Disease-associated mutations that alter the RNA structural ensemble by Halvorsen, Matthew, Martin, Joshua S, Broadaway, Sam, Laederach, Alain

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The Genetic Architecture of Obsessive-Compulsive Disorder: Contribution of Liability to OCD From Alleles Across the Frequency Spectrum by Mahjani, Behrang, Klei, Lambertus, Mattheisen, Manuel, Halvorsen, Matthew W, Reichenberg, Abraham, Roeder, Kathryn, Pedersen, Nancy L, Boberg, Julia, de Schipper, Elles, Bulik, Cynthia M, Landén, Mikael, Fundín, Bengt, Mataix-Cols, David, Sandin, Sven, Hultman, Christina M, Crowley, James J, Buxbaum, Joseph D, Rück, Christian, Devlin, Bernie, Grice, Dorothy E

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A burden of rare copy number variants in obsessive-compulsive disorder by Halvorsen, Matthew W, de Schipper, Elles, Bäckman, Julia, Strom, Nora I, Hagen, Kristen, Lindblad-Toh, Kerstin, Karlsson, Elinor K, Pedersen, Nancy L, Wallert, John, Bulik, Cynthia M, Fundín, Bengt, Landén, Mikael, Kvale, Gerd, Hansen, Bjarne, Haavik, Jan, Mattheisen, Manuel, Rück, Christian, Mataix-Cols, David, Crowley, James J

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Genome-Wide Association Study Meta-Analysis of 9619 Cases With Tic Disorders by Strom, Nora I., Halvorsen, Matthew W., Grove, Jakob, Ásbjörnsdóttir, Bergrún, Thorarensen, Ólafur, de Schipper, Elles, Bäckmann, Julia, Tian, Chao, Sul, Jae Hoon, Tsetsos, Fotis, Zelaya, Ivette, Osiecki, Lisa, Darrow, Sabrina M., Hirschtritt, Matthew E., Greenberg, Erica, Stuhrmann, Manfred, Dion, Yves, Rouleau, Guy, Aschauer, Harald, Stamenkovic, Mara, Schlögelhofer, Monika, Barr, Cathy L., Grados, Marco, Hinney, Anke, King, Robert A., Fernandez, Thomas V., Barta, Csaba, Tarnok, Zsanett, Nagy, Peter, Depienne, Christel, Worbe, Yulia, Hartmann, Andreas, Budman, Cathy L., Lyon, Gholson J., McMahon, William M., Batterson, James R., Malaty, Irene A., Okun, Michael S., Berlin, Cheston, Woods, Douglas W., Lee, Paul C., Jankovic, Joseph, Robertson, Mary M., Gilbert, Donald L., Brown, Lawrence W., Coffey, Barbara J., Hoekstra, Pieter J., Zinner, Samuel H., Luðvigsson, Pétur, Thorarensen, Ólafur, Atzmon, Gil, Barzilai, Nir, Moessner, Rainald, Ophoff, Roel, Pato, Carlos N., Knowles, James A., Buckner, Randy L., Willsey, Jeremy A., Tischfield, Jay A., Heiman, Gary A., Stefansson, Hreinn, Stefansson, Kári, Posthuma, Danielle, Pauls, David L., Freimer, Nelson B., Davis, Lea K., Paschou, Peristera, Coppola, Giovanni, Mathews, Carol A., Scharf, Jeremiah M., Agee, Michelle, Auton, Adam, Elson, Sarah L., Furlotte, Nicholas A., Hicks, Barry, Jewett, Ethan M., Jiang, Yunxuan, Kleinman, Aaron, Lin, Keng-Han, Litterman, Nadia K., McIntyre, Matthew H., McManus, Kimberly F., Mountain, Joanna L., Pitts, Steven J., Poznik, G. David, Sathirapongsasuti, J. Fah, Shelton, Janie F., Shringarpure, Suyash, Tung, Joyce Y., Wang, Xin, Als, Thomas Damm, Meier, Sandra M., Bybjerg-Grauholm, Jonas, Hougaard, David M., Werge, Thomas, Børglum, Anders D., Hinds, David A., Rück, Christian, Mataix-Cols, David, Mattheisen, Manuel

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Predicting remission after internet-delivered psychotherapy in patients with depression using machine learning and multi-modal data by Wallert, John, Boberg, Julia, Kaldo, Viktor, Mataix-Cols, David, Flygare, Oskar, Crowley, James J., Halvorsen, Matthew, Ben Abdesslem, Fehmi, Boman, Magnus, Andersson, Evelyn, Hentati Isacsson, Nils, Ivanova, Ekaterina, Rück, Christian

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ARFID Genes and Environment (ARFID-GEN): study protocol by Bulik, Cynthia M, Micali, Nadia, MacDermod, Casey M, Qi, Baiyu, Munn-Chernoff, Melissa A, Thornton, Laura M, White, Jennifer, Dinkler, Lisa, Pisetsky, Emily M, Johnson, Jessica, Devine, Katelin R, Ortiz, Shelby N, Silverman, Ava E, Berthold, Natasha, Dumain, Alexis, Guintivano, Jerry, Halvorsen, Matthew, Crowley, James J

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Author Correction: Increased burden of ultra-rare structural variants localizing to boundaries of topologically associated domains in schizophrenia by Halvorsen, Matthew, Huh, Ruth, Oskolkov, Nikolay, Wen, Jia, Netotea, Sergiu, Giusti-Rodriguez, Paola, Karlsson, Robert, Bryois, Julien, Nystedt, Björn, Ameur, Adam, Kähler, Anna K., Ancalade, NaEshia, Farrell, Martilias, Crowley, James J., Li, Yun, Magnusson, Patrik K. E., Gyllensten, Ulf, Hultman, Christina M., Sullivan, Patrick F., Szatkiewicz, Jin P.

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The potential of the riboSNitch in personalized medicine by Solem, Amanda C., Halvorsen, Matthew, Ramos, Silvia B. V., Laederach, Alain

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Polygenic Heterogeneity Across Obsessive-Compulsive Disorder Subgroups Defined by a Comorbid Diagnosis by Strom, Nora I, Grove, Jakob, Meier, Sandra M, Bækvad-Hansen, Marie, Becker Nissen, Judith, Damm Als, Thomas, Halvorsen, Matthew, Nordentoft, Merete, Mortensen, Preben B, Hougaard, David M, Werge, Thomas, Mors, Ole, Børglum, Anders D, Crowley, James J, Bybjerg-Grauholm, Jonas, Mattheisen, Manuel

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Swedish multimodal cohort of patients with anxiety or depression treated with internet-delivered psychotherapy (MULTI-PSYCH) by Boberg, Julia, Kaldo, Viktor, Mataix-Cols, David, Crowley, James J, Roelstraete, Bjorn, Halvorsen, Matthew, Forsell, Erik, Isacsson, Nils H, Sullivan, Patrick F, Svanborg, Cecilia, Andersson, Evelyn H, Lindefors, Nils, Kravchenko, Olly, Mattheisen, Manuel, Danielsdottir, Hilda B, Ivanova, Ekaterina, Boman, Magnus, Fernández de la Cruz, Lorena, Wallert, John, Rück, Christian

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Sudden unexpected death in asymptomatic infants due to PPA2 variants by Phoon, Colin K. L., Halvorsen, Matthew, Goldstein, David B., Rabin, Rachel, Cecchin, Frank, Crandall, Laura, Devinsky, Orrin

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W10. EXPLORING THE CONTRIBUTION OF POLYGENIC RISK SCORES TO EXPLAINING VARIANCE IN SYMPTOM LEVEL AFTER INTERNET-DELIVERED COGNITIVE BEHAVIORAL THERAPY FOR DEPRESSION AND ANXIETY DI... by Kravchenko, Olly, Boberg, Julia, Mataix-Cols, David, Crowley, James, Halvorsen, Matthew, Wallert, John, Rück, Christian

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T7. POLYGENIC RISK SCORES FOR PREDICTING SYMPTOM CHANGE AFTER INTERNET-DELIVERED COGNITIVE BEHAVIORAL THERAPY FOR DEPRESSION AND ANXIETY DISORDERS by Kravchenko, Olly, Boberg, Julia, Mataix-Cols, David, Crowley, James, Halvorsen, Matthew, Wallert, John, Rück, Christian

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Examination of the shared genetic basis of anorexia nervosa and obsessive–compulsive disorder by 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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De novo mutations in childhood cases of sudden unexplained death that disrupt intracellular Ca2+ regulation by Halvorsen, Matthew, Gould, Laura, Wang, Xiaohan, Grant, Gariel, Moya, Raquel, Rabin, Rachel, Ackerman, Michael J., Tester, David J., Lin, Peter T., Pappas, John G., Maurano, Matthew T., Goldstein, David B., Tsien, Richard W., Devinsky, Orrin

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Genomics of severe and treatment‐resistant obsessive–compulsive disorder treated with deep brain stimulation: A preliminary investigation by Chen, Long Long, Naesström, Matilda, Halvorsen, Matthew, Fytagoridis, Anders, Crowley, Stephanie B., Mataix‐Cols, David, Rück, Christian, Crowley, James J., Pascal, Diana

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Predicting eating disorder and anxiety symptoms using disorder-specific and transdiagnostic polygenic scores for anorexia nervosa and obsessive-compulsive disorder by Yilmaz, Zeynep, Schaumberg, Katherine, Halvorsen, Matthew, Goodman, Erica L., Brosof, Leigh C., Crowley, James J., Mathews, Carol A., Mattheisen, Manuel, Breen, Gerome, Bulik, Cynthia M., Micali, Nadia, Zerwas, Stephanie C.

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Increased burden of ultra-rare structural variants localizing to boundaries of topologically associated domains in schizophrenia by Halvorsen, Matthew, Huh, Ruth, Oskolkov, Nikolay, Wen, Jia, Netotea, Sergiu, Giusti-Rodriguez, Paola, Karlsson, Robert, Bryois, Julien, Nystedt, Björn, Ameur, Adam, Kähler, Anna K., Ancalade, NaEshia, Farrell, Martilias, Crowley, James J., Li, Yun, Magnusson, Patrik K. E., Gyllensten, Ulf, Hultman, Christina M., Sullivan, Patrick F., Szatkiewicz, Jin P.

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Multiple conformations are a conserved and regulatory feature of the RB1 5' UTR by Kutchko, Katrina M, Sanders, Wes, Ziehr, Ben, Phillips, Gabriela, Solem, Amanda, Halvorsen, Matthew, Weeks, Kevin M, Moorman, Nathaniel, Laederach, Alain

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Rare tandem repeat expansions associate with genes involved in synaptic and neuronal signaling functions in schizophrenia by Wen, Jia, Trost, Brett, Engchuan, Worrawat, Halvorsen, Matthew, Pallotto, Linda M., Mitina, Aleksandra, Ancalade, NaEshia, Farrell, Martilias, Backstrom, Ian, Guo, Keyi, Pellecchia, Giovanna, Thiruvahindrapuram, Bhooma, Giusti-Rodriguez, Paola, Rosen, Jonathan David, Li, Yun, Won, Hyejung, Magnusson, Patrik K. E., Gyllensten, Ulf, Bassett, Anne S., Hultman, Christina M., Sullivan, Patrick F., Yuen, Ryan K. C., Szatkiewicz, Jin P.

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