Soria JM - Search Results

1

Association of complement receptor 2 polymorphisms with innate resistance to HIV-1 infection.

Herrero R, Real LM, Rivero-Juárez A, Pineda JA, Camacho Á, Macías J, Laplana M, Konieczny P, Márquez FJ, Souto JC, Soria JM, Saulle I, Lo Caputo S, Biasin M, Rivero A, Fibla J, Caruz A. Herrero R, et al. Among authors: soria jm. Genes Immun. 2015 Mar;16(2):134-41. doi: 10.1038/gene.2014.71. Epub 2015 Jan 8. Genes Immun. 2015. PMID: 25569262

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 new locus on chromosome 18 that influences normal variation in activated protein C resistance phenotype and factor VIII activity and its relation to thrombosis susceptibility.

Soria JM, Almasy L, Souto JC, Buil A, Martinez-Sanchez E, Mateo J, Borrell M, Stone WH, Lathrop M, Fontcuberta J, Blangero J. Soria JM, et al. Blood. 2003 Jan 1;101(1):163-7. doi: 10.1182/blood-2002-06-1792. Epub 2002 Aug 15. Blood. 2003. PMID: 12393556 Free article.

9

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. Sabater-Lleal M, et al. Among authors: soria jm. Haematologica. 2003 Aug;88(8):906-13. Haematologica. 2003. PMID: 12935978

10

Association after linkage analysis indicates that homozygosity for the 46C-->T polymorphism in the F12 gene is a genetic risk factor for venous thrombosis.

Tirado I, Soria JM, Mateo J, Oliver A, Souto JC, Santamaria A, Felices R, Borrell M, Fontcuberta J. Tirado I, et al. Among authors: soria jm. Thromb Haemost. 2004 May;91(5):899-904. doi: 10.1160/TH03-10-0620. Thromb Haemost. 2004. PMID: 15116249

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