Similar articles for PMID: 27999448

Year	Number of Results
2004	1
2005	5
2006	3
2007	4
2008	2
2009	6
2010	8
2011	4
2012	6
2013	6
2014	4
2015	11
2016	5
2017	7
2018	2
2019	3
2020	3
2021	3
2022	1
2024	0

1

Thrombosis Related ABO, F5, MTHFR, and FGG Gene Polymorphisms in Morbidly Obese Patients.

Kupcinskiene K, Murnikovaite M, Varkalaite G, Juzenas S, Trepenaitis D, Petereit R, Maleckas A, Kupcinskas J, Macas A. Kupcinskiene K, et al. Dis Markers. 2016;2016:7853424. doi: 10.1155/2016/7853424. Epub 2016 Nov 23. Dis Markers. 2016. PMID: 27999448 Free PMC article.

2

Prevalence of F5 1691G>A, F2 20210G>A, and MTHFR 677C>T polymorphisms in Bosnian women with pregnancy loss.

Mahmutbegović E, Marjanović D, Medjedović E, Mahmutbegović N, Dogan S, Valjevac A, Czerska E, Pawińska-Matecka A, Madlani A, Adler G. Mahmutbegović E, et al. Bosn J Basic Med Sci. 2017 Nov 20;17(4):309-314. doi: 10.17305/bjbms.2017.1954. Bosn J Basic Med Sci. 2017. PMID: 28488549 Free PMC article.

3

MTHFR and F5 genetic variations have association with preeclampsia in Pakistani patients: a case control study.

Khidri FF, Waryah YM, Ali FK, Shaikh H, Ujjan ID, Waryah AM. Khidri FF, et al. BMC Med Genet. 2019 Oct 23;20(1):163. doi: 10.1186/s12881-019-0905-9. BMC Med Genet. 2019. PMID: 31646966 Free PMC article.

4

Effects of MTHFR c.677C>T, F2 c.20210G>A and F5 Leiden Polymorphisms in Gastroschisis.

Makhmudi A, Sadewa AH, Aryandono T, Chatterjee S, Heij HA, Gunadi. Makhmudi A, et al. J Invest Surg. 2016;29(2):88-92. doi: 10.3109/08941939.2015.1077908. Epub 2015 Sep 16. J Invest Surg. 2016. PMID: 26375922

5

Clinical impact of factor V Leiden, prothrombin G20210A, and MTHFR C677T mutations among sickle cell disease patients of Central India.

Nishank SS, Singh MP, Yadav R. Nishank SS, et al. Eur J Haematol. 2013 Nov;91(5):462-6. doi: 10.1111/ejh.12190. Epub 2013 Sep 16. Eur J Haematol. 2013. PMID: 23992124

6

ABO blood group but not haemostasis genetic polymorphisms significantly influence thrombotic risk: a study of 180 homozygotes for the Factor V Leiden mutation.

Procare-GEHT Group. Procare-GEHT Group. Br J Haematol. 2006 Dec;135(5):697-702. doi: 10.1111/j.1365-2141.2006.06353.x. Br J Haematol. 2006. PMID: 17107352 Free article.

7

Allelic polymorphism of F2, F5 and MTHFR genes in population of Ukraine.

Tatarskyy P, Kucherenko A, Livshits L. Tatarskyy P, et al. Tsitol Genet. 2010 May-Jun;44(3):3-8. Tsitol Genet. 2010. PMID: 20608153 Free article.

8

Methylenetetrahydrofolate reductase C677T and reduced folate carrier 80 G>A polymorphisms are associated with an increased risk of conotruncal heart defects.

Gong D, Gu H, Zhang Y, Gong J, Nie Y, Wang J, Zhang H, Liu R, Hu S, Zhang H. Gong D, et al. Clin Chem Lab Med. 2012 Feb 4;50(8):1455-61. doi: 10.1515/cclm-2011-0759. Clin Chem Lab Med. 2012. PMID: 22868813

9

Prevalence of genetic thrombophilic polymorphisms in the Sri Lankan population--implications for association study design and clinical genetic testing services.

Dissanayake VH, Weerasekera LY, Gammulla CG, Jayasekara RW. Dissanayake VH, et al. Exp Mol Pathol. 2009 Oct;87(2):159-62. doi: 10.1016/j.yexmp.2009.07.002. Epub 2009 Jul 8. Exp Mol Pathol. 2009. PMID: 19591822

10

Methylentetrahydrofolatereductase (rs1801133) polymorphism and psoriasis: contribution to oxidative stress, lipid peroxidation and correlation with vascular adhesion protein 1, preliminary report.

Asefi M, Vaisi-Raygani A, Khodarahmi R, Nemati H, Rahimi Z, Vaisi-Raygani H, Tavilani H, Pourmotabbed T. Asefi M, et al. J Eur Acad Dermatol Venereol. 2014 Sep;28(9):1192-8. doi: 10.1111/jdv.12262. Epub 2013 Sep 30. J Eur Acad Dermatol Venereol. 2014. PMID: 24118377

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Results by year

Text availability

Article attribute

Article type

Publication date

68 results

Results by year