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Igor V Morozov

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Articles 26
Citations 149
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Recent Articles
1.
Borisova T, Cherdonova A, Pshennikova V, Teryutin F, Morozov I, Bondar A, et al.
Sci Rep . 2024 Jul; 14(1):15342. PMID: 38961196
Mitochondrial forms account approximately 1-2% of all nonsyndromic cases of hearing loss (HL). One of the most common causative variants of mtDNA is the m.1555A > G variant of the...
2.
Vorobyova A, Morozov I, Vasilchikova T, Zakharov K, Ovchenkov Y, Chistyakov G, et al.
Inorg Chem . 2024 Mar; 63(11):5199-5207. PMID: 38447157
New nitrosonium manganese(II) nitrate, (NO)Mn(NO), has been synthesized and structurally characterized. In the temperature range of 45-298 K, the crystal is hexagonal (centrosymmetric sp. gr. 6/). Mn ions are assembled...
3.
Pshennikova V, Teryutin F, Cherdonova A, Borisova T, Solovyev A, Romanov G, et al.
Genes (Basel) . 2023 May; 14(5). PMID: 37239361
The (Cx26) gene pathogenic variants are associated with autosomal recessive deafness type 1A (DFNB1A, OMIM #220290). Direct sequencing of the gene among 165 hearing-impaired individuals living in the Baikal Lake...
4.
Maltsev M, Aksenova S, Morozov I, Minenkov Y, Osina E
J Comput Chem . 2023 Jan; 44(12):1189-1198. PMID: 36708239
Argon compounds play an important role in the mass spectrometry with inductively coupled plasma and other applications. At the same time, there is a little knowledge of their electronic terms...
5.
Vorobyova A, Danilovich I, Morozov I, Vasiliev A, Volkova O, Iqbal A, et al.
Materials (Basel) . 2022 Oct; 15(20). PMID: 36295129
The appearance of electrically neutral water molecules in the structure of cobalt dinitrate dihydrate, Co(NO)⋅2HO, drastically changes its magnetic properties as compared to its waterless counterpart, Co(NO). The title compound...
6.
Danilchenko V, Zytsar M, Maslova E, Bady-Khoo M, Barashkov N, Morozov I, et al.
Diagnostics (Basel) . 2021 Dec; 11(12). PMID: 34943614
Hereditary hearing loss (HL) is known to be highly locus/allelic heterogeneous, and the prevalence of different HL forms significantly varies among populations worldwide. Investigation of region-specific landscapes of hereditary HL...
7.
Lavrinenko Y, Levashov P, Minakov D, Morozov I, Valuev I
Phys Rev E . 2021 Nov; 104(4-2):045304. PMID: 34781451
A joint simulation method based on the wave packet molecular dynamics and density functional theory (WPMD-DFT) is applied to study warm dense deuterium (nonideal deuterium plasmas). This method was developed...
8.
Barashkov N, Konovalov F, Borisova T, Teryutin F, Solovyev A, Pshennikova V, et al.
Eur J Hum Genet . 2021 Mar; 29(6):965-976. PMID: 33767456
Congenital autosomal recessive cataract with unknown genetic etiology is one of the most common Mendelian diseases among the Turkic-speaking Yakut population (Eastern Siberia, Russia). To identify the genetic cause of...
9.
Zytsar M, Bady-Khoo M, Danilchenko V, Maslova E, Barashkov N, Morozov I, et al.
Genes (Basel) . 2020 Jul; 11(7). PMID: 32708339
The mutations in the gene (13q12.11, MIM 121011) encoding transmembrane protein connexin 26 (Cx26) account for a significant portion of hereditary hearing loss worldwide. Earlier we found a high prevalence...
10.
Dryomov S, Starikovskaya E, Nazhmidenova A, Morozov I, Sukernik R
BMC Evol Biol . 2020 Jul; 20(1):83. PMID: 32660486
Background: We have described the diversity of complete mtDNA sequences from 'relic' groups of the Russian Far East, primarily the Nivkhi (who speak a language isolate with no clear relatedness...