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Novel Genetic Risk Marker for Paranoid Schizophrenia in the Chromosomal Region 9q21.13 in Tatars: A Genome-Wide Association Analysis
Gareeva, A.E. (2024)
in higher functions, mainly to a change in cognitive functions and perception of reality. Both genetic
Genome-Wide Analysis of the Risk Association for the Development of Paranoid Schizophrenia in Russians: Search for Genetic Markers in the 1q43 Chromosomal Region
Gareeva, A.E. (2024)
Abstract: Schizophrenia is a highly hereditary disorder. Genetic risk is associated with a large
Genome-Wide Association Study: Analysis of Association of Polymorphic Loci in 4p15.2 and 20q13.31 Regions with Paranoid Schizophrenia
Gareeva, A.E. (2023)
of the genetic architecture of schizophrenia. The aim of this study was to study genetic risk factors
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)
topography and its thinning, stretching, and protrusion. The hereditary or genetic theory of keratoconus
MULTILOCUS ASSOCIATIONS OF INFLAMMATORY GENES WITH THE RISK OF TYPE 1 DIABETES
TIMASHEVA, Y.R., NASIBULLIN, T.R., MUSTAFINA, O.E., BALKHIYAROVA, Z.R., PROKOPENKO, I., AVZALETDINOVA, D.S., MORUGOVA, T.V. (2019)
Background Genome-wide association studies have captured a large proportion of genetic variation
Genetic Predisposition to Schizophrenia and Depressive Disorder Comorbidity
Shnayder, N.A., Novitsky, M.A., Neznanov, N.G., Limankin, O.V., Asadullin, A.R., Petrov, A.V., Dmitrenko, D.V., Narodova, E.A., Popenko, N.V., Nasyrova, R.F. (2022)
of the pathophysiology and/or genetic predictors of these mental disorders. The aim of this study was to review
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
МЕТОДЫ АНАЛИЗА ДНК
TECHNIQUES OF DNA ANALYSIS
Мухтарова, Л.Р., Мухаметзянова, А.А., Mukhtarova, L.R., Mukhametzyanova, A.A. (2024)
TECHNIQUES OF DNA ANALYSIS
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
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

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