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Наши публикации в журналах Q1

Opening up new horizons for psychiatric genetics in the Russian Federation: moving toward a national consortium. Fedorenko O.Y., Golimbet V.E., Ivanova S.А., Levchenko А., Gainetdinov R.R., Semke A.V., Simutkin G.G., Gareeva А.E., Glotov А.S., Gryaznova A., Iourov I.Y., Krupitsky E.M., Lebedev I.N., Mazo G.E., Kaleda V.G., Abramova L.I., Oleichik I.V., Nasykhova Y.A., Nasyrova R.F., Nikolishin A.E., Kasyanov E.D., Rukavishnikov G.V., Timerbulatov I.F., Brodyansky V.M., Vorsanova S.G., Yurov Y.B., et al. // Molecular Psychiatry. 2019. – P. 1-13. doi: 10.1038/s41380-019-0354-z (Impact factor 11,640)

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An experimental assay of the interactions of amino acids from orthologous sequences shaping a complex fitness landscape. Pokusaeva VO, Usmanova DR, Putintseva EV, Espinar L, Sarkisyan KS, Mishin AS, Povolotskaya IS, et al. (2019) PLoS Genet 15(4): e1008079. https://doi.org/10.1371/journal.pgen.1008079

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Effect of everolimus on renal function in patients with tuberous sclerosis complex: evidence from EXIST-1 and EXIST-2 Bissler JJ, Budde K, Sauter M, Franz DN, Zonnenberg BA, Frost MD, Belousova E, Berkowitz N, Ridolfi A, Christopher Kingswood J. Nephrology Dialysis Transplantation. 2019; Volume: 34 Issue: 6 Pages: 1000-1008 DOI: 10.1093/ndt/gfy132; https://academic.oup.com/ndt/article/34/6/1000/5056117

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CRISPR/Cas9-generated mouse model of Duchenne muscular dystrophy recapitulating a newly identified large 430 kb deletion in the human DMD geneю Egorova TV, Zotova ED, Reshetov DA, Polikarpova A, Vassilieva SG, Vlodavets DV, Gavrilov AA, Ulianov SV, Buchman VL, Deykin AV. Disease Models and Mechanisms. 04.2019; 12(4):037655. DOI: 10.1242/dmm.037655

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Advanced liver disease in Russian children and adolescents with chronic hepatitis C Turkova A., Volynets G.V., Crichton S., Skvortsova T.A., Panfilova V.N., Rogozina N.V., Khavkin A.I., Tumanova E.L., Indolfi G., Thorne C. Journal of Viral Hepatitis. 2019. Т. 26. № 7. С. 881-892. https://onlinelibrary.wiley.com/doi/full/10.1111/jvh.13093

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TSC-associated neuropsychiatric disorders (TAND): findings from the TOSCA natural history study. de Vries, PJ., Belousova E.D., Benedik M.P., Curatolo, P., Dahlin, M., D'Amato L., d'Augeres G.B., Ferreira J.C., Vries P.J., // ORPHANET JOURNAL OF RARE DISEASES. - 2018. - V.13. DOI: 10.1186/s13023-018-0901-8

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Chromosome instability in the neurodegenerating brain. Yurov Y.B., Vorsanova S.G., Iourov I.Y Frontiers in Genetics 2019. – Vol.10:892. – 4p. https://www.frontiersin.org/articles/10.3389/fgene.2019.00892/full

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Ontogenetic and pathogenetic views on somatic chromosomal mosaicism. Iourov I.Y., Vorsanova S.G., Yurov Y.B., Kutsev S.I. Genes 2019. – Vol.10, N379. – P. 1-25. https://www.mdpi.com/2073-4425/10/5/379

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The European Society for Paediatric Nephrology study of pediatric renal care in Europe: comparative analysis 1998-2017. Prikhodina L, Ehrich J, Shroff R, Topaloglu R, Levtchenko E; European Society for Paediatric Nephrology Pediatric Nephrology 2019 DOI: 10.1007/s00467-019-04378-5

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Angiomyolipoma rebound tumor growth after discontinuation of everolimus in patients with tuberous sclerosis complex or sporadic lymphangioleiomyomatosis. Bissler JJ, Nonomura N, Budde K, Zonnenberg B.A, Fischereder M, Voi M, Louveau A.L., Herbst F., Bebin E.M., Curatolo P, Zonta A., Belousova E. PlosOne. 2018;V 13; Issue 9; https://journals.plos.org/plosone/article/authors?id=10.1371/journal.pone.0201005

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Analysis of the Phenotypes in the Rett Networked Database. Frullanti E, Papa FT, Grillo E, Voinova V., et al. International Journal of Genomics 2019; 2019:6956934. DOI: 10.1155/2019/6956934; https://www.hindawi.com/journals/ijg/2019/6956934/

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Pilot data of serum proteins from children with autism spectrum disorders. Kaysheva A.L., Stepanov A.A., Kopylov A.T., Butkova T.V., Pleshakova T., Ryabtsev V.V., Iourov I.Y., Vorsanova S.G., Ivanov Y.D. Datain Brief 2019. - Vol. 27:1045582. - P.1-8. https://www.sciencedirect.com/science/article/pii/S2352340919309138

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