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Origin and diffusion of human Y chromosome haplogroup J1-M267
Sahakyan, H., Margaryan, A., Saag, L., Karmin, M., Flores, R., Haber, M., Kushniarevich, A., Khachatryan, Z., Bahmanimehr, A., Parik, J., Karafet, T., Yunusbayev, B., Reisberg, T., Solnik, A., Metspalu, E., Hovhannisyan, A., Khusnutdinova, E.K., Behar, D.M., Metspalu, M., Yepiskoposyan, L., Rootsi, S., Villems, R. (2021)
Human Y chromosome haplogroup J1-M267 is a common male lineage in West Asia. One high-frequency
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)
, Chukchi, and Yukaghirs), the highest carrier frequency of c.1621C>T p.(Gln541*) was found in the Yakut
GENETIC ASSOCIATION OF ADRA2A AND ADRB3 GENES WITH METABOLIC SYNDROME AMONG THE TATARS
Kochetova, O.V., Viktorova, T.V., Mustafina, O.E., Karpov, A.A., Khusnutdinova, E.K. (2015)
Genotype Frequency Distribution
РОЛЬ ГЕНОВ МИКРОРНК УЧАСТНИКОВ VHL-HIF1α ПУТИ В РАЗВИТИИ СВЕТЛОКЛЕТОЧНОГО РАКА ПОЧКИ
THE ROLE OF MIRNA GENES PARTICIPATING IN VHL-HIF1α IN CLEAR CELL RENAL CELL CARCINOMA
В.Н. Павлов, Гилязова, И.Р., Измайлов, А.А., Климентова, Е.А., Султанов, И.Р., Бермишева, М.А., Ахмадеев, З.Р., Нургалиева, А.Х., Ишбулатова, Г.В., Хуснутдинова, Э.К., V.N. Pavlov, Gilyazova, I.R., Izmailov, A.A., Klimentova, E.A, Sultanov, I.R., Bermishev, M.A., Akhmadeev, Z.R., Nurgalieva, A.Kh., Ishbulatova, G.V., Khusnutdinova, E.K. (2018)
ANTISOCIAL BEHAVIOR: NATURE VS. NURTURE
Kazantseva, A.V., Yakovleva, D.V., Davydova, Yu. D., Kosareva, A.R., Valinurov, R.G., Khusnutdinova, E.K. (2023)
ANTISOCIAL BEHAVIOR: NATURE VS. NURTURE
ANALYSIS OF CLINICAL MANIFESTATIONS OF NEUROFIBROMATOSIS TYPE 1 IN PATIENTS WITH NONSENSE PATHOGENIC VARIANTS IN THE NF1 GENE FROM THE REPUBLIC OF BASHKORTOSTAN
Mustafin, R.N., Bermisheva, M.A., Karunas, A.S., Akhmetshin, A.A., Monakhova, A.S., Khusnutdinova, E.K. (2025)
Relevance: neurofibromatosis type 1 (NF1) is a hereditary tumor syndrome occurring with a frequency
HEARING LOSS OF VOLGA-URAL REGION IN RUSSIA
Khusnutdinova, E.K., Dzhemileva, L.U., Lobov, S.L., Kuznetzov, D.U., Nazirova, A.G., Nurgalina, E.M., Barashkov, N.A., Fedorova, S.A. (2017)
carrier frequency of c.35delG, c.167delT and c.235delC mutations of the GJB2 gene in 17 populations
The Role of Polymorphic Variants of Gene Components of the PTEN/PI3K/AKT Signaling Pathway in the Development of Prostate Cancer
Gilyazova, I.R., Ivanova, E.A., Bermisheva, M.A., Loginova, M.V., Asadullina, D.D., Ishemgulov, R.R., Mustafin, A.T., Pavlov, V.N., Khusnutdinova, E.K. (2022)
result of comparison allele and genotype frequencies between the general sample of prostate cancer
THE ROLE OF THE POLYMORPHISM rs28362491 OF THE NFKB1 GENE IN THE GASTRIC CANCER DEVELOPMENT
Nurgalieva, A.Kh., Mustafin, S.A., Petrova, S.G., Ekomasova, N.V., Sakaeva, D.D., Fedorova, Y.Y., Abdeeva, G.R., Dzhaubermezov, M.A., Abdeev, R.R., Rakhimov, R.R., Khusnutdinova, E.K., Prokofyeva, D.S. (2024)
frequencies. Also, it has been established that for Tatars, allele D of the rs28362491 polymorphic locus
МАЖОРНАЯ МУТАЦИЯ В ГЕНЕ SPAST У ПАЦИЕНТОВ С АУТОСОМНО-ДОМИНАНТНОЙ СПАСТИЧЕСКОЙ ПАРАПЛЕГИЕЙ ИЗ РЕСПУБЛИКИ БАШКОРТОСТАН
MAJOR MUTATION IN THE SPAST GENE IN PATIENTS WITH AUTOSOMAL DOMINANT SPASTIC PARAPLEGIA FROM THE REPUBLIC OF BASHKORTOSTAN
KHIDIYATOVA, I.M., AKHMETGALEYEVA, A.F., YANKINA, M.A., KHUSNUTDINOVA, E.K., SHAVALIEVA, V.V., SAIFULLINA, E.V., MAGZHANOV, R.V., IDRISOVA, R.F., ХИДИЯТОВА И.М., АХМЕТГАЛЕЕВА А.Ф., САЙФУЛЛИНА Е.В., ИДРИСОВА Р.Ф., ЯНКИНА М.А., ШАВАЛИЕВА В.В., МАГЖАНОВ Р.В., ХУСНУТДИНОВА Э.К. (2019)
of Tatar ethnicity with a high frequency. In the general cohort of unrelated patients from

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