Enhanced Chemiluminescence Cannot Predict the Presence of Cryptosporidium parvum When Applied to Water-Quality Monitoring in an Agricultural Environment by Sawcer, K. E., Bodley-Tickell, A. T., Kitchen, S. E., Sturdee, A. P., Thorpe, G. H. G.

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Enhanced Chemiluminescence as an Indicator of Water Quality by Sawcer, K. E., Yeomans, W. E., Thorpe, G. H. G.

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The impact of environmental issues in the design and application of electricity meters by EDWARDS, A. M, SAWCER, K. E

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Locus for severity implicates CNS resilience in progression of multiple sclerosis by Stridh, Pernilla, McCauley, Jacob L., Saarela, Janna, van den Bosch, Aletta M. R., Beecham, Ashley H., Alfredsson, Lars, Alikhani, Katayoun, Amezcua, Lilyana, Andlauer, Till F. M., Ban, Maria, Barcellos, Lisa F., Barizzone, Nadia, Berge, Tone, Berthele, Achim, Bittner, Stefan, Bos, Steffan D., Briggs, Farren B. S., Caillier, Stacy J., Calabresi, Peter A., Caputo, Domenico, Carmona-Burgos, David X., Cavalla, Paola, Celius, Elisabeth G., Chinea, Angel R., Chitnis, Tanuja, Clarelli, Ferdinando, Comabella, Manuel, Comi, Giancarlo, Cotsapas, Chris, Cree, Bruce C. A., De Jager, Philip L., Delgado, Silvia R., Engel, Sinah, Esposito, Federica, Fabis-Pedrini, Marzena J., Fitzgerald, Kathryn C., Gasperi, Christiane, Gomez, Lissette, Gomez, Refujia, Hadjigeorgiou, Georgios, Held, Friederike, Henry, Roland G., Hillert, Jan, Huang, Jesse, Huitinga, Inge, Islam, Talat, Isobe, Noriko, Jagodic, Maja, Kermode, Allan G., Kilpatrick, Trevor J., Konidari, Ioanna, Kreft, Karim L., Lechner-Scott, Jeannette, Leone, Maurizio, Luessi, Felix, Manouchehrinia, Ali, Manrique, Clara P., Martinez, Andrea C., Martinez-Maldonado, Viviana, Mascia, Elisabetta, Metz, Luanne M., Midaglia, Luciana, Montalban, Xavier, Oksenberg, Jorge R., Oturai, Annette, Parnell, Grant P., Pericak-Vance, Margaret A., Piehl, Fredrik, Santaniello, Adam, Santoro, Silvia, Schaefer, Catherine, Sellebjerg, Finn, Shams, Hengameh, Shchetynsky, Klementy, Siokas, Vasileios, Søndergaard, Helle B., Sorosina, Melissa, Taylor, Bruce, Vandebergh, Marijne, Vecchio, Domizia, Wever, Dennis, Yong, V. Wee, Stewart, Graeme J., Compston, Alastair, Zipp, Frauke, Harbo, Hanne F., Hemmer, Bernhard, Goris, An, Smolders, Joost, Hauser, Stephen L., Kockum, Ingrid, Sawcer, Stephen J., Baranzini, Sergio E., Harroud, Adil, Blanco, Yolanda, Llufriu, Sara, Madireddy, Lohith, Saiz, Albert, Villoslada, Pablo, Stefánsson, Kári

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Host―microbe interactions have shaped the genetic architecture of inflammatory bowel disease by JOSTINS, Luke, RIPKE, Stephan, ESSERS, Jonah, MITROVIC, Mitja, NING, Kaida, CLEYNEN, Isabelle, THEATRE, Emilie, SPAIN, Sarah L, RAYCHAUDHURI, Soumya, GOYETTE, Philippe, ZHI WEI, ABRAHAM, Clara, WEERSMA, Rinse K, ACHKAR, Jean-Paul, AHMAD, Tariq, AMININEJAD, Leila, ANANTHAKRISHNAN, Ashwin N, ANDERSEN, Vibeke, ANDREWS, Jane M, BAIDOO, Leonard, BALSCHUN, Tobias, BAMPTON, Peter A, BITTON, Alain, DUERR, Richard H, BOUCHER, Gabrielle, BRAND, Stephan, BÜNING, Carsten, COHAIN, Ariella, CICHON, Sven, D'AMATO, Mauro, DE JONG, Dirk, DEVANEY, Kathy L, DUBINSKY, Marla, EDWARDS, Cathryn, MCGOVERN, Dermot P, ELLINGHAUS, David, FERGUSON, Lynnette R, FRANCHIMONT, Denis, FRANSEN, Karin, GEARRY, Richard, GEORGES, Michel, GIEGER, Christian, GLAS, Jürgen, HARITUNIANS, Talin, HART, Ailsa, HUI, Ken Y, HAWKEY, Chris, HEDL, Matija, XINLI HU, KARLSEN, Tom H, KUPCINSKAS, Limas, KUGATHASAN, Subra, LATIANO, Anna, LAUKENS, Debby, LAWRANCE, Ian C, LEES, Charlie W, LEE, James C, PHILIP SCHUMM, L, SHARMA, Yashoda, ANDERSON, Carl A

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Genetic variants are major determinants of CSF antibody levels in multiple sclerosis by Goris, An, Pauwels, Ine, Gustavsen, Marte W, van Son, Brechtje, Hilven, Kelly, Bos, Steffan D, Celius, Elisabeth Gulowsen, Berg-Hansen, Pål, Aarseth, Jan, Myhr, Kjell-Morten, D'Alfonso, Sandra, Barizzone, Nadia, Leone, Maurizio A, Martinelli Boneschi, Filippo, Sorosina, Melissa, Liberatore, Giuseppe, Kockum, Ingrid, Olsson, Tomas, Hillert, Jan, Alfredsson, Lars, Bedri, Sahl Khalid, Hemmer, Bernhard, Buck, Dorothea, Berthele, Achim, Knier, Benjamin, Biberacher, Viola, van Pesch, Vincent, Sindic, Christian, Bang Oturai, Annette, Søndergaard, Helle Bach, Sellebjerg, Finn, Jensen, Poul Erik H, Comabella, Manuel, Montalban, Xavier, Pérez-Boza, Jennifer, Malhotra, Sunny, Lechner-Scott, Jeannette, Broadley, Simon, Slee, Mark, Taylor, Bruce, Kermode, Allan G, Gourraud, Pierre-Antoine, Sawcer, Stephen J, Andreassen, Bettina Kullle, Dubois, Bénédicte, Harbo, Hanne F

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Using genome-wide complex trait analysis to quantify 'missing heritability' in Parkinson's disease by KELLER, Margaux F, SAAD, Mohamad, SCHULTE, Claudia, MOSKVINA, Valentina, DURR, Alexandra, HOLMANS, Peter, KILARSKI, Laura L, GUERREIRO, Rita, HERNANDEZ, Dena G, BRICE, Alexis, YLIKOTILA, Pauli, STEFANSSON, Hreinn, BRAS, Jose, MAJAMAA, Kari, MORRIS, Huw R, WILLIAMS, Nigel, GASSER, Thomas, HEUTINK, Peter, WOOD, Nicholas W, HARDY, John, MARTINEZ, Maria, SINGLETON, Andrew B, NALLS, Michael A, BETTELLA, Francesco, NICOLAOU, Nayia, SIMON-SANCHEZ, Javier, MITTAG, Florian, BÜCHEL, Finja, SHARMA, Manu, RAPHAEL GIBBS, J

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Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 Subphenotypes by Ruderfer, Douglas M., Boocock, James, Stahl, Eli A., Charney, Alexander W., Ori, Anil P.S., Alliey-Rodriguez, Ney, Anjorin, Adebayo, Badner, Judith A., Band, Gavin, Bruggeman, Richard, Buccola, Nancy G., Bumpstead, Suzannah J., Casas, Juan P., Chan, Raymond C.K., Chen, Ronald Y.L., Collier, David A., Cormican, Paul, Craddock, Nicholas, Crowley, James J., Curtis, David, Dannlowski, Udo, Davidson, Michael, Demontis, Ditte, Dronov, Serge, Elvsashagen, Torbjorn, Etain, Bruno, Fan, Chun Chieh, Forty, Liz, Fraser, Christine, Garnham, Julie, Gill, Michael, Gillman, Matthew, Gratten, Jacob, Gwilliam, Rhian, Hammer, Christian, Hansen, Thomas, Henskens, Frans A., Jamain, Stephane, Jankowski, Janusz, Joa, Inge, Julia, Antonio, Kandaswamy, Radhika, Kavanagh, David, Keller, Matthew C., Khrunin, Andrey, Lee, Phil H., Legge, Sophie E., Lencz, Todd, Levinson, Douglas F., Levy, Shawn E., Li, Tao, Lin, Kuang, Macek, Milan, McCarley, Robert W., McGuffin, Peter, McInnis, Melvin G., Meijer, Carin J., Melegh, Bela, Mesholam-Gately, Raquelle I., Myin-Germeys, Inez, Nicodemus, Kristin K., Nimgaonkar, Vishwajit, Nordin, Annelie, Nöthen, Markus M., Van Os, Jim, Owen, Michael J., Palmer, Colin N.A., Palotie, Aarno, Papadimitriou, George N., Pato, Michele T., Perlis, Roy H., Petryshen, Tracey L., Plomin, Robert, Potash, James B., Powell, John, Ramos-Quiroga, Josep Antoni, Rautanen, Anna, Reichenberg, Abraham, Ribases, Marta, Rice, John P., Richards, Alexander L., Ricketts, Michelle, Sanchez-Mora, Cristina, Sanders, Alan R., Schall, Ulrich, Serretti, Alessandro, Sham, Pak C., Straub, Richard E., Strauss, John S., Szatkiewicz, Jin P., Thompson, Robert C., Thorgeirsson, Thorgeir E., Treutlein, Jens, Vedder, Helmut, Wang, Qiang, Wu, Jing Qin, Sullivan, Patrick F., Wray, Naomi R., Sklar, Pamela, Kendler, Kenneth S.

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Genome-wide meta-analysis identifies six novel loci associated with habitual coffee consumption by Byrne, Enda M, Esko, Tõnu, Nalls, Michael A, Monda, Keri L, Amin, Najaf, Renstrom, Frida, Cavadino, Alana, Nolte, Ilja M, Teumer, Alexander, Yu, Kai, Marques-Vidal, Pedro, Manichaikul, Ani, Wojczynski, Mary K, Vink, Jacqueline M, Mikkilä, Vera, Eriksson, Joel, Musani, Solomon K, Geller, Frank, Luan, Jian'an, Garcia, Melissa E, Wright, Margaret J, Magnusson, Patrik Ke, Oostra, Ben A, Ikram, Mohammad Arfan, Uitterlinden, Andre G, Johansson, Ingegerd, Kaakinen, Marika, Milani, Lili, Power, Chris, Snieder, Harold, Stolk, Ronald P, Baumeister, Sebastian E, Biffar, Reiner, Gu, Fangyi, Kutalik, Zoltán, Forouhi, Nita G, Mihailov, Evelin, Lind, Lars, Lindgren, Cecilia, Michaëlsson, Karl, Morris, Andrew, Khaw, Kay-Tee, Wang, Jie Jin, Männistö, Satu, Perälä, Mia-Maria, Lehtimäki, Terho, Mozaffarian, Dariush, Psaty, Bruce M, Döring, Angela, Montgomery, Grant W, Melbye, Mads, Treur, Jorien L, Mellström, Dan, Hottenga, Jouke Jan, Prokopenko, Inga, Tönjes, Anke, Deloukas, Panos, Kanoni, Stavroula, Houston, Denise K, Liu, Yongmei, Mason, Marc A, Zonderman, Alan B, Franke, Lude, Kristal, Bruce S, Karjalainen, Juha, Reed, Danielle R, Westra, Harm-Jan, Saleheen, Danish, Harris, Tamara B, Dedoussis, George, Curhan, Gary, Pasquale, Louis R, Ordovas, Jose M, Peters, Ulrike, Ohlsson, Claes, Gieger, Christian, Martin, Nicholas G, Waldenberger, Melanie, Siscovick, David S, Raitakari, Olli, Hunter, David J, Kraft, Peter, Borecki, Ingrid B, Loos, Ruth Jf, Wareham, Nicholas J, Vollenweider, Peter, Caporaso, Neil, Grabe, Hans Jörgen, Neuhouser, Marian L, Wolffenbuttel, Bruce Hr, Hu, Frank B, Järvelin, Marjo-Riitta, Cupples, L Adrienne, Ridker, Paul M, van Duijn, Cornelia M, Metspalu, Andres, North, Kari E, Ingelsson, Erik, van Dam, Rob M, Chasman, Daniel I

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Complement genes contribute sex-biased vulnerability in diverse disorders by Kamitaki, Nolan, Sekar, Aswin, Handsaker, Robert E, de Rivera, Heather, Tooley, Katherine, Morris, David L, Taylor, Kimberly E, Whelan, Christopher W, Tombleson, Philip, Loohuis, Loes M Olde, Boehnke, Michael, Kimberly, Robert P, Kaufman, Kenneth M, Harley, John B, Langefeld, Carl D, Seidman, Christine E, Pato, Michele T, Pato, Carlos N, Ophoff, Roel A, Graham, Robert R, Criswell, Lindsey A, Vyse, Timothy J, McCarroll, Steven A

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Cross-ancestry genome-wide association analysis of corneal thickness strengthens link between complex and Mendelian eye diseases by Iglesias, Adriana I, Mishra, Aniket, Vitart, Veronique, Bykhovskaya, Yelena, Höhn, René, Springelkamp, Henriët, Cuellar-Partida, Gabriel, Gharahkhani, Puya, Bailey, Jessica N Cooke, Willoughby, Colin E, Li, Xiaohui, Yazar, Seyhan, Nag, Abhishek, Khawaja, Anthony P, Polašek, Ozren, Siscovick, David, Mitchell, Paul, Tham, Yih Chung, Haines, Jonathan L, Kearns, Lisa S, Hayward, Caroline, Shi, Yuan, van Leeuwen, Elisabeth M, Taylor, Kent D, Bonnemaijer, Pieter, Rotter, Jerome I, Martin, Nicholas G, Zeller, Tanja, Mills, Richard A, Souzeau, Emmanuelle, Staffieri, Sandra E, Jonas, Jost B, Schmidtmann, Irene, Boutin, Thibaud, Kang, Jae H, Lucas, Sionne E M, Wong, Tien Yin, Beutel, Manfred E, Wilson, James F, Uitterlinden, André G, Vithana, Eranga N, Foster, Paul J, Hysi, Pirro G, Hewitt, Alex W, Khor, Chiea Chuen, Pasquale, Louis R, Montgomery, Grant W, Klaver, Caroline C W, Aung, Tin, Pfeiffer, Norbert, Mackey, David A, Hammond, Christopher J, Cheng, Ching-Yu, Craig, Jamie E, Rabinowitz, Yaron S, Wiggs, Janey L, Burdon, Kathryn P, van Duijn, Cornelia M, MacGregor, Stuart

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Comparative performances of machine learning methods for classifying Crohn Disease patients using genome-wide genotyping data by Romagnoni, Alberto, Jégou, Simon, Van Steen, Kristel, Wainrib, Gilles, Hugot, Jean-Pierre

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Unraveling Multiple MHC Gene Associations with Systemic Lupus Erythematosus: Model Choice Indicates a Role for HLA Alleles and Non-HLA Genes in Europeans by MORRIS, David L, TAYLOR, Kimberly E, PONS-ESTEL, Bernardo A, GREGERSEN, Peter K, HARLEY, John B, HAUSER, Stephen L, HOM, Geoffrey, LANGEFELD, Carl D, NOBLE, Janelle A, RIOUX, John D, SELDIN, Michael F, CRISWELL, Lindsey A, FERNANDO, Michelle M. A, VYSE, Timothy J, NITITHAM, Joanne, ALARCON-RIQUELME, Marta E, BARCELLOS, Lisa F, BEHRENS, Timothy W, COTSAPAS, Chris, GAFFNEY, Patrick M, GRAHAM, Robert R

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Discovery and functional prioritization of Parkinson's disease candidate genes from large-scale whole exome sequencing by Jansen, Iris E, Ye, Hui, Heetveld, Sasja, Lechler, Marie C, Michels, Helen, Seinstra, Renée I, Lubbe, Steven J, Drouet, Valérie, Lesage, Suzanne, Majounie, Elisa, Gibbs, J Raphael, Nalls, Mike A, Ryten, Mina, Botia, Juan A, Vandrovcova, Jana, Simon-Sanchez, Javier, Castillo-Lizardo, Melissa, Rizzu, Patrizia, Blauwendraat, Cornelis, Chouhan, Amit K, Li, Yarong, Yogi, Puja, Amin, Najaf, van Duijn, Cornelia M, Morris, Huw R, Brice, Alexis, Singleton, Andrew B, David, Della C, Nollen, Ellen A, Jain, Shushant, Shulman, Joshua M, Heutink, Peter

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Ischemic stroke is associated with the ABO locus: The EuroCLOT study by Williams, Frances M. K., Carter, Angela M., Hysi, Pirro G., Surdulescu, Gabriela, Hodgkiss, Dylan, Soranzo, Nicole, Traylor, Matthew, Bevan, Steve, Dichgans, Martin, Rothwell, Peter M. W., Sudlow, Cathie, Farrall, Martin, Silander, Kaisa, Kaunisto, Mari, Wagner, Peter, Saarela, Olli, Kuulasmaa, Kari, Virtamo, Jarmo, Salomaa, Veikko, Amouyel, Philippe, Arveiler, Dominique, Ferrieres, Jean, Wiklund, Per-Gunnar, Arfan Ikram, M., Hofman, Albert, Boncoraglio, Giorgio B., Parati, Eugenio A., Helgadottir, Anna, Gretarsdottir, Solveig, Thorsteinsdottir, Unnur, Thorleifsson, Gudmar, Stefansson, Kari, Seshadri, Sudha, DeStefano, Anita, Gschwendtner, Andreas, Psaty, Bruce, Longstreth, Will, Mitchell, Braxton D., Cheng, Yu-Ching, Clarke, Robert, Ferrario, Marco, Bis, Joshua C., Levi, Christopher, Attia, John, Holliday, Elizabeth G., Scott, Rodney J., Fornage, Myriam, Sharma, Pankaj, Furie, Karen L., Rosand, Jonathan, Nalls, Mike, Meschia, James, Mosely, Thomas H., Evans, Alun, Palotie, Aarno, Markus, Hugh S., Grant, Peter J., Spector, Tim D.

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NR1H3 p.Arg415Gln Is Not Associated to Multiple Sclerosis Risk by Antel, Jack, Ban, Maria, Baranzini, Sergio, Barcellos, Lisa, Barizzone, Nadia, Beecham, Ashley, Berge, Tone, Bernardinelli, Luisa, Booth, David, Bos, Steffan, Buck, Dorothea, Butkiewicz, Mariusz, Celius, Elisabeth G., Comabella, Manuel, Compston, Alastair, Dedham, Katrina, Cotsapas, Chris, D’ Alfonso, Sandra, De Jager, Phil, Dubois, Benedicte, Duquette, Pierre, Fontaine, Bertrand, Gasperi, Christiane, Gil, Elia, Goris, An, Gourraud, Pierre Antoine, Graetz, Christiane, Gyllenberg, Alexandra, Hadjigeorgiou, Georgios, Hafler, David, Hribko, Deanna, Haines, Jonathan, Harbo, Hanne, Hauser, Stephen, Warto, Shannon, Hawkins, Clive, Hemmer, Bernhard, Henry, Roland, Hintzen, Rogier, Horakova, Dana, Ivinson, Adrian, Howard, Melissa, Jelcic, Ilijas, Kaskow, Belinda, Kira, Jun-Ichi, Kleinova, Pavlina, Kockum, Ingrid, Kucerova, Karolina, Lill, Christina, Luessi, Felix, Malhotra, Sunny, Martin, Roland, Martinelli, Filippo, Matsushita, Takuya, McCabe, Cristin, McCauley, Jacob, Mescheriakkova, Julia, Mitrovic, Mitja, Moen, Stine-Marit, Montalban, Xavier, Muhlau, Mark, Nakmura, Yuri, Oksenberg, Jorge, Olsson, Tomas, Oturai, Annette, Palotie, Aarno, Patsopoulos, Nikolaos, Pavlicova, Jana, Pericak-Vance, Peggy, Piehl, Fredrik, Rebeix, Isabelle, Rioux, John, Saarela, Janna, Sawcer, Stephen, Sellebjerg, Finn, Sondergaard, Helle Bach, Sorensen, Per Soelberg, Sospedra, Mireia, Spurkland, Anne, Stewart, Graeme, Taylor, Bruce, Uitterlinden, Andre, Van Duijn, Cornelia, Zipp, Frauke

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Insights into the genetic architecture of early stage age-related macular degeneration: a genome-wide association study meta-analysis by Holliday, Elizabeth G, Smith, Albert V, Cornes, Belinda K, Buitendijk, Gabriëlle H S, Jensen, Richard A, Sim, Xueling, Aspelund, Thor, Aung, Tin, Baird, Paul N, Boerwinkle, Eric, Cheng, Ching Yu, van Duijn, Cornelia M, Eiriksdottir, Gudny, Gudnason, Vilmundur, Harris, Tamara, Hewitt, Alex W, Inouye, Michael, Jonasson, Fridbert, Klein, Barbara E K, Launer, Lenore, Li, Xiaohui, Liew, Gerald, Lumley, Thomas, McElduff, Patrick, McKnight, Barbara, Mitchell, Paul, Psaty, Bruce M, Rochtchina, Elena, Rotter, Jerome I, Scott, Rodney J, Tay, Wanting, Taylor, Kent, Teo, Yik Ying, Uitterlinden, André G, Viswanathan, Ananth, Xie, Sophia, Vingerling, Johannes R, Klaver, Caroline C W, Tai, E Shyong, Siscovick, David, Klein, Ronald, Cotch, Mary Frances, Wong, Tien Y, Attia, John, Wang, Jie Jin

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NeuroX, a fast and efficient genotyping platform for investigation of neurodegenerative diseases by Nalls, Mike A, Bras, Jose, Hernandez, Dena G, Keller, Margaux F, Majounie, Elisa, Renton, Alan E, Saad, Mohamad, Jansen, Iris, Guerreiro, Rita, Lubbe, Steven, Plagnol, Vincent, Gibbs, J. Raphael, Schulte, Claudia, Pankratz, Nathan, Sutherland, Margaret, Bertram, Lars, Lill, Christina M, DeStefano, Anita L, Faroud, Tatiana, Eriksson, Nicholas, Tung, Joyce Y, Edsall, Connor, Nichols, Noah, Brooks, Janet, Arepalli, Sampath, Pliner, Hannah, Letson, Chris, Heutink, Peter, Martinez, Maria, Gasser, Thomas, Traynor, Bryan J, Wood, Nick, Hardy, John, Singleton, Andrew B

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Common variant at 16p11.2 conferring risk of psychosis by Steinberg, Stacy, de Jong, S, Mattheisen, M, Demontis, D, Jamain, S, Papiol, S, Vassos, E, Giegling, I, Breuer, R, Fraser, G, Melle, Ingrid, Djurovic, Srdjan, Agartz, Ingrid, Suvisaari, J, Lonnqvist, J, Paunio, T, Hansen, T, Ingason, A, Pirinen, M, Strengman, E, Orntoft, T, Didriksen, M, Hollegaard, MV, Nordentoft, M, Abramova, L, Arrojo, M, Sanjuan, J, Arango, C, Etain, B, Bellivier, F, Meary, A, Schurhoff, F, Szoke, A, Ribolsi, M, Magni, V, Siracusano, A, Sperling, S, Rossner, M, Christiansen, C, Kiemeney, LA, Veldink, J, Curran, S, Bolton, P, Staal, W, Rehnstrom, K, Kilpinen, H, Freitag, CM, Meyer, J, Magnusson, P, Saemundsen, E, Martsenkovska, I, Paketchieva, K, Durmishi, N, Naneishvili, N, Mikeladze, N, Surguladze, S, Farmer, A, Mitchell, PB, Wright, A, Fullerton, JM, Montgomery, GW, Martin, NG, van Winkel, R, Kenis, G, De Hert, M, Rethelyi, JM, Bitter, I, Terenius, L, Jonsson, EG, Bakker, S, van Os, J, Jablensky, A, Bramon, E, Powell, J, Murray, R, Corvin, A, Gill, M, Morris, D, O'Neill, FA, Riley, B, Owen, MJ, O'Donovan, MC, Kong, A, Ehrenreich, H, Carracedo, A, Golimbet, V, Andreassen, Ole Andreas, Mors, O, Mortensen, PB, Werge, T, Nothen, MM, Cichon, S, Ruggeri, M, Tosato, S, Palotie, A, St Clair, D, Rujescu, D, Collier, DA, Stefansson, H, Stefánsson, Kári

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CNV analysis in a large schizophrenia sample implicates deletions at 16p12.1 and SLC1A1 and duplications at 1p36.33 and CGNL1 by Rees, Elliott, Walters, James T R, Chambert, Kimberly D, O'Dushlaine, Colm, Szatkiewicz, Jin, Richards, Alexander L, Georgieva, Lyudmila, Mahoney-Davies, Gerwyn, Legge, Sophie E, Moran, Jennifer L, Genovese, Giulio, Levinson, Douglas, Morris, Derek W, Cormican, Paul, Kendler, Kenneth S, O'Neill, Francis A, Riley, Brien, Gill, Michael, Corvin, Aiden, Sklar, Pamela, Hultman, Christina, Pato, Carlos, Pato, Michele, Sullivan, Patrick F, Gejman, Pablo V, McCarroll, Steven A, O'Donovan, Michael C, Owen, Michael J, Kirov, George

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