Monomeric C-Reactive Protein in Serum With Markedly Elevated CRP Levels Shares Common Calcium-Dependent Ligand Binding Properties With an in vitro Dissociated Form of C-Reactive Pr... von Williams, Robert D, Moran, Jennifer A, Fryer, Anthony A, Littlejohn, Jamie R, Williams, Harry M, Greenhough, Trevor J, Shrive, Annette K

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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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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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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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Polygenic transmission disequilibrium confirms that common and rare variation act additively to create risk for autism spectrum disorders von Weiner, Daniel J, Wigdor, Emilie M, Ripke, Stephan, Walters, Raymond K, Kosmicki, Jack A, Grove, Jakob, Samocha, Kaitlin E, Goldstein, Jacqueline I, Okbay, Aysu, Bybjerg-Grauholm, Jonas, Werge, Thomas, Hougaard, David M, Taylor, Jacob, Skuse, David, Devlin, Bernie, Anney, Richard, Sanders, Stephan J, Bishop, Somer, Mortensen, Preben Bo, Børglum, Anders D, Smith, George Davey, Daly, Mark J, Robinson, Elise B

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Comorbidity of Severe Psychotic Disorders With Measures of Substance Use von Hartz, Sarah M, Pato, Carlos N, Medeiros, Helena, Cavazos-Rehg, Patricia, Sobell, Janet L, Knowles, James A, Bierut, Laura J, Pato, Michele T

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Large-scale genome-wide association analysis of bipolar disorder identifies a new susceptibility locus near ODZ4 von Sklar, Pamela, Ripke, Stephan, Scott, Laura J, Andreassen, Ole A, Cichon, Sven, Craddock, Nick, Edenberg, Howard J, Nurnberger, John I, Rietschel, Marcella, Blackwood, Douglas, Corvin, Aiden, Flickinger, Matthew, Guan, Weihua, Mattingsdal, Morten, McQuillin, Andrew, Kwan, Phoenix, Wienker, Thomas F, Daly, Mark, Dudbridge, Frank, Holmans, Peter A, Lin, Danyu, Burmeister, Margit, Greenwood, Tiffany A, Hamshere, Marian L, Muglia, Pierandrea, Smith, Erin N, Zandi, Peter P, Nievergelt, Caroline M, McKinney, Rebecca, Shilling, Paul D, Schork, Nicholas J, Bloss, Cinnamon S, Foroud, Tatiana, Koller, Daniel L, Gershon, Elliot S, Liu, Chunyu, Badner, Judith A, Scheftner, William A, Lawson, William B, Nwulia, Evaristus A, Hipolito, Maria, Coryell, William, Rice, John, Byerley, William, McMahon, Francis J, Schulze, Thomas G, Berrettini, Wade, Lohoff, Falk W, Potash, James B, Mahon, Pamela B, McInnis, Melvin G, Zöllner, Sebastian, Zhang, Peng, Craig, David W, Szelinger, Szabocls, Barrett, Thomas B, Breuer, René, Meier, Sandra, Strohmaier, Jana, Witt, Stephanie H, Tozzi, Federica, Farmer, Anne, McGuffin, Peter, Strauss, John, Xu, Wei, Kennedy, James L, Vincent, John B, Matthews, Keith, Day, Richard, Ferreira, Manuel A, O'Dushlaine, Colm, Perlis, Roy, Raychaudhuri, Soumya, Ruderfer, Douglas, Lee, Phil H, Smoller, Jordan W, Li, Jun, Absher, Devin, Bunney, William E, Barchas, Jack D, Schatzberg, Alan F, Jones, Edward G, Meng, Fan, Thompson, Robert C, Watson, Stanley J, Myers, Richard M, Akil, Huda, Boehnke, Michael, Chambert, Kim, Moran, Jennifer, Scolnick, Ed, Djurovic, Srdjan, Melle, Ingrid, Morken, Gunnar, Gill, Michael, Morris, Derek, Quinn, Emma, Mühleisen, Thomas W, Degenhardt, Franziska A, Mattheisen, Manuel

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A Randomized Trial of Urodynamic Testing before Stress-Incontinence Surgery von Nager, Charles W, Brubaker, Linda, Litman, Heather J, Zyczynski, Halina M, Varner, R. Edward, Amundsen, Cindy, Sirls, Larry T, Norton, Peggy A, Arisco, Amy M, Chai, Toby C, Zimmern, Philippe, Barber, Matthew D, Dandreo, Kimberly J, Menefee, Shawn A, Kenton, Kimberly, Lowder, Jerry, Richter, Holly E, Khandwala, Salil, Nygaard, Ingrid, Kraus, Stephen R, Johnson, Harry W, Lemack, Gary E, Mihova, Marina, Albo, Michael E, Mueller, Elizabeth, Sutkin, Gary, Wilson, Tracey S, Hsu, Yvonne, Rozanski, Thomas A, Rickey, Leslie M, Rahn, David, Tennstedt, Sharon, Kusek, John W, Gormley, E. Ann

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Identification of Pathways for Bipolar Disorder: A Meta-analysis von Nurnberger, John I, Koller, Daniel L, Jung, Jeesun, Edenberg, Howard J, Foroud, Tatiana, Guella, Ilaria, Vawter, Marquis P, Kelsoe, John R

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Validation of Electronic Health Record Phenotyping of Bipolar Disorder Cases and Controls von Castro, Victor M., Minnier, Jessica, Murphy, Shawn N., Kohane, Isaac, Churchill, Susanne E., Gainer, Vivian, Cai, Tianxi, Hoffnagle, Alison G., Dai, Yael, Block, Stefanie, Weill, Sydney R., Nadal-Vicens, Mireya, Pollastri, Alisha R., Rosenquist, J. Niels, Goryachev, Sergey, Ongur, Dost, Sklar, Pamela, Perlis, Roy H., Smoller, Jordan W., Smoller, Jordan W., Perlis, Roy H., Lee, Phil Hyoun, Castro, Victor M., Hoffnagle, Alison G., Sklar, Pamela, Stahl, Eli A., Purcell, Shaun M., Ruderfer, Douglas M., Charney, Alexander W., Roussos, Panos, Pato, Carlos, Pato, Michele, Medeiros, Helen, Sobel, Janet, Craddock, Nick, Jones, Ian, Forty, Liz, DiFlorio, Arianna, Green, Elaine, Jones, Lisa, Dunjewski, Katherine, Landén, Mikael, Hultman, Christina, Juréus, Anders, Bergen, Sarah, Svantesson, Oscar, McCarroll, Steven, Moran, Jennifer, Chambert, Kimberly, Belliveau, Richard A.

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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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Predictors of Outcomes in Patients With Mild Ischemic Stroke Symptoms: MaRISS von Romano, Jose G., Gardener, Hannah, Campo-Bustillo, Iszet, Khan, Yosef, Tai, Sofie, Riley, Nikesha, Smith, Eric E., Sacco, Ralph L., Khatri, Pooja, Alger, Heather M., Mac Grory, Brian, Gulati, Deepak, Sangha, Navdeep S., Craig, Jeffrey M., Olds, Karin E., Benesch, Curtis G., Kelly, Adam G., Brehaut, Scott S., Kansara, Amit C., Schwamm, Lee H.

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A Rare Functional Noncoding Variant at the GWAS-Implicated MIR137/MIR2682 Locus Might Confer Risk to Schizophrenia and Bipolar Disorder von Duan, Jubao, Shi, Jianxin, Fiorentino, Alessia, Leites, Catherine, Chen, Xiangning, Moy, Winton, Chen, Jingchun, Alexandrov, Boian S., Usheva, Anny, He, Deli, Freda, Jessica, O’Brien, Niamh L., Gejman, Pablo V., Sanders, Alan R., Duan, Jubao, Levinson, Douglas F., Shi, Jianxin, Buccola, Nancy G., Mowry, Bryan J., Freedman, Robert, Olincy, Ann, Amin, Farooq, Black, Donald W., Silverman, Jeremy M., Byerley, William F., Svrakic, Dragan M., Cloninger, C. Robert, Pato, Michele T., Sobell, Janet L., Medeiros, Helena, Abbott, Colony, Skar, Brooke, Buckley, Peter F., Bromet, Evelyn J., Escamilla, Michael A., Fanous, Ayman H., Lehrer, Douglas S., Macciardi, Fabio, Malaspina, Dolores, McCarroll, Steve A., Marder, Stephen R., Moran, Jennifer, Morley, Christopher P., Nicolini, Humberto, Perkins, Diana O., Purcell, Shaun M., Rapaport, Mark H., Sklar, Pamela, Smoller, Jordan W., Knowles, James A., Pato, Carlos N., McQuillin, Andrew, Sanders, Alan R., Gershon, Elliot S., DeLisi, Lynn E., Bishop, Alan R., Gurling, Hugh M.D., Pato, Michele T., Levinson, Douglas F., Kendler, Kenneth S., Pato, Carlos N., Gejman, Pablo V.

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Elevated polygenic burden for autism is associated with differential DNA methylation at birth von Hannon, Eilis, Schendel, Diana, Ladd-Acosta, Christine, Grove, Jakob, Hansen, Christine Søholm, Andrews, Shan V, Hougaard, David Michael, Bresnahan, Michaeline, Mors, Ole, Hollegaard, Mads Vilhelm, Bækvad-Hansen, Marie, Hornig, Mady, Mortensen, Preben Bo, Børglum, Anders D, Werge, Thomas, Pedersen, Marianne Giørtz, Nordentoft, Merete, Buxbaum, Joseph, Daniele Fallin, M, Bybjerg-Grauholm, Jonas, Reichenberg, Abraham, Mill, Jonathan

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Frequency and Prognostic Significance of Clinical Fluctuations Before Hospital Arrival in Stroke von Romano, Jose G., Gardener, Hannah, Smith, Eric E., Campo-Bustillo, Iszet, Khan, Yosef, Tai, Sofie, Riley, Nikesha, Sacco, Ralph L., Khatri, Pooja, Alger, Heather M., Mac Grory, Brian, Gulati, Deepak, Sangha, Navdeep S., Olds, Karin E., Benesch, Curtis G., Kelly, Adam G., Brehaut, Scott S., Kansara, Amit C., Schwamm, Lee H.

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Schizophrenia susceptibility alleles are enriched for alleles that affect gene expression in adult human brain von Richards, A L, Jones, L, Moskvina, V, Kirov, G, Gejman, P V, Levinson, D F, Sanders, A R, Purcell, S, Visscher, P M, Craddock, N, Owen, M J, Holmans, P, O'Donovan, M C

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GWA study data mining and independent replication identify cardiomyopathy-associated 5 (CMYA5) as a risk gene for schizophrenia von Chen, X, Lee, G, Maher, B S, Fanous, A H, Chen, J, Zhao, Z, Guo, A, van den Oord, E, Sullivan, P F, Shi, J, Levinson, D F, Gejman, P V, Sanders, A, Duan, J, Owen, M J, Craddock, N J, O'Donovan, M C, Blackman, J, Lewis, D, Kirov, G K, Qin, W, Schwab, S, Wildenauer, D, Chowdari, K, Nimgaonkar, V, Straub, R E, Weinberger, D R, O'Neill, F A, Walsh, D, Bronstein, M, Darvasi, A, Lencz, T, Malhotra, A K, Rujescu, D, Giegling, I, Werge, T, Hansen, T, Ingason, A, Nöethen, M M, Rietschel, M, Cichon, S, Djurovic, S, Andreassen, O A, Cantor, R M, Ophoff, R, Corvin, A, Morris, D W, Gill, M, Pato, C N, Pato, M T, Macedo, A, Gurling, H M D, McQuillin, A, Pimm, J, Hultman, C, Lichtenstein, P, Sklar, P, Purcell, S M, Scolnick, E, St Clair, D, Blackwood, D H R, Kendler, K S

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Disentangling polygenic associations between attention-deficit/hyperactivity disorder, educational attainment, literacy and language von Verhoef, Ellen, Demontis, Ditte, Burgess, Stephen, Shapland, Chin Yang, Dale, Philip S., Okbay, Aysu, Neale, Benjamin M., Faraone, Stephen V., Stergiakouli, Evie, Davey Smith, George, Fisher, Simon E., Børglum, Anders D., St Pourcain, Beate

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Schizophrenia-associated somatic copy-number variants from 12,834 cases reveal recurrent NRXN1 and ABCB11 disruptions von Maury, Eduardo A, Sherman, Maxwell A, Genovese, Giulio, Gilgenast, Thomas G, Kamath, Tushar, Burris, S J, Rajarajan, Prashanth, Flaherty, Erin, Akbarian, Schahram, Chess, Andrew, McCarroll, Steven A, Loh, Po-Ru, Phillips-Cremins, Jennifer E, Brennand, Kristen J, Macosko, Evan Z, Walters, James T R, O'Donovan, Michael, Sullivan, Patrick, Sebat, Jonathan, Lee, Eunjung A, Walsh, Christopher A

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Two non-synonymous markers in PTPN21 , identified by genome-wide association study data-mining and replication, are associated with schizophrenia von Chen, Jingchun, Lee, Grace, Fanous, Ayman H, Zhao, Zhongming, Jia, Peilin, O'Neill, Anthony, Walsh, Dermot, Kendler, Kenneth S, Chen, Xiangning, The International Schizophrenia Consortium

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