Natalia Bogdanova

Analysis of more than 400,000 women provides case-control evidence for BRCA1 and BRCA2 variant classification

Large-scale meta-analysis and precision functional assays identify FANCM regions in which PTVs confer different risks for ER-negative and triple-negative breast cancer

Understanding the genetic complexity of puberty timing across the allele frequency spectrum

Integrative multi-omics analyses to identify the genetic and functional mechanisms underlying ovarian cancer risk regions

Polygenic score distribution differences across European ancestry populations: implications for breast cancer risk prediction

Differences in polygenic score distributions in European ancestry populations: implications for breast cancer risk prediction

Co-observation of germline pathogenic variants in breast cancer predisposition genes: Results from analysis of the BRIDGES sequencing dataset

Publisher Correction: Understanding the genetic complexity of puberty timing across the allele frequency spectrum

Large-scale genome-wide association study of 398,238 women unveils seven novel loci associated with high-grade serous epithelial ovarian cancer risk

Analysis of more than 400,000 women provides case-control evidence for BRCA1 and BRCA2 variant classification

Analysis of variants in untranslated and promoter regions and breast cancer risk using whole genome sequencing data

Aggregation tests identify new gene associations with breast cancer in populations with diverse ancestry

FANCM missense variants and breast cancer risk: a case-control association study of 75,156 European women

Evaluation of European-based polygenic risk score for breast cancer in Ashkenazi Jewish women in Israel

Understanding the genetic complexity of puberty timing across the allele frequency spectrum

Spectrum and Frequency of Germline FANCM Protein-Truncating Variants in 44,803 European Female Breast Cancer Cases

Pathology of Tumors Associated With Pathogenic Germline Variants in 9 Breast Cancer Susceptibility Genes

Physical activity, sedentary time and breast cancer risk: a Mendelian randomisation study

Polygenic risk modeling for prediction of epithelial ovarian cancer risk

Breast cancer risks associated with missense variants in breast cancer susceptibility genes

Individual radiosensitivity reflected by γ-H2AX and 53BP1 foci predicts outcome in PSMA-targeted radioligand therapy

Rare germline copy number variants (CNVs) and breast cancer risk

Copy Number Variants Are Ovarian Cancer Risk Alleles at Known and Novel Risk Loci

Correction: Polygenic risk modeling for prediction of epithelial ovarian cancer risk

Mendelian randomisation study of smoking exposure in relation to breast cancer risk

Functional annotation of the 2q35 breast cancer risk locus implicates a structural variant in influencing activity of a long-range enhancer element

Gene-Environment Interactions Relevant to Estrogen and Risk of Breast Cancer: Can Gene-Environment Interactions Be Detected Only among Candidate SNPs from Genome-Wide Association Studies?

CYP3A7*1C allele: linking premenopausal oestrone and progesterone levels with risk of hormone receptor-positive breast cancers

Breast cancer risks associated with missense variants in breast cancer susceptibility genes

Rare copy number variants (CNVs) and breast cancer risk