QIMR Berghofer Medical Research Institute

Mutations of the BRAF gene in human cancer

GCTA: A Tool for Genome-wide Complex Trait Analysis

Finding the missing heritability of complex diseases

Common polygenic variation contributes to risk of schizophrenia and bipolar disorder

Host–microbe interactions have shaped the genetic architecture of inflammatory bowel disease

Common SNPs explain a large proportion of the heritability for human height

Association of missense and 5′-splice-site mutations in tau with the inherited dementia FTDP-17

Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index

Obesity is globally prevalent and highly heritable, but its underlying genetic factors remain largely elusive. To identify genetic loci for obesity susceptibility, we examined a...

Five Years of GWAS Discovery

The past five years have seen many scientific and biological discoveries made through the experimental design of genome-wide association studies (GWASs). These studies were aime...

Defining the role of common variation in the genomic and biological architecture of adult human height