- Gažiová M, Sládeček T, Pös O, Števko M, Krampl W, Pös Z, Hekel R, Hlavačka M, Kucharík M, Radvánszky J, Budiš J, Szemes T (2022): Automated prediction of the clinical impact of structural copy number variations. Sci Rep. 12(1):555. doi: 10.1038/s41598-021-04505-z. (IF.2020: 4.380 – Q1) (0 citácií)
- Hekel R, Budis J, Kucharik M, Radvanszky J, Pös Z, Szemes T. (2021): Privacy-preserving storage of sequenced genomic data. BMC Genomics. 22(1):712. (IF.2020: 3.969 – Q2)
- Forgacova N, Gazdarica J, Budis J, Radvanszky J, Szemes T. (2021): Repurposing non-invasive prenatal testing data: Population study of single nucleotide variants associated with colorectal cancer and Lynch syndrome. Oncol Lett. 22(5):779. (IF.2020: 2.967 – Q4)
- Radvanszky J*, Hyblova M, Radvanska E, Spalek P, Valachova A, Magyarova G, Bognar C, Polak E, Szemes T, Kadasi L. (2021): Characterisation of Non-Pathogenic Premutation-Range Myotonic Dystrophy Type 2 Alleles. J Clin Med. 2021 Aug 31;10(17):3934. (IF.2020: 4.241 – Q1)
- Pecimonova M*, Radvanszky J, Smolak D, Budis J, Lichvar M, Kristinova D, Rozova I, Turna J, Szemes T. (2021): Admixed phenotype of NEDD4L associated periventricular nodular heterotopia: A case report. Medicine (Baltimore). 2021 Jun 4;100(22):e26136. (IF.2020: 1.889 – Q2)
- Pös O, Radvanszky J*, Buglyó G, Pös Z, Rusnakova D, Nagy B, Szemes T (2021): DNA copy number variation: Main characteristics, evolutionary significance, and pathological aspects. Biomed J. 44(5):548-559. (IF.2020: 4.910 – Q2) (8 citácií)
- Pös O, Radvanszky J*, Styk J, Pös Z, Buglyó G, Kajsik M, Budis J, Nagy B, Szemes T (2021): Copy Number Variation: Methods and Clinical Applications. Appl. Sci. 2021, 11(2), 819; https://doi.org/10.3390/app11020819. (IF.2020: 2.679 – Q2/Q3)
