Therapeutic hypothermia is not dead, but hibernating by Freedman, Jr, Robert J, Schock, Robert B, Peacock, W Frank

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Cool is Hot!...But Then What? by Freedman Jr, Robert J.

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The current practice of intra-aortic balloon counterpulsation: results from the Benchmark Registry by Ferguson, James J, Cohen, Marc, Freedman, Robert J, Stone, Gregg W, Miller, Michael F, Joseph, Debra L, Ohman, E.Magnus

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Comparison of outcomes after 8 vs. 9.5 French size intra-aortic balloon counterpulsation catheters based on 9,332 patients in the prospective Benchmark® registry by Cohen, Marc, Ferguson III, James J., Freedman Jr, Robert J., Miller, Michael F., Reddy, Ramachandra C., Ohman, E. Magnus, Stone, Gregg W., Christenson, Jan, Joseph, Debra L.

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Hypothermia: A crack in the refrigerator door by Freedman Jr, Robert J.

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Intra-aortic balloon counterpulsation: No longer bottom-up technology? by Freedman Jr, Robert J.

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Intra-aortic balloon counterpulsation in US and non-US centres: results of the Benchmark® Registry by Cohen, Marc, Urban, Philip, Christenson, Jan T., Joseph, Debra L., Freedman, Robert J., Miller, Michael F., Ohman, E.Magnus, Reddy, Ramachandra C., Stone, Gregg W., Ferguson, James J.

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Biological insights from 108 schizophrenia-associated genetic loci by Neale, Benjamin M, Pers, Tune H, Agartz, Ingrid, Agerbo, Esben, Amin, Farooq, Bergen, Sarah E, Bigdeli, Tim B, Buckner, Randy L, Cai, Guiqing, Catts, Stanley V, Chan, Raymond C. K, Chen, Eric Y. H, Cheng, Wei, Cheung, Eric F. C, Ann Chong, Siow, Robert Cloninger, C, Cohen, Nadine, Crowley, James J, Davidson, Michael, Davis, Kenneth L, Del Favero, Jurgen, Demontis, Ditte, Dinan, Timothy, Djurovic, Srdjan, Drapeau, Elodie, Eriksson, Johan, Escott-Price, Valentina, Friedl, Marion, Fromer, Menachem, Genovese, Giulio, Georgieva, Lyudmila, Giusti-Rodriguez, Paola, Gopal, Srihari, Gratten, Jacob, Hammer, Christian, Hofman, Andrea, Hougaard, David M, Julia, Antonio, Klovins, Janis, Ausrele Kucinskiene, Zita, Hong Lee, S, Lerer, Bernard, Limborska, Svetlana, Lubinski, Jan, Macek Jr, Milan, Magnusson, Patrik K. E, Mattheisen, Manuel, McDonald, Colm, Michie, Patricia T, Milanova, Vihra, Mokrab, Younes, Muller-Myhsok, Bertram, Nenadic, Igor, Nordin, Annelie, Van Os, Jim, Endophenotypes International Consortium, Psychosis, Parkhomenko, Elena, Pejovic-Milovancevic, Milica, Pimm, Jonathan, Price, Alkes, Purcell, Shaun M, Quested, Digby, Rasmussen, Henrik B, Roffman, Joshua L, Schubert, Christian R, Schwab, Sibylle G, Scott, Rodney J, Seidman, Larry J, Silverman, Jeremy M, Smoller, Jordan W, Steinberg, Stacy, Strengman, Eric, Strohmaier, Jana, Svrakic, Dragan M, Soderman, Erik, Thirumalai, Srinivas, Toncheva, Draga, Tosato, Sarah, Veijola, Juha, Walsh, Dermot, Weiser, Mark, Wolen, Aaron R, Zheng, Xuebin, Wray, Naomi R, Visscher, Peter M, Trust Case-Control Consortium, Wellcome, Andreassen, Ole A, Blackwood, Douglas H. R, Esko, Tonu, Gill, Michael, Jablensky, Assen V, McCarroll, Steven A, Mowry, Bryan J, Owen, Michael J, Pato, Carlos N, Posthuma, Danielle, Rujescu, Dan, Sham, Pak C, Sklar, Pamela, St Clair, David

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Placental genomics mediates genetic associations with complex health traits and disease by Bhattacharya, Arjun, Freedman, Anastasia N., Avula, Vennela, Harris, Rebeca, Liu, Weifang, Pan, Calvin, Lusis, Aldons J., Joseph, Robert M., Smeester, Lisa, Hartwell, Hadley J., Kuban, Karl C. K., Marsit, Carmen J., Li, Yun, O’Shea, T. Michael, Fry, Rebecca C., Santos, Hudson P.

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Spatial and Temporal Mapping of De Novo Mutations in Schizophrenia to a Fetal Prefrontal Cortical Network by Gulsuner, Suleyman, Walsh, Tom, Watts, Amanda C., Lee, Ming K., Thornton, Anne M., Casadei, Silvia, Rippey, Caitlin, Shahin, Hashem, Braff, David, Cadenhead, Kristin S., Calkins, Monica E., Dobie, Dorcas J., Freedman, Robert, Green, Michael, Greenwood, Tiffany, Gur, Raquel E., Gur, Ruben C., Lazzeroni, Laura, Light, Gregory, Nuechterlein, Keith, Olincy, Ann, Radant, Al, Ray, Amrita, Schork, Nik, Seidman, Larry J., Siever, Larry, Silverman, Jeremy, Stone, William S., Sugar, Catherine, Swerdlow, Neal, Tsuang, Debby, Tsuang, Ming, Turetsky, Bruce, Aduroja, Tolulope, Allen, Trina, Bradford, L. Diane, Calkins, Monica E., Devlin, Bernie, Edwards, Neil B., Ganguli, Rohan, Go, Rodney C.P., Gur, Raquel E., Gur, Ruben C., Kwentus, Joseph, Lahti, Adrienne C., Lyons, Paul, Mathos, Kim, May, Roberta, McLeod-Bryant, Steve, McEvoy, Joseph P., Montgomery-Barefield, Laura, Nimgaonkar, Vishwajit L., O’Jile, Judith, Santos, Al, Savage, Robert M., Swanson, Charles L., Wilson, William, Nimgaonkar, Vishwajit L., Go, Rodney C.P., Savage, Robert M., Swerdlow, Neal R., Gur, Raquel E., Braff, David L., King, Mary-Claire, McClellan, Jon M.

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Schizophrenia risk from complex variation of complement component 4 by Sekar, Aswin, Bialas, Allison R., de Rivera, Heather, Davis, Avery, Hammond, Timothy R., Kamitaki, Nolan, Tooley, Katherine, Presumey, Jessy, Baum, Matthew, Van Doren, Vanessa, Genovese, Giulio, Rose, Samuel A., Handsaker, Robert E., Daly, Mark J., Carroll, Michael C., Stevens, Beth, McCarroll, Steven A.

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Association of the Age at Menarche with Site-Specific Cancer Risks in Pooled Data from Nine Cohorts by Fuhrman, Barbara J, Moore, Steven C, Byrne, Celia, Makhoul, Issam, Kitahara, Cari M, Berrington de González, Amy, Linet, Martha S, Weiderpass, Elisabete, Adami, Hans-Olov, Freedman, Neal D, Liao, Linda M, Matthews, Charles E, Stolzenberg-Solomon, Rachael Z, Gaudet, Mia M, Patel, Alpa V, Lee, I-Min, Buring, Julie E, Wolk, Alicja, Larsson, Susanna C, Prizment, Anna E, Robien, Kim, Spriggs, Michael, Check, David P, Murphy, Neil, Gunter, Marc J, Van Dusen, Jr, Harold L, Ziegler, Regina G, Hoover, Robert N

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Genomic Relationships, Novel Loci, and Pleiotropic Mechanisms across Eight Psychiatric Disorders by 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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Heritability of the Severity of Diabetic Retinopathy: The FIND-Eye Study by Arar, Nedal H, Freedman, Barry I, Adler, Sharon G, Iyengar, Sudha K, Chew, Emily Y, Davis, Mathew D, Satko, Scott G, Bowden, Donald W, Duggirala, Ravi, Elston, Robert C, Guo, Xiuxing, Hanson, Robert L, Igo, Robert P., Jr, Ipp, Eli, Kimmel, Paul L, Knowler, William C, Molineros, Julio, Nelson, Robert G, Pahl, Madeleine V, Quade, Shannon R. E, Rasooly, Rebekah S, Rotter, Jerome I, Saad, Mohammed F, Scavini, Marina, Schelling, Jeffrey R, Sedor, John R, Shah, Vallabh O, Zager, Philip G, Abboud, Hanna E, on behalf of Family Investigation of Nephropathy and Diabetes Research Group

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Patterns of gray matter atrophy in genetic frontotemporal dementia: results from the GENFI study by Cash, David M., Bocchetta, Martina, Thomas, David L., Dick, Katrina M., van Swieten, John C., Borroni, Barbara, Galimberti, Daniela, Masellis, Mario, Tartaglia, Maria Carmela, Rowe, James B., Graff, Caroline, Tagliavini, Fabrizio, Frisoni, Giovanni B., Laforce, Robert, Finger, Elizabeth, de Mendonça, Alexandre, Sorbi, Sandro, Rossor, Martin N., Ourselin, Sebastien, Rohrer, Jonathan D., Andersson, Christin, Archetti, Silvana, Arighi, Andrea, Benussi, Luisa, Black, Sandra, Cosseddu, Maura, Fallström, Marie, Ferreira, Carlos, Fenoglio, Chiara, Fox, Nick, Freedman, Morris, Fumagalli, Giorgio, Gazzina, Stefano, Ghidoni, Roberta, Grisoli, Marina, Jelic, Vesna, Jiskoot, Lize, Keren, Ron, Lombardi, Gemma, Maruta, Carolina, Mead, Simon, Meeter, Lieke, van Minkelen, Rick, Nacmias, Benedetta, Öijerstedt, Linn, Padovani, Alessandro, Panman, Jessica, Pievani, Michela, Polito, Cristina, Premi, Enrico, Prioni, Sara, Rademakers, Rosa, Redaelli, Veronica, Rogaeva, Ekaterina, Rossi, Giacomina, Rossor, Martin, Scarpini, Elio, Tang-Wai, David, Tartaglia, Carmela, Thonberg, Hakan, Tiraboschi, Pietro, Verdelho, Ana, Warren, Jason

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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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Modeling Linkage Disequilibrium Increases Accuracy of Polygenic Risk Scores by Gusev, Alexander, Ripke, Stephan, Walters, James T.R., Agartz, Ingrid, Albus, Margot, Bene, Judit, Bevilacqua, Elizabeth, Bigdeli, Tim B., Bruggeman, Richard, Buckner, Randy L., Carr, Vaughan J., Catts, Stanley V., Chan, Raymond C.K., Cheng, Wei, Cohen, Nadine, Curtis, David, Dikeos, Dimitris, Dinan, Timothy, Eriksson, Johan, Escott-Price, Valentina, Franke, Lude, Godard, Stephanie, Goldstein, Jacqueline I., de Haan, Lieuwe, Hartmann, Annette M., Hoffmann, Per, Hofman, Andrea, Hollegaard, Mads V., Hougaard, David M., Ikeda, Masashi, Kim, Yunjung, Kucinskas, Vaidutis, Laurent, Claudine, Limborska, Svetlana, Loughland, Carmel M., Macek, Milan, Marsal, Sara, Mattheisen, Manuel, Milanova, Vihra, Mors, Ole, Mortensen, Preben B., Olsen, Line, Parkhomenko, Elena, Paunio, Tiina, Pimm, Jonathan, Purcell, Shaun M., Reichenberg, Abraham, Reimers, Mark A., Richards, Alexander L., Roussos, Panos, Ruderfer, Douglas M., Sigurdsson, Engilbert, Silverman, Jeremy M., So, Hon-Cheong, Spencer, Chris C.A., Stefansson, Hreinn, Straub, Richard E., Strengman, Eric, Strohmaier, Jana, Svrakic, Dragan M., Tosato, Sarah, Veijola, Juha, Walsh, Dermot, Wang, Dai, Weiser, Mark, Wolen, Aaron R., Wong, Emily H.M., Stefansson, Kari, Andreassen, Ole A., Ehrenreich, Hannelore, Gill, Michael, Hultman, Christina M., Jablensky, Assen V., McQuillin, Andrew, Pato, Carlos N., Rietschel, Marcella, Sham, Pak C., Sklar, Pamela, Weinberger, Daniel R., Daly, Mark J., Crisponi, Laura, Figueroa, Jonine, Gaudet, Mia M., Hall, Per, Hein, Rebecca, Irwanto, Astrid, Johansson, Mattias, Lund, Eiliv, Peto, Julian, Rahman, Nazneen, Southey, Melissa C., Travis, Ruth, Waisfisz, Quinten, Pato, Carlos, Stahl, Eli, Belbin, Gillian, Kenny, Eimear E., Purcell, Shaun, Chasman, Daniel, Neale, Benjamin

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Sex-Dependent Shared and Nonshared Genetic Architecture Across Mood and Psychotic Disorders by Alexander, Madeline, Amin, Farooq, Bacanu, Silviu A., Bergen, Sarah E., Cai, Guiqing, Chambert, Kimberly D., Chen, Eric Y.H., Cloninger, C. Robert, Cohen, David, Cormican, Paul, Djurovic, Srdjan, Drapeau, Elodie, Durmishi, Naser, Genovese, Giulio, Herms, Stefan, Hofman, Andrea, Kalaydjieva, Luba, Kim, Yunjung, Kuzelova-Ptackova, Hana, Liang, Kung-Yee, Lönnqvist, Jouko, Maher, Brion S., Meier, Sandra, Milanova, Vihra, Parkhomenko, Elena, Paunio, Tiina, Purcell, Shaun M., Quested, Digby, Rasmussen, Henrik B., Richards, Alexander L., Roussos, Panos, Sim, Kang, So, Hon-Cheong, Strengman, Eric, Strohmaier, Jana, Svrakic, Dragan M., Tosato, Sarah, Weiser, Mark, Zimprich, Fritz, Wray, Naomi R., Stefansson, Kari, Visscher, Peter M., Liu, Jianjun, McQuillin, Andrew, Rujescu, Dan, Sullivan, Patrick F., Barroso, Ines, Mathew, Christopher G., Trembath, Richard C., Su, Zhan, Bumpstead, Suzannah J., Gillman, Matthew, McCann, Owen T., Iyegbe, Conrad, Milani, Lili, Palotie, Aarno, Sanders, Alan R., Bramon, Elvira, Lee, Jimmy, Breen, Gerome, Whitehead Pavlides, Jennifer M., Pedersen, Carsten Bøcker, Bøen, Erlend, Coryell, William, Dobbyn, Amanda L., Garnham, Julie, Pedersen, Marianne Giørtz, Gordon-Smith, Katherine, Kupka, Ralph, Martinsson, Lina, McKay, James D., Meng, Fan, Mullins, Niamh, Rivera, Margarita, Shehktman, Tatyana, Spijker, Anne T., Streit, Fabian, Vedder, Helmut, Weickert, Thomas W., Zandi, Peter, Zöllner, Sebastian, Kogevinas, Manolis, Nöthen, Markus M., Smeland, Olav B., Andreassen, Ole A., Abdellaoui, Abdel, Andlauer, Till F.M., Eley, Thalia C., Lind, Penelope A., Mostafavi, Sara, Smith, Daniel J., Wellmann, Jürgen, Hayward, Caroline, Schaefer, Catherine, Boomsma, Dorret I., Willemsen, Gonneke, Teumer, Alexander, Van der Auwera, Sandra, Blokland, Gabriëlla A.M., Plath, Niels

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Genome-Wide Association of CKD Progression: The Chronic Renal Insufficiency Cohort Study by Parsa, Afshin, Kanetsky, Peter A, Xiao, Rui, Gupta, Jayanta, Mitra, Nandita, Limou, Sophie, Xie, Dawei, Xu, Huichun, Anderson, Amanda Hyre, Ojo, Akinlolu, Kusek, John W, Lora, Claudia M, Hamm, L Lee, He, Jiang, Sandholm, Niina, Jeff, Janina, Raj, Dominic E, Böger, Carsten A, Bottinger, Erwin, Salimi, Shabnam, Parekh, Rulan S, Adler, Sharon G, Langefeld, Carl D, Bowden, Donald W, Groop, Per-Henrik, Forsblom, Carol, Freedman, Barry I, Lipkowitz, Michael, Fox, Caroline S, Winkler, Cheryl A, Feldman, Harold I

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A Comparison of Ten Polygenic Score Methods for Psychiatric Disorders Applied Across Multiple Cohorts by Ni, Guiyan, Wang, Ying, Ge, Tian, Smoller, Jordan W., Ripke, Stephan, Farh, Kai-How, Holmans, Peter A., Agartz, Ingrid, Belliveau, Richard A., Bigdeli, Tim B., Black, Donald W., Buckner, Randy L., Cheng, Wei, Degenhardt, Franziska, Dudbridge, Frank, Eichhammer, Peter, Farrell, Martilias S., Frank, Josef, Freedman, Robert, Friedl, Marion, Giegling, Ina, Giusti-Rodríguez, Paola, Gratten, Jacob, Hartmann, Annette M., Hollegaard, Mads V., Kahn, René S., Karachanak-Yankova, Sena, Kavanagh, David, Keller, Matthew C., Kennedy, James L., Knowles, James A., Kucinskiene, Zita Ausrele, Li, Tao, Loughland, Carmel M., Lubinski, Jan, Maier, Wolfgang, Mallet, Jacques, Michie, Patricia T., Myin-Germeys, Inez, Nertney, Deborah A., Nicodemus, Kristin K., Nikitina-Zake, Liene, O’Callaghan, Eadbhard, O’Dushlaine, Colm, Pejovic-Milovancevic, Milica, Pocklington, Andrew J., Powell, John, Pulver, Ann E., Ruderfer, Douglas M., Salomaa, Veikko, Shi, Jianxin, Sim, Kang, Slominsky, Petr, Spencer, Chris C.A., Stahl, Eli A., Steinberg, Stacy, Stogmann, Elisabeth, Suvisaari, Jaana, Williams, Nigel M., Witt, Stephanie H., Wormley, Brandon K., Blackwood, Douglas H.R., Bramon, Elvira, Buxbaum, Joseph D., Esko, Tõnu, Gurling, Hugh, Moran, Jennifer L., Mowry, Bryan J., Owen, Michael J., Petryshen, Tracey L., Weinberger, Daniel R., Byrne, Enda M., Abdellaoui, Abdel, Andlauer, Till F.M., Castelao, Enrique, Derks, Eske M., Foo, Jerome C., Forstner, Andreas J., Hall, Lynsey S., Homuth, Georg, Jansen, Rick, Jones, Ian, Jones, Lisa A., Kretzschmar, Warren W., McGuffin, Peter, Mihailov, Evelin, Mostafavi, Sara, Nivard, Michel G., O’Reilly, Paul F., Quiroz, Jorge A., Smith, Daniel J., Thompson, Wesley, Treutlein, Jens, Umbricht, Daniel, Wu, Yang, Zhang, Futao, Grabe, Hans J., Hayward, Caroline, Lewis, Glyn, Wray, Naomi R.

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