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<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">cardiotomsk</journal-id><journal-title-group><journal-title xml:lang="ru">Сибирский журнал клинической и экспериментальной медицины</journal-title><trans-title-group xml:lang="en"><trans-title>Siberian Journal of Clinical and Experimental Medicine</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">2713-2927</issn><issn pub-type="epub">2713-265X</issn><publisher><publisher-name>TSU publishing</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.29001/2073-8552-2021-36-4-37-44</article-id><article-id custom-type="elpub" pub-id-type="custom">cardiotomsk-1281</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>ОБЗОРЫ И ЛЕКЦИИ</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>REVIEWS AND LECTURES</subject></subj-group></article-categories><title-group><article-title>Современные исследования генетики многофакторных заболеваний, связанных с нарушением когнитивных функций человека</article-title><trans-title-group xml:lang="en"><trans-title>Recent studies of the genetics of complex diseases associated with impaired cognitive functions</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0003-2690-8802</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Бочарова</surname><given-names>А. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Bocharova</surname><given-names>A. V.</given-names></name></name-alternatives><bio xml:lang="ru"><p> младший научный сотрудник, лаборатория эволюционной генетики</p><p> 634050, Российская Федерация, Томск, ул. Набережная реки Ушайки, 10 </p></bio><bio xml:lang="en"><p> Junior Research Scientist, Laboratory of Evolutionary Genetics</p><p> 10, Ushaika River Embankment str., Tomsk, 634050, Russian Federation </p></bio><email xlink:type="simple">anna.bocharova@medgenetics.ru</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-5166-331X</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Степанов</surname><given-names>В. А.</given-names></name><name name-style="western" xml:lang="en"><surname>Stepanov</surname><given-names>V. A.</given-names></name></name-alternatives><bio xml:lang="ru"><p> д-р биол. наук, профессор, чл.-корр. РАН, директор Томского национального исследовательского медицинского центра Российской академии наук; профессор кафедры генетики и клеточной биологии, Институт биологии, экологии, почвоведения, сельского и лесного хозяйства, Национальный исследовательский Томский государственный университет. </p><p> 634050, Российская Федерация, Томск, ул. Набережная реки Ушайки, 10 </p></bio><bio xml:lang="en"><p> Dr. Sci. (Biol.), Professor, Corresponding Member of the Russian Academy of Sciences, Director; Professor, Department of Genetics and Cell Biology, Institute of Biology, Ecology, Soil Science, Agriculture, and Forestry, National Research Tomsk State University </p><p> 10, Ushaika River Embankment str., Tomsk, 634050, Russian Federation </p></bio><email xlink:type="simple">vadim.stepanov@medgenetics.ru</email><xref ref-type="aff" rid="aff-2"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>Научно-исследовательский институт медицинской генетики, Томский национальный исследовательский медицинский центр Российской академии наук</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Tomsk National Research Medical Center, Russian Academy of Sciences </institution><country>Russian Federation</country></aff></aff-alternatives><aff-alternatives id="aff-2"><aff xml:lang="ru"><institution>Научно-исследовательский институт медицинской генетики, Томский национальный исследовательский медицинский центр Российской академии наук</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Tomsk National Research Medical Center, Russian Academy of Sciences</institution><country>Russian Federation</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2021</year></pub-date><pub-date pub-type="epub"><day>01</day><month>01</month><year>2022</year></pub-date><volume>36</volume><issue>4</issue><fpage>37</fpage><lpage>44</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Бочарова А.В., Степанов В.А., 2022</copyright-statement><copyright-year>2022</copyright-year><copyright-holder xml:lang="ru">Бочарова А.В., Степанов В.А.</copyright-holder><copyright-holder xml:lang="en">Bocharova A.V., Stepanov V.A.</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.sibjcem.ru/jour/article/view/1281">https://www.sibjcem.ru/jour/article/view/1281</self-uri><abstract><p> В представленной работе обобщены данные современных исследований, связанных с поиском генетической компоненты широко распространенных социально  значимых заболеваний, которые приводят к нарушениям  когнитивных функций человека. Основное внимание уделено таким патологиям многофакторной природы, как шизофрения (ШЗ) и болезнь Альцгеймера (БА). В статье приводится подробный анализ широкого спектра методов  современной генетики: от близнецовых до эпигенетических исследований. </p></abstract><trans-abstract xml:lang="en"><p> The present work summarizes data of recent studies related to the search for the genetic component of complex diseases leading to impaired cognitive functions. The main attention is paid to such pathologies as schizophrenia and Alzheimer’s disease. The article provides a detailed analysis of a wide range of modern genetics methods: from twin studies to epigenetic research. </p></trans-abstract><kwd-group xml:lang="ru"><kwd>шизофрения</kwd><kwd>болезнь Альцгеймера</kwd><kwd>генетические исследования</kwd><kwd>когнитивные функции</kwd></kwd-group><kwd-group xml:lang="en"><kwd>schizophrenia</kwd><kwd>Alzheimer’s disease</kwd><kwd>genetic research</kwd><kwd>cognitive function</kwd></kwd-group><funding-group><funding-statement xml:lang="ru">исследование выполнено за счет средств федерального бюджета Научно-исследовательского института медицинской генетики, Томский национальный исследовательский медицинский центр Российской академии наук</funding-statement><funding-statement xml:lang="en">the study was conducted at the cost of the federal budget of Research Institute of Medical Genetics, Tomsk National Research Medical Center, Russian Academy of Sciences</funding-statement></funding-group></article-meta></front><back><ref-list><title>References</title><ref id="cit1"><label>1</label><citation-alternatives><mixed-citation xml:lang="ru">Cardno A.G., Gottesman I.I. Twin studies of schizophrenia: from bowand-arrow concordances to star wars Mx and functional genomics. Am. J. Med. Genet. 2000;97(1):12–17.</mixed-citation><mixed-citation xml:lang="en">Cardno A.G., Gottesman I.I. Twin studies of schizophrenia: from bowand-arrow concordances to star wars Mx and functional genomics. Am. J. Med. Genet. 2000;97(1):12–17.</mixed-citation></citation-alternatives></ref><ref id="cit2"><label>2</label><citation-alternatives><mixed-citation xml:lang="ru">Hilker R., Helenius D., Fagerlund B., Skytthe A., Christensen K., Werge T.M. et al. Heritability of schizophrenia and schizophrenia spectrum based on the Nationwide Danish Twin Register. Biol. Psychiatry. 2018;83(6):492–498. DOI: 10.1016/j.biopsych.2017.08.017.</mixed-citation><mixed-citation xml:lang="en">Hilker R., Helenius D., Fagerlund B., Skytthe A., Christensen K., Werge T.M. et al. Heritability of schizophrenia and schizophrenia spectrum based on the Nationwide Danish Twin Register. Biol. Psychiatry. 2018;83(6):492–498. DOI: 10.1016/j.biopsych.2017.08.017.</mixed-citation></citation-alternatives></ref><ref id="cit3"><label>3</label><citation-alternatives><mixed-citation xml:lang="ru">Besteher B., Brambilla P., Nenadić I. Twin studies of brain structure and cognition in schizophrenia. Neurosci. Biobehav. Rev. 2020;109:103–113. DOI: 10.1016/j.neubiorev.2019.12.021.</mixed-citation><mixed-citation xml:lang="en">Besteher B., Brambilla P., Nenadić I. Twin studies of brain structure and cognition in schizophrenia. Neurosci. Biobehav. Rev. 2020;109:103–113. DOI: 10.1016/j.neubiorev.2019.12.021.</mixed-citation></citation-alternatives></ref><ref id="cit4"><label>4</label><citation-alternatives><mixed-citation xml:lang="ru">Sullivan P.F., Kendler K.S., Neale M.C. Schizophrenia as a complex trait: evidence from a meta-analysis of twin studies. Arch. Gen. Psychiatry. 2003;6(12):1187–1192. DOI: 10.1001/archpsyc.60.12.1187.</mixed-citation><mixed-citation xml:lang="en">Sullivan P.F., Kendler K.S., Neale M.C. Schizophrenia as a complex trait: evidence from a meta-analysis of twin studies. Arch. Gen. Psychiatry. 2003;6(12):1187–1192. DOI: 10.1001/archpsyc.60.12.1187.</mixed-citation></citation-alternatives></ref><ref id="cit5"><label>5</label><citation-alternatives><mixed-citation xml:lang="ru">Lambert J.C., Ibrahim-Verbaas C.A., Harold D., Naj A.C., Sims R., Bellenguez C. et al. Meta-analysis of 74,046 individuals identifi es 11 new susceptibility loci for Alzheimer’s disease. Nat. Genet. 2013;45(12):1452–1458. DOI: 10.1038/ng.2802.</mixed-citation><mixed-citation xml:lang="en">Lambert J.C., Ibrahim-Verbaas C.A., Harold D., Naj A.C., Sims R., Bellenguez C. et al. Meta-analysis of 74,046 individuals identifi es 11 new susceptibility loci for Alzheimer’s disease. Nat. Genet. 2013;45(12):1452–1458. DOI: 10.1038/ng.2802.</mixed-citation></citation-alternatives></ref><ref id="cit6"><label>6</label><citation-alternatives><mixed-citation xml:lang="ru">Степанов В.А., Бочарова А.В., Марусин А.В., Жукова Н.Г., Алифирова В.М., Жукова И.А. Репликативный анализ ассоциаций генетических маркеров когнитивных признаков с болезнью Альцгеймера в российской популяции. Молекулярная биология. 2014;48(6):952–962. DOI: 10.7868/S0026898414060160.</mixed-citation><mixed-citation xml:lang="en">Stepanov V.A., Bocharova A.V., Marusin A.V., Zhukova N.G., Alifi rova V.M., Zhukova I.A. Replicative association analysis of genetic markers of cognitive traits with Alzheimer’s disease in the Russian population. Molecular Biology. 2014;48(6):952–962 (In Russ.). DOI: 10.1134/S0026893314060168.</mixed-citation></citation-alternatives></ref><ref id="cit7"><label>7</label><citation-alternatives><mixed-citation xml:lang="ru">Бочарова А.В., Степанов В.А., Марусин А.В., Харьков В.Н., Вагайцева К.В., Федоренко О.Ю. и др. Анализ ассоциаций генетических маркеров шизофрении и ее когнитивных эндофенотипов. Генетика. 2017;53(1):100–108. DOI: 10.7868/S0016675817010039.</mixed-citation><mixed-citation xml:lang="en">Bocharova A.V., Stepanov V.A., Marusin A.V., Kharkov V.N., Vagaitseva K.V., Fedorenko O.Yu. et al. Association study of genetic markers of schizophrenia and its cognitive endophenotypes. Russian Journal of Genetics. 2017;53(1):139–146 (In Russ.). DOI: 10.1134/S1022795417010033.</mixed-citation></citation-alternatives></ref><ref id="cit8"><label>8</label><citation-alternatives><mixed-citation xml:lang="ru">Rajan K.B., Weuve J., Barnes L.L., Wilson R.S., Evans D.A. Prevalence and incidence of clinically diagnosed Alzheimer’s disease dementia from 1994 to 2012 in a population study. Alzheimers Dement. 2019;15(1):1–7. DOI: 10.1016/j.jalz.2018.07.216.</mixed-citation><mixed-citation xml:lang="en">Rajan K.B., Weuve J., Barnes L.L., Wilson R.S., Evans D.A. Prevalence and incidence of clinically diagnosed Alzheimer’s disease dementia from 1994 to 2012 in a population study. Alzheimers Dement. 2019;15(1):1–7. DOI: 10.1016/j.jalz.2018.07.216.</mixed-citation></citation-alternatives></ref><ref id="cit9"><label>9</label><citation-alternatives><mixed-citation xml:lang="ru">Samper-Ternent R., Kuo Y.F., Ray L.A., Ottenbacher K.J., Markides K.S., Al Snih S. Prevalence of health conditions and predictors of mortality in oldest old Mexican Americans and non-Hispanic whites. J. Am. Med. Dir. Assoc. 2012;13(3):254–259. DOI: 10.1016/j.jamda.2010.07.010.</mixed-citation><mixed-citation xml:lang="en">Samper-Ternent R., Kuo Y.F., Ray L.A., Ottenbacher K.J., Markides K.S., Al Snih S. Prevalence of health conditions and predictors of mortality in oldest old Mexican Americans and non-Hispanic whites. J. Am. Med. Dir. Assoc. 2012;13(3):254–259. DOI: 10.1016/j.jamda.2010.07.010.</mixed-citation></citation-alternatives></ref><ref id="cit10"><label>10</label><citation-alternatives><mixed-citation xml:lang="ru">Bigdeli T.B., Genovese G., Georgakopoulos P., Meyers J.L., Peterson R.E.,Iyegbe C.O. et al. Contributions of common genetic variants to risk of schizophrenia among individuals of African and Latino ancestry. Mol. Psychiatry. 2019(10):2455–2467. DOI: 10.1038/s41380-019-0517-y.</mixed-citation><mixed-citation xml:lang="en">Bigdeli T.B., Genovese G., Georgakopoulos P., Meyers J.L., Peterson R.E.,Iyegbe C.O. et al. Contributions of common genetic variants to risk of schizophrenia among individuals of African and Latino ancestry. Mol. Psychiatry. 2019(10):2455–2467. DOI: 10.1038/s41380-019-0517-y.</mixed-citation></citation-alternatives></ref><ref id="cit11"><label>11</label><citation-alternatives><mixed-citation xml:lang="ru">Lam M., Chen C.Y., Li Z., Martin A.R., Bryois J., Ma X. et al. Comparative genetic architectures of schizophrenia in East Asian and European populations. Nat. Genet. 2019;51(12):1670–1678. DOI: 10.1038/s41588-019-0512-x.</mixed-citation><mixed-citation xml:lang="en">Lam M., Chen C.Y., Li Z., Martin A.R., Bryois J., Ma X. et al. Comparative genetic architectures of schizophrenia in East Asian and European populations. Nat. Genet. 2019;51(12):1670–1678. DOI: 10.1038/s41588-019-0512-x.</mixed-citation></citation-alternatives></ref><ref id="cit12"><label>12</label><citation-alternatives><mixed-citation xml:lang="ru">Schizophrenia Working Group of the Psychiatric Genomics Consortium. Biological insights from 108 schizophrenia-associated genetic loci. Nature. 2014;511(7510):421–427. DOI: 10.1038/nature13595.</mixed-citation><mixed-citation xml:lang="en">Schizophrenia Working Group of the Psychiatric Genomics Consortium. Biological insights from 108 schizophrenia-associated genetic loci. Nature. 2014;511(7510):421–427. DOI: 10.1038/nature13595.</mixed-citation></citation-alternatives></ref><ref id="cit13"><label>13</label><citation-alternatives><mixed-citation xml:lang="ru">Pardiñas A.F., Holmans P., Pocklington A.J., Escott-Price V., Ripke S., Carrera N. et al. Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection. Nat. Genet. 2018;50(3):381–389. DOI: 10.1038/s41588-018-0059-2.</mixed-citation><mixed-citation xml:lang="en">Pardiñas A.F., Holmans P., Pocklington A.J., Escott-Price V., Ripke S., Carrera N. et al. Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection. Nat. Genet. 2018;50(3):381–389. DOI: 10.1038/s41588-018-0059-2.</mixed-citation></citation-alternatives></ref><ref id="cit14"><label>14</label><citation-alternatives><mixed-citation xml:lang="ru">Федоренко О.Ю., Иванова С.А. Новый взгляд на генетику нейро-когнитивного дефицита при шизофрении. Журнал неврологии и психиатрии им. C.C. Корсакова. 2020;120(8):183–192. DOI: 10.17116/jnevro2020120081183.</mixed-citation><mixed-citation xml:lang="en">Fedorenko O.Y., Ivanova S.A. A new look at the genetics of neurocognitive defi cits in schizophrenia. Zh. Nevrol. Psikhiatr. Im. S.S. Korsakova. 2020;120(8):183–192 (In Russ.). DOI: 10.17116/jnevro2020120081183.</mixed-citation></citation-alternatives></ref><ref id="cit15"><label>15</label><citation-alternatives><mixed-citation xml:lang="ru">Nho K., Kim S., Horgusluoglu E., Risacher S.L., Shen L., Kim D. et al. Association analysis of rare variants near the APOE region with CSF and neuroimaging biomarkers of Alzheimer’s disease. BMC Medical Genomics. 2017;10(1):29. DOI: 10.1186/s12920-017-0267-0.</mixed-citation><mixed-citation xml:lang="en">Nho K., Kim S., Horgusluoglu E., Risacher S.L., Shen L., Kim D. et al. Association analysis of rare variants near the APOE region with CSF and neuroimaging biomarkers of Alzheimer’s disease. BMC Medical Genomics. 2017;10(1):29. DOI: 10.1186/s12920-017-0267-0.</mixed-citation></citation-alternatives></ref><ref id="cit16"><label>16</label><citation-alternatives><mixed-citation xml:lang="ru">Kong A., Frigge M.L., Masson G., Besenbacher S., Sulem P., Magnusson G. et al. Rate of de novo mutations and the importance of father’s age to disease risk. Nature. 2012; 488(7412):471–475. DOI: 10.1038/nature11396.</mixed-citation><mixed-citation xml:lang="en">Kong A., Frigge M.L., Masson G., Besenbacher S., Sulem P., Magnusson G. et al. Rate of de novo mutations and the importance of father’s age to disease risk. Nature. 2012; 488(7412):471–475. DOI: 10.1038/nature11396.</mixed-citation></citation-alternatives></ref><ref id="cit17"><label>17</label><citation-alternatives><mixed-citation xml:lang="ru">Girard S.L., Gauthier J., Noreau A., Xiong L., Zhou S., Jouan L. et al. Increased exonic de novo mutation rate in individuals with schizophrenia. Nat. Genet. 2011;43(9):860–863. DOI: 10.1038/ng.886.</mixed-citation><mixed-citation xml:lang="en">Girard S.L., Gauthier J., Noreau A., Xiong L., Zhou S., Jouan L. et al. Increased exonic de novo mutation rate in individuals with schizophrenia. Nat. Genet. 2011;43(9):860–863. DOI: 10.1038/ng.886.</mixed-citation></citation-alternatives></ref><ref id="cit18"><label>18</label><citation-alternatives><mixed-citation xml:lang="ru">Xu B., Roos J.L., Dexheimer P., Boone B., Plummer B., Levy S. et al. Exome sequencing supports a de novo mutational paradigm for schizophrenia. Nat. Genet. 2011;43(9):864–868. DOI: 10.1038/ng.902.</mixed-citation><mixed-citation xml:lang="en">Xu B., Roos J.L., Dexheimer P., Boone B., Plummer B., Levy S. et al. Exome sequencing supports a de novo mutational paradigm for schizophrenia. Nat. Genet. 2011;43(9):864–868. DOI: 10.1038/ng.902.</mixed-citation></citation-alternatives></ref><ref id="cit19"><label>19</label><citation-alternatives><mixed-citation xml:lang="ru">Purcell S.M., Moran J.L., Fromer M., Ruderfer D., Solovieff N., Roussos P. et al. A polygenic burden of rare disruptive mutations in schizophrenia. Nature. 2014;506(7487):185–190. DOI: 10.1038/nature12975.</mixed-citation><mixed-citation xml:lang="en">Purcell S.M., Moran J.L., Fromer M., Ruderfer D., Solovieff N., Roussos P. et al. A polygenic burden of rare disruptive mutations in schizophrenia. Nature. 2014;506(7487):185–190. DOI: 10.1038/nature12975.</mixed-citation></citation-alternatives></ref><ref id="cit20"><label>20</label><citation-alternatives><mixed-citation xml:lang="ru">Vega-Sevey J.G., Martínez-Magaña J.J., Genis-Mendoza A.D., Escamilla M., Lanzagorta N., Tovilla-Zarate C.A. et al. Copy number variants in siblings of Mexican origin concordant for schizophrenia or bipolar disorder. Psychiatry Res. 2020;291:113018. DOI: 10.1016/j.psychres.2020.113018.</mixed-citation><mixed-citation xml:lang="en">Vega-Sevey J.G., Martínez-Magaña J.J., Genis-Mendoza A.D., Escamilla M., Lanzagorta N., Tovilla-Zarate C.A. et al. Copy number variants in siblings of Mexican origin concordant for schizophrenia or bipolar disorder. Psychiatry Res. 2020;291:113018. DOI: 10.1016/j.psychres.2020.113018.</mixed-citation></citation-alternatives></ref><ref id="cit21"><label>21</label><citation-alternatives><mixed-citation xml:lang="ru">Stefansson H., Rujescu D., Cichon S., Pietiläinen O.P., Ingason A., Steinberg S. et al. Large recurrent microdeletions associated with schizophrenia. Nature. 2008;455(7210):232–236. DOI: 10.1038/nature07229.</mixed-citation><mixed-citation xml:lang="en">Stefansson H., Rujescu D., Cichon S., Pietiläinen O.P., Ingason A., Steinberg S. et al. Large recurrent microdeletions associated with schizophrenia. Nature. 2008;455(7210):232–236. DOI: 10.1038/nature07229.</mixed-citation></citation-alternatives></ref><ref id="cit22"><label>22</label><citation-alternatives><mixed-citation xml:lang="ru">International Schizophrenia Consortium. Rare chromosomal deletions and duplications increase risk of schizophrenia. Nature. 2008;455(7210):237–241. DOI: 10.1038/nature07239.</mixed-citation><mixed-citation xml:lang="en">International Schizophrenia Consortium. Rare chromosomal deletions and duplications increase risk of schizophrenia. Nature. 2008;455(7210):237–241. DOI: 10.1038/nature07239.</mixed-citation></citation-alternatives></ref><ref id="cit23"><label>23</label><citation-alternatives><mixed-citation xml:lang="ru">Heinzen E.L., Need A.C., Hayden K.M., Chiba-Falek O., Roses A.D., Strittmatter W.J. et al. Genome-wide scan of copy number variation in late-onset Alzheimer’s disease. J. Alzheimers Dis. 2010;19(1):69–77. DOI: 10.3233/JAD-2010-1212.</mixed-citation><mixed-citation xml:lang="en">Heinzen E.L., Need A.C., Hayden K.M., Chiba-Falek O., Roses A.D., Strittmatter W.J. et al. Genome-wide scan of copy number variation in late-onset Alzheimer’s disease. J. Alzheimers Dis. 2010;19(1):69–77. DOI: 10.3233/JAD-2010-1212.</mixed-citation></citation-alternatives></ref><ref id="cit24"><label>24</label><citation-alternatives><mixed-citation xml:lang="ru">Zheng X., Demirci F.Y., Barmada M.M., Richardson G.A., Lopez O.L., Sweet R.A. et al. A rare duplication on chromosome 16p11.2 is identified in patients with psychosis in Alzheimer’s disease. PLoS One. 2014;9(11):e111462. DOI: 10.1371/journal.pone.0111462.</mixed-citation><mixed-citation xml:lang="en">Zheng X., Demirci F.Y., Barmada M.M., Richardson G.A., Lopez O.L., Sweet R.A. et al. A rare duplication on chromosome 16p11.2 is identified in patients with psychosis in Alzheimer’s disease. PLoS One. 2014;9(11):e111462. DOI: 10.1371/journal.pone.0111462.</mixed-citation></citation-alternatives></ref><ref id="cit25"><label>25</label><citation-alternatives><mixed-citation xml:lang="ru">Hollingworth P., Sweet R., Sims R., Harold D., Russo G., Abraham R. et al. Genomewide association study of Alzheimer’s disease with psychotic symptoms. Mol. Psychiatry. 2012;17(12):1316–1327. DOI: 10.1038/mp.2011.125.</mixed-citation><mixed-citation xml:lang="en">Hollingworth P., Sweet R., Sims R., Harold D., Russo G., Abraham R. et al. Genomewide association study of Alzheimer’s disease with psychotic symptoms. Mol. Psychiatry. 2012;17(12):1316–1327. DOI: 10.1038/mp.2011.125.</mixed-citation></citation-alternatives></ref><ref id="cit26"><label>26</label><citation-alternatives><mixed-citation xml:lang="ru">De Jager P.L., Srivastava G., Lunnon K., Burgess J., Schalkwyk L.C., Yu L. et al. Alzheimer’s disease: Early alterations in brain DNA methylation at ANK1, BIN1, RHBDF2 and other loci. Nat. Neurosci. 2014;17(9):1156–1163. DOI: 10.1038/nn.3786.</mixed-citation><mixed-citation xml:lang="en">De Jager P.L., Srivastava G., Lunnon K., Burgess J., Schalkwyk L.C., Yu L. et al. Alzheimer’s disease: Early alterations in brain DNA methylation at ANK1, BIN1, RHBDF2 and other loci. Nat. Neurosci. 2014;17(9):1156–1163. DOI: 10.1038/nn.3786.</mixed-citation></citation-alternatives></ref><ref id="cit27"><label>27</label><citation-alternatives><mixed-citation xml:lang="ru">Abdolmaleky H.M., Cheng K.H., Russo A., Smith C.L., Faraone S.V., Wilcox M. et al. Hypermethylation of the reelin (RELN) promoter in the brain of schizophrenic patients: A preliminary report. Am. J. Med. Genet. B Neuropsychiatr. Genet. 2005; 134B(1):60–66. DOI: 10.1002/ajmg.b.30140.</mixed-citation><mixed-citation xml:lang="en">Abdolmaleky H.M., Cheng K.H., Russo A., Smith C.L., Faraone S.V., Wilcox M. et al. Hypermethylation of the reelin (RELN) promoter in the brain of schizophrenic patients: A preliminary report. Am. J. Med. Genet. B Neuropsychiatr. Genet. 2005; 134B(1):60–66. DOI: 10.1002/ajmg.b.30140.</mixed-citation></citation-alternatives></ref><ref id="cit28"><label>28</label><citation-alternatives><mixed-citation xml:lang="ru">Huang H.S., Akbarian S. GAD1 mRNA expression and DNA methylation in prefrontal cortex of subjects with schizophrenia. PLoS One. 2007;2(8):e809. DOI: 10.1371/journal.pone.0000809.</mixed-citation><mixed-citation xml:lang="en">Huang H.S., Akbarian S. GAD1 mRNA expression and DNA methylation in prefrontal cortex of subjects with schizophrenia. PLoS One. 2007;2(8):e809. DOI: 10.1371/journal.pone.0000809.</mixed-citation></citation-alternatives></ref><ref id="cit29"><label>29</label><citation-alternatives><mixed-citation xml:lang="ru">Carrard A., Salzmann A., Malafosse A., Karege F. Increased DNA methylation status of the serotonin receptor 5HTR1A gene promoter in schizophrenia and bipolar disorder. J. Affect. Disord. 2011;132(3):450–453. DOI: 10.1016/j.jad.2011.03.018.</mixed-citation><mixed-citation xml:lang="en">Carrard A., Salzmann A., Malafosse A., Karege F. Increased DNA methylation status of the serotonin receptor 5HTR1A gene promoter in schizophrenia and bipolar disorder. J. Affect. Disord. 2011;132(3):450–453. DOI: 10.1016/j.jad.2011.03.018.</mixed-citation></citation-alternatives></ref><ref id="cit30"><label>30</label><citation-alternatives><mixed-citation xml:lang="ru">Alfimova M., Kondratyev N., Golov A., Golimbet V. Profiling haplotype specific CpG and CpH methylation within a schizophrenia GWAS locus on chromosome 14 in schizophrenia and healthy subjects. Sci. Rep. 2020;10(1):4704. DOI: 10.1038/s41598-020-61671-2.</mixed-citation><mixed-citation xml:lang="en">Alfimova M., Kondratyev N., Golov A., Golimbet V. Profiling haplotype specific CpG and CpH methylation within a schizophrenia GWAS locus on chromosome 14 in schizophrenia and healthy subjects. Sci. Rep. 2020;10(1):4704. DOI: 10.1038/s41598-020-61671-2.</mixed-citation></citation-alternatives></ref><ref id="cit31"><label>31</label><citation-alternatives><mixed-citation xml:lang="ru">Rao J.S., Keleshian V.L., Klein S., Rapoport S.I. Epigenetic modifications in frontal cortex from Alzheimer’s disease and bipolar disorder patients. Transl. Psychiatry. 2012;2(7):e132. DOI: 10.1038/tp.2012.55.</mixed-citation><mixed-citation xml:lang="en">Rao J.S., Keleshian V.L., Klein S., Rapoport S.I. Epigenetic modifications in frontal cortex from Alzheimer’s disease and bipolar disorder patients. Transl. Psychiatry. 2012;2(7):e132. DOI: 10.1038/tp.2012.55.</mixed-citation></citation-alternatives></ref><ref id="cit32"><label>32</label><citation-alternatives><mixed-citation xml:lang="ru">Gräff J., Rei D., Guan J.S., Wang W.Y., Seo J., Hennig K.M. et al. An epigenetic blockade of cognitive functions in the neurodegenerating brain. Nature. 2012;483(7388): 222–226. DOI: 10.1038/nature10849.</mixed-citation><mixed-citation xml:lang="en">Gräff J., Rei D., Guan J.S., Wang W.Y., Seo J., Hennig K.M. et al. An epigenetic blockade of cognitive functions in the neurodegenerating brain. Nature. 2012;483(7388): 222–226. DOI: 10.1038/nature10849.</mixed-citation></citation-alternatives></ref><ref id="cit33"><label>33</label><citation-alternatives><mixed-citation xml:lang="ru">Benes F.M., Lim B., Matzilevich D., Walsh J.P., Subburaju S., Minns M. Regulation of the GABA cell phenotype in hippocampus of schizophrenics and bipolars. Proc. Natl. Acad. Sci. USA. 2007;104(24):10164–10169. DOI: 10.1073/pnas.0703806104.</mixed-citation><mixed-citation xml:lang="en">Benes F.M., Lim B., Matzilevich D., Walsh J.P., Subburaju S., Minns M. Regulation of the GABA cell phenotype in hippocampus of schizophrenics and bipolars. Proc. Natl. Acad. Sci. USA. 2007;104(24):10164–10169. DOI: 10.1073/pnas.0703806104.</mixed-citation></citation-alternatives></ref><ref id="cit34"><label>34</label><citation-alternatives><mixed-citation xml:lang="ru">Jakovcevski M., Bharadwaj R., Straubhaar J., Gao G., Gavin D.P., Jakovcevski I. et al. Prefrontal cortical dysfunction after overexpression of histone deacetylase 1. Biol. Psychiatry. 2013;74(9):696–705. DOI: 10.1016/j.biopsych.2013.03.020.</mixed-citation><mixed-citation xml:lang="en">Jakovcevski M., Bharadwaj R., Straubhaar J., Gao G., Gavin D.P., Jakovcevski I. et al. Prefrontal cortical dysfunction after overexpression of histone deacetylase 1. Biol. Psychiatry. 2013;74(9):696–705. DOI: 10.1016/j.biopsych.2013.03.020.</mixed-citation></citation-alternatives></ref><ref id="cit35"><label>35</label><citation-alternatives><mixed-citation xml:lang="ru">Kurita M., Holloway T., García-Bea A., Kozlenkov A., Friedman A.K., Moreno J.L. et al. HDAC2 regulates atypical antipsychotic responses through the modulation of mGlu2 promoter activity. Nat. Neurosci. 2012;15(9):1245–1254. DOI: 10.1038/nn.3181.</mixed-citation><mixed-citation xml:lang="en">Kurita M., Holloway T., García-Bea A., Kozlenkov A., Friedman A.K., Moreno J.L. et al. HDAC2 regulates atypical antipsychotic responses through the modulation of mGlu2 promoter activity. Nat. Neurosci. 2012;15(9):1245–1254. DOI: 10.1038/nn.3181.</mixed-citation></citation-alternatives></ref><ref id="cit36"><label>36</label><citation-alternatives><mixed-citation xml:lang="ru">Mitchell A.C., Javidfar B., Pothula V., Ibi D., Shen E.Y., Peter C.J. et al. MEF2C transcription factor is associated with the genetic and epigenetic risk architecture of schizophrenia and improves cognition in mice. Mol. Psychiatry. 2018;23(1):123–132. DOI: 10.1038/mp.2016.254.</mixed-citation><mixed-citation xml:lang="en">Mitchell A.C., Javidfar B., Pothula V., Ibi D., Shen E.Y., Peter C.J. et al. MEF2C transcription factor is associated with the genetic and epigenetic risk architecture of schizophrenia and improves cognition in mice. Mol. Psychiatry. 2018;23(1):123–132. DOI: 10.1038/mp.2016.254.</mixed-citation></citation-alternatives></ref><ref id="cit37"><label>37</label><citation-alternatives><mixed-citation xml:lang="ru">Fiore R., Khudayberdiev S., Saba R., Schratt G. MicroRNA function in the nervous system. Prog. Mol. Biol. Transl. Sci. 2011;102:47–100. DOI: 10.1016/B978-0-12-415795-8.00004-0.</mixed-citation><mixed-citation xml:lang="en">Fiore R., Khudayberdiev S., Saba R., Schratt G. MicroRNA function in the nervous system. Prog. Mol. Biol. Transl. Sci. 2011;102:47–100. DOI: 10.1016/B978-0-12-415795-8.00004-0.</mixed-citation></citation-alternatives></ref><ref id="cit38"><label>38</label><citation-alternatives><mixed-citation xml:lang="ru">Nunez-Iglesias J., Liu C.C., Morgan T.E., Finch C.E., Zhou X.J. Joint genome-wide profiling of miRNA and mRNA expression in Alzheimer’s disease cortex reveals altered miRNA regulation. PLoS One. 2010;5(2):e8898. DOI: 10.1371/journal.pone.0008898.</mixed-citation><mixed-citation xml:lang="en">Nunez-Iglesias J., Liu C.C., Morgan T.E., Finch C.E., Zhou X.J. Joint genome-wide profiling of miRNA and mRNA expression in Alzheimer’s disease cortex reveals altered miRNA regulation. PLoS One. 2010;5(2):e8898. DOI: 10.1371/journal.pone.0008898.</mixed-citation></citation-alternatives></ref><ref id="cit39"><label>39</label><citation-alternatives><mixed-citation xml:lang="ru">Fan X., Liu Y., Jiang J., Ma Z., Wu H., Liu T. et al. miR-20a promotes proliferation and invasion by targeting APP in human ovarian cancer cells. Acta Biochim. Biophys. Sin. 2010;42(5):318–324. DOI: 10.1093/abbs/gmq026.</mixed-citation><mixed-citation xml:lang="en">Fan X., Liu Y., Jiang J., Ma Z., Wu H., Liu T. et al. miR-20a promotes proliferation and invasion by targeting APP in human ovarian cancer cells. Acta Biochim. Biophys. Sin. 2010;42(5):318–324. DOI: 10.1093/abbs/gmq026.</mixed-citation></citation-alternatives></ref><ref id="cit40"><label>40</label><citation-alternatives><mixed-citation xml:lang="ru">Vilardo E., Barbato C., Ciotti M., Cogoni C., Ruberti F. MicroRNA-101 regulates amyloid precursor protein expression in hippocampal neurons. J. Biol. Chem. 2010;285(24):18344–18351. DOI: 10.1074/jbc.M110.112664.</mixed-citation><mixed-citation xml:lang="en">Vilardo E., Barbato C., Ciotti M., Cogoni C., Ruberti F. MicroRNA-101 regulates amyloid precursor protein expression in hippocampal neurons. J. Biol. Chem. 2010;285(24):18344–18351. DOI: 10.1074/jbc.M110.112664.</mixed-citation></citation-alternatives></ref><ref id="cit41"><label>41</label><citation-alternatives><mixed-citation xml:lang="ru">Smith P., Al Hashimi A., Girard J., Delay C., Hébert S.S. In vivo regulation of amyloid precursor protein neuronal splicing by microRNAs. J. Neurochem. 2011;116(2):240–247. DOI: 10.1111/j.1471-4159.2010.07097.x.</mixed-citation><mixed-citation xml:lang="en">Smith P., Al Hashimi A., Girard J., Delay C., Hébert S.S. In vivo regulation of amyloid precursor protein neuronal splicing by microRNAs. J. Neurochem. 2011;116(2):240–247. DOI: 10.1111/j.1471-4159.2010.07097.x.</mixed-citation></citation-alternatives></ref><ref id="cit42"><label>42</label><citation-alternatives><mixed-citation xml:lang="ru">Guo A., Sun J., Jia P., Zhao Z. A novel microRNA and transcription factor mediated regulatory network in schizophrenia. BMC Syst. Biol. 2010;4:10. DOI: 10.1186/1752-0509-4-10.</mixed-citation><mixed-citation xml:lang="en">Guo A., Sun J., Jia P., Zhao Z. A novel microRNA and transcription factor mediated regulatory network in schizophrenia. BMC Syst. Biol. 2010;4:10. DOI: 10.1186/1752-0509-4-10.</mixed-citation></citation-alternatives></ref><ref id="cit43"><label>43</label><citation-alternatives><mixed-citation xml:lang="ru">Zhu Y., Kalbfleisch T., Brennan M.D., Li Y. A microRNA gene is hosted in an intron of a schizophrenia-susceptibility gene. Schizophr. Res. 2009;109(1–3):86–89. DOI: 10.1016/j.schres.2009.01.022.</mixed-citation><mixed-citation xml:lang="en">Zhu Y., Kalbfleisch T., Brennan M.D., Li Y. A microRNA gene is hosted in an intron of a schizophrenia-susceptibility gene. Schizophr. Res. 2009;109(1–3):86–89. DOI: 10.1016/j.schres.2009.01.022.</mixed-citation></citation-alternatives></ref><ref id="cit44"><label>44</label><citation-alternatives><mixed-citation xml:lang="ru">Mellios N., Huang H.S., Baker S.P., Galdzicka M., Ginns E., Akbarian S. Molecular determinants of dysregulated GABAergic gene expression in the prefrontal cortex of subjects with schizophrenia. Biol. Psychiatry. 2009;65(12):1006–1014. DOI: 10.1016/j.biopsych.2008.11.019.</mixed-citation><mixed-citation xml:lang="en">Mellios N., Huang H.S., Baker S.P., Galdzicka M., Ginns E., Akbarian S. Molecular determinants of dysregulated GABAergic gene expression in the prefrontal cortex of subjects with schizophrenia. Biol. Psychiatry. 2009;65(12):1006–1014. DOI: 10.1016/j.biopsych.2008.11.019.</mixed-citation></citation-alternatives></ref><ref id="cit45"><label>45</label><citation-alternatives><mixed-citation xml:lang="ru">Алфимова М.В., Кондратьев Н.В., Голов А.К., Голимбет В.Е. Метилирование ДНК в локусе MIR137HG, ассоциированном с шизофренией и интеллектом, может быть связано с заболеванием и когнитивными функциями. Генетика. 2019;55(2):207–213. DOI: 10.1134/S0016675819020036.</mixed-citation><mixed-citation xml:lang="en">Alfimova M.V., Kondratiev N.V., Golov A.K., Golimbet V.E. DNA methylation at the schizophrenia and intelligence GWAS-implicated MIR137HG locus may be associated with disease and cognitive functions. Russian Journal of Genetics. 2019;55(2):232–237 (In Russ.). DOI: 10.1134/S0026898418050026.</mixed-citation></citation-alternatives></ref><ref id="cit46"><label>46</label><citation-alternatives><mixed-citation xml:lang="ru">Hoffmann A., Ziller M., Spengler D. Childhood-onset schizophrenia: Insights from induced pluripotent stem cells. Int. J. Mol. Sci. 2018;19(12):3829. DOI: 10.3390/ijms19123829.</mixed-citation><mixed-citation xml:lang="en">Hoffmann A., Ziller M., Spengler D. Childhood-onset schizophrenia: Insights from induced pluripotent stem cells. Int. J. Mol. Sci. 2018;19(12):3829. DOI: 10.3390/ijms19123829.</mixed-citation></citation-alternatives></ref><ref id="cit47"><label>47</label><citation-alternatives><mixed-citation xml:lang="ru">Lee K.M., Hawi Z.H., Parkington H.C., Parish C.L., Kumar P.V., Polo J.M. et al. The application of human pluripotent stem cells to model the neuronal and glial components of neurodevelopmental disorders. Mol. Psychiatry. 2020;25(2):368–378. DOI: 10.1038/s41380-019-0495-0.</mixed-citation><mixed-citation xml:lang="en">Lee K.M., Hawi Z.H., Parkington H.C., Parish C.L., Kumar P.V., Polo J.M. et al. The application of human pluripotent stem cells to model the neuronal and glial components of neurodevelopmental disorders. Mol. Psychiatry. 2020;25(2):368–378. DOI: 10.1038/s41380-019-0495-0.</mixed-citation></citation-alternatives></ref><ref id="cit48"><label>48</label><citation-alternatives><mixed-citation xml:lang="ru">Gottesman I.I., Gould T.D. The endophenotype concept in psychiatry: etymology &amp; strategic intentions. Am. J. Psychiatry. 2003;160:636–645. DOI: 10.1176/appi.ajp.160.4.636.</mixed-citation><mixed-citation xml:lang="en">Gottesman I.I., Gould T.D. The endophenotype concept in psychiatry: etymology &amp; strategic intentions. Am. J. Psychiatry. 2003;160:636–645. DOI: 10.1176/appi.ajp.160.4.636.</mixed-citation></citation-alternatives></ref><ref id="cit49"><label>49</label><citation-alternatives><mixed-citation xml:lang="ru">Greenwood T.A., Swerdlow N.R., Gur R.E., Cadenhead K.S., Calkins M.E., Dobie D.J. et al. Genome-wide linkage analyses of 12 endophenotypes for schizophrenia from the Consortium on the Genetics of Schizophrenia. Am. J. Psychiatry. 2013;170(5):521–532. DOI: 10.1176/appi.ajp.2012.12020186.</mixed-citation><mixed-citation xml:lang="en">Greenwood T.A., Swerdlow N.R., Gur R.E., Cadenhead K.S., Calkins M.E., Dobie D.J. et al. Genome-wide linkage analyses of 12 endophenotypes for schizophrenia from the Consortium on the Genetics of Schizophrenia. Am. J. Psychiatry. 2013;170(5):521–532. DOI: 10.1176/appi.ajp.2012.12020186.</mixed-citation></citation-alternatives></ref><ref id="cit50"><label>50</label><citation-alternatives><mixed-citation xml:lang="ru">Manoach D.S., Agam Y. Neural markers of errors as endophenotypes in neuropsychiatric disorders. Front. Hum. Neurosci. 2013;7:350. DOI: 10.3389/fnhum.2013.00350.</mixed-citation><mixed-citation xml:lang="en">Manoach D.S., Agam Y. Neural markers of errors as endophenotypes in neuropsychiatric disorders. Front. Hum. Neurosci. 2013;7:350. DOI: 10.3389/fnhum.2013.00350.</mixed-citation></citation-alternatives></ref><ref id="cit51"><label>51</label><citation-alternatives><mixed-citation xml:lang="ru">Knowles E.E., Carless M.A., de Almeida M.A., Curran J.E., McKay D.R., Sprooten E. et al. Genome-wide significant localization for working and spatial memory: Identifying genes for psychosis using models of cognition. Am. J. Med. Genet. B Neuropsychiatr. Genet. 2014;165B(1):84–95. DOI: 10.1002/ajmg.b.32211.</mixed-citation><mixed-citation xml:lang="en">Knowles E.E., Carless M.A., de Almeida M.A., Curran J.E., McKay D.R., Sprooten E. et al. Genome-wide significant localization for working and spatial memory: Identifying genes for psychosis using models of cognition. Am. J. Med. Genet. B Neuropsychiatr. Genet. 2014;165B(1):84–95. DOI: 10.1002/ajmg.b.32211.</mixed-citation></citation-alternatives></ref><ref id="cit52"><label>52</label><citation-alternatives><mixed-citation xml:lang="ru">Zhang P., Zhang N., Fang S., He J., Fan L., Luo X. et al. Factor structure and measurement invariance of the Chinese version of the Snaith-Hamilton Pleasure Scale (SHAPS) in non-clinical and clinical populations. J. Affect. Disord. 2021;281:759–766. DOI: 10.1016/j.jad.2020.11.068.</mixed-citation><mixed-citation xml:lang="en">Zhang P., Zhang N., Fang S., He J., Fan L., Luo X. et al. Factor structure and measurement invariance of the Chinese version of the Snaith-Hamilton Pleasure Scale (SHAPS) in non-clinical and clinical populations. J. Affect. Disord. 2021;281:759–766. DOI: 10.1016/j.jad.2020.11.068.</mixed-citation></citation-alternatives></ref><ref id="cit53"><label>53</label><citation-alternatives><mixed-citation xml:lang="ru">Bradley E.R., Tai M., Hankin M., Woolley J.D. Preliminary evidence that oxytocin does not improve mentalizing in women with schizophrenia. Horm. Behav. 2021;128:104915. DOI: 10.1016/j.yhbeh.2020.104915.</mixed-citation><mixed-citation xml:lang="en">Bradley E.R., Tai M., Hankin M., Woolley J.D. Preliminary evidence that oxytocin does not improve mentalizing in women with schizophrenia. Horm. Behav. 2021;128:104915. DOI: 10.1016/j.yhbeh.2020.104915.</mixed-citation></citation-alternatives></ref><ref id="cit54"><label>54</label><citation-alternatives><mixed-citation xml:lang="ru">Stevens B.W., DiBattista A.M., William Rebeck G., Green A.E. A gene-brain-cognition pathway for the effect of an Alzheimer׳s risk gene on working memory in young adults. Neuropsychologia. 2014;61:143–149. DOI: 10.1016/j.neuropsychologia.2014.06.021.</mixed-citation><mixed-citation xml:lang="en">Stevens B.W., DiBattista A.M., William Rebeck G., Green A.E. A gene-brain-cognition pathway for the effect of an Alzheimer׳s risk gene on working memory in young adults. Neuropsychologia. 2014;61:143–149. DOI: 10.1016/j.neuropsychologia.2014.06.021.</mixed-citation></citation-alternatives></ref><ref id="cit55"><label>55</label><citation-alternatives><mixed-citation xml:lang="ru">Johansson L. Can stress increase Alzheimer’s disease risk in women? Expert. Rev. Neurother. 2014;4(2):123–125. DOI:10.1586/14737175.2014.878651.</mixed-citation><mixed-citation xml:lang="en">Johansson L. Can stress increase Alzheimer’s disease risk in women? Expert. Rev. Neurother. 2014;4(2):123–125. DOI:10.1586/14737175.2014.878651.</mixed-citation></citation-alternatives></ref><ref id="cit56"><label>56</label><citation-alternatives><mixed-citation xml:lang="ru">Киренская А.В., Сторожева З.И., Ткаченко А.А. Нейрофизиологические эндофенотипы шизофрении как инструмент для изучения внимания и контроля поведения: перспективы исследований и диагностики. СПб.: Нестор-История; 2015:336.</mixed-citation><mixed-citation xml:lang="en">Kirenskaya A.V., Storozheva Z.I., Tkachenko A.A. Neurophysiological endophenotypes of schizophrenia as a tool for studying attention and behavior control: research and diagnostic perspectives. St. Petesburg: Nestor-History; 2015:336 (In Russ.).</mixed-citation></citation-alternatives></ref><ref id="cit57"><label>57</label><citation-alternatives><mixed-citation xml:lang="ru">Macedo A., Gómez C., Rebelo M.Â., Poza J., Gomes I., Martins S. et al. Risk variants in three Alzheimer’s disease genes show association with EEG endophenotypes. J. Alzheimers Dis. 2021;80(1):209–223. DOI: 10.3233/JAD-200963.</mixed-citation><mixed-citation xml:lang="en">Macedo A., Gómez C., Rebelo M.Â., Poza J., Gomes I., Martins S. et al. Risk variants in three Alzheimer’s disease genes show association with EEG endophenotypes. J. Alzheimers Dis. 2021;80(1):209–223. DOI: 10.3233/JAD-200963.</mixed-citation></citation-alternatives></ref><ref id="cit58"><label>58</label><citation-alternatives><mixed-citation xml:lang="ru">Refisch A., Chung H.Y., Komatsuzaki S., Schumann A., Mühleisen T.W., Nöthen M.M. et al. A common variation in HCN1 is associated with heart rate variability in schizophrenia. Schizophr. Res. 2021;229:73–79. DOI: 10.1016/j.schres.2020.11.017.</mixed-citation><mixed-citation xml:lang="en">Refisch A., Chung H.Y., Komatsuzaki S., Schumann A., Mühleisen T.W., Nöthen M.M. et al. A common variation in HCN1 is associated with heart rate variability in schizophrenia. Schizophr. Res. 2021;229:73–79. DOI: 10.1016/j.schres.2020.11.017.</mixed-citation></citation-alternatives></ref><ref id="cit59"><label>59</label><citation-alternatives><mixed-citation xml:lang="ru">Kohl S., Heekeren K., Klosterkötter J., Kuhn J. Prepulse inhibition in psychiatric disorders-apart from schizophrenia. J. Psychiatr. Res. 2013;47(4):445–452. DOI: 10.1016/j.jpsychires.2012.11.018.</mixed-citation><mixed-citation xml:lang="en">Kohl S., Heekeren K., Klosterkötter J., Kuhn J. Prepulse inhibition in psychiatric disorders-apart from schizophrenia. J. Psychiatr. Res. 2013;47(4):445–452. DOI: 10.1016/j.jpsychires.2012.11.018.</mixed-citation></citation-alternatives></ref><ref id="cit60"><label>60</label><citation-alternatives><mixed-citation xml:lang="ru">Kim Y., Noh Y.W., Kim K., Kim E. Hyperactive ACC-MDT pathway suppresses prepulse inhibition in mice. Schizophr. Bull. 2021;47(1):31–43.DOI: 10.1093/schbul/sbaa090.</mixed-citation><mixed-citation xml:lang="en">Kim Y., Noh Y.W., Kim K., Kim E. Hyperactive ACC-MDT pathway suppresses prepulse inhibition in mice. Schizophr. Bull. 2021;47(1):31–43.DOI: 10.1093/schbul/sbaa090.</mixed-citation></citation-alternatives></ref><ref id="cit61"><label>61</label><citation-alternatives><mixed-citation xml:lang="ru">Fagan A.M., Mintun M.A., Mach R.H., Lee S.Y., Dence C.S., Shah A.R. et al. Inverse relation between in vivo amyloid imaging load and cerebrospinal fl uid Abeta42 in humans. Ann. Neurol. 2006;59(3):512–519. DOI: 10.1002/ana.20730.</mixed-citation><mixed-citation xml:lang="en">Fagan A.M., Mintun M.A., Mach R.H., Lee S.Y., Dence C.S., Shah A.R. et al. Inverse relation between in vivo amyloid imaging load and cerebrospinal fl uid Abeta42 in humans. Ann. Neurol. 2006;59(3):512–519. DOI: 10.1002/ana.20730.</mixed-citation></citation-alternatives></ref><ref id="cit62"><label>62</label><citation-alternatives><mixed-citation xml:lang="ru">Cruchaga C., Kauwe J.S., Mayo K., Spiegel N., Bertelsen S., Nowotny P. et al. SNPs associated with cerebrospinal fl uid phospho-tau levels infl uence rate of decline in Alzheimer’s disease. PLoS Genet. 2010;6(9):e1001101. DOI: 10.1371/journal.pgen.1001101.</mixed-citation><mixed-citation xml:lang="en">Cruchaga C., Kauwe J.S., Mayo K., Spiegel N., Bertelsen S., Nowotny P. et al. SNPs associated with cerebrospinal fl uid phospho-tau levels infl uence rate of decline in Alzheimer’s disease. PLoS Genet. 2010;6(9):e1001101. DOI: 10.1371/journal.pgen.1001101.</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>
