a pooled analysis of 42,510 cases and 40,577 controls from the Breast Cancer Association Consortium in HUMAN GENETICS
  • 2015-12 Microelements as diagnostic markers of pancreatic cancer in HEREDITARY CANCER IN CLINICAL PRACTICE
  • 2015-12 Serum concentrations of Cu, Se, Fe and Zn in patients diagnosed with pancreatic cancer in HEREDITARY CANCER IN CLINICAL PRACTICE
  • 2015-12 Iron as diagnostic marker of cancer in HEREDITARY CANCER IN CLINICAL PRACTICE
  • 2015-12 Cis-eQTL analysis and functional validation of candidate susceptibility genes for high-grade serous ovarian cancer in NATURE COMMUNICATIONS
  • 2015-12 Selenium as diagnostic marker of cancers in HEREDITARY CANCER IN CLINICAL PRACTICE
  • 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 Zinc as diagnostic marker of cancers in HEREDITARY CANCER IN CLINICAL PRACTICE
  • 2015-12 Copper as diagnostic marker of cancers in HEREDITARY CANCER IN CLINICAL PRACTICE
  • 2015-12 Magnesium as a diagnostic marker of cancer in HEREDITARY CANCER IN CLINICAL PRACTICE
  • 2015-12 Common germline polymorphisms associated with breast cancer-specific survival in BREAST CANCER RESEARCH
  • 2015-12 The influence of selenium concentration and variations in selenoprotein genes on the CHEK2-dependent cancers in HEREDITARY CANCER IN CLINICAL PRACTICE
  • 2015-11 Large-scale genomic analyses link reproductive aging to hypothalamic signaling, breast cancer susceptibility and BRCA1-mediated DNA repair in NATURE GENETICS
  • 2015-08 Genome-wide significant risk associations for mucinous ovarian carcinoma in NATURE GENETICS
  • 2015-06 Germline RECQL mutations are associated with breast cancer susceptibility 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
  • 2015-02 Prevalence of BRCA1 and BRCA2 germline mutations in patients with triple-negative breast cancer in BREAST CANCER RESEARCH AND TREATMENT
  • 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
  • 2014-12 Large deletion causing von Hippel-Lindau disease and hereditary breast cancer syndrome in HEREDITARY CANCER IN CLINICAL PRACTICE
  • 2014-12 Evidence that breast cancer risk at the 2q35 locus is mediated through IGFBP5 regulation in NATURE COMMUNICATIONS
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