Rare-variant collapsing analyses reveal novel risk genes for arterial and venous cardiovascular diseases in the UK biobank

Thromb Res. 2023 Sep:229:86-89. doi: 10.1016/j.thromres.2023.06.030. Epub 2023 Jul 4.

Authors

Bengt Zöller¹, Eric Manderstedt², Christina Lind-Halldén³, Christer Halldén²

Affiliations

¹ Center for Primary Health Care Research, Department of Clinical Sciences, Lund University and Region Skåne, Malmö, Sweden. Electronic address: [email protected].
² Center for Primary Health Care Research, Department of Clinical Sciences, Lund University and Region Skåne, Malmö, Sweden.
³ Department of Environmental Science and Bioscience, Kristianstad University, Kristianstad, Sweden.

PMID: 37421682
DOI: 10.1016/j.thromres.2023.06.030

No abstract available

Keywords: Cardiovascular diseases; Genetics; Mutation; Whole exome sequencing.

Publication types

Letter

MeSH terms

Arteries
Biological Specimen Banks
Cardiovascular Diseases* / genetics
Genetic Predisposition to Disease
Genetic Variation
Humans
United Kingdom / epidemiology