Bengt Zöller
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- 2023
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Mark
Rare-variant collapsing analyses of arterial hypertension in the UK biobank
- Contribution to journal › Letter
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Mark
Multimorbidity can run in families - What are implications for clinical practice?
- Contribution to journal › Debate/Note/Editorial
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Mark
Rare-variant collapsing analyses reveal novel risk genes for arterial and venous cardiovascular diseases in the UK biobank
- Contribution to journal › Letter
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Mark
Contribution of rare genetic variants to heart failure and cardiomyopathy in the UK Biobank
- Contribution to journal › Letter
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Mark
The role of fibrinolysis in vascular diseases in UK biobank
- Contribution to journal › Letter
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Mark
Familial risk of vasospastic angina : a nationwide family study in Sweden
- Contribution to journal › Article
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Mark
Familial aggregation of multimorbidity in Sweden: national explorative family study
- Contribution to journal › Article
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Mark
“C1-inhibitor levels and Venous Thromboembolism : Results from a Mendelian Randomization Study”: comment from Grover et al
- Contribution to journal › Letter
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Mark
A hypothesis - generating Swedish extended national cross-sectional family study of multimorbidity severity and venous thromboembolism
- Contribution to journal › Article
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Mark
Rare-variant collapsing and bioinformatic analyses for amyloidosis, dementia and Parkinson’s disease in the UK biobank reveal novel susceptibility loci
- Contribution to journal › Letter
