Resultados de procura - Glessner, Joseph T.
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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 2014Text -
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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 2022Text -
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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 2022Text -
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PennCNV: An integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data por Wang, Kai, Li, Mingyao, Hadley, Dexter, Liu, Rui, Glessner, Joseph, Grant, Struan F.A., Hakonarson, Hakon, Bucan, Maja
Publicado 2007Text -
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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 2014Text -
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Microdeletions and Microduplications in Patients with Congenital Heart Disease and Multiple Congenital Anomalies por Goldmuntz, Elizabeth, Paluru, Prasuna, Glessner, Joseph, Hakonarson, Hakon, Biegel, Jaclyn A., White, Peter S., Gai, Xiaowu, Shaikh, Tamim H.
Publicado 2011Text -
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Microduplications at the 15q11.2 BP1–BP2 locus are enriched in patients with anorexia nervosa por Chang, Xiao, qu, Huiqi, Liu, Yichuan, Glessner, Joseph, Hou, Cuiping, Wang, Fengxiang, Li, Jin, Sleiman, Patrick, Hakonarson, Hakon
Publicado 2019Text -
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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 2020Text -
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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 2021Text