Natalia V Bogdanova


Ontology type: schema:Person     


Person Info

NAME

Natalia V

SURNAME

Bogdanova

Publications in SciGraph latest 50 shown

  • 2019-12 Shared heritability and functional enrichment across six solid cancers in NATURE COMMUNICATIONS
  • 2018-07 A transcriptome-wide association study of 229,000 women identifies new candidate susceptibility genes for breast cancer in NATURE GENETICS
  • 2018-02 Ethnic Features of Genetic Susceptibility to Breast Cancer in RUSSIAN JOURNAL OF GENETICS
  • 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
  • 2017-05 Genetic modifiers of CHEK2*1100delC-associated breast cancer risk in GENETICS IN MEDICINE
  • 2017-04 Analysis of a RECQL splicing mutation, c.1667_1667+3delAGTA, in breast cancer patients and controls from Central Europe in FAMILIAL CANCER
  • 2017-02 Assessment of an APOBEC3B truncating mutation, c.783delG, in patients with breast cancer in BREAST CANCER RESEARCH AND TREATMENT
  • 2016-12 Genetic predisposition to ductal carcinoma in situ of the breast 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 search for new candidate genes involved in ovarian cancer pathogenesis by exome sequencing in RUSSIAN JOURNAL OF GENETICS
  • 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
  • 2016-07 Assessing the genetic architecture of epithelial ovarian cancer histological subtypes in HUMAN GENETICS
  • 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
  • 2016-01 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 Cis-eQTL analysis and functional validation of candidate susceptibility genes for high-grade serous ovarian cancer 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
  • 2015-08 Genome-wide significant risk associations for mucinous ovarian carcinoma 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
  • 2015-03 Prevalence of the BLM nonsense mutation, p.Q548X, in ovarian cancer patients from Central and Eastern Europe in FAMILIAL CANCER
  • 2015-02 Identification of six new susceptibility loci for invasive epithelial ovarian cancer in NATURE GENETICS
  • 2014-12 Functional deficiency of NBN, the Nijmegen breakage syndrome protein, in a p.R215W mutant breast cancer cell line in BMC CANCER
  • 2014-12 Evidence that breast cancer risk at the 2q35 locus is mediated through IGFBP5 regulation in NATURE COMMUNICATIONS
  • 2014-12 The frequency of the BLM*p.Q548X (c.1642C > T) mutation in breast cancer patients from Russia in BREAST CANCER RESEARCH AND TREATMENT
  • 2014-06 Genetic variation at CYP3A is associated with age at menarche and breast cancer risk: a case-control study in BREAST CANCER RESEARCH
  • 2014-06 Double heterozygotes among breast cancer patients analyzed for BRCA1, CHEK2, ATM, NBN/NBS1, and BLM germ-line mutations in BREAST CANCER RESEARCH AND TREATMENT
  • 2014-06 Prevalence of PALB2 mutation c.509_510delGA in unselected breast cancer patients from Central and Eastern Europe in FAMILIAL CANCER
  • 2014-05 Genome-wide association study of subtype-specific epithelial ovarian cancer risk alleles using pooled DNA in HUMAN GENETICS
  • 2014-02 FGF receptor genes and breast cancer susceptibility: results from the Breast Cancer Association Consortium in BRITISH JOURNAL OF CANCER
  • 2014-01 Frequency of CHEK2 gene mutations in breast cancer patients from Republic of Bashkortostan in MOLECULAR BIOLOGY
  • 2013-12 Hereditary breast cancer: ever more pieces to the polygenic puzzle in HEREDITARY CANCER IN CLINICAL PRACTICE
  • 2013-12 Epigenetic analysis leads to identification of HNF1B as a subtype-specific susceptibility gene for ovarian cancer in NATURE COMMUNICATIONS
  • 2013-04 GWAS meta-analysis and replication identifies three new susceptibility loci for ovarian cancer in NATURE GENETICS
  • 2013-04 Large-scale genotyping identifies 41 new loci associated with breast cancer risk in NATURE GENETICS
  • 2013-04 Genome-wide association studies identify four ER negative–specific breast cancer risk loci 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
  • 2013-01 Nonsense mutation p.Q548X in BLM, the gene mutated in Bloom’s syndrome, is associated with breast cancer in Slavic populations in BREAST CANCER RESEARCH AND TREATMENT
  • 2012-03 Genome-wide association analysis identifies three new breast cancer susceptibility loci in NATURE GENETICS
  • 2011-12 Mutation analysis of the SLX4/FANCP gene in hereditary breast cancer in BREAST CANCER RESEARCH AND TREATMENT
  • 2011-04 PALB2 mutations in German and Russian patients with bilateral breast cancer in BREAST CANCER RESEARCH AND TREATMENT
  • 2010-12 TOPBP1 missense variant Arg309Cys and breast cancer in a German hospital-based case-control study in JOURNAL OF NEGATIVE RESULTS IN BIOMEDICINE
  • 2010-10 Common variants at 19p13 are associated with susceptibility to ovarian cancer in NATURE GENETICS
  • 2010-07 Erratum to: BAK, BAX, and NBK/BIK Proapoptotic Gene Alterations in Iranian Patients with Ataxia Telangiectasia in JOURNAL OF CLINICAL IMMUNOLOGY
  • 2010-01 BAK, BAX, and NBK/BIK Proapoptotic Gene Alterations in Iranian Patients with Ataxia Telangiectasia in JOURNAL OF CLINICAL IMMUNOLOGY
  • 2009-11 A nonsense mutation (E1978X) in the ATM gene is associated with breast cancer in BREAST CANCER RESEARCH AND TREATMENT
  • 2009-09 Synergistic interaction of variants in CHEK2 and BRCA2 on breast cancer risk in BREAST CANCER RESEARCH AND TREATMENT
  • 2009-06 TGFB1 gene polymorphism Leu10Pro (c.29T>C), prostate cancer incidence and quality of life in patients treated with brachytherapy in WORLD JOURNAL OF UROLOGY
  • 2009-05 Newly discovered breast cancer susceptibility loci on 3p24 and 17q23.2 in NATURE GENETICS
  • Affiliations

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