Author: Lambertus Klei

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Preprints

Large-scale exome sequencing study implicates both developmental and functional changes in the neurobiology of autism

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Common risk variants identified in autism spectrum disorder

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  • In genetics: 28
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Limited contribution of rare, noncoding variation to autism spectrum disorder from sequencing of 2,076 genomes in quartet families

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  • In genomics: 703
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Rare coding variation illuminates the allelic architecture, risk genes, cellular expression patterns, and phenotypic context of autism

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  • In neurology: 52
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Whole-genome and RNA sequencing reveal variation and transcriptomic coordination in the developing human prefrontal cortex

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  • In neuroscience: 1,669
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Semi-soft Clustering of Single Cell Data

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Genome-wide association study identifies new locus associated with OCD

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  • In psychiatry and clinical psychology: 263
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Functional connectome fingerprinting accuracy in youths and adults is similar when examined on the same day and 1.5 years apart

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  • In neuroscience: 8,897
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Genome-Wide Association Identifies the First Risk Loci for Psychosis in Alzheimer Disease

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How rare and common risk variation jointly affect liability for autism spectrum disorder

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The genetic architecture of obsessive-compulsive disorder: alleles across the frequency spectrum contribute liability to OCD

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Transcriptome alterations are enriched for synapse-associated genes in the striatum of subjects with obsessive-compulsive disorder

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  • In neuroscience: 18,420
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Genetic maternal effects contributes to the risk of Tourette's disorder

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