Searching for new genes associated with the familial hypercholesterolemia phenotype using whole-genome sequencing and machine learning
Ivanoshchuk, D. E., Kolker, A. B., Timoshchenko, O. V., Semaev, S. E., Shakhtshneider, E. V.
Published in Vavilovskiĭ zhurnal genetiki i selekt͡s︡ii (01.09.2023)
Published in Vavilovskiĭ zhurnal genetiki i selekt͡s︡ii (01.09.2023)
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Journal Article
Polymorphism of the GLIS3 gene in a Caucasian population and among individuals with carbohydrate metabolism disorders in Russia
Shakhtshneider, E V, Mikhailova, S V, Ivanoshchuk, D E, Orlov, P S, Ovsyannikova, A K, Rymar, O D, Ragino, Yu I, Voevoda, M I
Published in BMC research notes (02.04.2018)
Published in BMC research notes (02.04.2018)
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Screening of West Siberian patients with primary congenital glaucoma for CYP1B1 gene mutations
Ivanoshchuk, D E, Mikhailova, S V, Fenkova, O G, Shakhtshneider, E V, Fursova, A Z, Bychkov, I Y, Voevoda, M I
Published in Vavilovskiĭ zhurnal genetiki i selekt͡s︡ii (01.12.2020)
Published in Vavilovskiĭ zhurnal genetiki i selekt͡s︡ii (01.12.2020)
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Journal Article
A rare splice site mutation in the gene encoding glucokinase/hexokinase 4 in a patient with MODY type 2
Ivanoshchuk, D E, Shakhtshneider, E V, Ovsyannikova, A K, Mikhailova, S V, Rymar, O D, Oblaukhova, V I, Yurchenko, A A, Voevoda, M I
Published in Vavilovskiĭ zhurnal genetiki i selekt͡s︡ii (01.05.2020)
Published in Vavilovskiĭ zhurnal genetiki i selekt͡s︡ii (01.05.2020)
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Journal Article
Molecular genetics of maturity-onset diabetes of the young
Voevoda, M I, Ivanova, A A, Shakhtshneider, E V, Ovsyannikova, A K, Mikhailova, S V, Astrakova, K S, Voevoda, S M, Rymar, O D
Published in Terapevtic̆eskii arhiv (01.01.2016)
Published in Terapevtic̆eskii arhiv (01.01.2016)
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Journal Article
Analysis of polymorphism of innate immunity receptor genes in patients with coronary atherosclerosis and in a population sample from Novosibirsk
Mikhailova, S. V., Ivanoshchuk, D. E., Orlov, P. S., Latyntseva, L. D., Kashtanova, E. V., Polonskaya, Ya. V., Ragino, Yu. I., Shakhtshneider, E. V.
Published in Sibirskiĭ nauchnyĭ medit︠s︡inskiĭ zhurnal (30.08.2023)
Published in Sibirskiĭ nauchnyĭ medit︠s︡inskiĭ zhurnal (30.08.2023)
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Journal Article
The frequency of metabolic syndrome and its individual components in women aged 25–45 years, depending on the level of prolactin
Rymar, O. D., Voevoda, S. M., Shakhtshneider, E. V., Stakhneva, E. M., Mustafina, S. V., Shcherbakova, L. V.
Published in Ozhirenie i metabolizm (24.07.2021)
Published in Ozhirenie i metabolizm (24.07.2021)
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Journal Article
GCK-MODY diabetes course in persons over 18 years of age: prospective observation
Ovsyannikova, A. K., Shakhtshneider, E. V., Ivanoshchuk, D. E., Voevoda, M. I., Rymar, O. D.
Published in Sakharnyĭ diabet (14.07.2021)
Published in Sakharnyĭ diabet (14.07.2021)
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Journal Article
Biochemical, molecular genetic and clinical aspects of COVID-2019
Kashtanova, E. V., Shakhtshneider, E. V., Kruchinina, M. V., Logvinenko, I. I., Striukova, E. V., Ragino, Yu. I.
Published in Bi͡u︡lletenʹ Sibirskoĭ medit͡s︡iny (12.04.2021)
Published in Bi͡u︡lletenʹ Sibirskoĭ medit͡s︡iny (12.04.2021)
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Journal Article
spectrum of mutations in the low-density lipoprotein receptor gene in the Russian population
Voevoda, M. I, Kulikov, I. V, Shakhtshneider, E. V, Maksimov, V. N, Pilipenko, I. V, Tereschenko, I. P, Kobzev, V. F, Romaschenko, A. G, Nikitin, Yu. P
Published in Russian journal of genetics (01.10.2008)
Published in Russian journal of genetics (01.10.2008)
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Journal Article
A Case of Maturity Onset Diabetes of the Young (MODY3) in a Family with a Novel HNF1A Gene Mutation in Five Generations
Ovsyannikova, A. K., Rymar, O. D., Ivanoshchuk, D. E., Mikhailova, Svetlana V., Shakhtshneider, E. V., Orlov, P. S., Malakhina, E. S., Voevoda, M. I.
Published in Diabetes therapy (01.02.2018)
Published in Diabetes therapy (01.02.2018)
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Journal Article
Role of IL13 genetic polymorphism in the development of bronchial asthma in children
Tereschenko, S. Yu, Smolnikova, M. V., Kasparov, E. V., Shakhtshneider, E. V., Malinchik, M. A., Konopleva, O. S., Smirnova, S. V.
Published in Medit͡s︡inskai͡a︡ immunologii͡a (01.12.2020)
Published in Medit͡s︡inskai͡a︡ immunologii͡a (01.12.2020)
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Journal Article
Analysis of f5 gene polymorphism in men with coronary atherosclerosis using whole exome sequencing
Striukova, E. S., Shakhtshneider, E. V., Ivanoshchuk, D. E., Ragino, Yu. I., Polonskaya, Ya. V., Murashov, I. S., Volkov, A. M., Kurguzov, A. V., Chernyavsky, A. M., Valeev, E. S., Maksimov, V. N., Kashtanova, E. V.
Published in Ateroskleroz (03.05.2021)
Published in Ateroskleroz (03.05.2021)
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Journal Article
Association of Level of Proprotein Convertase Subtilisin/Kexin Type 9 with Intima-Media Thickness in Patients with Familial Hypercholesterolemia
Benimetskaya, K. S., Ragino, Yu. I., Shakhtshneider, E. V., Makarenkova, K. V., Shchepina, Yu. V., Stakhneva, E. M., Voevoda, M. I.
Published in Bulletin of experimental biology and medicine (01.06.2017)
Published in Bulletin of experimental biology and medicine (01.06.2017)
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ANALYSIS OF DIFFERENTIAL ExPRESSION OF MATRIx METALLOPROTEASES IN STABLE AND UNSTABLE ATHEROSCLEROTIC LESIONS BY A METHOD OF FULL GENOME SEQUENCING OF RNA: PILOT STUDY
Ivanoschuk, D. Е., Ragino, Yu. I., Shakhtshneider, E. V., Mikhailova, S. V., Fishman, V. S., Polonskaya, Ya. V., Kashtanova, E. V., Chernyavsky, A. M., Murashov, I. S., Voevoda, М. I.
Published in Rossiĭskiĭ kardiologicheskiĭ zhurnal (09.09.2018)
Published in Rossiĭskiĭ kardiologicheskiĭ zhurnal (09.09.2018)
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Proprotein Convertase Subtilisin/Kexin-Type 9 (PCSK9) New Opportunities of Lipid-Lowering Therapy
Astrakova, K S, Ragino, Yu I, Shakhtshneider, E V, Voevoda, M I
Published in Kardiologiia (27.09.2016)
Published in Kardiologiia (27.09.2016)
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Blood Levels of Proprotein Convertase Subtilisin/Kexin Type 9 (PCSK9) in Men from Different Population Groups and Its Relation to Unfavorable Long-Term Prognosis
Ragino, Yu I, Astrakova, K S, Shakhtshneider, E V, Stakhneva, E M, Gafarov, V V, Bogatyrev, S N, Voevoda, M I
Published in Kardiologiia (01.04.2017)
Published in Kardiologiia (01.04.2017)
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