Aarno Palotie

Analysis of protein-coding genetic variation in 60,706 humans

De novo mutations in schizophrenia implicate synaptic networks

A framework for the interpretation of de novo mutation in human disease

The contribution of rare variants to risk of schizophrenia in individuals with and without intellectual disability

Quantifying the Impact of Rare and Ultra-rare Coding Variation across the Phenotypic Spectrum

There is a limited understanding about the impact of rare protein-truncating variants across multiple phenotypes. We explore the impact of this class of variants on 13 quantitat...

Ultra-rare disruptive and damaging mutations influence educational attainment in the general population

A reference panel of 64,976 haplotypes for genotype imputation

The functional spectrum of low-frequency coding variation

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 on 8p12 and 1q24.2 confer risk of schizophrenia