Identification of the same factor V gene mutation in 47 out of 50 thrombosis-prone families with inherited resistance to activated protein C. B Zöller, PJ Svensson, X He, B Dahlbäck The Journal of clinical investigation 94 (6), 2521-2524, 1994 | 601 | 1994 |
Linkage between inherited resistance to activated protein C and factor V gene mutation in venous thrombosis B Zöller, B Dahlbäck The Lancet 343 (8912), 1536-1538, 1994 | 553 | 1994 |
Resistance to activated protein C as an additional genetic risk factor in hereditary deficiency of protein S B Zoller, A Berntsdotter, PG de Frutos, B Dahlbäck Blood 85 (12), 3518-3523, 1995 | 444 | 1995 |
Risk of pulmonary embolism in patients with autoimmune disorders: a nationwide follow-up study from Sweden B Zöller, X Li, J Sundquist, K Sundquist The Lancet 379 (9812), 244-249, 2012 | 408 | 2012 |
The 20210 A allele of the prothrombin gene is a common risk factor among Swedish outpatients with verified deep venous thrombosis A Hillarp, B Zӧller, PJ Svensson, B Dahlbäck Thrombosis and Haemostasis 78 (09), 0990-0992, 1997 | 335 | 1997 |
Thrombophilia as a multigenic disease B Zoller, PG de Frutos, A Hillarp, B Dahlback Haematologica 84 (1), 59-70, 1999 | 318 | 1999 |
Epidemiology of valvular heart disease in a Swedish nationwide hospital-based register study P Andell, X Li, A Martinsson, C Andersson, M Stagmo, B Zöller, ... Heart 103 (21), 1696-1703, 2017 | 298 | 2017 |
Cardiovascular risk factors associated with venous thromboembolism J Gregson, S Kaptoge, T Bolton, L Pennells, P Willeit, S Burgess, S Bell, ... JAMA cardiology 4 (2), 163-173, 2019 | 261 | 2019 |
Evaluation of the relationship between protein S and C4b-binding protein isoforms in hereditary protein S deficiency demonstrating type I and type III deficiencies to be … B Zoller, P Garcia de Frutos, B Dahlback | 226 | 1995 |
Risk of subsequent ischemic and hemorrhagic stroke in patients hospitalized for immune-mediated diseases: a nationwide follow-up study from Sweden B Zöller, X Li, J Sundquist, K Sundquist BMC neurology 12, 1-9, 2012 | 207 | 2012 |
Autoimmune diseases and venous thromboembolism: a review of the literature B Zöller, X Li, J Sundquist, K Sundquist American journal of cardiovascular disease 2 (3), 171, 2012 | 204 | 2012 |
Risk of haemorrhagic and ischaemic stroke in patients with cancer: a nationwide follow-up study from Sweden B Zöller, J Ji, J Sundquist, K Sundquist European journal of cancer 48 (12), 1875-1883, 2012 | 202 | 2012 |
Differential regulation of alpha and beta chains of C4b-binding protein during acute-phase response resulting in stable plasma levels of free anticoagulant protein S P Garcia de Frutos, RI Alim, Y Hardig, B Zoller, B Dahlback | 192 | 1994 |
Risk of subsequent coronary heart disease in patients hospitalized for immune-mediated diseases: a nationwide follow-up study from Sweden B Zöller, X Li, J Sundquist, K Sundquist PloS one 7 (3), e33442, 2012 | 171 | 2012 |
Increased risks of coronary heart disease and stroke among spousal caregivers of cancer patients J Ji, B Zöller, K Sundquist, J Sundquist Circulation 125 (14), 1742-1747, 2012 | 161 | 2012 |
Risk of coronary heart disease in patients with cancer: a nationwide follow-up study from Sweden B Zöller, J Ji, J Sundquist, K Sundquist European journal of cancer 48 (1), 121-128, 2012 | 160 | 2012 |
Determination of 14 circulating microRNAs in Swedes and Iraqis with and without diabetes mellitus type 2 X Wang, J Sundquist, B Zöller, AA Memon, K Palmér, K Sundquist, ... PloS one 9 (1), e86792, 2014 | 157 | 2014 |
Age-and gender-specific familial risks for venous thromboembolism: a nationwide epidemiological study based on hospitalizations in Sweden B Zöller, X Li, J Sundquist, K Sundquist Circulation 124 (9), 1012-1020, 2011 | 154 | 2011 |
A common thrombomodulin amino acid dimorphism is associated with myocardial infarction L Norlund, J Holm, B Zöller, AK Öhlin Thrombosis and haemostasis 77 (02), 248-251, 1997 | 143 | 1997 |
Clarification of the risk for venous thrombosis associated with hereditary protein S deficiency by investigation of a large kindred with a characterized gene defect RE Simmonds, H Ireland, DA Lane, B Zoller, PG de Frutos, B Dahlback Annals of internal medicine 128 (1), 8-14, 1998 | 132 | 1998 |