Natalia V. Bogdanova
Carl Neuberg Str. 1
Hannover, NI 30625, Germany
Hannover, NI 30625, Germany
Last Updated: 09/26/2026
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Found 170 publications
PRANA: A Deep Learning Method for Adapting Polygenic Risk Scores to Diverse Ethnic Groups.
Journal: medRxiv : the preprint server for health sciences
Published: July 29, 2026
Author Correction: Functional mechanisms underlying pleiotropic risk alleles at the 19p13.1 breast-ovarian cancer susceptibility locus.
Journal: Nature communications
Published: September 09, 2025
Threshold-Based Overlap of Breast Cancer High-Risk Classification Using Family History, Polygenic Risk Scores, and Traditional Risk Models in 180,398 Women.
Journal: Cancers
Published: September 09, 2025
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.
Journal: Breast (Edinburgh, Scotland)
Published: July 09, 2025
Overlap of high-risk individuals across family history, genetic & non-genetic breast cancer risk models: Analysis of 180,398 women from European & Asian ancestries.
Journal: medRxiv : the preprint server for health sciences
Published: March 17, 2025
Analysis of more than 400,000 women provides case-control evidence for BRCA1 and BRCA2 variant classification.
Journal: medRxiv : the preprint server for health sciences
Published: September 16, 2024
Analysis of more than 400,000 women provides case-control evidence for BRCA1 and BRCA2 variant classification.
Journal: Nature communications
Published: September 02, 2024
Polygenic score distribution differences across European ancestry populations: implications for breast cancer risk prediction.
Journal: Breast cancer research : BCR
Published: August 12, 2024
Synonymous rpsH variants: the common denominator in Escherichia coli adapting to ionizing radiation.
Synonymous rpsH variants: the common denominator in Escherichia coli adapting to ionizing radiation.
Journal: NAR genomics and bioinformatics
Published: May 29, 2024
Co-observation of germline pathogenic variants in breast cancer predisposition genes: Results from analysis of the BRIDGES sequencing dataset.
Journal: American journal of human genetics
Published: March 29, 2024
Large-scale genome-wide association study of 398,238 women unveils seven novel loci associated with high-grade serous epithelial ovarian cancer risk.
Journal: medRxiv : the preprint server for health sciences
Published: March 18, 2024
Last Updated: 09/26/2026