Surveying the contribution of rare variants to the genetic architecture of human disease through exome sequencing of 177,882 UK Biobank participants
Authors
Quanli Wang,
Ryan DhindsaKeren Carss,
Andrew Harper,
Abhishek Nag,
Ioanna Tachmazidou,
Dimitrios Vitsios,
Sri Deevi,
Alex Mackay,
Daniel Muthas,
Michael Hühn,
Susan Monkley,
Henric Olsson,
Sebastian Wasilewski,
Katherine Smith,
Ruth March,
Adam Platt,
Carolina Haefliger,
Steve Petrovski,
AstraZeneca Initiative +18 authors
,
Slavé Petrovski Tip Tip