Hypnotic Interrogation, Pretrial Preparation, and Witness Testimony during Direct and Cross-Examination by Spanos, Nicholas P, Quigley, Celia A, Gwynn, Maxwell I, Glatt, Richard L, Perlini, Arthur H

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Genetic correlations among psychiatric and immune‐related phenotypes based on genome‐wide association data by Tylee, Daniel S., Sun, Jiayin, Hess, Jonathan L., Tahir, Muhammad A., Sharma, Esha, Malik, Rainer, Worrall, Bradford B., Levine, Andrew J., Martinson, Jeremy J., Nejentsev, Sergey, Speed, Doug, Fischer, Annegret, Mick, Eric, Walker, Brian R., Crawford, Andrew, Grant, Struan F. A., Polychronakos, Constantin, Bradfield, Jonathan P., Sleiman, Patrick M. A., Hakonarson, Hakon, Ellinghaus, Eva, Elder, James T., Tsoi, Lam C., Trembath, Richard C., Barker, Jonathan N., Franke, Andre, Dehghan, Abbas, Faraone, Stephen V., Glatt, Stephen J.

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Convalescent plasma in the treatment of moderate to severe COVID-19 pneumonia: a randomized controlled trial (PROTECT-Patient Trial) by van den Berg, Karin, Glatt, Tanya Nadia, Vermeulen, Marion, Little, Francesca, Swanevelder, Ronel, Barrett, Claire, Court, Richard, Bremer, Marise, Nyoni, Cynthia, Swarts, Avril, Mmenu, Cordelia, Crede, Thomas, Kritzinger, Gerdien, Naude, Jonathan, Szymanski, Patryk, Cowley, James, Moyo-Gwete, Thandeka, Moore, Penny L., Black, John, Singh, Jaimendra, Bhiman, Jinal N., Baijnath, Prinita, Mody, Priyesh, Malherbe, Jacques, Potgieter, Samantha, van Vuuren, Cloete, Maasdorp, Shaun, Wilkinson, Robert J., Louw, Vernon J., Wasserman, Sean

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Association of the OPRM1 Variant rs1799971 (A118G) with Non-Specific Liability to Substance Dependence in a Collaborative de novo Meta-Analysis of European-Ancestry Cohorts by Schwantes-An, Tae-Hwi, Zhang, Juan, Chen, Li-Shiun, Hartz, Sarah M., Chen, Xiangning, Coon, Hilary, Frank, Josef, Kamens, Helen M., Konte, Bettina, Kovanen, Leena, Latvala, Antti, Legrand, Lisa N., Maher, Brion S., Melroy, Whitney E., Nelson, Elliot C., Reid, Mark W., Shen, Pei-Hong, Yang, Bao-Zhu, Andrews, Judy A., Aveyard, Paul, Brown, Sandra A., Cichon, Sven, Corley, Robin P., Dahmen, Norbert, Degenhardt, Louisa, Gaebel, Wolfgang, Giegling, Ina, Glatt, Stephen J., Grucza, Richard A., Hardin, Jill, Hartmann, Annette M., Heath, Andrew C., Herms, Stefan, Hoffmann, Per, Hops, Hyman, Ising, Marcus, Johnson, Eric O., Johnstone, Elaine, Kaneva, Radka P., Kendler, Kenneth S., Kiefer, Falk, Kranzler, Henry R., Krauter, Ken S., Levran, Orna, Lucae, Susanne, Maier, Wolfgang, Mann, Karl, Martin, Nicholas G., Mattheisen, Manuel, Montgomery, Grant W., Murphy, Michael F., Neale, Michael C., Nikolov, Momchil A., Nishita, Denise, Nöthen, Markus M., Nurnberger, John, Partonen, Timo, Pergadia, Michele L., Reynolds, Maureen, Ridinger, Monika, Rose, Richard J., Rouvinen-Lagerström, Noora, Scherbaum, Norbert, Schmäl, Christine, Soyka, Michael, Stallings, Michael C., Steffens, Michael, Treutlein, Jens, Tsuang, Ming, Wall, Tamara L., Wodarz, Norbert, Yuferov, Vadim, Zill, Peter, Bergen, Andrew W., Chen, Jingchun, Cinciripini, Paul M., Edenberg, Howard J., Ehringer, Marissa A., Ferrell, Robert E., Gelernter, Joel, Goldman, David, Hewitt, John K., Hopfer, Christian J., Iacono, William G., Kaprio, Jaakko, Kremensky, Ivo M., Madden, Pamela A.F., McGue, Matt, Munafò, Marcus R., Philibert, Robert A., Rietschel, Marcella, Roy, Alec, Rujescu, Dan, Saarikoski, Sirkku T., Swan, Gary E., Todorov, Alexandre A., Vanyukov, Michael M., Weiss, Robert B., Bierut, Laura J., Saccone, Nancy L.

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Rare coding variants in 10 genes confer substantial risk for schizophrenia by 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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Human Platelet Phenolsulfotransferases: cDNA Cloning, Stable Expression in V79 Cells, and Identification of a Novel Allelic Variant of the Phenol-Sulfating Form by Jones, A.L., Hagen, M., Coughtrie, M.W.H., Roberts, R.C., Glatt, H.

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Pyrimethamine for Primary Prophylaxis of Toxoplasmic Encephalitis in Patients with Human Immunodeficiency Virus Infection: A Double-Blind, Randomized Trial by Leport, Catherine, Ch⩽ne, Geneviève, Morlat, Philippe, Luft, Benjamin J., Rousseau, Franck, Pueyo, Sophie, Hafner, Richard, Miro, Jose, Aubertin, Jean, Salamon, Roger, Vildé, Jean-Louis

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Letters by Glatt, Mark, Atkins, Richard L, Diane Asseo Griliches

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Comments on Some Reorganization Provisions of the Pending Bankruptcy Bills by COOGAN, PETER F., BROUDE, RICHARD, GLATT, HERMAN

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