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Association and Gene-Gene Interactions Study of Late-Onset Alzheimer's Disease in the Russian Population.
Genes (Basel). 2021 Oct 19;12(10):1647. doi: 10.3390/genes12101647.
Genes (Basel). 2021.
PMID: 34681041
Free PMC article.
Case Report: A Novel Homozygous Variant of the SERPINF1 Gene in Rare Osteogenesis Imperfecta Type VI.
Zhalsanova IZ, Postrigan AE, Valiakhmetov NR, Kolesnikov NA, Zhigalina DI, Zarubin AA, Petrova VV, Minaycheva LI, Seitova GN, Skryabin NA, Stepanov VA.
Zhalsanova IZ, et al. Among authors: minaycheva li.
Int J Mol Sci. 2023 Apr 3;24(7):6672. doi: 10.3390/ijms24076672.
Int J Mol Sci. 2023.
PMID: 37047644
Free PMC article.
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A comparison of neuropsychological performance between US and Russia: preparing for a global clinical trial.
Hayden KM, Makeeva OA, Newby LK, Plassman BL, Markova VV, Dunham A, Romero HR, Melikyan ZA, Germain CM, Welsh-Bohmer KA, Roses AD; TOMSK-DUKE Study Group Investigators.
Hayden KM, et al.
Alzheimers Dement. 2014 Nov;10(6):760-768.e1. doi: 10.1016/j.jalz.2014.02.008. Epub 2014 Jul 22.
Alzheimers Dement. 2014.
PMID: 25066497
Free PMC article.
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PGT-M for spinocerebellar ataxia type 1: development of a STR panel and a report of two clinical cases.
Soloveva EV, Skleimova MM, Minaycheva LI, Garaeva AF, Zhigalina DI, Churkin EO, Okkel YV, Timofeeva OS, Petrov IA, Seitova GN, Lebedev IN, Stepanov VA.
Soloveva EV, et al. Among authors: minaycheva li.
J Assist Reprod Genet. 2024 Apr 5. doi: 10.1007/s10815-024-03105-w. Online ahead of print.
J Assist Reprod Genet. 2024.
PMID: 38578603
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Analysis of Association of Genetic Markers in the LUZP2 and FBXO40 Genes with the Normal Variability in Cognitive Performance in the Elderly.
Stepanov V, Vagaitseva K, Bocharova A, Marusin A, Markova V, Minaycheva L, Makeeva O.
Stepanov V, et al. Among authors: minaycheva l.
Int J Alzheimers Dis. 2018 Apr 19;2018:2686045. doi: 10.1155/2018/2686045. eCollection 2018.
Int J Alzheimers Dis. 2018.
PMID: 29850221
Free PMC article.
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Delineation of Clinical Manifestations of the Inherited Xq24 Microdeletion Segregating with sXCI in Mothers: Two Novel Cases with Distinct Phenotypes Ranging from UBE2A Deficiency Syndrome to Recurrent Pregnancy Loss.
Tolmacheva EN, Kashevarova AA, Nazarenko LP, Minaycheva LI, Skryabin NA, Lopatkina ME, Nikitina TV, Sazhenova EA, Belyaeva EO, Fonova EA, Salyukova OA, Tarabykin VS, Lebedev IN.
Tolmacheva EN, et al. Among authors: minaycheva li.
Cytogenet Genome Res. 2020;160(5):245-254. doi: 10.1159/000508050. Epub 2020 May 30.
Cytogenet Genome Res. 2020.
PMID: 32485717
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