Dana Gabrikova
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Explore the profile of Dana Gabrikova including associated specialties, affiliations and a list of published articles.
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14
Citations
157
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Recent Articles
1.
Stiburkova B, Gabrikova D, Cepek P, Simek P, Kristian P, Cordoba-Lanus E, et al.
Nucleosides Nucleotides Nucleic Acids
. 2016 Dec;
35(10-12):529-535.
PMID: 27906637
The Roma represents a transnational ethnic group, with a current European population of 8-10 million. The evolutionary process that had the greatest impact on the gene pool of the Roma...
2.
Gabrikova D, Bernasovska J, Sokolova J, Stiburkova B
Urolithiasis
. 2015 Jun;
43(5):441-5.
PMID: 26033041
Renal hypouricemia is a rare heterogeneous inherited disorder characterized by impaired tubular uric acid transport with severe complications, such as acute kidney injury. Type 1 and 2 are caused by...
3.
Bozikova A, Gabrikova D, Pitonak J, Bernasovska J, Macekova S, Lohajova-Behulova R
Genet Test Mol Biomarkers
. 2014 Dec;
19(2):98-102.
PMID: 25549181
Aims: Hereditary as well as acquired thrombophilia is associated with a higher incidence of severe obstetric complications such as preeclampsia, spontaneous pregnancy loss, placental abruption, and fetal growth retardation. The...
4.
Ivanov I, Azmanov D, Ivanova M, Chamova T, Pacheva I, Panova M, et al.
Mol Genet Metab
. 2014 Aug;
113(1-2):76-83.
PMID: 25087164
Investigation of 31 of Roma patients with congenital lactic acidosis (CLA) from Bulgaria identified homozygosity for the R446* mutation in the PDHX gene as the most common cause of the...
5.
Petrejcikova E, Carnogurska J, Hronska D, Bernasovska J, Boronova I, Gabrikova D, et al.
Anthropol Anz
. 2014 Jul;
71(3):275-85.
PMID: 25065120
Human Y-chromosome haplogroups are important markers used mainly in population genetic studies. The haplogroups are defined by several SNPs according to the phylogeny and international nomenclature. The alternative method to...
6.
Gabrikova D, Mistrik M, Bernasovska J, Bozikova A, Behulova R, Tothova I, et al.
J Appl Genet
. 2013 Sep;
54(4):455-60.
PMID: 23996628
Autosomal recessive forms of Charcot-Marie-Tooth disease (CMT) account for less than 10 % of all CMT cases, but are more frequent in the populations with a high rate of consanguinity....
7.
Bozikova A, Gabrikova D, Sovicova A, Behulova R, Macekova S, Boronova I, et al.
J Thromb Thrombolysis
. 2012 May;
34(3):406-9.
PMID: 22562116
Factor V Leiden and prothrombin G20210A are the two most prevalent causes of inherited thrombophilia. The prevalence of these mutations varies widely in healthy Caucasian population. The aim of our...
8.
Gabrikova D, Bernasovska J, Macekova S, Bozikova A, Bernasovsky I, Balisinova A, et al.
J Appl Genet
. 2012 Feb;
53(2):183-7.
PMID: 22354660
The aim of this study was to assess the frequencies of three hemochromatosis gene (HFE) mutations in ethnic Roma/Gypsies in Slovakia. A cohort of 367 individuals representing general population and...
9.
Macekova S, Bernasovsky I, Gabrikova D, Bozikova A, Bernasovska J, Boronova I, et al.
Am J Phys Anthropol
. 2011 Oct;
147(1):30-4.
PMID: 21989907
The rs9939609 SNP located in the first intron of the fat mass and obesity associated gene (FTO) has been found to be associated with common obesity mainly in populations of...
10.
Frojmark A, Schuster J, Sobol M, Entesarian M, Kilander M, Gabrikova D, et al.
Am J Hum Genet
. 2011 Jun;
88(6):852-860.
PMID: 21665003
Inherited and isolated nail malformations are rare and heterogeneous conditions. We identified two consanguineous pedigrees in which some family members were affected by isolated nail dysplasia that suggested an autosomal-recessive...