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Issue Date	Title	Author(s)
2022	Klinefelter syndrome mosaicism in boys with neurodevelopmental disorders: a cohort study and an extension of the hypothesis	Vorsanova, S. G.; Demidova, I. A.; Kolotii, A. D.; Kurinnaia, O. S.; Iourov, I. Y.
2022	COVID-19 and aging-related genome (chromosome) instability in the brain: another possible time-bomb of SARS-CoV-2 infection	Iourov, I. Y.; Vorsanova, S. G.
2022	Synaptic vesicle binding of α-synuclein is modulated by β- and γ-synucleins	Carnazza, K. E.; Komer, L. E.; Ying Xue Xie; Andre Pineda; Buchman, V. L.
2022	Therapeutic potential of highly functional codon‑optimized microutrophin for muscle‑specific expression	Starikova, A. V.; Skopenkova, V. V.; Polikarpova, A. V.; Reshetov, D. A.; Soldatov, V. O.
2022	Clinical and genetic characteristics of preeclampsia	Golovchenko, O. V.; Abramova, M. Yu.; Orlova, V. S.; Batlutskaya, I. V.; Sorokina, I. N.
2022	Polymorphisms of the filaggrin gene are associated with atopic dermatitis in the Caucasian population of Central Russia	Churnosov, M.; Belyaeva, T.; Reshetnikov, E.; Dvornyk, V.; Ponomarenko, I.
2022	ALS-linked cytoplasmic FUS assemblies are compositionally different from physiological stress granules and sequester hnRNPA3, a novel modifier of FUS toxicity	Haiyan An; Gioana Litscher; Naruaki Watanabe; Wenbin Wei; Buchman, V. L.
2022	Analysis of associations of polymorphic loci of the LOXL1 gene with the development of primary open-angle glaucoma in women of the Central Chernozem region of Russia	Eliseeva, N. V.; Ponomarenko, I.; Churnosov, M.
2022	Comprehensive statistical and bioinformatics analysis in the deciphering of putative mechanisms by which lipid-associated GWAS loci contribute to coronary artery disease	Lazarenko, V.; Churilin, M.; Azarova, Yu.; Klyosova, E.; Churnosov, M.
2022	Genetic variation at the catalytic subunit of glutamate cysteine ligase contributes to the susceptibility to sporadic colorectal cancer: a pilot study	Bykanova, M. A.; Solodilova, M. A.; Azarova, I. E.; Klyosova, E. Y.; Churnosov, M.