Common variants in polygenic schizophrenia

por Glessner, Joseph T, Hakonarson, Hakon
Publicado 2009

ParseCNV integrative copy number variation association software with quality tracking

por Glessner, Joseph T., Li, Jin, Hakonarson, Hakon
Publicado 2013

Mendelian randomization study of obesity and type 2 diabetes in hospitalized COVID-19 patients

por Qu, Hui-Qi, Qu, Jingchun, Glessner, Joseph, Hakonarson, Hakon
Publicado 2022

Circulating LIGHT (TNFSF14) and Interleukin-18 Levels in Sepsis-Induced Multi-Organ Injuries

por Qu, Hui-Qi, Snyder, James, Connolly, John, Glessner, Joseph, Kao, Charlly, Sleiman, Patrick, Hakonarson, Hakon
Publicado 2022

Large Copy-Number Variations Are Enriched in Cases With Moderate to Extreme Obesity

por Wang, Kai, Li, Wei-Dong, Glessner, Joseph T., Grant, Struan F.A., Hakonarson, Hakon, Price, R. Arlen
Publicado 2010

GWAS meta analysis identifies TSNARE1 as a novel Schizophrenia / Bipolar susceptibility locus

por Sleiman, Patrick, Wang, Dai, Glessner, Joseph, Hadley, Dexter, Gur, Raquel E., Cohen, Nadine, Li, Qingqin, Hakonarson, Hakon
Publicado 2013

Genome-Wide Association Study of Maternal and Inherited Loci for Conotruncal Heart Defects

por Agopian, A. J., Mitchell, Laura E., Glessner, Joseph, Bhalla, Angela D., Sewda, Anshuman, Hakonarson, Hakon, Goldmuntz, Elizabeth
Publicado 2014

Expansion of Schizophrenia Gene Network Knowledge Using Machine Learning Selected Signals From Dorsolateral Prefrontal Cortex and Amygdala RNA-seq Data

por Liu, Yichuan, Qu, Hui-Qi, Chang, Xiao, Tian, Lifeng, Glessner, Joseph, Sleiman, Patrick A. M., Hakonarson, Hakon
Publicado 2022

An electronic health record (EHR) phenotype algorithm to identify patients with attention deficit hyperactivity disorders (ADHD) and psychiatric comorbidities

por Slaby, Isabella, Hain, Heather S., Abrams, Debra, Mentch, Frank D., Glessner, Joseph T., Sleiman, Patrick M. A., Hakonarson, Hakon
Publicado 2022

Copy number variation analysis in the context of electronic medical records and large-scale genomics consortium efforts

por Connolly, John J., Glessner, Joseph T., Almoguera, Berta, Crosslin, David R., Jarvik, Gail P., Sleiman, Patrick M., Hakonarson, Hakon
Publicado 2014

Mitochondrial DNA haplogroups and risk of attention deficit and hyperactivity disorder in European Americans

por Chang, Xiao, Liu, Yichuan, Mentch, Frank, Glessner, Joseph, Qu, Huiqi, Nguyen, Kenny, Sleiman, Patrick M. A., Hakonarson, Hakon
Publicado 2020

MONTAGE: a new tool for high-throughput detection of mosaic copy number variation

por Glessner, Joseph T., Chang, Xiao, Liu, Yichuan, Li, Jin, Khan, Munir, Wei, Zhi, Sleiman, Patrick M. A., Hakonarson, Hakon
Publicado 2021

Genetic correlations between COVID-19 and a variety of traits and diseases

por Chang, Xiao, Li, Yun, Nguyen, Kenny, Qu, Huiqi, Liu, Yichuan, Glessner, Joseph, Sleiman, Patrick M.A., Hakonarson, Hakon
Publicado 2021

Metabolomic profiling for dyslipidemia in pediatric patients with sickle cell disease, on behalf of the IHCC consortium

por Qu, Hui-Qi, Glessner, Joseph, Qu, Jingchun, Mentch, Frank, Campbell, Ian, Sleiman, Patrick, Connolly, John J, Hakonarson, Hakon
Publicado 2022

Modeling genetic inheritance of copy number variations

por Wang, Kai, Chen, Zhen, Tadesse, Mahlet G., Glessner, Joseph, Grant, Struan F. A., Hakonarson, Hakon, Bucan, Maja, Li, Mingyao
Publicado 2008

Machine Learning Reduced Gene/Non-Coding RNA Features That Classify Schizophrenia Patients Accurately and Highlight Insightful Gene Clusters

por Liu, Yichuan, Qu, Hui-Qi, Chang, Xiao, Tian, Lifeng, Qu, Jingchun, Glessner, Joseph, Sleiman, Patrick M. A., Hakonarson, Hakon
Publicado 2021

Discovery of Novel Host Molecular Factors Underlying HBV/HCV Infection

por Huang, Xubo, Glessner, Joseph T., Huang, Jinxia, Zhou, Desheng, March, Michael E., Wang, Hongna, Xia, Qianghua, Hakonarson, Hakon, Li, Jin
Publicado 2021

COVID-19 in pediatrics: Genetic susceptibility

por Glessner, Joseph T., Chang, Xiao, Mentch, Frank, Qu, Huiqi, Abrams, Debra J., Thomas, Alexandria, Sleiman, Patrick M. A., Hakonarson, Hakon
Publicado 2022

Adjustment of genomic waves in signal intensities from whole-genome SNP genotyping platforms

por Diskin, Sharon J., Li, Mingyao, Hou, Cuiping, Yang, Shuzhang, Glessner, Joseph, Hakonarson, Hakon, Bucan, Maja, Maris, John M., Wang, Kai
Publicado 2008

Association of Rare Recurrent Copy Number Variants With Congenital Heart Defects Based on Next-Generation Sequencing Data From Family Trios

por Liu, Yichuan, Chang, Xiao, Glessner, Joseph, Qu, Huiqi, Tian, Lifeng, Li, Dong, Nguyen, Kenny, Sleiman, Patrick M. A., Hakonarson, Hakon
Publicado 2019