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

Zöller, Bengt LU orcid ; Manderstedt, Eric LU ; Lind-Halldén, Christina LU and Halldén, Christer LU (2023) In Thrombosis Research 229. p.86-89
Please use this url to cite or link to this publication:
author
; ; and
organization
publishing date
type
Contribution to journal
publication status
published
subject
keywords
Cardiovascular diseases, Genetics, Mutation, Whole exome sequencing
in
Thrombosis Research
volume
229
pages
4 pages
publisher
Elsevier
external identifiers
  • pmid:37421682
  • scopus:85164399915
ISSN
0049-3848
DOI
10.1016/j.thromres.2023.06.030
language
English
LU publication?
yes
id
d3a3ba45-22c8-409c-aacb-6ef19d7db32f
date added to LUP
2023-09-04 10:56:14
date last changed
2024-04-20 02:29:02
@article{d3a3ba45-22c8-409c-aacb-6ef19d7db32f,
  author       = {{Zöller, Bengt and Manderstedt, Eric and Lind-Halldén, Christina and Halldén, Christer}},
  issn         = {{0049-3848}},
  keywords     = {{Cardiovascular diseases; Genetics; Mutation; Whole exome sequencing}},
  language     = {{eng}},
  pages        = {{86--89}},
  publisher    = {{Elsevier}},
  series       = {{Thrombosis Research}},
  title        = {{Rare-variant collapsing analyses reveal novel risk genes for arterial and venous cardiovascular diseases in the UK biobank}},
  url          = {{http://dx.doi.org/10.1016/j.thromres.2023.06.030}},
  doi          = {{10.1016/j.thromres.2023.06.030}},
  volume       = {{229}},
  year         = {{2023}},
}