Neuromagnetic Oscillations Predict Evoked-Response Latency Delays and Core Language Deficits in Autism Spectrum Disorders von Edgar, J. Christopher, Khan, Sarah Y., Blaskey, Lisa, Chow, Vivian Y., Rey, Michael, Gaetz, William, Cannon, Katelyn M., Monroe, Justin F., Cornew, Lauren, Qasmieh, Saba, Liu, Song, Welsh, John P., Levy, Susan E., Roberts, Timothy P. L.

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Auditory Magnetic Mismatch Field Latency: A Biomarker for Language Impairment in Autism von Roberts, Timothy P.L, Cannon, Katelyn M, Tavabi, Kambiz, Blaskey, Lisa, Khan, Sarah Y, Monroe, Justin F, Qasmieh, Saba, Levy, Susan E, Edgar, J. Christopher

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Missing and delayed auditory responses in young and older children with autism spectrum disorders von Edgar, J Christopher, Lanza, Matthew R, Daina, Aleksandra B, Monroe, Justin F, Khan, Sarah Y, Blaskey, Lisa, Cannon, Katelyn M, Jenkins, 3rd, Julian, Qasmieh, Saba, Levy, Susan E, Roberts, Timothy P L

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Resting-State Alpha in Autism Spectrum Disorder and Alpha Associations with Thalamic Volume von Edgar, J. Christopher, Heiken, Kory, Chen, Yu-Han, Herrington, John D., Chow, Vivian, Liu, Song, Bloy, Luke, Huang, Mingxiong, Pandey, Juhi, Cannon, Katelyn M., Qasmieh, Saba, Levy, Susan E., Schultz, Robert T., Roberts, Timothy P. L.

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Reprogramming the antigen specificity of B cells using genome-editing technologies von Voss, James E, Gonzalez-Martin, Alicia, Andrabi, Raiees, Fuller, Roberta P, Murrell, Ben, McCoy, Laura E, Porter, Katelyn, Huang, Deli, Li, Wenjuan, Sok, Devin, Le, Khoa, Briney, Bryan, Chateau, Morgan, Rogers, Geoffrey, Hangartner, Lars, Feeney, Ann J, Nemazee, David, Cannon, Paula, Burton, Dennis R

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MEG detection of delayed auditory evoked responses in autism spectrum disorders: towards an imaging biomarker for autism von Roberts, Timothy P.L., Khan, Sarah Y., Rey, Mike, Monroe, Justin F., Cannon, Katelyn, Blaskey, Lisa, Woldoff, Sarah, Qasmieh, Saba, Gandal, Mike, Schmidt, Gwen L., Zarnow, Deborah M., Levy, Susan E., Edgar, J. Christopher

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Multi-ancestry genome-wide association meta-analysis of Parkinson’s disease von Kim, Jonggeol Jeffrey, Vitale, Dan, Otani, Diego Véliz, Lian, Michelle Mulan, Heilbron, Karl, Iwaki, Hirotaka, Lake, Julie, Solsberg, Caroline Warly, Leonard, Hampton, Makarious, Mary B., Tan, Eng-King, Singleton, Andrew B., Bandres-Ciga, Sara, Noyce, Alastair J., Blauwendraat, Cornelis, Nalls, Mike A., Foo, Jia Nee, Mata, Ignacio

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Predictors of initial management failure in traumatic hemothorax: A prospective multicenter cohort analysis von Beyer, Carl A., Byrne, James P., Moore, Sarah A., McLauchlan, Nathaniel R., Rezende-Neto, Joao B., Schroeppel, Thomas J., Dodgion, Christopher, Inaba, Kenji, Seamon, Mark J., Cannon, Jeremy W., Afif, Iman, Beyer, Carl A., Cannon, Jeremy W., McLauchlan, Nathaniel R., Seamon, Mark J., Prakash, Priya S., Moore, Sarah A., Byrne, James P., Rezende-Neto, Joao B., Trpcic, Sandy, Semprun, Carlos, Dunn, Julie A., Smoot, Brittany, Schmitzer, Peggy, Jenkins, Donald H., Cardenas, Tatiana, DeRosa, Mark, Barry, Lauran, Pedraza, Santiago, Talathoti, Naresh, Coimbra, Raul, Mukherjee, Kaushik, Farnsworth, Joshua, Luo-Owen, Xian, Wild, Jeffrey, Young, Katelyn, Cole, Joshua, Torres, Denise, Schroeppel, Thomas J., Lee, Jeanne, Curry, Terry G., Skarupa, David J., Mull, Jennifer, Sabra, Michel J., Carrick, Matthew M., Rodkey, Kathy, Moore, Forrest O., Ward, Jeanette, Geng, Thomas, Lapham, David, Ong, Adrian, Piccinini, Alice, Inaba, Kenji, Dodgion, Christopher, Walsh, Pamela, Gooley, Brian, Schwartz, Tim, Shraga, Sarrina, Haan, James M., Lightwine, Kelly, Burris, Jennifer, Agrawal, Vaidehi, Hartline, Cassie

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Genetic analysis and natural history of Parkinson's disease due to the LRRK2 G2019S variant von Kmiecik, Matthew J, Micheletti, Steven, Coker, Daniella, Heilbron, Karl, Shi, Jingchunzi, Stagaman, Keaton, Filshtein Sonmez, Teresa, Fontanillas, Pierre, Shringarpure, Suyash, Wetzel, Madeleine, Rowbotham, Helen M, Cannon, Paul, Shelton, Janie F, Hinds, David A, Tung, Joyce Y, Holmes, Michael V, Aslibekyan, Stella, Norcliffe-Kaufmann, Lucy

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