Cauda equina syndrome : Factors affecting long-term functional and sphincteric outcome by MCCARTHY, Michael J. H, AYLOTT, Caspar E. W, GREVITT, Michael P, HEGARTY, James

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Long-term outcome after surgical treatment of Scheuermann’s Kyphosis (SK) by Debnath, Ujjwal K., Quraishi, Nasir A., McCarthy, Michael J. H., McConnell, J. R., Mehdian, S. M. H., Shetaiwi, Ali, Grevitt, Michael P., Webb, John K.

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A Comparison of Magnetic Resonance Imaging Muscle Fat Content in the Lumbar Paraspinal Muscles with Patient-Reported Outcome Measures in Patients with Lumbar Degenerative Disk Dise... by Bhadresha, Ashwin, Lawrence, Owen John, McCarthy, Michael J. H.

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Correction to: Long-term outcome after surgical treatment of Scheuermann’s Kyphosis (SK) by Debnath, Ujjwal K., Quraishi, Nasir A., McCarthy, Michael J. H., McConnell, J. R., Mehdian, S. M. H., Shetaiwi, Ali, Grevitt, Michael P., Webb, John K.

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Two stage one component revision in infected total hip replacements - two case reports and literature review by Faroug, Radwane, Shah, Yousaf, McCarthy, Michael J H, Halawa, Maher

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The influence of the energy of trauma, the timing of decompression, and the impact of grade of SCI on outcome by McCarthy, Michael JH, Gatehouse, Simon, Steel, Monica, Goss, Ben, Williams, Richard

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A genome-wide association study of pulmonary function measures in the Framingham Heart Study by Wilk, Jemma B, Chen, Ting-Hsu, Gottlieb, Daniel J, Walter, Robert E, Nagle, Michael W, Brandler, Brian J, Myers, Richard H, Borecki, Ingrid B, Silverman, Edwin K, Weiss, Scott T, O'Connor, George T

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Genome-wide association analysis identifies variants associated with nonalcoholic fatty liver disease that have distinct effects on metabolic traits by Speliotes, Elizabeth K, Yerges-Armstrong, Laura M, Wu, Jun, Hernaez, Ruben, Kim, Lauren J, Palmer, Cameron D, Gudnason, Vilmundur, Eiriksdottir, Gudny, Garcia, Melissa E, Launer, Lenore J, Nalls, Michael A, Clark, Jeanne M, Mitchell, Braxton D, Shuldiner, Alan R, Butler, Johannah L, Tomas, Marta, Hoffmann, Udo, Hwang, Shih-Jen, Massaro, Joseph M, O'Donnell, Christopher J, Sahani, Dushyant V, Salomaa, Veikko, Schadt, Eric E, Schwartz, Stephen M, Siscovick, David S, Voight, Benjamin F, Carr, J Jeffrey, Feitosa, Mary F, Harris, Tamara B, Fox, Caroline S, Smith, Albert V, Kao, W H Linda, Hirschhorn, Joel N, Borecki, Ingrid B

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A meta-analysis of gene expression signatures of blood pressure and hypertension by Huan, Tianxiao, Esko, Tõnu, Peters, Marjolein J, Pilling, Luke C, Schramm, Katharina, Schurmann, Claudia, Chen, Brian H, Liu, Chunyu, Joehanes, Roby, Johnson, Andrew D, Yao, Chen, Ying, Sai-Xia, Courchesne, Paul, Milani, Lili, Raghavachari, Nalini, Wang, Richard, Liu, Poching, Reinmaa, Eva, Dehghan, Abbas, Hofman, Albert, Uitterlinden, André G, Hernandez, Dena G, Bandinelli, Stefania, Singleton, Andrew, Melzer, David, Metspalu, Andres, Carstensen, Maren, Grallert, Harald, Herder, Christian, Meitinger, Thomas, Peters, Annette, Roden, Michael, Waldenberger, Melanie, Dörr, Marcus, Felix, Stephan B, Zeller, Tanja, Vasan, Ramachandran, O'Donnell, Christopher J, Munson, Peter J, Yang, Xia, Prokisch, Holger, Völker, Uwe, van Meurs, Joyce B J, Ferrucci, Luigi, Levy, Daniel

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Genome-wide association of body fat distribution in African ancestry populations suggests new loci by Liu, Ching-Ti, Monda, Keri L, Taylor, Kira C, Lange, Leslie, Demerath, Ellen W, Palmas, Walter, Wojczynski, Mary K, Ellis, Jaclyn C, Vitolins, Mara Z, Liu, Simin, Papanicolaou, George J, Irvin, Marguerite R, Xue, Luting, Griffin, Paula J, Nalls, Michael A, Adeyemo, Adebowale, Liu, Jiankang, Li, Guo, Ruiz-Narvaez, Edward A, Chen, Wei-Min, Chen, Fang, Henderson, Brian E, Millikan, Robert C, Ambrosone, Christine B, Strom, Sara S, Guo, Xiuqing, Andrews, Jeanette S, Sun, Yan V, Mosley, Thomas H, Yanek, Lisa R, Shriner, Daniel, Haritunians, Talin, Rotter, Jerome I, Speliotes, Elizabeth K, Smith, Megan, Rosenberg, Lynn, Mychaleckyj, Josyf, Nayak, Uma, Spruill, Ida, Garvey, W Timothy, Pettaway, Curtis, Nyante, Sarah, Bandera, Elisa V, Britton, Angela F, Zonderman, Alan B, Rasmussen-Torvik, Laura J, Chen, Yii-Der Ida, Ding, Jingzhong, Lohman, Kurt, Kritchevsky, Stephen B, Zhao, Wei, Peyser, Patricia A, Kardia, Sharon L R, Kabagambe, Edmond, Broeckel, Ulrich, Chen, Guanjie, Zhou, Jie, Wassertheil-Smoller, Sylvia, Neuhouser, Marian L, Rampersaud, Evadnie, Psaty, Bruce, Kooperberg, Charles, Manson, Joann E, Kuller, Lewis H, Ochs-Balcom, Heather M, Johnson, Karen C, Sucheston, Lara, Ordovas, Jose M, Palmer, Julie R, Haiman, Christopher A, McKnight, Barbara, Howard, Barbara V, Becker, Diane M, Bielak, Lawrence F, Liu, Yongmei, Allison, Matthew A, Grant, Struan F A, Burke, Gregory L, Patel, Sanjay R, Schreiner, Pamela J, Borecki, Ingrid B, Evans, Michele K, Taylor, Herman, Sale, Michele M, Howard, Virginia, Carlson, Christopher S, Rotimi, Charles N, Cushman, Mary, Harris, Tamara B, Reiner, Alexander P, Cupples, L Adrienne, North, Kari E, Fox, Caroline S

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Differential responses to lithium in hyperexcitable neurons from patients with bipolar disorder by Mertens, Jerome, Wang, Qiu-Wen, Kim, Yongsung, Yu, Diana X, Pham, Son, Yang, Bo, Zheng, Yi, Diffenderfer, Kenneth E, Zhang, Jian, Soltani, Sheila, Eames, Tameji, Schafer, Simon T, Boyer, Leah, Marchetto, Maria C, Nurnberger, John I, Calabrese, Joseph R, Ødegaard, Ketil J, McCarthy, Michael J, Zandi, Peter P, Alda, Martin, Alba, Martin, Nievergelt, Caroline M, Mi, Shuangli, Brennand, Kristen J, Kelsoe, John R, Gage, Fred H, Yao, Jun

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Pooled sequencing of 531 genes in inflammatory bowel disease identifies an associated rare variant in BTNL2 and implicates other immune related genes by Prescott, Natalie J, Lehne, Benjamin, Stone, Kristina, Lee, James C, Taylor, Kirstin, Knight, Jo, Papouli, Efterpi, Mirza, Muddassar M, Simpson, Michael A, Spain, Sarah L, Lu, Grace, Fraternali, Franca, Bumpstead, Suzannah J, Gray, Emma, Amar, Ariella, Bye, Hannah, Green, Peter, Chung-Faye, Guy, Hayee, Bu'Hussain, Pollok, Richard, Satsangi, Jack, Parkes, Miles, Barrett, Jeffrey C, Mansfield, John C, Sanderson, Jeremy, Lewis, Cathryn M, Weale, Michael E, Schlitt, Thomas, Mathew, Christopher G

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Synaptic, transcriptional and chromatin genes disrupted in autism by De Rubeis, Silvia, He, Xin, Goldberg, Arthur P, Poultney, Christopher S, Samocha, Kaitlin, Cicek, A Erucment, Kou, Yan, Liu, Li, Fromer, Menachem, Walker, Susan, Singh, Tarinder, Klei, Lambertus, Kosmicki, Jack, Shih-Chen, Fu, Aleksic, Branko, Biscaldi, Monica, Bolton, Patrick F, Brownfeld, Jessica M, Cai, Jinlu, Campbell, Nicholas G, Carracedo, Angel, Chahrour, Maria H, Chiocchetti, Andreas G, Coon, Hilary, Crawford, Emily L, Curran, Sarah R, Dawson, Geraldine, Duketis, Eftichia, Fernandez, Bridget A, Gallagher, Louise, Geller, Evan, Guter, Stephen J, Hill, R Sean, Ionita-Laza, Juliana, Jimenz Gonzalez, Patricia, Kilpinen, Helena, Klauck, Sabine M, Kolevzon, Alexander, Lee, Irene, Lei, Irene, Lei, Jing, Lehtimäki, Terho, Lin, Chiao-Feng, Ma'ayan, Avi, Marshall, Christian R, McInnes, Alison L, Neale, Benjamin, Owen, Michael J, Ozaki, Noriio, Parellada, Mara, Parr, Jeremy R, Purcell, Shaun, Puura, Kaija, Rajagopalan, Deepthi, Rehnström, Karola, Reichenberg, Abraham, Sabo, Aniko, Sachse, Michael, Sanders, Stephan J, Schafer, Chad, Schulte-Rüther, Martin, Skuse, David, Stevens, Christine, Szatmari, Peter, Tammimies, Kristiina, Valladares, Otto, Voran, Annette, Li-San, Wang, Weiss, Lauren A, Willsey, A Jeremy, Yu, Timothy W, Yuen, Ryan K C, Cook, Edwin H, Freitag, Christine M, Gill, Michael, Hultman, Christina M, Lehner, Thomas, Palotie, Aaarno, Schellenberg, Gerard D, Sklar, Pamela, State, Matthew W, Sutcliffe, James S, Walsh, Christiopher A, Scherer, Stephen W, Zwick, Michael E, Barett, Jeffrey C, Cutler, David J, Roeder, Kathryn, Devlin, Bernie, Daly, Mark J, Buxbaum, Joseph D

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Biological interpretation of genome-wide association studies using predicted gene functions by Pers, Tune H, Karjalainen, Juha M, Chan, Yingleong, Westra, Harm-Jan, Wood, Andrew R, Yang, Jian, Lui, Julian C, Vedantam, Sailaja, Gustafsson, Stefan, Esko, Tonu, Frayling, Tim, Speliotes, Elizabeth K, Boehnke, Michael, Raychaudhuri, Soumya, Fehrmann, Rudolf S N, Hirschhorn, Joel N, Franke, Lude

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A genomic mutational constraint map using variation in 76,156 human genomes by Chen, Siwei, Francioli, Laurent C, Goodrich, Julia K, Collins, Ryan L, Kanai, Masahiro, Wang, Qingbo, Alföldi, Jessica, Watts, Nicholas A, Vittal, Christopher, Gauthier, Laura D, Poterba, Timothy, Wilson, Michael W, Tarasova, Yekaterina, Phu, William, Grant, Riley, Yohannes, Mary T, Koenig, Zan, Farjoun, Yossi, Banks, Eric, Donnelly, Stacey, Gabriel, Stacey, Gupta, Namrata, Ferriera, Steven, Tolonen, Charlotte, Novod, Sam, Bergelson, Louis, Roazen, David, Ruano-Rubio, Valentin, Covarrubias, Miguel, Llanwarne, Christopher, Petrillo, Nikelle, Wade, Gordon, Jeandet, Thibault, Munshi, Ruchi, Tibbetts, Kathleen, O'Donnell-Luria, Anne, Solomonson, Matthew, Seed, Cotton, Martin, Alicia R, Talkowski, Michael E, Rehm, Heidi L, Daly, Mark J, Tiao, Grace, Neale, Benjamin M, MacArthur, Daniel G, Karczewski, Konrad 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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Genetic effects on gene expression across human tissues by Battle, Alexis, Brown, Christopher D, Engelhardt, Barbara E, Montgomery, Stephen B

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Transfusion of Plasma, Platelets, and Red Blood Cells in a 1:1:1 vs a 1:1:2 Ratio and Mortality in Patients With Severe Trauma: The PROPPR Randomized Clinical Trial by Holcomb, John B, Tilley, Barbara C, Baraniuk, Sarah, Fox, Erin E, Wade, Charles E, Podbielski, Jeanette M, del Junco, Deborah J, Brasel, Karen J, Bulger, Eileen M, Callcut, Rachael A, Cohen, Mitchell Jay, Cotton, Bryan A, Fabian, Timothy C, Inaba, Kenji, Kerby, Jeffrey D, Muskat, Peter, O’Keeffe, Terence, Rizoli, Sandro, Robinson, Bryce R. H, Scalea, Thomas M, Schreiber, Martin A, Stein, Deborah M, Weinberg, Jordan A, Callum, Jeannie L, Hess, John R, Matijevic, Nena, Miller, Christopher N, Pittet, Jean-Francois, Hoyt, David B, Pearson, Gail D, Leroux, Brian, van Belle, Gerald

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Early mobilization and recovery in mechanically ventilated patients in the ICU: a bi-national, multi-centre, prospective cohort study by Hodgson, Carol, Bellomo, Rinaldo, Berney, Susan, Bailey, Michael, Buhr, Heidi, Denehy, Linda, Harrold, Megan, Higgins, Alisa, Presneill, Jeff, Saxena, Manoj, Skinner, Elizabeth, Young, Paul, Webb, Steven

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Genome-wide association and Mendelian randomisation analysis provide insights into the pathogenesis of heart failure by Shah, Sonia, Roselli, Carolina, Lin, Honghuang, Fatemifar, Ghazaleh, Hedman, Åsa K, Morley, Michael P, Verweij, Niek, Dehghan, Abbas, Almgren, Peter, Ärnlöv, Johan, Backman, Joshua D, Biggs, Mary L, Bloom, Heather L, Brown, Michael R, Buckbinder, Leonard, Chasman, Daniel I, Chen, Xing, Chen, Xu, Chung, Jonathan, Chutkow, William, Delgado, Graciela E, Denaxas, Spiros, Dörr, Marcus, Dudley, Samuel C, Dunn, Michael E, Felix, Stephan B, Finan, Chris, Ghanbari, Mohsen, Ghasemi, Sahar, Giedraitis, Vilmantas, Giulianini, Franco, Gottdiener, John S, Gross, Stefan, Guðbjartsson, Daníel F, van der Harst, Pim, Hyde, Craig L, Ingelsson, Erik, Jukema, J Wouter, Khaw, Kay-Tee, Kleber, Marcus E, Køber, Lars, Koekemoer, Andrea, Langenberg, Claudia, Lind, Lars, London, Barry, Lovering, Ruth C, Luan, Jian'an, Magnusson, Patrik, Mahajan, Anubha, Melander, Olle, Mordi, Ify R, Morgan, Thomas, Morris, Andrew D, Morris, Andrew P, Morrison, Alanna C, Nagle, Michael W, Niessner, Alexander, O'Donoghue, Michelle L, Owens, Anjali T, Palmer, Colin N A, Parry, Helen M, Portilla-Fernandez, Eliana, Psaty, Bruce M, Rice, Kenneth M, Ridker, Paul M, Romaine, Simon P R, Salo, Perttu, Salomaa, Veikko, Smith, Nicholas L, Stender, Steen, Stott, David J, Svensson, Per, Taylor, Kent D, Teumer, Alexander, Thorgeirsson, Guðmundur, Thorsteinsdottir, Unnur, Tyl, Benoit, Uitterlinden, Andre G, Veluchamy, Abirami, Völker, Uwe, Voors, Adriaan A, Wang, Xiaosong, Waterworth, Dawn, Weiss, Raul, Wiggins, Kerri L, Xing, Heming, Yerges-Armstrong, Laura M, Yu, Bing, Zannad, Faiez, Zhao, Jing Hua, Hemingway, Harry, Samani, Nilesh J, Malarstig, Anders, Asselbergs, Folkert W, Kuchenbaecker, Karoline, Lang, Chim C, Stefansson, Kari, Smith, J Gustav, Swerdlow, Daniel I, Lumbers, R Thomas

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