Analysis of protein-coding genetic variation in 60,706 humans von Lek, Monkol, Karczewski, Konrad J., Minikel, Eric V., Samocha, Kaitlin E., Banks, Eric, Fennell, Timothy, O’Donnell-Luria, Anne H., Ware, James S., Hill, Andrew J., Cummings, Beryl B., Tukiainen, Taru, Birnbaum, Daniel P., Kosmicki, Jack A., Duncan, Laramie E., Estrada, Karol, Zhao, Fengmei, Zou, James, Pierce-Hoffman, Emma, Berghout, Joanne, Cooper, David N., Deflaux, Nicole, DePristo, Mark, Do, Ron, Flannick, Jason, Fromer, Menachem, Gauthier, Laura, Goldstein, Jackie, Gupta, Namrata, Howrigan, Daniel, Kiezun, Adam, Kurki, Mitja I., Moonshine, Ami Levy, Natarajan, Pradeep, Orozco, Lorena, Peloso, Gina M., Poplin, Ryan, Rivas, Manuel A., Ruano-Rubio, Valentin, Rose, Samuel A., Ruderfer, Douglas M., Shakir, Khalid, Stenson, Peter D., Stevens, Christine, Thomas, Brett P., Tiao, Grace, Tusie-Luna, Maria T., Weisburd, Ben, Won, Hong-Hee, Yu, Dongmei, Altshuler, David M., Ardissino, Diego, Boehnke, Michael, Danesh, John, Donnelly, Stacey, Elosua, Roberto, Florez, Jose C., Gabriel, Stacey B., Getz, Gad, Glatt, Stephen J., Hultman, Christina M., Kathiresan, Sekar, Laakso, Markku, McCarroll, Steven, McCarthy, Mark I., McGovern, Dermot, McPherson, Ruth, Neale, Benjamin M., Palotie, Aarno, Purcell, Shaun M., Saleheen, Danish, Scharf, Jeremiah M., Sklar, Pamela, Sullivan, Patrick F., Tuomilehto, Jaakko, Tsuang, Ming T., Watkins, Hugh C., Wilson, James G., Daly, Mark J., MacArthur, Daniel G.

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Genomic Relationships, Novel Loci, and Pleiotropic Mechanisms across Eight Psychiatric Disorders von Tucker-Drob, Elliot M., Yu, Dongmei, Ge, Tian, Derks, Eske M., Keski-Rahkonen, Anna, Kirov, George, Asherson, Philip, Baldursson, Gísli, Bybjerg-Grauholm, Jonas, Churchhouse, Claire, Crosbie, Jennifer, Demontis, Ditte, Grove, Jakob, Martin, Joanna, McGough, James J., Pedersen, Carsten B., Poulsen, Jesper B., Rothenberger, Aribert, Schachar, Russell, Turley, Patrick, Arking, Dan E., Collins, Ryan L., Coon, Hilary, Delorme, Richard, Hope, Sigrun, Nyegaard, Mette, Pinto, Dalila, Qvist, Per, Talkowski, Michael E., Albani, Diego, Alda, Martin, Bass, Nicholas, Bauer, Michael, Cichon, Sven, Clarke, Toni-Kim, Czerski, Piotr M., Fischer, Sascha B., Frank, Josef, Goes, Fernando S., Holland, Dominic, Jones, Lisa A., Joachim, Oedegaard Ketil, Maaser, Anna, Malt, Ulrik F., McMahon, Francis J., Montgomery, Grant W., Myers, Richard M., Nöthen, Markus M., Perry, Amy, Vieta, Eduard, Aschauer, Harald, Bencko, Vladimir, Burghardt, Roland, Carlberg, Laura, Guo, Yiran, Klump, Kelly L., Le Hellard, Stephanie, Monteleone, Alessio Maria, Seitz, Jochen, Treasure, Janet, Wade, Tracey D., Wichmann, H-Erich, Woodside, D. Blake, Grabe, Hans J., Horn, Carsten, Penninx, Brenda WJH, Schulte, Eva C., Smith, Daniel J., Alexander, Madeline, Begemann, Martin, Campion, Dominique, Ehrenreich, Hannelore, Murphy, Kieran C., Riley, Brien, Sham, Pak C., van Os, Jim, Weiser, Mark, Brown, Lawrence W., Cheon, Keun-Ah, Denys, Damiaan, Gilbert, Donald L., Grados, Marco A., Ibanez-Gomez, Laura, King, Robert A., Leventhal, Bennett L., Okun, Michael S., Piras, Federica, Robertson, Mary, Samuels, Jack F., Spalletta, Gianfranco, Stein, Dan J., Stewart, S Evelyn, Storch, Eric A., Stranger, Barbara, Tübing, Jennifer, Visscher, Frank, Wagner, Michael, Santangelo, Susan L., Thornton, Laura M., Neale, Benjamin M.

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Analysis of shared heritability in common disorders of the brain von Anttila, Verneri, Bulik-Sullivan, Brendan, Finucane, Hilary K, Walters, Raymond K, Bras, Jose, Duncan, Laramie, Escott-Price, Valentina, Falcone, Guido J, Gormley, Padhraig, Malik, Rainer, Patsopoulos, Nikolaos A, Ripke, Stephan, Wei, Zhi, Yu, Dongmei, Lee, Phil H, Turley, Patrick, Grenier-Boley, Benjamin, Chouraki, Vincent, Kamatani, Yoichiro, Berr, Claudine, Letenneur, Luc, Hannequin, Didier, Amouyel, Philippe, Boland, Anne, Deleuze, Jean-François, Duron, Emmanuelle, Vardarajan, Badri N, Reitz, Christiane, Goate, Alison M, Huentelman, Matthew J, Kamboh, M Ilyas, Larson, Eric B, Rogaeva, Ekaterina, St George-Hyslop, Peter, Hakonarson, Hakon, Kukull, Walter A, Farrer, Lindsay A, Barnes, Lisa L, Beach, Thomas G, Demirci, F Yesim, Head, Elizabeth, Hulette, Christine M, Jicha, Gregory A, Kauwe, John S K, Kaye, Jeffrey A, Leverenz, James B, Levey, Allan I, Lieberman, Andrew P, Pankratz, Vernon S, Poon, Wayne W, Quinn, Joseph F, Saykin, Andrew J, Schneider, Lon S, Smith, Amanda G, Sonnen, Joshua A, Stern, Robert A, Van Deerlin, Vivianna M, Van Eldik, Linda J, Harold, Denise, Russo, Giancarlo, Rubinsztein, David C, Bayer, Anthony, Tsolaki, Magda, Proitsi, Petra, Fox, Nick C, Hampel, Harald, Owen, Michael J, Mead, Simon, Passmore, Peter, Morgan, Kevin, Nöthen, Markus M, Rossor, Martin, Lupton, Michelle K, Hoffmann, Per, Kornhuber, Johannes, Lawlor, Brian, McQuillin, Andrew, Al-Chalabi, Ammar, Bis, Joshua C, Ruiz, Agustin, Boada, Mercè, Seshadri, Sudha, Beiser, Alexa, Rice, Kenneth, van der Lee, Sven J, De Jager, Philip L, Geschwind, Daniel H, Riemenschneider, Matthias, Riedel-Heller, Steffi, Rotter, Jerome I, Ransmayr, Gerhard, Hyman, Bradley T, Cruchaga, Carlos, Alegret, Montserrat, Winsvold, Bendik, Palta, Priit, Farh, Kai-How, Cuenca-Leon, Ester, Furlotte, Nicholas, Kurth, Tobias

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Examination of the shared genetic basis of anorexia nervosa and obsessive–compulsive disorder von Yilmaz, Zeynep, Halvorsen, Matthew, Bryois, Julien, Yu, Dongmei, Thornton, Laura M., Zerwas, Stephanie, Micali, Nadia, Moessner, Rainald, Burton, Christie L., Zai, Gwyneth, Erdman, Lauren, Kas, Martien J., Arnold, Paul D., Davis, Lea K., Knowles, James A., Breen, Gerome, Scharf, Jeremiah M., Nestadt, Gerald, Mathews, Carol A., Bulik, Cynthia M., Mattheisen, Manuel, Crowley, James J.

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Cross-Disorder Genome-Wide Analyses Suggest a Complex Genetic Relationship Between Tourette’s Syndrome and OCD von Yu, Dongmei, Davis, Lea K., Gamazon, Eric R., Derks, Eske M., Evans, Patrick, Crane, Jacquelyn, Osiecki, Lisa, Gerber, Gloria, Haddad, Stephen, McGrath, Lauren M., Mayerfeld, Catherine, Arepalli, Sampath, Barlassina, Cristina, Barr, Cathy L., Black, Donald W., Bloch, Michael H., Brentani, Helena, Camarena, Beatriz, Campbell, Desmond D., Cavallini, Maria C., Chavira, Denise A., Cook, Edwin H., Cookson, M.R., Cullen, Bernadette, Denys, Damiaan, Dion, Yves, Eapen, Valsama, Egberts, Karin, Fernandez, Thomas, Fournier, Eduardo, Garrido, Helena, Geller, Daniel, Girard, Simon L., Grabe, Hans J., Greenberg, Benjamin D., Heiman, Gary A., Hemmings, Sian M.J., Herrera, Luis D., Hezel, Dianne M., Jankovic, Joseph, Kremeyer, Barbara, Lanzagorta, Nuria, Lowe, Thomas L., Lupoli, Sara, Macciardi, Fabio, Maier, Wolfgang, Manunta, Paolo, Marconi, Maurizio, McCracken, James T., Mesa Restrepo, Sandra C., Moessner, Rainald, Moorjani, Priya, Morgan, Jubel, Muller, Heike, Murphy, Dennis L., Naarden, Allan L., Nurmi, Erika, Ochoa, William Cornejo, Pato, Carlos N., Piacentini, John, Pittenger, Christopher, Rauch, Scott L., Renner, Tobias, Reus, Victor I., Riddle, Mark A., Romero, Roxana, Rosenberg, David, Ruhrmann, Stephan, Sabatti, Chiara, Salvi, Erika, Samuels, Jack, Sandor, Paul, Sheppard, Brooke, Singer, Harvey S., Stein, Dan J., Strengman, Eric, Tischfield, Jay A., Turiel, Maurizio, Vallada, Homero, Veenstra-VanderWeele, Jeremy, Walitza, Susanne, Wang, Ying, Weale, Mike, Weiss, Robert, Wendland, Jens R., Westenberg, Herman G.M., Shugart, Yin Yao, Hounie, Ana G., Wagner, Michael, Ruiz-Linares, Andres, Cath, Danielle C., Posthuma, Danielle, Heutink, Peter, Hanna, Gregory L., Conti, David V., Arnold, Paul D., Freimer, Nelson B., Stewart, S. Evelyn, Knowles, James A., Pauls, David L.

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Partitioning the heritability of Tourette syndrome and obsessive compulsive disorder reveals differences in genetic architecture von Davis, Lea K, Yu, Dongmei, Keenan, Clare L, Gamazon, Eric R, Konkashbaev, Anuar I, Derks, Eske M, Neale, Benjamin M, Yang, Jian, Lee, S Hong, Evans, Patrick, Barr, Cathy L, Bellodi, Laura, Benarroch, Fortu, Berrio, Gabriel Bedoya, Bienvenu, Oscar J, Bloch, Michael H, Blom, Rianne M, Bruun, Ruth D, Budman, Cathy L, Camarena, Beatriz, Campbell, Desmond, Cappi, Carolina, Cardona Silgado, Julio C, Cath, Danielle C, Cavallini, Maria C, Chavira, Denise A, Chouinard, Sylvain, Conti, David V, Cook, Edwin H, Coric, Vladimir, Cullen, Bernadette A, Deforce, Dieter, Delorme, Richard, Dion, Yves, Edlund, Christopher K, Egberts, Karin, Falkai, Peter, Fernandez, Thomas V, Gallagher, Patience J, Garrido, Helena, Geller, Daniel, Girard, Simon L, Grabe, Hans J, Grados, Marco A, Greenberg, Benjamin D, Gross-Tsur, Varda, Haddad, Stephen, Heiman, Gary A, Hemmings, Sian M J, Hounie, Ana G, Illmann, Cornelia, Jankovic, Joseph, Jenike, Michael A, Kennedy, James L, King, Robert A, Kremeyer, Barbara, Kurlan, Roger, Lanzagorta, Nuria, Leboyer, Marion, Leckman, James F, Lennertz, Leonhard, Liu, Chunyu, Lochner, Christine, Lowe, Thomas L, Macciardi, Fabio, McCracken, James T, McGrath, Lauren M, Mesa Restrepo, Sandra C, Moessner, Rainald, Morgan, Jubel, Muller, Heike, Murphy, Dennis L, Naarden, Allan L, Ochoa, William Cornejo, Ophoff, Roel A, Osiecki, Lisa, Pakstis, Andrew J, Pato, Michele T, Pato, Carlos N, Piacentini, John, Pittenger, Christopher, Pollak, Yehuda, Rauch, Scott L, Renner, Tobias J, Reus, Victor I, Richter, Margaret A, Riddle, Mark A, Robertson, Mary M, Romero, Roxana, Rosàrio, Maria C, Rosenberg, David, Rouleau, Guy A, Ruhrmann, Stephan, Ruiz-Linares, Andres, Sampaio, Aline S, Samuels, Jack, Sandor, Paul, Sheppard, Brooke, Singer, Harvey S, Smit, Jan H

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Sex differences in the genetic architecture of obsessive–compulsive disorder von Khramtsova, Ekaterina A., Heldman, Raphael, Derks, Eske M., Yu, Dongmei, Davis, Lea K., Stranger, Barbara E.

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Elevated common variant genetic risk for tourette syndrome in a densely-affected pedigree von Halvorsen, Matthew, Szatkiewicz, Jin, Mudgal, Poorva, Yu, Dongmei, Nordsletten, Ashley E., Mataix-Cols, David, Mathews, Carol A., Scharf, Jeremiah M., Mattheisen, Manuel, Robertson, Mary M., McQuillin, Andrew, Crowley, James J.

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Investigating Shared Genetic Basis Across Tourette Syndrome and Comorbid Neurodevelopmental Disorders Along the Impulsivity-Compulsivity Spectrum von Yang, Zhiyu, Wu, Hanrui, Lee, Phil H., Tsetsos, Fotis, Davis, Lea K., Yu, Dongmei, Lee, Sang Hong, Dalsgaard, Søren, Haavik, Jan, Barta, Csaba, Zayats, Tetyana, Eapen, Valsamma, Wray, Naomi R., Devlin, Bernie, Daly, Mark, Neale, Benjamin, Børglum, Anders D., Crowley, James J., Scharf, Jeremiah, Mathews, Carol A., Faraone, Stephen V., Franke, Barbara, Mattheisen, Manuel, Smoller, Jordan W., Paschou, Peristera

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Identification of a Novel Gene on Chromosome 7q11.2 Interrupted by a Translocation Breakpoint in a Pair of Autistic Twins von Sultana, Razia, Yu, Chang-En, Yu, Jun, Munson, Jeffery, Chen, Donghui, Hua, Wenhui, Estes, Annette, Cortes, Fanny, de la Barra, Flora, Yu, Dongmei, Haider, Syed T., Trask, Barbara J., Green, Eric D., Raskind, Wendy H., Disteche, Christine M., Wijsman, Ellen, Dawson, Geraldine, Storm, Daniel R., Schellenberg, Gerard D., Villacres, Enrique C.

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Effects of a Macro-Nutrient Preload on Type 2 Diabetic Patients von Li, Chun-Jun, Norstedt, Gunnar, Hu, Zhao-Gian, Yu, Pei, Li, Dai-Qing, Li, Jing, Yu, Qian, Sederholm, Magnus, Yu, De-Min

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Effect of fiber pretreatment condition on the interfacial strength and mechanical properties of wood fiber/PP composites von Wu, Jingshen, Yu, Demei, Chan, Chi-Ming, Kim, Jangkyo, Mai, Yiu-Wing

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Study on morphology, crystallization behaviors of highly filled maleated polyethylene-layered silicate nanocomposites von Xie, Yunchuan, Yu, Demei, Kong, Jie, Fan, Xiaodong, Qiao, Wenqiang

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Tuberculosis Developing in a Patient With Long-term High Dose Inhaled Corticosteroid Use: A Case Report von Sobere Yu, Karen, DM, De Guia, Teresita, DM

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A multi-objective optimization model of the partner selection problem in a virtual enterprise and its solution with genetic algorithms von Fuqing, Zhao, Yi, Hong, Dongmei, Yu

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Reelin, a guidance signal for the regeneration of the entorhino-hippocampal path von Wu, Ping, Li, Ming-shan, Yu, Dong-ming, Deng, Jin-bo

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The dielectric and mechanical properties of a potassium-titanate-whisker-reinforced PP/PA blend von Yu, Demei, Wu, Jingshen, Zhou, Limin, Xie, Darong, Wu, Songzheng

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CHARACTERIZING AN INVERSE AXIS BETWEEN ORTHOGONAL SOURCES OF GENETIC RISK von Davis, L, Lee, SH, Gamazon, E, Im, HK, Yu, DM, McGrath, L, Williams, S, Cook, E, Sullivan, P, Sutcliffe, J, Knowles, J, Mathews, C, Scharf, J, Wray, N, Cox, N

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Joint oligogenic segregation and linkage analysis using bayesian Markov chain Monte Carlo methods von WIJSMAN, Ellen M, DONGMEI YU

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Fracture toughness and fracture mechanisms of pbt/pc/im blends. Part V Effect of PBT-PC interfacial strength on the fracture and tensile properties of the PBT/PC blends von Wu, J, Wang, K, Yu, D

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