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Founder vs. non-founder BRCA1/2 pathogenic alleles: the analysis of Belarusian breast and ovarian cancer patients and review of other studies on ethnically homogenous populations

Familial cancer, 2023, Vol.22 (1), p.19-30

2023

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The Effect of Inactivating Heterozygous Mutation in NBS1 Gene on DNA Damage and Repair Markers and Apoptosis Markers in Mice

Bulletin of experimental biology and medicine, 2023-06, Vol.175 (2), p.234-238

2023

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Spectrum of APC and MUTYH germ‐line mutations in Russian patients with colorectal malignancies

Clinical genetics, 2018-05, Vol.93 (5), p.1015-1021

2018

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The role of molecular diagnostics in the choice of therapy for biliary tract cancers

Sibirskiĭ onkologicheskiĭ zhurnal, 2024-03, Vol.23 (1), p.130-141

2024

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Clinical characteristics of ovarian cancer relapse in BRCA1/2 germ-line mutation carriers and non-carriers

Annals of oncology, 2018-10, Vol.29, p.viii354-viii354

2018

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Immune checkpoint inhibitors for the treatment of solid tumors in HIV-infected patients: is it worth the risk?

Sibirskiĭ onkologicheskiĭ zhurnal, 2023-02, Vol.22 (1), p.141-150

2023

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Sequencing of KRAS and NRAS in 1501 colorectal carcinomas reveals significant share of mutations, which are not included in common diagnostic kits

Annals of oncology, 2018-10, Vol.29, p.viii195-viii195

2018

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Final results of the concordance analysis of PD-L1 immunohistochemistry (IHC) assays and polymerase chain reaction (PCR) in non-small lung cancer (NSCLC) patients

Annals of oncology, 2018-10, Vol.29, p.viii507-viii507

2018

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PALB2 germ-line mutations in Russian breast cancer patients: Identification of recurrent alleles and analysis of phenotypic characteristics of the tumors

Annals of oncology, 2018-10, Vol.29, p.viii76-viii76

2018

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Distinct functional consequences of HER2 gene amplification in colorectal and lung adenocarcinomas

Annals of oncology, 2018-10, Vol.29, p.viii27-viii27

2018

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Neoadjuvant eribulin plus carboplatin vs. paclitaxel plus carboplatin in patients with triple-negative breast cancer (TNBC)

Annals of oncology, 2018-10, Vol.29, p.viii88-viii89

2018

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Lung cancers carrying distinct ALK fusion variants demonstrate similar responsiveness to ALK tyrosine kinase inhibitors

Annals of oncology, 2018-10, Vol.29, p.viii502-viii502

2018

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HRD-negative high-grade carcinoma of the ovary in BRCA2 pathogenic variant carrier

Sibirskiĭ onkologicheskiĭ zhurnal, 2024-05, Vol.23 (2), p.139-146

2024

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CCND1 and FGFR1 gene amplifications are associated with reduced benefit from aromatase inhibitors in metastatic breast cancer

Clinical & translational oncology, 2021-04, Vol.23 (4), p.874-881

2021

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Evolution of systemic treatment for hormone-sensitive breast cancer: from sequential use of single agents to the upfront administration of drug combinations

Opukholi zhenskoĭ reproduktivnoĭ sistemy, 2016-09, Vol.12 (2), p.46-51

Imyanitov, E. N.

2016

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BRCA1/2 mutation spectrum in Armenian patients with breast and ovarian cancers

Sibirskiĭ onkologicheskiĭ zhurnal, 2024-01, Vol.22 (6), p.83-91

2024

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Predictive and prognostic features of early and locally advanced PIK3CA-mutated luminal HER2-negative breast cancer

Opukholi zhenskoĭ reproduktivnoĭ sistemy, 2024-01, Vol.19 (4), p.63-74

2024

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Hereditary predisposition to kidney cancer: cancer syndromes, multisystemic disorders, and nephropathies

Sechenovskiĭ vestnik, 2023-08, Vol.14 (2), p.5-20

2023

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Meta- and Pooled Analysis of GSTT1 and Lung Cancer: A HuGE-GSEC Review

American journal of epidemiology, 2006-12, Vol.164 (11), p.1027-1042

2006

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Hereditary ovarian cancer

Sibirskiĭ onkologicheskiĭ zhurnal, 2022-11, Vol.21 (5), p.123-134

2022

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Current approaches to systemic treatment of BRCA-associated triple-negative breast cancer

Uspehi molekulârnoj onkologii, 2023-10, Vol.10 (3), p.8-14

2023

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Monitoring of the presence of EGFR-mutated DNA during EGFR-targeted therapy may assist in the prediction of treatment outcome

Cancer treatment and research communications, 2022, Vol.31, p.100524-100524, Article 100524

2022

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Molecular diagnosis in oncology

Molecular biology (New York), 2008-10, Vol.42 (5), p.687-698

Imyanitov, E. N

2008

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Assessment of resection margins during breast-conserving surgery using multimodal optical coherence tomography

Opukholi zhenskoĭ reproduktivnoĭ sistemy, 2023-08, Vol.19 (2), p.34-46

2023

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Reactivaion of immune-related colitis during targeted therapy in a patient with metastatic cutaneous melanoma

Sibirskiĭ onkologicheskiĭ zhurnal, 2022-11, Vol.21 (5), p.162-167

2022

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Founder vs. non-founder BRCA1/2 pathogenic alleles: the analysis of Belarusian breast and ovarian cancer patients and review of other studies on ethnically homogenous populations

The Effect of Inactivating Heterozygous Mutation in NBS1 Gene on DNA Damage and Repair Markers and Apoptosis Markers in Mice

Spectrum of APC and MUTYH germ‐line mutations in Russian patients with colorectal malignancies

The role of molecular diagnostics in the choice of therapy for biliary tract cancers

Clinical characteristics of ovarian cancer relapse in BRCA1/2 germ-line mutation carriers and non-carriers

Immune checkpoint inhibitors for the treatment of solid tumors in HIV-infected patients: is it worth the risk?

Sequencing of KRAS and NRAS in 1501 colorectal carcinomas reveals significant share of mutations, which are not included in common diagnostic kits

Final results of the concordance analysis of PD-L1 immunohistochemistry (IHC) assays and polymerase chain reaction (PCR) in non-small lung cancer (NSCLC) patients

PALB2 germ-line mutations in Russian breast cancer patients: Identification of recurrent alleles and analysis of phenotypic characteristics of the tumors

Distinct functional consequences of HER2 gene amplification in colorectal and lung adenocarcinomas

Neoadjuvant eribulin plus carboplatin vs. paclitaxel plus carboplatin in patients with triple-negative breast cancer (TNBC)

Lung cancers carrying distinct ALK fusion variants demonstrate similar responsiveness to ALK tyrosine kinase inhibitors

HRD-negative high-grade carcinoma of the ovary in BRCA2 pathogenic variant carrier

CCND1 and FGFR1 gene amplifications are associated with reduced benefit from aromatase inhibitors in metastatic breast cancer

Evolution of systemic treatment for hormone-sensitive breast cancer: from sequential use of single agents to the upfront administration of drug combinations

BRCA1/2 mutation spectrum in Armenian patients with breast and ovarian cancers

Predictive and prognostic features of early and locally advanced PIK3CA-mutated luminal HER2-negative breast cancer

Hereditary predisposition to kidney cancer: cancer syndromes, multisystemic disorders, and nephropathies

Meta- and Pooled Analysis of GSTT1 and Lung Cancer: A HuGE-GSEC Review

Hereditary ovarian cancer

Current approaches to systemic treatment of BRCA-associated triple-negative breast cancer

Monitoring of the presence of EGFR-mutated DNA during EGFR-targeted therapy may assist in the prediction of treatment outcome

Molecular diagnosis in oncology

Assessment of resection margins during breast-conserving surgery using multimodal optical coherence tomography

Reactivaion of immune-related colitis during targeted therapy in a patient with metastatic cutaneous melanoma

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