Showing 1 - 11 results of 11 for search 'Christina Lind-Halldén', query time: 0.03s Refine Results
  1. 1
    Contribution of rare genetic variants to heart failure and cardiomyopathy in the UK Biobank

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

    Published 2023-10-01
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  2. 2
    Bioinformatic and rare‐variant collapsing analyses for type 1 and type 2 diabetes in the UK Biobank reveal novel pleiotropic susceptibility loci

    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

    Published 2023-09-01
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  3. 3
    Genetic Variation in the von Willebrand Factor Gene in Swedish von Willebrand Disease Patients

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

    Published 2018-01-01
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  4. 4
    Common and Rare Variants in Genes Associated with von Willebrand Factor Level Variation: No Accumulation of Rare Variants in Swedish von Willebrand Disease Patients

    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

    Published 2020-10-01
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  5. 5
    Genetic variation in the C-type lectin receptor CLEC4M in type 1 von Willebrand Disease patients.

    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

    Published 2018-01-01
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  6. 6
    Contribution of rare and common coding variants to haematological malignancies in the UK biobank

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

    Published 2023-01-01
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  7. 7
    Detection of mosaics in hemophilia A by deep Ion Torrent sequencing and droplet digital PCR

    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

    Published 2020-10-01
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  8. 8
    Targeted re-sequencing of F8, F9 and VWF: Characterization of Ion Torrent data and clinical implications for mutation screening.

    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

    Published 2019-01-01
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  9. 9
    Chronic Rhinosinusitis Patients Show Accumulation of Genetic Variants in PARS2.

    Chronic Rhinosinusitis Patients Show Accumulation of Genetic Variants in PARS2. by Viktor Henmyr, Christina Lind-Halldén, Christer Halldén, Torbjörn Säll, Daniel Carlberg, Claus Bachert, Lars-Olaf Cardell

    Published 2016-01-01
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  10. 10
    Classic Thrombophilias and Thrombotic Risk Among Middle‐Aged and Older Adults: A Population‐Based Cohort Study

    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

    Published 2022-02-01
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  11. 11
    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

    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

    Published 2022-10-01
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