-
2
-
-
0033653710
-
Genetic susceptibility to thrombosis and its relationship to physiological risk factors: the GAIT study. Genetic analysis of idiopathic thrombophilia
-
Souto J.C., Almasy L., Borrell M., et al. Genetic susceptibility to thrombosis and its relationship to physiological risk factors: the GAIT study. Genetic analysis of idiopathic thrombophilia. Am. J. Hum. Genet. 2000, 67:1452-1459.
-
(2000)
Am. J. Hum. Genet.
, vol.67
, pp. 1452-1459
-
-
Souto, J.C.1
Almasy, L.2
Borrell, M.3
-
3
-
-
13244287947
-
Familial segregation of venous thromboembolism
-
Heit J.A., Phelps M.A., Ward S.A., et al. Familial segregation of venous thromboembolism. J. Thromb. Haemost. 2004, 2:731-736.
-
(2004)
J. Thromb. Haemost.
, vol.2
, pp. 731-736
-
-
Heit, J.A.1
Phelps, M.A.2
Ward, S.A.3
-
4
-
-
18244384262
-
A quantitative-trait locus in the human factor XII gene influences both plasma factor XII levels and susceptibility to thrombotic disease
-
Soria J.M., Almasy L., Souto J.C., et al. A quantitative-trait locus in the human factor XII gene influences both plasma factor XII levels and susceptibility to thrombotic disease. Am. J. Hum. Genet. 2002, 70:567-574.
-
(2002)
Am. J. Hum. Genet.
, vol.70
, pp. 567-574
-
-
Soria, J.M.1
Almasy, L.2
Souto, J.C.3
-
5
-
-
77954752114
-
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
-
Buil A., Trégouët D.A., Souto J.C., 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. Blood 2010, 115:4644-4650.
-
(2010)
Blood
, vol.115
, pp. 4644-4650
-
-
Buil, A.1
Trégouët, D.A.2
Souto, J.C.3
-
6
-
-
0034603799
-
Genetic determinants of hemostasis phenotypes in Spanish families
-
Souto J.C., Almasy L., Borrell M., et al. Genetic determinants of hemostasis phenotypes in Spanish families. Circulation 2000, 101:1546-1551.
-
(2000)
Circulation
, vol.101
, pp. 1546-1551
-
-
Souto, J.C.1
Almasy, L.2
Borrell, M.3
-
7
-
-
0346733120
-
Genetic determinants of iron metabolism plasma phenotypes and their relationship with risk of thrombosis
-
Souto J.C., Remacha A., Buil A., et al. Genetic determinants of iron metabolism plasma phenotypes and their relationship with risk of thrombosis. Haematologica 2003, 88:1436-1438.
-
(2003)
Haematologica
, vol.88
, pp. 1436-1438
-
-
Souto, J.C.1
Remacha, A.2
Buil, A.3
-
8
-
-
84887587702
-
Biomarkers for prediction of venous thromboembolism in cancer
-
Pabinger I., Thaler J., Ay C. Biomarkers for prediction of venous thromboembolism in cancer. Blood 2013, 122:2011-2018.
-
(2013)
Blood
, vol.122
, pp. 2011-2018
-
-
Pabinger, I.1
Thaler, J.2
Ay, C.3
-
9
-
-
76549120858
-
High hematocrit as a risk factor for venous thrombosis. Cause or innocent bystander?
-
Schreijer A.J.M., Reitsma P.H., Cannegieter S.C. High hematocrit as a risk factor for venous thrombosis. Cause or innocent bystander?. Haematologica 2010, 95:182-184.
-
(2010)
Haematologica
, vol.95
, pp. 182-184
-
-
Schreijer, A.J.M.1
Reitsma, P.H.2
Cannegieter, S.C.3
-
10
-
-
76549088896
-
Hematocrit and risk of venous thromboembolism in a general population. The Tromsø study
-
Brækkan S.K., Mathiesen E.B., Njølstad I., et al. Hematocrit and risk of venous thromboembolism in a general population. The Tromsø study. Haematologica 2010, 95:270-275.
-
(2010)
Haematologica
, vol.95
, pp. 270-275
-
-
Brækkan, S.K.1
Mathiesen, E.B.2
Njølstad, I.3
-
11
-
-
78649351035
-
Red cells playing as activated platelets in thalassemia intermedia
-
Mannucci P.M. Red cells playing as activated platelets in thalassemia intermedia. J. Thromb. Haemost. 2010, 8:2149-2151.
-
(2010)
J. Thromb. Haemost.
, vol.8
, pp. 2149-2151
-
-
Mannucci, P.M.1
-
12
-
-
84877739011
-
The role of the red cell membrane in thrombin generation
-
Whelihan M.F., Mann K.G. The role of the red cell membrane in thrombin generation. Thromb. Res. 2013, 131:377-382.
-
(2013)
Thromb. Res.
, vol.131
, pp. 377-382
-
-
Whelihan, M.F.1
Mann, K.G.2
-
14
-
-
84868204046
-
Association between B-group vitamins and venous thrombosis: systematic review and meta-analysis of epidemiological studies
-
Zhou K., Zhao R., Geng Z., et al. Association between B-group vitamins and venous thrombosis: systematic review and meta-analysis of epidemiological studies. J. Thromb. Thrombolysis 2012, 34:459-467.
-
(2012)
J. Thromb. Thrombolysis
, vol.34
, pp. 459-467
-
-
Zhou, K.1
Zhao, R.2
Geng, Z.3
-
15
-
-
33847671755
-
Haptoglobin genotype is a determinant of iron, lipid peroxidation, and macrophage accumulation in the atherosclerotic plaque
-
Levy A.P., Levy J.E., Kalet-Litman S., et al. Haptoglobin genotype is a determinant of iron, lipid peroxidation, and macrophage accumulation in the atherosclerotic plaque. Arterioscler. Thromb. Vasc. Biol. 2007, 27:134-140.
-
(2007)
Arterioscler. Thromb. Vasc. Biol.
, vol.27
, pp. 134-140
-
-
Levy, A.P.1
Levy, J.E.2
Kalet-Litman, S.3
-
16
-
-
27844483410
-
Haptoglobin phenotype 2-2 as a potentially new risk factor for spontaneous venous thromboembolism
-
Vormittag R., Vukovich T., Mannhalter C., et al. Haptoglobin phenotype 2-2 as a potentially new risk factor for spontaneous venous thromboembolism. Haematologica 2005, 90:1557-1561.
-
(2005)
Haematologica
, vol.90
, pp. 1557-1561
-
-
Vormittag, R.1
Vukovich, T.2
Mannhalter, C.3
-
17
-
-
33947497535
-
In vivo and in vitro studies establishing haptoglobin as a major susceptibility gene for diabetic vascular disease
-
Asleh R., AP L. In vivo and in vitro studies establishing haptoglobin as a major susceptibility gene for diabetic vascular disease. Vasc. Health Risk Manag. 2005, 1:19-28.
-
(2005)
Vasc. Health Risk Manag.
, vol.1
, pp. 19-28
-
-
Asleh, R.1
AP, L.2
-
18
-
-
84889648423
-
The contribution of red blood cells to thrombin generation in sickle cell disease: meizothrombin generation on sickled red blood cells
-
Whelihan M.F., Mooberry M.J., Zachary V., et al. The contribution of red blood cells to thrombin generation in sickle cell disease: meizothrombin generation on sickled red blood cells. J. Thromb. Haemost. 2013, 11:2187-2189.
-
(2013)
J. Thromb. Haemost.
, vol.11
, pp. 2187-2189
-
-
Whelihan, M.F.1
Mooberry, M.J.2
Zachary, V.3
-
19
-
-
85017153592
-
Genetic associations with plasma B12, B6, and folate levels in an ischemic stroke population from the vitamin intervention for stroke prevention (VISP) trial
-
Keene K.L., Chen W.M., Chen F., et al. Genetic associations with plasma B12, B6, and folate levels in an ischemic stroke population from the vitamin intervention for stroke prevention (VISP) trial. Front Public Health 2014, 2:112.
-
(2014)
Front Public Health
, vol.2
, pp. 112
-
-
Keene, K.L.1
Chen, W.M.2
Chen, F.3
-
20
-
-
79955936239
-
Vitamin B12 deficiency, hyperhomocysteinemia and thrombosis: a case and control study
-
Remacha A.F., Souto J.C., Piñana J.L., et al. Vitamin B12 deficiency, hyperhomocysteinemia and thrombosis: a case and control study. Int. J. Hematol. 2011, 93:458-464.
-
(2011)
Int. J. Hematol.
, vol.93
, pp. 458-464
-
-
Remacha, A.F.1
Souto, J.C.2
Piñana, J.L.3
-
21
-
-
0036938917
-
Enhanced risk of thrombotic disease in patients with acquired vitamin B12 and/or folate deficiency: role of hyperhomocysteinemia
-
Remacha A.F., Souto J.C., Rámila E., et al. Enhanced risk of thrombotic disease in patients with acquired vitamin B12 and/or folate deficiency: role of hyperhomocysteinemia. Ann. Hematol. 2002, 81:616-621.
-
(2002)
Ann. Hematol.
, vol.81
, pp. 616-621
-
-
Remacha, A.F.1
Souto, J.C.2
Rámila, E.3
-
22
-
-
0036148263
-
Thromboplastin-thrombomodulin-mediated time and serum folate levels are genetically correlated with the risk of thromboembolic disease: results from the GAIT Project
-
Souto J.C., Almasy L., Borrell M., et al. Thromboplastin-thrombomodulin-mediated time and serum folate levels are genetically correlated with the risk of thromboembolic disease: results from the GAIT Project. Thromb. Haemost. 2002, 87:68-73.
-
(2002)
Thromb. Haemost.
, vol.87
, pp. 68-73
-
-
Souto, J.C.1
Almasy, L.2
Borrell, M.3
-
23
-
-
0142135569
-
Search for new thrombosis-related genes through intermediate phenotypes. Genetic and household effects
-
Souto J.C. Search for new thrombosis-related genes through intermediate phenotypes. Genetic and household effects. Pathophysiol. Haemost. Thromb. 2002, 32:338-340.
-
(2002)
Pathophysiol. Haemost. Thromb.
, vol.32
, pp. 338-340
-
-
Souto, J.C.1
-
24
-
-
28944435358
-
Genomewide linkage analysis of soluble transferrin receptor plasma levels
-
Remacha A.F., Souto J.C., Soria J.M., et al. Genomewide linkage analysis of soluble transferrin receptor plasma levels. Ann. Hematol. 2006, 85:25-28.
-
(2006)
Ann. Hematol.
, vol.85
, pp. 25-28
-
-
Remacha, A.F.1
Souto, J.C.2
Soria, J.M.3
-
25
-
-
84964352114
-
-
Available at:. Accessed March 30, 2014.
-
International Physical Activity Questionnaire (IPAQ). Available at:. Accessed March 30, 2014. http://www.ipaq.ki.se.
-
-
-
-
27
-
-
0035160177
-
Genetic regulation of plasma levels of vitamin K-dependent proteins involved in hemostasis: results from the GAIT Project. Genetic analysis of idiopathic thrombophilia
-
Souto J.C., Almasy L., Blangero J., et al. Genetic regulation of plasma levels of vitamin K-dependent proteins involved in hemostasis: results from the GAIT Project. Genetic analysis of idiopathic thrombophilia. Thromb. Haemost. 2001, 85:88-92.
-
(2001)
Thromb. Haemost.
, vol.85
, pp. 88-92
-
-
Souto, J.C.1
Almasy, L.2
Blangero, J.3
-
28
-
-
0030056295
-
Genetic and environmental correlations among hormone levels and measures of body fat accumulation and topography
-
Comuzzie A.G., Blangero J., Mahaney M.C., et al. Genetic and environmental correlations among hormone levels and measures of body fat accumulation and topography. J. Clin. Endocrinol. Metab. 1996, 81:597-600.
-
(1996)
J. Clin. Endocrinol. Metab.
, vol.81
, pp. 597-600
-
-
Comuzzie, A.G.1
Blangero, J.2
Mahaney, M.C.3
-
29
-
-
0031966959
-
Multipoint quantitative-trait linkage analysis in general pedigrees
-
Almasy L., Blangero J. Multipoint quantitative-trait linkage analysis in general pedigrees. Am. J. Hum. Genet. 1998, 62:1198-1211.
-
(1998)
Am. J. Hum. Genet.
, vol.62
, pp. 1198-1211
-
-
Almasy, L.1
Blangero, J.2
-
30
-
-
84907319426
-
Asymptotic properties of maximum likelihood estimators and likelihood ratio tests under nonstandard conditions
-
Self S., Liang K. Asymptotic properties of maximum likelihood estimators and likelihood ratio tests under nonstandard conditions. J. Am. Stat. Assoc. 1987, 82:605-610.
-
(1987)
J. Am. Stat. Assoc.
, vol.82
, pp. 605-610
-
-
Self, S.1
Liang, K.2
-
31
-
-
0033966370
-
Genetic influences on F cells and other hematologic variables: a twin heritability study
-
Garner C., Tatu T., Reittie J.E., et al. Genetic influences on F cells and other hematologic variables: a twin heritability study. Blood 2000, 95:342-346.
-
(2000)
Blood
, vol.95
, pp. 342-346
-
-
Garner, C.1
Tatu, T.2
Reittie, J.E.3
-
32
-
-
33748039452
-
Heritability of cardiovascular and personality traits in 6,148 sardinians
-
Pilia G., Chen W.M., Scuteri A., et al. Heritability of cardiovascular and personality traits in 6,148 sardinians. PLoS Genet. 2006, 2.
-
(2006)
PLoS Genet.
, vol.2
-
-
Pilia, G.1
Chen, W.M.2
Scuteri, A.3
-
33
-
-
84990252549
-
Quantitative trait locus linkage analysis in a large Amish pedigree identifies novel candidate loci for erythrocyte traits
-
Hinckley J.D., Abbott D., Burns T.L., et al. Quantitative trait locus linkage analysis in a large Amish pedigree identifies novel candidate loci for erythrocyte traits. Mol. Genet. Genomic Med. 2013, 1:131-141.
-
(2013)
Mol. Genet. Genomic Med.
, vol.1
, pp. 131-141
-
-
Hinckley, J.D.1
Abbott, D.2
Burns, T.L.3
-
34
-
-
50849144857
-
Variation of hemoglobin levels in normal Italian populations from genetic isolates
-
Sala C., Ciullo M., Lanzara C., et al. Variation of hemoglobin levels in normal Italian populations from genetic isolates. Haematologica 2008, 93:1372-1375.
-
(2008)
Haematologica
, vol.93
, pp. 1372-1375
-
-
Sala, C.1
Ciullo, M.2
Lanzara, C.3
-
35
-
-
13244296993
-
Evidence for a gene influencing haematocrit on chromosome 6q23-24: genomewide scan in the Framingham heart study
-
Lin J.P., O'Donnell C.J., Levy D., et al. Evidence for a gene influencing haematocrit on chromosome 6q23-24: genomewide scan in the Framingham heart study. J. Med. Genet. 2005, 42:75-79.
-
(2005)
J. Med. Genet.
, vol.42
, pp. 75-79
-
-
Lin, J.P.1
O'Donnell, C.J.2
Levy, D.3
-
36
-
-
50849133580
-
Variability and heritability of hemoglobin concentration: an opportunity to improve understanding of anemia in older adults
-
Patel K.V. Variability and heritability of hemoglobin concentration: an opportunity to improve understanding of anemia in older adults. Haematologica 2008, 93:1281-1283.
-
(2008)
Haematologica
, vol.93
, pp. 1281-1283
-
-
Patel, K.V.1
-
37
-
-
0033374163
-
Genetic and environmental causes of variation in basal levels of blood cells
-
Evans D.M., Frazer I.H., Martin N.G. Genetic and environmental causes of variation in basal levels of blood cells. Twin Res. 1999, 2:250-257.
-
(1999)
Twin Res.
, vol.2
, pp. 250-257
-
-
Evans, D.M.1
Frazer, I.H.2
Martin, N.G.3
-
38
-
-
84893131979
-
Lessons and implications from genome-wide association studies (GWAS) findings of blood cell phenotypes
-
Chami N., Lettre G. Lessons and implications from genome-wide association studies (GWAS) findings of blood cell phenotypes. Genes (Basel) 2014, 5:51-64.
-
(2014)
Genes (Basel)
, vol.5
, pp. 51-64
-
-
Chami, N.1
Lettre, G.2
-
39
-
-
84875813976
-
Genetic determinants of haemolysis in sickle cell anaemia
-
Milton J.N., Rooks H., Drasar E., et al. Genetic determinants of haemolysis in sickle cell anaemia. Br. J. Haematol. 2013, 161:270-278.
-
(2013)
Br. J. Haematol.
, vol.161
, pp. 270-278
-
-
Milton, J.N.1
Rooks, H.2
Drasar, E.3
-
40
-
-
84857769490
-
A genome-wide association study identifies rs2000999 as a strong genetic determinant of circulating haptoglobin levels
-
Froguel P., Ndiaye N.C., Bonnefond A., et al. A genome-wide association study identifies rs2000999 as a strong genetic determinant of circulating haptoglobin levels. PLoS One 2012, 7.
-
(2012)
PLoS One
, vol.7
-
-
Froguel, P.1
Ndiaye, N.C.2
Bonnefond, A.3
-
41
-
-
75449090777
-
Heritability of serum iron measures in the hemochromatosis and iron overload screening (HEIRS) family study
-
McLaren C.E., Barton J.C., Eckfeldt J.H., et al. Heritability of serum iron measures in the hemochromatosis and iron overload screening (HEIRS) family study. Am. J. Hematol. 2010, 85:101-105.
-
(2010)
Am. J. Hematol.
, vol.85
, pp. 101-105
-
-
McLaren, C.E.1
Barton, J.C.2
Eckfeldt, J.H.3
-
42
-
-
33748501230
-
Heritability of serum iron, ferritin and transferrin saturation in a genetically isolated population, the Erasmus Rucphen family (ERF) study
-
Njajou O.T., Alizadeh B.Z., Aulchenko Y., et al. Heritability of serum iron, ferritin and transferrin saturation in a genetically isolated population, the Erasmus Rucphen family (ERF) study. Hum. Hered. 2006, 61:222-228.
-
(2006)
Hum. Hered.
, vol.61
, pp. 222-228
-
-
Njajou, O.T.1
Alizadeh, B.Z.2
Aulchenko, Y.3
-
43
-
-
84879082514
-
Implication of the proprotein convertases in iron homeostasis: proprotein convertase 7 sheds human transferrin receptor 1 and furin activates hepcidin
-
Guillemot J., Canuel M., Essalmani R., et al. Implication of the proprotein convertases in iron homeostasis: proprotein convertase 7 sheds human transferrin receptor 1 and furin activates hepcidin. Hepatology 2013, 57:2514-2524.
-
(2013)
Hepatology
, vol.57
, pp. 2514-2524
-
-
Guillemot, J.1
Canuel, M.2
Essalmani, R.3
-
44
-
-
84896696808
-
The contribution of diet and genotype to iron status in women: a classical twin study
-
Fairweather-Tait S.J., Guile G.R., Valdes A.M., et al. The contribution of diet and genotype to iron status in women: a classical twin study. PLoS One 2013, 8.
-
(2013)
PLoS One
, vol.8
-
-
Fairweather-Tait, S.J.1
Guile, G.R.2
Valdes, A.M.3
-
46
-
-
34547850403
-
The heritability of plasma homocysteine, and the influence of genetic variation in the homocysteine methylation pathway
-
Siva A., De Lange M., Clayton D., et al. The heritability of plasma homocysteine, and the influence of genetic variation in the homocysteine methylation pathway. QJM 2007, 100:495-499.
-
(2007)
QJM
, vol.100
, pp. 495-499
-
-
Siva, A.1
De Lange, M.2
Clayton, D.3
-
47
-
-
84878263496
-
Dietary supplement use and smoking are important correlates of biomarkers of water-soluble vitamin status after adjusting for sociodemographic and lifestyle variables in a representative sample of U.S. adults
-
Pfeiffer C.M., Sternberg M.R., Schleicher R.L., et al. Dietary supplement use and smoking are important correlates of biomarkers of water-soluble vitamin status after adjusting for sociodemographic and lifestyle variables in a representative sample of U.S. adults. J. Nutr. 2013, 143:957S-965S.
-
(2013)
J. Nutr.
, vol.143
, pp. 957S-965S
-
-
Pfeiffer, C.M.1
Sternberg, M.R.2
Schleicher, R.L.3
-
49
-
-
34547913499
-
Evaluation of iron deficiency in young women in relation to oral contraceptive use
-
Casabellata G., Di Santolo M., Banfi G., et al. Evaluation of iron deficiency in young women in relation to oral contraceptive use. Contraception 2007, 76:200-207.
-
(2007)
Contraception
, vol.76
, pp. 200-207
-
-
Casabellata, G.1
Di Santolo, M.2
Banfi, G.3
-
50
-
-
78650055834
-
Prediction of venous thromboembolism in cancer patients
-
Ay C., Dunkler D., Marosi C., et al. Prediction of venous thromboembolism in cancer patients. Blood 2010, 116:5377-5382.
-
(2010)
Blood
, vol.116
, pp. 5377-5382
-
-
Ay, C.1
Dunkler, D.2
Marosi, C.3
-
51
-
-
43449115194
-
Development and validation of a predictive model for chemotherapy-associated thrombosis
-
Khorana A.A., Kuderer N.M., Culakova E., et al. Development and validation of a predictive model for chemotherapy-associated thrombosis. Blood 2008, 111:4902-4907.
-
(2008)
Blood
, vol.111
, pp. 4902-4907
-
-
Khorana, A.A.1
Kuderer, N.M.2
Culakova, E.3
|