1 – 10 of 46
- show: 10
- |
- sort: year (new to old)
Close
Embed this list
<iframe src=""
width=""
height=""
allowtransparency="true"
frameborder="0">
</iframe>
- 2023
-
Mark
Genetics of circulating inflammatory proteins identifies drivers of immune-mediated disease risk and therapeutic targets
- Contribution to journal › Article
- 2022
-
Mark
Comprehensive genome-wide association study of different forms of hernia identifies more than 80 associated loci
- Contribution to journal › Article
- 2021
-
Mark
Genetic regulation of spermine oxidase activity and cancer risk : a Mendelian randomization study
- Contribution to journal › Article
-
Mark
The genomics of heart failure : design and rationale of the HERMES consortium
- Contribution to journal › Article
-
Mark
Mendelian randomisation identifies alternative splicing of the FAS death receptor as a mediator of severe COVID-19
(2021)
- Working paper/Preprint › Preprint in preprint archive
- 2020
-
Mark
Genetic and In Vitro Inhibition of PCSK9 and Calcific Aortic Valve Stenosis
- Contribution to journal › Article
- 2019
-
Mark
Roadmap for a precision-medicine initiative in the Nordic region
(2019) In Nature Genetics
- Contribution to journal › Debate/Note/Editorial
- 2018
-
Mark
Haplotype Sharing Provides Insights into Fine-Scale Population History and Disease in Finland
- Contribution to journal › Article
- 2017
-
Mark
Rare and low-frequency coding variants alter human adult height
- Contribution to journal › Article
-
Mark
Systematic Evaluation of Pleiotropy Identifies 6 Further Loci Associated With Coronary Artery Disease
- Contribution to journal › Article