Anna A. Bukaeva

2, Abricosovsky Side Street
Moscow, MOW 119991, Russian Federation

Last Updated: 09/26/2026

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Found 12 publications

Extended Germline Profiling of Cancer Predisposition and Homologous Recombination Repair Genes in 275 Russian Patients with Triple-Negative Breast Cancer.

Extended Germline Profiling of Cancer Predisposition and Homologous Recombination Repair Genes in 275 Russian Patients with Triple-Negative Breast Cancer.

Journal: Biomedicines

Published: June 10, 2026

Genetic Determinants of Severe Hypertriglyceridemia: Rare Variants in LPL, APOC2, APOA5, GPIHBP1, LMF1, APOE and Polygenic Risk.

Genetic Determinants of Severe Hypertriglyceridemia: Rare Variants in LPL, APOC2, APOA5, GPIHBP1, LMF1, APOE and Polygenic Risk.

Journal: International journal of molecular sciences

Published: April 27, 2026

Neoantigen-Driven Immunotherapy in Triple-Negative Breast Cancer: Emerging Strategies and Clinical Potential.

Neoantigen-Driven Immunotherapy in Triple-Negative Breast Cancer: Emerging Strategies and Clinical Potential.

Journal: Biomedicines

Published: July 18, 2025

On Penetrance Estimation in Family, Clinical, and Population Cohorts.

On Penetrance Estimation in Family, Clinical, and Population Cohorts.

Journal: Circulation. Genomic and precision medicine

Published: March 28, 2025

A Novel Bradycardia-Associated Variant in HCN4 as a Candidate Modifier in Type 3 Long QT Syndrome: Case Report and Deep In Silico Analysis.

A Novel Bradycardia-Associated Variant in HCN4 as a Candidate Modifier in Type 3 Long QT Syndrome: Case Report and Deep In Silico Analysis.

Journal: Biomedicines

Published: March 03, 2025

The Yield of Genetic Testing and Putative Genetic Factors of Disease Heterogeneity in Long QT Syndrome Patients.

The Yield of Genetic Testing and Putative Genetic Factors of Disease Heterogeneity in Long QT Syndrome Patients.

Journal: International journal of molecular sciences

Published: September 25, 2024

A Rare Coincidence of Three Inherited Diseases in a Family with Cardiomyopathy and Multiple Extracardiac Abnormalities.

A Rare Coincidence of Three Inherited Diseases in a Family with Cardiomyopathy and Multiple Extracardiac Abnormalities.

Journal: International journal of molecular sciences

Published: June 21, 2024

A Splice Variant of the MYH7 Gene Is Causative in a Family with Isolated Left Ventricular Noncompaction Cardiomyopathy.

A Splice Variant of the MYH7 Gene Is Causative in a Family with Isolated Left Ventricular Noncompaction Cardiomyopathy.

Journal: Genes

Published: July 28, 2022

A Case of Severe Left-Ventricular Noncompaction Associated with Splicing Altering Variant in the FHOD3 Gene.

A Case of Severe Left-Ventricular Noncompaction Associated with Splicing Altering Variant in the FHOD3 Gene.

Journal: Genes

Published: December 15, 2021

The LDLR, APOB, and PCSK9 Variants of Index Patients with Familial Hypercholesterolemia in Russia.

The LDLR, APOB, and PCSK9 Variants of Index Patients with Familial Hypercholesterolemia in Russia.

Journal: Genes

Published: December 16, 2020

Allelic Dropout Is a Common Phenomenon That Reduces the Diagnostic Yield of PCR-Based Sequencing of Targeted Gene Panels.

Allelic Dropout Is a Common Phenomenon That Reduces the Diagnostic Yield of PCR-Based Sequencing of Targeted Gene Panels.

Journal: Frontiers in genetics

Published: October 23, 2020

Low mutation rate in the TTN gene in paediatric patients with dilated cardiomyopathy - a pilot study.

Low mutation rate in the TTN gene in paediatric patients with dilated cardiomyopathy - a pilot study.

Journal: Scientific reports

Published: March 18, 2019

Showing 1-12 of 12

Last Updated: 09/26/2026