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  1. Article ; Online: PSReliP: an integrated pipeline for analysis and visualization of population structure and relatedness based on genome-wide genetic variant data.

    Solovieva, Elena / Sakai, Hiroaki

    BMC bioinformatics

    2023  Volume 24, Issue 1, Page(s) 135

    Abstract: Background: Population structure and cryptic relatedness between individuals (samples) are two major factors affecting false positives in genome-wide association studies (GWAS). In addition, population stratification and genetic relatedness in genomic ... ...

    Abstract Background: Population structure and cryptic relatedness between individuals (samples) are two major factors affecting false positives in genome-wide association studies (GWAS). In addition, population stratification and genetic relatedness in genomic selection in animal and plant breeding can affect prediction accuracy. The methods commonly used for solving these problems are principal component analysis (to adjust for population stratification) and marker-based kinship estimates (to correct for the confounding effects of genetic relatedness). Currently, many tools and software are available that analyze genetic variation among individuals to determine population structure and genetic relationships. However, none of these tools or pipelines perform such analyses in a single workflow and visualize all the various results in a single interactive web application.
    Results: We developed PSReliP, a standalone, freely available pipeline for the analysis and visualization of population structure and relatedness between individuals in a user-specified genetic variant dataset. The analysis stage of PSReliP is responsible for executing all steps of data filtering and analysis and contains an ordered sequence of commands from PLINK, a whole-genome association analysis toolset, along with in-house shell scripts and Perl programs that support data pipelining. The visualization stage is provided by Shiny apps, an R-based interactive web application. In this study, we describe the characteristics and features of PSReliP and demonstrate how it can be applied to real genome-wide genetic variant data.
    Conclusions: The PSReliP pipeline allows users to quickly analyze genetic variants such as single nucleotide polymorphisms and small insertions or deletions at the genome level to estimate population structure and cryptic relatedness using PLINK software and to visualize the analysis results in interactive tables, plots, and charts using Shiny technology. The analysis and assessment of population stratification and genetic relatedness can aid in choosing an appropriate approach for the statistical analysis of GWAS data and predictions in genomic selection. The various outputs from PLINK can be used for further downstream analysis. The code and manual for PSReliP are available at https://github.com/solelena/PSReliP .
    MeSH term(s) Animals ; Genome-Wide Association Study/methods ; Software ; Genomics/methods ; Genome ; Workflow
    Language English
    Publishing date 2023-04-05
    Publishing country England
    Document type Journal Article
    ZDB-ID 2041484-5
    ISSN 1471-2105 ; 1471-2105
    ISSN (online) 1471-2105
    ISSN 1471-2105
    DOI 10.1186/s12859-023-05169-4
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article: Lechenie bol'nykh s posledstviyami cherepno-mozgovoi travmy.

    Solovieva, E Yu / Karneev, A N / Amelina, I P

    Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova

    2023  Volume 123, Issue 3, Page(s) 26–33

    Abstract: Traumatic brain injury (TBI) is one of the leading causes of neurological morbidity, disability and mortality in all age groups of the population. As a result of the general increase in the number of cases of brain injuries, there is a significant ... ...

    Title translation Treatment of diseases with consequences of traumatic brain injury.
    Abstract Traumatic brain injury (TBI) is one of the leading causes of neurological morbidity, disability and mortality in all age groups of the population. As a result of the general increase in the number of cases of brain injuries, there is a significant increase in the consequences of TBI, the dominant part of which is asthenic, vegetative, cognitive, emotional and liquorodynamic disorders. Therapeutic measures in the long-term period of TBI should be carried out intensively as in the first 12 months. after TBI, and in the future, considering the ongoing processes of morphofunctional maturation of the CNS and high brain plasticity, especially in childhood. Syndromic treatment should be differentiated and pathogenetically substantiated. The article covers in detail the modern methods of drug therapy in patients with remote residual effects of brain injury. The high efficiency of the use of the neuroprotective drug Cortexin in the correction of the consequences of TBI was shown.
    MeSH term(s) Humans ; Brain Injuries, Traumatic/complications ; Brain Injuries, Traumatic/drug therapy ; Brain Injuries ; Longitudinal Studies ; Neuronal Plasticity ; Neuroprotective Agents
    Chemical Substances Neuroprotective Agents
    Language Russian
    Publishing date 2023-02-16
    Publishing country Russia (Federation)
    Document type English Abstract ; Journal Article
    ZDB-ID 1201462-x
    ISSN 2309-4729 ; 1997-7298 ; 0044-4588
    ISSN (online) 2309-4729
    ISSN 1997-7298 ; 0044-4588
    DOI 10.17116/jnevro202312303126
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article: Okislitel'nyĭ stress i vospalenie kak zven'ia odnoĭ tsepi u bol'nykh s khronicheskimi tserebrovaskuliarnymi zabolevaniiami.

    Amelina, I P / Solovieva, E Yu

    Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova

    2019  Volume 119, Issue 4, Page(s) 106–114

    Abstract: Cerebrovascular diseases (CVD) are the main cause of death and permanent disability. The urgency of the problem of chronic CVD is associated with an increase of the absolute number of elderly and senile age in the population, a trend towards slowly ... ...

    Title translation Oxidative stress and inflammation as links in a chain in patients with chronic cerebrovascular diseases.
    Abstract Cerebrovascular diseases (CVD) are the main cause of death and permanent disability. The urgency of the problem of chronic CVD is associated with an increase of the absolute number of elderly and senile age in the population, a trend towards slowly increasing, sluggish pathological processes. It is obvious that any somatic disease in such patients is comorbid to cerebrovascular diseases that suggests a unified mechanism of the pathogenesis for both the main and concomitant diseases. The article notes that microangiopathy is the most common cause of CVD. The main etiopathogenetic factor affecting cerebral vessels of small caliber is endothelial dysfunction, systemic inflammation and oxidative stress. Understanding the molecular components that underlie functional abnormalities and damage of small blood vessels gives the key to the modern strategies in therapy, forming the foundation for an adequate pathogenetically justified therapy. This impact should be gradual, complex and aimed at correcting pathochemical disorders in general and neurotransmitter imbalance in particular. The drug dipyridamole, which has pleiotropic effects, can be considered as one of the pathogenetically justified means in complex drug therapy in patients with CVD.
    MeSH term(s) Aged ; Cerebrovascular Disorders/immunology ; Cerebrovascular Disorders/metabolism ; Chronic Disease ; Comorbidity ; Humans ; Inflammation ; Oxidative Stress
    Language Russian
    Publishing date 2019-06-03
    Publishing country Russia (Federation)
    Document type Journal Article
    ZDB-ID 1201462-x
    ISSN 2309-4729 ; 1997-7298 ; 0044-4588
    ISSN (online) 2309-4729
    ISSN 1997-7298 ; 0044-4588
    DOI 10.17116/jnevro2019119041106
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article: Vizualizatsiya mozgovoi aktivnosti s pomoshch'yu fMRT u patsientki s sub"ektivnym kognitivnym snizheniem.

    Solovieva, E Yu / Vorob'eva, O V / Fateeva, V V / Skipetrova, L A

    Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova

    2023  Volume 123, Issue 4, Page(s) 125–129

    Abstract: In clinical practice, subjective cognitive decline (SCD) is often difficult to diagnose because it is not detected by standard neuropsychological and cognitive tests.The described clinical case is presented to demonstrate the difficulties of diagnosis ... ...

    Title translation Imaging of brain activity using fMRI in a patient with subjective cognitive decline.
    Abstract In clinical practice, subjective cognitive decline (SCD) is often difficult to diagnose because it is not detected by standard neuropsychological and cognitive tests.The described clinical case is presented to demonstrate the difficulties of diagnosis and treatment choice in a patient with SCD. fMRI might be considered as an instrumental method to analyze the functional relationship between the activity of brain structures and cerebral circulation in patients with SCD. Patient clinical and neuropsychological data with a detailed description of fMRI with a cognitive paradigm are presented. The article is focused on the early diagnosis of SCD and the prognostic assessment of the transition of SCD to dementia.
    MeSH term(s) Humans ; Magnetic Resonance Imaging ; Cognitive Dysfunction/etiology ; Neuropsychological Tests ; Brain/diagnostic imaging
    Language Russian
    Publishing date 2023-04-21
    Publishing country Russia (Federation)
    Document type English Abstract ; Journal Article
    ZDB-ID 1201462-x
    ISSN 2309-4729 ; 1997-7298 ; 0044-4588
    ISSN (online) 2309-4729
    ISSN 1997-7298 ; 0044-4588
    DOI 10.17116/jnevro2023123041125
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article: Developing core marker sets for effective genomic-assisted selection in wheat and barley breeding programs.

    Ishikawa, Goro / Sakai, Hiroaki / Mizuno, Nobuyuki / Solovieva, Elena / Tanaka, Tsuyoshi / Matsubara, Kazuki

    Breeding science

    2022  Volume 72, Issue 3, Page(s) 257–266

    Abstract: Wheat ( ...

    Abstract Wheat (
    Language English
    Publishing date 2022-06-29
    Publishing country Japan
    Document type Journal Article
    ZDB-ID 1190370-3
    ISSN 1344-7610 ; 0536-3683
    ISSN 1344-7610 ; 0536-3683
    DOI 10.1270/jsbbs.22004
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article: Vliyanie khronicheskoi boli pri osteoartrite na risk razvitiya serdechno-sosudistykh zabolevanii i sovremennye sposoby ikh lekarstvennoi profilaktiki.

    Sarvilina, I V / Danilov, Al B / Tkacheva, O N / Gromova, O A / Solovieva, E Yu / Dudinskaya, E N / Rozanov, A V / Kartashova, E A

    Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova

    2023  Volume 123, Issue 5, Page(s) 20–30

    Abstract: The purpose of the review of scientific medical literature was to evaluate the data of the epidemiology of osteoarthritis (OA) and cardiovascular diseases (CVD) with the analysis of risk factors, pathophysiological and pathobiochemical mechanisms of the ... ...

    Title translation Influence of chronic pain in osteoarthritis on the risk of cardiovascular diseases and modern methods of drug prevention.
    Abstract The purpose of the review of scientific medical literature was to evaluate the data of the epidemiology of osteoarthritis (OA) and cardiovascular diseases (CVD) with the analysis of risk factors, pathophysiological and pathobiochemical mechanisms of the relationship between OA and the risk of developing CVD in the presence of chronic pain, modern strategies for screening and management of this cohort of patients, the mechanism of action and pharmacological effects of chondroitin sulfate (CS). Conclusions were drawn about the need for additional clinical and observational studies of the efficacy and safety of the parenteral form of CS (Chondroguard) in patients with chronic pain in OA and CVD, improvement of clinical recommendations for the treatment of chronic pain in patients with OA and cardiovascular risk, with special attention to interventions that eliminate mobility restrictions in patients and the inclusion of basic and adjuvant therapy with DMOADs to achieve the goals of multipurpose monotherapy in patients with contraindications to standard therapy drugs.
    MeSH term(s) Humans ; Chronic Pain/drug therapy ; Chronic Pain/epidemiology ; Chronic Pain/etiology ; Cardiovascular Diseases/epidemiology ; Cardiovascular Diseases/etiology ; Cardiovascular Diseases/prevention & control ; Osteoarthritis/complications ; Osteoarthritis/drug therapy ; Osteoarthritis/epidemiology ; Chondroitin Sulfates ; Combined Modality Therapy
    Chemical Substances Chondroitin Sulfates (9007-28-7)
    Language Russian
    Publishing date 2023-06-14
    Publishing country Russia (Federation)
    Document type Review ; English Abstract ; Journal Article
    ZDB-ID 1201462-x
    ISSN 2309-4729 ; 1997-7298 ; 0044-4588
    ISSN (online) 2309-4729
    ISSN 1997-7298 ; 0044-4588
    DOI 10.17116/jnevro202312305120
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article: Family case of Potocki-Lupski syndrome.

    Kolbasin, L N / Dubrovskaya, T A / Salnikova, G B / Solovieva, E N / Donnikov, M Yu / Illarionov, R A / Glotov, A S / Kovalenko, L V / Belotserkovtseva, L D

    Molecular cytogenetics

    2024  Volume 17, Issue 1, Page(s) 6

    Abstract: Background: Potocki-Lupski syndrome (PTLS, OMIM # 610883) is a rare genetic developmental disorder resulting from a partial heterozygous microduplication at chromosome 17p11.2. The condition is characterized by a wide variability of clinical expression, ...

    Abstract Background: Potocki-Lupski syndrome (PTLS, OMIM # 610883) is a rare genetic developmental disorder resulting from a partial heterozygous microduplication at chromosome 17p11.2. The condition is characterized by a wide variability of clinical expression, which can make its clinical and molecular diagnosis challenging.
    Case presentation: We report here a family (mother and her two children) diagnosed with PTLS. When examining children, neurological and psychological (neuropsychiatric) manifestations (speech delay, mild mental retardation), motor disorders, craniofacial dysmorphism (microcephaly, dolichocephaly, triangular face, wide bulging forehead, long chin, antimongoloid slant, "elfin" ears) were revealed. The suspected clinical diagnosis was confirmed by MLPA and CMA molecular genetic testing which revealed the presence of a segmental aneusomy; microduplication in the 17p11.2 region.
    Conclusions: Children with PTLS can have a clinically recognizable and specific phenotype: craniofacial dysmorphism, motor and neurological manifestations, which may implicate a possible genetic disease to the attending physician. Moreover, each child with this syndrome is unique and may have a different clinical picture. The management of such patients requires a multidisciplinary team approach, including medical genetic counseling.
    Language English
    Publishing date 2024-03-22
    Publishing country England
    Document type Journal Article
    ZDB-ID 2420849-8
    ISSN 1755-8166
    ISSN 1755-8166
    DOI 10.1186/s13039-024-00673-5
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article ; Online: GGDonto ontology as a knowledge-base for genetic diseases and disorders of glycan metabolism and their causative genes.

    Solovieva, Elena / Shikanai, Toshihide / Fujita, Noriaki / Narimatsu, Hisashi

    Journal of biomedical semantics

    2018  Volume 9, Issue 1, Page(s) 14

    Abstract: Background: Inherited mutations in glyco-related genes can affect the biosynthesis and degradation of glycans and result in severe genetic diseases and disorders. The Glyco-Disease Genes Database (GDGDB), which provides information about these diseases ... ...

    Abstract Background: Inherited mutations in glyco-related genes can affect the biosynthesis and degradation of glycans and result in severe genetic diseases and disorders. The Glyco-Disease Genes Database (GDGDB), which provides information about these diseases and disorders as well as their causative genes, has been developed by the Research Center for Medical Glycoscience (RCMG) and released in April 2010. GDGDB currently provides information on about 80 genetic diseases and disorders caused by single-gene mutations in glyco-related genes. Many biomedical resources provide information about genetic disorders and genes involved in their pathogenesis, but resources focused on genetic disorders known to be related to glycan metabolism are lacking. With the aim of providing more comprehensive knowledge on genetic diseases and disorders of glycan biosynthesis and degradation, we enriched the content of the GDGDB database and improved the methods for data representation.
    Results: We developed the Genetic Glyco-Diseases Ontology (GGDonto) and a RDF/SPARQL-based user interface using Semantic Web technologies. In particular, we represented the GGDonto content using Semantic Web languages, such as RDF, RDFS, SKOS, and OWL, and created an interactive user interface based on SPARQL queries. This user interface provides features to browse the hierarchy of the ontology, view detailed information on diseases and related genes, and find relevant background information. Moreover, it provides the ability to filter and search information by faceted and keyword searches.
    Conclusions: Focused on the molecular etiology, pathogenesis, and clinical manifestations of genetic diseases and disorders of glycan metabolism and developed as a knowledge-base for this scientific field, GGDonto provides comprehensive information on various topics, including links to aid the integration with other scientific resources. The availability and accessibility of this knowledge will help users better understand how genetic defects impact the metabolism of glycans as well as how this impaired metabolism affects various biological functions and human health. In this way, GGDonto will be useful in fields related to glycoscience, including cell biology, biotechnology, and biomedical, and pharmaceutical research.
    MeSH term(s) Databases, Genetic ; Disease/genetics ; Gene Ontology ; Internet ; Knowledge Bases ; Mutation ; Polysaccharides/biosynthesis ; Polysaccharides/metabolism ; User-Computer Interface
    Chemical Substances Polysaccharides
    Language English
    Publishing date 2018-04-18
    Publishing country England
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2548651-2
    ISSN 2041-1480 ; 2041-1480
    ISSN (online) 2041-1480
    ISSN 2041-1480
    DOI 10.1186/s13326-018-0182-0
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  9. Article: [From the conception of «oxidizing stress» to the conception of «cell signaling modulation»].

    Solovieva, E Yu / Chipova, D T

    Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova

    2015  Volume 115, Issue 8, Page(s) 105–111

    Abstract: We discuss the current conception of "oxidizing stress" which covers a wide group of various interrelated phenomena including higher production of reactive oxygen species (ROS) and oxidative damage of cellular molecular components. Currently the term of ... ...

    Abstract We discuss the current conception of "oxidizing stress" which covers a wide group of various interrelated phenomena including higher production of reactive oxygen species (ROS) and oxidative damage of cellular molecular components. Currently the term of oxidizing stress is used for the description of pro-oxidant and antioxidant imbalance, with the prevalence of the former, that results in the damage of biological molecules and cellular structures. However ROS do not play a single role in oxidative metabolism. There are also active nitrogen forms, reactive forms of carbon, chlorine and sulphur. These highly reactive molecules are involved in many reactions and play a great role in the regulation of different metabolic processes in the body. These reactions underlie such pathological processes as heart ischemia, atherosclerosis, cerebral ischemia and different types of inflammation. An effect of highly reactive molecules on the destruction of biologically important molecular in different stressful conditions is determined by the reactions they are involved in. But the balance of oxidizers and antioxidants should not be considered as a unified system because main cellular redox systems are not in the redox equilibrium. In this view, a search for an optimal oxidizer that impacts on the modulation of cellular signal pathways related with ROS development is the most effective way in the development of antioxidant therapy.
    MeSH term(s) Antioxidants/pharmacology ; Antioxidants/therapeutic use ; Atherosclerosis/metabolism ; Brain Ischemia/metabolism ; Humans ; Inflammation/metabolism ; Myocardial Ischemia/metabolism ; Oxidation-Reduction ; Oxidative Stress ; Reactive Oxygen Species/metabolism ; Signal Transduction
    Chemical Substances Antioxidants ; Reactive Oxygen Species
    Language Russian
    Publishing date 2015
    Publishing country Russia (Federation)
    Document type English Abstract ; Journal Article ; Review
    ZDB-ID 1201462-x
    ISSN 2309-4729 ; 1997-7298 ; 0044-4588
    ISSN (online) 2309-4729
    ISSN 1997-7298 ; 0044-4588
    DOI 10.17116/jnevro201511581105-111
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  10. Article: Odnostoronniĭ kriptoftal'm (kliniko-morfologicheskoe issledovanie).

    Kulbaev, N D / Solovieva, E P / Kutushev, R Z / Volgareva, E A

    Vestnik oftalmologii

    2019  Volume 135, Issue 2, Page(s) 102–107

    Abstract: Cryptophthalmos is a rare ocular cup malformation, which is classified among autosomal dominant inherited diseases, but often it occurs sporadically. The pathology is characterized by the absence of eyelids or palpebral fissure or their hypoplasia, as ... ...

    Title translation Unilateral cryptophthalmos (a clinical and morphological study).
    Abstract Cryptophthalmos is a rare ocular cup malformation, which is classified among autosomal dominant inherited diseases, but often it occurs sporadically. The pathology is characterized by the absence of eyelids or palpebral fissure or their hypoplasia, as well as by abnormal development of the eye, especially of its anterior segment. The article describes a case of total cryptophthalmos without any associated malformations, with macrophthalmos on the right eye and abortive cryptophthalmos on the left in a one-year old girl. A pathomorphological investigation of the enucleated right eyeball was carried out.
    MeSH term(s) Eyelids ; Female ; Humans ; Infant ; Microphthalmos ; Orbit
    Language Russian
    Publishing date 2019-06-19
    Publishing country Russia (Federation)
    Document type Case Reports ; Journal Article
    ZDB-ID 962921-x
    ISSN 0042-465X
    ISSN 0042-465X
    DOI 10.17116/oftalma2019135021102
    Database MEDical Literature Analysis and Retrieval System OnLINE

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