Human Genome Epidemiology Literature Finder
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Records 1 - 10 (of 10 Records) |
| Query Trace: Thromboembolism and F12[original query] |
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| Association after linkage analysis indicates that homozygosity for the 46C-->T polymorphism in the F12 gene is a genetic risk factor for venous thrombosis. Thrombosis and haemostasis 2004 May 91 (5): 899-904. Tirado Isabel, Soria José Manuel, Mateo José, Oliver Artur, Souto Juan Carlos, Santamaria Amparo, Felices Rosa, Borrell Montserrat, Fontcuberta Jor |
| Rapid triplex asymmetric real-time PCR hybridization probe assay for the joint genotyping of F2, F5 and F12. Clinical biochemistry 2009 Aug 42 (12): 1317-24. Martínez-Serra J, Gutierrez A, Amat J C, Galmés B, Vila A, Julia M, López H, Bautista A M, Truyols C, Ros T, Navarro M, Canaro M, Díaz M, Besalduch |
| Paternal endothelial protein C receptor 219Gly variant as a mild and limited risk factor for deep vein thrombosis during pregnancy. Journal of thrombosis and haemostasis : JTH 2010 Apr 8 (4): 707-13. Galanaud J P, Cochery-Nouvellon E, Alonso S, Chauleur C, Mercier E, Lissalde-Lavigne G, Fabbro-Peray P, Reny J L, Mares P, Dauzat M, Quere I, Gris J |
| The factor XII -4C>T variant and risk of common thrombotic disorders: A HuGE review and meta-analysis of evidence from observational studies. American journal of epidemiology 2011 Jan 173 (2): 136-44. Johnson Candice Y, Tuite Ashleigh, Morange Pierre E, Tregouet David A, Gagnon Fran |
| Thrombin generation as an intermediate phenotype for venous thrombosis. Thrombosis and haemostasis 2010 1 103 (1): 114-22. Segers Olivier, van Oerle René van, ten Cate Hugo ten, Rosing Jan, Castoldi Elisabet |
| Single nucleotide polymorphisms and the risk of venous thrombosis: results from a Danish case-cohort study. British journal of haematology 2012 Nov . El-Galaly TC, Severinsen MT, Overvad K, Steffensen R, Vistisen AK, Tjønneland A, Kristensen SR |
| Multilocus genetic risk scores for venous thromboembolism risk assessment. Journal of the American Heart Association 2014 Oct 3 (5): e001060. Soria José Manuel, Morange Pierre-Emmanuel, Vila Joan, Souto Juan Carlos, Moyano Manel, Trégouët David-Alexandre, Mateo José, Saut Noémi, Salas Eduardo, Elosua Rober |
| A genetic association study of activated partial thromboplastin time in European Americans and African Americans: the ARIC Study. Human molecular genetics 2015 Apr 24 (8): 2401-8. Weng Lu-Chen, Cushman Mary, Pankow James S, Basu Saonli, Boerwinkle Eric, Folsom Aaron R, Tang Weiho |
| The prevalence of heterozygous F12 mutations in Chinese population and its relevance to incidents of thrombosis. BMC medical genetics 2018 Mar 19 (1): 50. Wu Xi, Ding Qiulan, Wang Xuefeng, Dai Jing, Wu Wenm |
Genetic Profile of Endotoxemia Reveals an Association With Thromboembolism and Stroke.
Journal of the American Heart Association 2021 Oct e022482. Leskelä Jaakko, Toppila Iiro, Härma Mari-Anne, Palviainen Teemu, Salminen Aino, Sandholm Niina, Pietiäinen Milla, Kopra Elisa, Pais de Barros Jean-Paul, , Lassenius Mariann I, Kumar Anmol, Harjutsalo Valma, Roslund Kajsa, Forsblom Carol, Loukola Anu, Havulinna Aki S, Lagrost Laurent, Salomaa Veikko, Groop Per-Henrik, Perola Markus, Kaprio Jaakko, Lehto Markku, Pussinen Pirkko |
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