Dr. Hilary Coon
Dr. Hilary Coon’s Select Publications
Bilder, D.A. et al. Early Second Trimester Maternal Serum Steroid-Related Biomarkers Associated with Autism Spectrum Disorder. J Autism Dev Disord 49, 4572-4583 (2019). doi:10.1007/s10803-019-04162-2
Das, S.C. et al. DiI-mediated analysis of presynaptic and postsynaptic structures in human postmortem brain tissue. J Comp Neurol 527, 3087-3098 (2019). doi:10.1002/cne.24722
Kirby, A.V. et al. A 20-year study of suicide death in a statewide autism population. Autism Res 12, 658-666 (2019). doi:10.1002/aur.2076
Nobre, C., Gehlenborg, N., Coon, H. & Lex, A. Lineage: Visualizing Multivariate Clinical Data in Genealogy Graphs. IEEE Trans Vis Comput Graph 25, 1543-1558 (2019). doi:10.1109/tvcg.2018.2811488
Shade, J., Coon, H. & Docherty, A.R. Ethical implications of using biobanks and population databases for genetic suicide research. Am J Med Genet B Neuropsychiatr Genet 180, 601-608 (2019). doi:10.1002/ajmg.b.32718
An, J.Y. et al. Genome-wide de novo risk score implicates promoter variation in autism spectrum disorder. Science 362(2018). doi:10.1126/science.aat6576
Coon, H. et al. Genome-wide significant regions in 43 Utah high-risk families implicate multiple genes involved in risk for completed suicide. Mol Psychiatry (2018). doi:10.1038/s41380-018-0282-3
Farley, M. et al. Mid-life social outcomes for a population-based sample of adults with ASD. Autism Res 11, 142-152 (2018). doi:10.1002/aur.1897
Keeshin, B.R., Gray, D., Zhang, C., Presson, A.P. & Coon, H. Youth Suicide Deaths: Investigation of Clinical Predictors in a Statewide Sample. Suicide Life Threat Behav 48, 601-612 (2018). doi:10.1111/sltb.12386
Lin, C.Y. et al. Allele-specific expression in a family quartet with autism reveals mono-to-biallelic switch and novel transcriptional processes of autism susceptibility genes. Sci Rep 8, 4277 (2018). doi:10.1038/s41598-018-22753-4
Waller, R.G. et al. Novel pedigree analysis implicates DNA repair and chromatin remodeling in multiple myeloma risk. PLoS Genet 14, e1007111 (2018). doi:10.1371/journal.pgen.1007111
Autism Spectrum Disorders Working Group of The Psychiatric Genomics Consortium. Meta-analysis of GWAS of over 16,000 individuals with autism spectrum disorder highlights a novel locus at 10q24.32 and a significant overlap with schizophrenia. Mol Autism 8, 21 (2017). doi:10.1186/s13229-017-0137-9
Christensen, E.D. et al. Sudden infant death “syndrome”-Insights and future directions from a Utah population database analysis. Am J Med Genet A 173, 177-182 (2017). doi:10.1002/ajmg.a.37994
Figueroa, K.P. et al. Genetic analysis of age at onset variation in spinocerebellar ataxia type 2. Neurol Genet 3, e155 (2017). doi:10.1212/nxg.0000000000000155
Lim, E.T. et al. Rates, distribution and implications of postzygotic mosaic mutations in autism spectrum disorder. Nat Neurosci 20, 1217-1224 (2017). doi:10.1038/nn.4598
Weiner, D.J. et al. Polygenic transmission disequilibrium confirms that common and rare variation act additively to create risk for autism spectrum disorders. Nat Genet 49, 978-985 (2017). doi:10.1038/ng.3863