Search Results - Glessner, Joseph T.

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  1. 1
    Common variants in polygenic schizophrenia

    Common variants in polygenic schizophrenia by Glessner, Joseph T, Hakonarson, Hakon

    Published 2009
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  2. 2
    ParseCNV integrative copy number variation association software with quality tracking

    ParseCNV integrative copy number variation association software with quality tracking by Glessner, Joseph T., Li, Jin, Hakonarson, Hakon

    Published 2013
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  3. 3
    Mendelian randomization study of obesity and type 2 diabetes in hospitalized COVID-19 patients

    Mendelian randomization study of obesity and type 2 diabetes in hospitalized COVID-19 patients by Qu, Hui-Qi, Qu, Jingchun, Glessner, Joseph, Hakonarson, Hakon

    Published 2022
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  4. 4
    Phasing of Many Thousands of Genotyped Samples

    Phasing of Many Thousands of Genotyped Samples by Williams, Amy L., Patterson, Nick, Glessner, Joseph, Hakonarson, Hakon, Reich, David

    Published 2012
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  5. 5
    Circulating LIGHT (TNFSF14) and Interleukin-18 Levels in Sepsis-Induced Multi-Organ Injuries

    Circulating LIGHT (TNFSF14) and Interleukin-18 Levels in Sepsis-Induced Multi-Organ Injuries by Qu, Hui-Qi, Snyder, James, Connolly, John, Glessner, Joseph, Kao, Charlly, Sleiman, Patrick, Hakonarson, Hakon

    Published 2022
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  6. 6
    Large Copy-Number Variations Are Enriched in Cases With Moderate to Extreme Obesity

    Large Copy-Number Variations Are Enriched in Cases With Moderate to Extreme Obesity by Wang, Kai, Li, Wei-Dong, Glessner, Joseph T., Grant, Struan F.A., Hakonarson, Hakon, Price, R. Arlen

    Published 2010
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  7. 7
    GWAS meta analysis identifies TSNARE1 as a novel Schizophrenia / Bipolar susceptibility locus

    GWAS meta analysis identifies TSNARE1 as a novel Schizophrenia / Bipolar susceptibility locus by Sleiman, Patrick, Wang, Dai, Glessner, Joseph, Hadley, Dexter, Gur, Raquel E., Cohen, Nadine, Li, Qingqin, Hakonarson, Hakon

    Published 2013
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  8. 8
    Genome-Wide Association Study of Maternal and Inherited Loci for Conotruncal Heart Defects

    Genome-Wide Association Study of Maternal and Inherited Loci for Conotruncal Heart Defects by Agopian, A. J., Mitchell, Laura E., Glessner, Joseph, Bhalla, Angela D., Sewda, Anshuman, Hakonarson, Hakon, Goldmuntz, Elizabeth

    Published 2014
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  9. 9
    Circulating LIGHT (TNFSF14) and Interleukin-18 Levels in Sepsis-Induced Multi-Organ Injuries

    Circulating LIGHT (TNFSF14) and Interleukin-18 Levels in Sepsis-Induced Multi-Organ Injuries by Qu, Hui-Qi, Snyder, James, Connolly, John, Glessner, Joseph, Kao, Charlly, Sleiman, Patrick M.A., Hakonarson, Hakon

    Published 2022
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  10. 10
    Expansion of Schizophrenia Gene Network Knowledge Using Machine Learning Selected Signals From Dorsolateral Prefrontal Cortex and Amygdala RNA-seq Data

    Expansion of Schizophrenia Gene Network Knowledge Using Machine Learning Selected Signals From Dorsolateral Prefrontal Cortex and Amygdala RNA-seq Data by Liu, Yichuan, Qu, Hui-Qi, Chang, Xiao, Tian, Lifeng, Glessner, Joseph, Sleiman, Patrick A. M., Hakonarson, Hakon

    Published 2022
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  11. 11
    An electronic health record (EHR) phenotype algorithm to identify patients with attention deficit hyperactivity disorders (ADHD) and psychiatric comorbidities

    An electronic health record (EHR) phenotype algorithm to identify patients with attention deficit hyperactivity disorders (ADHD) and psychiatric comorbidities by Slaby, Isabella, Hain, Heather S., Abrams, Debra, Mentch, Frank D., Glessner, Joseph T., Sleiman, Patrick M. A., Hakonarson, Hakon

    Published 2022
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  12. 12
    PennCNV: An integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data

    PennCNV: An integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data by Wang, Kai, Li, Mingyao, Hadley, Dexter, Liu, Rui, Glessner, Joseph, Grant, Struan F.A., Hakonarson, Hakon, Bucan, Maja

    Published 2007
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  13. 13
    Copy number variation analysis in the context of electronic medical records and large-scale genomics consortium efforts

    Copy number variation analysis in the context of electronic medical records and large-scale genomics consortium efforts by Connolly, John J., Glessner, Joseph T., Almoguera, Berta, Crosslin, David R., Jarvik, Gail P., Sleiman, Patrick M., Hakonarson, Hakon

    Published 2014
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  14. 14
    Microdeletions and Microduplications in Patients with Congenital Heart Disease and Multiple Congenital Anomalies

    Microdeletions and Microduplications in Patients with Congenital Heart Disease and Multiple Congenital Anomalies by Goldmuntz, Elizabeth, Paluru, Prasuna, Glessner, Joseph, Hakonarson, Hakon, Biegel, Jaclyn A., White, Peter S., Gai, Xiaowu, Shaikh, Tamim H.

    Published 2011
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  15. 15
    Microduplications at the 15q11.2 BP1–BP2 locus are enriched in patients with anorexia nervosa

    Microduplications at the 15q11.2 BP1–BP2 locus are enriched in patients with anorexia nervosa by Chang, Xiao, qu, Huiqi, Liu, Yichuan, Glessner, Joseph, Hou, Cuiping, Wang, Fengxiang, Li, Jin, Sleiman, Patrick, Hakonarson, Hakon

    Published 2019
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  16. 16
    Mitochondrial DNA haplogroups and risk of attention deficit and hyperactivity disorder in European Americans

    Mitochondrial DNA haplogroups and risk of attention deficit and hyperactivity disorder in European Americans by Chang, Xiao, Liu, Yichuan, Mentch, Frank, Glessner, Joseph, Qu, Huiqi, Nguyen, Kenny, Sleiman, Patrick M. A., Hakonarson, Hakon

    Published 2020
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  17. 17
    MONTAGE: a new tool for high-throughput detection of mosaic copy number variation

    MONTAGE: a new tool for high-throughput detection of mosaic copy number variation by Glessner, Joseph T., Chang, Xiao, Liu, Yichuan, Li, Jin, Khan, Munir, Wei, Zhi, Sleiman, Patrick M. A., Hakonarson, Hakon

    Published 2021
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  18. 18
    Genetic correlations between COVID-19 and a variety of traits and diseases

    Genetic correlations between COVID-19 and a variety of traits and diseases by Chang, Xiao, Li, Yun, Nguyen, Kenny, Qu, Huiqi, Liu, Yichuan, Glessner, Joseph, Sleiman, Patrick M.A., Hakonarson, Hakon

    Published 2021
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  19. 19
    Modeling genetic inheritance of copy number variations

    Modeling genetic inheritance of copy number variations by Wang, Kai, Chen, Zhen, Tadesse, Mahlet G., Glessner, Joseph, Grant, Struan F. A., Hakonarson, Hakon, Bucan, Maja, Li, Mingyao

    Published 2008
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  20. 20
    Machine Learning Reduced Gene/Non-Coding RNA Features That Classify Schizophrenia Patients Accurately and Highlight Insightful Gene Clusters

    Machine Learning Reduced Gene/Non-Coding RNA Features That Classify Schizophrenia Patients Accurately and Highlight Insightful Gene Clusters by Liu, Yichuan, Qu, Hui-Qi, Chang, Xiao, Tian, Lifeng, Qu, Jingchun, Glessner, Joseph, Sleiman, Patrick M. A., Hakonarson, Hakon

    Published 2021
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