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The Combination of Chromosomal Reorganization and Inherited Point Mutation Has Led to the Development of a Rare Clinical Phenotype in a Patient with Disorder of Sex Differentiation and Neuromuscular Pathology

Cytology and genetics, 2022-10, Vol.56 (5), p.417-422

2022

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Polymorphic Variants of the UGT1A1, MTHFR, GSTP, and ITPA Genes and Response to Platinum-Based Chemotherapy in Patients with Bladder Cancer

Cytology and genetics, 2024-10, Vol.58 (5), p.404-410

2024

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Distribution of Genotypes for the rs12979860 Polymorphism of the IFNL Gene among Children with COVID-19 in Ukraine

Cytology and genetics, 2023-12, Vol.57 (6), p.579-586

2023

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Children of Chernobyl Cleanup Workers do not Show Elevated Rates of Mutations in Minisatellite Alleles

Radiation research, 2001-01, Vol.155 (1), p.74-80

2001

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Genetic Modifiers of the Spinal Muscular Atrophy Phenotype

Cytology and genetics, 2020-03, Vol.54 (2), p.130-136

2020

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Analysis of Relative Average Length of Telomeres in Leukocytes of Women with COVID-19

Cytology and genetics, 2022, Vol.56 (6), p.526-529

2022

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Laboratory-biochemical features of the course of chronic hepatitis C with polymorphism rs11536889 + 3725G/C of TLR-4 gene

Journal of education, health and sport, 2020-04, Vol.10 (4), p.254-261

2020

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Relationship between the Prevalence of ACE1 I/D Polymorphism Genotype II and Covid-19 Morbidity, Mortality in Ukraine and in Some Europe Countries

Cytology and genetics, 2021, Vol.55 (5), p.427-432

2021

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Origin of dystrophin gene deletions in Duchenne and Becker muscular dystrophy patients from Ukraine

Cytology and genetics, 2017-05, Vol.51 (3), p.185-191

2017

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TGFBI Gene Mutation Analysis in Families with Hereditary Corneal Dystrophies from Ukraine

Ophthalmologica (Basel), 2004-11, Vol.218 (6), p.411-414

2004

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Investigation of rs11536889 + 3725G/C Polymorphism of the TLR4 Gene in Patients with Autoimmune and Chronic Viral Hepatitis C

Cytology and genetics, 2019-07, Vol.53 (4), p.300-306

2019

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TGFBI gene mutations in the Ukrainian patients with inherited corneal stromal dystrophies

Russian journal of genetics, 2008-10, Vol.44 (10), p.1208-1211

2008

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Association of the leukemia inhibitory factor gene polymorphism rs929271 with idiopathic mild intellectual disability

Biopolimery i kletka, 2015, Vol.31 (1), p.34-37

2015

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ANALYSIS CYP21A2 GENE MUTATIONS TECHNIQUE IN PATIENTS WITH CONGENITAL ADRENAL HYPERPLASIA

Biotechnologia acta, 2014-01, Vol.7 (1), p.75-79

2014

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ZNF527 GENE rs386809049 ANALYSIS IN POPULATION OF UKRAINE

TSitologiia i genetika, 2015-07, Vol.49 (4), p.35

2015

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IFNL4 polymorphism as a predictor of chronic hepatitis C treatment efficiency in Ukrainian patients

Cytology and genetics, 2016, Vol.50 (5), p.330-333

2016

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IL1beta, IL6 and IL8 gene polymorphisms involvement in recurrent corneal erosion in patients with hereditary stromal corneal dystrophies

TSitologiia i genetika, 2013-05, Vol.47 (3), p.42

2013

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Implementation of the quantitative Real-Time PCR for the molecular-genetic diagnostics of spinal muscular atrophy

Biopolimery i kletka, 2010, Vol.26 (1), p.51-55

2010

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Polymorphism of trinucleotide repeats in loci DM, DRPLA and SCA1 in East European populations

European journal of human genetics : EJHG, 2001-11, Vol.9 (11), p.829-835

2001

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IFN-λ-3 (IL28B) genotyping by restriction fragment length polymorphism method: detection polymorphism of rs12979860

Biopolimery i kletka, 2011, Vol.27 (3), p.231-234

2011

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Study of possible role of CYP1A1, GSTT1, GSTM1, GSTP1, NAT2 and ADRB2 genes polymorphisms in bronchial asthma development in children

Biopolimery i kletka, 2011, Vol.27 (1), p.66-73

2011

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Comparative analysis of associations of polymorphic genes F2, F5, GP1BA and ACE with the risk of stroke development in Russian and Ukrainian populations

Molekulârnaâ genetika, mikrobiologiâ i virusologiâ, 2013 (1), p.20

2013

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Analysis of 17p11.2 chromosome region rearrangements in CMT1 patients from Ukraine

Cytology and genetics, 2009, Vol.43 (1), p.28-32

2009

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Human genome mutation and rearrangement studies – the way to investigate monogenic and complex disease pathogenesis

Biopolimery i kletka, 2013, Vol.29 (4), p.330-338

2013

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Allelic polymorphism of FMR1 gene CGG-repeat region in patients with impairment of natural and stimulated ovulation

TSitologiia i genetika, 2010-11, Vol.44 (6), p.45

2010

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The Combination of Chromosomal Reorganization and Inherited Point Mutation Has Led to the Development of a Rare Clinical Phenotype in a Patient with Disorder of Sex Differentiation and Neuromuscular Pathology

Polymorphic Variants of the UGT1A1, MTHFR, GSTP, and ITPA Genes and Response to Platinum-Based Chemotherapy in Patients with Bladder Cancer

Distribution of Genotypes for the rs12979860 Polymorphism of the IFNL Gene among Children with COVID-19 in Ukraine

Children of Chernobyl Cleanup Workers do not Show Elevated Rates of Mutations in Minisatellite Alleles

Genetic Modifiers of the Spinal Muscular Atrophy Phenotype

Analysis of Relative Average Length of Telomeres in Leukocytes of Women with COVID-19

Laboratory-biochemical features of the course of chronic hepatitis C with polymorphism rs11536889 + 3725G/C of TLR-4 gene

Relationship between the Prevalence of ACE1 I/D Polymorphism Genotype II and Covid-19 Morbidity, Mortality in Ukraine and in Some Europe Countries

Origin of dystrophin gene deletions in Duchenne and Becker muscular dystrophy patients from Ukraine

TGFBI Gene Mutation Analysis in Families with Hereditary Corneal Dystrophies from Ukraine

Investigation of rs11536889 + 3725G/C Polymorphism of the TLR4 Gene in Patients with Autoimmune and Chronic Viral Hepatitis C

TGFBI gene mutations in the Ukrainian patients with inherited corneal stromal dystrophies

Association of the leukemia inhibitory factor gene polymorphism rs929271 with idiopathic mild intellectual disability

ANALYSIS CYP21A2 GENE MUTATIONS TECHNIQUE IN PATIENTS WITH CONGENITAL ADRENAL HYPERPLASIA

ZNF527 GENE rs386809049 ANALYSIS IN POPULATION OF UKRAINE

IFNL4 polymorphism as a predictor of chronic hepatitis C treatment efficiency in Ukrainian patients

IL1beta, IL6 and IL8 gene polymorphisms involvement in recurrent corneal erosion in patients with hereditary stromal corneal dystrophies

Implementation of the quantitative Real-Time PCR for the molecular-genetic diagnostics of spinal muscular atrophy

Polymorphism of trinucleotide repeats in loci DM, DRPLA and SCA1 in East European populations

IFN-λ-3 (IL28B) genotyping by restriction fragment length polymorphism method: detection polymorphism of rs12979860

Study of possible role of CYP1A1, GSTT1, GSTM1, GSTP1, NAT2 and ADRB2 genes polymorphisms in bronchial asthma development in children

Comparative analysis of associations of polymorphic genes F2, F5, GP1BA and ACE with the risk of stroke development in Russian and Ukrainian populations

Analysis of 17p11.2 chromosome region rearrangements in CMT1 patients from Ukraine

Human genome mutation and rearrangement studies – the way to investigate monogenic and complex disease pathogenesis

Allelic polymorphism of FMR1 gene CGG-repeat region in patients with impairment of natural and stimulated ovulation

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