Piekuse L - Search Results

1

A New Baltic Population-Specific Human Genetic Marker in the PMCA4 Gene.

Stavusis J, Inashkina I, Lace B, Pelnena D, Limborska S, Khrunin A, Kucinskas V, Krumina A, Piekuse L, Zorn B, Fodina V, Punab M, Erenpreiss J. Stavusis J, et al. Among authors: piekuse l. Hum Hered. 2016;82(3-4):140-146. doi: 10.1159/000481434. Epub 2017 Nov 2. Hum Hered. 2016. PMID: 29131013

2

Association studies of candidate genes and cleft lip and palate taking into consideration geographical origin.

Lace B, Kempa I, Piekuse L, Grinfelde I, Klovins J, Pliss L, Krumina A, Vieira AR. Lace B, et al. Among authors: piekuse l. Eur J Oral Sci. 2011 Dec;119(6):413-7. doi: 10.1111/j.1600-0722.2011.00877.x. Epub 2011 Oct 15. Eur J Oral Sci. 2011. PMID: 22112025

3

Analysis of possible genetic risk factors contributing to development of childhood acute lymphoblastic leukaemia in the Latvian population.

Kreile M, Piekuse L, Rots D, Dobele Z, Kovalova Z, Lace B. Kreile M, et al. Among authors: piekuse l. Arch Med Sci. 2016 Jun 1;12(3):479-85. doi: 10.5114/aoms.2016.59920. Epub 2016 May 18. Arch Med Sci. 2016. PMID: 27279837 Free PMC article.

4

Association between inherited monogenic liver disorders and chronic hepatitis C.

Piekuse L, Kreile M, Zarina A, Steinberga Z, Sondore V, Keiss J, Lace B, Krumina A. Piekuse L, et al. World J Hepatol. 2014 Feb 27;6(2):92-7. doi: 10.4254/wjh.v6.i2.92. World J Hepatol. 2014. PMID: 24575168 Free PMC article.

5

Genetic variation spectrum in ATP7B gene identified in Latvian patients with Wilson disease.

Zarina A, Tolmane I, Kreile M, Chernushenko A, Cernevska G, Pukite I, Micule I, Krumina Z, Krumina A, Rozentale B, Piekuse L. Zarina A, et al. Among authors: piekuse l. Mol Genet Genomic Med. 2017 Jun 7;5(4):405-409. doi: 10.1002/mgg3.297. eCollection 2017 Jul. Mol Genet Genomic Med. 2017. PMID: 28717664 Free PMC article.

6

From clinical and biochemical to molecular genetic diagnosis of Wilson disease in Latvia.

Krumina A, Keiss J, Sondore V, Chernushenko A, Cernevska G, Zarina A, Micule I, Piekuse L, Kreile M, Lace B, Krumina Z, Rozentale B. Krumina A, et al. Among authors: piekuse l. Genetika. 2008 Oct;44(10):1379-84. Genetika. 2008. PMID: 19062534

7

Lack of association between polymorphisms in genes MTHFR and MDR1 with risk of childhood acute lymphoblastic leukemia.

Kreile M, Rots D, Piekuse L, Cebura E, Grutupa M, Kovalova Z, Lace B. Kreile M, et al. Among authors: piekuse l. Asian Pac J Cancer Prev. 2014;15(22):9707-11. doi: 10.7314/apjcp.2014.15.22.9707. Asian Pac J Cancer Prev. 2014. PMID: 25520092 Free article.

8

Genetic variants in COL2A1, COL11A2, and IRF6 contribute risk to nonsyndromic cleft palate.

Nikopensius T, Jagomägi T, Krjutskov K, Tammekivi V, Saag M, Prane I, Piekuse L, Akota I, Barkane B, Krumina A, Ambrozaityte L, Matuleviciene A, Kucinskiene ZA, Lace B, Kucinskas V, Metspalu A. Nikopensius T, et al. Among authors: piekuse l. Birth Defects Res A Clin Mol Teratol. 2010 Sep;88(9):748-56. doi: 10.1002/bdra.20700. Birth Defects Res A Clin Mol Teratol. 2010. PMID: 20672350

9

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: piekuse l. 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

10

Elevated serum levels of homocysteine as an early prognostic factor of psychiatric disorders in children and adolescents.

Kevere L, Purvina S, Bauze D, Zeibarts M, Andrezina R, Rizevs A, Jelisejevs S, Piekuse L, Kreile M, Purvins I. Kevere L, et al. Among authors: piekuse l. Schizophr Res Treatment. 2012;2012:373261. doi: 10.1155/2012/373261. Epub 2012 Oct 2. Schizophr Res Treatment. 2012. PMID: 23091720 Free PMC article.

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