Brain gene co-expression networks link complement signaling with convergent synaptic pathology in schizophrenia

od Kim, Minsoo, Haney, Jillian R., Zhang, Pan, Hernandez, Leanna M., Wang, Lee-kai, Perez-Cano, Laura, Olde Loohuis, Loes M., de la Torre-Ubieta, Luis, Gandal, Michael J.
izdano v Nat Neurosci (2021)

Inherited and de novo genetic risk for autism impacts shared networks

od Ruzzo, Elizabeth K., Pérez-Cano, Laura, Jung, Jae-Yoon, Wang, Lee-kai, Kashef-Haghighi, Dorna, Hartl, Chris, Singh, Chanpreet, Xu, Jin, Hoekstra, Jackson N., Leventhal, Olivia, Leppa, Virpi M., Gandal, Michael J., Paskov, Kelley, Stockham, Nate, Polioudakis, Damon, Lowe, Jennifer K., Prober, David A., Geschwind, Daniel H., Wall, Dennis P.
izdano v Cell (2019)

Diagnostic utility of transcriptome sequencing for rare Mendelian diseases

od Lee, Hane, Huang, Alden Y., Wang, Lee-kai, Yoon, Amanda J., Renteria, Genecee, Eskin, Ascia, Signer, Rebecca H., Dorrani, Naghmeh, Nieves-Rodriguez, Shirley, Wan, Jijun, Douine, Emilie D., Woods, Jeremy D., Dell’Angelica, Esteban C., Fogel, Brent L., Martin, Martin G., Butte, Manish J., Parker, Neil H., Wang, Richard T., Shieh, Perry B., Wong, Derek A., Gallant, Natalie, Singh, Kathryn E., Asher, Y. Jane Tavyev, Sinsheimer, Janet S., Krakow, Deborah, Loo, Sandra K., Allard, Patrick, Papp, Jeanette C., Palmer, Christina G. S., Martinez-Agosto, Julian A., Nelson, Stanley F.
izdano v Genet Med (2019)