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По вашему запросу найдено документов: 817

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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)

in certain populations by specific genetic background and population structure. At least, the data from

Association of inflammation gene polymorphism with increased risk of metabolic syndrome in tatar ethnic group

Kochetova, Olga V., Avzaletdinova, Diana S., Korytina, Gulnaz F. (2022)

genetic polymorphisms

The Genetic Markers of Knee Osteoarthritis in Women from Russia

Tyurin, Anton, Akhiiarova, Karina, Minniakhmetov, Ildar, Mokrysheva, Natalia, Khusainova, Rita (2024)

to the clinical and ethnic heterogeneity of the studied populations. To find the genetic markers

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)

the genetic cause of congenital cataract spread in this population, we performed whole-exome sequencing

Erratum: Author Correction: A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers (Nature communications (2021) 12 1 (1078))

Breast cancer (BC) risk for BRCA1 and BRCA2 mutation carriers varies by genetic and familial

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)

An association study was performed for genetic polymorphisms in ADRB3 (rs4994) and ADRA2A (rs

The frequent variant A57F in the GNE gene in patients from Russia has Finno-Ugric Mari origin

Subbotin, Dmitrii, Ionova, Sofya, Marakhonov, Andrey, Saifullina, Elena, Borovikov, Artem, Akhmadeeva, Leila, Chausova, Polina, Ryzhkova, Oksana, Zinchenko, Rena, Kutsev, Sergey, Murtazina, Aysylu (2024)

variants from historically isolated populations is important for molecular genetic diagnosis. This approach

CLINICAL FORMS OF HUNTINGTON’S DISEASE IN THE PATIENTS FROM REPUBLIC OF BASHKORTOSTAN

Magzhanov, R., Saifullina, E. (2014)

at an early stage of the illness. In different populations the clinical characteristics of patients with HD

Mendelian Randomization Analysis Identifies Inverse Causal Relationship between External Eating and Metabolic Phenotypes

Timasheva, Yanina, Balkhiyarova, Zhanna, Avzaletdinova, Diana, Morugova, Tatyana, Korytina, Gulnaz F., Nouwen, Arie, Prokopenko, Inga, Kochetova, Olga (2024)

phenotypes remain unclear. We aimed to identify genetic variants linked to eating behaviour and investigate

ГЕНЕТИЧЕСКИЕ ОСОБЕННОСТИ ПОПУЛЯЦИИ, ПРОЖИВАЮЩЕЙ НА ТЕРРИТОРИИ РЕСПУБЛИКИ БАШКОРТОСТАН

GENETIC CHARACTERISTICS OF THE POPULATION LIVING IN THE TERRITORY OF THE REPUBLIC OF BASHKORTOSTAN

Логинова, М.А., Парамонов, И.В., В.Н. Павлов, Сафуанова, Г.Ш., Loginova, M.A., Paramonov, I.V., Pavlov, V.N., Safuanova, G.Sh. (Вестник трансплантологии и искусственных органов, 2016)

in the studied population; one was registered in the WHO Nomenclature Committee for Factors of the HLA System

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