Eric Manderstedt

Publication Activity (10 Years)

Years Active: 2018-2023
Publications (10 Years): 6

Top Topics

Prognostic Factors

Venous Thromboembolism

Top Venues

Journal of thrombosis and haemostasis : JTH

Journal of human hypertension

Research and practice in thrombosis and haemostasis

This page only lists publications with an associated author ORCID identifier.

Publications

Bengt Zöller, Eric Manderstedt, Christina Lind-Halldén, Christer Halldén
Rare-variant collapsing analyses of arterial hypertension in the UK biobank. Journal of human hypertension (2023)
Eric Manderstedt, Christer Halldén, Christina Lind-Halldén, Johan Elf, Peter J Svensson, Gunnar Engström, Olle Melander, Aris Baras, Luca A Lotta, Bengt Zöller, null null
Thrombotic risk determined by rare and common SERPINA1 variants in a population-based cohort study. Journal of thrombosis and haemostasis : JTH 20 (6) (2022)
Eric Manderstedt, Christer Halldén, Christina Lind-Halldén, Johan Elf, Peter J Svensson, Gunnar Engström, Olle Melander, Aris Baras, Luca A Lotta, Bengt Zöller, null null
Thrombomodulin (THBD) gene variants and thrombotic risk in a population-based cohort study. Journal of thrombosis and haemostasis : JTH 20 (4) (2022)
Eric Manderstedt, Christina Lind-Halldén, Christer Halldén, Johan Elf, Peter J Svensson, Gunnar Engström, Olle Melander, Aris Baras, Luca A Lotta, Bengt Zöller, null null
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. Research and practice in thrombosis and haemostasis 6 (7) (2022)
Eric Manderstedt, Christina Lind-Halldén, Rolf C R Ljung, Jan Astermark, Christer Halldén
Identification of F8 rearrangements in carrier and non-carrier mothers of haemophilia A patients. Haemophilia : the official journal of the World Federation of Hemophilia 27 (5) (2021)
Eric Manderstedt, Christina Lind-Halldén, Stefan Lethagen, Christer Halldén
Genetic variation in the C-type lectin receptor CLEC4M in type 1 von Willebrand Disease patients. PloS one 13 (2) (2018)