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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: baranov vs. 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.
The spectrum of pathogenic variants of the ATP7B gene in Wilson disease in the Russian Federation.
Balashova MS, Tuluzanovskaya IG, Glotov OS, Glotov AS, Barbitoff YA, Fedyakov MA, Alaverdian DA, Ivashchenko TE, Romanova OV, Sarana AM, Scherbak SG, Baranov VS, Filimonov MI, Skalny AV, Zhuchenko NA, Ignatova TM, Asanov AY. Balashova MS, et al. Among authors: baranov vs. J Trace Elem Med Biol. 2020 May;59:126420. doi: 10.1016/j.jtemb.2019.126420. Epub 2019 Oct 25. J Trace Elem Med Biol. 2020. PMID: 31708252
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: baranov vs. 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
Targeted sequencing analysis of ACVR2A gene identifies novel risk variants associated with preeclampsia.
Glotov AS, Kazakov SV, Vashukova ES, Pakin VS, Danilova MM, Nasykhova YA, Masharsky AE, Mozgovaya EV, Eremeeva DR, Zainullina MS, Baranov VS. Glotov AS, et al. Among authors: baranov vs. J Matern Fetal Neonatal Med. 2019 Sep;32(17):2790-2796. doi: 10.1080/14767058.2018.1449204. Epub 2018 Mar 21. J Matern Fetal Neonatal Med. 2019. PMID: 29506428 Free article.
Analysis of the Spectrum of ACE2 Variation Suggests a Possible Influence of Rare and Common Variants on Susceptibility to COVID-19 and Severity of Outcome.
Shikov AE, Barbitoff YA, Glotov AS, Danilova MM, Tonyan ZN, Nasykhova YA, Mikhailova AA, Bespalova ON, Kalinin RS, Mirzorustamova AM, Kogan IY, Baranov VS, Chernov AN, Pavlovich DM, Azarenko SV, Fedyakov MA, Tsay VV, Eismont YA, Romanova OV, Hobotnikov DN, Vologzhanin DA, Mosenko SV, Ponomareva TA, Talts YA, Anisenkova AU, Lisovets DG, Sarana AM, Urazov SP, Scherbak SG, Glotov OS. Shikov AE, et al. Among authors: baranov vs. Front Genet. 2020 Sep 29;11:551220. doi: 10.3389/fgene.2020.551220. eCollection 2020. Front Genet. 2020. PMID: 33133145 Free PMC article.
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: baranov vs. Front Genet. 2019 Nov 20;10:1164. doi: 10.3389/fgene.2019.01164. eCollection 2019. Front Genet. 2019. PMID: 31824569 Free PMC article.
234 results