Journal Articles

Source: ncbi.nlm.nih.gov/pubmed?term=soria,%20jose%20manuel.

2012 — 2016

[1] G. Athanasiadis, L. Arranz, A. Ziyatdinov, H. Brunel, M. Camacho, J. Malouf, N. H. Sosa, L. Vila, J. Casademont and J. M. Soria. “Exploring correlation between bone metabolism markers and densitometric traits in extended families from Spain”. In: Bone 90 (May. 2016). [DOI:10.1016/j.bone.2016.05.009] [PubMed:27241279] , pp. 1-6.

[2] A. Engert, C. Balduini, A. Brand, B. Coiffier, C. Cordonnier, H. Dohner, T. D. de Wit, S. Eichinger, W. Fibbe, T. Green, F. de Haas, A. Iolascon, T. Jaffredo, F. Rodeghiero, G. Salles, J. J. Schuringa, A. Engert, C. Balduini, A. Brand, B. Coiffier, et al. “The European Hematology Association Roadmap for European Hematology Research: a consensus document”. In: Haematologica 101.2 (Feb. 2016). [DOI:10.3324/haematol.2015.136739] [PubMed:26819058] , pp. 115-208.

[3] N. Hernandez-de Sosa, G. Athanasiadis, J. Malouf, A. Laiz, A. Marin, S. Herrera, J. Farrerons, J. M. Soria and J. Casademont. “Genetic Contribution of Femoral Neck Bone Geometry to the Risk of Developing Osteoporosis: A Family-Based Study”. In: PLoS ONE 11.5 (2016). [PubMed Central:PMC4862643] [DOI:10.1371/journal.pone.0154833] [PubMed:27163365] , p. e0154833.

[4] D. A. Hinds, A. Buil, D. Ziemek, A. Martinez-Perez, R. Malik, L. Folkersen, M. Germain, A. Malarstig, A. Brown, J. M. Soria, M. Dichgans, N. Bing, A. Franco-Cereceda, J. C. Souto, E. T. Dermitzakis, A. Hamsten, B. B. Worrall, J. Y. Tung and M. Sabater-Lleal. “Genome-wide association analysis of self-reported events in 6135 individuals and 252 827 controls identifies 8 loci associated with thrombosis”. In: Hum. Mol. Genet. (Feb. 2016). [DOI:10.1093/hmg/ddw037] [PubMed:26908601] .

[5] L. Martin-Fernandez, A. Ziyatdinov, M. Carrasco, J. A. Millon, A. Martinez-Perez, N. Vilalta, H. Brunel, M. Font, A. Hamsten, J. C. Souto and J. M. Soria. “Genetic Determinants of Thrombin Generation and Their Relation to Venous Thrombosis: Results from the GAIT-2 Project”. In: PLoS ONE 11.1 (2016). [PubMed Central:PMC4718515] [DOI:10.1371/journal.pone.0146922] [PubMed:26784699] , p. e0146922.

[6] A. F. Remacha, N. Vilalta, M. P. Sarda, J. Millon, N. Pujol-Moix, A. Ziyatdinov, J. Fontcuberta, J. Nomdedeu, J. M. Soria and J. C. Souto. “Erytrocyte-related phenotypes and genetic susceptibility to thrombosis”. In: Blood Cells Mol. Dis. 59 (Jul. 2016). [DOI:10.1016/j.bcmd.2016.04.006] [PubMed:27282566] , pp. 44-48.

[7] M. Vazquez-Santiago, A. Ziyatdinov, N. Pujol-Moix, H. Brunel, A. Morera, J. M. Soria and J. C. Souto. “Age and gender effects on 15 platelet phenotypes in a Spanish population”. In: Comput. Biol. Med. 69 (Feb. 2016). [DOI:10.1016/j.compbiomed.2015.12.023] [PubMed:26773944] , pp. 226-233.

[8] A. Ziyatdinov, H. Brunel, A. Martinez-Perez, A. Buil, A. Perera and J. M. Soria. “solarius: an R interface to SOLAR for variance component analysis in pedigrees”. In: Bioinformatics 32.12 (Jun. 2016). [DOI:10.1093/bioinformatics/btw080] [PubMed:27153684] , pp. 1901-1902.

[9] M. Franberg, K. Gertow, A. Hamsten, J. Lagergren, B. Sennblad, H. Watkins, A. Hamsten, R. Collins, U. Seedorf, M. G. Franzosi, J. Hager, F. Green, M. Parker, J. M. Soria, E. Tremoli, J. Bjorkegren, A. Walentinsson, C. Finocchiaro, A. Goel, M. Farral, et al. “Discovering Genetic Interactions in Large-Scale Association Studies by Stage-wise Likelihood Ratio Tests”. In: PLoS Genet. 11.9 (Sep. 2015). [PubMed Central:PMC4581725] [DOI:10.1371/journal.pgen.1005502] [PubMed:26402789] , p. e1005502.

[10] N. Pujol-Moix, M. Vazquez-Santiago, A. Morera, A. Ziyatdinov, A. Remacha, J. F. Nomdedeu, J. Fontcuberta, J. M. Soria and J. C. Souto. “Genetic determinants of platelet large-cell ratio, immature platelet fraction, and other platelet-related phenotypes”. In: Thromb. Res. 136.2 (Aug. 2015). [DOI:10.1016/j.thromres.2015.06.016] [PubMed:26148565] , pp. 361-366.

[11] J. M. Soria and S. Lopez. “[The genetics of thrombosis in cancer]”. In: Med Clin (Barc) 144 Suppl 1 (Jan. 2015). [DOI:10.1016/S0025-7753(15)30015-4] [PubMed:25771089] , pp. 26-30.

[12] G. Athanasiadis, J. Malouf, N. Hernandez-Sosa, L. Martin-Fernandez, M. Catalan, J. Casademont and J. M. Soria. “Linkage and association analyses using families identified a locus affecting an osteoporosis-related trait”. In: Bone 60 (Mar. 2014). [DOI:10.1016/j.bone.2013.12.010] [PubMed:24334171] , pp. 98-103.

[13] N. Hernandez-de Sosa, G. Athanasiadis, J. Malouf, A. Laiz, A. Marin, S. Herrera, J. Farrerons, J. M. Soria and J. Casademont. “Heritability of bone mineral density in a multivariate family-based study”. In: Calcif. Tissue Int. 94.6 (Jun. 2014). [DOI:10.1007/s00223-014-9852-9] [PubMed:24687525] , pp. 590-596.

[14] S. Lopez, A. Buil, J. C. Souto, J. Casademont, A. Martinez-Perez, L. Almasy and J. M. Soria. “A genome-wide association study in the genetic analysis of idiopathic thrombophilia project suggests sex-specific regulation of mitochondrial DNA levels”. In: Mitochondrion 18 (Sep. 2014). [DOI:10.1016/j.mito.2014.09.004] [PubMed:25240745] , pp. 34-40.

[15] J. M. Soria, P. E. Morange, J. Vila, J. C. Souto, M. Moyano, D. A. Tregouet, J. Mateo, N. Saut, E. Salas and R. Elosua. “Multilocus genetic risk scores for venous thromboembolism risk assessment”. In: J Am Heart Assoc 3.5 (Oct. 2014). [PubMed Central:PMC4323784] [DOI:10.1161/JAHA.114.001060] [PubMed:25341889] , p. e001060.

[16] J. C. Souto, G. Pena, A. Ziyatdinov, A. Buil, S. Lopez, J. Fontcuberta and J. M. Soria. “A genomewide study of body mass index and its genetic correlation with thromboembolic risk. Results from the GAIT project”. In: Thromb. Haemost. 112.5 (Nov. 2014). [DOI:10.1160/TH14-03-0275] [PubMed:25118907] , pp. 1036-1043.

[17] M. E. de la Morena-Barrio, A. Buil, A. I. Anton, I. Martinez-Martinez, A. Minano, R. Gutierrez-Gallego, J. Navarro-Fernandez, S. Aguila, J. C. Souto, V. Vicente, J. M. Soria and J. Corral. “Identification of antithrombin-modulating genes. Role of LARGE, a gene encoding a bifunctional glycosyltransferase, in the secretion of proteins?”. In: PLoS ONE 8.5 (2013). [PubMed Central:PMC3660365] [DOI:10.1371/journal.pone.0064998] [PubMed:23705025] , p. e64998.

[18] M. Camacho, A. Martinez-Perez, A. Buil, L. Siguero, S. Alcolea, S. Lopez, J. Fontcuberta, J. C. Souto, L. Vila and J. M. Soria. “Genetic determinants of 5-lipoxygenase pathway in a Spanish population and their relationship with cardiovascular risk”. In: Atherosclerosis 224.1 (Sep. 2012). [DOI:10.1016/j.atherosclerosis.2012.07.001] [PubMed:22835628] , pp. 129-135.

[19] M. C. Garcia-Dabrio, N. Pujol-Moix, A. Martinez-Perez, J. Fontcuberta, J. C. Souto, J. M. Soria and J. F. Nomdedeu. “Influence of age, gender and lifestyle in lymphocyte subsets: report from the Spanish Gait-2 Study”. In: Acta Haematol. 127.4 (2012). [DOI:10.1159/000337051] [PubMed:22538526] , pp. 244-249.

[20] A. Helgadottir, S. Gretarsdottir, G. Thorleifsson, H. Holm, R. S. Patel, T. Gudnason, G. T. Jones, A. M. van Rij, D. J. Eapen, A. F. Baas, D. A. Tregouet, P. E. Morange, J. Emmerich, B. Lindblad, A. Gottsater, L. A. Kiemeny, J. S. Lindholt, N. Sakalihasan, R. E. Ferrell, D. J. Carey, et al. “Apolipoprotein(a) genetic sequence variants associated with systemic atherosclerosis and coronary atherosclerotic burden but not with venous thromboembolism”. In: J. Am. Coll. Cardiol. 60.8 (Aug. 2012). [DOI:10.1016/j.jacc.2012.01.078] [PubMed:22898070] , pp. 722-729.

[21] S. Lopez, A. Buil, J. C. Souto, J. Casademont, J. Blangero, A. Martinez-Perez, J. Fontcuberta, M. Lathrop, L. Almasy and J. M. Soria. “Sex-specific regulation of mitochondrial DNA levels: genome-wide linkage analysis to identify quantitative trait loci”. In: PLoS ONE 7.8 (2012). [PubMed Central:PMC3423410] [DOI:10.1371/journal.pone.0042711] [PubMed:22916149] , p. e42711.

[22] M. Sabater-Lleal, A. Martinez-Perez, A. Buil, L. Folkersen, J. C. Souto, M. Bruzelius, M. Borrell, J. Odeberg, A. Silveira, P. Eriksson, L. Almasy, A. Hamsten and J. M. Soria. “A genome-wide association study identifies KNG1 as a genetic determinant of plasma factor XI Level and activated partial thromboplastin time”. In: Arterioscler. Thromb. Vasc. Biol. 32.8 (Aug. 2012). [DOI:10.1161/ATVBAHA.112.248492] [PubMed:22701019] , pp. 2008-2016.

[23] J. C. Souto and J. M. Soria. “Predicting individual risk of venous thrombosis”. In: Blood 120.3 (Jul. 2012). [DOI:10.1182/blood-2012-06-433243] [PubMed:22821999] , pp. 500-501.

* — 2011

[1] G. Athanasiadis, A. Buil, J. C. Souto, M. Borrell, S. Lopez, A. Martinez-Perez, M. Lathrop, J. Fontcuberta, L. Almasy and J. M. Soria. “A genome-wide association study of the Protein C anticoagulant pathway”. In: PLoS ONE 6.12 (2011). [PubMed Central:PMC3247258] [DOI:10.1371/journal.pone.0029168] [PubMed:22216198] , p. e29168.

[2] J. A. Guerrero, J. Rivera, T. Quiroga, A. Martinez-Perez, A. I. Anton, C. Martinez, O. Panes, V. Vicente, D. Mezzano, J. M. Soria and J. Corral. “Novel loci involved in platelet function and platelet count identified by a genome-wide study performed in children”. In: Haematologica 96.9 (Sep. 2011). [PubMed Central:PMC3166104] [DOI:10.3324/haematol.2011.042077] [PubMed:21546496] , pp. 1335-1343.

[3] H. Brunel, J. J. Gallardo-Chacon, A. Buil, M. Vallverdu, J. M. Soria, P. Caminal and A. Perera. “MISS: a non-linear methodology based on mutual information for genetic association studies in both population and sib-pairs analysis”. In: Bioinformatics 26.15 (Aug. 2010). [DOI:10.1093/bioinformatics/btq273] [PubMed:20562420] , pp. 1811-1818.

[4] A. Buil, D. A. Tregouet, J. C. Souto, N. Saut, M. Germain, M. Rotival, L. Tiret, F. Cambien, M. Lathrop, T. Zeller, M. C. Alessi, S. Rodriguez de Cordoba, T. Munzel, P. Wild, J. Fontcuberta, F. Gagnon, J. Emmerich, L. Almasy, S. Blankenberg, J. M. Soria, et al. “C4BPB/C4BPA is a new susceptibility locus for venous thrombosis with unknown protein S-independent mechanism: results from genome-wide association and gene expression analyses followed by case-control studies”. In: Blood 115.23 (Jun. 2010). [PubMed Central:PMC2890187] [DOI:10.1182/blood-2010-01-263038] [PubMed:20212171] , pp. 4644-4650.

[5] F. Calafell, L. Almasy, M. Sabater-Lleal, A. Buil, C. Mordillo, A. Ramirez-Soriano, M. Sikora, J. C. Souto, J. Blangero, J. Fontcuberta and J. M. Soria. “Sequence variation and genetic evolution at the human F12 locus: mapping quantitative trait nucleotides that influence FXII plasma levels”. In: Hum. Mol. Genet. 19.3 (Feb. 2010). [PubMed Central:PMC2798724] [DOI:10.1093/hmg/ddp517] [PubMed:19933701] , pp. 517-525.

[6] M. Sabater-Lleal, M. Chillon, C. Mordillo, A. Martinez, E. Gil, J. Mateo, J. Blangero, L. Almasy, J. Fontcuberta and J. M. Soria. “Combined cis-regulator elements as important mechanism affecting FXII plasma levels”. In: Thromb. Res. 125.2 (Feb. 2010). [PubMed Central:PMC2906145] [DOI:10.1016/j.thromres.2009.08.019] [PubMed:19786295] , pp. 55-60.

[7] L. Vila, A. Martinez-Perez, M. Camacho, A. Buil, S. Alcolea, N. Pujol-Moix, M. Soler, R. Anton, J. C. Souto, J. Fontcuberta and J. M. Soria. “Heritability of thromboxane A2 and prostaglandin E2 biosynthetic machinery in a Spanish population”. In: Arterioscler. Thromb. Vasc. Biol. 30.1 (Jan. 2010). [PubMed Central:PMC2831176] [DOI:10.1161/ATVBAHA.109.193219] [PubMed:19850905] , pp. 128-134.

[8] I. Arbesu and J. M. Soria. “Update to Soria et al.’s “F7 gene and clotting factor VII levels” (2005): genetic determinants of quantitative traits in thrombotic disease”. In: Hum. Biol. 81.5-6 (Dec. 2009). [DOI:10.3378/027.081.0628] [PubMed:20504203] , pp. 869-874.

[9] A. Buil, A. Martinez-Perez, A. Perera-Lluna, L. Rib, P. Caminal and J. M. Soria. “A new gene-based association test for genome-wide association studies”. In: BMC Proc 3 Suppl 7 (2009). [PubMed Central:PMC2795904] [PubMed:20017997] , p. S130.

[10] A. Malarstig, A. Buil, J. C. Souto, R. Clarke, F. Blanco-Vaca, J. Fontcuberta, J. Peden, M. Andersen, A. Silveira, S. Barlera, U. Seedorf, H. Watkins, L. Almasy, A. Hamsten and J. M. Soria. “Identification of ZNF366 and PTPRD as novel determinants of plasma homocysteine in a family-based genome-wide association study”. In: Blood 114.7 (Aug. 2009). [PubMed Central:PMC2727417] [DOI:10.1182/blood-2009-04-215269] [PubMed:19525478] , pp. 1417-1422.

[11] J. M. Soria, L. Almasy, J. C. Souto, M. Sabaterlleal, J. Fontcuberta, J. Blangero, J. M. Soria, L. Almasy, J. C. Souto, M. Sabaterlleal, J. Fontcuberta and J. Blangero. “The F7 gene and clotting factor VII levels: dissection of a human quantitative trait locus. 2005”. In: Hum. Biol. 81.5-6 (Dec. 2009). [DOI:10.3378/027.081.0627] [PubMed:20504202] , pp. 853-867.

[12] S. Lopez, A. Buil, J. Ordonez, J. C. Souto, L. Almasy, M. Lathrop, J. Blangero, F. Blanco-Vaca, J. Fontcuberta and J. M. Soria. “Genome-wide linkage analysis for identifying quantitative trait loci involved in the regulation of lipoprotein a (Lpa) levels”. In: Eur. J. Hum. Genet. 16.11 (Nov. 2008). [PubMed Central:PMC2749722] [DOI:10.1038/ejhg.2008.114] [PubMed:18560444] , pp. 1372-1379.

[13] M. Sabater-Lleal, A. Buil, J. C. Souto, L. Alamsy, M. Borrell, M. Lathrop, J. Blangero, J. Fontcuberta and J. M. Soria. “A genome-wide exploration suggests an oligogenic model of inheritance for the TAFI activity and its antigen levels”. In: Hum. Genet. 124.1 (Aug. 2008). [PubMed Central:PMC2592198] [DOI:10.1007/s00439-008-0527-3] [PubMed:18563448] , pp. 81-88.

[14] M. Lopez, P. Giraldo, P. Alvarez, R. Cornudella, M. Pocovi, A. Martinez, J. Fontcuberta and J. M. Soria. “Multiplex assay for genetic testing of thrombophilia: a method for routine clinical care”. In: J. Clin. Lab. Anal. 21.6 (2007). [DOI:10.1002/jcla.20183] [PubMed:18022930] , pp. 349-355.

[15] C. Mordillo, E. Martinez-Marchan, J. Fontcuberta and J. M. Soria. “Molecular analysis of multiple genetic variants in Spanish FXII-deficient families”. In: Haematologica 92.11 (Nov. 2007). [DOI:10.3324/haematol.11388] [PubMed:18024408] , pp. 1569-1572.

[16] A. Perera, A. Buil, M. C. Di Bernardo, M. Sabater-Lleal, L. Pattini, J. C. Souto, J. Fontcuberta, M. Vallverdu, J. M. Soria and P. Caminal. “Clustering of individuals given SNPs similarity based on normalized mutual information: F7 SNPs in the GAIT sample”. In: Conf Proc IEEE Eng Med Biol Soc 2007 (2007). [DOI:10.1109/IEMBS.2007.4352238] [PubMed:18001904] , pp. 123-126.

[17] M. Sabater-Lleal, M. Chillon, T. E. Howard, E. Gil, L. Almasy, J. Blangero, J. Fontcuberta and J. M. Soria. “Functional analysis of the genetic variability in the F7 gene promoter”. In: Atherosclerosis 195.2 (Dec. 2007). [DOI:10.1016/j.atherosclerosis.2006.12.031] [PubMed:17292373] , pp. 262-268.

[18] J. Corral, R. Gonzalez-Conejero, J. M. Soria, J. R. Gonzalez-Porras, E. Perez-Ceballos, R. Lecumberri, V. Roldan, J. C. Souto, A. Minano, D. Hernandez-Espinosa, I. Alberca, J. Fontcuberta and V. Vicente. “A nonsense polymorphism in the protein Z-dependent protease inhibitor increases the risk for venous thrombosis”. In: Blood 108.1 (Jul. 2006). [PubMed Central:PMC1895831] [DOI:10.1182/blood-2005-08-3249] [PubMed:16527896] , pp. 177-183.

[19] A. Perera, M. Vallverdu, F. Claria, J. M. Soria and P. Caminal. “DNA binding sites characterization by means of Rényi entropy measures on nucleotide transitions”. In: Conf Proc IEEE Eng Med Biol Soc 1 (2006). [DOI:10.1109/IEMBS.2006.260482] [PubMed:17946719] , pp. 5783-5786.

[20] A. F. Remacha, J. C. Souto, J. M. Soria, A. Buil, M. P. Sarda, M. Lathrop, J. Blangero, L. Almasy and J. Fontcuberta. “Genomewide linkage analysis of soluble transferrin receptor plasma levels”. In: Ann. Hematol. 85.1 (Jan. 2006). [DOI:10.1007/s00277-005-1092-7] [PubMed:16132911] , pp. 25-28.

[21] M. Sabater-Lleal, J. M. Soria, J. Bertranpetit, L. Almasy, J. Blangero, J. Fontcuberta and F. Calafell. “Human F7 sequence is split into three deep clades that are related to FVII plasma levels”. In: Hum. Genet. 118.6 (Feb. 2006). [DOI:10.1007/s00439-005-0045-5] [PubMed:16292673] , pp. 741-751.

[22] J. C. Souto and J. M. Soria. “Plasma homocysteine and the genetics of cardiovascular disease”. In: Future Cardiol 2.2 (Mar. 2006). [DOI:10.2217/14796678.2.2.169] [PubMed:19804073] , pp. 169-178.

[23] A. Santamaria, J. M. Soria, I. Tirado, J. Mateo, I. Coll, J. C. Souto and J. Fontcuberta. “Double heterozygosity for Factor V Leiden and Factor V Cambridge mutations associated with low levels of activated protein C resistance in a Spanish thrombophilic family”. In: Thromb. Haemost. 93.6 (Jun. 2005). [DOI:10.1267/THRO05061193] [PubMed:15968408] , pp. 1193-1195.

[24] J. M. Soria, L. Almasy, J. C. Souto, A. Buil, M. Lathrop, J. Blangero and J. Fontcuberta. “A genome search for genetic determinants that influence plasma fibrinogen levels”. In: Arterioscler. Thromb. Vasc. Biol. 25.6 (Jun. 2005). [DOI:10.1161/01.ATV.0000161927.38739.6f] [PubMed:15761192] , pp. 1287-1292.

[25] J. M. Soria, L. Almasy, J. C. Souto, M. Sabater-Lleal, J. Fontcuberta and J. Blangero. “The F7 gene and clotting factor VII levels: dissection of a human quantitative trait locus”. In: Hum. Biol. 77.5 (Oct. 2005). [PubMed:16596941] , pp. 561-575.

[26] J. M. Soria and J. Fontcuberta. “New approaches and future prospects for evaluating genetic risk of thrombosis”. In: Haematologica 90.9 (Sep. 2005). [PubMed:16154845] , pp. 1212-1222.

[27] J. C. Souto, F. Blanco-Vaca, J. M. Soria, A. Buil, L. Almasy, J. Ordonez-Llanos, J. M. Martin-Campos, M. Lathrop, W. Stone, J. Blangero and J. Fontcuberta. “A genomewide exploration suggests a new candidate gene at chromosome 11q23 as the major determinant of plasma homocysteine levels: results from the GAIT project”. In: Am. J. Hum. Genet. 76.6 (Jun. 2005). [PubMed Central:PMC1196452] [DOI:10.1086/430409] [PubMed:15849667] , pp. 925-933.

[28] I. Tirado, J. Mateo, J. M. Soria, A. Oliver, E. Martinez-Sanchez, C. Vallve, M. Borrell, T. Urrutia and J. Fontcuberta. “The ABO blood group genotype and factor VIII levels as independent risk factors for venous thromboembolism”. In: Thromb. Haemost. 93.3 (Mar. 2005). [DOI:10.1160/TH04-04-0251] [PubMed:15735796] , pp. 468-474.

[29] D. M. Warren, J. M. Soria, J. C. Souto, A. Comuzzie, J. Fontcuberta, J. Blangero, J. W. MacCluer and L. Almasy. “Heritability of hemostasis phenotypes and their correlation with type 2 diabetes status in Mexican Americans”. In: Hum. Biol. 77.1 (Feb. 2005). [PubMed:16114812] , pp. 1-15.

[30] A. Buil, J. M. Soria, J. C. Souto, L. Almasy, M. Lathrop, J. Blangero and J. Fontcuberta. “Protein C levels are regulated by a quantitative trait locus on chromosome 16: results from the Genetic Analysis of Idiopathic Thrombophilia (GAIT) Project”. In: Arterioscler. Thromb. Vasc. Biol. 24.7 (Jul. 2004). [DOI:10.1161/01.ATV.0000132408.13064.09] [PubMed:15142863] , pp. 1321-1325.

[31] J. Esparza-Gordillo, J. M. Soria, A. Buil, L. Almasy, J. Blangero, J. Fontcuberta and S. Rodriguez de Cordoba. “Genetic and environmental factors influencing the human factor H plasma levels”. In: Immunogenetics 56.2 (May. 2004). [DOI:10.1007/s00251-004-0660-7] [PubMed:15118848] , pp. 77-82.

[32] A. Santamaria, J. Mateo, I. Tirado, A. Oliver, R. Belvis, J. Marti-Fabregas, R. Felices, J. M. Soria, J. C. Souto and J. Fontcuberta. “Homozygosity of the T allele of the 46 C->T polymorphism in the F12 gene is a risk factor for ischemic stroke in the Spanish population”. In: Stroke 35.8 (Aug. 2004). [DOI:10.1161/01.STR.0000133127.68041.a3] [PubMed:15232129] , pp. 1795-1799.

[33] I. Tirado, J. M. Soria, J. Mateo, A. Oliver, J. C. Souto, A. Santamaria, R. Felices, M. Borrell and J. Fontcuberta. “Association after linkage analysis indicates that homozygosity for the 46C->T polymorphism in the F12 gene is a genetic risk factor for venous thrombosis”. In: Thromb. Haemost. 91.5 (May. 2004). [DOI:10.1160/TH03-10-0620] [PubMed:15116249] , pp. 899-904.

[34] L. Almasy, J. M. Soria, J. C. Souto, I. Coll, D. Bacq, A. Faure, J. Mateo, M. Borrell, X. Munoz, N. Sala, W. H. Stone, M. Lathrop, J. Fontcuberta and J. Blangero. “A quantitative trait locus influencing free plasma protein S levels on human chromosome 1q: results from the Genetic Analysis of Idiopathic Thrombophilia (GAIT) project”. In: Arterioscler. Thromb. Vasc. Biol. 23.3 (Mar. 2003). [DOI:10.1161/01.ATV.0000055740.22563.C5] [PubMed:12615682] , pp. 508-511.

[35] J. Esparza-Gordillo, J. M. Soria, A. Buil, J. C. Souto, L. Almasy, J. Blangero, J. Fontcuberta and S. R. de Cordoba. “Genetic determinants of variation in the plasma levels of the C4b-binding protein (C4BP) in Spanish families”. In: Immunogenetics 54.12 (Mar. 2003). [DOI:10.1007/s00251-003-0537-1] [PubMed:12671737] , pp. 862-866.

[36] M. Sabater-Lleal, E. Martinez-Marchan, E. Martinez-Sanchez, M. Coll, C. Vallve, J. Mateo, J. C. Souto, J. Fontcuberta and J. M. Soria. “Complexity of the genetic contribution to factor VII deficiency in two Spanish families: clinical and biological implications”. In: Haematologica 88.8 (Aug. 2003). [PubMed:12935978] , pp. 906-913.

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