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Results: 1 to 20 of 50

References for PMC Articles for PubMed (Select 20735728)

1.

APOE/C1/C4/C2 gene cluster genotypes, haplotypes and lipid levels in prospective coronary heart disease risk among UK healthy men.

Ken-Dror G, Talmud PJ, Humphries SE, Drenos F.

Mol Med. 2010 Sep-Oct;16(9-10):389-99. doi: 10.2119/molmed.2010.00044. Epub 2010 May 20.

2.

Genotype-phenotype relationship of F7 R353Q polymorphism and plasma factor VII coagulant activity in Asian Indian families predisposed to coronary artery disease.

Shanker J, Perumal G, Maitra A, Rao VS, Natesha BK, John S, Hebbagodi S, Kakkar VV.

J Genet. 2009 Dec;88(3):291-7.

3.

Gene-centric association signals for lipids and apolipoproteins identified via the HumanCVD BeadChip.

Talmud PJ, Drenos F, Shah S, Shah T, Palmen J, Verzilli C, Gaunt TR, Pallas J, Lovering R, Li K, Casas JP, Sofat R, Kumari M, Rodriguez S, Johnson T, Newhouse SJ, Dominiczak A, Samani NJ, Caulfield M, Sever P, Stanton A, Shields DC, Padmanabhan S, Melander O, Hastie C, Delles C, Ebrahim S, Marmot MG, Smith GD, Lawlor DA, Munroe PB, Day IN, Kivimaki M, Whittaker J, Humphries SE, Hingorani AD; ASCOT investigators; NORDIL investigators; BRIGHT Consortium.

Am J Hum Genet. 2009 Nov;85(5):628-42. doi: 10.1016/j.ajhg.2009.10.014.

4.

Integrated associations of genotypes with multiple blood biomarkers linked to coronary heart disease risk.

Drenos F, Talmud PJ, Casas JP, Smeeth L, Palmen J, Humphries SE, Hingorani AD.

Hum Mol Genet. 2009 Jun 15;18(12):2305-16. doi: 10.1093/hmg/ddp159. Epub 2009 Mar 31.

5.

Concept, design and implementation of a cardiovascular gene-centric 50 k SNP array for large-scale genomic association studies.

Keating BJ, Tischfield S, Murray SS, Bhangale T, Price TS, Glessner JT, Galver L, Barrett JC, Grant SF, Farlow DN, Chandrupatla HR, Hansen M, Ajmal S, Papanicolaou GJ, Guo Y, Li M, Derohannessian S, de Bakker PI, Bailey SD, Montpetit A, Edmondson AC, Taylor K, Gai X, Wang SS, Fornage M, Shaikh T, Groop L, Boehnke M, Hall AS, Hattersley AT, Frackelton E, Patterson N, Chiang CW, Kim CE, Fabsitz RR, Ouwehand W, Price AL, Munroe P, Caulfield M, Drake T, Boerwinkle E, Reich D, Whitehead AS, Cappola TP, Samani NJ, Lusis AJ, Schadt E, Wilson JG, Koenig W, McCarthy MI, Kathiresan S, Gabriel SB, Hakonarson H, Anand SS, Reilly M, Engert JC, Nickerson DA, Rader DJ, Hirschhorn JN, Fitzgerald GA.

PLoS One. 2008;3(10):e3583. doi: 10.1371/journal.pone.0003583. Epub 2008 Oct 31.

6.

The paradoxical association between inherited factor VII deficiency and venous thrombosis.

Marty S, Barro C, Chatelain B, Fimbel B, Tribout B, Reynaud J, Schved JF, Giansily-Blaizot M.

Haemophilia. 2008 May;14(3):564-70. doi: 10.1111/j.1365-2516.2007.01647.x. Epub 2008 Feb 13.

PMID:
18282149
7.

Relationship between markers of activated coagulation, their correlation with inflammation, and association with coronary heart disease (NPHSII).

Miller GJ, Ireland HA, Cooper JA, Bauer KA, Morrissey JH, Humphries SE, Esnouf MP.

J Thromb Haemost. 2008 Feb;6(2):259-67. Epub 2007 Oct 29.

PMID:
17973650
8.

Coagulation factor VII gene haplotypes, obesity-related traits, and cardiovascular risk in young women.

Reiner AP, Carlson CS, Rieder MJ, Siscovick DS, Liu K, Chandler WL, Green D, Schwartz SM, Nickerson DA.

J Thromb Haemost. 2007 Jan;5(1):42-9. Epub 2006 Oct 16.

PMID:
17059418
9.

A comparison of phasing algorithms for trios and unrelated individuals.

Marchini J, Cutler D, Patterson N, Stephens M, Eskin E, Halperin E, Lin S, Qin ZS, Munro HM, Abecasis GR, Donnelly P; International HapMap Consortium.

Am J Hum Genet. 2006 Mar;78(3):437-50. Epub 2006 Jan 26.

10.

Efficiency and power in genetic association studies.

de Bakker PI, Yelensky R, Pe'er I, Gabriel SB, Daly MJ, Altshuler D.

Nat Genet. 2005 Nov;37(11):1217-23. Epub 2005 Oct 23.

PMID:
16244653
11.

Accounting for decay of linkage disequilibrium in haplotype inference and missing-data imputation.

Stephens M, Scheet P.

Am J Hum Genet. 2005 Mar;76(3):449-62. Epub 2005 Jan 31.

12.

Cohort Profile: the Whitehall II study.

Marmot M, Brunner E.

Int J Epidemiol. 2005 Apr;34(2):251-6. Epub 2004 Dec 2. No abstract available.

13.

Influence of polymorphisms in the factor VII gene promoter on activated factor VII levels and on the risk of myocardial infarction in advanced coronary atherosclerosis.

Bozzini C, Girelli D, Bernardi F, Ferraresi P, Olivieri O, Pinotti M, Martinelli N, Manzato F, Friso S, Villa G, Pizzolo F, Beltrame F, Corrocher R.

Thromb Haemost. 2004 Sep;92(3):541-9.

PMID:
15351850
14.

A functional haplotype in the 5' flanking region of the factor VII gene is associated with an increased risk of coronary heart disease.

Carew JA, Basso F, Miller GJ, Hawe E, Jackson AA, Humphries SE, Bauer KA.

J Thromb Haemost. 2003 Oct;1(10):2179-85.

PMID:
14521602
15.

Thrombosis in inherited factor VII deficiency.

Mariani G, Herrmann FH, Schulman S, Batorova A, Wulff K, Etro D, Dolce A, Auerswald G, Astermark J, Schved JF, Ingerslev J, Bernardi F; International Factor VII Deficiency Study Group.

J Thromb Haemost. 2003 Oct;1(10):2153-8.

PMID:
14521598
16.

Complexity of the genetic contribution to factor VII deficiency in two Spanish families: clinical and biological implications.

Sabater-Lleal M, Martínez-Marchán E, Martínez-Sánchez E, Coll M, Vallvé C, Mateo J, Souto JC, Fontcuberta J, Soria JM.

Haematologica. 2003 Aug;88(8):906-13.

17.

Polymorphic changes in the 5' flanking region of factor VII have a combined effect on promoter strength.

Kudaravalli R, Tidd T, Pinotti M, Ratti A, Santacroce R, Margaglione M, Dallapiccola B, Bernardi F, Fortina P, Devoto M, Pollak ES.

Thromb Haemost. 2002 Nov;88(5):763-7.

PMID:
12428091
18.

Genetic linkage and transmission disequilibrium of marker haplotypes at chromosome 1q41 in human systemic lupus erythematosus.

Graham RR, Langefeld CD, Gaffney PM, Ortmann WA, Selby SA, Baechler EC, Shark KB, Ockenden TC, Rohlf KE, Moser KL, Brown WM, Gabriel SE, Messner RP, King RA, Horak P, Elder JT, Stuart PE, Rich SS, Behrens TW.

Arthritis Res. 2001;3(5):299-305. Epub 2001 Jul 17.

19.

Factor VII polymorphisms and myocardial infarction: what is special in Italians? REGRESS study group. Regression Growth Evaluation Statin Study.

Nederhand RJ, de Maat MP, Jukema JW; Regression Growth Evaluation Statin Study group.

Thromb Haemost. 2001 Apr;85(4):746-7. No abstract available.

PMID:
11341517
20.

A new statistical method for haplotype reconstruction from population data.

Stephens M, Smith NJ, Donnelly P.

Am J Hum Genet. 2001 Apr;68(4):978-89. Epub 2001 Mar 9.

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