Construction Law Graduate Studies around the World von Bell, Matthew, Gerber, Paula, Evans, Phil, Kirsh, Harvey J, Barrington, Louise, Britton, Philip, Green, Martin, McAdam, Brodie, Davenport, Dierdre, Ndekugri, Issaka, Frilet, Marc, Chan, Edwin H, Chao-Duivis, Monika, Auchie, Derek P, Chan, Philip, Sklar, Stanley P

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Molecular Landscape and Actionable Alterations in a Genomically Guided Cancer Clinical Trial: National Cancer Institute Molecular Analysis for Therapy Choice (NCI-MATCH) von Flaherty, Keith T, Gray, Robert J, Chen, Alice P, Li, Shuli, McShane, Lisa M, Patton, David, Hamilton, Stanley R, Williams, P Mickey, Iafrate, A John, Sklar, Jeffrey, Mitchell, Edith P, Harris, Lyndsay N, Takebe, Naoko, Sims, David J, Coffey, Brent, Fu, Tony, Routbort, Mark, Zwiebel, James A, Rubinstein, Larry V, Little, Richard F, Arteaga, Carlos L, Comis, Robert, Abrams, Jeffrey S, O'Dwyer, Peter J, Conley, Barbara A

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Analytical Validation of the Next-Generation Sequencing Assay for a Nationwide Signal-Finding Clinical Trial: Molecular Analysis for Therapy Choice Clinical Trial von Lih, Chih-Jian, Harrington, Robin D, Sims, David J, Harper, Kneshay N, Bouk, Courtney H, Datta, Vivekananda, Yau, Jonathan, Singh, Rajesh R, Routbort, Mark J, Luthra, Rajyalakshmi, Patel, Keyur P, Mantha, Geeta S, Krishnamurthy, Savitri, Ronski, Karyn, Walther, Zenta, Finberg, Karin E, Canosa, Sandra, Robinson, Hayley, Raymond, Amelia, Le, Long P, McShane, Lisa M, Polley, Eric C, Conley, Barbara A, Doroshow, James H, Iafrate, A John, Sklar, Jeffrey L, Hamilton, Stanley R, Williams, P Mickey

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The NCI-MATCH trial: lessons for precision oncology von O’Dwyer, Peter J., Gray, Robert J., Flaherty, Keith T., Chen, Alice P., Li, Shuli, Wang, Victoria, McShane, Lisa M., Patton, David R., Tricoli, James V., Williams, P. Mickey, Iafrate, A. John, Sklar, Jeffrey, Mitchell, Edith P., Takebe, Naoko, Sims, David J., Coffey, Brent, Fu, Tony, Routbort, Mark, Rubinstein, Larry V., Little, Richard F., Arteaga, Carlos L., Marinucci, Donna, Hamilton, Stanley R., Conley, Barbara A., Harris, Lyndsay N., Doroshow, James H.

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Modeling Linkage Disequilibrium Increases Accuracy of Polygenic Risk Scores von Gusev, Alexander, Ripke, Stephan, Walters, James T.R., Agartz, Ingrid, Albus, Margot, Bene, Judit, Bevilacqua, Elizabeth, Bigdeli, Tim B., Bruggeman, Richard, Buckner, Randy L., Carr, Vaughan J., Catts, Stanley V., Chan, Raymond C.K., Cheng, Wei, Cohen, Nadine, Curtis, David, Dikeos, Dimitris, Dinan, Timothy, Eriksson, Johan, Escott-Price, Valentina, Franke, Lude, Godard, Stephanie, Goldstein, Jacqueline I., de Haan, Lieuwe, Hartmann, Annette M., Hoffmann, Per, Hofman, Andrea, Hollegaard, Mads V., Hougaard, David M., Ikeda, Masashi, Kim, Yunjung, Kucinskas, Vaidutis, Laurent, Claudine, Limborska, Svetlana, Loughland, Carmel M., Macek, Milan, Marsal, Sara, Mattheisen, Manuel, Milanova, Vihra, Mors, Ole, Mortensen, Preben B., Olsen, Line, Parkhomenko, Elena, Paunio, Tiina, Pimm, Jonathan, Purcell, Shaun M., Reichenberg, Abraham, Reimers, Mark A., Richards, Alexander L., Roussos, Panos, Ruderfer, Douglas M., Sigurdsson, Engilbert, Silverman, Jeremy M., So, Hon-Cheong, Spencer, Chris C.A., Stefansson, Hreinn, Straub, Richard E., Strengman, Eric, Strohmaier, Jana, Svrakic, Dragan M., Tosato, Sarah, Veijola, Juha, Walsh, Dermot, Wang, Dai, Weiser, Mark, Wolen, Aaron R., Wong, Emily H.M., Stefansson, Kari, Andreassen, Ole A., Ehrenreich, Hannelore, Gill, Michael, Hultman, Christina M., Jablensky, Assen V., McQuillin, Andrew, Pato, Carlos N., Rietschel, Marcella, Sham, Pak C., Sklar, Pamela, Weinberger, Daniel R., Daly, Mark J., Crisponi, Laura, Figueroa, Jonine, Gaudet, Mia M., Hall, Per, Hein, Rebecca, Irwanto, Astrid, Johansson, Mattias, Lund, Eiliv, Peto, Julian, Rahman, Nazneen, Southey, Melissa C., Travis, Ruth, Waisfisz, Quinten, Pato, Carlos, Stahl, Eli, Belbin, Gillian, Kenny, Eimear E., Purcell, Shaun, Chasman, Daniel, Neale, Benjamin

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Gene expression imputation across multiple brain regions provides insights into schizophrenia risk von Huckins, Laura M., Dobbyn, Amanda, Ruderfer, Douglas M., Hoffman, Gabriel, Wang, Weiqing, Pardiñas, Antonio F., Rajagopal, Veera M., Als, Thomas D., T. Nguyen, Hoang, Girdhar, Kiran, Boocock, James, Roussos, Panos, Fromer, Menachem, Kramer, Robin, Domenici, Enrico, Gamazon, Eric R., Purcell, Shaun, Demontis, Ditte, Børglum, Anders D., Walters, James T. R., O’Donovan, Michael C., Sullivan, Patrick, Owen, Michael J., Devlin, Bernie, Sieberts, Solveig K., Cox, Nancy J., Im, Hae Kyung, Sklar, Pamela, Stahl, Eli A.

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The Genetics of the Mood Disorder Spectrum: Genome-wide Association Analyses of More Than 185,000 Cases and 439,000 Controls von de Leeuw, Christiaan A., McQuillin, Andrew, Ripke, Stephan, Trzaskowski, Maciej, Agerbo, Esben, Alliey-Rodriguez, Ney, Andlauer, Till F.M., Awasthi, Swapnil, Badner, Judith A., Bækvad-Hansen, Marie, Bøen, Erlend, Castelao, Enrique, Cerrato, Felecia, Cervantes, Pablo, Colodro-Conde, Lucía, Davies, Gail, Del-Favero, Jurgen, Dumont, Ashley, Fischer, Sascha B., Foo, Jerome C., Forty, Liz, Gordon, Scott D., Green, Melissa J., Grove, Jakob, Hansen, Christine Søholm, Hansen, Thomas F., Heilbronner, Urs, van Hemert, Albert M., Hipolito, Maria, Hoffmann, Per, Holland, Dominic, Jamain, Stéphane, Jansen, Rick, Johnson, Jessica S., de Jong, Simone, Hassan Kiadeh, Farnush Farhadi, Kraft, Julia, Krogh, Jesper, Lawson, William B., Li, Yihan, Maaser, Anna, MacKinnon, Dean F., Mahon, Pamela B., Maier, Robert M., Medland, Sarah E., Mehta, Divya, Mihailov, Evelin, Montgomery, Grant W., Mullins, Niamh, Nyholt, Dale R., Ösby, Urban, Peterson, Roseann E., Pistis, Giorgio, Reinbold, Céline S., Ryu, Euijung, Schoevers, Robert, Schork, Nicholas J., Schulte, Eva C., Shehktman, Tatyana, Streit, Fabian, Thompson, Robert C., Traylor, Matthew, Vedder, Helmut, Viktorin, Alexander, Visscher, Peter M., Watson, Stanley J., Weinsheimer, Shantel Marie, Wu, Yang, Zhang, Peng, Agartz, Ingrid, Backlund, Lena, Bellivier, Frank, Blackwood, Douglas H.R., Domenici, Enrico, Fullerton, Janice M., Goes, Fernando, Hayward, Caroline, Hultman, Christina M., Jones, Ian, Kahn, René S., Kloiber, Stefan, Leboyer, Marion, Li, Qingqin S., Lucae, Susanne, Madden, Pamela A.F., Magnusson, Patrik K., Martin, Nicholas G., Mortensen, Preben Bo, Neale, Benjamin M., Nordentoft, Merete, O'Donovan, Michael C., Pato, Carlos, Pato, Michele T., Penninx, Brenda W.J. H., Posthuma, Danielle, Stefansson, Kari, Vieta, Eduard, Di Florio, Arianna, Ophoff, Roel A., Wray, Naomi R.

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Genome-wide association study identifies five new schizophrenia loci von Ripke, Stephan, Sanders, Alan R, Kendler, Kenneth S, Levinson, Douglas F, Sklar, Pamela, Holmans, Peter A, Lin, Dan-Yu, Duan, Jubao, Ophoff, Roel A, Andreassen, Ole A, Scolnick, Edward, Cichon, Sven, St Clair, David, Corvin, Aiden, Gurling, Hugh, Werge, Thomas, Rujescu, Dan, Blackwood, Douglas H R, Pato, Carlos N, Malhotra, Anil K, Purcell, Shaun, Dudbridge, Frank, Neale, Benjamin M, Rossin, Lizzy, Visscher, Peter M, Posthuma, Danielle, Ruderfer, Douglas M, Fanous, Ayman, Stefansson, Hreinn, Steinberg, Stacy, Mowry, Bryan J, Golimbet, Vera, De Hert, Marc, Jonsson, Erik G, Bitter, Istvan, Pietilaeinen, Olli P H, Collier, David A, Tosato, Sarah, Agartz, Ingrid, Albus, Margot, Alexander, Madeline, Amdur, Richard L, Amin, Farooq, Bass, Nicholas, Bergen, Sarah E, Black, Donald W, Boerglum, Anders D, Brown, Matthew A, Bruggeman, Richard, Buccola, Nancy G

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Partitioning Heritability of Regulatory and Cell-Type-Specific Variants across 11 Common Diseases von Trynka, Gosia, Stahl, Eli, Neale, Benjamin M., Farh, Kai-How, Pers, Tune H., Albus, Margot, Cahn, Wiepke, Cai, Guiqing, Carr, Vaughan J., Carrera, Noa, Cheng, Wei, Cheung, Eric F.C., Cohen, David, Cormican, Paul, Craddock, Nick, Demontis, Ditte, Djurovic, Srdjan, Donohoe, Gary, Dudbridge, Frank, Durmishi, Naser, Eriksson, Johan, Farrell, Martilias S., Freimer, Nelson B., Fromer, Menachem, Godard, Stephanie, Goldstein, Jacqueline I., Grove, Jakob, Hartmann, Annette M., Henskens, Frans A., Herms, Stefan, Hirschhorn, Joel N., Hoffmann, Per, Hougaard, David M., Ikeda, Masashi, Julià, Antonio, Kelly, Brian J., Kennedy, James L., Kucinskas, Vaidutis, Kuzelova-Ptackova, Hana, Laurent, Claudine, Lee, S. Hong, Li, Tao, Lieberman, Jeffrey, Limborska, Svetlana, Loughland, Carmel M., Lnnqvist, Jouko, Marsal, Sara, McCarley, Robert W., Meijer, Carin J., Melegh, Bela, Melle, Ingrid, Milani, Lili, Mors, Ole, Myin-Germeys, Inez, Nikitina-Zake, Liene, O’Callaghan, Eadbhard, O’Dushlaine, Colm, O’Neill, F. Anthony, Oh, Sang-Yun, Pantelis, Christos, Parkhomenko, Elena, Perkins, Diana O., Powell, John, Quested, Digby, Salomaa, Veikko, Schubert, Christian R., Shi, Jianxin, Sigurdsson, Engilbert, Sim, Kang, Stogmann, Elisabeth, Strengman, Eric, Suvisaari, Jaana, Thirumalai, Srinivas, Veijola, Juha, Walsh, Dermot, Weiser, Mark, Witt, Stephanie H., Wong, Emily H.M., Wu, Jing Qin, Stefansson, Kari, Blackwood, Douglas H.R., Ehrenreich, Hannelore, Gurling, Hugh, Hultman, Christina M., Kirov, George, Malhotra, Anil K., McCarroll, Steven A., McQuillin, Andrew, Palotie, Aarno, Rietschel, Marcella, Sham, Pak C., O’Donovan, Michael C., Bergen, Sarah, Magnusson, Patrik K.E., Scolnick, Edward, Purcell, Shaun M., Pasaniuc, Bogdan, Sullivan, Patrick F., Raychaudhuri, Soumya, Price, Alkes L.

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Identification of Pathways for Bipolar Disorder: A Meta-analysis von Nurnberger, John I, Koller, Daniel L, Jung, Jeesun, Edenberg, Howard J, Foroud, Tatiana, Guella, Ilaria, Vawter, Marquis P, Kelsoe, John R

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Estimation of Genetic Correlation via Linkage Disequilibrium Score Regression and Genomic Restricted Maximum Likelihood von Moser, Gerhard, Ripke, Stephan, Walters, James T.R., Farh, Kai-How, Bulik-Sullivan, Brendan, Collier, David A., Agartz, Ingrid, Amin, Farooq, Begemann, Martin, Buccola, Nancy G., Byerley, William, Carr, Vaughan J., Carrera, Noa, Catts, Stanley V., Chong, Siow Ann, Craddock, Nick, Crowley, James J., Curtis, David, Davidson, Michael, Davis, Kenneth L., Demontis, Ditte, Dinan, Timothy, Donohoe, Gary, Drapeau, Elodie, Essioux, Laurent, Fanous, Ayman H., Franke, Lude, Georgieva, Lyudmila, Godard, Stephanie, Hammer, Christian, Hansen, Mark, Hansen, Thomas, Henskens, Frans A., Hirschhorn, Joel N., Hollegaard, Mads V., Hougaard, David M., Ikeda, Masashi, Joa, Inge, Juliá, Antonio, Kahn, René S., Karachanak-Yankova, Sena, Karjalainen, Juha, Khrunin, Andrey, Li, Miaoxin, Lieberman, Jeffrey, Lönnqvist, Jouko, Mattheisen, Manuel, Mattingsda, Morten, McDonald, Colm, Melle, Ingrid, Milanova, Vihra, Mokrab, Younes, Murray, Robin M., Nenadic, Igor, O’Neill, F. Anthony, Van Os, Jim, Papio, Sergi, Parkhomenko, Elena, Perkins, Diana O., Pietiläinenl, Olli, Pulver, Ann E., Purcell, Shaun M., Rasmussen, Henrik B., Reichenberg, Abraham, Richards, Alexander L., Ruderfer, Douglas M., Salomaa, Veikko, Sanders, Alan R., Scott, Rodney J., Silverman, Jeremy M., Smoller, Jordan W., So, Hon-Cheong, Spencer, Chris C.A., Stefansson, Hreinn, Stogmann, Elisabeth, Strengman, Eric, Svrakic, Dragan M., Söderman, Erik, Toncheva, Draga, Veijola, Juha, Walsh, Dermot, Weiser, Mark, Wildenauer, Dieter B., Williams, Nigel M., Williams, Stephanie, Witt, Stephanie H., Wolen, Aaron R., Xi, Hualin Simon, Zai, Clement C., Stefansson, Kari, Blackwood, Douglas H.R., Buxbaum, Joseph D., Esko, Tõnu, Gill, Michael, McQuillin, Andrew, Moran, Jennifer L., Petryshen, Tracey L., Rietsche, Marcella, Sham, Pak C., Weinberger, Daniel R.

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Schizophrenia risk conferred by rare protein-truncating variants is conserved across diverse human populations von Liu, Dongjing, Meyer, Dara, Fennessy, Brian, Feng, Claudia, Cheng, Esther, Johnson, Jessica S., Park, You Jeong, Rieder, Marysia-Kolbe, Ascolillo, Steven, de Pins, Agathe, Dobbyn, Amanda, Lebovitch, Dannielle, Moya, Emily, Nguyen, Tan-Hoang, Wilkins, Lillian, Hassan, Arsalan, Burdick, Katherine E., Buxbaum, Joseph D., Domenici, Enrico, Frangou, Sophia, Hartmann, Annette M., Laurent-Levinson, Claudine, Malhotra, Dheeraj, Pato, Carlos N., Pato, Michele T., Ressler, Kerry, Roussos, Panos, Rujescu, Dan, Arango, Celso, Bertolino, Alessandro, Blasi, Giuseppe, Bocchio-Chiavetto, Luisella, Campion, Dominique, Carr, Vaughan, Fullerton, Janice M., Gennarelli, Massimo, González-Peñas, Javier, Levinson, Douglas F., Mowry, Bryan, Nimgaokar, Vishwajit L., Pergola, Giulio, Rampino, Antonio, Cervilla, Jorge A., Rivera, Margarita, Schwab, Sibylle G., Wildenauer, Dieter B., Daly, Mark, Neale, Benjamin, Singh, Tarjinder, O’Donovan, Michael C., Owen, Michael J., Walters, James T., Ayub, Muhammad, Malhotra, Anil K., Lencz, Todd, Sullivan, Patrick F., Sklar, Pamela, Stahl, Eli A., Huckins, Laura M., Charney, Alexander W.

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A polygenic resilience score moderates the genetic risk for schizophrenia von Hess, Jonathan L., Tylee, Daniel S., Mattheisen, Manuel, Børglum, Anders D., Als, Thomas D., Grove, Jakob, Werge, Thomas, Mortensen, Preben Bo, Mors, Ole, Nordentoft, Merete, Hougaard, David M., Byberg-Grauholm, Jonas, Bækvad-Hansen, Marie, Greenwood, Tiffany A., Tsuang, Ming T., Curtis, David, Steinberg, Stacy, Sigurdsson, Engilbert, Stefánsson, Hreinn, Stefánsson, Kári, Edenberg, Howard J., Holmans, Peter, Faraone, Stephen V., Glatt, Stephen J.

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Analytical Validation of the Next-Generation Sequencing Assay for a Nationwide Signal-Finding Clinical Trial von Lih, Chih-Jian, Harrington, Robin D, Sims, David J, Harper, Kneshay N, Bouk, Courtney H, Datta, Vivekananda, Yau, Jonathan, Singh, Rajesh R, Routbort, Mark J, Luthra, Rajyalakshmi, Patel, Keyur P, Mantha, Geeta S, Krishnamurthy, Savitri, Ronski, Karyn, Walther, Zenta, Finberg, Karin E, Canosa, Sandra, Robinson, Hayley, Raymond, Amelia, Le, Long P, McShane, Lisa M, Polley, Eric C, Conley, Barbara A, Doroshow, James H, Iafrate, A. John, Sklar, Jeffrey L, Hamilton, Stanley R, Williams, P. Mickey

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Doravirine versus ritonavir-boosted darunavir in antiretroviral-naive adults with HIV-1 (DRIVE-FORWARD): 48-week results of a randomised, double-blind, phase 3, non-inferiority tri... von Squires, Kathleen, Cahn, Pedro, Lombaard, Johan, DeJesus, Edwin, Lai, Ming-Tain, Rodgers, Anthony, Kumar, Sushma, Sklar, Peter, Nguyen, Bach-Yen, Hanna, George J, Hwang, Carey, Martins, Marcelo, Bloch, Mark Theo, Baker, David Alfred, Roth, Norman, Moore, Richard James, McMahon, James, Rieger, Armin, Zoufaly, Alexander, Zangerle, Robert, Smaill, Fiona, Rachlis, Anita, Perez, Carlos, Campos Barker, Maria Isabel E., Wolff Reyes, Marcelo, Laursen, Alex Lund, Molina, Jean-Michel, Yazdanpanah, Yazdan, Cotte, Laurent, Raffi, Francois, Morlat, Philippe, Girard, Pierre-Marie, Katlama, Christine, Rockstroh, Juergen K., Arasteh, Keikawus, Stoehr, Albrecht, Stellbrink, Hans-Juergen, Stoll, Matthias, Schuermann, Dirk, Faetkenheuer, Gerd, Bogner, Johannes, Gori, Andrea, Coltan, Gabriel, Constandis, Felicia, Erscoiu, Simona Manuela, Pokrovsky, Vadim Valentinovich, Shuldyakov, Andrey Anatolyevich, Ryamova, Elena Pavlovna, Kulagin, Valeriy Viktorovich, Tsybakova, Olga Aleksandrovna, Orlova-Morozova, Elena, Shimonova, Tatyana Evgenyevna, Kozyrev, Oleg Anatolyevich, Orrell, Catherine, Lombaard, Johannes Jurgens, Botes, Margaretha Elizabeth, Portilla, Joaquin, Gatell, Josep Maria, Perez, Maria Jesus, Arribas, Jose Ramon, Negredo, Eugenia, Podzamczer, Daniel, Troya, Jesus, De los Santos, Ignacio, Berenguer, Juan, Williams, Ian G., Johnson, Margaret A., Schembri, Gabriel, Gompels, Mark, Fox, Julie Meriel, Taylor, Steven John, Kegg, Stephen, Hagins, Debbie P., Osiyemi, Olayemi O., Prelutsky, David James, Ramgopal, Moti N., Dretler, Robin, DeJesus, Edwin, Sloan, Louis, Lewis, Stanley T., Clay, Patrick G., Bellos, Nicholaos C., Montero, Jose, Creticos, Catherine, Shamblaw, David, Valdes, Martin, Felizarta, Franco Antonio, Slim, Jihad, Lalezari, Jacob Paul, Ruane, Peter Jerome, Cade, Jerry L., Campo, Rafael E., Blick, Gary, Mayer, Cynthia, Daar, Eric, Kumar, Princy N., Swindells, Susan, Castro, Jose Guillermo, Santiago, Lizette, Santana-Bagur, Jorge L.

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Publisher Correction: Gene expression imputation across multiple brain regions provides insights into schizophrenia risk von Huckins, Laura M., Dobbyn, Amanda, Ruderfer, Douglas M., Hoffman, Gabriel, Wang, Weiqing, Pardiñas, Antonio F., Rajagopal, Veera M., Als, Thomas D., T. Nguyen, Hoang, Girdhar, Kiran, Boocock, James, Roussos, Panos, Fromer, Menachem, Kramer, Robin, Domenici, Enrico, Gamazon, Eric R., Purcell, Shaun, Demontis, Ditte, Børglum, Anders D., Walters, James T. R., O’Donovan, Michael C., Sullivan, Patrick, Owen, Michael J., Devlin, Bernie, Sieberts, Solveig K., Cox, Nancy J., Im, Hae Kyung, Sklar, Pamela, Stahl, Eli A.

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Genetic Schizophrenia Risk Variants Jointly Modulate Total Brain and White Matter Volume von Terwisscha van Scheltinga, Afke F, Bakker, Steven C, van Haren, Neeltje E.M, Derks, Eske M, Buizer-Voskamp, Jacobine E, Boos, Heleen B.M, Cahn, Wiepke, Hulshoff Pol, Hilleke E, Ripke, Stephan, Ophoff, Roel A, Kahn, René S

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Rare coding variants in 10 genes confer substantial risk for schizophrenia von Singh, Tarjinder, Poterba, Timothy, Curtis, David, Akil, Huda, Al Eissa, Mariam, Barchas, Jack D., Bass, Nicholas, Bigdeli, Tim B., Breen, Gerome, Bromet, Evelyn J., Buckley, Peter F., Bunney, William E., Bybjerg-Grauholm, Jonas, Byerley, William F., Chapman, Sinéad B., Chen, Wei J., Churchhouse, Claire, Craddock, Nicholas, Cusick, Caroline M., DeLisi, Lynn, Dodge, Sheila, Escamilla, Michael A., Eskelinen, Saana, Fanous, Ayman H., Faraone, Stephen V., Fiorentino, Alessia, Francioli, Laurent, Gabriel, Stacey B., Gage, Diane, Taliun, Sarah A. Gagliano, Ganna, Andrea, Genovese, Giulio, Glahn, David C., Grove, Jakob, Hall, Mei-Hua, Hämäläinen, Eija, Heyne, Henrike O., Holi, Matti, Hougaard, David M., Howrigan, Daniel P., Huang, Hailiang, Hwu, Hai-Gwo, Kahn, René S., Kang, Hyun Min, Karczewski, Konrad J., Kirov, George, Knowles, James A., Lee, Francis S., Lehrer, Douglas S., Lescai, Francesco, Malaspina, Dolores, Marder, Stephen R., McCarroll, Steven A., McIntosh, Andrew M., Medeiros, Helena, Milani, Lili, Morley, Christopher P., Morris, Derek W., Bo Mortensen, Preben, Myers, Richard M., Nordentoft, Merete, O’Brien, Niamh L., Olivares, Ana Maria, Ongur, Dost, Ouwehand, Willem H., Palmer, Duncan S., Paunio, Tiina, Quested, Digby, Rapaport, Mark H., Rees, Elliott, Rollins, Brandi, Satterstrom, F. Kyle, Schatzberg, Alan, Scolnick, Edward, Scott, Laura J., Sharp, Sally I., Sklar, Pamela, Smoller, Jordan W., Sobell, Janet l., Solomonson, Matthew, Stevens, Christine R., Suvisaari, Jaana, Tiao, Grace, Watson, Stanley J., Watts, Nicholas A., Blackwood, Douglas H., Børglum, Anders D., Cohen, Bruce M., Corvin, Aiden P., Esko, Tõnu, Freimer, Nelson B., Glatt, Stephen J., Hultman, Christina M., McQuillin, Andrew, Palotie, Aarno, Pato, Carlos N., Pato, Michele T., Pulver, Ann E., St. Clair, David, Tsuang, Ming T.

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Design and development of the molecular analysis for Therapy Choice (NCI-MATCH) Designated Laboratory Network von Tricoli, James V., Zane, Linda, Harrington, Robin, Yee, Laura, Harper, Kneshay N., Chang, Ting-Chia, Harris, Lyndsay, Chen, Alice P., Flaherty, Keith, O'Dwyer, Peter J., Conley, Barbara A., Winter, Cynthia, Lee, Jennifer, Williams, Paul M., Sklar, Jeffrey, Patton, David, Tsongalis, Gregory J., Hamilton, Stanley R., Iafrate, A. John, Karlovich, Chris Alan

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Abstract B007: Concordance between tumor tissue and plasma genotyping in NCI-MATCH Trial (EAY131) von Gouda, Mohamed A, Janku, Filip, Yuan, Ying, Drusbosky, Leylah, Chen, Alice P, Patel, Keyur, Hamilton, Stanley R, Routbort, Mark, Williams, P. Mickey, Iafrate, John, Sklar, Jeffrey, Coffey, Brent, Little, Richard F, Arteaga, Carlos L, Abrams, Jeffrey S, O’Dwyer, Peter J, Flaherty, Keith T, Harris, Lyndsay N, Meric-Bernstam, Funda

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