Katalóg evidencie publikačnej činnosti PU

ID záznamu:	PU.Prešov.2015062313204948
Kategória:	ADC
Autor:	Bôžiková Alexandra (40%)
Autor:	Dojčáková Dana (25%)
Autor:	Pitoňák Jozef (5%)
Autor:	Bernasovská Jarmila (10%)
Autor:	Mačeková Soňa (10%)
Autor:	Behulová Regína (10%)
Názov:	Ethnic differences in the Association of thrombophilic polymorphisms with obstetric complications in Slovak and Roma (Gypsy) populations [print, elektronický dokument]
Zdroj:	Genetic Testing and Molecular Biomarkers [print, elektronický dokument]
Lokácia:	Roč. 19, č. 2. - New York : Mary Ann Liebert, (2015), s. 98-102
ISSN:	1945-0265. - ISSN 1945-0257
URL:	http://online.liebertpub.com/toc/gtmb/19/2
Ohlas:	[1] 2018. JUSIĆ, A., BALIĆ, D., AVDIĆ, A. et al. The association of factor V G1961A (Factor V Leiden), prothrombin G20210A, MTHFR C677T and pai-1 4G/5G polymorphisms with recurrent pregnancy loss in Bosnian women. In Medicinski Glasnik, ISSN 1840-0132. 2018, vol. 15, no. 2, s. 158-163.
Ohlas:	[1] 2018. DLUSKI, D., MIERZYńSKI, R., PONIEDZIALEK-CZAJKOWSKA, E. et al. Adverse pregnancy outcomes and inherited thrombophilia. In Journal of perinatal medicine, ISSN 0300-5577. 2018, vol. 46, no. 4, s. 411-417.
Ohlas:	[1] 2016. AYDIN, H., GUNAY, M., CELIK, G. et al. Evaluation of Factor V Leiden, Prothrombin G20210A, MTHFR C677T and MTHFR A1298C gene polymorphisms in retinopathy of prematurity in a Turkish cohort. In Ophthalmic genetics, ISSN 1381-6810. 2016, vol. 37, no. 4, s. 415-418.
Ohlas:	[1] 2019. FIATAL, S., PIKÓ, P., KÓSA, Z. et al. Genetic profiling revealed an increased risk of venous thrombosis in the Hungarian Roma population. In Thrombosis research, ISSN 0049-3848. 2019, vol. 179, s. 44.
Ohlas:	[1] 2019. TRIFONOVA, E.A., SWAROVSKAYA, M.G., GANZHA, O.A. et al. The interaction effect of angiogenesis and endothelial dysfunction-related gene variants increases the susceptibility of recurrent pregnancy loss. In Journal of assisted reproduction and genetics, ISSN 1058-0468. 2019, vol. 36, no. 4, s. 717-726.
Ohlas:	[1] 2019. TRASCA, L.F., PATRASCU, N., BRUJA, R. et al. Therapeutic implications of inherited thrombophilia in pregnancy. In American journal of therapeutics, ISSN 1075-2765. 2019, roč. 26, č. 3, s. E364-E374. SCOPUS;WOS:000467748200010.
Ohlas:	[1] 2021. RESHETNIKOV, Evgeny A. Rs34845949 polymorphism of the SASH1 gene is associated with the risk of preeclampsia. In Research results in biomedicine, ISSN 2658-6533. 2021, roč. 7, č. 1, s. 44-55. SCOPUS.
Ohlas:	[1] 2019. DUGALIC, S., PETRONIJEVIC, M., STEFANOVIC, A. et al. Perinatal complications related to inherited thrombophilia: review of evidence in different regions of the world. In Journal of maternal-fetal & neonatal medicine, ISSN 1476-7058. 2019, roč. 34, č. 15, s. 2567-2576. SCOPUS;WOS:000487433700001.
Ohlas:	[1] 2020. ALKHURIJI, A., ALRAQIBAH, A.A.M., ALHARBI, A.A. et al. Two polymorphisms in methylenetetrahydrofolate reductase gene (C677T and A1298C) frequently associated with recurrent spontaneous abortion show no association in Saudi women. In Biocell, ISSN 0327-9545. 2020, roč. 44, č. 4, s. 613-621. SCOPUS;WOS:000604967300015.
Ohlas:	[1] 2023. HU, Y., WANG, A., YI, K. MTHFR A1298C polymorphism and risk of Preeclampsia: a meta-analysis. In Clinical and experimental obstetrics & gynecology, ISSN 0390-6663. 2023, roč. 50, č. 12, art no. 266. WOS:001141729600001; SCOPUS.
Oblasť výskumu:	130