T. Darlington

发表

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

H. Coon, A. Shabalin, A. McIntosh, 2019, bioRxiv.

Meta-analytic approaches for examining complexity and heterogeneity in studies of adolescent development.

E. Tanner‐Smith, N. Parr, M. Schweer-Collins, 2019, Journal of adolescence.

Combined genome-wide linkage and targeted association analysis of head circumference in autism spectrum disorder families

H. Coon, A. Paterson, T. Dyer, 2017, Journal of Neurodevelopmental Disorders.

Mesolimbic transcriptional response to hedonic substitution of voluntary exercise and voluntary ethanol consumption

M. Ehringer, R. Cox, T. Darlington, 2014, Behavioural Brain Research.

Genome-wide association study of suicide death: Results from a first wave of Utah completed suicide data (N = 1,420)

Daniel E. Adkins, H. Coon, A. Shabalin, 2017 .

Evidence for Association Between Low Frequency Variants in CHRNA6/CHRNB3 and Antisocial Drug Dependence

Phillip A. Richmond, J. Hewitt, R. Corley, 2016, Behavior Genetics.

Complex Multifactorial Genetic Diseases

T. Darlington, Daniel J Howrigan, Nancy William, 2018 .

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

H. Coon, N. Camp, J. Morgan, 2017, bioRxiv.

Genetic risk factors in two Utah pedigrees at high risk for suicide

W. McMahon, H. Coon, N. Camp, 2013, Translational Psychiatry.

Shared genomic segments in high-risk multigenerational pedigrees with gastroschisis.

N. Camp, M. Feldkamp, S. Krikov, 2019, Birth defects research.

Novel pedigree analysis implicates DNA repair and chromatin remodeling in multiple myeloma risk

H. Coon, N. Camp, C. Vachon, 2017, bioRxiv.

Genetic and environmental influences on alcohol behaviors: insight from the mouse transcriptome

T. Darlington, 2013 .

Evidence for Association Between Low Frequency Variants in CHRNA6/CHRNB3 and Antisocial Drug Dependence

Phillip A. Richmond, J. Hewitt, R. Corley, 2016, Behavior genetics.

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

Ken R. Smith, H. Coon, N. Camp, 2018, Molecular Psychiatry.

Identifying rare variants for genetic risk through a combined pedigree and phenotype approach: application to suicide and asthma

H. Coon, N. Camp, D. Yurgelun-Todd, 2014, Translational Psychiatry.

Identification of genome-wide significant shared genomic segments in large extended Utah families at high risk for completed suicide

Nicola J. Camp, Todd M. Darlington, Hilary Coon, 2017 .

Neurexin 1 variants as risk factors for suicide death

Ken R. Smith, H. Coon, N. Camp, 2021, Molecular Psychiatry.

Voluntary wheel running reduces voluntary consumption of ethanol in mice: identification of candidate genes through striatal gene expression profiling

M. Ehringer, X. Gallego, R. Cox, 2016, Genes, brain, and behavior.

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

Ken R. Smith, H. Coon, N. Camp, 2018, bioRxiv.

Transcriptome analysis of Inbred Long Sleep and Inbred Short Sleep mice

R. Radcliffe, T. Phang, M. Ehringer, 2013, Genes, brain, and behavior.

Novel pedigree analysis implicates DNA repair and chromatin 1 remodeling in Multiple Myeloma risk 2

H. Coon, N. Camp, C. Vachon, 2017 .

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

Daniel E. Adkins, H. Coon, A. Shabalin, 2017, bioRxiv.