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Transforming growth factor beta 1 is a novel susceptibility gene for adolescent idiopathic scoliosis

Spine (Philadelphia, Pa. 1976), 2013-05, Vol.38 (12), p.E699-E704

2013

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A comprehensive study revealed SNP-SNP interactions and a sex-dependent relationship between polymorphisms of the CYP2J2 gene and hypertension risk

Hypertension research, 2019-02, Vol.42 (2), p.257-272

2019

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Polymorphism of SERF2, the gene encoding a heat-resistant obscure (Hero) protein with chaperone activity, is a novel link in ischemic stroke

IBRO neuroscience reports, 2023-06, Vol.14, p.453-461

2023

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The C718T polymorphism in the 3'-untranslated region of glutathione peroxidase-4 gene is a predictor of cerebral stroke in patients with essential hypertension

Hypertension research, 2012-05, Vol.35 (5), p.507-512

2012

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A polymorphic variant of rs440837 A>G in the ZBTB10 gene is associated with the occurrence of moderately differentiated breast cancer

Ginekologiâ (Moskva. Online), 2024-09, Vol.26 (3), p.249-253

2024

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The etiopathogenesis of uterine leiomyomas: A review

Ginekologiâ (Moskva. Online), 2023-04, Vol.25 (1), p.22-30

2023

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A comprehensive contribution of genes for aryl hydrocarbon receptor signaling pathway to hypertension susceptibility

Pharmacogenetics and genomics, 2017-02, Vol.27 (2), p.57-69

2017

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Polymorphic variants of the PPP1R21 gene associated with the level of sex hormone-binding globulin and the risk of various stages of breast cancer

Ginekologiâ (Moskva. Online), 2024-05, Vol.26 (1), p.89-94

2024

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Lipid-associated GWAS loci as important markers of the risk, severity, and clinical course of peripheral artery disease

Expert review of molecular diagnostics, 2024-10, p.1-12

2024

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Polymorphism of LYPLAL1 and TGFA Genes Associated With Progression of Knee Osteoarthritis in Residents Central Chernozem Region of Russia

Travmatologii͡a︡ i ortopedii͡a︡ Rossii, 2022-12, Vol.28 (4), p.42-53

2022

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Genome-wide Studies of knee Osteoarthritis: Review

Travmatologii͡a︡ i ortopedii͡a︡ Rossii, 2021-12, Vol.27 (4), p.131-144

2021

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Association of matrix metalloproteinase gene polymorphisms with different biological subtypes of breast cancer

Ginekologiâ (Moskva. Online), 2022-11, Vol.24 (5), p.393-398

2022

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Genetic variation at the catalytic subunit of glutamate cysteine ligase contributes to the susceptibility to sporadic colorectal cancer: a pilot study

Molecular biology reports, 2022-07, Vol.49 (7), p.6145-6154

2022

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Association between HSPA8 Gene Variants and Ischemic Stroke: A Pilot Study Providing Additional Evidence for the Role of Heat Shock Proteins in Disease Pathogenesis

Genes, 2023-05, Vol.14 (6), p.1171

2023

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The insertion-deletion polymorphism of the ACE gene is associated with increased blood pressure in women at the end of pregnancy

Journal of the renin-angiotensin-aldosterone system, 2015-09, Vol.16 (3), p.623-632

2015

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Polymorphism of the maternal EGF gene is associated with the fetal growth retardation: a prospective comparative study

Ginekologiâ (Moskva. Online), 2021-12, Vol.23 (6), p.554-558

2021

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The rs5918 polymorphism in the ITGB3 gene increases the risk for preeclampsia in pregnant women with fetal growth retardation

Ginekologiâ (Moskva. Online), 2021-09, Vol.23 (4), p.330-334

2021

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The polymorphic locus rs1799945 of the HFE gene determines the risk of severe preeclampsia

Ginekologiâ (Moskva. Online), 2023-07, Vol.25 (2), p.234-238

2023

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Altered erythrocyte membrane protein composition mirrors pleiotropic effects of hypertension susceptibility genes and disease pathogenesis

Journal of hypertension, 2015-11, Vol.33 (11), p.2265-2277

2015

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Synergism between the N -acetyltransferase 2 gene and oxidant exposure increases the risk of idiopathic male infertility

Reproductive biomedicine online, 2014-09, Vol.29 (3), p.362-369

2014

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Smoking Status Modifies the Relation Between CYP1A12C Gene Polymorphism and Idiopathic Male Infertility: The Importance of Gene–Environment Interaction Analysis for Genetic Studies of the Disease

Reproductive sciences (Thousand Oaks, Calif.), 2013-11, Vol.20 (11), p.1302-1307

2013

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Estimation of candidate genes in the development of a combination of endometrial hyperplasia and uterine fi broids

Medical Herald of the South of Russia, 2017-12, Vol.8 (4), p.68-73

2017

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The role of obesity in the implementation of genetic predisposition to the development of essential hypertension in men

Ozhirenie i metabolizm, 2019-12, Vol.16 (4), p.66-72

2019

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Study of the associations between polymorphic markers rs1800629 TNFa, rs909253 Lta, rs767455 TNFR1, rs1061624 TNFR2 and the development of type 2 diabetes

Sakharnyĭ diabet, 2017-08, Vol.20 (3), p.166-171

2017

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Modern concepts of etiology, pathogenesis and risk factors for preeclampsia

Journal of obstetrics and women's diseases, 2021-11, Vol.70 (5), p.105-116

2021

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Transforming growth factor beta 1 is a novel susceptibility gene for adolescent idiopathic scoliosis

A comprehensive study revealed SNP-SNP interactions and a sex-dependent relationship between polymorphisms of the CYP2J2 gene and hypertension risk

Polymorphism of SERF2, the gene encoding a heat-resistant obscure (Hero) protein with chaperone activity, is a novel link in ischemic stroke

The C718T polymorphism in the 3'-untranslated region of glutathione peroxidase-4 gene is a predictor of cerebral stroke in patients with essential hypertension

A polymorphic variant of rs440837 A>G in the ZBTB10 gene is associated with the occurrence of moderately differentiated breast cancer

The etiopathogenesis of uterine leiomyomas: A review

A comprehensive contribution of genes for aryl hydrocarbon receptor signaling pathway to hypertension susceptibility

Polymorphic variants of the PPP1R21 gene associated with the level of sex hormone-binding globulin and the risk of various stages of breast cancer

Lipid-associated GWAS loci as important markers of the risk, severity, and clinical course of peripheral artery disease

Polymorphism of LYPLAL1 and TGFA Genes Associated With Progression of Knee Osteoarthritis in Residents Central Chernozem Region of Russia

Genome-wide Studies of knee Osteoarthritis: Review

Association of matrix metalloproteinase gene polymorphisms with different biological subtypes of breast cancer

Genetic variation at the catalytic subunit of glutamate cysteine ligase contributes to the susceptibility to sporadic colorectal cancer: a pilot study

Association between HSPA8 Gene Variants and Ischemic Stroke: A Pilot Study Providing Additional Evidence for the Role of Heat Shock Proteins in Disease Pathogenesis

The insertion-deletion polymorphism of the ACE gene is associated with increased blood pressure in women at the end of pregnancy

Polymorphism of the maternal EGF gene is associated with the fetal growth retardation: a prospective comparative study

The rs5918 polymorphism in the ITGB3 gene increases the risk for preeclampsia in pregnant women with fetal growth retardation

The polymorphic locus rs1799945 of the HFE gene determines the risk of severe preeclampsia

Altered erythrocyte membrane protein composition mirrors pleiotropic effects of hypertension susceptibility genes and disease pathogenesis

Synergism between the N -acetyltransferase 2 gene and oxidant exposure increases the risk of idiopathic male infertility

Smoking Status Modifies the Relation Between CYP1A12C Gene Polymorphism and Idiopathic Male Infertility: The Importance of Gene–Environment Interaction Analysis for Genetic Studies of the Disease

Estimation of candidate genes in the development of a combination of endometrial hyperplasia and uterine fi broids

The role of obesity in the implementation of genetic predisposition to the development of essential hypertension in men

Study of the associations between polymorphic markers rs1800629 TNFa, rs909253 Lta, rs767455 TNFR1, rs1061624 TNFR2 and the development of type 2 diabetes

Modern concepts of etiology, pathogenesis and risk factors for preeclampsia

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