Comparison of Uncontrolled and Device-Induced Therapeutic Hypothermia in Newborn Infants with Hypoxic Ischemic Encephalopathy by A. A. Zarubin, E. S. Filippov, A. S. Vanyarkina, O. G. Ivanova, A. A. Shishkina

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The Effect of Severe Birth Asphyxia on the Hemostasis System in Newborns During the First Hour of Life by I. E. Golub, A. A. Zarubin, N. I. Micheeva, A. S. Vanyarkina, O. G. Ivanova

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Changes in DNA methylation profile in liver tissue during progression of HCV-induced fibrosis to hepatocellular carcinoma by I. A. Goncharova, A. A. Zarubin, N. P. Babushkina, I. A. Koroleva, M. S. Nazarenko

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Blocks identical by descent in the genomes of the indigenous population of Siberia demonstrate genetic links between populations by N. A. Kolesnikov, V. N. Kharkov, K. V. Vagaitseva, A. A. Zarubin, V. A. Stepanov

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The Tasks of Modeling the Changes in Audiences of Modern Information and Communication Services by Methods of Cellular Automata by A.A. Zarubin, O.E. Kyzyurov, S.D. Pavlov, I.R. Patrushev, A.A. Saveleva

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HYPOXIC-ISCHEMIC ENCEPHALOPATHY IN NEONATES BORN TO SEVERE BIRTH ASPHYXIA by A. A. Zarubin, N. I. Mikheeva, E. S. Filippov, T. A. Belogorova, A. S. Vanyarkina, A. A. Shishkin

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Structure and origin of Tuvan gene pool according to autosome SNP and Y-chromosome haplogroups by V. A. Stepanov, N. A. Kolesnikov, L. V. Valikhova, A. A. Zarubin, I. Yu. Khitrinskaya, V. N. Kharkov

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Relationship of the gene pool of the Khants with the peoples of Western Siberia, Cis-Urals and the Altai-Sayan Region according to the data on the polymorphism of autosomic locus a... by V. N. Kharkov, N. A. Kolesnikov, L. V. Valikhova, A. A. Zarubin, M. G. Svarovskaya, A. V. Marusin, I. Yu. Khitrinskaya, V. A. Stepanov

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New mutation of the TP53 gene associated with the hereditary breast cancer in a young Tuvinian woman by P. A. Gervas, A. Yu. Molokov, A. A. Zarubin, A. A. Ponomareva, N. N. Babyshkina, V. A. Belyavskaya, L. F. Pisareva, E. L. Choynzonov, N. V. Cherdyntseva

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Deoxyribonucleic acid methylation in the enhancer region of the CDKN2A/2B and CDKN2B-AS1 genes in blood vessels and cells in patients with carotid atherosclerosis by Yu. A. Koroleva, A. V. Markov, I. A. Goncharova, A. A. Sleptsov, N. P. Babushkina, N. R. Valiakhmetov, D. V. Sharysh, A. A. Zarubin, M. S. Kuznetsov, B. N. Kozlov, M. S. Nazarenko

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A novel germline mutation of the <i>PALB2</i> gene in a young Yakut breast cancer woman by P. A. Gervas, A. Yu. Molokov, A. A. Zarubin, A. A. Ivanova, D. G. Tikhonov, N. S. Kipriyanova, A. N. Egorov, L. D. Zhuikova, N. A. Shefer, E. B. Topolnitskiy, V. A. Belyavskaya, L. F. Pisareva, E. L. Choynzonov, N. V. Cherdyntseva

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Diagnostic yield of chromosomal microarray and trio whole exome sequencing in congenital brain anomalies by E. A. Fonova, A. A. Kashevarova, M. E. Lopatkina, A. A. Sivtsev, A. A. Zarubin, V. V. Demeneva, G. N. Seitova, L. I. Minaycheva, O. A. Salyukova, S. V. Fadyushina, V. V. Petrova, E. O. Belyaeva, L. P. Nazarenko, I. N. Lebedev

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Combined whole exome sequencing and chromosomal microarray analysis improve clinical interpretation of genomic variants in patients with intellectual disability by A. A. Kashevarova, E. O. Belyaeva, E. A. Fonova, M. E. Lopatkina, O. Y. Vasilyeva, D. A. Fedotov, A. A. Zarubin, A. A. Sivtsev, V. V. Demeneva, O. A. Salyukova, V. V. Petrova, S. V. Fadiushina, L. I. Minaycheva, G. N. Seitova, L. P. Nazarenko, I. N. Lebedev

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Generation of an induced pluripotent stem cell line ICGi030-A from a Wilson's disease patient carrying a frameshift mutation p.Lys1013fs and missense mutation p.H1069Q in the ATP7B... by D.I. Zhigalina, A.A. Malakhova, O.Yu. Vasilyeva, E.V. Grigor'eva, A.A. Sivtsev, N.A. Kolesnikov, M.E. Lopatkina, R.R. Savchenko, I.Zh. Zhalsanova, A.E. Postrigan', A.A. Zarubin, T.V. Nikitina, A.O. Bueverov, P.O. Bogomolov, S.M. Zakian, N.A. Skryabin

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