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Functional annotation of the 2q35 breast cancer risk locus implicates a structural variant in influencing activity of a long-range enhancer element
Baxter, J.S., Johnson, N., Tomczyk, K, Gillespie, A., Maguire, S., Brough, R., Fachal, L, Michailidou, K., Bolla, M.K., Wang, Q., Dennis, J., Ahearn, T.U., Bermisheva, M. (2021)
(signal 1), 5 (signal 2), and 42 (signal 3) credible causal variants at these loci. We used publicly
ROLE OF ALLELIC GENES OF MATRIX METALLOPROTEINASES AND THEIR TISSUE INHIBITORS IN THE RISK OF PEPTIC ULCER DISEASE DEVELOPMENT
Shaymardanova, E.Kh., Nurgalieva, A.Kh., Khidiyatova, I.M., Gabbasova, L.V., Kuramshina, O.A., Kryukova, A.Ya., Sagitov, R.B., Munasipov, F.R., Khusnutdinova, E.Kh. (2016)
of Bashkortostan. Associations of polymorphic variants rs1799750 and rs494379 of gene MMP1, rs3025058 of gene MMP3
Whole Exome Sequencing Study Suggests an Impact of FANCA, CDH1 and VEGFA Genes on Diffuse Gastric Cancer Development
Nurgalieva, A., Galliamova, L., Ekomasova, N., Yankina, M., Sakaeva, D., Valiev, R., Prokofyeva, D., Dzhaubermezov, M., Fedorova, Y., Khusnutdinov, S., Khusnutdinova, E. (2023)
stomach tissue from the same patient. Three pathogenic variants were identified: c.1320+1G>A in the CDH1
АССОЦИАЦИЯ АЛЛЕЛЬНЫХ ВАРИАНТОВ ГЕНОВ, УЧАСТВУЮЩИХ В МЕТАБОЛИЗМЕ ГЛЮКОКОРТИКОСТЕРОИДОВ, С РАЗВИТИЕМ БРОНХИАЛЬНОЙ АСТМЫ
ASSOCIATION BETWEEN ALLELIC VARIANTS OF THE GENES INVOLVED IN GLUCOCORTICOIDS METABOLISM AND ASTHMA
ФЕДОРОВА, Ю.Ю., КАРУНАС, А.С., МУРЗИНА, Р.Р., САВЕЛЬЕВА, О.Н., ГИМАЛОВА, Г.Ф., ГАТИЯТУЛЛИН, Р.Ф., ЭТКИНА, Э.И., ХУСНУТДИНОВА, Э.К., Fedorova Y.Y.,, Karunas A.S.,, Gimalova G.F.,, Khusnutdinova E.K., Savelieva O.N., Murzina R.R., Gatiyatullin R.F., Etkina E.I. (2019)
ASSOCIATION BETWEEN ALLELIC VARIANTS OF THE GENES INVOLVED IN GLUCOCORTICOIDS METABOLISM AND ASTHMA
THE ROLE OF TRANSPOSABLE ELEMENTS IN THE ASSOCIATION OF POLYMORPHIC VARIANTS WITH MULTIFACTORIAL DISEASES
Mustafin, R.N. (2024)
THE ROLE OF TRANSPOSABLE ELEMENTS IN THE ASSOCIATION OF POLYMORPHIC VARIANTS WITH MULTIFACTORIAL
МОЛЕКУЛЯРНО-ГЕНЕТИЧЕСКИЕ ИССЛЕДОВАНИЯ ФУНКЦИОНИРОВАНИЯ ПОЛИМОРФНЫХ ВАРИАНТОВ ГЕНОВ ЦИТОКИНОВОЙ СЕТИ И БИОТРАНСФОРМАЦИИ КСЕНОБИОТИКОВ ПРИ ОНКОПАТОЛОГИИ
MOLECULAR GENETICS STUDY FUNCTIONING POLYMORPHIC GENE VARIANTS CYTOKINE NETWORK AND BIOTRANSFORMATION OF XENOBIOTICS FOR CANCER
Е. В. Воробьева, E. V. Vorobyeva, Э. М. Васильева, E. M. Vasilyeva, Г. Ф. Галикеева, G F. Galikeeva, В. Ю. Горбунова, V. Y. Gorbunova (Креативная хирургия и онкология, №4, 2017)
MOLECULAR GENETICS STUDY FUNCTIONING POLYMORPHIC GENE VARIANTS CYTOKINE NETWORK
FINE-MAPPING OF 150 BREAST CANCER RISK REGIONS IDENTIFIES 191 LIKELY TARGET GENES
FACHAL, L., KAR, S., TYRER, J.P., GHOUSSAINI, M., HARRINGTON, P.A., HEALEY, C.S., MAYES, R., SHAH, M., PHAROAH, P.D.P., EASTON, D.F., DUNNING, A.M., ASCHARD, H., JIANG, X., TAMIMI, R.M., KHUSNUTDINOVA, E., BIAŁKOWSKA, K., и др. соавторы (2020)
Genome-wide association studies have identified breast cancer risk variants in over 150 genomic
THE RELATIONSHIP OF THE IMMUNE RESPONSE MEDIATOR GENES' POLYMORPHIC VARIANTS WITH THE METHOTREXATE EFFICACY IN JUVENILE IDIOPATHIC ARTHRITIS
NAZAROVA, L.SH., DANILKO, K.V., MALIEVSKY, V.A., KARIMOV, D.O., BAKIROV, A.B., VIKTOROVA, T.V. (2020)
, PADI4 rs2240336) variants with the methotrexate efficacy in juvenile idiopathic arthritis (JIA
Investigating the role of osteoprotegerin gene polymorphic variants in osteoporosis
Yalaev, B.I., Tyurin, A.V., Mirgalieva, R.I., Khusnutdinova, E.K., Khusainova, R.I. (2021)
- Polymorphic variants rs3134069, rs3102734, rs7844539 and rs3102734 are potential markers of the risk
Autosomal recessive cataract (CTRCT18) in the Yakut population isolate of Eastern Siberia: a novel founder variant in the FYCO1 gene
Barashkov, N.A., Konovalov, F.A., Borisova, T.V., Teryutin, F.M., Solovyev, A.V., Pshennikova, V.G., Sapojnikova, N.V., Vychuzhina, L.S., Romanov, G.P., Gotovtsev, N.N., Morozov, I.V., Bondar, A.A., Platonov, F.A., Burtseva, T.E., Khusnutdinova, E.K., Posukh, O.L., Fedorova, S.A. (2021)
this variant in a homozygous state in 25 out of 29 Yakut families with congenital cataract (86%). Among 424

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