A Method for Variant Agnostic Detection of SARS-CoV-2, Rapid Monitoring of Circulating Variants, and Early Detection of Emergent Variants Such as Omicron by Lai, Eric, Kennedy, Emily B, Lozach, Jean, Hayashibara, Kathleen, Davis-Turak, Jeremy, Becker, David, Brzoska, Pius, Cassens, Tyler, Diamond, Evan, Gandhi, Manoj, Greninger, Alexander L, Hajian, Pooneh, Leonetti, Nicole A, Nguyen, Jason M, O'Donovan, K M Clair, Peck, Troy, Ramirez, 3rd, Jimmy M, Roychoudhury, Pavitra, Sandoval, Efren, Wesselman, Cassandra, Wesselman, Timothy, White, Simon, Williams, Stephen, Wong, David, Yu, Yufei, Creager, Richard S

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Improved Detection of Common Variants Associated with Schizophrenia by Leveraging Pleiotropy with Cardiovascular-Disease Risk Factors by Andreassen, Ole A., Djurovic, Srdjan, Thompson, Wesley K., Schork, Andrew J., Kendler, Kenneth S., O’Donovan, Michael C., Rujescu, Dan, Werge, Thomas, van de Bunt, Martijn, Morris, Andrew P., McCarthy, Mark I., Roddey, J. Cooper, McEvoy, Linda K., Desikan, Rahul S., Dale, Anders M.

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Genetic utility of broadly defined bipolar schizoaffective disorder as a diagnostic concept by Hamshere, M. L., Green, E. K., Jones, I. R., Jones, L., Moskvina, V., Kirov, G., Grozeva, D., Nikolov, I., Vukcevic, D., Caesar, S., Gordon-Smith, K., Fraser, C., Russell, E., Breen, G., Clair, D. St, Collier, D. A., Young, A. H., Ferrier, I. N., Farmer, A., McGuffin, P., Holmans, P. A., Owen, M. J., O'Donovan, M. C., Craddock, N.

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DNA methylation meta-analysis reveals cellular alterations in psychosis and markers of treatment-resistant schizophrenia by Hannon, Eilis, Dempster, Emma L, Mansell, Georgina, Burrage, Joe, Bass, Nick, Bohlken, Marc M, Corvin, Aiden, Curtis, Charles J, Dempster, David, Di Forti, Marta, Dinan, Timothy G, Donohoe, Gary, Gaughran, Fiona, Gill, Michael, Gillespie, Amy, Gunasinghe, Cerisse, Hulshoff, Hilleke E, Hultman, Christina M, Johansson, Viktoria, Kahn, René S, Kaprio, Jaakko, Kenis, Gunter, Kowalec, Kaarina, MacCabe, James, McDonald, Colm, McQuillin, Andrew, Morris, Derek W, Murphy, Kieran C, Mustard, Colette J, Nenadic, Igor, O'Donovan, Michael C, Quattrone, Diego, Richards, Alexander L, Rutten, Bart Pf, St Clair, David, Therman, Sebastian, Toulopoulou, Timothea, Van Os, Jim, Waddington, John L, Sullivan, Patrick, Vassos, Evangelos, Breen, Gerome, Collier, David Andrew, Murray, Robin M, Schalkwyk, Leonard S, Mill, Jonathan

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Common polygenic variation contributes to risk of schizophrenia and bipolar disorder by Purcell, Shaun M, Wray, Naomi R, Stone, Jennifer L, Visscher, Peter M, O'Donovan, Michael C, Sullivan, Patrick F, Sklar, Pamela

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Rare chromosomal deletions and duplications increase risk of schizophrenia by Stone, Jennifer L., O'Donovan, Michael C., Gurling, Hugh, Kirov, George K., Blackwood, Douglas H. R., Corvin, Aiden, Craddock, Nick J., Gill, Michael, Hultman, Christina M., Lichtenstein, Paul, McQuillin, Andrew, Pato, Carlos N., Ruderfer, Douglas M., Owen, Michael J., St Clair, David, Sullivan, Patrick F., Sklar, Pamela, Purcell, Shaun M.

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Genome-wide association study reveals greater polygenic loading for schizophrenia in cases with a family history of illness by Bigdeli, Tim B., Ripke, Stephan, Bacanu, Silviu-Alin, Lee, Sang Hong, Wray, Naomi R., Gejman, Pablo V., Rietschel, Marcella, Cichon, Sven, St Clair, David, Corvin, Aiden, Kirov, George, McQuillin, Andrew, Gurling, Hugh, Rujescu, Dan, Andreassen, Ole A., Werge, Thomas, Blackwood, Douglas H. R., Pato, Carlos N., Pato, Michele T., Malhotra, Anil K., O'Donovan, Michael C., Kendler, Kenneth S., Fanous, Ayman H.

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Expression analysis in a rat psychosis model identifies novel candidate genes validated in a large case–control sample of schizophrenia by Ingason, A, Giegling, I, Hartmann, A M, Genius, J, Konte, B, Friedl, M, Ripke, S, Sullivan, P F, St. Clair, D, Collier, D A, O'Donovan, M C, Mirnics, K, Rujescu, D

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Polygenic dissection of the bipolar phenotype by Hamshere, M L, O'Donovan, M C, Jones, I R, Jones, L, Kirov, G, Green, E K, Moskvina, V, Grozeva, D, Bass, N, McQuillin, A, Gurling, H, St Clair, D, Young, A H, Ferrier, I N, Farmer, A, McGuffin, P, Sklar, P, Purcell, S, Holmans, P A, Owen, M J, Craddock, N

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DISC1 exon 11 rare variants found more commonly in schizoaffective spectrum cases than controls by Green, E.K., Grozeva, D., Sims, R., Raybould, R., Forty, L., Gordon-Smith, K., Russell, E., St. Clair, D., Young, A.H., Ferrier, I.N., Kirov, G., Jones, I., Jones, L, Owen, M.J., O'Donovan, M.C., Craddock, N.

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Additive Genetic Variation in Schizophrenia Risk Is Shared by Populations of African and European Descent by de Candia, Teresa R., Lee, S. Hong, Yang, Jian, Browning, Brian L., Gejman, Pablo V., Levinson, Douglas F., Mowry, Bryan J., Hewitt, John K., Goddard, Michael E., O’Donovan, Michael C., Purcell, Shaun M., Posthuma, Danielle, Visscher, Peter M., Wray, Naomi R., Keller, Matthew C.

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Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls by Clayton, David G, Cardon, Lon R, Duncanson, Audrey, Ouwehand, Willem H, Todd, John A, Donnelly, Peter, Easton, Doug, Evans, David, Morris, Andrew P, Spencer, Chris C. A, Boorman, James P, Cant, Barbara, Everson, Ursula, Hussey, Judith M, Knight, Alexandra S, Nutland, Sarah, Stevens, Helen E, Watkins, Nicholas A, Jones, Richard W, Ring, Susan M, Breen, Gerome, Caesar, Sian, Green, Elaine K, Grozeva, Detelina, Jones, Ian R, Kirov, George, Moskvina, Valentina, Nikolov, Ivan, Collier, David A, Farmer, Anne, Williamson, Richard, Young, Allan H, Ball, Stephen G, Balmforth, Anthony J, Bishop, D. Timothy, Iles, Mark M, Dixon, Richard J, Stevens, Suzanne, Thompson, John R, Bredin, Francesca, Tremelling, Mark, Drummond, Hazel, Nimmo, Elaine R, Fisher, Sheila A, Forbes, Alastair, Lewis, Cathryn M, Prescott, Natalie J, Barbour, Jamie, Mohiuddin, M. Khalid, Mansfield, John C, Cummings, Fraser R, Connell, John, Dobson, Richard, Gungadoo, Johannie, Newhouse, Stephen J, Barton, Anne, Bruce, Ian N, John, Sally L, Potter, Catherine, Silman, Alan J, Symmons, Deborah P. M, Dunger, David B, Widmer, Barry, Frayling, Timothy M, Lango, Hana, Perry, John R. B, Groves, Christopher J, Rayner, Nigel W, Timpson, Nicholas J, Zeggini, Eleftheria, Newport, Melanie, Vannberg, Fredrik, Farrar, Claire, Wordsworth, Paul, Brown, Matthew A, Franklyn, Jayne A, Heward, Joanne M, Simmonds, Matthew J, Seal, Sheila, Stratton, Michael R, Ban, Maria, Conway, David, Chaney, Amy, Ghori, Mohammed J. R, Gwilliam, Rhian, Hunt, Sarah E, McGinnis, Ralph, Potter, Simon, Whittaker, Pamela, Widden, Claire, Withers, David, Hallgrimsdottir, Ingileif B, Vukcevic, Damjan, Bentley, David, Caulfield, Mark, Compston, Alistair, Farrall, Martin, Hall, Alistair S, Hattersley, Andrew T, Mathew, Christopher G

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An inherited duplication at the gene p21 Protein-Activated Kinase 7 (PAK7) is a risk factor for psychosis by Morris, Derek W, Pearson, Richard D, Cormican, Paul, Kenny, Elaine M, O'Dushlaine, Colm T, Perreault, Louis-Philippe Lemieux, Giannoulatou, Eleni, Tropea, Daniela, Maher, Brion S, Wormley, Brandon, Kelleher, Eric, Fahey, Ciara, Molinos, Ines, Bellini, Stefania, Pirinen, Matti, Strange, Amy, Freeman, Colin, Thiselton, Dawn L, Elves, Rachel L, Regan, Regina, Ennis, Sean, Dinan, Timothy G, McDonald, Colm, Murphy, Kieran C, O'Callaghan, Eadbhard, Waddington, John L, Walsh, Dermot, O'Donovan, Michael, Grozeva, Detelina, Craddock, Nick, Stone, Jennifer, Scolnick, Ed, Purcell, Shaun, Sklar, Pamela, Coe, Bradley, Eichler, Evan E, Ophoff, Roel, Buizer, Jacobine, Szatkiewicz, Jin, Hultman, Christina, Sullivan, Patrick, Gurling, Hugh, Mcquillin, Andrew, St Clair, David, Rees, Elliott, Kirov, George, Walters, James, Blackwood, Douglas, Johnstone, Mandy, Donohoe, Gary, O'Neill, Francis A, Kendler, Kenneth S, Gill, Michael, Riley, Brien P, Spencer, Chris C A, Corvin, Aiden

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Mosaic copy number variation in schizophrenia by Ruderfer, Douglas M, Chambert, Kim, Moran, Jennifer, Talkowski, Michael, Chen, Elizabeth S, Gigek, Carolina, Gusella, James F, Blackwood, Douglas H, Corvin, Aiden, Gurling, Hugh M, Hultman, Christina M, Kirov, George, Magnusson, Patrick, O'Donovan, Michael C, Owen, Michael J, Pato, Carlos, St Clair, David, Sullivan, Patrick F, Purcell, Shaun M, Sklar, Pamela, Ernst, Carl

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Evaluation of a Susceptibility Gene for Schizophrenia: Genotype Based Meta-Analysis of RGS4 Polymorphisms from Thirteen Independent Samples by Talkowski, Michael E., Seltman, Howard, Bassett, Anne S., Brzustowicz, Linda M., Chen, Xiangning, Chowdari, Kodavali V., Collier, David A., Cordeiro, Quirino, Corvin, Aiden P., Deshpande, Smita N., Egan, Michael F., Gill, Michael, Kendler, Kenneth S., Kirov, George, Heston, Leonard L., Levitt, Pat, Lewis, David A., Li, Tao, Mirnics, Karoly, Morris, Derek W., Norton, Nadine, O'Donovan, Michael C., Owen, Michael J., Richard, Christian, Semwal, Prachi, Sobell, Janet L., St Clair, David, Straub, Richard E., Thelma, B.K., Vallada, Homero, Weinberger, Daniel R., Williams, Nigel M., Wood, Joel, Zhang, Feng, Devlin, Bernie, Nimgaonkar, Vishwajit L.

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New data and an old puzzle: the negative association between schizophrenia and rheumatoid arthritis by Lee, S Hong, Byrne, Enda M, Hultman, Christina M, Kähler, Anna, Vinkhuyzen, Anna A E, Ripke, Stephan, Andreassen, Ole A, Frisell, Thomas, Gusev, Alexander, Hu, Xinli, Karlsson, Robert, Mantzioris, Vasilis X, McGrath, John J, Mehta, Divya, Stahl, Eli A, Zhao, Qiongyi, Kendler, Kenneth S, Sullivan, Patrick F, Price, Alkes L, O'Donovan, Michael, Okada, Yukinori, Mowry, Bryan J, Raychaudhuri, Soumya, Wray, Naomi R, Byerley, William, Cahn, Wiepke, Cantor, Rita M, Cichon, Sven, Cormican, Paul, Curtis, David, Djurovic, Srdjan, Escott-Price, Valentina, Gejman, Pablo V, Georgieva, Lyudmila, Giegling, Ina, Hansen, Thomas F, Ingason, Andrés, Kim, Yunjung, Konte, Bettina, Lee, Phil H, McIntosh, Andrew, McQuillin, Andrew, Morris, Derek W, Nöthen, Markus M, O'Dushlaine, Colm, Olincy, Ann, Olsen, Line, Pato, Carlos N, Pato, Michele T, Pickard, Benjamin S, Posthuma, Danielle, Rasmussen, Henrik B, Rietschel, Marcella, Rujescu, Dan, Schulze, Thomas G, Silverman, Jeremy M, Thirumalai, Srinivasa, Werge, Thomas, Agartz, Ingrid, Amin, Farooq, Azevedo, Maria H, Bass, Nicholas, Black, Donald W, Blackwood, Douglas H R, Bruggeman, Richard, Buccola, Nancy G, Choudhury, Khalid, Cloninger, Robert C, Corvin, Aiden, Craddock, Nicholas, Daly, Mark J, Datta, Susmita, Donohoe, Gary J, Duan, Jubao, Dudbridge, Frank, Fanous, Ayman, Freedman, Robert, Freimer, Nelson B, Friedl, Marion, Gill, Michael, Gurling, Hugh, De Haan, Lieuwe, Hamshere, Marian L, Hartmann, Annette M, Holmans, Peter A, Kahn, René S, Keller, Matthew C, Kenny, Elaine, Kirov, George K, Krabbendam, Lydia, Krasucki, Robert, Lawrence, Jacob, Lencz, Todd, Levinson, Douglas F, Lieberman, Jeffrey A, Lin, Dan-Yu, Linszen, Don H, Magnusson, Patrik K E, Maier, Wolfgang, Malhotra, Anil K

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Network-assisted investigation of combined causal signals from genome-wide association studies in schizophrenia by Jia, Peilin, Wang, Lily, Fanous, Ayman H, Pato, Carlos N, Edwards, Todd L, Zhao, Zhongming

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Runs of homozygosity implicate autozygosity as a schizophrenia risk factor by Keller, Matthew C, Simonson, Matthew A, Ripke, Stephan, Neale, Ben M, Gejman, Pablo V, Howrigan, Daniel P, Lee, Sang Hong, Lencz, Todd, Levinson, Douglas F, Sullivan, Patrick F

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Investigation of the genetic association between quantitative measures of psychosis and schizophrenia: a polygenic risk score analysis by Derks, Eske M, Vorstman, Jacob A S, Ripke, Stephan, Kahn, Rene S, Ophoff, Roel A

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Re-evaluation of putative rheumatoid arthritis susceptibility genes in the post-genome wide association study era and hypothesis of a key pathway underlying susceptibility by Barton, Anne, Thomson, Wendy, Ke, Xiayi, Eyre, Steve, Hinks, Anne, Bowes, John, Gibbons, Laura, Plant, Darren, Wilson, Anthony G., Marinou, Ioanna, Morgan, Ann, Emery, Paul, Steer, Sophia, Hocking, Lynne, Reid, David M., Wordsworth, Paul, Harrison, Pille, Worthington, Jane

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