Canlyniadau Chwilio - Glessner, Joseph T.
- Dangos 1 - 20 canlyniadau o 129
- Ewch i'r Dudalen Nesaf
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GWAS meta analysis identifies TSNARE1 as a novel Schizophrenia / Bipolar susceptibility locus gan Sleiman, Patrick, Wang, Dai, Glessner, Joseph, Hadley, Dexter, Gur, Raquel E., Cohen, Nadine, Li, Qingqin, Hakonarson, Hakon
Cyhoeddwyd 2013Text -
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Genome-Wide Association Study of Maternal and Inherited Loci for Conotruncal Heart Defects gan Agopian, A. J., Mitchell, Laura E., Glessner, Joseph, Bhalla, Angela D., Sewda, Anshuman, Hakonarson, Hakon, Goldmuntz, Elizabeth
Cyhoeddwyd 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 gan Liu, Yichuan, Qu, Hui-Qi, Chang, Xiao, Tian, Lifeng, Glessner, Joseph, Sleiman, Patrick A. M., Hakonarson, Hakon
Cyhoeddwyd 2022Text -
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An electronic health record (EHR) phenotype algorithm to identify patients with attention deficit hyperactivity disorders (ADHD) and psychiatric comorbidities gan Slaby, Isabella, Hain, Heather S., Abrams, Debra, Mentch, Frank D., Glessner, Joseph T., Sleiman, Patrick M. A., Hakonarson, Hakon
Cyhoeddwyd 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 gan Wang, Kai, Li, Mingyao, Hadley, Dexter, Liu, Rui, Glessner, Joseph, Grant, Struan F.A., Hakonarson, Hakon, Bucan, Maja
Cyhoeddwyd 2007Text -
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Copy number variation analysis in the context of electronic medical records and large-scale genomics consortium efforts gan Connolly, John J., Glessner, Joseph T., Almoguera, Berta, Crosslin, David R., Jarvik, Gail P., Sleiman, Patrick M., Hakonarson, Hakon
Cyhoeddwyd 2014Text -
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Microdeletions and Microduplications in Patients with Congenital Heart Disease and Multiple Congenital Anomalies gan Goldmuntz, Elizabeth, Paluru, Prasuna, Glessner, Joseph, Hakonarson, Hakon, Biegel, Jaclyn A., White, Peter S., Gai, Xiaowu, Shaikh, Tamim H.
Cyhoeddwyd 2011Text -
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Microduplications at the 15q11.2 BP1–BP2 locus are enriched in patients with anorexia nervosa gan Chang, Xiao, qu, Huiqi, Liu, Yichuan, Glessner, Joseph, Hou, Cuiping, Wang, Fengxiang, Li, Jin, Sleiman, Patrick, Hakonarson, Hakon
Cyhoeddwyd 2019Text -
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Mitochondrial DNA haplogroups and risk of attention deficit and hyperactivity disorder in European Americans gan Chang, Xiao, Liu, Yichuan, Mentch, Frank, Glessner, Joseph, Qu, Huiqi, Nguyen, Kenny, Sleiman, Patrick M. A., Hakonarson, Hakon
Cyhoeddwyd 2020Text -
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Machine Learning Reduced Gene/Non-Coding RNA Features That Classify Schizophrenia Patients Accurately and Highlight Insightful Gene Clusters gan Liu, Yichuan, Qu, Hui-Qi, Chang, Xiao, Tian, Lifeng, Qu, Jingchun, Glessner, Joseph, Sleiman, Patrick M. A., Hakonarson, Hakon
Cyhoeddwyd 2021Text