Modeling the patient journey from injury to community reintegration for persons with acute traumatic spinal cord injury in a Canadian centre by Santos, Argelio, Gurling, James, Dvorak, Marcel F, Noonan, Vanessa K, Fehlings, Michael G, Burns, Anthony S, Lewis, Rachel, Soril, Lesley, Fallah, Nader, Street, John T, Bélanger, Lise, Townson, Andrea, Liang, Liping, Atkins, Derek

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Modeling the Patient Journey from Injury to Community Reintegration for Persons with Acute Traumatic Spinal Cord Injury in a Canadian Centre: e72552 by Santos, Argelio, Gurling, James, Dvorak, Marcel F, Noonan, Vanessa K, Fehlings, Michael G, Burns, Anthony S, Lewis, Rachel, Soril, Lesley, Fallah, Nader, Street, John T

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Comment: The grocery adjudicator is playing a long game by Gurling, James

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Comment: Supermarkets could find themselves in the political spotlight by Gurling, James

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Beware the one-club golfer by Gurling, James

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SOAP BOX by Carswell, Douglas

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SOAP BOX by Zetter, Lionel

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Genome-wide association study of bipolar disorder in Canadian and UK populations corroborates disease loci including SYNE1 and CSMD1 by Xu, Wei, Cohen-Woods, Sarah, Chen, Qian, Noor, Abdul, Knight, Jo, Hosang, Georgina, Parikh, Sagar V, De Luca, Vincenzo, Tozzi, Federica, Muglia, Pierandrea, Forte, Julia, McQuillin, Andrew, Hu, Pingzhao, Gurling, Hugh M D, Kennedy, James L, McGuffin, Peter, Farmer, Anne, Strauss, John, Vincent, John B

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New insights into the genetic etiology of Alzheimer's disease and related dementias by Amin, Najaf, Naj, Adam C, Grenier-Boley, Benjamin, Boland, Anne, van der Lee, Sven J, Yang, Qiong, de Rojas, Itziar, Yaqub, Amber, Chapuis, Julien, Alarcón-Martín, Emilio, Tsolaki, Anthoula, Antúnez, Carmen, Bailly, Henri, Barral, Sandra, Pastor, Ana Belén, Below, Jennifer E, Benussi, Luisa, Binetti, Giuliano, Boada, Mercè, Bråthen, Geir, Bresner, Catherine, Brodaty, Henry, Brusco, Luis Ignacio, Burholt, Vanessa, Cuccaro, Michael L, Clark, Christopher, Custodero, Carlo, Dalmasso, Maria Carolina, Daniele, Antonio, Debette, Stéphanie, Dichgans, Martin, Escott-Price, Valentina, Ferreira, Catarina B, Fladby, Tormod, Fließbach, Klaus, García-Alberca, Jose Maria, Garcia-Madrona, Sebastian, Garcia-Ribas, Guillermo, Giegling, Ina, Grande, Giulia, Gudnason, Vilmundur, Haapasalo, Annakaisa, Hampel, Harald, Hanon, Olivier, Hardy, John, Harwood, Janet, Hoffmann, Per, Hulsman, Marc, Kilander, Lena, Kornhuber, Johannes, Lage, Carmen, Love, Seth, Löwemark, Malin, Marquié, Marta, Mead, Simon, Medina, Miguel, Mir, Pablo, Mol, Merel, Ngandu, Tiia, Ortega, Gemma, Paolo, Caffarra, Pasquier, Florence, Pastor, Pau, Polak, Thomas, Priller, Josef, Thomassen, Jesper Qvist, Rainero, Innocenzo, Rajabli, Farid, Reinders, Marcel J T, Reitz, Christiane, Rongve, Arvid, Rosende-Roca, Maitée, Rujescu, Dan, Sakka, Paraskevi, Sánchez-Arjona, María Bernal, Sánchez-Valle, Raquel, Scamosci, Michela, Scheltens, Philip, Scherbaum, Norbert, Snijders, Gijsje J L, Spalletta, Gianfranco, Tartan, Juan Pablo, Tárraga, Lluís, Tesí, Niccolo, Traykov, Latchezar, Ulstein, Ingun, van Rooij, Jeroen, van Swieten, John, Vandenberghe, Rik, Wagner, Michael, Wiltfang, Jens, Yannakoulia, Mary, Zulaica, Miren, Sachdev, Perminder, Ikram, M Arfan, de Mendonça, Alexandre, Hort, Jakub, Ingelsson, Martin, Sims, Rebecca, Ruiz, Agustín

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Improved imputation of low-frequency and rare variants using the UK10K haplotype reference panel by Huang, Jie, Howie, Bryan, McCarthy, Shane, Memari, Yasin, Walter, Klaudia, Min, Josine L., Danecek, Petr, Malerba, Giovanni, Trabetti, Elisabetta, Zheng, Hou-Feng, Gambaro, Giovanni, Richards, J. Brent, Durbin, Richard, Timpson, Nicholas J., Marchini, Jonathan, Soranzo, Nicole

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Estimation of Genetic Correlation via Linkage Disequilibrium Score Regression and Genomic Restricted Maximum Likelihood by Moser, Gerhard, Ripke, Stephan, Walters, James T.R., Farh, Kai-How, Bulik-Sullivan, Brendan, Collier, David A., Agartz, Ingrid, Amin, Farooq, Begemann, Martin, Buccola, Nancy G., Byerley, William, Carr, Vaughan J., Carrera, Noa, Catts, Stanley V., Chong, Siow Ann, Craddock, Nick, Crowley, James J., Curtis, David, Davidson, Michael, Davis, Kenneth L., Demontis, Ditte, Dinan, Timothy, Donohoe, Gary, Drapeau, Elodie, Essioux, Laurent, Fanous, Ayman H., Franke, Lude, Georgieva, Lyudmila, Godard, Stephanie, Hammer, Christian, Hansen, Mark, Hansen, Thomas, Henskens, Frans A., Hirschhorn, Joel N., Hollegaard, Mads V., Hougaard, David M., Ikeda, Masashi, Joa, Inge, Juliá, Antonio, Kahn, René S., Karachanak-Yankova, Sena, Karjalainen, Juha, Khrunin, Andrey, Li, Miaoxin, Lieberman, Jeffrey, Lönnqvist, Jouko, Mattheisen, Manuel, Mattingsda, Morten, McDonald, Colm, Melle, Ingrid, Milanova, Vihra, Mokrab, Younes, Murray, Robin M., Nenadic, Igor, O’Neill, F. Anthony, Van Os, Jim, Papio, Sergi, Parkhomenko, Elena, Perkins, Diana O., Pietiläinenl, Olli, Pulver, Ann E., Purcell, Shaun M., Rasmussen, Henrik B., Reichenberg, Abraham, Richards, Alexander L., Ruderfer, Douglas M., Salomaa, Veikko, Sanders, Alan R., Scott, Rodney J., Silverman, Jeremy M., Smoller, Jordan W., So, Hon-Cheong, Spencer, Chris C.A., Stefansson, Hreinn, Stogmann, Elisabeth, Strengman, Eric, Svrakic, Dragan M., Söderman, Erik, Toncheva, Draga, Veijola, Juha, Walsh, Dermot, Weiser, Mark, Wildenauer, Dieter B., Williams, Nigel M., Williams, Stephanie, Witt, Stephanie H., Wolen, Aaron R., Xi, Hualin Simon, Zai, Clement C., Stefansson, Kari, Blackwood, Douglas H.R., Buxbaum, Joseph D., Esko, Tõnu, Gill, Michael, McQuillin, Andrew, Moran, Jennifer L., Petryshen, Tracey L., Rietsche, Marcella, Sham, Pak C., Weinberger, Daniel R.

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A Rare Functional Noncoding Variant at the GWAS-Implicated MIR137/MIR2682 Locus Might Confer Risk to Schizophrenia and Bipolar Disorder by 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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Genomewide Association Studies: History, Rationale, and Prospects for Psychiatric Disorders by Cichon, Sven, Craddock, Nick, Daly, Mark, Faraone, Stephen V, Gejman, Pablo V, Kelsoe, John, Lehner, Thomas, Levinson, Douglas F, Moran, Audra, Sklar, Pamela, Sullivan, Patrick F

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Whole-genome sequence-based analysis of thyroid function by Taylor, Peter N., Porcu, Eleonora, Chew, Shelby, Campbell, Purdey J., Traglia, Michela, Brown, Suzanne J., Mullin, Benjamin H., Shihab, Hashem A., Min, Josine, Walter, Klaudia, Memari, Yasin, Huang, Jie, Barnes, Michael R., Beilby, John P., Charoen, Pimphen, Danecek, Petr, Dudbridge, Frank, Forgetta, Vincenzo, Greenwood, Celia, Grundberg, Elin, Johnson, Andrew D., Hui, Jennie, Lim, Ee M., McCarthy, Shane, Muddyman, Dawn, Panicker, Vijay, Perry, John R.B., Bell, Jordana T., Yuan, Wei, Relton, Caroline, Gaunt, Tom, Schlessinger, David, Abecasis, Goncalo, Cucca, Francesco, Surdulescu, Gabriela L., Woltersdorf, Wolfram, Zeggini, Eleftheria, Zheng, Hou-Feng, Toniolo, Daniela, Dayan, Colin M., Naitza, Silvia, Walsh, John P., Spector, Tim, Davey Smith, George, Durbin, Richard, Brent Richards, J., Sanna, Serena, Soranzo, Nicole, Timpson, Nicholas J., Wilson, Scott G.

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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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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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Low-frequency variation in TP53 has large effects on head circumference and intracranial volume by Haworth, Simon, Shapland, Chin Yang, Hayward, Caroline, Prins, Bram P., Felix, Janine F., Medina-Gomez, Carolina, Rivadeneira, Fernando, Wang, Carol, Ahluwalia, Tarunveer S., Vrijheid, Martine, Guxens, Mònica, Sunyer, Jordi, Tachmazidou, Ioanna, Walter, Klaudia, Iotchkova, Valentina, Jackson, Andrew, Cleal, Louise, Huffmann, Jennifer, Min, Josine L., Sass, Lærke, Timmers, Paul R. H. J., Davey Smith, George, Fisher, Simon E., Wilson, James F., Cole, Tim J., Fernandez-Orth, Dietmar, Bønnelykke, Klaus, Bisgaard, Hans, Pennell, Craig E., Jaddoe, Vincent W. V., Dedoussis, George, Timpson, Nicholas, Zeggini, Eleftheria, Vitart, Veronique, St Pourcain, Beate

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A polygenic resilience score moderates the genetic risk for schizophrenia by Hess, Jonathan L., Tylee, Daniel S., Mattheisen, Manuel, Børglum, Anders D., Als, Thomas D., Grove, Jakob, Werge, Thomas, Mortensen, Preben Bo, Mors, Ole, Nordentoft, Merete, Hougaard, David M., Byberg-Grauholm, Jonas, Bækvad-Hansen, Marie, Greenwood, Tiffany A., Tsuang, Ming T., Curtis, David, Steinberg, Stacy, Sigurdsson, Engilbert, Stefánsson, Hreinn, Stefánsson, Kári, Edenberg, Howard J., Holmans, Peter, Faraone, Stephen V., Glatt, Stephen J.

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Mutations in GDP-Mannose Pyrophosphorylase B Cause Congenital and Limb-Girdle Muscular Dystrophies Associated with Hypoglycosylation of α-Dystroglycan by Carss, Keren J., Stevens, Elizabeth, Foley, A. Reghan, Cirak, Sebahattin, Riemersma, Moniek, Torelli, Silvia, Hoischen, Alexander, Willer, Tobias, van Scherpenzeel, Monique, Moore, Steven A., Messina, Sonia, Bertini, Enrico, Bönnemann, Carsten G., Abdenur, Jose E., Grosmann, Carla M., Kesari, Akanchha, Punetha, Jaya, Quinlivan, Ros, Waddell, Leigh B., Young, Helen K., Wraige, Elizabeth, Yau, Shu, Brodd, Lina, Feng, Lucy, Sewry, Caroline, MacArthur, Daniel G., North, Kathryn N., Hoffman, Eric, Stemple, Derek L., Hurles, Matthew E., van Bokhoven, Hans, Campbell, Kevin P., Lefeber, Dirk J., Lin, Yung-Yao, Muntoni, Francesco

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Genome-Wide Association Study of Suicide Attempts in Mood Disorder Patients by Perlis, Roy H, Huang, Jie, Purcell, Shaun, Fava, Maurizio, Rush, A. John, Sullivan, Patrick F, Hamilton, Steven P, McMahon, Francis J, Schulze, Thomas, Potash, James B, Zandi, Peter P, Willour, Virginia L, Penninx, Brenda W, Boomsma, Dorret I, Vogelzangs, Nicole, Middeldorp, Christel M, Rietschel, Marcella, Nöthen, Markus, Cichon, Sven, Gurling, Hugh, Bass, Nick, McQuillin, Andrew, Hamshere, Marian, Craddock, Nick, Sklar, Pamela, Smoller, Jordan W

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