Author

Leslie Jerominski

University of Utah

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Genetics· 4

Signature Assays, Organisms & Methods

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Organism:human· 4 Approach:statistical model· 4 Research Focus:GWAS / association mapping· 2 Assay:whole-genome sequencing· 2 Research Focus:differential expression· 1 Research Focus:gene regulatory network inference· 1 Assay:GWAS summary statistics· 1 Approach:matrix factorization· 1

Frequent Co-Authors

Hilary H CooniD· 4 shared Amanda V. BakianiD· 3 shared Andrey A. ShabaliniD· 3 shared Anna R. DochertyiD· 3 shared Brooks R KeeshiniD· 3 shared Danli CheniD· 3 shared Douglas GrayiD· 3 shared Emily DiBlasiiD· 3 shared

Activity by Year

2017-2021 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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4 shared papersGenetics

Hilary H CoonORCID

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4 papers

Recent·Most cited

Rare protein coding variants implicate genes involved in risk of suicide death

Emily DiBlasi, Andrey A. Shabalin, Eric T. Monson, Brooks R Keeshin, Amanda V. Bakian, Anne V. Kirby, Elliott Ferris, Danli Chen, Nancy William, Eoin Gaj, Michael Klein, Leslie Jerominski, William Brandon Callor, Erik D. Christensen, Ken Robert Smith, , Hilary H Coon

The paper identifies five rare SNPs associated with suicide death using genetic data from the USGRS and controls, highlighting their potential role in suicide risk and related biological processes.

American Journal of Medical Genetics Part B Neuropsychiatric Genetics · May 27, 2021Peer-reviewedGenetics

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

Anna R. Docherty, Andrey A. Shabalin, Emily DiBlasi, Eric T. Monson, Niamh Mullins, Daniel E. Adkins, Silviu‐Alin Bacanu, Amanda V. Bakian, Sheila E. Crowell, Danli Chen, Todd M. Darlington, William Brandon Callor, Erik D. Christensen, Douglas Gray, Brooks R Keeshin, , Hilary H Coon

This paper conducts a genome-wide association study of suicide death and shows polygenic scores predict suicide case-control status and related psychiatric traits.

American Journal of Psychiatry · Oct 1, 2020Peer-reviewedGenetics

Genomewide significant regions in 43 Utah high-risk families implicate multiple genes involved in risk for completed suicide

Hilary H Coon, Todd M. Darlington, Emily DiBlasi, William Brandon Callor, Elliott Ferris, Alison M. Fraser, Zhe Yu, Nancy William, Sujan Chandra Das, Sheila E. Crowell, Danli Chen, John S. Anderson, Michael Klein, Leslie Jerominski, Dale S. Cannon, , Douglas Gray

The paper identifies 207 genes associated with completed suicide using genomic data from 43 high-risk Utah families, finding four significant variants linked to suicide risk.

Molecular Psychiatry · Oct 23, 2018Peer-reviewedGenetics

High-risk Autism Spectrum Disorder Utah pedigrees: a novel Shared Genomic Segments analysis.

Todd M. Darlington, Deborah A. Bilder, Jubel Morgan, Leslie Jerominski, Venkatesh Rajamanickam, Rob Sargent, Nicola J. Camp, Hilary H Coon

The paper uses a new pedigree analysis method to identify shared genomic segments in high-risk ASD families, finding one genome-wide significant segment and several suggestive regions.

bioRxiv · May 9, 2017 · PreprintGenetics