Utkus A - Search Results

1

Dynamics of Physiological, Biochemical and Psychological Markers during Single Session of Virtual Reality-Based Respiratory Biofeedback Relaxation.

Mazgelytė E, Zagorskaja J, Dereškevičiūtė E, Petrėnas T, Kaminskas A, Songailienė J, Utkus A, Chomentauskas G, Karčiauskaitė D. Mazgelytė E, et al. Among authors: utkus a. Behav Sci (Basel). 2022 Nov 28;12(12):482. doi: 10.3390/bs12120482. Behav Sci (Basel). 2022. PMID: 36546965 Free PMC article.

2

Epilepsy subtype-specific copy number burden observed in a genome-wide study of 17 458 subjects.

Niestroj LM, Perez-Palma E, Howrigan DP, Zhou Y, Cheng F, Saarentaus E, Nürnberg P, Stevelink R, Daly MJ, Palotie A, Lal D; Epi25 Collaborative. Niestroj LM, et al. Brain. 2020 Jul 1;143(7):2106-2118. doi: 10.1093/brain/awaa171. Brain. 2020. PMID: 32568404 Free PMC article.

3

Sub-genic intolerance, ClinVar, and the epilepsies: A whole-exome sequencing study of 29,165 individuals.

Epi25 Collaborative. Electronic address: jm4279@cumc.columbia.edu; Epi25 Collaborative. Epi25 Collaborative. Electronic address: jm4279@cumc.columbia.edu, et al. Am J Hum Genet. 2021 Jun 3;108(6):965-982. doi: 10.1016/j.ajhg.2021.04.009. Epub 2021 Apr 30. Am J Hum Genet. 2021. PMID: 33932343 Free PMC article.

4

Variation in FGF1, FOXE1, and TIMP2 genes is associated with nonsyndromic cleft lip with or without cleft palate.

Nikopensius T, Kempa I, Ambrozaitytė L, Jagomägi T, Saag M, Matulevičienė A, Utkus A, Krjutškov K, Tammekivi V, Piekuse L, Akota I, Barkane B, Krumina A, Klovins J, Lace B, Kučinskas V, Metspalu A. Nikopensius T, et al. Among authors: utkus a. Birth Defects Res A Clin Mol Teratol. 2011 Apr;91(4):218-25. doi: 10.1002/bdra.20791. Epub 2011 Apr 1. Birth Defects Res A Clin Mol Teratol. 2011. PMID: 21462296

5

Molecular basis of cystic fibrosis in Lithuania: incomplete CFTR mutation detection by PCR-based screening protocols.

Giannattasio S, Bobba A, Jurgelevicius V, Vacca RA, Lattanzio P, Merafina RS, Utkus A, Kucinskas V, Marra E. Giannattasio S, et al. Among authors: utkus a. Genet Test. 2006 Fall;10(3):169-73. doi: 10.1089/gte.2006.10.169. Genet Test. 2006. PMID: 17020467

6

Hereditary lymphedema type I associated with VEGFR3 mutation: the first de novo case and atypical presentations.

Ghalamkarpour A, Morlot S, Raas-Rothschild A, Utkus A, Mulliken JB, Boon LM, Vikkula M. Ghalamkarpour A, et al. Among authors: utkus a. Clin Genet. 2006 Oct;70(4):330-5. doi: 10.1111/j.1399-0004.2006.00687.x. Clin Genet. 2006. PMID: 16965327

7

Comments on biological asymmetry.

Opitz JM, Utkus A. Opitz JM, et al. Among authors: utkus a. Am J Med Genet. 2001 Jul 15;101(4):359-69. Am J Med Genet. 2001. PMID: 11471160

8

Athlome Project Consortium: a concerted effort to discover genomic and other "omic" markers of athletic performance.

Pitsiladis YP, Tanaka M, Eynon N, Bouchard C, North KN, Williams AG, Collins M, Moran CN, Britton SL, Fuku N, Ashley EA, Klissouras V, Lucia A, Ahmetov II, de Geus E, Alsayrafi M; Athlome Project Consortium. Pitsiladis YP, et al. Physiol Genomics. 2016 Mar;48(3):183-90. doi: 10.1152/physiolgenomics.00105.2015. Epub 2015 Dec 29. Physiol Genomics. 2016. PMID: 26715623 Free PMC article. Review.

9

Sub-genic intolerance, ClinVar, and the epilepsies: A whole-exome sequencing study of 29,165 individuals.

Epi25 Collaborative. Electronic address: jm4279@cumc.columbia.edu; Epi25 Collaborative. Epi25 Collaborative. Electronic address: jm4279@cumc.columbia.edu, et al. Am J Hum Genet. 2021 Oct 7;108(10):2024. doi: 10.1016/j.ajhg.2021.08.008. Am J Hum Genet. 2021. PMID: 34626584 Free PMC article. No abstract available.

10

Polygenic burden in focal and generalized epilepsies.

Leu C, Stevelink R, Smith AW, Goleva SB, Kanai M, Ferguson L, Campbell C, Kamatani Y, Okada Y, Sisodiya SM, Cavalleri GL, Koeleman BPC, Lerche H, Jehi L, Davis LK, Najm IM, Palotie A, Daly MJ, Busch RM; Epi25 Consortium; Lal D. Leu C, et al. Brain. 2019 Nov 1;142(11):3473-3481. doi: 10.1093/brain/awz292. Brain. 2019. PMID: 31608925 Free PMC article.

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