Christer Halldén (Former)
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- 2023
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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
- 2022
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Mark
Classic Thrombophilias and Thrombotic Risk Among Middle-Aged and Older Adults : A Population-Based Cohort Study
(
- Contribution to journal › Article
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Mark
Thrombotic Risk Determined by Protein C Receptor (PROCR) Variants among Middle-Aged and Older Adults : A Population-Based Cohort Study
(
- Contribution to journal › Article
- 2021
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Mark
Droplet digital PCR and mile-post analysis for the detection of F8 int1h inversions
(
- Contribution to journal › Article
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Mark
Thrombotic Risk Determined by STAB 2 Variants in a Population-Based Cohort Study
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- Contribution to journal › Letter
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Mark
Identification of F8 rearrangements in carrier and non-carrier mothers of haemophilia A patients
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- Contribution to journal › Letter
- 2020
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Mark
Detection of F8 int22h inversions using digital droplet PCR and mile-post assays
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- Contribution to journal › Article
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Mark
Detection of mosaics in hemophilia A by deep Ion Torrent sequencing and droplet digital PCR
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- Contribution to journal › Article
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Mark
Genetic risk factors for venous thromboembolism
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- Contribution to journal › Scientific review
- 2019
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Mark
Targeted re-sequencing of F8, F9 and VWF : Characterization of Ion Torrent data and clinical implications for mutation screening
(
- Contribution to journal › Article
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Mark
Next-Generation Sequencing of 17 Genes Associated with Venous Thromboembolism Reveals a Deficit of Non-Synonymous Variants in Procoagulant Genes
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- Contribution to journal › Article
- 2018
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Mark
Genetic Variation in the Syntaxin-Binding Protein STXBP5 in Type 1 von Willebrand Disease Patients
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- Contribution to journal › Article
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Mark
Genetic variation in the C-type lectin receptor CLEC4M in type 1 von Willebrand Disease patients
(
- Contribution to journal › Article
- 2017
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Mark
Genetic variation of the Toll-like receptors in a Swedish allergic rhinitis case population
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- Contribution to journal › Article
- 2016
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Mark
Origin of mutation in sporadic cases of severe haemophilia A in Sweden.
(
- Contribution to journal › Article
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Mark
Chronic rhinosinusitis patients show accumulation of genetic variants in PARS2
(
- Contribution to journal › Article
- 2014
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Mark
Genetic Variation in KLK2 and KLK3 Is Associated with Concentrations of hK2 and PSA in Serum and Seminal Plasma in Young Men
(
- Contribution to journal › Article
- 2013
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Mark
Copy number variants in the kallikrein gene cluster.
(
- Contribution to journal › Article
- 2012
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Mark
Evaluation of Multiple Risk-Associated Single Nucleotide Polymorphisms Versus Prostate-Specific Antigen at Baseline to Predict Prostate Cancer in Unscreened Men
(
- Contribution to journal › Article
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Mark
Toll-like receptor gene polymorphisms are associated with allergic rhinitis: a case control study
(
- Contribution to journal › Article