A multi-omic analysis of MCF10A cells provides a resource for integrative assessment of ligand-mediated molecular and phenotypic responses von Gross, Sean M., Dane, Mark A., Smith, Rebecca L., Devlin, Kaylyn L., McLean, Ian C., Derrick, Daniel S., Mills, Caitlin E., Subramanian, Kartik, London, Alexandra B., Torre, Denis, Evangelista, John Erol, Clarke, Daniel J. B., Xie, Zhuorui, Erdem, Cemal, Lyons, Nicholas, Natoli, Ted, Pessa, Sarah, Lu, Xiaodong, Mullahoo, James, Li, Jonathan, Adam, Miriam, Wassie, Brook, Liu, Moqing, Kilburn, David F., Liby, Tiera A., Bucher, Elmar, Sanchez-Aguila, Crystal, Daily, Kenneth, Omberg, Larsson, Wang, Yunguan, Jacobson, Connor, Yapp, Clarence, Chung, Mirra, Vidovic, Dusica, Lu, Yiling, Schurer, Stephan, Lee, Albert, Pillai, Ajay, Subramanian, Aravind, Papanastasiou, Malvina, Fraenkel, Ernest, Feiler, Heidi S., Mills, Gordon B., Jaffe, Jake D., Ma’ayan, Avi, Birtwistle, Marc R., Sorger, Peter K., Korkola, James E., Gray, Joe W., Heiser, Laura M.

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Comprehensive multi-omic profiling of somatic mutations in malformations of cortical development von Chung, Changuk, Yang, Xiaoxu, Bae, Taejeong, Vong, Keng Ioi, Mittal, Swapnil, Donkels, Catharina, Westley Phillips, H., Li, Zhen, Marsh, Ashley P. L., Breuss, Martin W., Ball, Laurel L., Garcia, Camila Araújo Bernardino, George, Renee D., Gu, Jing, Xu, Mingchu, Barrows, Chelsea, James, Kiely N., Stanley, Valentina, Nidhiry, Anna S., Khoury, Sami, Howe, Gabrielle, Riley, Emily, Xu, Xin, Copeland, Brett, Wang, Yifan, Kim, Se Hoon, Kang, Hoon-Chul, Schulze-Bonhage, Andreas, Haas, Carola A., Urbach, Horst, Prinz, Marco, Limbrick, David D., Gurnett, Christina A., Smyth, Matthew D., Sattar, Shifteh, Nespeca, Mark, Gonda, David D., Imai, Katsumi, Takahashi, Yukitoshi, Chen, Hsin-Hung, Tsai, Jin-Wu, Conti, Valerio, Guerrini, Renzo, Devinsky, Orrin, Silva, Wilson A., Machado, Helio R., Mathern, Gary W., Abyzov, Alexej, Baldassari, Sara, Baulac, Stéphanie, Gleeson, Joseph G.

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Control-independent mosaic single nucleotide variant detection with DeepMosaic von Yang, Xiaoxu, Xu, Xin, Breuss, Martin W., Antaki, Danny, Ball, Laurel L., Chung, Changuk, Shen, Jiawei, Li, Chen, George, Renee D., Wang, Yifan, Bae, Taejeong, Cheng, Yuhe, Abyzov, Alexej, Wei, Liping, Alexandrov, Ludmil B., Sebat, Jonathan L., Gleeson, Joseph G.

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Using brain cell-type-specific protein interactomes to interpret neurodevelopmental genetic signals in schizophrenia von Liu, Ruize, Nacu, Eugeniu, Petrossian, Natalie, Ching, Joshua K.T., Malolepsza, Edyta, Egri, Shawn B., Apffel, Annie M., Neale, Benjamin M., Farh, Kai-How, Huang, Hailiang, Albus, Margot, Bacanu, Silviu A., Belliveau, Richard A., Bergen, Sarah E., Buckner, Randy L., Cahn, Wiepke, Cai, Guiqing, Catts, Stanley V., Chambert, Kimberley D., Chen, Eric Y.H., Cloninger, C. Robert, Duan, Jubao, Durmishi, Naser, Eichhammer, Peter, Farrell, Martilias S., Frank, Josef, Friedman, Joseph I., Genovese, Giulio, Giegling, Ina, Giusti-Rodríguez, Paola, Golimbet, Vera, Hartmann, Annette M., Herms, Stefan, Hofman, Andrea, Hollegaard, Mads V., Karachanak-Yankova, Sena, Keller, Matthew C., Kennedy, James L., Kim, Yunjung, Konte, Bettina, Kucinskas, Vaidutis, Kucinskiene, Zita Ausrele, Laurent, Claudine, Legge, Sophie E., Loughland, Carmel M., Lubinski, Jan, Macek, Milan, Maier, Wolfgang, Mesholam-Gately, Raquelle I., Metspalu, Andres, Mors, Ole, Myin-Germeys, Inez, Nertney, Deborah A., Nicodemus, Kristin K., Oh, Sang-Yun, Pantelis, Christos, Parkhomenko, Elena, Pocklington, Andrew J., Powell, John, Quested, Digby, Rasmussen, Henrik B., Richards, Alexander L., Salomaa, Veikko, Schulze, Thomas G., Sigurdsson, Engilbert, Sim, Kang, Stahl, Eli A., Stogmann, Elisabeth, Strengman, Eric, Suvisaari, Jaana, Szatkiewicz, Jin P., Tosato, Sarah, Webb, Bradley T., Witt, Stephanie H., Wormley, Brandon K., Zheng, Xuebin, Zimprich, Fritz, Wray, Naomi R., Andreassen, Ole A., Cichon, Sven, Knight, Jo, Levinson, Douglas F., McQuillin, Andrew, Moran, Jennifer L., Owen, Michael J., Petryshen, Tracey L., Posthuma, Danielle, Rujescu, Dan, Sham, Pak C., Werge, Thomas, Qin, Shengying, Sawa, Akira, Glatt, Stephen J., Tang, Jinsong, Liu, Ruize, Horiuchi, Yasue, Myung, Woojae, Ozeki, Yuji, Kim, Se Hyun, Fornelos, Nadine

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ASXL1 Mutations Promote Myeloid Transformation Through Inhibition of PRC2-Mediated Gene Repression von Abdel-Wahab, Omar, Adli, Mazhar, Saunders, Lindsay, Gao, Jie, Shih, Alan H., Pandey, Suveg, Jaffe, Jake, Zhao, Xinyang, Perna, Fabiana, Carroll, Martin, Melnick, Ari, Nimer, Stephen D., Aifantis, Iannis, Bernstein, Bradley, Levine, Ross L

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Antibody-mediated rejection of human orthotopic liver allografts. A study of liver transplantation across ABO blood group barriers von Demetris, AJ, Jaffe, R, Tzakis, A, Ramsey, G, Todo, S, Belle, S, Esquivel, C, Shapiro, R, Markus, B, Mroczek, E

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Recurrent hepatitis B in liver allograft recipients. Differentiation between viral hepatitis B and rejection von Demetris, AJ, Jaffe, R, Sheahan, DG, Burnham, J, Spero, J, Iwatsuki, S, Van Theil, DH, Starzl, TE

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Occurrence of cytomegalovirus hepatitis in liver transplant patients von Bronsther, Oscar, Makowka, Leonard, Jaffe, Ronald, Demetris, A. Jake, Breinig, Mary Kay, Ho, Monto, Esquivel, Carlos O., Gordon, Robert D., Iwatsuki, Shunzaburo, Tzakis, Andreas, Marsh Jr, James W., Mazzaferro, Vincenzo, Van Thiel, David, Starzl, Thomas E.

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