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2015 1
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Page 1
CyberGenomics: Application of Behavioral Genetics in Cybersecurity.
Domarkienė I, Ambrozaitytė L, Bukauskas L, Rančelis T, Sütterlin S, Knox BJ, Maennel K, Maennel O, Parish K, Lugo RG, Brilingaitė A. Domarkienė I, et al. Among authors: rancelis t. Behav Sci (Basel). 2021 Nov 1;11(11):152. doi: 10.3390/bs11110152. Behav Sci (Basel). 2021. PMID: 34821613 Free PMC article. Review.
Molecular and Functional Characterisation of a Novel Intragenic 12q24.21 Deletion Resulting in MED13L Haploinsufficiency Syndrome.
Siavrienė E, Petraitytė G, Mikštienė V, Maldžienė Ž, Sasnauskienė A, Žitkutė V, Ambrozaitytė L, Rančelis T, Utkus A, Kučinskas V, Preikšaitienė E. Siavrienė E, et al. Among authors: rancelis t. Medicina (Kaunas). 2023 Jun 29;59(7):1225. doi: 10.3390/medicina59071225. Medicina (Kaunas). 2023. PMID: 37512036 Free PMC article.
Putative protective genomic variation in the Lithuanian population.
Žukauskaitė G, Domarkienė I, Rančelis T, Kavaliauskienė I, Baronas K, Kučinskas V, Ambrozaitytė L. Žukauskaitė G, et al. Among authors: rancelis t. Genet Mol Biol. 2024 Apr 15;47(2):e20230030. doi: 10.1590/1678-4685-GMB-2023-0030. eCollection 2024. Genet Mol Biol. 2024. PMID: 38626572 Free PMC article.
Novel GLI3 variant causes Greig cephalopolysyndactyly syndrome in three generations of a Lithuanian family.
Siavrienė E, Mikštienė V, Radzevičius D, Maldžienė Ž, Rančelis T, Petraitytė G, Tamulytė G, Kavaliauskienė I, Šarkinas L, Utkus A, Kučinskas V, Preikšaitienė E. Siavrienė E, et al. Among authors: rancelis t. Mol Genet Genomic Med. 2019 Sep;7(9):e878. doi: 10.1002/mgg3.878. Epub 2019 Jul 20. Mol Genet Genomic Med. 2019. PMID: 31325247 Free PMC article.
PIGN-Related Disease in Two Lithuanian Families: A Report of Two Novel Pathogenic Variants, Molecular and Clinical Characterisation.
Siavrienė E, Maldžienė Ž, Mikštienė V, Petraitytė G, Rančelis T, Dapkūnas J, Burnytė B, Benušienė E, Sasnauskienė A, Grikinienė J, Griškevičiūtė E, Utkus A, Preikšaitienė E. Siavrienė E, et al. Among authors: rancelis t. Medicina (Kaunas). 2022 Oct 26;58(11):1526. doi: 10.3390/medicina58111526. Medicina (Kaunas). 2022. PMID: 36363484 Free PMC article.
Donor Splice Site Variant in SLC9A6 Causes Christianson Syndrome in a Lithuanian Family: A Case Report.
Petraitytė G, Mikštienė V, Siavrienė E, Cimbalistienė L, Maldžienė Ž, Rančelis T, Vaitėnienė EM, Ambrozaitytė L, Dapkūnas J, Dzindzalieta R, Pranckevičienė E, Kučinskas V, Utkus A, Preikšaitienė E. Petraitytė G, et al. Among authors: rancelis t. Medicina (Kaunas). 2022 Feb 26;58(3):351. doi: 10.3390/medicina58030351. Medicina (Kaunas). 2022. PMID: 35334527 Free PMC article.
Compound heterozygous c.598_612del and c.1746-20C > G CAPN3 genotype cause autosomal recessive limb-girdle muscular dystrophy-1: a case report.
Siavrienė E, Petraitytė G, Burnytė B, Morkūnienė A, Mikštienė V, Rančelis T, Utkus A, Kučinskas V, Preikšaitienė E. Siavrienė E, et al. Among authors: rancelis t. BMC Musculoskelet Disord. 2021 Dec 4;22(1):1020. doi: 10.1186/s12891-021-04920-3. BMC Musculoskelet Disord. 2021. PMID: 34863162 Free PMC article.
16 results