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Year | Number of Results |
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2016 | 2 |
2017 | 1 |
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Page 1
Pilot Screening of Cell-Free mtDNA in NIPT: Quality Control, Variant Calling, and Haplogroup Determination.
Genes (Basel). 2021 May 14;12(5):743. doi: 10.3390/genes12050743.
Genes (Basel). 2021.
PMID: 34069212
Free PMC article.
Case report: Preimplantation genetic testing for infantile GM1 gangliosidosis.
Zagaynova VA, Nasykhova YA, Tonyan ZN, Danilova MM, Dvoynova NM, Lazareva TE, Ivashchenko TE, Shabanova ES, Krikheli IO, Lesik EA, Bespalova ON, Kogan IY, Glotov AS.
Zagaynova VA, et al. Among authors: ivashchenko te.
Front Genet. 2024 Feb 9;15:1344051. doi: 10.3389/fgene.2024.1344051. eCollection 2024.
Front Genet. 2024.
PMID: 38404665
Free PMC article.
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Reproductive History of a Woman With 8p and 18p Genetic Imbalance and Minor Phenotypic Abnormalities.
Pendina AA, Shilenkova YV, Talantova OE, Efimova OA, Chiryaeva OG, Malysheva OV, Dudkina VS, Petrova LI, Serebryakova EA, Shabanova ES, Mekina ID, Komarova EM, Koltsova AS, Tikhonov AV, Tral TG, Tolibova GK, Osinovskaya NS, Krapivin MI, Petrovskaia-Kaminskaia AV, Korchak TS, Ivashchenko TE, Glotov OS, Romanova OV, Shikov AE, Urazov SP, Tsay VV, Eismont YA, Scherbak SG, Sagurova YM, Vashukova ES, Kozyulina PY, Dvoynova NM, Glotov AS, Baranov VS, Gzgzyan AM, Kogan IY.
Pendina AA, et al. Among authors: ivashchenko te.
Front Genet. 2019 Nov 20;10:1164. doi: 10.3389/fgene.2019.01164. eCollection 2019.
Front Genet. 2019.
PMID: 31824569
Free PMC article.
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Whole‑exome sequencing in Russian children with non‑type 1 diabetes mellitus reveals a wide spectrum of genetic variants in MODY‑related and unrelated genes.
Glotov OS, Serebryakova EA, Turkunova ME, Efimova OA, Glotov AS, Barbitoff YA, Nasykhova YA, Predeus AV, Polev DE, Fedyakov MA, Polyakova IV, Ivashchenko TE, Shved NY, Shabanova ES, Tiselko AV, Romanova OV, Sarana AM, Pendina AA, Scherbak SG, Musina EV, Petrovskaia-Kaminskaia AV, Lonishin LR, Ditkovskaya LV, Zhelenina LА, Tyrtova LV, Berseneva OS, Skitchenko RK, Suspitsin EN, Bashnina EB, Baranov VS.
Glotov OS, et al. Among authors: ivashchenko te.
Mol Med Rep. 2019 Dec;20(6):4905-4914. doi: 10.3892/mmr.2019.10751. Epub 2019 Oct 16.
Mol Med Rep. 2019.
PMID: 31638168
Free PMC article.
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Frequency and Spectrum of MED12 Exon 2 Mutations in Multiple Versus Solitary Uterine Leiomyomas From Russian Patients.
Osinovskaya NS, Malysheva OV, Shved NY, Ivashchenko TE, Sultanov IY, Efimova OA, Yarmolinskaya MI, Bezhenar VF, Baranov VS.
Osinovskaya NS, et al. Among authors: ivashchenko te.
Int J Gynecol Pathol. 2016 Nov;35(6):509-515. doi: 10.1097/PGP.0000000000000255.
Int J Gynecol Pathol. 2016.
PMID: 26630226
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Catechol-O-methyltransferase Val158Met polymorphism is associated with increased risk of multiple uterine leiomyomas either positive or negative for MED12 exon 2 mutations.
Dzhemlikhanova LK, Efimova OA, Osinovskaya NS, Parfenyev SE, Niauri DA, Sultanov IY, Malysheva OV, Pendina AA, Shved NY, Ivashchenko TE, Yarmolinskaya MI, Kakhiani MI, Gorovaya EA, Tkachenko AN, Baranov VS.
Dzhemlikhanova LK, et al. Among authors: ivashchenko te.
J Clin Pathol. 2017 Mar;70(3):233-236. doi: 10.1136/jclinpath-2016-203976. Epub 2016 Aug 4.
J Clin Pathol. 2017.
PMID: 27491313
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