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GENETIC ASPECTS OF KERATOCONUS DEVELOPMENT
Bikbova, M.M., Usubova, E.L., Oganisyana, K.Kh., Lobov, S.L., Khasanovad, R.R., Dzhemilevab, L.U., Khusnutdinova, E.K. (2017)
Exome sequencing study of Russian breast cancer patients suggests a predisposing role for USP39
Kuligina, E.S., Sokolenko, A.P., Bizin, I.V., Romanko, A.A., Zagorodnev, K.A., Anisimova, M.O., Krylova, D.D., Anisimova, E.I., Mantseva, M.A., Varma, A.K., Hasan, S.K., Ni, V.I., Koloskov, A.V., Suspitsin, E.N., Venina, A.R., Aleksakhina, S.N., Sokolova, T.N., Milanović, A.M., Schürmann, P., Prokofyeva, D.S., Bermisheva, M.A., Khusnutdinova, E.K., Bogdanova, N., Dörk, T., Imyanitov, E.N. (2020)
MICRORNA-200 FAMILY EXPRESSION ANALYSIS IN METASTATIC CLEAR CELL RENAL CELL CARCINOMA PATIENTS
GILYAZOVA, I.R., KLIMENTOVA, E.A., BERMISHEVA, M.A., KHUSNUTDINOVA, E.K., IZMAILOV, A.A., GALIMOVA, E.F., SAFIULLIN, R.I., GALIMOV, S.N., PAVLOV, V.N., BULYGIN, K.V. (2020)
RECONSTRUCTION OF SNP HAPLOTYPES WITH MUTATION C.-23+1G>A IN HUMAN GENE GJB2 (CHROMOSOME 13) IN SOME POPULATIONS OF EURASIA
Solovyev, A.V., Barashkov, N.A., Bady-Khoo, M.S., Zytsar, M.V., Posukh, O.L., Romanov, G.P., Rafailov, A.M., Sazonov, N.N., Alexeev, A.N., Dzhemileva, L.U., Khusnutdinova, E.K., Fedorova, S.A. (2017)
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)
OPINIONS OF HEARING PARENTS ABOUT THE CAUSES OF HEARING IMPAIRMENT OF THEIR CHILDREN WITH BIALLELIC GJB2 MUTATIONS
Solovyev, A.V., Dzhemileva, L.U., Posukh, O.L., Barashkov, N.A., Bady-Khoo, M.S., Lobov, S.L., Popova, N.Y., Romanov, G.P., Sazonov, N.N., Bondar, A.A., Morozov, I.V., Tomsky, M.I., Fedorova, S.A., Khusnutdinova, E.K. (2017)
of their deafness filled by their parents. Most of the parents at 78% (CI 68.4–85.4%) attributed their children’s HI
COMPARISON OF PREDICTIVE IN SILICO TOOLS ON MISSENSE VARIANTS IN GJB2, GJB6, AND GJB3 GENES ASSOCIATED WITH AUTOSOMAL RECESSIVE DEAFNESS 1A (DFNB1A)
PSHENNIKOVA, V.G., BARASHKOV, N.A., ROMANOV, G.P., TERYUTIN, F.M., SOLOV'EV, A.V., GOTOVTSEV, N.N., NIKANOROVA, A.A., FEDOROVA, S.A., NAKHODKIN, S.S., SAZONOV, N.N., MOROZOV, I.V., BONDAR, A.A., POSUKH, O.L, DZHEMILEVA, L.U., KHUSNUTDINOVA, E.K. (2019)
ASSOCIATION BETWEEN ALLELIC VARIANTS OF THE GENES INVOLVED IN GLUCOCORTICOIDS METABOLISM AND ASTHMA
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)
THE ROLE OF OXYTOCIN RECEPTOR (OXTR) GENE POLYMORPHISMS IN THE DEVELOPMENT OF AGGRESSIVE BEHAVIOR IN HEALTHY INDIVIDUALS
DAVYDOVA, YU. D., KAZANTSEVA, A. V., ENIKEEVA, R. F., MUSTAFIN, R.N., ENIKEEVA, R. F., LOBASKOVA, M. M., MALYKH, S. B., GILYAZOVA, I.R., KHUSNUTDINOVA, E.K. (2020)
ЧАСТОТА ВЫЯВЛЕНИЯ МУТАЦИИ 5382INSC ГЕНА BRCA1
Бермишева, М.А., Зиннатуллина, Г.Ф., Ганцев, Ш.Х., Кочанова, В.А., Попов, О.С., Доерк, Т., Хуснутдинова, Э.К., Bermisheva, M.A., Zinnatullina, G.F., Gantsev, Sh.Kh., Kochanova, V.A., Popov, O.S., Doer, T., Khusnutdinova, E.K (2008)

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