Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2009 1
2010 1
2011 1
2014 1
2016 5
2017 5
2018 5
2019 2
2020 3
2021 6
2022 5
2023 7
2024 1

Text availability

Article attribute

Article type

Publication date

Search Results

38 results

Results by year

Filters applied: . Clear all
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: ambrozaityte l. 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: ambrozaityte l. Medicina (Kaunas). 2023 Jun 29;59(7):1225. doi: 10.3390/medicina59071225. Medicina (Kaunas). 2023. PMID: 37512036 Free PMC article.
Kearns-Sayre syndrome case. Novel 5,9 kb mtDNA deletion.
Grigalionienė K, Burnytė B, Balkelienė D, Ambrozaitytė L, Utkus A. Grigalionienė K, et al. Among authors: ambrozaityte l. Mol Genet Genomic Med. 2023 Jan;11(1):e2059. doi: 10.1002/mgg3.2059. Epub 2022 Oct 1. Mol Genet Genomic Med. 2023. PMID: 36181358 Free PMC article.
X-linked juvenile retinoschisis: phenotypic and genetic characterization.
Strupaitė R, Ambrozaitytė L, Cimbalistienė L, Ašoklis R, Utkus A. Strupaitė R, et al. Among authors: ambrozaityte l. Int J Ophthalmol. 2018 Nov 18;11(11):1875-1878. doi: 10.18240/ijo.2018.11.22. eCollection 2018. Int J Ophthalmol. 2018. PMID: 30450322 Free PMC article.
HINT1 neuropathy in Lithuania: clinical, genetic, and functional profiling.
Malcorps M, Amor-Barris S, Burnyte B, Vilimiene R, Armirola-Ricaurte C, Grigalioniene K, Ekshteyn A, Morkuniene A, Vaitkevicius A, De Vriendt E, Baets J, Scherer SS, Ambrozaityte L, Utkus A, Jordanova A, Peeters K. Malcorps M, et al. Among authors: ambrozaityte l. Orphanet J Rare Dis. 2022 Oct 14;17(1):374. doi: 10.1186/s13023-022-02541-0. Orphanet J Rare Dis. 2022. PMID: 36242072 Free PMC article.
38 results