T-CELLS FOR THERAPY von DE BETS JOZEF EDUARD MARIA ANTONIUS, HAMEL DAVID M

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Support for the habitat amount hypothesis from a global synthesis of species density studies von Watling, James I., Arroyo‐Rodríguez, Victor, Pfeifer, Marion, Baeten, Lander, Banks‐Leite, Cristina, Cisneros, Laura M., Fang, Rebecca, Hamel‐Leigue, A. Caroli, Lachat, Thibault, Leal, Inara R., Lens, Luc, Possingham, Hugh P., Raheem, Dinarzarde C., Ribeiro, Danilo B., Slade, Eleanor M., Urbina‐Cardona, J. Nicolas, Wood, Eric M., Fahrig, Lenore, Storch, David

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Vascular dysfunction—The disregarded partner of Alzheimer's disease von Sweeney, Melanie D., Montagne, Axel, Sagare, Abhay P., Nation, Daniel A., Schneider, Lon S., Chui, Helena C., Harrington, Michael G., Pa, Judy, Law, Meng, Wang, Danny J.J., Jacobs, Russell E., Doubal, Fergus N., Ramirez, Joel, Black, Sandra E., Nedergaard, Maiken, Benveniste, Helene, Dichgans, Martin, Iadecola, Costantino, Love, Seth, Bath, Philip M., Markus, Hugh S., Salman, Rustam A., Allan, Stuart M., Quinn, Terence J., Kalaria, Rajesh N., Werring, David J., Carare, Roxana O., Touyz, Rhian M., Williams, Steve C.R., Moskowitz, Michael A., Katusic, Zvonimir S., Lutz, Sarah E., Lazarov, Orly, Minshall, Richard D., Rehman, Jalees, Davis, Thomas P., Wellington, Cheryl L., González, Hector M., Yuan, Chun, Lockhart, Samuel N., Hughes, Timothy M., Chen, Christopher L.H., Sachdev, Perminder, O'Brien, John T., Skoog, Ingmar, Pantoni, Leonardo, Gustafson, Deborah R., Biessels, Geert Jan, Wallin, Anders, Smith, Eric E., Mok, Vincent, Wong, Adrian, Passmore, Peter, Barkof, Frederick, Muller, Majon, Breteler, Monique M.B., Román, Gustavo C., Hamel, Edith, Seshadri, Sudha, Gottesman, Rebecca F., van Buchem, Mark A., Arvanitakis, Zoe, Schneider, Julie A., Drewes, Lester R., Hachinski, Vladimir, Finch, Caleb E., Toga, Arthur W., Wardlaw, Joanna M., Zlokovic, Berislav V.

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Mutation Detection in Patients with Retinal Dystrophies Using Targeted Next Generation Sequencing von Weisschuh, Nicole, Mayer, Anja K, Strom, Tim M, Kohl, Susanne, Glöckle, Nicola, Schubach, Max, Andreasson, Sten, Bernd, Antje, Birch, David G, Hamel, Christian P, Heckenlively, John R, Jacobson, Samuel G, Kamme, Christina, Kellner, Ulrich, Kunstmann, Erdmute, Maffei, Pietro, Reiff, Charlotte M, Rohrschneider, Klaus, Rosenberg, Thomas, Rudolph, Günther, Vámos, Rita, Varsányi, Balázs, Weleber, Richard G, Wissinger, Bernd

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Loss-of-Function Mutations in Euchromatin Histone Methyl Transferase 1 ( EHMT1) Cause the 9q34 Subtelomeric Deletion Syndrome von Kleefstra, Tjitske, Brunner, Han G., Amiel, Jeanne, Oudakker, Astrid R., Nillesen, Willy M., Magee, Alex, Geneviève, David, Cormier-Daire, Valérie, van Esch, Hilde, Fryns, Jean-Pierre, Hamel, Ben C.J., Sistermans, Erik A., de Vries, Bert B.A., van Bokhoven, Hans

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Mutations involved in Aicardi-Goutières syndrome implicate SAMHD1 as regulator of the innate immune response von Bodemer, Christine, Vanderver, Adeline, Bertini, Enrico, Hamel, Ben C J, van der Knaap, Marjo S, Heiberg, Arvid, Orcesi, Simona, Tan, Tiong Y, Lagae, Lieven, Manfield, Iain W, Whittaker, Elizabeth, Lamb, Teresa, Gornall, Hannah, Cazorla, Angels Garcia, Rice, Gillian I, Hunter, Matthew, Shalev, Stavit A, Marom, Daphna, Rasmussen, Magnhild, Desguerre, Isabelle, Crow, Yanick J, Lourenco, Charles M, Bonthron, David T, Ali, Manir, Fuller, Jonathan C, Soler, Doriette M, Bond, Jacquelyn, Jackson, Richard M, Couthard, Lydia R, Wakeling, Emma L, Gener, Blanca, Brockmann, Knut, Landrieu, Pierre G, Fazzi, Elisa, Carr, Ian M, van der Merwe, William, Shinawi, Marwan, Kumar, Ram, Spiegel, Ronen, Briggs, Tracy A, Attard-Montalto, Simon P, Asipu, Aruna, Brueton, Louise A, Wassmer, Evangeline, Brunette, Rebecca L, Lebon, Pierre, Stetson, Daniel B, McDermott, Michael F, Aeby, Alec, Corry, Peter C, Prendiville, Julie S

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Development of AMSTAR: a measurement tool to assess the methodological quality of systematic reviews von Shea, Beverley J, Grimshaw, Jeremy M, Wells, George A, Boers, Maarten, Andersson, Neil, Hamel, Candyce, Porter, Ashley C, Tugwell, Peter, Moher, David, Bouter, Lex M

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Gene Patenting — The Supreme Court Finally Speaks von Kesselheim, Aaron S, Cook-Deegan, Robert M, Winickoff, David E, Mello, Michelle M

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X-Linked Mental Retardation and Autism Are Associated with a Mutation in the NLGN4 Gene, a Member of the Neuroligin Family von Laumonnier, Frédéric, Bonnet-Brilhault, Frédérique, Gomot, Marie, Blanc, Romuald, David, Albert, Moizard, Marie-Pierre, Raynaud, Martine, Ronce, Nathalie, Lemonnier, Eric, Calvas, Patrick, Laudier, Béatrice, Chelly, Jamel, Fryns, Jean-Pierre, Ropers, Hans-Hilger, Hamel, Ben C.J., Andres, Christian, Barthélémy, Catherine, Moraine, Claude, Briault, Sylvain

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AMSTAR is a reliable and valid measurement tool to assess the methodological quality of systematic reviews von Shea, Beverley J, Hamel, Candyce, Wells, George A, Bouter, Lex M, Kristjansson, Elizabeth, Grimshaw, Jeremy, Henry, David A, Boers, Maarten

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Planetary Ices and the Linear Mixing Approximation von Bethkenhagen, M., Meyer, E. R., Hamel, S., Nettelmann, N., French, M., Scheibe, L., Ticknor, C., Collins, L. A., Kress, J. D., Fortney, J. J., Redmer, R.

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Profile: The KEMRI/CDC Health and Demographic Surveillance System—Western Kenya von ODHIAMBO, Frank O, LASERSON, Kayla F, OMBOK, Maurice, LINDBLADE, Kimberly, DESAI, Meghna, TER KUILE, Feiko, PHILLIPS-HOWARD, Penelope, EIJK, Anna M.van, ROSEN, Daniel, HIGHTOWER, Allen, OFWARE, Peter, MUTTAI, Hellen, SEWE, Maquins, NAHLEN, Bernard, DECOCK, Kevin, SLUTSKER, Laurence, BREIMAN, Robert F, VULULE, John M, HAMEL, Mary J, FEIKIN, Daniel R, ADAZU, Kubaje, OGWANG, Sheila, OBOR, David, AMEK, Nyaguara, BAYOH, Nabie

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New Guidelines for Statistical Reporting in the Journal von Harrington, David, D’Agostino, Ralph B, Gatsonis, Constantine, Hogan, Joseph W, Hunter, David J, Normand, Sharon-Lise T, Drazen, Jeffrey M, Hamel, Mary Beth

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Safety and efficacy of losmapimod in facioscapulohumeral muscular dystrophy (ReDUX4): a randomised, double-blind, placebo-controlled phase 2b trial von Tawil, Rabi, Wagner, Kathryn R, Hamel, Johanna I, Leung, Doris G, Statland, Jeffrey M, Wang, Leo H, Genge, Angela, Sacconi, Sabrina, Lochmüller, Hanns, Reyes-Leiva, David, Diaz-Manera, Jordi, Alonso-Perez, Jorge, Muelas, Nuria, Vilchez, Juan J, Pestronk, Alan, Gibson, Summer, Goyal, Namita A, Hayward, Lawrence J, Johnson, Nicholas, LoRusso, Samantha, Freimer, Miriam, Shieh, Perry B, Subramony, S H, van Engelen, Baziel, Kools, Joost, Leinhard, Olof Dahlqvist, Widholm, Per, Morabito, Christopher, Moxham, Christopher M, Cadavid, Diego, Mellion, Michelle L, Odueyungbo, Adefowope, Tracewell, William G, Accorsi, Anthony, Ronco, Lucienne, Gould, Robert J, Shoskes, Jennifer, Rojas, Luis Alejandro, Jiang, John G

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NK-like T cells and plasma cytokines, but not anti-viral serology, define immune fingerprints of resilience and mild disability in exceptional aging von Vallejo, Abbe N, Hamel, Jr, David L, Mueller, Robert G, Ives, Diane G, Michel, Joshua J, Boudreau, Robert M, Newman, Anne B

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Ex vivo comparison of pin placement with patient‐specific drill guides or freehand technique in canine cadaveric spines von Guevara, Francisco, Foss, Kari D., Harper, Tisha A. M., Moran, Clara A., Hague, Devon W., Hamel, Philip E. S., Schaeffer, David J., McCoy, Annette M.

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Absence of GP130 cytokine receptor signaling causes extended Stuve-Wiedemann syndrome von Chen, Yin-Huai, Grigelioniene, Giedre, Newton, Phillip T., Gullander, Jacob, Elfving, Maria, Hammarsjo, Anna, Batkovskyte, Dominyka, Alsaif, Hessa S., Kurdi, Wesam I. Y., Abdulwahab, Firdous, Shanmugasundaram, Veerabahu, Devey, Luke, Bacrot, Severine, Brodszki, Jana, Huber, Celine, Hamel, Ben, Gisselsson, David, Papadogiannakis, Nikos, Jedrycha, Katarina, Gurtl-Lackner, Barbara, Chagin, Andrei S., Nishimura, Gen, Aschenbrenner, Dominik, Alkuraya, Fowzan S., Laurence, Arian, Cormier-Daire, Valerie, Uhlig, Holm H.

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Neuroinflammation, mitochondrial defects and neurodegeneration in mucopolysaccharidosis III type C mouse model von Martins, Carla, Hůlková, Helena, Dridi, Larbi, Dormoy-Raclet, Virginie, Grigoryeva, Lubov, Choi, Yoo, Langford-Smith, Alexander, Wilkinson, Fiona L, Ohmi, Kazuhiro, DiCristo, Graziella, Hamel, Edith, Ausseil, Jerôme, Cheillan, David, Moreau, Alain, Svobodová, Eva, Hájková, Zuzana, Tesařová, Markéta, Hansíková, Hana, Bigger, Brian W, Hrebícek, Martin, Pshezhetsky, Alexey V

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Mutations in the gene encoding the 3′-5′ DNA exonuclease TREX1 cause Aicardi-Goutières syndrome at the AGS1 locus von Bonthron, David T, Lindahl, Tomas, Ali, Manir, Ponsot, Gerard, Robins, Peter, Voit, Thomas, van Bokhoven, Hans, Barnes, Deborah E, Livingston, John H, Massey, Roger F, Crow, Yanick J, Parmar, Rekha, Lebon, Pierre, Jackson, Andrew P, Hayward, Bruce E, Hamel, Ben C, Leitch, Andrea, Klepper, Joerg, Cowan, Frances M, Frints, Suzanne G, Black, Deborah N, Lynch, Sally Ann, Meritet, Jean François, Brunner, Han G, Corry, Peter C, Michaud, Jacques L

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Effect of Phosphodiesterase-5 Inhibition on Exercise Capacity and Clinical Status in Heart Failure With Preserved Ejection Fraction: A Randomized Clinical Trial von Redfield, Margaret M, Chen, Horng H, Borlaug, Barry A, Semigran, Marc J, Lee, Kerry L, Lewis, Gregory, LeWinter, Martin M, Rouleau, Jean L, Bull, David A, Mann, Douglas L, Deswal, Anita, Stevenson, Lynne W, Givertz, Michael M, Ofili, Elizabeth O, O’Connor, Christopher M, Felker, G. Michael, Goldsmith, Steven R, Bart, Bradley A, McNulty, Steven E, Ibarra, Jenny C, Lin, Grace, Oh, Jae K, Patel, Manesh R, Kim, Raymond J, Tracy, Russell P, Velazquez, Eric J, Anstrom, Kevin J, Hernandez, Adrian F, Mascette, Alice M, Braunwald, Eugene

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