Soria JM - Search Results

1

A genome-wide association study in the genetic analysis of idiopathic thrombophilia project suggests sex-specific regulation of mitochondrial DNA levels.

López S, Buil A, Souto JC, Casademont J, Martinez-Perez A, Almasy L, Soria JM. López S, et al. Among authors: soria jm. Mitochondrion. 2014 Sep;18:34-40. doi: 10.1016/j.mito.2014.09.004. Epub 2014 Sep 18. Mitochondrion. 2014. PMID: 25240745

2

Homozygotes for prothrombin gene 20210 A allele in a thrombophilic family without clinical manifestations of venous thromboembolism.

Souto JC, Mateo J, Soria JM, Llobet D, Coll I, Borrell M, Fontcuberta J. Souto JC, et al. Among authors: soria jm. Haematologica. 1999 Jul;84(7):627-32. Haematologica. 1999. PMID: 10406905

3

Linkage analysis demonstrates that the prothrombin G20210A mutation jointly influences plasma prothrombin levels and risk of thrombosis.

Soria JM, Almasy L, Souto JC, Tirado I, Borell M, Mateo J, Slifer S, Stone W, Blangero J, Fontcuberta J. Soria JM, et al. Blood. 2000 May 1;95(9):2780-5. Blood. 2000. PMID: 10779421 Free article.

4

Functional effects of the ABO locus polymorphism on plasma levels of von Willebrand factor, factor VIII, and activated partial thromboplastin time.

Souto JC, Almasy L, Muñiz-Diaz E, Soria JM, Borrell M, Bayén L, Mateo J, Madoz P, Stone W, Blangero J, Fontcuberta J. Souto JC, et al. Among authors: soria jm. Arterioscler Thromb Vasc Biol. 2000 Aug;20(8):2024-8. doi: 10.1161/01.atv.20.8.2024. Arterioscler Thromb Vasc Biol. 2000. PMID: 10938027

5

Genetic susceptibility to thrombosis and its relationship to physiological risk factors: the GAIT study. Genetic Analysis of Idiopathic Thrombophilia.

Souto JC, Almasy L, Borrell M, Blanco-Vaca F, Mateo J, Soria JM, Coll I, Felices R, Stone W, Fontcuberta J, Blangero J. Souto JC, et al. Among authors: soria jm. Am J Hum Genet. 2000 Dec;67(6):1452-9. doi: 10.1086/316903. Epub 2000 Oct 19. Am J Hum Genet. 2000. PMID: 11038326 Free PMC article.

6

Risk of thrombosis associated with oral contraceptives of women from 97 families with inherited thrombophilia: high risk of thrombosis in carriers of the G20210A mutation of the prothrombin gene.

Santamaría A, Mateo J, Oliver A, Menéndez B, Souto JC, Borrell M, Soria JM, Tirado I, Fontcuberta J. Santamaría A, et al. Among authors: soria jm. Haematologica. 2001 Sep;86(9):965-71. Haematologica. 2001. PMID: 11532625

7

Contribution of prothrombin 20210A allele and factor V Leiden mutation to thrombosis risk in thrombophilic families with other hemostatic deficiencies.

Tirado I, Mateo J, Soria JM, Oliver A, Borrell M, Coll I, Vallvé C, Souto JC, Martínez-Sánchez E, Fontcuberta J. Tirado I, et al. Among authors: soria jm. Haematologica. 2001 Nov;86(11):1200-8. Haematologica. 2001. PMID: 11694407

8

A quantitative-trait locus in the human factor XII gene influences both plasma factor XII levels and susceptibility to thrombotic disease.

Soria JM, Almasy L, Souto JC, Bacq D, Buil A, Faure A, Martínez-Marchán E, Mateo J, Borrell M, Stone W, Lathrop M, Fontcuberta J, Blangero J. Soria JM, et al. Am J Hum Genet. 2002 Mar;70(3):567-74. doi: 10.1086/339259. Epub 2002 Jan 22. Am J Hum Genet. 2002. PMID: 11805911 Free PMC article.

9

Thromboplastin-thrombomodulin-mediated time and serum folate levels are genetically correlated with the risk of thromboembolic disease: results from the GAIT project.

Souto JC, Almasy L, Borrell M, Stone WH, Blanco-Vaca F, Soria JM, Blangero J, Fontcuberta J. Souto JC, et al. Among authors: soria jm. Thromb Haemost. 2002 Jan;87(1):68-73. Thromb Haemost. 2002. PMID: 11848458

10

Identification of a large deletion and three novel mutations in exon 13 of the factor V gene in a Spanish family with normal factor V coagulant and anticoagulant properties.

Soria JM, Blangero J, Souto JC, Martínez-Sánchez E, Martínez-Marchán E, Coll I, Tirado I, Cercós A, Almasy L, Fontcuberta J. Soria JM, et al. Hum Genet. 2002 Jul;111(1):59-65. doi: 10.1007/s00439-002-0746-y. Epub 2002 Jun 18. Hum Genet. 2002. PMID: 12136237

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