Søgeresultater - Glessner, Joseph T.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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