A Phase II Randomized Study of HIV-Specific T-Cell Gene Therapy in Subjects with Undetectable Plasma Viremia on Combination Antiretroviral Therapy von Deeks, Steven G., Wagner, Bridget, Anton, Peter A., Mitsuyasu, Ronald T., Scadden, David T., Huang, Christine, Macken, Catherine, Richman, Douglas D., Christopherson, Cindy, June, Carl H., Lazar, Richard, Broad, David F., Jalali, Sayeh, Hege, Kristen M.

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The Mode and Duration of Anti-CD28 Costimulation Determine Resistance to Infection by Macrophage-Tropic Strains of Human Immunodeficiency Virus Type 1 In Vitro von Creson, J R, Lin, A A, Li, Q, Broad, D F, Roberts, M R, Anderson, S J

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Long-term in vivo survival of receptor-modified syngeneic T cells in patients with human immunodeficiency virus infection von WALKER, R. E, BECHTEL, C. M, LEITMAN, S. F, PALENSKY, J, WITTES, J, DAVEY, R. T, FALLOON, J, POLIS, M. A, KOVACS, J. A, BROAD, D. F, LEVINE, B. L, ROBERTS, M. R, NATARAJAN, V, MASUR, H, LANE, H. C, BASELER, M, HEGE, K. M, METCALF, J. A, STEVENS, R, HAZEN, A, BLAESE, R. M, CHEN, C. C

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Classification of Trimethoprim‐Resistant Dihydrofolate Reductases Mediated by R‐Plasmids Using Isoelectric Focussing von BROAD, David F., SMITH, John T.

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Autism spectrum disorder and attention deficit hyperactivity disorder have a similar burden of rare protein-truncating variants von Satterstrom, F. Kyle, Walters, Raymond K., Singh, Tarjinder, Wigdor, Emilie M., Lescai, Francesco, Demontis, Ditte, Kosmicki, Jack A., Grove, Jakob, Stevens, Christine, Bybjerg-Grauholm, Jonas, Bækvad-Hansen, Marie, Palmer, Duncan S., Maller, Julian B., Nordentoft, Merete, Mors, Ole, Robinson, Elise B., Hougaard, David M., Werge, Thomas M., Bo Mortensen, Preben, Neale, Benjamin M., Børglum, Anders D., Daly, Mark J.

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Genetic risk for autism spectrum disorders and neuropsychiatric variation in the general population von Robinson, Elise B, St Pourcain, Beate, Anttila, Verneri, Kosmicki, Jack A, Bulik-Sullivan, Brendan, Grove, Jakob, Maller, Julian, Samocha, Kaitlin E, Sanders, Stephan J, Ripke, Stephan, Martin, Joanna, Hollegaard, Mads V, Werge, Thomas, Hougaard, David M, Neale, Benjamin M, Evans, David M, Skuse, David, Mortensen, Preben Bo, Børglum, Anders D, Ronald, Angelica, Smith, George Davey, Daly, Mark J

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Genome-wide association study identifies 16 genomic regions associated with circulating cytokines at birth von Wang, Yunpeng, Nudel, Ron, Benros, Michael E., Skogstrand, Kristin, Fishilevich, Simon, Lancet, Doron, Sun, Jiangming, Hougaard, David M., Andreassen, Ole A., Mortensen, Preben Bo, Buil, Alfonso, Hansen, Thomas F., Thompson, Wesley K., Werge, Thomas

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Rare coding variation provides insight into the genetic architecture and phenotypic context of autism von Fu, Jack M., Satterstrom, F. Kyle, Peng, Minshi, Brand, Harrison, Collins, Ryan L., Dong, Shan, Wamsley, Brie, Klei, Lambertus, Wang, Lily, Hao, Stephanie P., Stevens, Christine R., Cusick, Caroline, Babadi, Mehrtash, Banks, Eric, Collins, Brett, Dodge, Sheila, Gabriel, Stacey B., Gauthier, Laura, Lee, Samuel K., Liang, Lindsay, Ljungdahl, Alicia, Mahjani, Behrang, Sloofman, Laura, Smirnov, Andrey N., Barbosa, Mafalda, Betancur, Catalina, Brusco, Alfredo, Chung, Brian H. Y., Cook, Edwin H., Cuccaro, Michael L., Domenici, Enrico, Ferrero, Giovanni Battista, Gargus, J. Jay, Herman, Gail E., Hertz-Picciotto, Irva, Maciel, Patricia, Manoach, Dara S., Passos-Bueno, Maria Rita, Persico, Antonio M., Renieri, Alessandra, Sutcliffe, James S., Tassone, Flora, Trabetti, Elisabetta, Campos, Gabriele, Cardaropoli, Simona, Carli, Diana, Chan, Marcus C. Y., Fallerini, Chiara, Giorgio, Elisa, Girardi, Ana Cristina, Hansen-Kiss, Emily, Lee, So Lun, Lintas, Carla, Ludena, Yunin, Nguyen, Rachel, Pavinato, Lisa, Pericak-Vance, Margaret, Pessah, Isaac N., Schmidt, Rebecca J., Smith, Moyra, Costa, Claudia I. S., Trajkova, Slavica, Wang, Jaqueline Y. T., Yu, Mullin H. C., Cutler, David J., De Rubeis, Silvia, Buxbaum, Joseph D., Daly, Mark J., Devlin, Bernie, Roeder, Kathryn, Sanders, Stephan J., Talkowski, Michael E.

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Safety and Efficacy of NVX-CoV2373 Covid-19 Vaccine von Heath, Paul T, Galiza, Eva P, Baxter, David N, Boffito, Marta, Browne, Duncan, Burns, Fiona, Chadwick, David R, Clark, Rebecca, Cosgrove, Catherine, Galloway, James, Goodman, Anna L, Heer, Amardeep, Higham, Andrew, Iyengar, Shalini, Jamal, Arham, Jeanes, Christopher, Kalra, Philip A, Kyriakidou, Christina, McAuley, Daniel F, Meyrick, Agnieszka, Minassian, Angela M, Minton, Jane, Moore, Patrick, Munsoor, Imrozia, Nicholls, Helen, Osanlou, Orod, Packham, Jonathan, Pretswell, Carol H, San Francisco Ramos, Alberto, Saralaya, Dinesh, Sheridan, Ray P, Smith, Richard, Soiza, Roy L, Swift, Pauline A, Thomson, Emma C, Turner, Jeremy, Viljoen, Marianne E, Albert, Gary, Cho, Iksung, Dubovsky, Filip, Glenn, Greg, Rivers, Joy, Robertson, Andreana, Smith, Kathy, Toback, Seth

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SYT1-associated neurodevelopmental disorder: a case series von Baker, Kate, Gordon, Sarah L, Melland, Holly, Bumbak, Fabian, Scott, Daniel J, Jiang, Tess J, Owen, David, Turner, Bradley J, Boyd, Stewart G, Rossi, Mari, Al-Raqad, Mohammed, Elpeleg, Orly, Peck, Dawn, Mancini, Grazia M S, Wilke, Martina, Zollino, Marcella, Marangi, Giuseppe, Weigand, Heike, Borggraefe, Ingo, Haack, Tobias, Stark, Zornitza, Sadedin, Simon, Tan, Tiong Yang, Jiang, Yunyun, Gibbs, Richard A, Ellingwood, Sara, Amaral, Michelle, Kelley, Whitley, Kurian, Manju A, Cousin, Michael A, Raymond, F Lucy

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Shared molecular neuropathology across major psychiatric disorders parallels polygenic overlap von Gandal, Michael J, Haney, Jillian R, Parikshak, Neelroop N, Leppa, Virpi, Ramaswami, Gokul, Hartl, Chris, Schork, Andrew J, Appadurai, Vivek, Buil, Alfonso, Werge, Thomas M, Liu, Chunyu, White, Kevin P, Horvath, Steve, Geschwind, Daniel H

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Genome-wide analyses of ADHD identify 27 risk loci, refine the genetic architecture and implicate several cognitive domains von Demontis, Ditte, Walters, G. Bragi, Athanasiadis, Georgios, Walters, Raymond, Therrien, Karen, Nielsen, Trine Tollerup, Farajzadeh, Leila, Voloudakis, Georgios, Bendl, Jaroslav, Zeng, Biau, Zhang, Wen, Grove, Jakob, Als, Thomas D., Duan, Jinjie, Satterstrom, F. Kyle, Bybjerg-Grauholm, Jonas, Bækved-Hansen, Marie, Gudmundsson, Olafur O., Magnusson, Sigurdur H., Baldursson, Gisli, Davidsdottir, Katrin, Haraldsdottir, Gyda S., Agerbo, Esben, Hoffman, Gabriel E., Dalsgaard, Søren, Martin, Joanna, Ribasés, Marta, Boomsma, Dorret I., Soler Artigas, Maria, Roth Mota, Nina, Howrigan, Daniel, Medland, Sarah E., Zayats, Tetyana, Rajagopal, Veera M., Nordentoft, Merete, Mors, Ole, Hougaard, David M., Mortensen, Preben Bo, Daly, Mark J., Faraone, Stephen V., Stefansson, Hreinn, Roussos, Panos, Franke, Barbara, Werge, Thomas, Neale, Benjamin M., Stefansson, Kari, Børglum, Anders D.

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Evolution of genes and genomes on the Drosophila phylogeny von Clark, Andrew G, Eisen, Michael B, Smith, Douglas R, Bergman, Casey M, Oliver, Brian, Markow, Therese A, Kaufman, Thomas C, Kellis, Manolis, Gelbart, William, Iyer, Venky N, Pollard, Daniel A, Sackton, Timothy B, Larracuente, Amanda M, Singh, Nadia D, Abad, Jose P, Abt, Dawn N, Adryan, Boris, Aguade, Montserrat, Akashi, Hiroshi, Anderson, Wyatt W, Aquadro, Charles F, Ardell, David H, Arguello, Roman, Artieri, Carlo G, Barbash, Daniel A, Barker, Daniel, Barsanti, Paolo, Batterham, Phil, Batzoglou, Serafim, Begun, Dave, Bhutkar, Arjun, Blanco, Enrico, Bosak, Stephanie A, Bradley, Robert K, Brand, Adrianne D, Brent, Michael R, Brooks, Angela N, Brown, Randall H, Butlin, Roger K, Caggese, Corrado, Calvi, Brian R, Bernardo de Carvalho, A, Caspi, Anat, Castrezana, Sergio, Celniker, Susan E, Chang, Jean L, Chapple, Charles, Chatterji, Sourav, Chinwalla, Asif, Civetta, Alberto, Clifton, Sandra W, Comeron, Josep M, Costello, James C, Coyne, Jerry A, Daub, Jennifer, David, Robert G, Delcher, Arthur L, Delehaunty, Kim, Do, Chuong B, Ebling, Heather, Edwards, Kevin, Eickbush, Thomas, Evans, Jay D, Filipski, Alan, Findeiss, Sven, Freyhult, Eva, Fulton, Lucinda, Fulton, Robert, Garcia, Ana C L, Gardiner, Anastasia, Garfield, David A, Garvin, Barry E, Gibson, Greg, Gilbert, Don, Gnerre, Sante, Godfrey, Jennifer, Good, Robert, Gotea, Valer, Gravely, Brenton, Greenberg, Anthony J, Griffiths-Jones, Sam, Gross, Samuel, Guigo, Roderic, Gustafson, Erik A, Haerty, Wilfried, Hahn, Matthew W, Halligan, Daniel L, Halpern, Aaron L, Halter, Gillian M, Han, Mira V, Heger, Andreas, Hillier, LaDeana, Hinrichs, Angie S, Holmes, Ian, Hoskins, Roger A, Hubisz, Melissa J, Hultmark, Dan, Huntley, Melanie A, Jaffe, David B, Jagadeeshan, Santosh

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Quantifying the Impact of Rare and Ultra-rare Coding Variation across the Phenotypic Spectrum von Ganna, Andrea, Satterstrom, F. Kyle, Zekavat, Seyedeh M., Das, Indraniel, Kurki, Mitja I., Churchhouse, Claire, Alfoldi, Jessica, Martin, Alicia R., Havulinna, Aki S., Byrnes, Andrea, Thompson, Wesley K., Nielsen, Philip R., Karczewski, Konrad J., Saarentaus, Elmo, Rivas, Manuel A., Gupta, Namrata, Pietiläinen, Olli, Emdin, Connor A., Lescai, Francesco, Bybjerg-Grauholm, Jonas, Flannick, Jason, Mercader, Josep M., Udler, Miriam, Laakso, Markku, Salomaa, Veikko, Hultman, Christina, Ripatti, Samuli, Hämäläinen, Eija, Moilanen, Jukka S., Körkkö, Jarmo, Kuismin, Outi, Nordentoft, Merete, Hougaard, David M., Mors, Ole, Werge, Thomas, Mortensen, Preben Bo, MacArthur, Daniel, Daly, Mark J., Sullivan, Patrick F., Locke, Adam E., Palotie, Aarno, Børglum, Anders D., Kathiresan, Sekar, Neale, Benjamin M.

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Genome-wide association study of school grades identifies genetic overlap between language ability, psychopathology and creativity von Rajagopal, Veera M., Ganna, Andrea, Coleman, Jonathan R. I., Allegrini, Andrea, Voloudakis, Georgios, Grove, Jakob, Als, Thomas D., Horsdal, Henriette T., Petersen, Liselotte, Appadurai, Vivek, Schork, Andrew, Buil, Alfonso, Bulik, Cynthia M., Bybjerg-Grauholm, Jonas, Bækvad-Hansen, Marie, Hougaard, David M., Mors, Ole, Nordentoft, Merete, Werge, Thomas, Mortensen, Preben Bo, Breen, Gerome, Roussos, Panos, Plomin, Robert, Agerbo, Esben, Børglum, Anders D., Demontis, Ditte

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A Genetic Investigation of Sex Bias in the Prevalence of Attention-Deficit/Hyperactivity Disorder von Walters, Raymond K., Lee, S. Hong, Brikell, Isabell, Ghirardi, Laura, Larsson, Henrik, Lichtenstein, Paul, Bell, Robert K., Bryc, Katarzyna, Fontanillas, Pierre, Hromatka, Bethann S., Huber, Karen E., Litterman, Nadia K., McIntyre, Matthew H., Mountain, Joanna L., Pitts, Steven J., Vacic, Vladimir, Anney, Richard J.L., Vasquez, Alejandro Arias, Arranz, Maria Jesús, Banaschewski, Tobias, Banaschewski, Tobias J., Mortensen, Preben Bo, Børglum, Anders, Charach, Alice, Crosbie, Jennifer, Dalsgaard, Soeren, Demontis, Ditte, Dempfle, Astrid, Elia, Josephine, Faraone, Stephen V., Franke, Barbara, Freitag, Christine, Gelernter, Joel, Grevet, Eugenio, Haavik, Jan, Hakonarson, Hakon, Hawi, Ziarih, Hinney, Anke, Holmans, Peter, Ickowitz, Abel, Kent, Lindsey, Kittel-Schneider, Sarah, Langley, Kate, Lesch, Klaus-Peter, Loo, Sandra K., Martin, Joanna, Medland, Sarah E., Mulas, Fernando, Mulligan, Aisling, O’Donovan, Michael C., Oades, Robert D., Palmason, Haukur, Rhode, Luis, Roeyers, Herbert, Romanos, Marcel, Romanos, Jasmin, Rothenberger, Aribert, Schäfer, Helmut, Scherag, André, Schimmelmann, Benno G., Sergeant, Joseph, Smalley, Susan L., Sonuga-Barke, Edmund J.S., Steinhausen, Hans-Christoph, Sullivan, Patrick F., Todorov, Alexandre, Waldman, Irwin, Wang, Yufeng, Warnke, Andreas, Williams, Nigel, Witt, Stephanie H., Yang, Li, Agerbo, Esben, Belliveau, Rich, Børglum, Anders D., Chambert, Kimberly, Dalsgaard, Søren, Dumont, Ashley, Goldstein, Jacqueline, Grove, Jakob, Howrigan, Daniel P., Huang, Hailiang, Martin, Alicia R., Mattheisen, Manuel, Moran, Jennifer, Mors, Ole, Pallesen, Jonatan, Poterba, Timothy, Poulsen, Jesper Buchhave, Robinson, Elise B., Satterstrom, F. Kyle, Stevens, Christine, Turley, Patrick, Pedersen, Marianne Giørtz, Mors, Ole, Nordentoft, Merete, Hougaard, David M., Bybjerg-Grauholm, Jonas, Franke, Barbara, Neale, Benjamin M.

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Genome-wide analyses of self-reported empathy: correlations with autism, schizophrenia, and anorexia nervosa von Warrier, Varun, Toro, Roberto, Chakrabarti, Bhismadev, Børglum, Anders D, Grove, Jakob, Hinds, David A., Bourgeron, Thomas, Baron-Cohen, Simon

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Physical, cognitive, and mental health impacts of COVID-19 after hospitalisation (PHOSP-COVID): a UK multicentre, prospective cohort study von Howard, Luke, Abel, K, Altmann, D, Angyal, A, Ashworth, M, Assefa-Kebede, H, Baldry, E, Baldwin, D, Barratt, S, Bishop, L, Broome, M, Brown, M, Burns, G, Chetham, L, Choudhury, G, Coburn, Z, Cole, J, Connor, L, Coupland, C, Cross, A, Dalton, M, Davies, G A, Deakin, B, Defres, S, Diver, S, Dobson, S L, Drain, S, Fairbairn, S, Glossop, J, Greenhalgh, A, Gupta, A, Haggar, A, Harris, V, Harrison, E M, Hart, N, Heller, S, Hosseini, A, Hufton, E, Hussell, T, Ient, A, Ingram, L, Jacob, J, Johnston, D, Kausar, Z, Kelly, S, Khan, F, Korszun, A, Kwan, J, Laing, C, Lamlum, H, Lawrie, A, Lim, L, Lipman, M, Mackay, C, Man, W, Mayet, J, McAuley, H J C, McCann, G P, Mcgarvey, L, McGinness, J, McGuinness, H, McIvor, E, McNarry, M, Mitchell, J, Mohamed, A, Molyneaux, P L, Newell, H, Nicoll, D, Openshaw, P J M, Paradowski, K, Pariante, C, Pendlebury, J, Plekhanova, T, Quint, J, Qureshi, H, Rahman, N, Richardson, M, Rowland, M J, Russell, E, Sage, E K, Shaw, V, Southern, D, Spencer, L G, Stadon, L, Stockley, J, Storrie, A, Summers, C, Taylor, C, Turtle, L, Ugwuoke, R, Wall, E, Watson, J, Welch, C, Wilkinson, D, Williams-Howard, S A, Willis, G, Witham, M, Woods, J, Yasmin, S, Yousuf, A J

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Analysis of 6,515 exomes reveals the recent origin of most human protein-coding variants von Fu, Wenqing, O’Connor, Timothy D., Jun, Goo, Kang, Hyun Min, Abecasis, Goncalo, Leal, Suzanne M., Gabriel, Stacey, Rieder, Mark J., Altshuler, David, Shendure, Jay, Nickerson, Deborah A., Bamshad, Michael J., NHLBI Exome Sequencing Project, Akey, Joshua M.

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Safety and immunogenicity of concomitant administration of COVID-19 vaccines (ChAdOx1 or BNT162b2) with seasonal influenza vaccines in adults in the UK (ComFluCOV): a multicentre,... von Cappel-Porter, Heike, Culliford, Lucy, Emmett, Stevan R, Hutton, David, Jacobsen, Nick, Joyce, Katherine, Kaminski, Rachel, Libri, Vincenzo, Middleditch, Alex, McCullagh, Liz, Moran, Ed, Thirard, Russell, Snape, Matthew D, Finn, Adam, Rogers, Chris A, Adams, Kirsty, Alaee, Seema, Aley, Parvinder K., Allum, Emma, Anthony, Sally, Awal, Tanya, Barron, Charlotte, Bennett, Lorna, Bishop, Sarah, Bodalia, Pritesh, Bowyer, Catherine, Bray, Jonathan J.H., Burge, Sharon, Chohan, Gurjit, Close, Adrianne, Coleman, Tom, Cowley, Claire, Cranfield, Charlotte, Cross, Eleanor, D'Arcangelo, Silvia, David Otter, Ashley, Davies, Kate, Davies, Louisa, Driver, Kimberley, Evans, Mim, Evans, Isabel, Feltham, Sally, Ford, Jamie, Gooch, Karen E., Goodwin, Jayne, Halliday, Alice, Harrhy, Sarah, Haxton, Lesley, Haynes, Matthew, Hazell, Mae, Hembrough, Tracey, Hewson, Jacqueline, Hicks, Bethany, Hill, Michelle, Hills, Alex, Hua, Cheryl, Iftikhar, Hina, Iqbal, Attya, Jones, Nicola, Kellett Wright, Johanna, Kidd, Sarah, Knibbs, Lucy, Langton, Helen, Lewis-Clarke, Phoebe, Maclean, Kirsty, Manning, Nicola, Marriott, Anthony, McFadzean, Isobel Joy, McLaughlin, Maeve, Mills, Bianca, Norman, Chris, Nyland, Kerry, Owen, Diana, Paterson, Jemma, Pegler, Suzannah, Rampling, Tommy, Rea, David, Regan, Karen, Riaz, Tawassal, Ricamara, Marivic, Rice, Danielle, Roots, Marianne, Salem, Ahmed, Salter-Hewitt, Jade, Shankland, Sara, Silva, Louise, Smith, Joyce, Stringer, Rebecca, Talbot, Helen, Taylor, Sarah Louise, Thomas, Amy, Tilzey, Grace, Turner, Kelly, Tyler, Jenny, Wale, Katharine, Warnes, Barbara, Whittley, Sarah, Williams, Jennie, Williamson, Kevin, Yim, Yee Ting Nicole

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