Ngā hua rapu - Glessner, Joseph T.
- E whakaatu ana i te 1 - 20 hua o te 129
- Haere ki te Whārangi Whai Ake
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GWAS meta analysis identifies TSNARE1 as a novel Schizophrenia / Bipolar susceptibility locus mā Sleiman, Patrick, Wang, Dai, Glessner, Joseph, Hadley, Dexter, Gur, Raquel E., Cohen, Nadine, Li, Qingqin, Hakonarson, Hakon
I whakaputaina 2013Text -
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Genome-Wide Association Study of Maternal and Inherited Loci for Conotruncal Heart Defects mā Agopian, A. J., Mitchell, Laura E., Glessner, Joseph, Bhalla, Angela D., Sewda, Anshuman, Hakonarson, Hakon, Goldmuntz, Elizabeth
I whakaputaina 2014Text -
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Circulating LIGHT (TNFSF14) and Interleukin-18 Levels in Sepsis-Induced Multi-Organ Injuries mā Qu, Hui-Qi, Snyder, James, Connolly, John, Glessner, Joseph, Kao, Charlly, Sleiman, Patrick M.A., Hakonarson, Hakon
I whakaputaina 2022Text -
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Expansion of Schizophrenia Gene Network Knowledge Using Machine Learning Selected Signals From Dorsolateral Prefrontal Cortex and Amygdala RNA-seq Data mā Liu, Yichuan, Qu, Hui-Qi, Chang, Xiao, Tian, Lifeng, Glessner, Joseph, Sleiman, Patrick A. M., Hakonarson, Hakon
I whakaputaina 2022Text -
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An electronic health record (EHR) phenotype algorithm to identify patients with attention deficit hyperactivity disorders (ADHD) and psychiatric comorbidities mā Slaby, Isabella, Hain, Heather S., Abrams, Debra, Mentch, Frank D., Glessner, Joseph T., Sleiman, Patrick M. A., Hakonarson, Hakon
I whakaputaina 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 mā Wang, Kai, Li, Mingyao, Hadley, Dexter, Liu, Rui, Glessner, Joseph, Grant, Struan F.A., Hakonarson, Hakon, Bucan, Maja
I whakaputaina 2007Text -
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Copy number variation analysis in the context of electronic medical records and large-scale genomics consortium efforts mā Connolly, John J., Glessner, Joseph T., Almoguera, Berta, Crosslin, David R., Jarvik, Gail P., Sleiman, Patrick M., Hakonarson, Hakon
I whakaputaina 2014Text -
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Microdeletions and Microduplications in Patients with Congenital Heart Disease and Multiple Congenital Anomalies mā Goldmuntz, Elizabeth, Paluru, Prasuna, Glessner, Joseph, Hakonarson, Hakon, Biegel, Jaclyn A., White, Peter S., Gai, Xiaowu, Shaikh, Tamim H.
I whakaputaina 2011Text -
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Microduplications at the 15q11.2 BP1–BP2 locus are enriched in patients with anorexia nervosa mā Chang, Xiao, qu, Huiqi, Liu, Yichuan, Glessner, Joseph, Hou, Cuiping, Wang, Fengxiang, Li, Jin, Sleiman, Patrick, Hakonarson, Hakon
I whakaputaina 2019Text -
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Mitochondrial DNA haplogroups and risk of attention deficit and hyperactivity disorder in European Americans mā Chang, Xiao, Liu, Yichuan, Mentch, Frank, Glessner, Joseph, Qu, Huiqi, Nguyen, Kenny, Sleiman, Patrick M. A., Hakonarson, Hakon
I whakaputaina 2020Text -
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Machine Learning Reduced Gene/Non-Coding RNA Features That Classify Schizophrenia Patients Accurately and Highlight Insightful Gene Clusters mā Liu, Yichuan, Qu, Hui-Qi, Chang, Xiao, Tian, Lifeng, Qu, Jingchun, Glessner, Joseph, Sleiman, Patrick M. A., Hakonarson, Hakon
I whakaputaina 2021Text