Natalia N. Antonenkova

MI 223040, Belarus

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 71 publications

PRANA: A Deep Learning Method for Adapting Polygenic Risk Scores to Diverse Ethnic Groups.

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

Threshold-Based Overlap of Breast Cancer High-Risk Classification Using Family History, Polygenic Risk Scores, and Traditional Risk Models in 180,398 Women.

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

Overlap of high-risk individuals across family history, genetic & non-genetic breast cancer risk models: Analysis of 180,398 women from European & Asian ancestries.

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

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

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

Journal: Breast cancer research : BCR

Published: August 12, 2024

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

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

Journal: medRxiv : the preprint server for health sciences

Published: February 27, 2024

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

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

Journal: Cancers

Published: April 17, 2023

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

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

Journal: European journal of human genetics : EJHG

Published: July 15, 2022

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

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

Journal: American journal of human genetics

Published: July 13, 2022

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

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

Journal: Genome medicine

Published: May 05, 2022

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

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

Journal: European journal of human genetics : EJHG

Published: March 22, 2022

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

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

Journal: Journal of the National Cancer Institute

Published: January 28, 2022

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

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

Journal: Communications biology

Published: June 08, 2021

Showing 1-12 of 71

Last Updated: 09/26/2026