Author: Francesco Lescai

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Preprints

Exome sequencing identifies rare coding variants in 10 genes which confer substantial risk for schizophrenia

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Quantifying the impact of rare and ultra-rare coding variation across the phenotypic spectrum

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  • In genetics: 253
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ASD and ADHD have a similar burden of rare protein-truncating variants

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  • In genetics: 438
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Estimating the functional impact of INDELs in transcription factor binding sites: a genome-wide landscape

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  • In bioinformatics: 4,890
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Meta-analysis of Scandinavian Schizophrenia Exomes

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  • In genetics: 2,765
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