About Our Research
Principal investigator Hillary Coon, PhD, leads multidisciplinary studies of risks leading to complex psychiatric conditions. Current work primarily focuses on risks leading to suicide mortality. Dr. Coon began collaborating on this study more than 25 years ago, subsequently taking the lead in building it into a unique research resource. The Utah Suicide Mortality Research Study (USMRS), now includes comprehensive health and exposure data and the world’s largest resource of biospecimens from suicide decedents.
Working to find risks associated with suicide mortality
Despite major advances in treatments for mental illnesses thought to be associated with risk, suicide mortality in the U.S. has increased dramatically since the late 1990’s. Over the last two decades, Dr. Coon has worked to establish collaborations and to build a comprehensive research study to bridge this critical knowledge gap, including statewide demographic, genealogical, environmental, and clinical data. Importantly, this resource now also includes the world’s largest resource of biospecimens from suicide decedents, enabling genetic and other biomarker discoveries.
This resource, the Utah Suicide Mortality Research Study (USMRS; https://rge.utah.edu.usmrs.php), now supports a diverse group of collaborative investigators dedicated to improving our understanding of risks leading to suicide through studies of the complex interactions among these comprehensive data elements.
Work funded by the NIH through 2030 focuses on several important topics. First, evidence of suicidal thoughts or behaviors (STBs) are currently the most robust predictors of suicide mortality. But how do we determine risks leading to suicide mortality for individuals where there is no evidence of STBs? Roughly half of suicide deaths fall into this category based on USMRS data and other recent, large, population-based studies. Even for those who exhibit STBs, fewer than 10% go on to die by suicide, posing a challenging problem to determine which individuals may be most at risk. For those with no evidence of STBs, knowledge of risks is currently even more difficult.
USMRS data can begin to approach these difficult questions. Recent findings have shown that suicide decedents without evidence of prior STBs were dramatically clinically different from those with evidence of prior STBs, exhibiting significantly fewer diagnoses across the neuropsychiatric spectrum (https://pubmed.ncbi.nlm.nih.gov/40020535/). Subsequent work showed that these dramatic clinical differences were not attributable to poor access to healthcare. Rather, suicide decedents without prior STBs also showed significantly lower underlying polygenic liabilities to many neuropsychiatric conditions (https://pubmed.ncbi.nlm.nih.gov/40385453, now in press).This work represents a paradigm shift in our assumptions about suicide risk, broadening our scope of risk discovery beyond neuropsychiatric clinical / genetic risks to include other novel risks associated with physical health and increased attention on the important contributions of exposures.
Additional new work will focus on discovery of physiological and mechanistic aspects leading to risk of suicide mortality. Other NIH funding anticipated to start in early 2026 will use a strategy of analyzing homogeneous subtypes, including unique Utah genealogical data that allows ascertainment of extended families at high risk of suicide death where familial transmission of genetic variation leading to risk can follow the successful design of prior work in Utah that has led to genetic discoveries for cancer and heart diseases. Other subtypes will also be studied defined by extreme psychiatric risks, but also by dysregulated physiological stress responses, recognizing our other work that has suggested that risks go beyond neuropsychiatric vulnerabilities.
As part of her deep passion, Dr. Coon will also pursue work to help maintain the USMRS and to ensure its sustainability for future discoveries by many investigators. The USMRS, which is now partially supported by the University of Utah Office of the Vice President for Research, rests on strong, long-term collaborations with the Utah State Office of the Medical Examiner, the Utah Population Database, investigators at Intermountain Health, the University of Utah Clinical and Translational Science Institute, and the University of Utah Office for Research Integrity and Compliance.
Dr. Coon’s interests span other areas of complex disease. Her earlier work focused on neurodiversity, substance use, schizophrenia and bipolar disorder, pulmonary disorders, and cardiovascular disorders. These areas of work continue to influence her perspectives on analytical strategies and on the integration of studies across mental and physical health. She also retains a long-term interest in research ethics and has served for more than two decades on the University of Utah Institutional Review Board
Learn more about our research
Project 1: R01MH123489 (Coon)
Prediction of suicide death using electronic health records and polygenic scores
This study uses electronic heath records, demographic information, environmental exposures, familial risks, and genetic differences to define and characterize subgroups at high risk of suicide mortality.
This study will help us to better understand the risks of suicide in those both with and without prior evidence of suicidality.
Sponsored by the National Institute of Mental Health (NIMH). Project duration: 7/15/2020 -6/30/2025, with renewal 7/1/2025-6/30/2030
Project 2: R0lMH122412 (Coon)
Genetic risk discovery using WGS from a population-based resource of 10,000 suicide deaths with DNA
This study uses whole-genome sequencing data to identify and characterize genetic variants that lead to suicide mortality risk. Genomic regions studied are prioritized using evidence of sharing among suicide deaths within very high-risk extended families.
A competitive renewal of this project scored in the top 5th percentile in the NIH review process, and will therefore likely receive continued NIH funding from 2026 – 2031
Sponsored by the National Institute of Mental Health (NIMH). Project duration: 4/1/2020 to 3/31/2026
Project 3: UU Vice President for Research (Coon)
Sustainability support for Utah Suicide Mortality Research Study (USMRS)
Funding will be used for these goals:
- Strategic planning
- Data/statistical infrastructure
- Wet lab infrastructure and ongoing sample collection/processing.
- Dissemination and community partnerships.
Dr. Hilary Coon has, over the course of two decades, worked to build a large, comprehensive, and unique collaborative research resource to study factors leading to risk of suicide mortality. Work using this resource has resulted in transformative knowledge about suicide mortality, and supports a network of investigators spanning many departments across the University of Utah. The USMRS, which is now partially supported by the University of Utah Office of the Vice President for Research, rests on strong collaborations with the Utah State Office of the Medical Examiner, the Utah Population Database, investigators at Intermountain Health, the University of Utah Clinical and Translational Science Institute, and the University of Utah Office for Research Integrity and Compliance.
Sponsored by the University of Utah Office of the Vice President for Research. Project duration: 1/21/2025-1/21/2030
Project 4: Margolis Foundation (Coon)
Unique Utah Research Resources to Reveal Risks for Suicide and Accidental Overdose
This project investigates the similarities and differences in risks of overdose and suicide mortality. Preliminary data will be used to support future funding and research endeavors.
Project duration:12/2023-1/2025
Project 5: Center for Genomic Medicine (Coon)
Functional genomic risk variants associated with substance use disorders in deceased individuals who did not die by suicide: a comparison to suicide deaths
This project uses archived blood samples from non-suicide deaths to build a resource for current and future comparative studies.
Project duration: 9/2023-9/2024
Project 6: CTSI Seed grant, (Coon)
Community Consultation on Research Use of Autopsy Blood Spots in Utah
This study goals includes work to define critical issues and create guidelines for future community-engaged research efforts of archived blood spots from Utah non-suicide decedents.
Project 7: AFSP BSG-1-005-18 (Willour/Coon)
Suicide risk in bipolar disorder
This study investigates the clinical and genetic risks of individuals with bipolar disorder who die by suicide compared to those with bipolar disorder but no suicidality. It will help identify unique risk factors for individuals with bipolar disorder.
Sponsored by the American Foundation for Suicide Prevention. Project duration: 11/1/2019-10/31/2023
Project 8: Utah Department of Substance Abuse and Mental Health (Coon)
Risk discovery for suicidality and mixed substance use
This project develops resources to inform future studies of suicide mortality with co-occuring substance abuse. It will help identify unique or compounding risk factors for people with substance use disorders.
Project duration: 2021-2025
Co-Investigator projects
- R01MH132733 (Mullins) 9/1/2023-8/31/2028, NIMH, Utah subaward. Title: Establishing the Suicide Working Group of the Psychiatric Genomics Consortium to elucidate the genetics and biology of suicide outcomes.
- R01HD112836 (Workalemahu) NIH/NIA. 9/15/2023-5/31/2028. Title: Inherited and de novo genetic variants relevant to familial, recurrent and sporadic stillbirth. This project investigates genetic risks leading to stillbirth by utilizing unique Utah data.
- R01MH134284 (Docherty) 5/15/2024-2/28/2029, NIMH. Title: Building resources for the diversification of genetic data on suicide death. Goals: This project develops resources for studying suicide mortality in India.
- R01ES032028 (Bakian) 7/15/2021-6/30/2026, NIH/NIEHS. Title: The influence of multiple environmental exposures on suicide risk. Goals: This project considers demographic, clinical, and genetic factors to investigate the effects of exposures on risks of suicide mortality.
- R01MH123619 (Docherty) 7/15/2020- 7/31/2025, NIMH. Title: Genome-wide association analysis of suicide death. Goals: use extensive Utah data to explore common genomic variation leading to risk of suicide mortality.
- RF1AG073189 (Burt) 8/15/21-7/31/24, NIH/NIA. Title: Quantifying the contributions of mitochondrial DNA to Alzheimer’s Disease and related conditions of aging. Goals: This project employs novel model-fitting strategies to Utah epidemiological data to explore associations between variations in mitochondrial DNA and Alzheimer’s Disease risk.
Current early career awards
Primary mentor
- K23MH123934 (Kirby) 4/1/2021-3/31/2025 NIMH. Title: Participatory research for suicide prevention in autism
- Brain & Behavior Foundation (Monson) 1/1/2023-1/1/2025 $105,000 Title: Clinical and Genetic Trauma-Related Risk Factors Leading to Suicide Death
Co-mentor
- K18MD019159 (Goldstein) 9/23/2023-8/31/2025 NIH $1,097,970, Title: Preventing firearm suicide deaths.
Meet our research team
Principal Investigator
Hilary Coon, PhD
Hilary Coon, PhD, is a Benning Endowed Presidential Professor with appointments in Psychiatry, Bioinformatics, Neurobiology, and Genetic Epidemiology. Dr. Coon uses unique Utah research resources to study genetic and environmental risks leading to complex psychiatric conditions. Currently, her work is focused on risks leading to suicide mortality.
Selected Publications
- Coon H, Shabalin A, DiBlasi E, Monson ET, Han S, Kaufman EA, Chen D, Kious B, Molina N, Yu Z, Staley M, Crockett DK, Colbert SM, Mullins N, Bakian AV, Docherty AR, Keeshin B. Absence of nonfatal suicidal behavior preceding suicide death reveals differences in clinical risks. In press, Psychiatry Research; 2025 May; 347:116391. doi: 10.1016/j.psychres.2025.116391. PMID: 40020535; PMCID: PMC11976895.
- Bakian AV, Chen D, Zhang C, Hanson HA, Docherty AR, Keeshin B, Gray D, Smith KR, VanDerslice JA, Yu DZ, Zhang Y, Coon H. A population-wide analysis of the familial risk of suicide in Utah, USA. Psychol Med. 2023 Mar;53(4):1448-1457. doi: 10.1017/S0033291721003020. PMID: 37010215; PMCID: PMC10009406.
- Han S, DiBlasi E, Monson ET, Shabalin A, Ferris E, Chen D, Fraser A, Yu Z, Staley M, Callor WB, Christensen ED, Crockett DK, Li QS, Willour V, Bakian AV, Keeshin B, Docherty AR, Eilbeck K, Coon H. Whole-genome sequencing analysis of suicide deaths integrating brain-regulatory eQTLs data to identify risk loci and genes. Mol Psychiatry. 2023 Sep;28(9):3909-3919. doi: 10.1038/s41380-023-02282-x. Epub 2023 Oct 4. PMID: 37794117; PMCID: PMC10730410.
- DiBlasi E, Kaufman EA, Webster S, Hagn EE, Shabalin AA, Chen D, Han S, Jawish R, Monson ET, Staley MJ, Keeshin BR, Docherty AR, Bakian AV, Okifuji A, Coon H. Phenome-wide diagnostic comparison among suicide deaths and living individuals with chronic pain diagnoses. BMC Med. 2024 Dec 2;22(1):568. doi: 10.1186/s12916-024-03794-1. PMID: 39617899; PMCID: PMC11610288.
- Das SC, Schulmann A, Callor WB, Jerominski L, Panicker MM, Christensen ED, Bunney WE, Williams ME, Coon H, Vawter MP. Altered transcriptomes, cell type proportions, and dendritic spine morphology in hippocampus of suicide decedents. J Affect Disord. 2024 Dec 15;367:118-128. doi: 10.1016/j.jad.2024.08.144. Epub 2024 Aug 25. PMID: 39191313.
- Coon H, Shabalin A, Bakian AV, DiBlasi E, Monson ET, Kirby A, Chen D, Fraser A, Yu Z, Staley M, Callor WB, Christensen ED, Crowell SE, Gray D, Crockett DK, Li QS, Keeshin B, Docherty AR. 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 Apr;189(3-4):60-73. doi: 10.1002/ajmg.b.32890. Epub 2022 Feb 24. PMID: 35212135; PMCID: PMC9149029.
- Li QS, Shabalin AA, DiBlasi E, Gopal S, Canuso CM; FinnGen, International Suicide Genetics Consortium; Palotie A, Drevets WC, Docherty AR, Coon H. Genome-wide association study meta-analysis of suicide death and suicidal behavior. Mol Psychiatry. 2023 Feb;28(2):891-900. doi: 10.1038/s41380-022-01828-9. Epub 2022 Oct 17. PMID: 36253440; PMCID: PMC9908547.
- DiBlasi E, Shabalin AA, Nicholas TJ, Monson ET, Ferris E, Yefimov L, Han S, Baird LM, Callor WB, Staley MJ, Li Q, Willour VL, Coon H. Intragenic deletions from whole genome sequencing of 1054 suicide deaths. medRxiv [Preprint]. 2025 Mar 6:2025.02.28.25323104. doi: 10.1101/2025.02.28.25323104. PMID: 40093239; PMCID: PMC11908330.
- Monson ET, Shabalin AA, Docherty AR, DiBlasi E, Bakian AV, Li QS, Gray D, Keeshin B, Crowell SE, Mullins N, Willour VL, Coon H. Assessment of suicide attempt and death in bipolar affective disorder: a combined clinical and genetic approach. Transl Psychiatry. 2021 Jul 7;11(1):379. doi: 10.1038/s41398-021-01500-w. PMID: 34234108; PMCID: PMC8263578.
- William N, Reissner C, Sargent R, Darlington TM, DiBlasi E, Li QS, Keeshin B, Callor WB, Ferris E, Jerominski L, Smith KR, Christensen ED, Gray DM, Camp NJ, Missler M, Williams ME, Coon H. Neurexin 1 variants as risk factors for suicide death. Mol Psychiatry. 2021 Dec;26(12):7436-7445. doi: 10.1038/s41380-021-01190-2. Epub 2021 Jun 25. PMID: 34168285; PMCID: PMC8709873.
Contact
Hilary Coon, PhD
Principal Investigator