Whole genome sequencing and variant discovery in the ASPIRE autism spectrum disorder cohort
Callaghan, Daniel Benjamin, Rogic, Sanja, Tan, Powell Patrick Cheng, Calli, Kristina, Qiao, Ying, Baldwin, Robert, Jacobson, Matthew, Belmadani, Manuel, Holmes, Nathan, Yu, Chang, Li, Yanchen, Li, Yingrui, Kurtzke, Franz‐Edward, Kuzeljevic, Boris, Yu, An Yi, Hudson, Melissa, Mcaughton, Amy J.M., Xu, Yuchen, Dionne‐Laporte, Alexandre, Girard, Simon, Liang, Ping, Separovic, Evica Rajcan, Liu, Xudong, Rouleau, Guy, Pavlidis, Paul, Lewis, M.E. Suzanne
Published in Clinical genetics (01.09.2019)
Published in Clinical genetics (01.09.2019)
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Journal Article
Transcriptome Sequencing of the Anterior Cingulate in Bipolar Disorder: Dysregulation of G Protein-Coupled Receptors
Cruceanu, Cristiana, Tan, Powell Patrick Cheng, Rogic, Sanja, Lopez, Juan Pablo, Torres-Platas, Susana Gabriela, Gigek, Carolina O., Alda, Martin, Rouleau, Guy A., Pavlidis, Paul, Turecki, Gustavo
Published in The American journal of psychiatry (01.11.2015)
Published in The American journal of psychiatry (01.11.2015)
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Journal Article
Interactive Exploration, Analysis, and Visualization of Complex Phenome-Genome Datasets with ASPIREdb
Tan, Powell Patrick Cheng, Rogic, Sanja, Zoubarev, Anton, McDonald, Cameron, Lui, Frances, Charathsandran, Gayathiri, Jacobson, Matthew, Belmadani, Manuel, Leong, Justin, Van Rossum, Thea, Portales-Casamar, Elodie, Qiao, Ying, Calli, Kristina, Liu, Xudong, Hudson, Melissa, Rajcan-Separovic, Evica, Lewis, ME Suzanne, Pavlidis, Paul
Published in Human mutation (01.08.2016)
Published in Human mutation (01.08.2016)
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Journal Article
Interactive exploration, analysis and visualization of complex phenomegenome datasets with ASPIREdb
Tan, Powell Patrick Cheng, Rogic, Sanja, Zoubarev, Anton, McDonald, Cameron, Lui, Frances, Charathsandran, Gayathiri, Jacobson, Matthew, Belmadani, Manuel, Leong, Justin, Van Rossum, Thea, Portales-Casamar, Elodie, Qiao, Ying, Calli, Kristina, Liu, Xudong, Hudson, Melissa, Rajcan-Separovic, Evica, Lewis, ME Suzanne, Pavlidis, Paul
Published in Human mutation (20.05.2016)
Published in Human mutation (20.05.2016)
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Journal Article