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

Year Number of Results
1999 1
2001 2
2005 1
2006 2
2007 2
2008 1
2011 1
2012 2
2013 4
2014 7
2015 5
2016 9
2017 10
2018 6
2019 12
2020 8
2021 17
2022 15
2023 12
2024 7
2025 1

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115 results

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Page 1
Intracerebral Hemorrhage Genetics.
Ekkert A, Šliachtenko A, Utkus A, Jatužis D. Ekkert A, et al. Among authors: utkus a. Genes (Basel). 2022 Jul 15;13(7):1250. doi: 10.3390/genes13071250. Genes (Basel). 2022. PMID: 35886033 Free PMC article. Review.
Perspectives in Sports Genomics.
Ginevičienė V, Utkus A, Pranckevičienė E, Semenova EA, Hall ECR, Ahmetov II. Ginevičienė V, et al. Among authors: utkus a. Biomedicines. 2022 Jan 27;10(2):298. doi: 10.3390/biomedicines10020298. Biomedicines. 2022. PMID: 35203507 Free PMC article. Review.
Fetal biometry: Relevance in obstetrical practice.
Žaliūnas B, Bartkevičienė D, Drąsutienė G, Utkus A, Kurmanavičius J. Žaliūnas B, et al. Among authors: utkus a. Medicina (Kaunas). 2017;53(6):357-364. doi: 10.1016/j.medici.2018.01.004. Epub 2018 Feb 9. Medicina (Kaunas). 2017. PMID: 29482879 Free article. Review.
Exome sequencing of 20,979 individuals with epilepsy reveals shared and distinct ultra-rare genetic risk across disorder subtypes.
Chen S, Abou-Khalil BW, Afawi Z, Ali QZ, Amadori E, Anderson A, Anderson J, Andrade DM, Annesi G, Arslan M, Auce P, Bahlo M, Baker MD, Balagura G, Balestrini S, Banks E, Barba C, Barboza K, Bartolomei F, Bass N, Baum LW, Baumgartner TH, Baykan B, Bebek N, Becker F, Bennett CA, Beydoun A, Bianchini C, Bisulli F, Blackwood D, Blatt I, Borggräfe I, Bosselmann C, Braatz V, Brand H, Brockmann K, Buono RJ, Busch RM, Caglayan SH, Canafoglia L, Canavati C, Castellotti B, Cavalleri GL, Cerrato F, Chassoux F, Cherian C, Cherny SS, Cheung CL, Chou IJ, Chung SK, Churchhouse C, Ciullo V, Clark PO, Cole AJ, Cosico M, Cossette P, Cotsapas C, Cusick C, Daly MJ, Davis LK, Jonghe P, Delanty N, Dennig D, Depondt C, Derambure P, Devinsky O, Di Vito L, Dickerson F, Dlugos DJ, Doccini V, Doherty CP, El-Naggar H, Ellis CA, Epstein L, Evans M, Faucon A, Feng YA, Ferguson L, Ferraro TN, Da Silva IF, Ferri L, Feucht M, Fields MC, Fitzgerald M, Fonferko-Shadrach B, Fortunato F, Franceschetti S, French JA, Freri E, Fu JM, Gabriel S, Gagliardi M, Gambardella A, Gauthier L, Giangregorio T, Gili T, Glauser TA, Goldberg E, Goldman A, Goldstein DB, Granata T, Grant R, Greenberg DA, Guerrini R, Gundogdu-Eken A, Gu… See abstract for full author list ➔ Chen S, et al. Among authors: utkus a. medRxiv [Preprint]. 2024 Sep 20:2023.02.22.23286310. doi: 10.1101/2023.02.22.23286310. medRxiv. 2024. Update in: Nat Neurosci. 2024 Oct;27(10):1864-1879. doi: 10.1038/s41593-024-01747-8. PMID: 36865150 Free PMC article. Updated. Preprint.
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: utkus a. Medicina (Kaunas). 2023 Jun 29;59(7):1225. doi: 10.3390/medicina59071225. Medicina (Kaunas). 2023. PMID: 37512036 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: utkus a. 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.
115 results