1 – 5 of 5
- show: 20
- |
- sort: year (new to old)
Close
Embed this list
<iframe src=" "
width=" "
height=" "
allowtransparency="true"
frameborder="0">
</iframe>
- 2020
-
Mark
The effect of LRRK2 loss-of-function variants in humans
(
- Contribution to journal › Article
-
Mark
Characterising the loss-of-function impact of 5’ untranslated region variants in 15,708 individuals
(
- Contribution to journal › Article
-
Mark
Enhancing rare variant interpretation in inherited arrhythmias through quantitative analysis of consortium disease cohorts and population controls
2020) In Genetics in Medicine(
- Contribution to journal › Article
- 2015
-
Mark
Recurrent Coding Sequence Variation Explains Only A Small Fraction of the Genetic Architecture of Colorectal Cancer.
(
- Contribution to journal › Article
-
Mark
Cardiometabolic effects of genetic upregulation of the interleukin 1 receptor antagonist: a Mendelian randomisation analysis
(
- Contribution to journal › Article