Aarno Palotie - Researcher Profile | RDL Research Database

Publications

7 shown

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

Monkol Lek , Konrad J. Karczewski , Eric Vallabh Minikel +76 more

2016 Nature 10077 citations

De novo mutations in schizophrenia implicate synaptic networks

Menachem Fromer , Andrew Pocklington , David H. Kavanagh +29 more

2014 Nature 1666 citations

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

Kaitlin E. Samocha , Elise Robinson , Stephan Sanders +23 more

2014 Nature Genetics 1091 citations

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

Tarjinder Singh , James Walters , Mandy Johnstone +20 more

2017 Nature Genetics 242 citations

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

Andrea Ganna , F. Kyle Satterstrom , Seyedeh M. Zekavat +41 more

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...

2018 Helda (University of Helsinki) 119 citations

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

Andrea Ganna , Giulio Genovese , Daniel P. Howrigan +29 more

2016 Nature Neuroscience 110 citations

A reference panel of 64,976 haplotypes for genotype imputation

Shane McCarthy , Sayantan Das , Warren W. Kretzschmar +97 more

2016 Nature Genetics 3126 citations

Frequent Co-Authors

Researcher Info

h-index: 7
Publications: 7
Citations: 16,431
Institution: Harvard University

External Links

ORCID Profile Google Scholar

Identifiers

ORCID: 0000-0002-2527-5874

Impact Metrics

h-index 7

h-index: Number of publications with at least h citations each.