日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

Genetic risk of chronic pain conditions associated with risk of suicide death through an integrative analysis of EHR and genomics data

通过对电子健康记录和基因组数据的综合分析,探讨慢性疼痛疾病的遗传风险与自杀死亡风险之间的关联

Han, Seonggyun; DiBlasi, Emily; Monson, Eric T; Shabalin, Andrey A; Baird, Lisa; Chen, Danli; Lamichhane, Dirga; Tharp, Doug; Ferris, Elliott; Yu, Zhe; Brandon Callor, W; Staley, Michael J; Li, Qingqin S; Willour, Virginia; Crockett, David K; Eilbeck, Karen; Bakian, Amanda V; Keeshin, Brooks R; Okifuji, Akiko; Coon, Hilary; Docherty, Anna R

Whole-genome sequencing analysis of suicide deaths integrating brain-regulatory eQTLs data to identify risk loci and genes

对自杀死亡案例进行全基因组测序分析,整合脑调控eQTL数据,以识别风险位点和基因。

Han, Seonggyun; DiBlasi, Emily; Monson, Eric T; Shabalin, Andrey; Ferris, Elliott; Chen, Danli; Fraser, Alison; Yu, Zhe; Staley, Michael; Callor, W Brandon; Christensen, Erik D; Crockett, David K; Li, Qingqin S; Willour, Virginia; Bakian, Amanda V; Keeshin, Brooks; Docherty, Anna R; Eilbeck, Karen; Coon, Hilary

The persistent homology of genealogical networks

谱系网络的持续同源性

Boyd, Zachary M; Callor, Nick; Gledhill, Taylor; Jenkins, Abigail; Snellman, Robert; Webb, Benjamin; Wonnacott, Raelynn

Altered transcriptomes, cell type proportions, and dendritic spine morphology in hippocampus of suicide deaths

自杀死亡者海马体中转录组、细胞类型比例和树突棘形态的改变

Das, Sujan C; Schulmann, Anton; Callor, William B; Jerominski, Leslie; Panicker, Mitradas M; Christensen, Erik D; Bunney, William E; Williams, Megan E; Coon, Hilary; Vawter, Marquis P

Neurexin 1 variants as risk factors for suicide death

神经连接蛋白1变异体作为自杀死亡的风险因素

Nancy William ,Carsten Reissner ,Robert Sargent ,Todd M Darlington ,Emily DiBlasi ,Qingqin S Li ,Brooks Keeshin ,William B Callor ,Elliott Ferris ,Leslie Jerominski ,Ken R Smith ,Erik D Christensen ,Douglas M Gray ,Nicola J Camp ,Markus Missler ,Megan E Williams ,Hilary Coon

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

罕见的蛋白质编码变异与自杀死亡风险相关的基因有关

DiBlasi, Emily; Shabalin, Andrey A; Monson, Eric T; Keeshin, Brooks R; Bakian, Amanda V; Kirby, Anne V; Ferris, Elliott; Chen, Danli; William, Nancy; Gaj, Eoin; Klein, Michael; Jerominski, Leslie; Callor, W Brandon; Christensen, Erik; Smith, Ken R; Fraser, Alison; Yu, Zhe; Gray, Douglas; Camp, Nicola J; Stahl, Eli A; Li, Qingqin S; Docherty, Anna R; Coon, Hilary

Genome-Wide Association Study of Suicide Death and Polygenic Prediction of Clinical Antecedents

全基因组关联研究与自杀死亡及临床前因的多基因预测

Docherty, Anna R; Shabalin, Andrey A; DiBlasi, Emily; Monson, Eric; Mullins, Niamh; Adkins, Daniel E; Bacanu, Silviu-Alin; Bakian, Amanda V; Crowell, Sheila; Chen, Danli; Darlington, Todd M; Callor, William B; Christensen, Erik D; Gray, Douglas; Keeshin, Brooks; Klein, Michael; Anderson, John S; Jerominski, Leslie; Hayward, Caroline; Porteous, David J; McIntosh, Andrew; Li, Qingqin; Coon, Hilary

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

犹他州 43 个高风险家庭的全基因组显著区域表明多个基因与自杀风险有关

Hilary Coon, Todd M Darlington, Emily DiBlasi, W Brandon Callor, Elliott Ferris, Alison Fraser, Zhe Yu, Nancy William, Sujan C Das, Sheila E Crowell, Danli Chen, John S Anderson, Michael Klein, Leslie Jerominski, Dale Cannon, Andrey Shabalin, Anna Docherty, Megan Williams, Ken R Smith, Brooks Keeshi

DiI-mediated analysis of presynaptic and postsynaptic structures in human postmortem brain tissue

利用DiI介导分析人类死后脑组织中的突触前和突触后结构

Das, Sujan C; Chen, Danli; Callor, William Brandon; Christensen, Eric; Coon, Hilary; Williams, Megan E

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

通过结合家系和表型分析方法识别遗传风险的罕见变异:以自杀和哮喘为例

Darlington, T M; Pimentel, R; Smith, K; Bakian, A V; Jerominski, L; Cardon, J; Camp, N J; Callor, W B; Grey, T; Singleton, M; Yandell, M; Renshaw, P F; Yurgelun-Todd, D A; Gray, D; Coon, H