Rare-variant collapsing analyses reveal novel risk genes for arterial and venous cardiovascular diseases in the UK biobank
Zöller, Bengt LU
; 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:
https://lup.lub.lu.se/record/d3a3ba45-22c8-409c-aacb-6ef19d7db32f
- author
- Zöller, Bengt
LU
; Manderstedt, Eric
LU
; Lind-Halldén, Christina
LU
and Halldén, Christer
LU
- organization
- publishing date
- 2023
- 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
-
- scopus:85164399915
- pmid:37421682
- 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
- 2025-11-17 07:00:01
@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}},
}