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1.
Mol Psychiatry ; 24(8): 1099-1111, 2019 08.
Artigo em Inglês | MEDLINE | ID: mdl-30664668

RESUMO

We provide an overview of the recent achievements in psychiatric genetics research in the Russian Federation and present genotype-phenotype, population, epigenetic, cytogenetic, functional, ENIGMA, and pharmacogenetic studies, with an emphasis on genome-wide association studies. The genetic backgrounds of mental illnesses in the polyethnic and multicultural population of the Russian Federation are still understudied. Furthermore, genetic, genomic, and pharmacogenetic data from the Russian Federation are not adequately represented in the international scientific literature, are currently not available for meta-analyses and have never been compared with data from other populations. Most of these problems cannot be solved by individual centers working in isolation but warrant a truly collaborative effort that brings together all the major psychiatric genetic research centers in the Russian Federation in a national consortium. For this reason, we have established the Russian National Consortium for Psychiatric Genetics (RNCPG) with the aim to strengthen the power and rigor of psychiatric genetics research in the Russian Federation and enhance the international compatibility of this research.The consortium is set up as an open organization that will facilitate collaborations on complex biomedical research projects in human mental health in the Russian Federation and abroad. These projects will include genotyping, sequencing, transcriptome and epigenome analysis, metabolomics, and a wide array of other state-of-the-art analyses. Here, we discuss the challenges we face and the approaches we will take to unlock the huge potential that the Russian Federation holds for the worldwide psychiatric genetics community.


Assuntos
Colaboração Intersetorial , Transtornos Mentais/epidemiologia , Transtornos Mentais/genética , Pesquisa Biomédica , Estudo de Associação Genômica Ampla , Humanos , Saúde Mental/etnologia , Federação Russa/epidemiologia
2.
J Appl Genet ; 53(4): 389-413, 2012 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-22941515

RESUMO

Suicide is thought to result from the harmful interaction of multiple factors that have social, environmental, neurobiological, and genetic backgrounds. Recent studies have suggested that genetic predisposition to suicidal behavior may be independent of the risk of suicide associated to mental disorders, such as affective disorders, schizophrenia, or alcohol dependence. Given the suicidal behavior heterogeneity and its hereditary complexity, the need to find demonstrable intermediate phenotypes that may make it possible to establish links between genes and suicide behaviors (endophenotypes) seems to be necessary. The main objective of this review was to consider the candidate endophenotypes of suicidal behaviors. Due to the recent advances in neuroimaging, we also characterize brain regions implicated in vulnerability to suicide behavior that are influenced by gene polymorphisms associated with suicidal behavior.


Assuntos
Endofenótipos/análise , Predisposição Genética para Doença , Suicídio/psicologia , Alelos , Encéfalo/metabolismo , Encéfalo/patologia , Transtorno Depressivo Maior/diagnóstico , Endofenótipos/metabolismo , Epigênese Genética , Estudos de Associação Genética , Humanos , Ácido Hidroxi-Indolacético/líquido cefalorraquidiano , Comportamento Impulsivo/genética , Comportamento Impulsivo/psicologia , Polimorfismo Genético , Fatores de Risco , Proteínas da Membrana Plasmática de Transporte de Serotonina/genética , Proteínas da Membrana Plasmática de Transporte de Serotonina/metabolismo , Triptofano Hidroxilase/genética , Triptofano Hidroxilase/metabolismo
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