Výsledky vyhledávání - Gockley, Jake

Origin and evolution of developmental enhancers in the mammalian neocortex Autor Emera, Deena, Yin, Jun, Reilly, Steven K., Gockley, Jake, Noonan, James P.

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The female protective effect in autism spectrum disorder is not mediated by a single genetic locus Autor Gockley, Jake, Willsey, A Jeremy, Dong, Shan, Dougherty, Joseph D, Constantino, John N, Sanders, Stephan J

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Massively parallel discovery of human-specific substitutions that alter enhancer activity Autor Uebbing, Severin, Gockley, Jake, Reilly, Steven K., Kocher, Acadia A., Geller, Evan, Gandotra, Neeru, Scharfe, Curt, Cotney, Justin, Noonan, James P.

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Multi-tissue neocortical transcriptome-wide association study implicates 8 genes across 6 genomic loci in Alzheimer’s disease Autor Gockley, Jake, Montgomery, Kelsey S., Poehlman, William L., Wiley, Jesse C., Liu, Yue, Gerasimov, Ekaterina, Greenwood, Anna K., Sieberts, Solveig K., Wingo, Aliza P., Wingo, Thomas S., Mangravite, Lara M., Logsdon, Benjamin A.

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The AD Knowledge Portal: A Repository for Multi‐Omic Data on Alzheimer's Disease and Aging Autor Greenwood, Anna K., Montgomery, Kelsey S., Kauer, Nicole, Woo, Kara H., Leanza, Zoe J., Poehlman, William L., Gockley, Jake, Sieberts, Solveig K., Bradic, Ljubomir, Logsdon, Benjamin A., Peters, Mette A., Omberg, Larsson, Mangravite, Lara M.

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Integrating human brain proteomes with genome-wide association data implicates new proteins in Alzheimer’s disease pathogenesis Autor Wingo, Aliza P., Liu, Yue, Gerasimov, Ekaterina S., Gockley, Jake, Logsdon, Benjamin A., Duong, Duc M., Dammer, Eric B., Robins, Chloe, Beach, Thomas G., Reiman, Eric M., Epstein, Michael P., De Jager, Philip L., Lah, James J., Bennett, David A., Seyfried, Nicholas T., Levey, Allan I., Wingo, Thomas S.

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Integrating human brain proteomes with genome-wide association data implicates novel proteins in post-traumatic stress disorder Autor Wingo, Thomas S., Gerasimov, Ekaterina S., Liu, Yue, Duong, Duc M., Vattathil, Selina M., Lori, Adriana, Gockley, Jake, Breen, Michael S., Maihofer, Adam X., Nievergelt, Caroline M., Koenen, Karestan C., Levey, Daniel F., Gelernter, Joel, Stein, Murray B., Ressler, Kerry J., Bennett, David A., Levey, Allan I., Seyfried, Nicholas T., Wingo, Aliza P.

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Brain proteome-wide association study implicates novel proteins in depression pathogenesis Autor Wingo, Thomas S., Liu, Yue, Gerasimov, Ekaterina S., Gockley, Jake, Logsdon, Benjamin A., Duong, Duc M., Dammer, Eric B., Lori, Adriana, Kim, Paul J., Ressler, Kerry J., Beach, Thomas G., Reiman, Eric M., Epstein, Michael P., De Jager, Philip L., Lah, James J., Bennett, David A., Seyfried, Nicholas T., Levey, Allan I., Wingo, Aliza P.

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Coexpression networks implicate human midfetal deep cortical projection neurons in the pathogenesis of autism Autor Willsey, A. Jeremy, Sanders, Stephan J., Li, Mingfeng, Dong, Shan, Tebbenkamp, Andrew T., Muhle, Rebecca A., Reilly, Steven K., Lin, Leon, Fertuzinhos, Sofia, Miller, Jeremy A., Murtha, Michael T., Bichsel, Candace, Niu, Wei, Cotney, Justin, Ercan-Sencicek, A. Gulhan, Gockley, Jake, Gupta, Abha, Han, Wenqi, He, Xin, Hoffman, Ellen, Klei, Lambertus, Lei, Jing, Liu, Wenzhong, Liu, Li, Lu, Cong, Xu, Xuming, Zhu, Ying, Mane, Shrikant M., Lein, Edward S., Wei, Liping, Noonan, James P., Roeder, Kathryn, Devlin, Bernie, Šestan, Nenad, State, Matthew W.

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Bone marrow microenvironments that contribute to patient outcomes in newly diagnosed multiple myeloma: A cohort study of patients in the Total Therapy clinical trials Autor Danziger, Samuel A., McConnell, Mark, Gockley, Jake, Young, Mary H., Rosenthal, Adam, Schmitz, Frank, Reiss, David J., Farmer, Phil, Alapat, Daisy V., Singh, Amrit, Ashby, Cody, Bauer, Michael, Ren, Yan, Smith, Kelsie, Couto, Suzana S., van Rhee, Frits, Davies, Faith, Zangari, Maurizio, Petty, Nathan, Orlowski, Robert Z., Dhodapkar, Madhav V., Copeland, Wilbert B., Fox, Brian, Hoering, Antje, Fitch, Alison, Newhall, Katie, Barlogie, Bart, Trotter, Matthew W. B., Hershberg, Robert M., Walker, Brian A., Dervan, Andrew P., Ratushny, Alexander V., Morgan, Gareth J.

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De novo insertions and deletions of predominantly paternal origin are associated with autism spectrum disorder Autor Dong, Shan, Walker, Michael F., Carriero, Nicholas J., DiCola, Michael, Willsey, A. Jeremy, Ye, Adam Y., Waqar, Zainulabedin, Gonzalez, Luis E., Overton, John D., Frahm, Stephanie, Keaney, John F., Teran, Nicole A., Dea, Jeanselle, Mandell, Jeffrey D., Bal, Vanessa Hus, Sullivan, Catherine A., DiLullo, Nicholas M., Khalil, Rehab O., Gockley, Jake, Yuksel, Zafer, Sertel, Sinem M., Ercan-Sencicek, A. Gulhan, Gupta, Abha R., Mane, Shrikant M., Sheldon, Michael, Brooks, Andrew I., Roeder, Kathryn, Devlin, Bernie, State, Matthew W., Wei, Liping, Sanders, Stephan J.

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