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A novel elastin gene frameshift mutation in a Russian family with cutis laxa: a case report.
BMC Dermatol. 2019 Jan 31;19(1):4. doi: 10.1186/s12895-019-0084-6.
BMC Dermatol. 2019.
PMID: 30704477
Free PMC article.
[A bioinformatic pipeline for NGS data analysis and mutation calling in human solid tumors].
Tsukanov KY, Krasnenko AY, Plakhina DA, Korostin DO, Churov AV, Druzhilovskaya OS, Rebrikov DV, Ilinsky VV.
Tsukanov KY, et al. Among authors: krasnenko ay.
Biomed Khim. 2017 Oct;63(5):413-417. doi: 10.18097/PBMC20176305413.
Biomed Khim. 2017.
PMID: 29080873
Russian.
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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 AA, Trofimova TA, Okuneva EG, Baryshnikova NV, Obuhova VA, Krasnenko AY, Tsukanov KY, Klimchuk OI, Surkova EI, Shatalov PA, Ilinsky VV.
Kozina AA, et al. Among authors: krasnenko ay.
BMC Nephrol. 2019 Oct 26;20(1):389. doi: 10.1186/s12882-019-1579-4.
BMC Nephrol. 2019.
PMID: 31655555
Free PMC article.
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A second update on mapping the human genetic architecture of COVID-19.
COVID-19 Host Genetics Initiative.
COVID-19 Host Genetics Initiative.
Nature. 2023 Sep;621(7977):E7-E26. doi: 10.1038/s41586-023-06355-3. Epub 2023 Sep 6.
Nature. 2023.
PMID: 37674002
Free PMC article.
No abstract available.
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Two novel PCDH19 mutations in Russian patients with epilepsy with intellectual disability limited to females: a case report.
Kozina AA, Okuneva EG, Baryshnikova NV, Fedonyuk ID, Kholin AA, Il'ina ES, Krasnenko AY, Stetsenko IF, Plotnikov NA, Klimchuk OI, Surkova EI, Ilinsky VV.
Kozina AA, et al. Among authors: krasnenko ay.
BMC Med Genet. 2020 Oct 21;21(1):209. doi: 10.1186/s12881-020-01119-6.
BMC Med Genet. 2020.
PMID: 33087045
Free PMC article.
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Neuronal ceroid lipofuscinosis in the Russian population: Two novel mutations and the prevalence of heterozygous carriers.
Kozina AA, Okuneva EG, Baryshnikova NV, Kondakova OB, Nikolaeva EA, Fedoniuk ID, Mikhailova SV, Krasnenko AY, Stetsenko IF, Plotnikov NA, Klimchuk OI, Popov YV, Surkova EI, Shatalov PA, Rakitko AS, Ilinsky VV.
Kozina AA, et al. Among authors: krasnenko ay.
Mol Genet Genomic Med. 2020 Jul;8(7):e1228. doi: 10.1002/mgg3.1228. Epub 2020 May 15.
Mol Genet Genomic Med. 2020.
PMID: 32412666
Free PMC article.
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A novel MFSD8 mutation in a Russian patient with neuronal ceroid lipofuscinosis type 7: a case report.
Kozina AA, Okuneva EG, Baryshnikova NV, Krasnenko AY, Tsukanov KY, Klimchuk OI, Kondakova OB, Larionova AN, Batysheva TT, Surkova EI, Shatalov PA, Ilinsky VV.
Kozina AA, et al. Among authors: krasnenko ay.
BMC Med Genet. 2018 Aug 25;19(1):151. doi: 10.1186/s12881-018-0669-7.
BMC Med Genet. 2018.
PMID: 30144815
Free PMC article.
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