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A new approach to estimating the prevalence of hereditary hearing loss: An analysis of the distribution of sign language users based on census data in Russia
Romanov, G.P., Pshennikova, V.G., Lashin, S.A., Solovyev, A.V., Teryutin, F.M., Cherdonova, A.M., Borisova, T.V., Sazonov, N.N., Khusnutdinova, E.K., Posukh, O.L., Fedorova, S.A., Barashkov, N.A. (2020)
of congenital hearing loss (HL) around the world. Sign language (SL) is known as the main type of communication
Study of the Role of Genes Involved in the Metabolism of Histamine in the Development of Allergic Respiratory Diseases
Savelieva, O.N., Karunas, A.S., Biktasheva, A.R., Vlasova, A.O., Khidiyatova, I.M., Etkina, E.I., Khusnutdinova, E.K. (2024)
. A significant increase in total IgE level was revealed in Russian patients with allergic airway
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
Герминальные мутации как возможные биомаркеры эффективности терапии ингибиторами контрольных точек иммунитета у пациентов с почечно-клеточной карциномой (мини-обзор)
Germline mutations as possible biomarkers of immune checkpoint inhibitor therapy efficacy in patients with renal cell carcinoma (mini review)
Гилязова, И.Р., Асадуллина, Д.Д., Иванова, Е.А., Рахимов, Р.Р., Измайлов, А.А., Бермишева, М.А., Гилязова, Г.Р., Шарифгалеев, И.А., Урманцев, М.Ф., Попова, Е.В., Сафиханов, Р.Я., Павлов, В.Н., Хуснутдинова, Э.К., Gilyazova, I.R., Asadullina, D.D., Ivanova, E.A., Rakhimov, R.R., Izmailov, A.A., Bermisheva, M.A., Gilyazova, G.R., Sharifgaleev, I.A., Urmantsev, M.F., Popova, E.V., Safikhanov, R.Ya., Pavlov, V.N., Khusnutdinova, E.K. (2022)
OPENING UP NEW HORIZONS FOR PSYCHIATRIC GENETICS IN THE RUSSIAN FEDERATION: MOVING TOWARD A NATIONAL CONSORTIUM
Fedorenko, O.Y., Golimbet, V.E., Ivanova, S.А., Levchenko, А., Gainetdinov, R.R., Semke, A.V., Simutkin, G.G., Gareeva, А.E., Glotov, А.S., Gryaznova, A., Iourov, I.Y., Krupitsky, E.M., Lebedev, I.N., Mazo, G.E., Kaleda, V.G., Abramova, L.I., Oleichik, I.V., Nasykhova, Y.A., Nasyrova, R.F., Nikolishin, A.E., Kasyanov, E.D., Rukavishnikov, G.V., Timerbulatov, I.F., Brodyansky, V.M., Vorsanova, S.G., Yurov, Y.B., Zhilyaeva, T.V., Sergeeva, A.V., Blokhina, E.A., Zvartau, E.E., Blagonravova, A.S., Aftanas, L.I., Bokhan, N.А., Kekelidze, Z.I., Klimenko, T.V., Anokhina, I.P., Khusnutdinova, E.K., Klyushnik, T.P., Neznanov, N.G., Stepanov, V.A., Schulze, T.G., Kibitov, А.О. (2019)
the major psychiatric genetic research centers in the Russian Federation in a national consortium
АНАЛИЗ РАСПРОСТРАНЕНИЯ ПОЛИМОРФНОГО ВАРИАНТА rs4988235 ГЕНА MCM6 В ТЮРКОЯЗЫЧНЫХ ПОПУЛЯЦИЯХ
ANALYSIS OF THE DISTRIBUTION OF THE POLYMORPHIC VARIANT OF rs4988235 OF THE MCM6 GENE IN TURKISHSPEAKING POPULATIONS
Джаубермезов, М.А., Екомасова, Н.В., Бучнев, Д.В., Токарева, Е.А., Хуснутдинова, Э.К., Dzhaubermezov, M.A., Ekomasova, N.V., Buchnev, D.V., Tokareva, E.A., Khusnutdinova, E.K. (2020)
A Replication Study of GWAS-Associated Variants in the TUFM, SH2B1, ZNF638, NEGR1, ATP2A1, EXOC4, and CSE1L Genes and Cognitive Abilities
Kazantseva, A.V., Davydova, Yu. D., Enikeeva, R.F., Takhirova, Z.R., Mustafin, R.N., Lobaskova, M.M., Malykh, S.B., Khusnutdinova, E.K. (2023)
of the most significant GWAS loci on spatial abilities in the Russian cohort (N = 1011, 18–25 years old) a set
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)
cohorts of Russian, Byelorussian, and German ancestry, comprising a total of 3216 cases and 2525 controls
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)
The c.-23+1G>A splice site mutation is one of the most frequent mutations of gene GJB2 (Cx26, 13q11
ANTISOCIAL BEHAVIOR: NATURE VS. NURTURE
Kazantseva, A.V., Yakovleva, D.V., Davydova, Yu. D., Kosareva, A.R., Valinurov, R.G., Khusnutdinova, E.K. (2023)
of REV3L, SORCS3, ZIC4, and XKR6 genetic variants on ASB in the Russian cohort under a moderating impact

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