Utkus A - Search Results

1

Analysis of Lithuanian CYP2D6 polymorphism and its relevance to psychiatric care of the local population.

Dlugauskas E, Strumila R, Lengvenyte A, Ambrozaityte L, Dagyte E, Molyte A, Navickas A, Utkus A. Dlugauskas E, et al. Among authors: utkus a. Nord J Psychiatry. 2019 Jan;73(1):31-35. doi: 10.1080/08039488.2018.1548648. Epub 2019 Jan 19. Nord J Psychiatry. 2019. PMID: 30661435

2

Heterogeneity of oral clefts in relation to associated congenital anomalies.

Matulevičienė A, Preikšaitienė E, Linkevičienė L, Radavičius M, Molytė A, Utkus A, Kučinskas V. Matulevičienė A, et al. Among authors: utkus a. Medicina (Kaunas). 2013;49(2):61-6. Medicina (Kaunas). 2013. PMID: 23888340 Free article.

3

Considering specific clinical features as evidence of pathogenic copy number variants.

Preiksaitiene E, Molytė A, Kasnauskiene J, Ciuladaite Z, Utkus A, Patsalis PC, Kučinskas V. Preiksaitiene E, et al. Among authors: utkus a. J Appl Genet. 2014 May;55(2):189-96. doi: 10.1007/s13353-014-0197-x. Epub 2014 Feb 18. J Appl Genet. 2014. PMID: 24535828

4

AMPD1 rs17602729 is associated with physical performance of sprint and power in elite Lithuanian athletes.

Ginevičienė V, Jakaitienė A, Pranculis A, Milašius K, Tubelis L, Utkus A. Ginevičienė V, et al. Among authors: utkus a. BMC Genet. 2014 May 17;15:58. doi: 10.1186/1471-2156-15-58. BMC Genet. 2014. PMID: 24885427 Free PMC article.

5

Association of BMP4 polymorphisms with non-syndromic cleft lip with or without cleft palate and isolated cleft palate in Latvian and Lithuanian populations.

Kempa I, Ambrozaitytė L, Stavusis J, Akota I, Barkane B, Krumina A, Matulevičienė A, Utkus A, Kučinskas V, Lace B. Kempa I, et al. Among authors: utkus a. Stomatologija. 2014;16(3):94-101. Stomatologija. 2014. PMID: 25471993 Free article.

6

Clinical, cytogenetic and molecular study of a case of ring chromosome 10.

Čiuladaitė Ž, Burnytė B, Vansevičiūtė D, Dagytė E, Kučinskas V, Utkus A. Čiuladaitė Ž, et al. Among authors: utkus a. Mol Cytogenet. 2015 Apr 21;8:29. doi: 10.1186/s13039-015-0124-9. eCollection 2015. Mol Cytogenet. 2015. PMID: 25922618 Free PMC article.

7

Frame shift mutations of the ZMPSTE24 gene in two siblings with restrictive dermopathy.

Matulevičienė A, Meškienė R, Morkūnienė A, Ambrozaitytė L, Meškauskas R, Garunkštienė R, Drazdienė N, Utkus A, Kučinskas V. Matulevičienė A, et al. Among authors: utkus a. Clin Dysmorphol. 2016 Jan;25(1):7-11. doi: 10.1097/MCD.0000000000000100. Clin Dysmorphol. 2016. PMID: 26379196

8

The high frequency of GJB2 gene mutation c.313_326del14 suggests its possible origin in ancestors of Lithuanian population.

Mikstiene V, Jakaitiene A, Byckova J, Gradauskiene E, Preiksaitiene E, Burnyte B, Tumiene B, Matuleviciene A, Ambrozaityte L, Uktveryte I, Domarkiene I, Rancelis T, Cimbalistiene L, Lesinskas E, Kucinskas V, Utkus A. Mikstiene V, et al. Among authors: utkus a. BMC Genet. 2016 Feb 19;17:45. doi: 10.1186/s12863-016-0354-9. BMC Genet. 2016. PMID: 26896187 Free PMC article.

9

A novel intronic splice site tafazzin gene mutation detected prenatally in a family with Barth syndrome.

Bakšienė M, Benušienė E, Morkūnienė A, Ambrozaitytė L, Utkus A, Kučinskas V. Bakšienė M, et al. Among authors: utkus a. Balkan J Med Genet. 2017 Mar 8;19(2):95-100. doi: 10.1515/bjmg-2016-0043. eCollection 2016 Dec 1. Balkan J Med Genet. 2017. PMID: 28289596 Free PMC article.

10

Identification of genetic causes of congenital neurodevelopmental disorders using genome wide molecular technologies.

Preikšaitienė E, Ambrozaitytė L, Maldžienė Ž, Morkūnienė A, Cimbalistienė L, Rančelis T, Utkus A, Kučinskas V. Preikšaitienė E, et al. Among authors: utkus a. Acta Med Litu. 2016;23(2):73-85. doi: 10.6001/actamedica.v23i2.3324. Acta Med Litu. 2016. PMID: 28356794 Free PMC article.

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