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New gene variants associated with venous thrombosis: a replication study in White and Black Americans.

Austin H, De Staercke C, Lally C, Bezemer ID, Rosendaal FR, Hooper WC.

J Thromb Haemost. 2011 Mar;9(3):489-95. doi: 10.1111/j.1538-7836.2011.04185.x.


Gene variants associated with deep vein thrombosis.

Bezemer ID, Bare LA, Doggen CJ, Arellano AR, Tong C, Rowland CM, Catanese J, Young BA, Reitsma PH, Devlin JJ, Rosendaal FR.

JAMA. 2008 Mar 19;299(11):1306-14. doi: 10.1001/jama.299.11.1306.


Association of F11 polymorphism rs2289252 with deep vein thrombosis and related phenotypes in population of Latvia.

Rovite V, Maurins U, Megnis K, Vaivade I, Pečulis R, Rits J, Prave S, Klovins J.

Thromb Res. 2014 Sep;134(3):659-63. doi: 10.1016/j.thromres.2014.07.011. Epub 2014 Jul 18.


Associations between polymorphisms in coagulation-related genes and venous thromboembolism: A meta-analysis with trial sequential analysis.

Jiang J, Liu K, Zou J, Ma H, Yang H, Zhang X, Jiao Y.

Medicine (Baltimore). 2017 Mar;96(13):e6537. doi: 10.1097/MD.0000000000006537. Review. Erratum in: Medicine (Baltimore). 2017 Jun 08;96(23):e7233.


Genetic variants associated with deep vein thrombosis: the F11 locus.

Li Y, Bezemer ID, Rowland CM, Tong CH, Arellano AR, Catanese JJ, Devlin JJ, Reitsma PH, Bare LA, Rosendaal FR.

J Thromb Haemost. 2009 Nov;7(11):1802-8. doi: 10.1111/j.1538-7836.2009.03544.x. Epub 2009 Jul 6.


F11 rs2289252T and rs2036914C Polymorphisms Increase the Activity of Factor XI in Post-trauma Patients with Fractures Despite Thromboprophylaxis.

Song N, Tian AX, Zhang JM, Jiang HQ, Zang JC, Ma XL.

Orthop Surg. 2016 Aug;8(3):377-82. doi: 10.1111/os.12262.


Single nucleotide polymorphisms and the risk of venous thrombosis: results from a Danish case-cohort study.

El-Galaly TC, Severinsen MT, Overvad K, Steffensen R, Vistisen AK, Tjønneland A, Kristensen SR.

Br J Haematol. 2013 Mar;160(6):838-41. doi: 10.1111/bjh.12132. Epub 2012 Nov 15.


Activity of coagulation factor XI in patients with spontaneous miscarriage: the presence of risk alleles.

Sokol J, Biringer K, Skerenova M, Stasko J, Kubisz P.

J Obstet Gynaecol. 2015;35(6):621-4. doi: 10.3109/01443615.2014.991284. Epub 2014 Dec 17.


Regulation of the F11, Klkb1, Cyp4v3 gene cluster in livers of metabolically challenged mice.

Safdar H, Cleuren AC, Cheung KL, Gonzalez FJ, Vos HL, Inoue Y, Reitsma PH, van Vlijmen BJ.

PLoS One. 2013 Sep 16;8(9):e74637. doi: 10.1371/journal.pone.0074637. eCollection 2013.


Variability of GP6 gene in patients with sticky platelet syndrome and deep venous thrombosis and/or pulmonary embolism.

Kotuličová D, Chudý P, Škereňová M, Ivanková J, Dobrotová M, Kubisz P.

Blood Coagul Fibrinolysis. 2012 Sep;23(6):543-7. doi: 10.1097/MBC.0b013e328355a808.


Prospective study of circulating factor XI and incident venous thromboembolism: The Longitudinal Investigation of Thromboembolism Etiology (LITE).

Folsom AR, Tang W, Roetker NS, Heckbert SR, Cushman M, Pankow JS.

Am J Hematol. 2015 Nov;90(11):1047-51. doi: 10.1002/ajh.24168.


Replication of a genetic risk score for venous thromboembolism in whites but not in African Americans.

Folsom AR, Tang W, Weng LC, Roetker NS, Cushman M, Basu S, Pankow JS.

J Thromb Haemost. 2016 Jan;14(1):83-8. doi: 10.1111/jth.13193. Epub 2015 Dec 29.


Venous thrombosis in relation to fibrinogen and factor VII genes among African-Americans.

Austin H, Hooper WC, Lally C, Dilley A, Ellingsen D, Wideman C, Wenger NK, Rawlins P, Silva V, Evatt B.

J Clin Epidemiol. 2000 Oct;53(10):997-1001.


Identification of coagulation gene 3'UTR variants that are potentially regulated by microRNAs.

Vossen CY, van Hylckama Vlieg A, Teruel-Montoya R, Salloum-Asfar S, de Haan H, Corral J, Reitsma P, Koeleman BPC, Martínez C.

Br J Haematol. 2017 Jun;177(5):782-790. doi: 10.1111/bjh.14629. Epub 2017 Apr 26.


The prevalence of the prothrombin gene variant C20209T in African-Americans and Caucasians and lack of association with venous thromboembolism.

Hooper WC, Roberts S, Dowling N, Austin H, Lally C, Whitsett C.

Thromb Res. 2006;118(6):767-8. Epub 2006 Feb 15. No abstract available.


Lipid trait-associated genetic variation is associated with gallstone disease in the diverse Third National Health and Nutrition Examination Survey (NHANES III).

Goodloe R, Brown-Gentry K, Gillani NB, Jin H, Mayo P, Allen M, McClellan B Jr, Boston J, Sutcliffe C, Schnetz-Boutaud N, Dilks HH, Crawford DC.

BMC Med Genet. 2013 Nov 21;14:120. doi: 10.1186/1471-2350-14-120.


Targeted sequencing to identify novel genetic risk factors for deep vein thrombosis: a study of 734 genes.

de Haan HG, van Hylckama Vlieg A, Lotta LA, Gorski MM, Bucciarelli P, Martinelli I, Baglin TP, Peyvandi F, Rosendaal FR; INVENT consortium.

J Thromb Haemost. 2018 Dec;16(12):2432-2441. doi: 10.1111/jth.14279. Epub 2018 Oct 16.


Next generation sequencing to dissect the genetic architecture of KNG1 and F11 loci using factor XI levels as an intermediate phenotype of thrombosis.

Martin-Fernandez L, Gavidia-Bovadilla G, Corrales I, Brunel H, Ramírez L, López S, Souto JC, Vidal F, Soria JM.

PLoS One. 2017 Apr 26;12(4):e0176301. doi: 10.1371/journal.pone.0176301. eCollection 2017.


Factor 11 single-nucleotide variants in women with heavy menstrual bleeding.

Wiewel-Verschueren S, Mulder AB, Meijer K, Mulder R.

J Obstet Gynaecol. 2017 Oct;37(7):912-918. doi: 10.1080/01443615.2017.1312303. Epub 2017 Jun 13. Review.


Chromosome 9p21 haplotypes and prognosis in white and black patients with coronary artery disease.

Gong Y, Beitelshees AL, Cooper-DeHoff RM, Lobmeyer MT, Langaee TY, Wu J, Cresci S, Province MA, Spertus JA, Pepine CJ, Johnson JA.

Circ Cardiovasc Genet. 2011 Apr;4(2):169-78. doi: 10.1161/CIRCGENETICS.110.959296. Epub 2011 Mar 3.

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