Author details

Full Name

Hilary Coon

Affiliation

ORCID

Career Start Year

1989

Papers

199

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
36800380	Whole-genome sequencing analysis in families with recurrent pregnancy loss: A pilot study.	PLoS One	2023
36161750	Familial aggregation of stillbirth: A pedigree analysis of a matched case-control study.	BJOG	2023
36253440	Genome-wide association study meta-analysis of suicide death and suicidal behavior.	Molecular Psychiatry	2023
37794117	Whole-genome sequencing analysis of suicide deaths integrating brain-regulatory eQTLs data to identify risk loci and genes.	Mol Psychiatry	2023
37777856	GWAS Meta-Analysis of Suicide Attempt: Identification of 12 Genome-Wide Significant Loci and Implication of Genetic Risks for Specific Health Factors.	Am J Psychiatry	2023
37032361	Neurite outgrowth deficits caused by rare PLXNB1 mutation in pediatric bipolar disorder.	Mol Psychiatry	2023
36778310	Altered transcriptomes, cell type proportions, and dendritic spine morphology in hippocampus of suicide deaths.		2023
36892557	Understanding heterogeneity in suicidal thoughts and behaviours and the implications for genetic studies - a commentary on Lannoy etÂ al. (2022).	J Child Psychol Psychiatry	2023
37010215	A population-wide analysis of the familial risk of suicide in Utah, USA.		2023
36940203	Genome-wide association study identifies four pan-ancestry loci for suicidal ideation in the Million Veteran Program.	PLoS Genet	2023
36804111	Phenotypic predictors of suicide subtypes from pre-to postdeployment in active duty military personnel.		2023
35347246	A genome-wide association study of suicide attempts in the million veterans program identifies evidence of pan-ancestry and ancestry-specific risk loci.	Mol Psychiatry	2022
35975759	Genetics and epigenetics of self-injurious thoughts and behaviors: Systematic review of the suicide literature and methodological considerations.	Am J Med Genet B Neuropsychiatr Genet	2022
34559220	Suicide and Psychosis: Results From a Population-Based Cohort of Suicide Death (N = 4380).	Schizophr Bull	2022
35212135	Extended familial risk of suicide death is associated with younger age at death and elevated polygenic risk of suicide.	Am J Med Genet B Neuropsychiatr Genet	2022
34472199	Ethical concerns relating to genetic risk scores for suicide.	Am J Med Genet B Neuropsychiatr Genet	2021
34234108	Assessment of suicide attempt and death in bipolar affective disorder: a combined clinical and genetic approach.	Transl Psychiatry	2021
33748530	Identifying suicidal subtypes and dynamic indicators of increasing and decreasing suicide risk in active duty military personnel: Study protocol.	Contemporary Clinical Trials Communications	2021
34168285	Neurexin 1 variants as risk factors for suicide death.	Molecular Psychiatry	2021
34042246	Rare protein-coding variants implicate genes involved in risk of suicide death.	Am J Med Genet B Neuropsychiatr Genet	2021
33513338	Mutation-specific pathophysiological mechanisms define different neurodevelopmental disorders associated with SATB1 dysfunction.	Am J Hum Genet	2021
33353974	Correction: Ethical and public health implications of genetic testing for suicide risk: family and survivor perspectives.	Genet Med	2021
33020592	Ethical and public health implications of genetic testing for suicide risk: family and survivor perspectives.	Genet Med	2021
34914455	Musical instrument engagement in adolescence predicts verbal ability 4 years later: A twin and adoption study.	Developmental Psychology	2021
34821019	Exploring the genetic overlap of suicide-related behaviors and substance use disorders.	American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics	2021
30353169	Genome-wide significant regions in 43 Utah high-risk families implicate multiple genes involved in risk for completed suicide.	Molecular Psychiatry	2020
32096122	Brief Report: Genetic Links Between Autism and Suicidal Behavior-A Preliminary Investigation.	Journal of Autism and Developmental Disorders	2020
32572023	The role of rare compound heterozygous events in autism spectrum disorder.	Transl Psychiatry	2020
30663277	A 20-year study of suicide death in a statewide autism population.	Autism Research	2019
29993603	Lineage: Visualizing Multivariate Clinical Data in Genealogy Graphs.	IEEE Trans Vis Comput Graph	2019
31482371	Correction to: Early Second Trimester Maternal Serum Steroidâ¿¿Related Biomarkers Associated with Autism Spectrum Disorder.	Journal of Autism and Developmental Disorders	2019
30779308	Ethical implications of using biobanks and population databases for genetic suicide research.	American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics	2019
31152449	DiI-mediated analysis of presynaptic and postsynaptic structures in human postmortem brain tissue.	Journal of Comparative Neurology	2019
29700473	An analytical framework for whole-genome sequence association studies and its implications for autism spectrum disorder.	Nat Genet	2018
28833472	Youth Suicide Deaths: Investigation of Clinical Predictors in a Statewide Sample.	Suicide and Life-Threatening Behavior	2018
30545852	Genome-wide de novo risk score implicates promoter variation in autism spectrum disorder.	Science	2018
29266823	Mid-life social outcomes for a population-based sample of adults with ASD.	Autism Research	2018
29389935	Novel pedigree analysis implicates DNA repair and chromatin remodeling in multiple myeloma risk.	PLoS Genet	2018
29523860	Allele-specific expression in a family quartet with autism reveals mono-to-biallelic switch and novel transcriptional processes of autism susceptibility genes.	Sci Rep	2018
28289475	Combined genome-wide linkage and targeted association analysis of head circumference in autism spectrum disorder families.	J Neurodev Disord	2017
28534046	Genetic analysis of age at onset variation in spinocerebellar ataxia type 2.	Neurology: Genetics	2017
27792857	Sudden infant death "syndrome"-Insights and future directions from a Utah population database analysis.	Am J Med Genet A	2017
27562213	VARPRISM: incorporating variant prioritization in tests of de novo mutation association.	Genome Med	2016
25744963	CYP2A6 Longitudinal Effects in Young Smokers.	Nicotine and Tobacco Research	2016
27423339	Male suspected suicide decedents in Utah: A comparison of Veterans and nonveterans.	Comprehensive Psychiatry	2016
27050036	Differential Vulnerability to Early-Life Parental Death: The Moderating Effects of Family Suicide History on Risks for Major Depression and Substance Abuse in Later Life.	Biodemography and Social Biology	2016
26392368	Association of the OPRM1 Variant rs1799971 (A118G) with Non-Specific Liability to Substance Dependence in a Collaborative de novo Meta-Analysis of European-Ancestry Cohorts.	Behav Genet	2016
26162628	A description of medical conditions in adults with autism spectrum disorder: A follow-up of the 1980s Utah/UCLA Autism Epidemiologic Study.	Autism	2016
26711810	APOH interacts with FTO to predispose to healthy thinness.	Human Genetics	2016
25241009	Spatial relative risk patterns of autism spectrum disorders in Utah.	Journal of Autism and Developmental Disorders	2015