selected publications
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academic article
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Analysis of shared heritability in common disorders of the brain.
Science.
360.
2018
Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection.
Nature Genetics.
50.
2018
Genetic risk for schizophrenia and autism, social impairment and developmental pathways to psychosis.
Translational Psychiatry.
8.
2018
Improving genetic prediction by leveraging genetic correlations among human diseases and traits.
Nature Communications.
9.
2018
Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects.
Nature Genetics.
49.
2017
Genome-wide association study of borderline personality disorder reveals genetic overlap with bipolar disorder, major depression and schizophrenia.
Translational Psychiatry.
7.
2017
No Reliable Association between Runs of Homozygosity and Schizophrenia in a Well-Powered Replication Study.
PLOS Genetics.
12.
2016
Modeling Linkage Disequilibrium Increases Accuracy of Polygenic Risk Scores.
American Journal of Human Genetics.
97.
2015
Partitioning heritability by functional annotation using genome-wide association summary statistics.
Nature Genetics.
47.
2015
Partitioning Heritability of Regulatory and Cell-Type-Specific Variants across 11 Common Diseases.
American Journal of Human Genetics.
95.
2014
Whole-Exome Sequencing Identifies Rare and Low-Frequency Coding Variants Associated with LDL Cholesterol.
American Journal of Human Genetics.
94.
2014
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dataset
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Descriptive data for the unimputed (post-QC) PGC replication data—ROHs defined as ≥ 110 consecutive homozygous SNPs or as ≥ 2.3 Mb long..
public-library-of-science.
2016
No Reliable Association between Runs of Homozygosity and Schizophrenia in a Well-Powered Replication Study.
public-library-of-science.
2016
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preprint
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Gene expression imputation across multiple brain regions reveals schizophrenia risk throughout development.
bioRxiv.
2017
Genome-wide association study identifies 30 Loci Associated with Bipolar Disorder.
bioRxiv.
2017
Genome-wide association study implicates CHRNA2 in cannabis use disorder.
bioRxiv.
2017
A contribution of novel CNVs to schizophrenia from a genome-wide study of 41,321 subjects: CNV Analysis Group and the Schizophrenia Working Group of the Psychiatric Genomics Consortium.
bioRxiv.
2016
Subtle stratification confounds estimates of heritability from rare variants.
bioRxiv.
2016
Haplotypes of common SNPs can explain missing heritability of complex diseases.
bioRxiv.
2015