Oksana D Rymar (O D Rymar, Oksana Rymar)

Publication Activity (10 Years)

Years Active: 2019-2023
Publications (10 Years): 10

Top Topics

Genome Wide Analysis

Tyrosine Kinase

Top Venues

Journal of personalized medicine

Problemy endokrinologii

Terapevticheskii arkhiv

This page only lists publications with an associated author ORCID identifier.

Publications

Dinara E Ivanoshchuk, Elena V Shakhtshneider, Svetlana V Mikhailova, Alla Ovsyannikova, Oksana D Rymar, Emil Valeeva, Pavel Orlov, Mikhail I Voevoda
The Mutation Spectrum of Rare Variants in the Gene of Adenosine Triphosphate (ATP)-Binding Cassette Subfamily C Member 8 in Patients with a MODY Phenotype in Western Siberia. Journal of personalized medicine 13 (2) (2023)
Dinara E Ivanoshchuk, Elena V Shakhtshneider, Svetlana V Mikhailova, Alla Ovsyannikova, Oksana D Rymar, Emil Valeeva, Pavel Orlov, Mikhail I Voevoda
The Mutation Spectrum of Rare Variants in the Gene of Adenosine Triphosphate (ATP)-Binding Cassette Subfamily C Member 8 in Patients with a MODY Phenotype in Western Siberia. Journal of personalized medicine 13 (2) (2023)
Dinara E Ivanoshchuk, Elena V Shakhtshneider, Svetlana V Mikhailova, Alla Ovsyannikova, Oksana D Rymar, Emil Valeeva, Pavel Orlov, Mikhail I Voevoda
The Mutation Spectrum of Rare Variants in the Gene of Adenosine Triphosphate (ATP)-Binding Cassette Subfamily C Member 8 in Patients with a MODY Phenotype in Western Siberia. Journal of personalized medicine 13 (2) (2023)
Eugeniia Vitalievna Striukova, Lilia V Shcherbakova, Oksana D Rymar, Alena Dmitrievna Khudiakova, Viktoriya Sergeevna Shramko, Yuliya Igorevna Ragino
Triglycerides, Obesity and Education Status Are Associated with the Risk of Developing Type 2 Diabetes in Young Adults, Cohort Study. Journal of personalized medicine 13 (9) (2023)
Dinara E Ivanoshchuk, Elena V Shakhtshneider, Svetlana V Mikhailova, Alla Ovsyannikova, Oksana D Rymar, Emil Valeeva, Pavel Orlov, Mikhail I Voevoda
The Mutation Spectrum of Rare Variants in the Gene of Adenosine Triphosphate (ATP)-Binding Cassette Subfamily C Member 8 in Patients with a MODY Phenotype in Western Siberia. Journal of personalized medicine 13 (2) (2023)
Elena Mazurenko, Oksana D Rymar, Victor Rerikh, Yuliya Khrapova, Artem Direev, Liliya Shcherbakova, Sofia Malyutina
Risk Factors for Chronic Non-Communicable Diseases and Osteoporotic Fractures in a Middle and Elderly-Aged Population. Journal of personalized medicine 12 (9) (2022)
K Yu Nikolaev, A I Shevela, Svetlana V Mustafina, Oksana D Rymar, A K Ovsyannikova, E M Zelenskaya, A Y Kovaleva, G I Lifshits
The Impact of Hypoglycemic Therapy on the Prognosis for Acute Coronary Syndrome in Patients with Type 2 Diabetes. Journal of personalized medicine 12 (5) (2022)
E S Mel'nikova, Oksana D Rymar, A A Ivanova, Svetlana V Mustafina, Marina Shapkina, M Bobak, Sophia Malyutina, Mikhail I Voevoda, Vladimir N Maksimov
[Association of polymorphisms of genes TCF7L2, FABP2, KCNQ1, ADIPOQ with the prognosis of the development of type 2 diabetes mellitus]. Terapevticheskii arkhiv 92 (10) (2020)
Elena Mazurenko, Sophia Malyutina, L V Shcherbakova, Svetlana V Mustafina, T M Nikitenko, Martin Bobak, Oksana D Rymar
[Erratum: The forearm fractures in patients with diabetes and without diabetes in population sample aged over 50 years (Novosibirsk) (Problems of Endocrinology (2019) 65(2) DOI: 10.14341/probl9799)]. Problemy endokrinologii 65 (4) (2019)
Elena Mazurenko, Sophia Malyutina, L V Shcherbakova, Svetlana V Mustafina, T M Nikitenko, Martin Bobak, Oksana D Rymar
[The forearm fractures in patients with diabetes and without diabetes in population sample aged over 50 years (Novosibirsk)]. Problemy endokrinologii 65 (2) (2019)