Torthaí cuardaigh - Glessner, Joseph T.

Common variants in polygenic schizophrenia de réir Glessner, Joseph T, Hakonarson, Hakon

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ParseCNV integrative copy number variation association software with quality tracking de réir 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 de réir Qu, Hui-Qi, Qu, Jingchun, Glessner, Joseph, Hakonarson, Hakon

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Phasing of Many Thousands of Genotyped Samples de réir 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 de réir 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 de réir 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 de réir 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 de réir 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 de réir 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 de réir 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 de réir 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 de réir 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 de réir 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 de réir 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 de réir 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 de réir 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 de réir 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 de réir 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 de réir 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 de réir Liu, Yichuan, Qu, Hui-Qi, Chang, Xiao, Tian, Lifeng, Qu, Jingchun, Glessner, Joseph, Sleiman, Patrick M. A., Hakonarson, Hakon

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