<?xml version="1.0" encoding="UTF-8"?>
<!DOCTYPE article PUBLIC "-//NLM//DTD JATS (Z39.96) Journal Publishing DTD v1.3 20210610//EN" "JATS-journalpublishing1-3.dtd">
<article article-type="research-article" dtd-version="1.3" xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xml:lang="ru"><front><journal-meta><journal-id journal-id-type="publisher-id">medgen</journal-id><journal-title-group><journal-title xml:lang="ru">Медицинская генетика</journal-title><trans-title-group xml:lang="en"><trans-title>Medical Genetics</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">2073-7998</issn><publisher><publisher-name>Publishing House «Genius Media» LLC</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.25557/2073-7998.2024.02.3-13</article-id><article-id custom-type="elpub" pub-id-type="custom">medgen-2417</article-id><article-categories><subj-group subj-group-type="heading"><subject>Research Article</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="ru"><subject>НАУЧНЫЙ ОБЗОР</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>REVIEW</subject></subj-group></article-categories><title-group><article-title>Роль геномики в прогнозировании нейропсихических расстройств</article-title><trans-title-group xml:lang="en"><trans-title>The role of genomics in predicting neuropsychic disorders</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Миннигалиев</surname><given-names>В. М.</given-names></name><name name-style="western" xml:lang="en"><surname>Minnigaliev</surname><given-names>V. M.</given-names></name></name-alternatives><bio xml:lang="ru"><p>450008, г.Уфа, ул. Ленина, д. 3</p></bio><bio xml:lang="en"><p>3, Lenina st., Ufa, 450008</p></bio><email xlink:type="simple">vkomissiya@inbox.ru</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Хамадуллина</surname><given-names>З. А.</given-names></name><name name-style="western" xml:lang="en"><surname>Khamadullina</surname><given-names>Z. A.</given-names></name></name-alternatives><bio xml:lang="ru"><p>450008, г.Уфа, ул. Ленина, д. 3</p></bio><bio xml:lang="en"><p>3, Lenina st., Ufa, 450008</p></bio><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Ширинян</surname><given-names>С. А.</given-names></name><name name-style="western" xml:lang="en"><surname>Shirinyan</surname><given-names>S. A.</given-names></name></name-alternatives><bio xml:lang="ru"><p>119048, г. Москва, ул. Трубецкая, д. 8, стр. 2</p></bio><bio xml:lang="en"><p>8-2, Trubetskaya st.,  Moscow, 119991</p></bio><xref ref-type="aff" rid="aff-2"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Бакиева</surname><given-names>А. А.</given-names></name><name name-style="western" xml:lang="en"><surname>Bakieva</surname><given-names>A. A.</given-names></name></name-alternatives><bio xml:lang="ru"><p>450008, г.Уфа, ул. Ленина, д. 3</p></bio><bio xml:lang="en"><p>3, Lenina st., Ufa, 450008</p></bio><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Исламова</surname><given-names>Э. И.</given-names></name><name name-style="western" xml:lang="en"><surname>Islamova</surname><given-names>E. I.</given-names></name></name-alternatives><bio xml:lang="ru"><p>344022, г. Ростов-на-Дону, пер. Нахичеванский, д. 29</p></bio><bio xml:lang="en"><p>29, Nakhichevansky Lane, Rostov-on-Don, 344022</p></bio><xref ref-type="aff" rid="aff-3"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Махортых</surname><given-names>Е. К.</given-names></name><name name-style="western" xml:lang="en"><surname>Makhortykh</surname><given-names>E. K.</given-names></name></name-alternatives><bio xml:lang="ru"><p>344022, г. Ростов-на-Дону, пер. Нахичеванский, д. 29</p></bio><bio xml:lang="en"><p>29, Nakhichevansky Lane, Rostov-on-Don, 344022</p></bio><xref ref-type="aff" rid="aff-3"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Гаязова</surname><given-names>Г. А.</given-names></name><name name-style="western" xml:lang="en"><surname>Gayazova</surname><given-names>G. A.</given-names></name></name-alternatives><bio xml:lang="ru"><p>450008, г.Уфа, ул. Ленина, д. 3</p></bio><bio xml:lang="en"><p>3, Lenina st., Ufa, 450008</p></bio><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Сагындыкова</surname><given-names>К. И.</given-names></name><name name-style="western" xml:lang="en"><surname>Sagyndykova</surname><given-names>K. I.</given-names></name></name-alternatives><bio xml:lang="ru"><p>450008, г.Уфа, ул. Ленина, д. 3</p></bio><bio xml:lang="en"><p>3, Lenina st., Ufa, 450008</p></bio><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Кукасова</surname><given-names>П. М.</given-names></name><name name-style="western" xml:lang="en"><surname>Kukasova</surname><given-names>P. M.</given-names></name></name-alternatives><bio xml:lang="ru"><p>450008, г.Уфа, ул. Ленина, д. 3</p></bio><bio xml:lang="en"><p>3, Lenina st., Ufa, 450008</p></bio><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Уморина</surname><given-names>Ю. О.</given-names></name><name name-style="western" xml:lang="en"><surname>Umorina</surname><given-names>Yu. O.</given-names></name></name-alternatives><bio xml:lang="ru"><p>430005, г. Саранск, ул. Большевистская, д. 68</p></bio><bio xml:lang="en"><p>68, Bolshevistskaya st., Saransk 430005, Republic of Mordovia</p></bio><xref ref-type="aff" rid="aff-4"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Чадаева</surname><given-names>Д. А.</given-names></name><name name-style="western" xml:lang="en"><surname>Chadaeva</surname><given-names>D. A.</given-names></name></name-alternatives><bio xml:lang="ru"><p>430005, г. Саранск, ул. Большевистская, д. 68</p></bio><bio xml:lang="en"><p>68, Bolshevistskaya st., Saransk 430005, Republic of Mordovia</p></bio><xref ref-type="aff" rid="aff-4"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Тишкина</surname><given-names>Е. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Tishkina</surname><given-names>E. V.</given-names></name></name-alternatives><bio xml:lang="ru"><p>430005, г. Саранск, ул. Большевистская, д. 68</p></bio><bio xml:lang="en"><p>68, Bolshevistskaya st., Saransk 430005, Republic of Mordovia</p></bio><xref ref-type="aff" rid="aff-4"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>Башкирский государственный медицинский университет</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Bashkir state medical university</institution><country>Russian Federation</country></aff></aff-alternatives><aff-alternatives id="aff-2"><aff xml:lang="ru"><institution>Первый Московский государственный медицинский университет им. И.М. Сеченова (Сеченовский университет)</institution><country>Россия</country></aff><aff xml:lang="en"><institution>I.M. Sechenov First Moscow state medical university</institution><country>Russian Federation</country></aff></aff-alternatives><aff-alternatives id="aff-3"><aff xml:lang="ru"><institution>Ростовский государственный медицинский университет</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Rostov state medical university</institution><country>Russian Federation</country></aff></aff-alternatives><aff-alternatives id="aff-4"><aff xml:lang="ru"><institution>Национальный исследовательский Мордовский государственный университет им. Н.П. Огарёва</institution><country>Россия</country></aff><aff xml:lang="en"><institution>National Research Ogarev Mordovia State University</institution><country>Russian Federation</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2024</year></pub-date><pub-date pub-type="epub"><day>25</day><month>03</month><year>2024</year></pub-date><volume>23</volume><issue>2</issue><fpage>3</fpage><lpage>13</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Миннигалиев В.М., Хамадуллина З.А., Ширинян С.А., Бакиева А.А., Исламова Э.И., Махортых Е.К., Гаязова Г.А., Сагындыкова К.И., Кукасова П.М., Уморина Ю.О., Чадаева Д.А., Тишкина Е.В., 2024</copyright-statement><copyright-year>2024</copyright-year><copyright-holder xml:lang="ru">Миннигалиев В.М., Хамадуллина З.А., Ширинян С.А., Бакиева А.А., Исламова Э.И., Махортых Е.К., Гаязова Г.А., Сагындыкова К.И., Кукасова П.М., Уморина Ю.О., Чадаева Д.А., Тишкина Е.В.</copyright-holder><copyright-holder xml:lang="en">Minnigaliev V.M., Khamadullina Z.A., Shirinyan S.A., Bakieva A.A., Islamova E.I., Makhortykh E.K., Gayazova G.A., Sagyndykova K.I., Kukasova P.M., Umorina Y.O., Chadaeva D.A., Tishkina E.V.</copyright-holder><license xml:lang="ru" license-type="creative-commons-attribution" xlink:href="https://creativecommons.org/licenses/by/4.0/" xlink:type="simple"><license-p>Данная работа распространяется под лицензией Creative Commons Attribution 4.0.</license-p></license><license xml:lang="en" license-type="creative-commons-attribution" xlink:href="https://creativecommons.org/licenses/by/4.0/" xlink:type="simple"><license-p>This work is licensed under a Creative Commons Attribution 4.0 License.</license-p></license></permissions><self-uri xlink:href="https://www.medgen-journal.ru/jour/article/view/2417">https://www.medgen-journal.ru/jour/article/view/2417</self-uri><abstract><p>Психические расстройства являются одним из важнейших вызовов для современной медицины. Несмотря на то, что психические заболевания не вносят значительного вклада в смертность населения, они оказывают важное влияние на качество жизни пациентов, а также на общественное здоровье и экономику. Согласно данным статистических исследований около 40% населения России имеют симптомы психических расстройств, а 5% нуждаются в лечении.  По мере развития психиатрической геномики продолжают развиваться и модели прогнозирования риска заболеваний. Накопление и статистический анализ больших данных, включающих результаты глубокого фенотипирования, картирования траекторий развития,   генотипирования большого количества индивидуумов будут способствовать пониманию факторов, которые, в конечном счете, играют важную роль в определении психического здоровья. Полигенные и полиэпигенетические показатели сами по себе, как и любой другой маркер, обладают ограниченной способностью прогнозировать состояние, для которого они были сгенерированы. Следует однако отметить, что оптимальный отбор генетических вариантов и других геномных маркеров, а также агрегирование связанных с ними весовых коэффициентов являются активными областями исследований. Постоянное совершенствование технологии (увеличение размера выборки GWAS и включение различных родословных, более высокое разрешение генотипирования и т.д.) влечет за собой постоянный пересмотр руководящих принципов для их расчета и интерпретации. Из-за недавнего появления нескольких методов, обсуждаемых в этом обзоре, доказательств их клинической полезности по-прежнему недостаточно, но поскольку технологии, лежащие в основе подходов функциональной геномики, продолжают совершенствоваться, необходимы дальнейшие исследования, посвященные оценке клинической полезности в психиатрии. Можно предположить, что некоторые из описанных здесь методов будут заменены более новыми подходами. Однако основная идея заключается в том, чтобы искать функциональные аспекты, а не руководствоваться исключительно подходами, основанными на данных.</p></abstract><trans-abstract xml:lang="en"><p>Today, mental disorders are one of the most important challenges for modern medicine. Despite the fact that mental illnesses do not significantly contribute to the mortality of the population, they have an important impact on the quality of life of each individual patient, as well as on public health and the economy of the country. According to statistical studies, about 40% of the Russian population has symptoms of mental disorders, and 5% need treatment.  As psychiatric genomics develops, disease risk prediction models based on biological structures continue to develop. Advances in the accessibility and complexity of big data, deep phenotyping, mapping of developmental trajectories, and the inclusion of large amounts of data on a large number of individuals will contribute to understanding the factors that ultimately play an important role in determining mental health. Polygenic and polyepigenetic indicators themselves, like any other marker, have a limited ability to predict the condition for which they were generated. It should be noted, however, that the optimal selection of genetic variants and other genomic markers, as well as the aggregation of related weights, are active areas of research. Continuous improvement of the technology (increasing the sample size of GWAS and the inclusion of different pedigrees, higher genotyping resolution, etc.) entails a constant revision of the guidelines for their calculation and interpretation. Due to the recent emergence of several methods discussed in this review, there is still insufficient evidence of their clinical usefulness, but as the technologies underlying functional genomics approaches continue to improve, further research is needed to assess clinical usefulness in psychiatry. It can be assumed that some of the methods described here will be replaced by newer approaches. However, the main idea is to include functional aspects rather than being guided solely by data-driven approaches.</p></trans-abstract><kwd-group xml:lang="ru"><kwd>генетика</kwd><kwd>геномика</kwd><kwd>психиатрия</kwd><kwd>прогнозирование</kwd><kwd>шизофрения</kwd><kwd>психические расстройства</kwd><kwd>болезнь  Альцгеймера</kwd></kwd-group><kwd-group xml:lang="en"><kwd>genetics</kwd><kwd>genomics</kwd><kwd>psychiatry</kwd><kwd>prognosis</kwd><kwd>schizophrenia</kwd><kwd>mental disorders</kwd><kwd>Alzheimer’s disease</kwd></kwd-group></article-meta></front><back><ref-list><title>References</title><ref id="cit1"><label>1</label><citation-alternatives><mixed-citation xml:lang="ru">Cкрипов В.С., Есина К.М. Комплексная оценка заболеваемости психическими расстройствами и расстройствами поведения в динамике за период 2015-2019 гг. в Российской Федерации. Социальные аспекты здоровья населения 2021; 67(4): 8.</mixed-citation><mixed-citation xml:lang="en">Skripov V.S., Esina K.M. Kompleksnaya otsenka zabolevayemosti psikhicheskimi rasstroystvami i rasstroystvami povedeniya v dinamike za period 2015-2019 gg. v Rossiyskoy Federatsii [Comprehensive assessment of mental disorders and behavioral disorders in the dynamics for the period 2015-2019. in Russian Federation]. Social’nye aspekty zdorov’a naselenia [Social aspects of population health  [serial online]. 2021; 67(4):8. (In Russ.).</mixed-citation></citation-alternatives></ref><ref id="cit2"><label>2</label><citation-alternatives><mixed-citation xml:lang="ru">Олейникова Т.А., Барыбина Е.С. Региональные различия показателей общей и первичной заболеваемости психическими расстройствами в России. Современные проблемы здравоохранения и медицинской статистики 2022; (3): 679-692.</mixed-citation><mixed-citation xml:lang="en">Oleinikova T.A., Barybina E.S. Regional’nyye razlichiya pokazateley obshchey i pervichnoy zabolevayemosti psikhicheskimi rasstroystvami v Rossii [Regional differences in the indicators of general and primary morbidity of mental disorders in Russia]. Sovremennyye problemy zdravookhraneniya i meditsinskoy statistiki  [ Modern problems of healthcare and medical statistics]. 2022; (3): 679-692. (In Russ.) doi: 10.24412/2312-2935-2022-3-679-692</mixed-citation></citation-alternatives></ref><ref id="cit3"><label>3</label><citation-alternatives><mixed-citation xml:lang="ru">Боровкова Е.И. Планирование семьи и преконцепционное консультирование. РМЖ. Мать и дитя 2019; 2(2): 131-134.</mixed-citation><mixed-citation xml:lang="en">Borovkova E.I. Planirovaniye sem’i i prekontseptsionnoye konsul’tirovaniye [Family planning and preconception consultation]. RMZH. Mat’ i ditya [Russian Journal of Woman and Child Health] 2019; 2(2): 131-134. (In Russ.)</mixed-citation></citation-alternatives></ref><ref id="cit4"><label>4</label><citation-alternatives><mixed-citation xml:lang="ru">Marigorta U.M., Gibson G. A simulation study of gene-by-environment interactions in GWAS implies ample hidden effects. Front Genet . 2014;5:225. doi: 10.3389/fgene.2014.00225.</mixed-citation><mixed-citation xml:lang="en">Marigorta U.M., Gibson G. A simulation study of gene-by-environment interactions in GWAS implies ample hidden effects. Front Genet . 2014;5:225. doi: 10.3389/fgene.2014.00225.</mixed-citation></citation-alternatives></ref><ref id="cit5"><label>5</label><citation-alternatives><mixed-citation xml:lang="ru">Zhang J., Yang J., Wen C. A. New SNP Genotyping Technology by Target SNP-Seq. Methods Mol Biol. 2023; 2638: 365-371. doi: 10.1007/978-1-0716-3024-2_26.</mixed-citation><mixed-citation xml:lang="en">Zhang J., Yang J., Wen C. A. New SNP Genotyping Technology by Target SNP-Seq. Methods Mol Biol.  2023; 2638: 365-371. doi: 10.1007/978-1-0716-3024-2_26.</mixed-citation></citation-alternatives></ref><ref id="cit6"><label>6</label><citation-alternatives><mixed-citation xml:lang="ru">Duncan L.E., Ostacher M., Ballon J. How genome-wide association studies (GWAS) made traditional candidate gene studies obsolete. Neuropsychopharmacology 2019; 44(9): 1518-1523. doi: 10.1038/s41386-019-0389-5.</mixed-citation><mixed-citation xml:lang="en">Duncan L.E., Ostacher M., Ballon J. How genome-wide association studies (GWAS) made traditional candidate gene studies obsolete. Neuropsychopharmacology 2019; 44(9): 1518-1523. doi: 10.1038/s41386-019-0389-5.</mixed-citation></citation-alternatives></ref><ref id="cit7"><label>7</label><citation-alternatives><mixed-citation xml:lang="ru">Subramanian I., Verma S., Kumar S., Jere A., Anamika K. Multiomics Data Integration, Interpretation, and Its Application. Bioinform Biol Insights 2020; 14: 1177932219899051. doi: 10.1177/1177932219899051.</mixed-citation><mixed-citation xml:lang="en">Subramanian I., Verma S., Kumar S., Jere A., Anamika K. Multiomics Data Integration, Interpretation, and Its Application.  Bioinform Biol Insights 2020; 14: 1177932219899051. doi: 10.1177/1177932219899051.</mixed-citation></citation-alternatives></ref><ref id="cit8"><label>8</label><citation-alternatives><mixed-citation xml:lang="ru">Баранова А.Н., Абраменко А.В., Смирнов T.А. Обзор полногеномных исследований поиска ассоциаций (GWAS) для выявления генетических факторов развития шизофрении. Международный научно-исследовательский журнал 2023; 2 (128): 81.</mixed-citation><mixed-citation xml:lang="en">Baranova A.N., Abramenko A.V., Smirnov T.A.  Obzor polnogenomnykh issledovaniy poiska assotsiatsiy (GWAS) dlya vyyavleniya geneticheskikh faktorov razvitiya shizofrenii [Review of genome-wide association search (WAS) studies to identify genetic factors in the development of schizophrenia]. Mezhdunarodnyj nauchno-issledovatel’skij zhurnal [International Scientific Research Journal]. 2023; 2 (128): 81 (In Russ.).</mixed-citation></citation-alternatives></ref><ref id="cit9"><label>9</label><citation-alternatives><mixed-citation xml:lang="ru">Watanabe K., Stringer S., Frei O., et al. A global overview of pleiotropy and genetic architecture in complex traits. Nat Genet. 2019;51(9):1339-1348. doi: 10.1038/s41588-019-0481-0.</mixed-citation><mixed-citation xml:lang="en">Watanabe K., Stringer S., Frei O., et al. A global overview of pleiotropy and genetic architecture in complex traits.  Nat Genet.  2019;51(9):1339-1348. doi: 10.1038/s41588-019-0481-0.</mixed-citation></citation-alternatives></ref><ref id="cit10"><label>10</label><citation-alternatives><mixed-citation xml:lang="ru">Buniello A., MacArthur J.A.L., Cerezo M., et al. The NHGRI-EBI GWAS Catalog of published genome-wide association studies, targeted arrays and summary statistics 2019. Nucleic Acids Res. 2019;47(D1):1005-1012. doi: 10.1093/nar/gky1120.</mixed-citation><mixed-citation xml:lang="en">Buniello A., MacArthur J.A.L., Cerezo M., et al. The NHGRI-EBI GWAS Catalog of published genome-wide association studies, targeted arrays and summary statistics 2019.  Nucleic Acids Res. 2019;47(D1):1005-1012. doi: 10.1093/nar/gky1120.</mixed-citation></citation-alternatives></ref><ref id="cit11"><label>11</label><citation-alternatives><mixed-citation xml:lang="ru">Visscher P.M., Wray N.R., Zhang Q., Sklar P., McCarthy M.I., Brown M.A., Yang J. 10 Years of GWAS Discovery: Biology, Function, and Translation. Am J Hum Genet. 2017;101(1):5-22. doi: 10.1016/j.ajhg.2017.06.005.</mixed-citation><mixed-citation xml:lang="en">Visscher P.M., Wray N.R., Zhang Q., Sklar P., McCarthy M.I., Brown M.A., Yang J. 10 Years of GWAS Discovery: Biology, Function, and Translation.  Am J Hum Genet.  2017;101(1):5-22. doi: 10.1016/j.ajhg.2017.06.005.</mixed-citation></citation-alternatives></ref><ref id="cit12"><label>12</label><citation-alternatives><mixed-citation xml:lang="ru">Trubetskoy V., Pardiñas A.F., Qi T., et al. Mapping genomic loci implicates genes and synaptic biology in schizophrenia. Nature. 2022;604(7906):502-508. doi: 10.1038/s41586-022-04434-5.</mixed-citation><mixed-citation xml:lang="en">Trubetskoy V., Pardiñas A.F., Qi T., et al. Mapping genomic loci implicates genes and synaptic biology in schizophrenia. Nature. 2022;604(7906):502-508. doi: 10.1038/s41586-022-04434-5.</mixed-citation></citation-alternatives></ref><ref id="cit13"><label>13</label><citation-alternatives><mixed-citation xml:lang="ru">Howard D.M., Adams M.J., Clarke T.K., et al. Genome-wide meta-analysis of depression identifies 102 independent variants and high-lights the importance of the prefrontal brain regions. Nat Neurosci. 2019;22(3):343-352. doi: 10.1038/s41593-018-0326-7.</mixed-citation><mixed-citation xml:lang="en">Howard D.M., Adams M.J., Clarke T.K., et al. Genome-wide meta-analysis of depression identifies 102 independent variants and high-lights the importance of the prefrontal brain regions. Nat Neurosci. 2019;22(3):343-352. doi: 10.1038/s41593-018-0326-7.</mixed-citation></citation-alternatives></ref><ref id="cit14"><label>14</label><citation-alternatives><mixed-citation xml:lang="ru">Кибитов А.О., Рукавишников Г.В., Мазо Г.Э., Крупицкий Е. М. Современные достижения и направления перспективного развития генетики и фармакогенетики психических заболеваний. Социальная и клиническая психиатрия 2020; 30(3): 100-112.</mixed-citation><mixed-citation xml:lang="en">Kibitov A.O., Rukavishnikov G.V., Mazo G.E., Krupitsky E. M. Sovremennyye dostizheniya i napravleniya perspektivnogo razvitiya genetiki i farmakogenetiki psikhicheskikh zabolevaniy [Modern achievements and directions of promising development of genetics and pharmacogenetics of mental diseases]. Social’naya i klinicheskaya psihiatriya [Social and clinical psychiatry]. 2020; 30(3): 100-112. (In Russ.)</mixed-citation></citation-alternatives></ref><ref id="cit15"><label>15</label><citation-alternatives><mixed-citation xml:lang="ru">Yu D., Sul J.H., Tsetsos F., et al. Interrogating the Genetic Determinants of Tourette’s Syndrome and Other Tic Disorders Through Genome-Wide Association Studies. Am J Psychiatry 2019; 176(3): 217-227. doi: 10.1176/appi.ajp.2018.18070857</mixed-citation><mixed-citation xml:lang="en">Yu D., Sul J.H., Tsetsos F., et al. Interrogating the Genetic Determinants of Tourette’s Syndrome and Other Tic Disorders Through Genome-Wide Association Studies.  Am J Psychiatry 2019; 176(3): 217-227. doi: 10.1176/appi.ajp.2018.18070857</mixed-citation></citation-alternatives></ref><ref id="cit16"><label>16</label><citation-alternatives><mixed-citation xml:lang="ru">Nievergelt C.M., Maihofer A.X., Klengel T., et al. International meta-analysis of PTSD genome-wide association studies identifies sex- and ancestry-specific genetic risk loci. Nat Commun. 2019; 10(1): 4558. doi: 10.1038/s41467-019-12576-w</mixed-citation><mixed-citation xml:lang="en">Nievergelt C.M., Maihofer A.X., Klengel T., et al. International meta-analysis of PTSD genome-wide association studies identifies sex- and ancestry-specific genetic risk loci.  Nat Commun.  2019; 10(1): 4558. doi: 10.1038/s41467-019-12576-w</mixed-citation></citation-alternatives></ref><ref id="cit17"><label>17</label><citation-alternatives><mixed-citation xml:lang="ru">Watson H.J., Yilmaz Z., Thornton L.M., et al. Genome-wide association study identifies eight risk loci and implicates metabo-psychiatric origins for anorexia nervosa. Nat Genet. 2019; 51(8): 1207-1214. doi: 10.1038/s41588-019-0439-2</mixed-citation><mixed-citation xml:lang="en">Watson H.J., Yilmaz Z., Thornton L.M., et al. Genome-wide association study identifies eight risk loci and implicates metabo-psychiatric origins for anorexia nervosa. Nat Genet. 2019; 51(8): 1207-1214. doi: 10.1038/s41588-019-0439-2</mixed-citation></citation-alternatives></ref><ref id="cit18"><label>18</label><citation-alternatives><mixed-citation xml:lang="ru">Jansen I.E., Savage J.E.., Watanabe K., et al. Genome-wide meta-analysis identifies new loci and functional pathways influencing Alzheimer’s disease risk. Nat Genet. 2019; 51(3): 404-413. doi: 10.1038/s41588-018-0311-9</mixed-citation><mixed-citation xml:lang="en">Jansen I.E., Savage J.E.., Watanabe K., et al. Genome-wide meta-analysis identifies new loci and functional pathways influencing Alzheimer’s disease risk. Nat Genet. 2019; 51(3): 404-413. doi: 10.1038/s41588-018-0311-9</mixed-citation></citation-alternatives></ref><ref id="cit19"><label>19</label><citation-alternatives><mixed-citation xml:lang="ru">Demontis D., Walters R.K., Martin J., et al. Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder. Nat Genet. 2019; 51(1): 63-75. doi: 10.1038/s41588-018-0269-7</mixed-citation><mixed-citation xml:lang="en">Demontis D., Walters R.K., Martin J., et al. Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder.  Nat Genet. 2019; 51(1): 63-75. doi: 10.1038/s41588-018-0269-7</mixed-citation></citation-alternatives></ref><ref id="cit20"><label>20</label><citation-alternatives><mixed-citation xml:lang="ru">Grove J., Ripke S., Als T.D., et al. Identification of common genetic risk variants for autism spectrum disorder. Nat Genet. 2019; 51(3): 431-444. doi: 10.1038/s41588-019-0344-8.</mixed-citation><mixed-citation xml:lang="en">Grove J., Ripke S., Als T.D., et al. Identification of common genetic risk variants for autism spectrum disorder. Nat Genet. 2019; 51(3): 431-444. doi: 10.1038/s41588-019-0344-8.</mixed-citation></citation-alternatives></ref><ref id="cit21"><label>21</label><citation-alternatives><mixed-citation xml:lang="ru">Ochoa D., Karim M., Ghoussaini M., Hulcoop D.G., McDonagh E.M., Dunham I. Human genetics evidence supports two-thirds of the 2021 FDA-approved drugs. Nat Rev Drug Discov. 2022;21(8):551. doi: 10.1038/d41573-022-00120-3.</mixed-citation><mixed-citation xml:lang="en">Ochoa D., Karim M., Ghoussaini M., Hulcoop D.G., McDonagh E.M., Dunham I. Human genetics evidence supports two-thirds of the 2021 FDA-approved drugs. Nat Rev Drug Discov. 2022;21(8):551. doi: 10.1038/d41573-022-00120-3.</mixed-citation></citation-alternatives></ref><ref id="cit22"><label>22</label><citation-alternatives><mixed-citation xml:lang="ru">Лимонова А.С., Ершова А.И., Киселева А.В., Раменский В.Е., Вяткин Ю.В., Куценко В.А., Мешков А.Н., Драпкина О.М. Оценка полигенного риска артериальной гипертензии. Кардиоваскулярная терапия и профилактика. 2022; 21(12): 3464. doi:10.15829/1728-8800-2022-3464</mixed-citation><mixed-citation xml:lang="en">Limonova A.S., Ershova A.I., Kiseleva A.V., Ramensky V.E., Vyatkin Yu.V., Kutsenko V.A., Meshkov A.N., Drapkina O.M. Otsenka poligennogo riska arterial’noy gipertenzii [Assessment of polygenic risk of hypertension].   Kardiovaskulyarnaya terapiya i profilaktika [ Cardiovascular Therapy and Prevention]. 2022;21(12):3464. (In Russ.)   doi:10.15829/1728-8800-2022-3464</mixed-citation></citation-alternatives></ref><ref id="cit23"><label>23</label><citation-alternatives><mixed-citation xml:lang="ru">Киселева А.В., Сопленкова А.Г., Куценко В.А., и др. Валидация шкал генетического риска ожирения на выборке населения регионов России. Кардиоваскулярная терапия и профилактика. 2023; 22(10): 3755. doi:10.15829/1728-8800-2023-3755.</mixed-citation><mixed-citation xml:lang="en">Kiseleva A.V., Soplenkova A.G., Kutsenko V.A., et al. Validatsiya shkal geneticheskogo riska ozhireniya na vyborke naseleniya regionov Rossii [Validation of genetic risk scores for obesity on a sample of the population of Russian regions].    Kardiovaskulyarnaya terapiya i profilaktika [ Cardiovascular Therapy and Prevention]. 2023;22(10):3755. (In Russ.)    doi:10.15829/1728-8800-2023-3755.</mixed-citation></citation-alternatives></ref><ref id="cit24"><label>24</label><citation-alternatives><mixed-citation xml:lang="ru">Wray N.R., Lin T., Austin J., McGrath J.J., Hickie I.B., Murray G.K., Visscher P.M. From Basic Science to Clinical Application of Polygenic Risk Scores: A Primer. JAMA Psychiatry. 2021;78(1):101-109. doi: 10.1001/jamapsychiatry.2020.3049</mixed-citation><mixed-citation xml:lang="en">Wray N.R., Lin T., Austin J., McGrath J.J., Hickie I.B., Murray G.K., Visscher P.M. From Basic Science to Clinical Application of Polygenic Risk Scores: A Primer. JAMA Psychiatry. 2021;78(1):101-109. doi: 10.1001/jamapsychiatry.2020.3049</mixed-citation></citation-alternatives></ref><ref id="cit25"><label>25</label><citation-alternatives><mixed-citation xml:lang="ru">Bevilacqua L., Doly S., Kaprio J., et al. A population-specific HTR2B stop codon predisposes to severe impulsivity. Nature . 2010;468(7327):1061-6. doi: 10.1038/nature09629.</mixed-citation><mixed-citation xml:lang="en">Bevilacqua L., Doly S., Kaprio J., et al. A population-specific HTR2B stop codon predisposes to severe impulsivity. Nature . 2010;468(7327):1061-6. doi: 10.1038/nature09629.</mixed-citation></citation-alternatives></ref><ref id="cit26"><label>26</label><citation-alternatives><mixed-citation xml:lang="ru">Колобкова Ю.А., Вигонт В.А., Шалыгин А.В., Казначеева Е.В. Болезнь Хантингтона: нарушения кальциевой сигнализации и модели для изучения развития патологии. Acta Naturae (русскоязычная версия). 2017; 9(2): 35-49.</mixed-citation><mixed-citation xml:lang="en">Kolobkova Yu.A., Vigant V.A., Shalygin A.V., Kaznacheeva E.V. Bolezn’ Khantingtona: narusheniya kal’tsiyevoy signalizatsii i modeli dlya izucheniya razvitiya patologii [Huntington’s disease: calcium signaling disorders and models for studying the development of pathology]. Acta Naturae (Russian version).  2017; 9 (2 (33): 35-49. (In Russ.).</mixed-citation></citation-alternatives></ref><ref id="cit27"><label>27</label><citation-alternatives><mixed-citation xml:lang="ru">Кузнецов К.О., Хайдарова Р.Р., Хабибуллина Р.Х., и др. Тестостерон и болезнь Альцгеймера. Проблемы Эндокринологии. 2022;68(5):97-107. doi:10.14341/probl13136</mixed-citation><mixed-citation xml:lang="en">Kuznetsov K.O., Khaidarova R.R., Khabibullina R.H., et al. Testosteron i bolezn’ Al’tsgeymera. [Testosterone and Alzheimer’s disease].    Problemy Endokrinologii [Problems of Endocrinology]. 2022;68(5):97-107. (In Russ.)   doi:10.14341/probl13136</mixed-citation></citation-alternatives></ref><ref id="cit28"><label>28</label><citation-alternatives><mixed-citation xml:lang="ru">Duncan L.E., Ostacher M., Ballon J. How genome-wide association studies (GWAS) made traditional candidate gene studies obsolete. Neuropsychopharmacology 2019; 44(9): 1518-1523. doi: 10.1038/s41386-019-0389-5.</mixed-citation><mixed-citation xml:lang="en">Duncan L.E., Ostacher M., Ballon J. How genome-wide association studies (GWAS) made traditional candidate gene studies obsolete. Neuropsychopharmacology 2019; 44(9): 1518-1523. doi: 10.1038/s41386-019-0389-5.</mixed-citation></citation-alternatives></ref><ref id="cit29"><label>29</label><citation-alternatives><mixed-citation xml:lang="ru">Zhang Y., Qi G., Park J.H., Chatterjee N. Estimation of complex effect-size distributions using summary-level statistics from genome-wide association studies across 32 complex traits. Nat Genet. 2018; 50(9): 1318-1326. doi: 10.1038/s41588-018-0193-x.</mixed-citation><mixed-citation xml:lang="en">Zhang Y., Qi G., Park J.H., Chatterjee N. Estimation of complex effect-size distributions using summary-level statistics from genome-wide association studies across 32 complex traits.  Nat Genet. 2018; 50(9): 1318-1326. doi: 10.1038/s41588-018-0193-x.</mixed-citation></citation-alternatives></ref><ref id="cit30"><label>30</label><citation-alternatives><mixed-citation xml:lang="ru">Boyle E.A., Li Y.I., Pritchard J.K. An Expanded View of Complex Traits: From Polygenic to Omnigenic. Cell 2017; 169(7): 1177-1186. doi: 10.1016/j.cell.2017.05.038.</mixed-citation><mixed-citation xml:lang="en">Boyle E.A., Li Y.I., Pritchard J.K. An Expanded View of Complex Traits: From Polygenic to Omnigenic. Cell 2017; 169(7): 1177-1186. doi: 10.1016/j.cell.2017.05.038.</mixed-citation></citation-alternatives></ref><ref id="cit31"><label>31</label><citation-alternatives><mixed-citation xml:lang="ru">International Schizophrenia Consortium; Purcell S.M., Wray N.R., Stone J.L., Visscher P.M., O’Donovan M.C., Sullivan P.F., Sklar P. Common polygenic variation contributes to risk of schizophrenia and bipolar disorder. Nature 2009; 460(7256): 748-52. doi: 10.1038/nature08185.</mixed-citation><mixed-citation xml:lang="en">International Schizophrenia Consortium; Purcell S.M., Wray N.R., Stone J.L., Visscher P.M., O’Donovan M.C., Sullivan P.F., Sklar P. Common polygenic variation contributes to risk of schizophrenia and bipolar disorder. Nature  2009; 460(7256): 748-52. doi: 10.1038/nature08185.</mixed-citation></citation-alternatives></ref><ref id="cit32"><label>32</label><citation-alternatives><mixed-citation xml:lang="ru">Chatterjee N., Shi .J, García-Closas M. Developing and evaluating polygenic risk prediction models for stratified disease prevention. Nat Rev Genet. 2016; 17(7): 392-406. doi: 10.1038/nrg.2016.27.</mixed-citation><mixed-citation xml:lang="en">Chatterjee N., Shi .J, García-Closas M. Developing and evaluating polygenic risk prediction models for stratified disease prevention.  Nat Rev Genet. 2016; 17(7): 392-406. doi: 10.1038/nrg.2016.27.</mixed-citation></citation-alternatives></ref><ref id="cit33"><label>33</label><citation-alternatives><mixed-citation xml:lang="ru">Batra A., Chen L.M., Wang Z., et al. Early Life Adversity and Polygenic Risk for High Fasting Insulin Are Associated With Childhood Impulsivity. Front Neurosci. 2021; 15: 704785. doi: 10.3389/fnins.2021.704785.</mixed-citation><mixed-citation xml:lang="en">Batra A., Chen L.M., Wang Z., et al. Early Life Adversity and Polygenic Risk for High Fasting Insulin Are Associated With Childhood Impulsivity.  Front Neurosci.  2021; 15: 704785. doi: 10.3389/fnins.2021.704785.</mixed-citation></citation-alternatives></ref><ref id="cit34"><label>34</label><citation-alternatives><mixed-citation xml:lang="ru">Ge T., Chen C.Y., Ni Y., Feng Y.A., Smoller J.W. Polygenic prediction via Bayesian regression and continuous shrinkage priors. Nat Commun. 2019; 10(1): 1776. doi: 10.1038/s41467-019-09718-5.</mixed-citation><mixed-citation xml:lang="en">Ge T., Chen C.Y., Ni Y., Feng Y.A., Smoller J.W. Polygenic prediction via Bayesian regression and continuous shrinkage priors.  Nat Commun.  2019; 10(1): 1776. doi: 10.1038/s41467-019-09718-5.</mixed-citation></citation-alternatives></ref><ref id="cit35"><label>35</label><citation-alternatives><mixed-citation xml:lang="ru">Ni G., Zeng J., Revez J.A., et al. A Comparison of Ten Polygenic Score Methods for Psychiatric Disorders Applied Across Multiple Cohorts. Biol Psychiatry 2021; 90(9): 611-620. doi: 10.1016/j.biopsych.2021.04.018.</mixed-citation><mixed-citation xml:lang="en">Ni G., Zeng J., Revez J.A., et al. A Comparison of Ten Polygenic Score Methods for Psychiatric Disorders Applied Across Multiple Cohorts.  Biol Psychiatry 2021; 90(9): 611-620. doi: 10.1016/j.biopsych.2021.04.018.</mixed-citation></citation-alternatives></ref><ref id="cit36"><label>36</label><citation-alternatives><mixed-citation xml:lang="ru">Lloyd-Jones L.R., Zeng J., Sidorenko J., et al. Improved polygenic prediction by Bayesian multiple regression on summary statistics. Nat Commun. 2019; 10(1): 5086. doi: 10.1038/s41467-019-12653-0.</mixed-citation><mixed-citation xml:lang="en">Lloyd-Jones L.R., Zeng J., Sidorenko J., et al. Improved polygenic prediction by Bayesian multiple regression on summary statistics.  Nat Commun.  2019; 10(1): 5086. doi: 10.1038/s41467-019-12653-0.</mixed-citation></citation-alternatives></ref><ref id="cit37"><label>37</label><citation-alternatives><mixed-citation xml:lang="ru">Кондратьева О.А., Карпулевич Е.А. Модификация метода расчета полигенных рисков с использованием графа вариации. Труды Института системного программирования РАН 2022; 34(2): 191-200. doi:10.15514/ISPRAS-2022-34(2)-15</mixed-citation><mixed-citation xml:lang="en">Kondrateva O.A., Karpulevich E.A. Modifikatsiya metoda rascheta poli-gennykh riskov s ispol’zovaniyem grafa variatsii [Modification of the Method for Calculating Polygenic Risks With Variation Graph]. Trudy Instituta sistemnogo programmirovaniya RAN  [Proceedings of the Institute for System Programming of the RAS (Proceedings of ISP RAS)] . 2022;34(2):191-200. (In Russ.)     doi:10.15514/ISPRAS-2022-34(2)-15</mixed-citation></citation-alternatives></ref><ref id="cit38"><label>38</label><citation-alternatives><mixed-citation xml:lang="ru">Ripke S., PGC SCZ WORKGROUP GWAS with over 70.000 cases and 100,000 controls. Eur Neuropsychopharmacol. 2019; 29: S814</mixed-citation><mixed-citation xml:lang="en">Ripke S., PGC SCZ WORKGROUP GWAS with over 70.000 cases and 100,000 controls.  Eur Neuropsychopharmacol. 2019; 29: S814</mixed-citation></citation-alternatives></ref><ref id="cit39"><label>39</label><citation-alternatives><mixed-citation xml:lang="ru">Desikan R.S., Fan C.C., Wang Y., et al. Genetic assessment of age-associated Alzheimer disease risk: Development and validation of a polygenic hazard score. PLoS Med. 2017; 14(3): e1002258. doi: 10.1371/journal.pmed.1002258</mixed-citation><mixed-citation xml:lang="en">Desikan R.S., Fan C.C., Wang Y., et al. Genetic assessment of age-associated Alzheimer disease risk: Development and validation of a polygenic hazard score.  PLoS Med.  2017; 14(3): e1002258. doi: 10.1371/journal.pmed.1002258</mixed-citation></citation-alternatives></ref><ref id="cit40"><label>40</label><citation-alternatives><mixed-citation xml:lang="ru">Mester R., Hou K., Ding Y., et al. Impact of cross-ancestry genetic architecture on GWASs in admixed populations. Am J Hum Genet. 2023; 110(6): 927-939. doi: 10.1016/j.ajhg.2023.05.001</mixed-citation><mixed-citation xml:lang="en">Mester R., Hou K., Ding Y., et al. Impact of cross-ancestry genetic architecture on GWASs in admixed populations.  Am J Hum Genet. 2023; 110(6): 927-939. doi: 10.1016/j.ajhg.2023.05.001</mixed-citation></citation-alternatives></ref><ref id="cit41"><label>41</label><citation-alternatives><mixed-citation xml:lang="ru">Perkins D.O., Olde Loohuis L., Barbee J., et al. Polygenic Risk Score Contribution to Psychosis Prediction in a Target Population of Persons at Clinical High Risk. Am J Psychiatry 2020; 177(2): 155-163. doi: 10.1176/appi.ajp.2019.18060721.</mixed-citation><mixed-citation xml:lang="en">Perkins D.O., Olde Loohuis L., Barbee J., et al. Polygenic Risk Score Contribution to Psychosis Prediction in a Target Population of Persons at Clinical High Risk.  Am J Psychiatry  2020; 177(2): 155-163. doi: 10.1176/appi.ajp.2019.18060721.</mixed-citation></citation-alternatives></ref><ref id="cit42"><label>42</label><citation-alternatives><mixed-citation xml:lang="ru">Byrne J.F., Mongan D., Murphy J., et al. Prognostic models predicting transition to psychotic disorder using blood-based biomarkers: a systematic review and critical appraisal. Transl Psychiatry 2023; 13(1): 333. doi: 10.1038/s41398-023-02623-y</mixed-citation><mixed-citation xml:lang="en">Byrne J.F., Mongan D., Murphy J., et al. Prognostic models predicting transition to psychotic disorder using blood-based biomarkers: a systematic review and critical appraisal. Transl Psychiatry  2023; 13(1): 333. doi: 10.1038/s41398-023-02623-y</mixed-citation></citation-alternatives></ref><ref id="cit43"><label>43</label><citation-alternatives><mixed-citation xml:lang="ru">Hernandez L.M., Kim M., Hoftman G.D., et al. Transcriptomic Insight Into the Polygenic Mechanisms Underlying Psychiatric Disorders. Biol Psychiatry 2021; 89(1): 54-64. doi: 10.1016/j.biopsych.2020.06.005</mixed-citation><mixed-citation xml:lang="en">Hernandez L.M., Kim M., Hoftman G.D., et al. Transcriptomic Insight Into the Polygenic Mechanisms Underlying Psychiatric Disorders.  Biol Psychiatry 2021; 89(1): 54-64. doi: 10.1016/j.biopsych.2020.06.005</mixed-citation></citation-alternatives></ref><ref id="cit44"><label>44</label><citation-alternatives><mixed-citation xml:lang="ru">Uffelmann E., Posthuma D. Emerging Methods and Resources for Biological Interrogation of Neuropsychiatric Polygenic Signal. Biol Psychiatry 2021; 89(1): 41-53. doi: 10.1016/j.biopsych.2020.05.022</mixed-citation><mixed-citation xml:lang="en">Uffelmann E., Posthuma D. Emerging Methods and Resources for Biological  Interrogation of Neuropsychiatric Polygenic Signal.  Biol Psychiatry 2021; 89(1): 41-53. doi: 10.1016/j.biopsych.2020.05.022</mixed-citation></citation-alternatives></ref><ref id="cit45"><label>45</label><citation-alternatives><mixed-citation xml:lang="ru">Bhattacharya A., Vo D.D., Jops C. et al. Isoform-level transcriptome-wide association uncovers genetic risk mechanisms for neuropsychiatric disorders in the human brain. Nat Genet. 2023. doi: 10.1038/s41588-023-01560-2</mixed-citation><mixed-citation xml:lang="en">Bhattacharya A., Vo D.D., Jops C. et al.  Isoform-level transcriptome-wide association uncovers genetic risk mechanisms for neuropsychiatric disorders in the human brain. Nat Genet. 2023. doi: 10.1038/s41588-023-01560-2</mixed-citation></citation-alternatives></ref><ref id="cit46"><label>46</label><citation-alternatives><mixed-citation xml:lang="ru">Girgenti M.J., Wang J., Ji D., et al. Transcriptomic organization of the human brain in post-traumatic stress disorder. Nat Neurosci. 2021; 24(1): 24-33. doi: 10.1038/s41593-020-00748-7</mixed-citation><mixed-citation xml:lang="en">Girgenti M.J., Wang J., Ji D., et al. Transcriptomic organization of the human brain in post-traumatic stress disorder.  Nat Neurosci. 2021; 24(1): 24-33. doi: 10.1038/s41593-020-00748-7</mixed-citation></citation-alternatives></ref><ref id="cit47"><label>47</label><citation-alternatives><mixed-citation xml:lang="ru">Zhang Y., Quick C., Yu K., et al. PTWAS: investigating tissue-relevant causal molecular mechanisms of complex traits using probabilistic TWAS analysis. Genome Biol. 2020; 21(1): 232. doi: 10.1186/s13059-020-02026-y</mixed-citation><mixed-citation xml:lang="en">Zhang Y., Quick C., Yu K., et al. PTWAS: investigating tissue-relevant causal molecular mechanisms of complex traits using probabilistic TWAS analysis. Genome Biol. 2020; 21(1): 232. doi: 10.1186/s13059-020-02026-y</mixed-citation></citation-alternatives></ref><ref id="cit48"><label>48</label><citation-alternatives><mixed-citation xml:lang="ru">Alpay B.A., Demetci P., Istrail S., Aguiar D. Combinatorial and statistical prediction of gene expression from haplotype sequence. Bioinformatics 2020; 36(1): 194-202. doi: 10.1093/bioinformatics/btaa318</mixed-citation><mixed-citation xml:lang="en">Alpay B.A., Demetci P., Istrail S., Aguiar D. Combinatorial and statistical prediction of gene expression from haplotype sequence. Bioinformatics  2020; 36(1): 194-202. doi: 10.1093/bioinformatics/btaa318</mixed-citation></citation-alternatives></ref><ref id="cit49"><label>49</label><citation-alternatives><mixed-citation xml:lang="ru">Koch L. Predicting mRNA levels from genome sequence. Nat Rev Genet. 2020; 21(8): 446-447. doi: 10.1038/s41576-020-0253-9.</mixed-citation><mixed-citation xml:lang="en">Koch L. Predicting mRNA levels from genome sequence. Nat Rev Genet. 2020; 21(8): 446-447. doi: 10.1038/s41576-020-0253-9.</mixed-citation></citation-alternatives></ref><ref id="cit50"><label>50</label><citation-alternatives><mixed-citation xml:lang="ru">Li B., Verma S.S., Veturi Y.C., Verma A., Bradford Y., Haas D.W., Ritchie M.D. Evaluation of PrediXcan for prioritizing GWAS associations and predicting gene expression. Pac Symp Biocomput. 2018; 23: 448-459.</mixed-citation><mixed-citation xml:lang="en">Li B., Verma S.S., Veturi Y.C., Verma A., Bradford Y., Haas D.W., Ritchie M.D. Evaluation of PrediXcan for prioritizing GWAS associations and predicting gene expression.  Pac Symp Biocomput.  2018; 23: 448-459.</mixed-citation></citation-alternatives></ref><ref id="cit51"><label>51</label><citation-alternatives><mixed-citation xml:lang="ru">Barbeira A.N., Pividori M., Zheng J., Wheeler H.E., Nicolae D.L., Im H.K. Integrating predicted transcriptome from multiple tissues improves association detection. PLoS Genet. 2019; 15(1): e1007889. doi: 10.1371/journal.pgen.1007889</mixed-citation><mixed-citation xml:lang="en">Barbeira A.N., Pividori M., Zheng J., Wheeler H.E., Nicolae D.L., Im H.K. Integrating predicted transcriptome from multiple tissues improves association detection. PLoS Genet. 2019; 15(1): e1007889. doi: 10.1371/journal.pgen.1007889</mixed-citation></citation-alternatives></ref><ref id="cit52"><label>52</label><citation-alternatives><mixed-citation xml:lang="ru">Shah K.P., Wheeler H.E., Gamazon E.R., Nicolae D.L., Cox N.J., Im H.K. Genetic predictors of gene expression associated with risk of bipolar disorder. bioRxiv. 2016 doi: 10.1101/043752</mixed-citation><mixed-citation xml:lang="en">Shah K.P., Wheeler H.E., Gamazon E.R., Nicolae D.L., Cox N.J., Im H.K. Genetic predictors of gene expression associated with risk of bipolar disorder.  bioRxiv. 2016 doi: 10.1101/043752</mixed-citation></citation-alternatives></ref><ref id="cit53"><label>53</label><citation-alternatives><mixed-citation xml:lang="ru">Yates D. Gene networking. Nat Rev Neurosci. 2021; 22(10): 589. doi: 10.1038/s41583-021-00522-z</mixed-citation><mixed-citation xml:lang="en">Yates D. Gene networking. Nat Rev Neurosci. 2021; 22(10): 589. doi: 10.1038/s41583-021-00522-z</mixed-citation></citation-alternatives></ref><ref id="cit54"><label>54</label><citation-alternatives><mixed-citation xml:lang="ru">Johnson M.R., Shkura K., Langley S.R., et al. Systems genetics identifies a convergent gene network for cognition and neurodevelopmental disease. Nat Neurosci. 2016; 19(2): 223-232. doi: 10.1038/nn</mixed-citation><mixed-citation xml:lang="en">Johnson M.R., Shkura K., Langley S.R., et al. Systems genetics identifies a convergent gene network for cognition and neurodevelopmental disease.  Nat Neurosci. 2016; 19(2): 223-232. doi: 10.1038/nn</mixed-citation></citation-alternatives></ref><ref id="cit55"><label>55</label><citation-alternatives><mixed-citation xml:lang="ru">Pergola G., Di Carlo P., D’Ambrosio E., et al. DRD2 co-expression network and a related polygenic index predict imaging, behavioral and clinical phenotypes linked to schizophrenia. Transl Psychiatry 2017; 7(1): e1006. doi: 10.1038/tp.2016.253</mixed-citation><mixed-citation xml:lang="en">Pergola G., Di Carlo P., D’Ambrosio E., et al.  DRD2 co-expression network and a related polygenic index predict imaging, behavioral and clinical phenotypes linked to schizophrenia.  Transl Psychiatry 2017; 7(1): e1006. doi: 10.1038/tp.2016.253</mixed-citation></citation-alternatives></ref><ref id="cit56"><label>56</label><citation-alternatives><mixed-citation xml:lang="ru">Gerring Z.F., Gamazon E.R., Derks E.M., Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium. A gene co-expression network-based analysis of multiple brain tissues reveals novel genes and molecular pathways underlying major depression. PLoS Genet. 2019; 15(7): e1008245. doi: 10.1371/journal.pgen.1008245</mixed-citation><mixed-citation xml:lang="en">Gerring Z.F., Gamazon E.R., Derks E.M., Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium. A gene co-expression network-based analysis of multiple brain tissues reveals novel genes and molecular pathways underlying major depression.  PLoS Genet. 2019; 15(7): e1008245. doi: 10.1371/journal.pgen.1008245</mixed-citation></citation-alternatives></ref><ref id="cit57"><label>57</label><citation-alternatives><mixed-citation xml:lang="ru">Restrepo-Lozano J.M., Pokhvisneva I., Wang Z., Patel S., Meaney M.J., Silveira P.P., Flores C. Corticolimbic DCC gene co-expression networks as predictors of impulsivity in children. Mol Psychiatry 2022; 27(6): 2742-2750. doi: 10.1038/s41380-022-01533-7</mixed-citation><mixed-citation xml:lang="en">Restrepo-Lozano J.M., Pokhvisneva I., Wang Z., Patel S., Meaney M.J., Silveira P.P., Flores C. Corticolimbic DCC gene co-expression networks as predictors of impulsivity in children. Mol Psychiatry  2022; 27(6): 2742-2750. doi: 10.1038/s41380-022-01533-7</mixed-citation></citation-alternatives></ref><ref id="cit58"><label>58</label><citation-alternatives><mixed-citation xml:lang="ru">Mucignat-Caretta C., Soravia G. Positive or negative environmental modulations on human brain development: the morphofunctional outcomes of music training or stress. Front Neurosci. 2023; 17: 1266766. doi: 10.3389/fnins.2023.1266766</mixed-citation><mixed-citation xml:lang="en">Mucignat-Caretta C., Soravia G. Positive or negative environmental modulations on human brain development: the morphofunctional outcomes of music training or stress.  Front Neurosci.  2023; 17: 1266766. doi: 10.3389/fnins.2023.1266766</mixed-citation></citation-alternatives></ref><ref id="cit59"><label>59</label><citation-alternatives><mixed-citation xml:lang="ru">McGill M.G., Pokhvisneva I., Clappison A.S., et al. Maternal Prenatal Anxiety and the Fetal Origins of Epigenetic Aging. Biol Psychiatry 2022; 91(3): 303-312. doi: 10.1016/j.biopsych.2021.07.025</mixed-citation><mixed-citation xml:lang="en">McGill M.G., Pokhvisneva I., Clappison A.S., et al. Maternal Prenatal Anxiety and the Fetal Origins of Epigenetic Aging. Biol Psychiatry  2022; 91(3): 303-312. doi: 10.1016/j.biopsych.2021.07.025</mixed-citation></citation-alternatives></ref><ref id="cit60"><label>60</label><citation-alternatives><mixed-citation xml:lang="ru">Belsky D.W., Domingue B.W., Wedow R., et al. Genetic analysis of social-class mobility in five longitudinal studies. Proc Natl Acad Sci USA 2018; 115(31): 7275-7284. doi: 10.1073/pnas.1801238115</mixed-citation><mixed-citation xml:lang="en">Belsky D.W., Domingue B.W., Wedow R., et al. Genetic analysis of social-class mobility in five longitudinal studies. Proc Natl Acad Sci USA  2018; 115(31): 7275-7284. doi: 10.1073/pnas.1801238115</mixed-citation></citation-alternatives></ref><ref id="cit61"><label>61</label><citation-alternatives><mixed-citation xml:lang="ru">Provençal N., Arloth J., Cattaneo A., et al. Glucocorticoid exposure during hippocampal neurogenesis primes future stress response by inducing changes in DNA methylation. Proc Natl Acad Sci USA 2020; 117(38): 23280-23285. doi: 10.1073/pnas.1820842116</mixed-citation><mixed-citation xml:lang="en">Provençal N., Arloth J., Cattaneo A., et al. Glucocorticoid exposure during hippocampal neurogenesis primes future stress response by inducing changes in DNA methylation.  Proc Natl Acad Sci USA 2020; 117(38): 23280-23285. doi: 10.1073/pnas.1820842116</mixed-citation></citation-alternatives></ref></ref-list><fn-group><fn fn-type="conflict"><p>The authors declare that there are no conflicts of interest present.</p></fn></fn-group></back></article>
