T. E. Ivashchenko
Russian Academy
35 Papers
82 Citations
T. E. Ivashchenko is an academic researcher from Russian Academy. The author has contributed to research in topics: Population & Allele. The author has an hindex of 7, co-authored 31 publications.
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Papers
Whole‑exome sequencing in Russian children with non‑type 1 diabetes mellitus reveals a wide spectrum of genetic variants in MODY‑related and unrelated genes
Oleg S. Glotov,Elena A. Serebryakova,Mariia E. Turkunova,Olga A. Efimova,Andrey S. Glotov,Yury A. Barbitoff,Yulia A. Nasykhova,Alexander V. Predeus,Dmitrii E. Polev,Mikhail A. Fedyakov,Irina V. Polyakova,T. E. Ivashchenko,Natalia Yu. Shved,Elena S. Shabanova,Alena V. Tiselko,Olga V. Romanova,Andrey M. Sarana,Anna A. Pendina,Sergey G. Scherbak,Ekaterina V. Musina,Anastasiia V. Petrovskaia‑Kaminskaia,Liubov R. Lonishin,Liliya V. Ditkovskaya,Liudmila А. Zhelenina,Ludmila V. Tyrtova,Olga Berseneva,Rostislav K. Skitchenko,Evgenii N. Suspitsin,Elena B. Bashnina,V. S. Baranov +29 more
TL;DR: The prevalence of GCK variants indicates that diagnostics of monogenic diabetes in Russian children may begin with testing for MODY2, highlighting the efficiency of using whole-exome sequencing in non-GCK-MODY cases.
Frequency and Spectrum of MED12 Exon 2 Mutations in Multiple Versus Solitary Uterine Leiomyomas From Russian Patients.
Natalia S. Osinovskaya,Olga V. Malysheva,Natalia Yu. Shved,T. E. Ivashchenko,Iskender Yu. Sultanov,Olga A. Efimova,Maria I. Yarmolinskaya,Vitaly F. Bezhenar,V. S. Baranov +8 more
TL;DR: The frequency and the spectrum of MED12 exon 2 mutations between multiple and solitary ULs from Russian patients are compared to suggest that to clearly understand UL pathogenesis, solitary and multiple tumors should probably be analyzed as separate sets.
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MED12 gene mutations in women with uterine myoma
N. S. Osinovskaya,T. E. Ivashchenko,A. K. Dolinskii,I. Yu. Sultanov,Svetlana Ghimbovschi,Eric P. Hoffman,V. F. Bezhenar,Vladislav S Baranov +7 more
TL;DR: It was shown that somatic mutations in the MED12 gene occur in 73% of cases with deletions of varying sizes and missense mutations being most common at codon 44.
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Catechol-O-methyltransferase Val158Met polymorphism is associated with increased risk of multiple uterine leiomyomas either positive or negative for MED12 exon 2 mutations
Lyailya Kh. Dzhemlikhanova,Olga A. Efimova,Natalia S. Osinovskaya,Sergey E. Parfenyev,Dariko A. Niauri,Iskender Yu. Sultanov,Olga V. Malysheva,Anna A. Pendina,Natalia Yu. Shved,T. E. Ivashchenko,Maria I. Yarmolinskaya,Maka I. Kakhiani,Ekaterina A. Gorovaya,Antonina N. Tkachenko,V. S. Baranov +14 more
TL;DR: Women with COMT Val/Val genotype are at high risk of developing multiple uterine fibroids either positive or negative for MED12 exon 2 mutations.
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•Journal Article
[Renin-angiotensin and kinin-bradykinin genes polymorphism effects on permanent arterial hypertension in children].
TL;DR: The method proved that polymorphism of renin-angiotensin and kinin-bradikynin gene systems renders essential influence on formation of stably raised arterial pressure in girls.
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