Author: Hilary Coon

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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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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: 560
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Genome-wide association study of suicide death and polygenic prediction of clinical antecedents

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  • In genomics: 928
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Lineage: Visualizing Multivariate Clinical Data in Genealogy Graphs

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  • In bioinformatics: 1,731
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DiI-mediated analysis of pre- and postsynaptic structures in human postmortem brain tissue

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  • In neuroscience: 5,088
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Genomewide significant regions in 43 Utah high-risk families implicate multiple genes involved in risk for completed suicide

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Novel pedigree analysis implicates DNA repair and chromatin remodeling in Multiple Myeloma risk

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Dissecting the shared genetic architecture of suicide attempt, psychiatric disorders and known risk factors

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  • In genetic and genomic medicine: 183
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Rare protein coding variants implicate genes involved in risk of suicide death

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