Некоторые публикации наших клиентов
GWAS of depression in 4,520 individuals from the Russian population highlights the role of MAGI2 (S-SCAM) in the gut-brain axis
Pinakhina D., Yermakovich D., Vergasova E., Kasyanov E., Rukavishnikov G., Rezapova V., Kolosov N., Sergushichev A., Popov I., Kovalenko E., Ilinskaya A., Kim A., Plotnikov N., Ilinsky V., Neznanov N., Mazo G., Kibitov A., Rakitko A., Artomov M.
Frontiers in Genetics (2023), 13:972196 doi.org/10.3389/fgene.2022.972196
Consolidation of metabolomic, proteomic, and GWAS data in connective model of schizophrenia
Kopylov A.T., Stepanov A.A., Butkova T.V., Malsagova K.A., Zakharova N.V., Kostyuk G.P., Elmuratov A.U., Kaysheva A.L.
Scientific Reports (2023), 13, 2139 doi.org/10.1038/s41598-023-29117-7
Validation of a DSM-5-based screening test using digital phenotyping in the Russian population
Kasyanov E.D., Verbitskaya E.V., Rakitko A.S., Ilyinsky V.V., Rukavishnikov G.V., Neznanov N.G., Kibitov A.O., Mazo G.E.
Zhurnal Nevrologii i Psikhiatrii Imeni S.S. Korsakova (2022), 122 (6. Vyp. 2): 64-70 doi.org/10.17116/jnevro202212206264
Apremilast Pharmacogenomics in Russian Patients with Moderate-to-Severe and Severe Psoriasis
Verbenko D.A., Karamova A.E., Artamonova O.G., Deryabin D.G., Rakitko A., Chernitsov A., Krasnenko A., Elmuratov A., Solomka V.S., Kubanov A.A.
Journal of Personalized Medicine (2021); 11(1):20. doi.org/10.3390/jpm11010020
Mapping the human genetic architecture of COVID-19
Increased risk of severe clinical course of COVID-19 in carriers of HLA-C*04:01
Weiner J., Suwalski P., Holtgrewe M., Rakitko A., Thibeault C., Müller M., Patriki D., Quedenau C., Krüger U., Ilinsky V., Popov I., et al.
EClinicalMedicine (2021), 40:101099. doi:10.1016/j.eclinm.2021.101099
Genome assembly using quantum and quantuminspired annealing
Boev A.S., Rakitko A.S., Usmanov S.R., Kobzeva A.N., Popov I.V., Ilinsky V.V., Kiktenko E.O., Fedorov A.K.
Scientific Reports (2021), 11, 13183 doi.org/10.1038/s41598-021-88321-5
Screening of Depressive Symptoms in a Russian General Population Sample: A Web-based Cross-sectional Study
Kibitov A.A., Rakitko A.S., Kasyanov E.D., Rukavishnikov G.V., Kozlova K.A., Ilinsky V.V., Neznanov N.G., Mazo G.E., Kibitov A.O.
Clinical Practice & Epidemiology in Mental Health (2021), 17: 205-211. doi.org/10.2174/1745017902117010205
Non-linear interaction between physical activity and polygenic risk score of body mass index in Danish and Russian populations
Borisevich D., Schnurr T.M., Engelbrechtsen L., Rakitko A., Ängquist L., Ilinsky V., Aadahl M., Grarup N., Pedersen O., Sørensen T.I.A., Hansen T.
PLoS One (2021), 16(10): e0258748. doi.org/10.1371/journal.pone.0258748
Neuronal ceroid lipofuscinosis in the Russian population: Two novel mutations and the prevalence of heterozygous carriers
Kozina A.A., Okuneva E.G., Baryshnikova N.V., Kondakova O.B., Nikolaeva E.A., Fedoniuk I.D., Mikhailova S.V., Krasnenko A.Y., Stetsenko I.F., Plotnikov N.A., Klimchuk O.I., Popov Y.V., Surkova E.I., Shatalov P.A., Rakitko A.S., Ilinsky V.V.
Molecular Genetics & Genomic Medicine (2020):e1228 doi.org/10.1002/mgg3.1228
Two novel PCDH19 mutations in Russian patients with epilepsy with intellectual disability limited to females: a case report
Kozina A.A., Okuneva E.G., Baryshnikova N.V., Fedonyuk I.D., Kholin A.A., Il'ina E.S., Krasnenko A.Y., Stetsenko I.F., Plotnikov N.A., Klimchuk O.I., Surkova E.I., Ilinsky V.V.
BMC Medical Genetics (2020), 21, 209. doi.org/10.1186/s12881-020-01119-6
Liddle syndrome due to a novel mutation in the γ subunit of the epithelial sodium channel (ENaC) in family from Russia: a case report
Kozina A.A., Trofimova T.A., Okuneva E.G., Baryshnikova N.V., Obuhova V.A., Krasnenko A.Y., Tsukanov K.Y., Klimchuk O.I., Surkova E.I., Shatalov P.A., Ilinsky V.V.
BMC Nephrology (2019), 20(1):389 doi.org/10.1186/s12882-019-1579-4
Compound heterozygous POMGNT1 mutations leading to muscular dystrophy-dystroglycanopathy type A3: a case report
Kondakova O.B., Krasnenko A.Yu., Tsukanov K.Yu., Klimchuk O.I., Korostin D.O., Davidova A.I., Batysheva T.T., Zhurkova N.V., Surkova E.I., Shatalov P.A., Ilinsky V.V.
BMC Pediatrics (2019), 19, 98 doi.org/10.1186/s12887-019-1470-2
Atypical onset of nephropathic infantile cystinosis in a Russian patient with rare CTNS mutation
Kozina A.A., Okuneva E.G., Baryshnikova N.V., Krasnenko A.Yu., Tsukanov K.Yu., Klimchuk O.I., Nikishina T.A., Fedoniuk I.D., Surkova E.I., Shatalov P.A., Ilinsky V.V.
Clinical Case Reports (2018); 6(9):1871-1876. doi.org/10.1002/ccr3.1678
A novel MFSD8 mutation in a Russian patient with neuronal ceroid lipofuscinosis type 7: a case report
Kozina A.A., Okuneva E.G., Baryshnikova N.V., Krasnenko A.Yu., Tsukanov K.Yu., Klimchuk O.I., Kondakova O.B., Larionova A.N., Batysheva T.T., Surkova E.I., Shatalov P.A., Ilinsky V.V.
BMC Medical Genetics (2018); 19(1):151. doi.org/10.1186/s12881-018-0669-7
Cytogenetic and Transcriptomic Analysis of Human Endometrial MSC Retaining Proliferative Activity after Sublethal Heat Shock
Shilina M.A., Grinchuk T.M., Anatskaya O.V., Vinogradov A.E., Alekseenko L. L, Elmuratov A. U., Nikolsky N.N.
Cells 2018, 7(11), 184; doi.org/10.3390/cells7110184
Draft Genome Sequence of Rhodococcus sp. Strain M8, Which Can Degrade a Broad Range of Nitriles
Consequences of early life stress on genomic landscape of H3K4me3 in prefrontal cortex of adult mice
Ershov, N.I., Bondar, N.P., Lepeshko, A.A., Reshetnikov, V.V., Ryabushkina, J.A., Merkulova, T.I.
BMC Genomics (2018) 19:1471-2164. doi.org/10.1186/s12864-018-4479-2
De novo assembling and primary analysis of genome and transcriptome of gray whale Eschrichtius robustus
Moskalev, A.А., Kudryavtseva, A.V., Graphodatsky, A.S., Beklemisheva, V.R., Serdyukova, N.A., Krutovsky, K.V., Sharov, V.V., Kulakovskiy, I.V., Lando, A.S., Kasianov, A.S., Kuzmin, D.A., Putintseva, Y.A., Feranchuk, S.I., Shaposhnikov, M.V., Fraifeld, V.E., Toren, D., Snezhkina, A.V., Sitnik, V.V.
BMC Evolutionary Biology (2017) 17:1471-2148. doi.org/10.1186/s12862-017-1103-z
Molecular Genetic Analysis of Human Endometrial Mesenchymal Stem Cells That Survived Sublethal Heat Shock
Vinogradov A.E., Shilina M.A., Anatskaya O.V., Alekseenko L.L, Fridlyanskaya I.I., Krasnenko A., Kim A., Korostin D., Ilynsky V., Elmuratov A., Tsyganov O., Grinchuk T.M., Nikolsky N.N.
Stem Cells International (2017) 2362630. doi.org/10.1155/2017/2362630
Genome analysis of Acidiplasma sp. MBA-1, a polyextremophilic archaeon predominant in the microbial community of a bioleaching reactor
Draft genome of the strain RCAM1026 Rhizobium leguminosarum bv. viciae
The dtd gene from Bacillus amyloliquefaciens encodes a putative d-tyrosyl-tRNATyr deacylase and is a selectable marker for Bacillus subtilis
2023 год