Publications
6 shownDemographic history and rare allele sharing among human populations
High-throughput sequencing technology enables population-level surveys of human genomic variation. Here, we examine the joint allele frequency distributions across continental h...
Integrating common and rare genetic variation in diverse human populations
Despite great progress in identifying genetic variants that influence human disease, most inherited risk remains unexplained. A more complete understanding requires genome-wide ...
Common variants at VRK2 and TCF4 conferring risk of schizophrenia
Common sequence variants have recently joined rare structural polymorphisms as genetic factors with strong evidence for association with schizophrenia. Here we extend our previo...
Frequent Co-Authors
Researcher Info
- h-index
- 6
- Publications
- 8
- Citations
- 13,467
- Institution
- Institute for Molecular Medicine Finland
External Links
Impact Metrics
h-index
6
h-index: Number of publications with at least h citations each.