Transcatheter Mitral-Valve Repair in Patients with Heart Failure von Stone, Gregg W, Lindenfeld, JoAnn, Abraham, William T, Kar, Saibal, Lim, D. Scott, Mishell, Jacob M, Whisenant, Brian, Grayburn, Paul A, Rinaldi, Michael, Kapadia, Samir R, Rajagopal, Vivek, Sarembock, Ian J, Brieke, Andreas, Marx, Steven O, Cohen, David J, Weissman, Neil J, Mack, Michael J

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Reviews von Faulkner, Alaric, Huey, Paul R., Babits, Lawrence E., Harrington, Faith, Pocius, Gerald L., Chapman, William, McCarthy, John Elizabeth P., Majewski, Teresita, Kent, Barry C., Orser, Charles E., Logan, Judith A.

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Admixture mapping in lupus identifies multiple functional variants within IFIH1 associated with apoptosis, inflammation, and autoantibody production von Molineros, Julio E, Maiti, Amit K, Sun, Celi, Looger, Loren L, Han, Shizhong, Kim-Howard, Xana, Glenn, Stuart, Adler, Adam, Kelly, Jennifer A, Niewold, Timothy B, Gilkeson, Gary S, Brown, Elizabeth E, Alarcón, Graciela S, Edberg, Jeffrey C, Petri, Michelle, Ramsey-Goldman, Rosalind, Reveille, John D, Vilá, Luis M, Freedman, Barry I, Tsao, Betty P, Criswell, Lindsey A, Jacob, Chaim O, Moore, Jason H, Vyse, Timothy J, Langefeld, Carl L, Guthridge, Joel M, Gaffney, Patrick M, Moser, Kathy L, Scofield, R Hal, Alarcón-Riquelme, Marta E, Williams, Scott M, Merrill, Joan T, James, Judith A, Kaufman, Kenneth M, Kimberly, Robert P, Harley, John B, Nath, Swapan K

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MicroRNA-3148 modulates allelic expression of toll-like receptor 7 variant associated with systemic lupus erythematosus von Deng, Yun, Zhao, Jian, Sakurai, Daisuke, Kaufman, Kenneth M, Edberg, Jeffrey C, Kimberly, Robert P, Kamen, Diane L, Gilkeson, Gary S, Jacob, Chaim O, Scofield, R Hal, Langefeld, Carl D, Kelly, Jennifer A, Ramsey-Goldman, Rosalind, Petri, Michelle A, Reveille, John D, Vilá, Luis M, Alarcón, Graciela S, Vyse, Timothy J, Pons-Estel, Bernardo A, Freedman, Barry I, Gaffney, Patrick M, Sivils, Kathy Moser, James, Judith A, Gregersen, Peter K, Anaya, Juan-Manuel, Niewold, Timothy B, Merrill, Joan T, Criswell, Lindsey A, Stevens, Anne M, Boackle, Susan A, Cantor, Rita M, Chen, Weiling, Grossman, Jeniffer M, Hahn, Bevra H, Harley, John B, Alarcόn-Riquelme, Marta E, Brown, Elizabeth E, Tsao, Betty P

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Human genetics in rheumatoid arthritis guides a high-throughput drug screen of the CD40 signaling pathway von Li, Gang, Diogo, Dorothée, Wu, Di, Spoonamore, Jim, Dancik, Vlado, Franke, Lude, Kurreeman, Fina, Rossin, Elizabeth J, Duclos, Grant, Hartland, Cathy, Zhou, Xuezhong, Li, Kejie, Liu, Jun, De Jager, Philip L, Siminovitch, Katherine A, Zhernakova, Alexandra, Raychaudhuri, Soumya, Bowes, John, Eyre, Steve, Padyukov, Leonid, Gregersen, Peter K, Worthington, Jane, Gupta, Namrata, Clemons, Paul A, Stahl, Eli, Tolliday, Nicola, Plenge, Robert M

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GeoSentinel surveillance of illness in returned travelers, 2007-2011 von Leder, K, Torresi, J, Libman, MD, Cramer, JP, Castelli, F, Schlagenhauf, P, Wilder-Smith, A, Wilson, ME, Keystone, JS, Schwartz, E, Barnett, ED, von Sonnenburg, F, Brownstein, JS, Cheng, AC, Sotir, MJ, Esposito, DH, Freedman, DO

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Characterization of the clinical and immunologic phenotype and management of 157 individuals with 56 distinct heterozygous NFKB1 mutations von Lorenzini, Tiziana, Fliegauf, Manfred, Klammer, Nils, Proietti, Michele, Bulashevska, Alla, Schejter, Yael D., Atschekzei, Faranaz, Stepensky, Polina, Pedroza, Luis A., van der Flier, Michiel, Martínez-Gallo, Mónica, Svec, Peter, Fischer, Ute, Ip, Winnie, Geha, Raif, Chou, Janet, Alosaimi, Mohammed, Weintraub, Lauren, Dos Santos Vilela, Maria Marluce, Holzinger, Dirk, Seidl, Maximilian, Lougaris, Vassilios, Plebani, Alessandro, Abolhassani, Hassan, Thaventhiran, James E., Warnatz, Klaus, Grimbacher, Bodo, Ashford, Sofie, Bacchelli, Chiara, Batista, Joana, Bibi, Shahnaz, Boardman, Barbara, Booth, Claire, Breen, Gerome, Burns, Siobhan O., Burren, Oliver S., Carss, Keren, Chambers, John, Cooper, Nichola, Davies, E.G., Dempster, John, Dewhurst, Eleanor F., Drewe, Elizabeth, Duarte, Daniel, Edgar, J. David M., Egner, William, El-Shanawany, Tariq, Erwood, Marie, Fox, James, Frontini, Mattia, Furnell, Abigail, Gaspar, H. Bobby, Gleadall, Nicholas S., Grigoriadou, Sofia, Hackett, Scott, Hague, Rosie, Haimel, Matthias, Hayman, Grant, Hu, Fengyuan, Huissoon, Aarnoud P., Jolles, Stephen, Kasanicki, Mary A., Kelleher, Peter, Klein, Nigel, Kreuzhuber, Roman, Kuijpers, Taco W., Kumararatne, Dinakantha, Allen, Hana Lango, Linger, Rachel, Lorenzo, Lorena E., Maimaris, Jesmeen, Martin, Jennifer, McDermott, Elizabeth M., Meacham, Stuart, Morrisson, Valerie, Nasir, Iman, Nejentsev, Sergey, Papadia, Sofia, Ponsford, Mark J., Quinn, Ellen, Quinti, Isabella, Rayner-Matthews, Paula J., Samani, Nilesh, Sanchis-Juan, Alba, Savic, Sinisa, Simpson, Michael A., Smith, Kenneth G.C., Thaventhiran, James E., Tilly, Tobias, Titterton, Catherine, Tuna, Salih, Urniaz, Rafal, von Ziegenweidt, Julie, Watt, Christopher, Welch, Steven B., Whitehorn, Deborah, Wood, Yvette, Workman, Sarita, Worth, Austen, Young, Timothy

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The UK10K project identifies rare variants in health and disease von Walter, Klaudia, Min, Josine L, Huang, Jie, Crooks, Lucy, Memari, Yasin, McCarthy, Shane, Perry, John R B, Xu, ChangJiang, Futema, Marta, Lawson, Daniel, Iotchkova, Valentina, Schiffels, Stephan, Hendricks, Audrey E, Danecek, Petr, Li, Rui, Floyd, James, Wain, Louise V, Barroso, Inês, Humphries, Steve E, Hurles, Matthew E, Zeggini, Eleftheria, Barrett, Jeffrey C, Plagnol, Vincent, Richards, J Brent, Greenwood, Celia M T, Timpson, Nicholas J, Durbin, Richard, Soranzo, Nicole

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Peripheral-Blood Stem Cells versus Bone Marrow from Unrelated Donors von Anasetti, Claudio, Logan, Brent R, Lee, Stephanie J, Waller, Edmund K, Weisdorf, Daniel J, Wingard, John R, Cutler, Corey S, Westervelt, Peter, Woolfrey, Ann, Couban, Stephen, Ehninger, Gerhard, Johnston, Laura, Maziarz, Richard T, Pulsipher, Michael A, Porter, David L, Mineishi, Shin, McCarty, John M, Khan, Shakila P, Anderlini, Paolo, Bensinger, William I, Leitman, Susan F, Rowley, Scott D, Bredeson, Christopher, Carter, Shelly L, Horowitz, Mary M, Confer, Dennis L

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Integrating de novo and inherited variants in 42,607 autism cases identifies mutations in new moderate-risk genes von Zhou, Xueya, Feliciano, Pamela, Shu, Chang, Wang, Tianyun, Astrovskaya, Irina, Hall, Jacob B., Obiajulu, Joseph U., Wright, Jessica R., Murali, Shwetha C., Xu, Simon Xuming, Brueggeman, Leo, Thomas, Taylor R., Marchenko, Olena, Fleisch, Christopher, Barns, Sarah D., Snyder, LeeAnne Green, Han, Bing, Chang, Timothy S., Turner, Tychele N., Harvey, William T., Nishida, Andrew, O’Roak, Brian J., Geschwind, Daniel H., Michaelson, Jacob J., Volfovsky, Natalia, Eichler, Evan E., Shen, Yufeng, Chung, Wendy K.

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The Prospective, Observational, Multicenter, Major Trauma Transfusion (PROMMTT) Study: Comparative Effectiveness of a Time-Varying Treatment With Competing Risks von Holcomb, John B, del Junco, Deborah J, Fox, Erin E, Wade, Charles E, Cohen, Mitchell J, Schreiber, Martin A, Alarcon, Louis H, Bai, Yu, Brasel, Karen J, Bulger, Eileen M, Cotton, Bryan A, Matijevic, Nena, Muskat, Peter, Myers, John G, Phelan, Herb A, White, Christopher E, Zhang, Jiajie, Rahbar, Mohammad H

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Common variants near MC4R are associated with fat mass, weight and risk of obesity von Day, Ian, Dermitzakis, Emmanouil T, Randall, Joshua C, Weedon, Michael N, Hinney, Anke, Evans, David M, Qi, Lu, Bennett, Amanda J, Munroe, Patricia B, Herrera, Blanca, Johnson, Toby, Elliott, Katherine S, Song, Kijoung, Zeggini, Eleftheria, Cauchi, Stéphane, Teichmann, Sarah A, Lindgren, Cecilia M, Brown, Morris, Sims, Matthew A, Karpe, Fredrik, O'Rahilly, Stephen, Hattersley, Andrew T, Scherag, André, Samani, Nilesh J, Keniry, Andrew, Li, Shengxu, Beckmann, Jacques S, Cooper, Cyrus, Caulfield, Mark J, Owen, Katharine R, Luben, Robert N, McGinnis, Ralph, Ghori, Jilur, Ness, Andrew R, Bochud, Murielle, Jarvelin, Marjo-Riitta, Hebebrand, Johannes, Ong, Ken K, Freathy, Rachel M, McArdle, Wendy L, Potter, Simon, Wareham, Nicholas J, Ganz Vogel, Carla I, Mooser, Vincent, Barroso, Inês, Deloukas, Panos, Waterworth, Dawn M, Bergmann, Sven, Elliott, Paul, Gwilliam, Rhian, Tobias, Jonathan H, Jolley, Jennifer D M, Morris, Andrew D, Loos, Ruth J F, Yuan, Xin, Smith, George Davey, Palmer, Colin N A, Groves, Christopher J, Dina, Christian, Syddall, Holly E, Waeber, Gerard, Zhao, Jing Hua, Sandhu, Manjinder S, Doney, Alex S F, Hunt, Sarah E, Pouta, Anneli, Speliotes, Elizabeth K, Connell, John M, Timpson, Nicholas J, Wallace, Chris, Attwood, Antony P, Hall, Alistair S, Khaw, Kay-Tee, Meyre, David, Vollenweider, Peter, Bingham, Sheila A, Berndt, Sonja I, Hadley, David, Rayner, Nigel W, Frayling, Timothy M, Sadaf Farooqi, I, Hirschhorn, Joel N, Strachan, David P, Inouye, Michael, Papadakis, Konstantinos, Ring, Susan M, Wraight, Vicki L, Willer, Cristen J, Marchini, Jonathan, Uda, Manuela, Nica, Alexandra C, Mangino, Massimo, Soranzo, Nicole, McCarthy, Mark I, De, Subhajyoti, Neville, Matthew J, Prokopenko, Inga, Wheeler, Eleanor, Heid, Iris M, Froguel, Philippe

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Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls von Clayton, David G, Cardon, Lon R, Duncanson, Audrey, Ouwehand, Willem H, Todd, John A, Donnelly, Peter, Easton, Doug, Evans, David, Morris, Andrew P, Spencer, Chris C. A, Boorman, James P, Cant, Barbara, Everson, Ursula, Hussey, Judith M, Knight, Alexandra S, Nutland, Sarah, Stevens, Helen E, Watkins, Nicholas A, Jones, Richard W, Ring, Susan M, Breen, Gerome, Caesar, Sian, Green, Elaine K, Grozeva, Detelina, Jones, Ian R, Kirov, George, Moskvina, Valentina, Nikolov, Ivan, Collier, David A, Farmer, Anne, Williamson, Richard, Young, Allan H, Ball, Stephen G, Balmforth, Anthony J, Bishop, D. Timothy, Iles, Mark M, Dixon, Richard J, Stevens, Suzanne, Thompson, John R, Bredin, Francesca, Tremelling, Mark, Drummond, Hazel, Nimmo, Elaine R, Fisher, Sheila A, Forbes, Alastair, Lewis, Cathryn M, Prescott, Natalie J, Barbour, Jamie, Mohiuddin, M. Khalid, Mansfield, John C, Cummings, Fraser R, Connell, John, Dobson, Richard, Gungadoo, Johannie, Newhouse, Stephen J, Barton, Anne, Bruce, Ian N, John, Sally L, Potter, Catherine, Silman, Alan J, Symmons, Deborah P. M, Dunger, David B, Widmer, Barry, Frayling, Timothy M, Lango, Hana, Perry, John R. B, Groves, Christopher J, Rayner, Nigel W, Timpson, Nicholas J, Zeggini, Eleftheria, Newport, Melanie, Vannberg, Fredrik, Farrar, Claire, Wordsworth, Paul, Brown, Matthew A, Franklyn, Jayne A, Heward, Joanne M, Simmonds, Matthew J, Seal, Sheila, Stratton, Michael R, Ban, Maria, Conway, David, Chaney, Amy, Ghori, Mohammed J. R, Gwilliam, Rhian, Hunt, Sarah E, McGinnis, Ralph, Potter, Simon, Whittaker, Pamela, Widden, Claire, Withers, David, Hallgrimsdottir, Ingileif B, Vukcevic, Damjan, Bentley, David, Caulfield, Mark, Compston, Alistair, Farrall, Martin, Hall, Alistair S, Hattersley, Andrew T, Mathew, Christopher G

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Clinical and mechanistic drivers of acute traumatic coagulopathy von Cohen, Mitchell Jay, Kutcher, Matt, Redick, Britt, Nelson, Mary, Call, Mariah, Knudson, M Margaret, Schreiber, Martin A, Bulger, Eileen M, Muskat, Peter, Alarcon, Louis H, Myers, John G, Rahbar, Mohammad H, Brasel, Karen J, Phelan, Herb A, del Junco, Deborah J, Fox, Erin E, Wade, Charles E, Holcomb, John B, Cotton, Bryan A, Matijevic, Nena

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Genome-wide association study identifies eight loci associated with blood pressure von Jackson, Anne U, Burton, Paul R, Di Gregorio, Alessandra, Mohlke, Karen L, Galan, Pilar, Syvänen, Ann-Christine, Marrugat, Jaume, Jarvelin, Marjo-Riitta, Newton-Cheh, Christopher, Meitinger, Thomas, Watkins, Hugh, Lucas, Gavin, Soranzo, Nicole, Tobin, Martin D, Wain, Louise V, Kooner, Jaspal S, Wallace, Chris, Altshuler, David, Najjar, Samer S, Zeggini, Eleftheria, Felix, Stephan B, Freimer, Nelson B, Laakso, Markku, Homuth, Georg, Ferrucci, Luigi, Brown, Morris, Snieder, Harold, Wichmann, H Erich, Orho-Melander, Marju, Chambers, John C, Valle, Timo T, van der Schouw, Yvonne T, Ernst, Florian, Strachan, David P, van der Harst, Pim, Kathiresan, Sekar, Romanazzi, Valeria, Dörr, Marcus, McArdle, Wendy L, Peden, John F, Beckmann, Jacques S, Song, Kijoung, Yuan, Xin, Melander, Olle, Coin, Lachlan, Lim, Noha, Barroso, Inês, Eyheramendy, Susana, O'Reilly, Paul F, Salomaa, Veikko, Gut, Ivo G, Tuomilehto, Jaakko, Peltonen, Leena, Morken, Mario A, Org, Elin, Luan, Jian'an, Panico, Salvatore, de Jong, Paul E, Schwartz, Stephen M, Matullo, Giuseppe, Wareham, Nicholas J, Seedorf, Udo, Laan, Maris, Uiterwaal, Cuno S, Boehnke, Michael, Farrall, Martin, Elosua, Roberto, Webster, John, Vollenweider, Peter, Reffelmann, Thorsten, Abecasis, Gonçalo R, Rettig, Rainer, Zhao, Jing Hua, Khaw, Kay-Tee, Elliott, Katherine S, Forouhi, Nita G, Voight, Benjamin F, Caulfield, Mark, Dominiczak, Anna, Munroe, Patricia B, Zhai, Guangju, Loos, Ruth JF, Sacerdote, Carlotta, Mooser, Vincent, Bergmann, Sven, Lakatta, Edward G, Bingham, Sheila A, Numans, Mattijs E, Völker, Uwe, Stringham, Heather M, Jousilahti, Pekka, Williams, Frances M, Clarke, Robert, Allione, Alessandra, Spector, Tim D, Elliott, Paul, Collins, Francis S, Lorbeer, Roberto, Sanna, Serena, Ricceri, Fulvio

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Mutations in GDP-Mannose Pyrophosphorylase B Cause Congenital and Limb-Girdle Muscular Dystrophies Associated with Hypoglycosylation of α-Dystroglycan von 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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Parent-of-origin-specific allelic associations among 106 genomic loci for age at menarche von Perry, John R. B., Ferreira, Teresa, Chasman, Daniel I., Esko, Tõnu, Thorleifsson, Gudmar, Albrecht, Eva, Ang, Wei Q., Corre, Tanguy, Cousminer, Diana L., Franceschini, Nora, Ganna, Andrea, Johnson, Andrew D., Kjellqvist, Sanela, Lunetta, Kathryn L., Porcu, Eleonora, Teumer, Alexander, Tikkanen, Emmi, Hottenga, Jouke-Jan, Pers, Tune H., Yerges-Armstrong, Laura M., Hua Zhao, Jing, Andrulis, Irene L., Anton-Culver, Hoda, Benitez, Javier, Blomqvist, Carl, Bolla, Manjeet K., Brenner, Hermann, Chang-Claude, Jenny, Chanock, Stephen, Chen, Jinhui, Chenevix-Trench, Georgia, Collée, J. Margriet, Davey Smith, George, Demerath, Ellen W., Dieffenbach, Aida K., Eriksson, Johan G., Flyger, Henrik, Franke, Lude, Gudbjartsson, Daniel F., Gudnason, Vilmundur, Guénel, Pascal, Guo, Suiqun, Hall, Per, Hartman, Catharina A., Heath, Andrew C., Hofman, Albert, Hooning, Maartje J., Hu, Frank B., Karasik, David, Kiel, Douglas P., Knight, Julia A., Kutalik, Zoltan, Lambrechts, Diether, Lindblom, Annika, Mägi, Reedik, Mannermaa, Arto, Martin, Nicholas G., Masson, Gisli, McArdle, Patrick F., Mihailov, Evelin, Nohr, Ellen A., Oostra, Ben A., Peacock, Munro, Peterlongo, Paolo, Peto, Julian, Postma, Dirkje S., Radice, Paolo, Rivadeneira, Fernando, Rose, Lynda M., Rudolph, Anja, Schlessinger, David, Sovio, Ulla, Tyrer, Jonathan, Vollenweider, Peter, Winqvist, Robert, Wolffenbuttel, Bruce H. R., Wright, Margaret J., Econs, Michael J., Loos, Ruth J. F., McCarthy, Mark I., Montgomery, Grant W., Rice, John P., Thorsteinsdottir, Unnur, van Duijn, Cornelia M., Alizadeh, Behrooz Z., Bergmann, Sven, Boerwinkle, Eric, Crisponi, Laura, Gasparini, Paolo, Gieger, Christian, Järvelin, Marjo-Riitta, Kraft, Peter, Ridker, Paul M., Snieder, Harold, Sørensen, Thorkild I. A., Spector, Tim D., Uitterlinden, André G., Zygmunt, Marek, Murray, Anna, Ong, Ken K.

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Mutations in TCF12, encoding a basic helix-loop-helix partner of TWIST1, are a frequent cause of coronal craniosynostosis von Sharma, Vikram P, Fenwick, Aimée L, Brockop, Mia S, McGowan, Simon J, Goos, Jacqueline A C, Hoogeboom, A Jeannette M, Brady, Angela F, Jeelani, Nu Owase, Lynch, Sally Ann, Mulliken, John B, Murray, Dylan J, Phipps, Julie M, Sweeney, Elizabeth, Tomkins, Susan E, Wilson, Louise C, Bennett, Sophia, Cornall, Richard J, Broxholme, John, Kanapin, Alexander, Johnson, David, Wall, Steven A, van der Spek, Peter J, Mathijssen, Irene M J, Maxson, Robert E, Twigg, Stephen R F, Wilkie, Andrew O M

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Brain tumor epidemiology: Consensus from the Brain Tumor Epidemiology Consortium von Bondy, Melissa L., Scheurer, Michael E., Malmer, Beatrice, Barnholtz‐Sloan, Jill S., Davis, Faith G., Il'yasova, Dora, Kruchko, Carol, McCarthy, Bridget J., Rajaraman, Preetha, Schwartzbaum, Judith A., Sadetzki, Siegal, Schlehofer, Brigitte, Tihan, Tarik, Wiemels, Joseph L., Wrensch, Margaret, Buffler, Patricia A.

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Resuscitate early with plasma and platelets or balance blood products gradually: findings from the PROMMTT study von del Junco, Deborah J, Holcomb, John B, Fox, Erin E, Brasel, Karen J, Phelan, Herb A, Bulger, Eileen M, Schreiber, Martin A, Muskat, Peter, Alarcon, Louis H, Cohen, Mitchell J, Cotton, Bryan A, Wade, Charles E, Myers, John G, Rahbar, Mohammad H

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