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International Ophthalmology|March 23, 2026
Study of circulating MiRNA expression in myopic patientsEdita Kunceviciene, Rasa Liutkeviciene, Brigita Budiene, et al.
Brain Sciences|June 24, 2022
<i>IL-10</i> Gene Polymorphisms and IL-10 Serum Levels in Patients with Multiple Sclerosis in LithuaniaUgne Masilionyte, Greta Gedvilaite, Kriste Kaikaryte, et al.
Stomatologija|July 25, 2020
Tendencies of FGFR2 rs2981582 polymorphism in patients with oral cancerVykintas Liutkevicius, Toma Tamauskaite, Alvita Vilkeviciute, et al.
In Vivo (Athens, Greece)|July 2, 2020
Association of Leukocyte Telomere Length and Genes Involved in its Regulation With Oral CarcinomaZaneta Jumatovaite, Albertas Kriauciunas, Alvita Vilkeviciute, et al.
Molecular Genetics & Genomic Medicine|July 16, 2020
Association of genetic variants at CETP, AGER, and CYP4F2 locus with the risk of atrophic age-related macular degenerationRasa Liutkeviciene, Alvita Vilkeviciute, Loresa Kriauciuniene, et al.
BMC Cancer|July 2, 2025
VEGFA (rs1570360, rs699947, rs3025033, rs2146323, rs3024997) genotypes in patients with laryngeal squamous cell carcinomaAgne Pasvenskaite, Alvita Vilkeviciute, Monika Duseikaite, et al.
Medicina (Kaunas, Lithuania)|January 8, 2025
Evaluating <i>TAB2, IKBKB,</i> and <i>IKBKG</i> Gene Polymorphisms and Serum Protein Levels and Their Association with Age-Related Macular Degeneration and Its Treatment EfficiencyAlvita Vilkeviciute, Enrika Pileckaite, Akvile Bruzaite, et al.
Scientific Reports|March 18, 2026
Genetic variants and serum biomarkers of CXCL8, MAP3K7, LTA/TNF, EXOC3L1, PROCR, and TRAF2 in Age-Related macular degeneration: associations with disease risk and therapeutic responseDzastina Cebatoriene, Alvita Vilkeviciute, Monika Duseikaite-Vidike, et al.
Diagnostics (Basel, Switzerland)|May 27, 2026
The Role of Kynurenine and 5-Hydroxytryptophan in Modulating Microbiota and Their Implications in Exudative Age-Related Macular DegenerationAlvita Vilkeviciute-Petraite, Akvile Bruzaite, Dzastina Cebatoriene, et al.
Medicina (Kaunas, Lithuania)|March 3, 2021
A Typical Case Presentation with Spontaneous Visual Recovery in Patient Diagnosed with Leber Hereditary Optic Neuropathy due to Rare Point Mutation in <i>MT-ND4</i> Gene (<i>m.11253T>C</i>) and Literature ReviewRasa Liutkeviciene, Agne Sidaraite, Lina Kuliaviene, et al.
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