Seismic design and hybrid tests of a full-scale three-story buckling-restrained braced frame using welded end connections and thin profile von Lin, Pao-Chun, Tsai, Keh-Chyuan, Wang, Kung-Juin, Yu, Yi-Jer, Wei, Chih-Yu, Wu, An-Chien, Tsai, Ching-Yi, Lin, Chih-Han, Chen, Jia-Chian, Schellenberg, Andreas H., Mahin, Stephen A., Roeder, Charles W.

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Real-Time Hybrid Simulation of Seismically Isolated Structures with Full-Scale Bearings and Large Computational Models von Sarebanha, Alireza, Schellenberg, Andreas H., Schoettler, Matthew J., Mosqueda, Gilberto, Mahin, Stephen A.

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Structural Finite Element Software Coupling Using Adapter Elements von Schellenberg, Andreas H., Huang, Yuli, Mahin, Stephen A.

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Hybrid shake table testing method: Theory, implementation and application to midlevel isolation von Schellenberg, Andreas H., Becker, Tracy C., Mahin, Stephen A.

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Hybrid shake table testing method: Theory, implementation and application to midlevel isolation von Schellenberg, Andreas H., Becker, Tracy C., Mahin, Stephen A.

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Deficiency of terminal ADP-ribose protein glycohydrolase TARG1/C6orf130 in neurodegenerative disease von Sharifi, Reza, Morra, Rosa, Denise Appel, C, Tallis, Michael, Chioza, Barry, Jankevicius, Gytis, Simpson, Michael A, Matic, Ivan, Ozkan, Ege, Golia, Barbara, Schellenberg, Matthew J, Weston, Ria, Williams, Jason G, Rossi, Marianna N, Galehdari, Hamid, Krahn, Juno, Wan, Alexander, Trembath, Richard C, Crosby, Andrew H, Ahel, Dragana, Hay, Ron, Ladurner, Andreas G, Timinszky, Gyula, Williams, R Scott, Ahel, Ivan

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RNA reference materials with defined viral RNA loads of SARS-CoV-2-A useful tool towards a better PCR assay harmonization von Vierbaum, Laura, Wojtalewicz, Nathalie, Grunert, Hans-Peter, Lindig, Vanessa, Duehring, Ulf, Drosten, Christian, Corman, Victor, Niemeyer, Daniela, Ciesek, Sandra, Rabenau, Holger F, Berger, Annemarie, Obermeier, Martin, Nitsche, Andreas, Michel, Janine, Mielke, Martin, Huggett, Jim, O'Sullivan, Denise, Busby, Eloise, Cowen, Simon, Vallone, Peter M, Cleveland, Megan H, Falak, Samreen, Kummrow, Andreas, Keller, Thomas, Schellenberg, Ingo, Zeichhardt, Heinz, Kammel, Martin

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Results of German external quality assessment schemes for SARS-CoV-2 antigen detection von Vierbaum, Laura, Wojtalewicz, Nathalie, Grunert, Hans-Peter, Zimmermann, Anika, Scholz, Annemarie, Goseberg, Sabine, Kaiser, Patricia, Duehring, Ulf, Drosten, Christian, Corman, Victor, Niemeyer, Daniela, Rabenau, Holger F., Obermeier, Martin, Nitsche, Andreas, Michel, Janine, Puyskens, Andreas, Huggett, Jim F., O’Sullivan, Denise M., Busby, Eloise, Cowen, Simon, Vallone, Peter M., Cleveland, Megan H., Falak, Samreen, Kummrow, Andreas, Schellenberg, Ingo, Zeichhardt, Heinz, Kammel, Martin

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Rates, distribution and implications of postzygotic mosaic mutations in autism spectrum disorder von Lim, Elaine T, Uddin, Mohammed, De Rubeis, Silvia, Chan, Yingleong, Kamumbu, Anne S, Zhang, Xiaochang, D'Gama, Alissa M, Kim, Sonia N, Hill, Robert Sean, Goldberg, Arthur P, Poultney, Christopher, Minshew, Nancy J, Kushima, Itaru, Aleksic, Branko, Ozaki, Norio, Parellada, Mara, Arango, Celso, Penzol, Maria J, Carracedo, Angel, Kolevzon, Alexander, Hultman, Christina M, Weiss, Lauren A, Fromer, Menachem, Chiocchetti, Andreas G, Freitag, Christine M, Church, George M, Scherer, Stephen W, Buxbaum, Joseph D, Walsh, Christopher A

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Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism von Satterstrom, F. Kyle, Breen, Michael S., Grove, Jakob, Klei, Lambertus, Xu, Xinyi, Norman, Utku, Brand, Harrison, Schwartz, Grace, Barbosa, Mafalda, Bybjerg-Grauholm, Jonas, Carracedo, Angel, Chiocchetti, Andreas G., Chung, Brian H.Y., Coon, Hilary, Cuccaro, Michael L., Dalla Bernardina, Bernardo, Domenici, Enrico, Dong, Shan, Freitag, Christine M., González-Peñas, Javier, Guter, Stephen, He, Xin, Herman, Gail E., Hertz-Picciotto, Irva, Hougaard, David M., Ionita-Laza, Iuliana, Jacob, Suma, Jamison, Jesslyn, Jugessur, Astanand, Kolevzon, Alexander, Kushima, Itaru, Lee, So Lun, Lehtimäki, Terho, Lim, Elaine T., Lipkin, W. Ian, Lopergolo, Diego, Lopes, Fátima, Ludena, Yunin, Maciel, Patricia, Meiri, Gal, Menashe, Idan, Miller, Judith, Montenegro, Eduarda M.S., Muglia, Pierandrea, Nordentoft, Merete, Ozaki, Norio, Palotie, Aarno, Parellada, Mara, Passos-Bueno, Maria Rita, Persico, Antonio M., Pessah, Isaac, Puura, Kaija, Renieri, Alessandra, Riberi, Evelise, Robinson, Elise B., Samocha, Kaitlin E., Sandin, Sven, Santangelo, Susan L., Schellenberg, Gerry, Scherer, Stephen W., Schmitt, Lauren, Silva, Isabela M.W., Singh, Tarjinder, Siper, Paige M., Soares, Gabriela, Susser, Ezra, Szatmari, Peter, Tang, Lara, Tassone, Flora, Teufel, Karoline, Trelles, Maria del Pilar, Werge, Thomas, Werling, Donna M., Wigdor, Emilie M., Yu, Mullin H.C., Zachi, Elaine, Agerbo, Esben, Als, Thomas Damm, Bækvad-Hansen, Marie, Belliveau, Rich, Cerrato, Felecia, Chambert, Kimberly, Churchhouse, Claire, Dumont, Ashley, Hansen, Christine S., Hauberg, Mads Engel, Hollegaard, Mads V., Howrigan, Daniel P., Maller, Julian, Mattheisen, Manuel, Moran, Jennifer, Pallesen, Jonatan, Poulsen, Jesper Buchhave, Ripke, Stephan, Gallagher, Louise, Gill, Michael, Zwick, Michael E., State, Matthew W., Daly, Mark J., Buxbaum, Joseph D.

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Opportunistic dried blood spot sampling validates and optimizes a pediatric population pharmacokinetic model of metronidazole von Randell, Rachel L, Balevic, Stephen J, Greenberg, Rachel G, Cohen-Wolkowiez, Michael, Thompson, Elizabeth J, Venkatachalam, Saranya, Smith, Michael J, Bendel, Catherine, Bliss, Joseph M, Chaaban, Hala, Chhabra, Rakesh, Dammann, Christiane E L, Downey, L Corbin, Hornik, Chi, Hussain, Naveed, Laughon, Matthew M, Lavery, Adrian, Moya, Fernando, Saxonhouse, Matthew, Sokol, Gregory M, Trembath, Andrea, Weitkamp, Joern-Hendrik, Hornik, Christoph P

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Meta-analysis of GWAS of over 16,000 individuals with autism spectrum disorder highlights a novel locus at 10q24.32 and a significant overlap with schizophrenia von The Psychiatric Genomics Consortium, The Autism Spectrum Disorders Working Group Of, Anney, Richard J L, Ripke, Stephan, Anttila, Verneri, Grove, Jakob, Holmans, Peter, Huang, Hailiang, Klei, Lambertus, Lee, Phil H, Medland, Sarah E, Neale, Benjamin, Robinson, Elise, Weiss, Lauren A, Zwaigenbaum, Lonnie, Yu, Timothy W, Wittemeyer, Kerstin, Willsey, a Jeremy, Wijsman, Ellen M, Werge, Thomas, Wassink, Thomas H, Waltes, Regina, Walsh, Christopher A, Wallace, Simon, Vorstman, Jacob a S, Vieland, Veronica J, Vicente, Astrid M, Vanengeland, Herman, Tsang, Kathryn, Thompson, Ann P, Szatmari, Peter, Svantesson, Oscar, Steinberg, Stacy, Stefansson, Kari, Stefansson, Hreinn, State, Matthew W, Soorya, Latha, Silagadze, Teimuraz, Scherer, Stephen W, Schellenberg, Gerard D, Sandin, Sven, Sanders, Stephan J, Saemundsen, Evald, Rouleau, Guy A, Rogé, Bernadette, Roeder, Kathryn, Roberts, Wendy, Reichert, Jennifer, Reichenberg, Abraham, Rehnström, Karola, Regan, Regina, Poustka, Fritz, Poultney, Christopher S, Piven, Joseph, Pinto, Dalila, Pericak-Vance, Margaret A, Pejovic-Milovancevic, Milica, Pedersen, Marianne Giørtz, Pedersen, Carsten Bøcker, Paterson, Andrew D, Parr, Jeremy R, Pagnamenta, Alistair T, Oliveira, Guiomar, Nurnberger, John I, Nordentoft, Merete, Murtha, Michael T, Mouga, Susana, Mortensen, Preben Bo, Mors, Ole, Morrow, Eric M, Moreno-De-Luca, Daniel, Monaco, Anthony P, Minshew, Nancy, Merikangas, Alison, Mcmahon, William M, Mcgrew, Susan G, Mattheisen, Manuel, Martsenkovsky, Igor, Martin, Donna M, Mane, Shrikant M, Magnusson, Pall, Magalhaes, Tiago, Maestrini, Elena, Lowe, Jennifer K, Lord, Catherine, Levitt, Pat, Martin, Christa Lese, Ledbetter, David H, Leboyer, Marion, Lecouteur, Ann S, Ladd-Acosta, Christine, Kolevzon, Alexander, Klauck, Sabine M, Jacob, Suma, Iliadou, Bozenna, Hultman, Christina M, Hougaard, David M, Hertz-Picciotto, Irva, Hendren, Robert, Hansen, Christine Søholm, Haines, Jonathan L

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Statistical and functional convergence of common and rare genetic influences on autism at chromosome 16p von Weiner, Daniel J., Ling, Emi, Erdin, Serkan, Tai, Derek J. C., Yadav, Rachita, Grove, Jakob, Fu, Jack M., Nadig, Ajay, Carey, Caitlin E., Baya, Nikolas, Bybjerg-Grauholm, Jonas, Berretta, Sabina, Macosko, Evan Z., Sebat, Jonathan, O’Connor, Luke J., Hougaard, David M., Børglum, Anders D., Talkowski, Michael E., McCarroll, Steven A., Robinson, Elise B.

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The impact of the metabotropic glutamate receptor and other gene family interaction networks on autism von Hadley, Dexter, Wu, Zhi-liang, Kao, Charlly, Kini, Akshata, Mohamed-Hadley, Alisha, Thomas, Kelly, Vazquez, Lyam, Qiu, Haijun, Mentch, Frank, Pellegrino, Renata, Kim, Cecilia, Connolly, John, Glessner, Joseph, Hakonarson, Hakon

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Synaptic, transcriptional, and chromatin genes disrupted in autism von De Rubeis, Silvia, He, Xin, Goldberg, Arthur P, Poultney, Christopher S, Samocha, Kaitlin, Cicek, A Ercument, Kou, Yan, Liu, Li, Fromer, Menachem, Walker, Susan, Singh, Tarjinder, Klei, Lambertus, Kosmicki, Jack, Fu, Shih-Chen, Aleksic, Branko, Biscaldi, Monica, Bolton, Patrick F, Brownfeld, Jessica M, Cai, Jinlu, Campbell, Nicholas J, Carracedo, Angel, Chahrour, Maria H, Chiocchetti, Andreas G, Coon, Hilary, Crawford, Emily L, Crooks, Lucy, Curran, Sarah R, Dawson, Geraldine, Duketis, Eftichia, Fernandez, Bridget A, Gallagher, Louise, Geller, Evan, Guter, Stephen J, Hill, R. Sean, Ionita-Laza, Iuliana, Gonzalez, Patricia Jimenez, Kilpinen, Helena, Klauck, Sabine M, Kolevzon, Alexander, Lee, Irene, Lei, Jing, Lehtimäki, Terho, Lin, Chiao-Feng, Ma'ayan, Avi, Marshall, Christian R, McInnes, Alison L, Neale, Benjamin, Owen, Michael J, Ozaki, Norio, Parellada, Mara, Parr, Jeremy R, Purcell, Shaun, Puura, Kaija, Rajagopalan, Deepthi, Rehnström, Karola, Reichenberg, Abraham, Sabo, Aniko, Sachse, Michael, Sanders, Stephan J, Schafer, Chad, Schulte-Rüther, Martin, Skuse, David, Stevens, Christine, Szatmari, Peter, Tammimies, Kristiina, Valladares, Otto, Voran, Annette, Wang, Li-San, Weiss, Lauren A, Willsey, A. Jeremy, Yu, Timothy W, Yuen, Ryan K.C, Cook, Edwin H, Freitag, Christine M, Gill, Michael, Hultman, Christina M, Lehner, Thomas, Palotie, Aarno, Schellenberg, Gerard D, Sklar, Pamela, State, Matthew W, Sutcliffe, James S, Walsh, Christopher A, Scherer, Stephen W, Zwick, Michael E, Barrett, Jeffrey C, Cutler, David J, Roeder, Kathryn, Devlin, Bernie, Daly, Mark J, Buxbaum, Joseph D

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Immune-related genetic enrichment in frontotemporal dementia: An analysis of genome-wide association studies von Broce, Iris J, Karch, Celeste M, Wen, Natalie, Fan, Chun C, Wang, Yunpeng, Hong Tan, Chin, Kouri, Naomi, Ross, Owen A, Höglinger, Günter U, Müller, Ulrich, Hardy, John, Momeni, Parastoo, Hess, Christopher P, Dillon, William P, Miller, Zachary A, Bonham, Luke W, Rabinovici, Gil D, Rosen, Howard J, Schellenberg, Gerard D, Franke, Andre, Karlsen, Tom Hemming, Veldink, Jan H, Ferrari, Raffaele, Yokoyama, Jennifer S, Miller, Bruce L, Andreassen, Ole Andreas, Dale, Anders, Desikan, Rahul S, Sugrue, Leo P

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Regioselectivity of the Pd-catalyzed synthesis of arylenevinylenes and its impact on polymer properties: Model reaction and polyreactions von Klingelhöfer, Stephanie, Schellenberg, Carsten, Pommerehne, Jörn, Bässler, Heinz, Greiner, Andreas, Heitz, Walter

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Immune-related genetic enrichment in frontotemporal dementia: An analysis of genome-wide association studies von Broce, Iris J, Karch, Celeste M, Wen, Natalie, Fan, Chun C, Wang, Yunpeng, Hong Tan, Chin, Kouri, Naomi, Ross, Owen A, Höglinger, Günter U, Müller, Ulrich, Hardy, John, Momeni, Parastoo, Hess, Christopher P, Dillon, William P, Miller, Zachary A, Bonham, Luke W, Rabinovici, Gil D, Rosen, Howard J, Schellenberg, Gerard D, Franke, Andre, Karlsen, Tom Hemming, Veldink, Jan H, Ferrari, Raffaele, Yokoyama, Jennifer S, Miller, Bruce L, Andreassen, Ole Andreas, Dale, Anders, Desikan, Rahul S, Sugrue, Leo P

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Synaptic, transcriptional and chromatin genes disrupted in autism von De Rubeis, Silvia, He, Xin, Poultney, Christopher S, Poultney, Christopher S, Samocha, Kaitlin, Samocha, Kaitlin, Ercument Cicek, A, Ercument Cicek, A, Kou, Yan, Liu, Li, Fromer, Menachem, Walker, Susan, Walker, Susan, Singh, Tarjinder, Singh, Tarjinder, Kosmicki, Jack, Fu, Shih-Chen, Aleksic, Branko, Aleksic, Branko, Biscaldi, Monica, Brownfeld, Jessica M, Brownfeld, Jessica M, Cai, Jinlu, Campbell, Nicholas G, Chahrour, Maria H, Chiocchetti, Andreas G, Coon, Hilary, Crooks, Lucy, Curran, Sarah R, Curran, Sarah R, Dawson, Geraldine, Dawson, Geraldine, Duketis, Eftichia, Fernandez, Bridget A, Gallagher, Louise, Geller, Evan, Guter, Stephen J, Sean Hill, R, Ionita-Laza, Iuliana, Jimenez Gonzalez, Patricia, Kilpinen, Helena, Kilpinen, Helena, Kolevzon, Alexander, Kolevzon, Alexander, Lei, Jing, Lehtimäki, Terho, Lin, Chiao-Feng, Lin, Chiao-Feng, Ma’ayan, Avi, Marshall, Christian R, Marshall, Christian R, McInnes, Alison L, McInnes, Alison L, Owen, Michael J, Ozaki, Norio, Parr, Jeremy R, Puura, Kaija, Rajagopalan, Deepthi, Rajagopalan, Deepthi, Rehnström, Karola, Reichenberg, Abraham, Sabo, Aniko, Sabo, Aniko, Sachse, Michael, Sanders, Stephan J, Schafer, Chad, Schulte-Rüther, Martin, Stevens, Christine, Szatmari, Peter, Szatmari, Peter, Tammimies, Kristiina, Valladares, Otto, Valladares, Otto, Voran, Annette, Wang, Li-San, Weiss, Lauren A, Weiss, Lauren A, Jeremy Willsey, A, Yu, Timothy W, Yu, Timothy W, Yuen, Ryan KC, Yuen, Ryan KC, Gill, Michael, Hultman, Christina M, Hultman, Christina M, Lehner, Thomas, Palotie, Aarno, Schellenberg, Gerard D, Sklar, Pamela, Sutcliffe, James S, Scherer, Stephen W, Zwick, Michael E, Barrett, Jeffrey C, Cutler, David J, Roeder, Kathryn, Devlin, Bernie, Daly, Mark J, Daly, Mark J, Buxbaum, Joseph D, Eapen, Valsamma

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Convergence of genes and cellular pathways dysregulated in autism spectrum disorders von Pinto, Dalila

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