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HLA-DRB111 and variants of the MHC class II locus are strong risk factors for systemic juvenile idiopathic arthritis

by Ombrello, Michael J., Remmers, Elaine F., Tachmazidou, Ioanna, Grom, Alexei, Foell, Dirk, Haas, Johannes-Peter, Martini, Alberto, Gattorno, Marco, Özen, Seza, Prahalad, Sampath, Zeft, Andrew S., Bohnsack, John F., Mellins, Elizabeth D., Ilowite, Norman T., Russo, Ricardo, Len, Claudio, Hilario, Maria Odete E., Oliveira, Sheila, Yeung, Rae S. M., Rosenberg, Alan, Wedderburn, Lucy R., Anton, Jordi, Schwarz, Tobias, Hinks, Anne, Bilginer, Yelda, Park, Jane, Cobb, Joanna, Satorius, Colleen L., Han, Buhm, Baskin, Elizabeth, Signa, Sara, Duerr, Richard H., Achkar, J. P., Kamboh, M. Ilyas, Kaufman, Kenneth M., Kottyan, Leah C., Pinto, Dalila, Scherer, Stephen W., Alarcón-Riquelme, Marta E., Docampo, Elisa, Estivill, Xavier, Gül, Ahmet, de Bakker, Paul I. W., Raychaudhuri, Soumya, Langefeld, Carl D., Thompson, Susan, Zeggini, Eleftheria, Thomson, Wendy, Kastner, Daniel L., Woo, Patricia, Achkar, J. P., Alarcón-Riquelme, Marta E., Allen, Roger, Anton, Jordi, Baskin, Elizabeth, Berg, Stefan, Bica, Bianca, Bilginer, Yelda, Bohnsack, John F., Cavalcanti, Andre, Chaitow, Jeffrey, Cobb, Joanna, Cuttica, Rubin, de Bakker, Paul I. W., Docampo, Elisa, Duerr, Richard, Ellis, Justine, Estivill, Xavier, Finkel, Terri H., Foell, Dirk, Gattorno, Marco, Grom, Alexei, Gül, Ahmet, Haas, Johannes-Peter, Hakonarson, Hakon, Han, Buhm, Hilario, Maria Odete E., Hinks, Anne, Ilowite, Norman T., Kamboh, M. Ilyas, Kaufman, Kenneth, Kottyan, Leah C., Langefeld, Carl, Len, Claudio, Martini, Alberto, Mellins, Elizabeth D., Minden, Kirstin, Murray, Kevin, Oliveira, Sheila, Ombrello, Michael J., Ozen, Seza, Park, Jane, Pinto, Dalila, Prahalad, Sampath, Quartier, Pierre, Raychaudhuri, Soumya, Rosenberg, Alan, Russo, Ricardo, Satorius, Colleen, Scherer, Stephen W.
Published in Proceedings of the National Academy of Sciences - PNAS (29.12.2015)

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The ENIGMA Consortium: large-scale collaborative analyses of neuroimaging and genetic data

by Vasquez, Alejandro Arias, Renteria, Miguel E., Agartz, Ingrid, Apostolova, Liana G., Bastin, Mark E., Bauer, Michael, Bearden, Carrie E., Binder, Elisabeth B., Bøen, Erlend, Bowman, Ian J., Brohawn, David G., Buitelaar, Jan, Carless, Melanie A., Ching, Christopher R. K., Conrod, Patricia, Depondt, Chantal, de Zubicaray, Greig I., Djurovic, Srdjan, Duggirala, Ravindranath, Dyer, Thomas D., Ekman, Carl Johan, Emsell, Louise, Fears, Scott, Fedko, Iryna, Fox, Peter T., Francks, Clyde, Frodl, Thomas, Frouin, Vincent, Godlewska, Beata, Haukvik, Unn K., Hickie, Ian B., Hoekstra, Pieter J., Homuth, Georg, Hulshoff Pol, Hilleke E., Hwang, Kristy S., Kim, Sungeun, Kochunov, Peter, Krämer, Bernd, Kwok, John B. J., Laje, Gonzalo, Landman, Bennett A., Lauriello, John, Li, Chiang-shan, Liberg, Benny, Liu, Xinmin, Macciardi, Fabio, Malt, Ulrik F., Mattheisen, Manuel, Meyer-Lindenberg, Andreas, Melle, Ingrid, Mohnke, Sebastian, Morris, Derek W., Mueller, Bryon A., Mühleisen, Thomas W., Müller-Myhsok, Bertram, Nichols, Thomas E., Oosterlaan, Jaap, Pandolfo, Massimo, Papmeyer, Martina, Pausova, Zdenka, Penninx, Brenda W., Peterson, Charles P., Potkin, Steven G., Rasmussen, Jerod, Rijpkema, Mark, Risacher, Shannon L., Roiz-Santiañez, Roberto, Romanczuk-Seiferth, Nina, Rujescu, Dan, Salami, Alireza, Scanlon, Cathy, Schmaal, Lianne, Schnack, Hugo G., Schork, Andrew J., Seidman, Larry, Shen, Li, Smoller, Jordan W., Sponheim, Scott R., Starr, John M., Sussmann, Jessika, Sämann, Philipp G., Teumer, Alexander, Toga, Arthur W., Trabzuni, Daniah, Turner, Jessica, Van den Heuvel, Martijn, van Eijk, Kristel, van Erp, Theo G. M., van Haren, Neeltje E. M., van ‘t Ent, Dennis, van Tol, Marie-Jose, Valdés Hernández, Maria C., Versace, Amelia, Weale, Michael E., Westlye, Lars T., Whelan, Christopher D., Wittfeld, Katharina, Zilles, David, Freimer, Nelson B., Lawrence, Natalia S.
Published in Brain imaging and behavior (01.06.2014)

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Genetic coding variant in complement factor B (CFB) is associated with increased risk for perianal Crohn’s disease and leads to impaired CFB cleavage and phagocytosis

by Stamps, Dalton T, Dube, Shishir, Li, Dalin, Yang, Shaohong, Landers, Carol J, Mengesha, Emebet, Murali, Ramachandran, Potdar, Alka A, Wolf, Andrea J, Botwin, Gregory J, Khrom, Michelle, Faubion, William A, Sandler, Robert S, Sartor, R Balfour, Brant, Steven R, Rioux, John D, Schumm, L Philip, Silverberg, Mark S, Zaghiyan, Karen, Melmed, Gil Y, Vasiliauskas, Eric A, Syal, Gaurav, Bonthala, Nirupama N, Targan, Stephan R, Michelsen, Kathrin S, Ahmad, Tariq, Amininejad, Leila, Andersen, Vibeke, Aumais, Guy, Baidoo, Leonard, Bayless, Theodore M, Bethge, Johannes, Boucher, Gabrielle, Brand, Stephan, Chew, Angela, Cho, Judy H, Cohain, Ariella, Jong, Dirk De, Denson, Lee A, Dewit, Olivier, D'Inca, Renata, Edwards, Cathryn, Ellinghaus, David, Festen, Eleonora A, Florin, Tim, Gieger, Christian, Goyette, Philippe, Green, Todd, Griffiths, Anne M, Hakonarson, Hakon, Hanigan, Katherine, Hart, Ailsa, Hayward, Nicholas K, Hugot, Jean-Pierre, Hui, Ken Y, Imielinski, Marcin, Jonaitis, Laimas, Jostins, Luke, Kiudelis, Gediminas, Krishnaprasad, Krupa, Kugathasan, Subra, Lee, James C, Lees, Charlie W, Leja, Marcis, Louis, Edouard, Mitrovic, Mitja, Ng, Aylwin, Ng, Siew C, Evelyn Ng, Sok Meng, Nikolaus, Susanna, Oikonomou, Ioannis, Phillips, Anne, Ponsioen, Cyriel Y, Prescott, Natalie J, Raychaudhuri, Soumya, Rieder, Florian, Rioux, John D, Ripke, Stephan, Russell, Richard K, Sanderson, Jeremy D, Satsangi, Jack, Schreiber, Stefan, Philip Schumm, L, Scott, Regan, Silverberg, Mark S, Simms, Lisa A, Spain, Sarah L, Sventoraityte, Jurgita, Torkvist, Leif, Tremelling, Mark, Vasiliauskas, Eric, Vermeire, Severine, Walters, Thomas, Wang, Kai, Wang, Ming-Hsi, Wei, Zhi, Winkelmann, Juliane, Zhang, Clarence K, Zhang, Wei, Zhao, Zhen Z
Published in Gut (01.11.2023)

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Epilepsy, hippocampal sclerosis and febrile seizures linked by common genetic variation around SCN1A

by Kasperavičiūtė, Dalia, Catarino, Claudia B., Matarin, Mar, Leu, Costin, Novy, Jan, Tostevin, Anna, Leal, Bárbara, Hessel, Ellen V. S., Hallmann, Kerstin, Hildebrand, Michael S., Dahl, Hans-Henrik M., Ryten, Mina, Trabzuni, Daniah, Ramasamy, Adaikalavan, Alhusaini, Saud, Doherty, Colin P., Dorn, Thomas, Hansen, Jörg, Krämer, Günter, Steinhoff, Bernhard J., Zumsteg, Dominik, Duncan, Susan, Kälviäinen, Reetta K., Eriksson, Kai J., Kantanen, Anne-Mari, Pandolfo, Massimo, Gruber-Sedlmayr, Ursula, Schlachter, Kurt, Reinthaler, Eva M., Stogmann, Elisabeth, Zimprich, Fritz, Théâtre, Emilie, Smith, Colin, O’Brien, Terence J., Meng Tan, K., Petrovski, Slave, Robbiano, Angela, Paravidino, Roberta, Zara, Federico, Striano, Pasquale, Sperling, Michael R., Buono, Russell J., Hakonarson, Hakon, Chaves, João, Costa, Paulo P., Silva, Berta M., da Silva, António M., de Graan, Pierre N. E., Koeleman, Bobby P. C., Becker, Albert, Schoch, Susanne, von Lehe, Marec, Reif, Philipp S., Rosenow, Felix, Becker, Felicitas, Weber, Yvonne, Lerche, Holger, Rössler, Karl, Buchfelder, Michael, Hamer, Hajo M., Kobow, Katja, Coras, Roland, Blumcke, Ingmar, Scheffer, Ingrid E., Berkovic, Samuel F., Weale, Michael E., Delanty, Norman, Depondt, Chantal, Cavalleri, Gianpiero L., Kunz, Wolfram S., Sisodiya, Sanjay M.
Published in Brain (London, England : 1878) (01.10.2013)

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IL1RN Variation Influences Both Disease Susceptibility and Response to Recombinant Human Interleukin‐1 Receptor Antagonist Therapy in Systemic Juvenile Idiopathic Arthritis

by Arthur, Victoria L., Grom, Alexei A., Foell, Dirk, Özen, Seza, Prahalad, Sampath, Mellins, Elizabeth D., Russo, Ricardo, Oliveira, Sheila, Yeung, Rae S. M., Rosenberg, Alan M., Minden, Kirsten, Kastner, Daniel L., Woo, Patricia, Ombrello, Michael J., Docampo, Elisa, Estivill, Xavier, Gattorno, Marco, Grom, Alexei, Gül, Ahmet, Haas, Johannes‐Peter, Kastner, Daniel L., Kottyan, Leah C., Langefeld, Carl D., Martini, Alberto, Ombrello, Michael J., Pinto, Dalila, Rosenberg, Alan, Russo, Ricardo, Scherer, Stephen W., Signa, Sara, Shuldiner, Emily, Tachmazidou, Ioanna, Thompson, Susan, Thomson, Wendy, Wedderburn, Lucy R., Woo, Patricia, Zeggini, Eleftheria, Chédeville, Gaëlle, Chetaille, Anne‐Laure, Dancey, Paul, Ellsworth, Janet, Guzman, Jaime, Jurencak, Roman, Schneider, Rayfel, Scherer, Stephen W., Spiegel, Lynn, Stringer, Elizabeth, Tucker, Lori B., Wintle, Richard F., Abinum, Mario, Bell, A., Hall, M., Hollingworth, Peter, Stewart, I., Woo, Patricia, Baildam, Eileen, Bishop, Nick, Brown, Lynsey, Davidson, Joyce, Friel, Elizabeth, Hadfield, Kelly, Lay, Mark, Lloyd, Olivia, Lydon, Carol, Makengo, Natasha, Moorcroft, Theresa, Price, Vicki, Venter, Katharine, Zelenovic, Jadranka, Foeldvari, Ivan, Foell, Dirk, Heiligenhaus, Arnd, Kallinich, Tilmann, Kümmerle‐Deschner, Jasmin, Minden, Kirsten, Mönkemöller, Kirsten, Elder, Melissa, Gottlieb, Beth S., Imundo, Lisa F., Miller, Michael L., Prather, Kristi, Singer, Nora G., Spalding, Steven J., Tarvin, Stacey E., Verbsky, James W., Wallace, Carol A., Cutts, Rebecca, Etheridge, Angela, Hinks, Anne, Howman, Ruth, Marshall, Lucy, Melville, Laura, Moncrieffe, Halima, Mulligan, Kathleen, Palman, Jason, Robinson, Emily, Simou, Stephanie, Stafford, Stefanie, Southwood, Tauny, Woo, Patricia
Published in Arthritis & rheumatology (Hoboken, N.J.) (01.08.2018)

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Developmental trajectories of neuroanatomical alterations associated with the 16p11.2 Copy Number Variations

by Cárdenas-de-la-Parra, Alonso, Martin-Brevet, Sandra, Moreau, Clara, Rodriguez-Herreros, Borja, Fonov, Vladimir S., Maillard, Anne M., Zürcher, Nicole R., Addor, Marie-Claude, Andrieux, Joris, Arveiler, Benoît, Baujatm, Geneviève, Sloan-Bénan, Frédérique, Belfiore, Marco, Bonneau, Dominique, Bouquillon, Sonia, Boute, Odile, Brusco, Alfredo, Busa, Tiffany, Caberg, Jean-Hubert, Campion, Dominique, Colombert, Vanessa, Cordier, Marie-Pierre, David, Albert, Debray, François-Guillaume, Delrue, Marie-Ange, Doco-Fenzy, Martine, Dunkhase-Heinl, Ulrike, Edery, Patrick, Fagerberg, Christina, Faivre, Laurence, Forzano, Francesca, Genevieve, David, Gérard, Marion, Giachino, Daniela, Guichet, Agnès, Guillin, Olivier, Héron, Delphine, Isidor, Bertrand, Jacquette, Aurélia, Jaillard, Sylvie, Journel, Hubert, Keren, Boris, Lacombe, Didier, Lebon, Sébastien, Le Caignec, Cédric, Lemaître, Marie-Pierre, Lespinasse, James, Mathieu-Dramart, Michèle, Mercier, Sandra, Mignot, Cyril, Missirian, Chantal, Petit, Florence, Pilekær Sørensen, Kristina, Pinson, Lucile, Plessis, Ghislaine, Prieur, Fabienne, Rooryck-Thambo, Caroline, Rossi, Massimiliano, Sanlaville, Damien, Schlott Kristiansen, Britta, Schluth-Bolard, Caroline, Till, Marianne, Van Haelst, Mieke, Van Maldergem, Lionel, Hadjikhani, Nouchine, Beckmann, Jacques S., Reymond, Alexandre, Draganski, Bogdan, Jacquemont, Sébastien, Collins, D. Louis
Published in NeuroImage (Orlando, Fla.) (01.12.2019)

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A Method to Exploit the Structure of Genetic Ancestry Space to Enhance Case-Control Studies

by Colombel, Jean-Frederick, Hugot, Jean-Pierre, Massey, Dunecan, Montgomery, Grant W., Oikonomou, Ioannis, Peeters, Harald, Proctor, Deborah D., Seibold, Frank, Törkvist, Leif, Andrews, Jane M., Bampton, Peter A., Florin, Timothy H., Krishnaprasad, Krupa, Radford-Smith, Graham, Simms, Lisa A., Laukens, Debby, Deslandres, Colette, Duerr, Richard H., Goyette, Philippe, Haritunians, Talin, Lahaie, Raymond G., Ng, Sok Meng, Rioux, John D., Aerts, Jan, Attwood, Anthony, Ball, Stephen G., Brown, Morris J., Burton, John, Byrnes, Jake, Cardin, Niall, Clee, Chris M., Coffey, Alison J., Dominiczak, Anna F., Evans, David M., Farmer, Anne, Ferrier, Nicol, Flynn, Edward, Franklyn, Jayne A., Frayling, Timothy M., Freathy, Rachel M., Gibbs, Polly, Gray, Emma, Howard, Philip, Hughes, Debbie, Hunt, Sarah, Jolley, Jennifer D., Jones, Lisa A., Kirov, George, Maller, Julian, Mansfield, John, McGuffin, Peter, McLay, Kirsten E., Mentzer, Alex, Munroe, Patricia B., Newman, William, Palotie, Aarno, Plagnol, Vincent, Prescott, Natalie J., Quail, Michael A., Reid, David M., Renwick, Anthony, Russell, Ellie, St Clair, David, Scott, Richard, Somaskantharajah, Elilan, Steer, Sophia, Symmons, Deborah P.M., Tobin, Martin D., Wain, Louise V., Walker, Mark, Wallace, Chris, Weedon, Michael N., Wilson, Anthony G., Yau, Chris, Young, Allan H., Brown, Matthew A., Gough, Stephen C.L., Satsangi, Jack, Ouwehand, Willem H., Parkes, Miles, Rahman, Nazneen, Samani, Nilesh J., Kwiatkowski, Dominic P., Donnelly, Peter, Bramon, Elvira, Casas, Juan P., Corvin, Aiden, Jankowski, Janusz, Markus, Hugh S., Palmer, Colin N.A., Plomin, Robert, Viswanathan, Ananth C., Spencer, Chris C.A., Blackburn, Hannah, Gillman, Matthew, McCann, Owen T., Waller, Matthew, Weston, Paul, Whittaker, Pamela, Roeder, Kathryn
Published in American journal of human genetics (05.05.2016)

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