Longitudinal molecular trajectories of diffuse glioma in adults von Barthel, Floris P., Johnson, Kevin C., Varn, Frederick S., Moskalik, Anzhela D., Tanner, Georgette, Kocakavuk, Emre, Anderson, Kevin J., Abiola, Olajide, Aldape, Kenneth, Alfaro, Kristin D., Alpar, Donat, Amin, Samirkumar B., Ashley, David M., Bandopadhayay, Pratiti, Barnholtz-Sloan, Jill S., Beroukhim, Rameen, Bock, Christoph, Brastianos, Priscilla K., Brat, Daniel J., Brodbelt, Andrew R., Bruns, Alexander F., Bulsara, Ketan R., Chakrabarty, Aruna, Chakravarti, Arnab, Chuang, Jeffrey H., Claus, Elizabeth B., Cochran, Elizabeth J., Connelly, Jennifer, Costello, Joseph F., Finocchiaro, Gaetano, Fletcher, Michael N., French, Pim J., Gan, Hui K., Gilbert, Mark R., Gould, Peter V., Grimmer, Matthew R., Iavarone, Antonio, Ismail, Azzam, Jenkinson, Michael D., Khasraw, Mustafa, Kim, Hoon, Kouwenhoven, Mathilde C. M., LaViolette, Peter S., Li, Meihong, Lichter, Peter, Ligon, Keith L., Lowman, Allison K., Malta, Tathiane M., Mazor, Tali, McDonald, Kerrie L., Molinaro, Annette M., Nam, Do-Hyun, Nayyar, Naema, Ng, Ho Keung, Ngan, Chew Yee, Niclou, Simone P., Niers, Johanna M., Noushmehr, Houtan, Noorbakhsh, Javad, Ormond, D. Ryan, Park, Chul-Kee, Poisson, Laila M., Rabadan, Raul, Radlwimmer, Bernhard, Rao, Ganesh, Reifenberger, Guido, Sa, Jason K., Schuster, Michael, Shaw, Brian L., Short, Susan C., Smitt, Peter A. Sillevis, Sloan, Andrew E., Smits, Marion, Suzuki, Hiromichi, Tabatabai, Ghazaleh, Van Meir, Erwin G., Watts, Colin, Weller, Michael, Wesseling, Pieter, Westerman, Bart A., Widhalm, Georg, Woehrer, Adelheid, Yung, W. K. Alfred, Zadeh, Gelareh, Huse, Jason T., De Groot, John F., Stead, Lucy F., Verhaak, Roel G. W.

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Recurrent somatic alterations of FGFR1 and NTRK2 in pilocytic astrocytoma von Jones, David T W, Hutter, Barbara, Jäger, Natalie, Korshunov, Andrey, Kool, Marcel, Warnatz, Hans-Jörg, Zichner, Thomas, Lambert, Sally R, Ryzhova, Marina, Quang, Dong Anh Khuong, Fontebasso, Adam M, Stütz, Adrian M, Hutter, Sonja, Zuckermann, Marc, Sturm, Dominik, Gronych, Jan, Lasitschka, Bärbel, Schmidt, Sabine, Şeker-Cin, Huriye, Witt, Hendrik, Sultan, Marc, Ralser, Meryem, Northcott, Paul A, Hovestadt, Volker, Bender, Sebastian, Pfaff, Elke, Stark, Sebastian, Faury, Damien, Schwartzentruber, Jeremy, Majewski, Jacek, Weber, Ursula D, Zapatka, Marc, Raeder, Benjamin, Schlesner, Matthias, Worth, Catherine L, Bartholomae, Cynthia C, von Kalle, Christof, Imbusch, Charles D, Radomski, Sylwester, Lawerenz, Chris, van Sluis, Peter, Koster, Jan, Volckmann, Richard, Versteeg, Rogier, Lehrach, Hans, Monoranu, Camelia, Winkler, Beate, Unterberg, Andreas, Herold-Mende, Christel, Milde, Till, Kulozik, Andreas E, Ebinger, Martin, Schuhmann, Martin U, Cho, Yoon-Jae, Pomeroy, Scott L, von Deimling, Andreas, Witt, Olaf, Taylor, Michael D, Wolf, Stephan, Karajannis, Matthias A, Eberhart, Charles G, Scheurlen, Wolfram, Hasselblatt, Martin, Ligon, Keith L, Kieran, Mark W, Korbel, Jan O, Yaspo, Marie-Laure, Brors, Benedikt, Felsberg, Jörg, Reifenberger, Guido, Collins, V Peter, Jabado, Nada, Eils, Roland, Lichter, Peter

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Histone H3.3G34-Mutant Interneuron Progenitors Co-opt PDGFRA for Gliomagenesis von Chen, Carol C.L., Deshmukh, Shriya, Jessa, Selin, Hadjadj, Djihad, Lisi, Véronique, Andrade, Augusto Faria, Faury, Damien, Jawhar, Wajih, Dali, Rola, Suzuki, Hiromichi, Pathania, Manav, A, Deli, Dubois, Frank, Woodward, Eleanor, Hébert, Steven, Coutelier, Marie, Karamchandani, Jason, Albrecht, Steffen, Brandner, Sebastian, De Jay, Nicolas, Gayden, Tenzin, Bajic, Andrea, Harutyunyan, Ashot S., Marchione, Dylan M., Mikael, Leonie G., Juretic, Nikoleta, Zeinieh, Michele, Russo, Caterina, Maestro, Nicola, Bassenden, Angelia V., Hauser, Peter, Virga, József, Bognar, Laszlo, Klekner, Almos, Zapotocky, Michal, Vicha, Ales, Krskova, Lenka, Vanova, Katerina, Zamecnik, Josef, Sumerauer, David, Ekert, Paul G., Ziegler, David S., Ellezam, Benjamin, Filbin, Mariella G., Blanchette, Mathieu, Hansford, Jordan R., Khuong-Quang, Dong-Anh, Berghuis, Albert M., Weil, Alexander G., Garcia, Benjamin A., Garzia, Livia, Mack, Stephen C., Beroukhim, Rameen, Ligon, Keith L., Taylor, Michael D., Bandopadhayay, Pratiti, Kramm, Christoph, Pfister, Stefan M., Korshunov, Andrey, Sturm, Dominik, Jones, David T.W., Salomoni, Paolo, Kleinman, Claudia L., Jabado, Nada

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Identification of a candidate tumour suppressor gene, MMAC1, at chromosome 10q23.3 that is mutated in multiple advanced cancers von Steck, Peter A., Pershouse, Mark A., Jasser, Samar A., Yung, W.K. Alfred, Lin, Huai, Ligon, Azra H., Langford, Lauren A., Baumgard, Michelle L., Hattier, Thomas, Davis, Thaylon, Frye, Cheryl, Hu, Rong, Swedlund, Bradley, Teng, David H.R., Tavtigian, Sean V.

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Interrogation of gossypol therapy in glioblastoma implementing cell line and patient-derived tumour models von Jarzabek, M A, Amberger-Murphy, V, Callanan, J J, Gao, C, Zagozdzon, A M, Shiels, L, Wang, J, Ligon, K L, Rich, B E, Dicker, P, Gallagher, W M, Prehn, J H M, Byrne, A T

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Mutations in GBA are associated with familial Parkinson disease susceptibility and age at onset von NICHOLS, W. C, PANKRATZ, N, MAREK, D. K, PAUCIULO, M. W, ELSAESSER, V. E, HALTER, C. A, RUDOLPH, A, WOJCIESZEK, J, PFEIFFER, R. F, FOROUD, T

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Meta-analysis of Parkinson's Disease: Identification of a novel locus, RIT2 von Pankratz, Nathan, Beecham, Gary W., DeStefano, Anita L., Dawson, Ted M., Doheny, Kimberly F., Factor, Stewart A., Hamza, Taye H., Hung, Albert Y., Hyman, Bradley T., Ivinson, Adrian J., Krainc, Dmitri, Latourelle, Jeanne C., Clark, Lorraine N., Marder, Karen, Martin, Eden R., Mayeux, Richard, Ross, Owen A., Scherzer, Clemens R., Simon, David K., Tanner, Caroline, Vance, Jeffery M., Wszolek, Zbigniew K., Zabetian, Cyrus P., Myers, Richard H., Payami, Haydeh, Scott, William K., Foroud, Tatiana

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Integration of cytogenetic landmarks into the draft sequence of the human genome von Cheung, V G, Nowak, N, Jang, W, Kirsch, I R, Zhao, S, Chen, X N, Furey, T S, Kim, U J, Kuo, W L, Olivier, M, Conroy, J, Kasprzyk, A, Massa, H, Yonescu, R, Sait, S, Thoreen, C, Snijders, A, Lemyre, E, Bailey, J A, Bruzel, A, Burrill, W D, Clegg, S M, Collins, S, Dhami, P, Friedman, C, Han, C S, Herrick, S, Lee, J, Ligon, A H, Lowry, S, Morley, M, Narasimhan, S, Osoegawa, K, Peng, Z, Plajzer-Frick, I, Quade, B J, Scott, D, Sirotkin, K, Thorpe, A A, Gray, J W, Hudson, J, Pinkel, D, Ried, T, Rowen, L, Shen-Ong, G L, Strausberg, R L, Birney, E, Callen, D F, Cheng, J F, Cox, D R, Doggett, N A, Carter, N P, Eichler, E E, Haussler, D, Korenberg, J R, Morton, C C, Albertson, D, Schuler, G, de Jong, P J, Trask, B J

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Myxopapillary ependymomas in children: imaging, treatment and outcomes von Bandopadhayay, Pratiti, Silvera, V. Michelle, Ciarlini, Pedro D. S. C., Malkin, Hayley, Bi, Wenya Linda, Bergthold, Guillaume, Faisal, Ahmed M., Ullrich, Nicole J., Marcus, Karen, Scott, R. Michael, Beroukhim, Rameen, Manley, Peter E., Chi, Susan N., Ligon, Keith L., Goumnerova, Liliana C., Kieran, Mark W.

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Exploring Expedition from Victoria to the Gulf of Carpentaria, under the Command of Mr. Robert O'Hara Burke von Howitt, A. W., Robert O'Hara Burke, King, John, Mueller, Fred, Wills, W. J., Wright, W., Brahé, William, Ligon, C. W. V., MacAdam, John, Smith, James, Mr. Archer

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Neuronal differentiation and cell-cycle programs mediate response to BET-bromodomain inhibition in MYC-driven medulloblastoma von Bandopadhayay, Pratiti, Piccioni, Federica, O’Rourke, Ryan, Ho, Patricia, Gonzalez, Elizabeth M., Buchan, Graham, Qian, Kenin, Gionet, Gabrielle, Girard, Emily, Coxon, Margo, Rees, Matthew G., Brenan, Lisa, Dubois, Frank, Shapira, Ofer, Greenwald, Noah F., Pages, Melanie, Balboni Iniguez, Amanda, Paolella, Brenton R., Meng, Alice, Sinai, Claire, Roti, Giovanni, Dharia, Neekesh V., Creech, Amanda, Tanenbaum, Benjamin, Khadka, Prasidda, Tracy, Adam, Tiv, Hong L., Hong, Andrew L., Coy, Shannon, Rashid, Rumana, Lin, Jia-Ren, Cowley, Glenn S., Lam, Fred C., Goodale, Amy, Lee, Yenarae, Schoolcraft, Kathleen, Vazquez, Francisca, Hahn, William C., Tsherniak, Aviad, Bradner, James E., Yaffe, Michael B., Milde, Till, Pfister, Stefan M., Qi, Jun, Schenone, Monica, Carr, Steven A., Ligon, Keith L., Kieran, Mark W., Santagata, Sandro, Olson, James M., Gokhale, Prafulla C., Jaffe, Jacob D., Root, David E., Stegmaier, Kimberly, Johannessen, Cory M., Beroukhim, Rameen

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Genomewide association study for susceptibility genes contributing to familial Parkinson disease von Pankratz, Nathan, Wilk, Jemma B, Latourelle, Jeanne C, DeStefano, Anita L, Halter, Cheryl, Pugh, Elizabeth W, Doheny, Kimberly F, Gusella, James F, Nichols, William C, Foroud, Tatiana, Myers, Richard H

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Clopidogrel as adjunctive antiplatelet therapy during coronary stenting von Mishkel, Gregory J, Aguirre, Frank V, Ligon, Robert W, Rocha-Singh, Krishna J, Lucore, Charles L

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AsthmaMap: an interactive knowledge repository for mechanisms of asthma von Mazein, A, Ivanova, O, Balaur, I, Ostaszewski, M, Berzhitskaya, V, Serebriyskaya, T, Ligon, T, Hasenauer, J, De Meulder, B, Overall, RW, Roy, L, Knowles, RG, Wheelock, CE, Dahlen, S-E, Chung, KF, Adcock, IM, Roberts, G, Djukanovic, R, Pellet, J, Gawron, P, Balling, R, Maitland-van der Zee, AH, Schneider, R, Sterk, PJ, Auffray, C

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Parkin dosage mutations have greater pathogenicity in familial PD than simple sequence mutations von PANKRATZ, N, KISSELL, D. K, PAUCIULO, M. W, HALTER, C. A, RUDOLPH, A, PFEIFFER, R. F, MARDER, K. S, FOROUD, T, NICHOLS, W. C

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Copy number variation in familial Parkinson disease von Pankratz, Nathan, Dumitriu, Alexandra, Hetrick, Kurt N, Sun, Mei, Latourelle, Jeanne C, Wilk, Jemma B, Halter, Cheryl, Doheny, Kimberly F, Gusella, James F, Nichols, William C, Myers, Richard H, Foroud, Tatiana, DeStefano, Anita L

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Variation in GIGYF2 is not associated with Parkinson disease von NICHOLS, W. C, KISSELL, D. K, FOROUD, T, PANKRATZ, N, PAUCIULO, M. W, ELSAESSER, V. E, CLARK, K. A, HALTER, C. A, RUDOLPH, A, WOJCIESZEK, J, PFEIFFER, R. F

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CB-04 EPIGENETIC REGULATION OF GLIOBLASTOMA TUMORIGENICITY: A HYBRID MODEL von Chen, C., Kozono, D., Li, J., Nitta, M., Sampetrean, O., Gonda, D., Kushwaha, D., Vandenberg, S., Ramakrishnan, V., Zhu, S., Furnari, F., Matsui, H., Harismendy, O., Cavenee, W., Mao, Y., Becher, O., Kwon, C.-H., Ligon, K., Saya, H., Carter, B.

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Genomewide association study for onset age in Parkinson disease von Latourelle, Jeanne C, Pankratz, Nathan, Dumitriu, Alexandra, Wilk, Jemma B, Goldwurm, Stefano, Pezzoli, Gianni, Mariani, Claudio B, DeStefano, Anita L, Halter, Cheryl, Gusella, James F, Nichols, William C, Myers, Richard H, Foroud, Tatiana

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Results of Treatment With Telmisartan‐Amlodipine in Hypertensive Patients von Littlejohn, Thomas W., Majul, Claudio R., Olvera, Rafael, Seeber, Mary, Kobe, Maureen, Guthrie, Robert, Oigman, Wille

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