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Single-Nucleotide Polymorphisms as Biomarkers of Antipsychotic-Induced Akathisia: Systematic Review
Nasyrova, Regina F, Vaiman, Elena E, Repkina, Vera V, Khasanova, Aiperi K, Asadullin, Azat R, Shipulin, German A, Altynbekov, Kuanysh S, Al-Zamil, Mustafa, Petrova, Marina M, Shnayder, Natalia A (2023)
genetic studies of the predisposition to the development of AIA. Objective: The goal of our study
The Genetic Markers of Knee Osteoarthritis in Women from Russia
Tyurin, Anton, Akhiiarova, Karina, Minniakhmetov, Ildar, Mokrysheva, Natalia, Khusainova, Rita (2024)
is the study of genetic markers of the disease, which have not been definitively established, due
«СОЛНЕЧНЫЕ» ЛЮДИ: СОЦИАЛИЗАЦИЯ
"SUNNY" PEOPLE: SOCIALIZATION
Габдуллина, М.И., Gabdullina, M.I. (2024)
genetics
НАСЛЕДСТВЕННЫЕ НАРУШЕНИЯ РЕЧИ
HEREDITARY SPEECH DISORDERS
Ершов, Н.М., Никифоров, Д.А., Ershov, N.M., Nikiforov, D.A. (2024)
genetic disorders
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 the prevalence of congenital HL. Since a significant part of congenital HL is due to genetic causes
Breast cancer risk genes - Association analysis in more than 113,000 women
Dorling, L., Carvalho, S., Allen, J., González-Neira, A., Luccarini, C., Wahlström, C., Pooley, K.A., Parsons, M.T., Fortuno, C., Wang, Q., Bolla, M.K., Dennis, J., Bermisheva, M., Khusnutdinova, E., Prokofyeva, D., other additional authors (2021)
BACKGROUND Genetic testing for breast cancer susceptibility is widely used, but for many genes
Germline Variants in Proto-Oncogenes and Tumor Suppressor Genes in Women with Cervical Cancer
Lenkova, Ksenia, Khusainova, Rita, Minyazeva, Raushaniya, Zaripova, Aliya, Gilyazova, Irina, Mokrysheva, Natalia, Minniakhmetov, Ildar (2024)
, characterized by genetic heterogeneity and a complex molecular landscape, both of which contribute to its
Integrating Common Risk Factors with Polygenic Scores Improves the Prediction of Type 2 Diabetes
Timasheva, Y., Balkhiyarova, Z., Avzaletdinova, D., Rassoleeva, I., Morugova, T.V., Korytina, G., Prokopenko, I., Kochetova, O. (2023)
We tested associations between 13 established genetic variants and type 2 diabetes (T2D) in 1371
ГЕНЕТИЧЕСКИЕ АСПЕКТЫ СИНДРОМА МАРФАНА
GENETIC ASPECTS OF MARFAN SYNDROME
Акрамов, А.А., Akramova, А.А. (2024)
GENETIC ASPECTS OF MARFAN SYNDROME
IN SEARCH FOR GENETIC MARKERS OF NON-FAMILIA SICK SINUS SYNDROME
Zagidullin, N., Plechev, V., Badykova, E., Badykov, M., Akhmadishina, L., Korytina, G., Sagitov, I. (2019)
Background Sick sinus syndrome (SSS) can result from genetic and environmental factors. More than a

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