Contribution of rare genetic variants to heart failure and cardiomyopathy in the UK Biobank by Bengt Zöller, Eric Manderstedt, Christina Lind‐Halldén, Christer Halldén

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Bioinformatic and rare‐variant collapsing analyses for type 1 and type 2 diabetes in the UK Biobank reveal novel pleiotropic susceptibility loci by Bengt Zöller, Eric Manderstedt, Christina Lind‐Halldén, Christer Halldén

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Genetic Variation in the von Willebrand Factor Gene in Swedish von Willebrand Disease Patients by Eric Manderstedt, Christina Lind-Halldén, Stefan Lethagen, Christer Halldén

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Common and Rare Variants in Genes Associated with von Willebrand Factor Level Variation: No Accumulation of Rare Variants in Swedish von Willebrand Disease Patients by Eric Manderstedt, Christina Lind-Halldén, Stefan Lethagen, Christer Halldén

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Genetic variation in the C-type lectin receptor CLEC4M in type 1 von Willebrand Disease patients. by Eric Manderstedt, Christina Lind-Halldén, Stefan Lethagen, Christer Halldén

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Contribution of rare and common coding variants to haematological malignancies in the UK biobank by Bengt Zöller, Eric Manderstedt, Christina Lind-Halldén, Christer Halldén

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Detection of mosaics in hemophilia A by deep Ion Torrent sequencing and droplet digital PCR by Eric Manderstedt, Rosanna Nilsson, Rolf Ljung, Christina Lind‐Halldén, Jan Astermark, Christer Halldén

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Targeted re-sequencing of F8, F9 and VWF: Characterization of Ion Torrent data and clinical implications for mutation screening. by Eric Manderstedt, Rosanna Nilsson, Christina Lind-Halldén, Rolf Ljung, Jan Astermark, Christer Halldén

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Tissue factor (F3) gene variants and thrombotic risk among middle-aged and older adults: A population-based cohort study by Eric Manderstedt, Christina Lind-Halldén, Christer Halldén, Johan Elf, Peter J. Svensson, Gunnar Engström, Olle Melander, Aris Baras, Luca A. Lotta, Bengt Zöller

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Classic Thrombophilias and Thrombotic Risk Among Middle‐Aged and Older Adults: A Population‐Based Cohort Study by Eric Manderstedt, Christina Lind‐Halldén, Christer Halldén, Johan Elf, Peter J. Svensson, Björn Dahlbäck, Gunnar Engström, Olle Melander, Aris Baras, Luca A. Lotta, Bengt Zöller

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Genetic variation of the blood coagulation regulator tissue factor pathway inhibitor and venous thromboembolism among middle‐aged and older adults: A population‐based cohort study... by Eric Manderstedt, Christina Lind‐Halldén, Christer Halldén, Johan Elf, Peter J. Svensson, Gunnar Engström, Olle Melander, Aris Baras, Luca A. Lotta, Bengt Zöller, for the Regeneron Genetics Center

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