Treffer 1 - 20 von 56 für Suche 'Anias, J', Suchdauer: 1,61s Treffer weiter einschränken
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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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    Monogenic early-onset lymphoproliferation and autoimmunity: Natural history of STAT3 gain-of-function syndrome von Leiding, Jennifer W., Vogel, Tiphanie P., Smith, Madison R., Carisey, Alexandre, Vargas-Hernández, Alexander, Silva-Carmona, Manuel, Neven, Bénédicte, Ronan Leahy, Timothy, Taskinen, Mervi, Kostyuchenko, Larysa, Scherbina, Anna, Bauer, Cindy S., Giovannini-Chami, Lisa, Romberg, Neil, Prince, Benjamin T., Bohnsack, John, Pachlopnik Schmid, Jana, Bahna, Sami, Brothers, Shannon, Chan, Alice Y., Chandrakasan, Shanmuganathan, Christiansen, Mette, Cole, Theresa, Desai, Mukesh M., Gottrand, Frédéric, Grimbacher, Bodo, Hoffman, Hal M., Guerrerio, Anthony L., Kainulainen, Leena, Lawrence, Monica G., Martelius, Timi, Neth, Olaf, Lugo Reyes, Saúl Oswaldo, Russell, Mark A., Schejter, Yael, Skevofilax, Effie, Suan, Daniel, Velasco, Helena, Walkovich, Kelly, Aleshkevich, Svetlana, Allende, Luis M., Atschekzei, Faranaz, Aygunes, Utku, Barlogis, Vincent, Belko, John, Bezrodnik, Liliana, Biebl, Ariane, Caldirola, Maria Soledad, Castelle, Martin, Cokugras, Haluk, Cox, Fionnuala, Dalgic, Buket, ASH Dalm, Virgil, Dujovny, Tal, Eken, Ahmet, Fabre, Alexandre, Fischer, Alain, Hannibal, Mark, Huppert, Laura, Karakoc-Aydiner, Elif, Pac Kisaarslan, Ayşenur, Kiykim, Ayca, Klocperk, Adam, Kuzmenko, Natalia, Lianou, Dimitra, Lorenz, Myriam Ricarda, Manson, Ania, Marega, Lia Furlaneto, Nolan, David, Norlin, Anna-Carin, Oleastro, Matias, Ozcan, Alper, Picard, Capucine, Polychronopoulou, Sophia, Quesada, Juan Francisco, Randall, Katrina L., Resin, Geraldine, Rodina, Yulia, Rohrlich, Pierre, Sachs, Johnathan, Sakovich, Inga, Santarlas, Christopher, Scheffler Mendoza, Selma C., Schwarz, Klaus, Sediva, Anna, Slatter, Mary, Sleasman, John, Suratannon, Narissara, Tanita, Kay, Travis, Stephen, Tsinti, Maria, Unal, Ekrem, Urdinez, Luciano, Vazquez-Gomez, Felisa, Weiss, Mitchell J., Zhang, Yu, Seppänen, Mikko R.J., Sogkas, Georgios, Milner, Joshua D., Forbes Satter, Lisa R.


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    Loss-of-function nuclear factor κB subunit 1 (NFKB1) variants are the most common monogenic cause of common variable immunodeficiency in Europeans von Tuijnenburg, Paul, Jansen, Machiel H., Carss, Keren J., Baxendale, Helen, Chandra, Anita, Seneviratne, Suranjith L., Oksenhendler, Eric, Tool, Anton T.J., Whitehorn, Deborah, Turro, Ernest, Thaventhiran, James E., Kuijpers, Taco W., Adhya, Zoe, Anantharachagan, Ariharan, Arumugakani, Gururaj, Bacchelli, Chiara, Baxendale, Helen, Bibi, Shahnaz, Booth, Claire, Browning, Michael, Burns, Siobhan, Clifford, Hayley, Cooper, Nichola, Davies, Sophie, Devlin, Lisa, Edgar, David, Egner, William, Ghurye, Rohit, Gilmour, Kimberley, Goddard, Sarah, Gordins, Pavel, Hackett, Scott, Hague, Rosie, Hayman, Grant, Jolles, Stephen, Jones, Julie, Kelleher, Peter, Klein, Nigel, Kuijpers, Taco, Kumararatne, Dinakantha, Laffan, James, Lango Allen, Hana, Lear, Sara, Longhurst, Hilary, Maimaris, Jesmeen, McDermott, Elizabeth, Morrisson, Valerie, Nasir, Iman, Noorani, Sadia, Oksenhendler, Eric, Ponsford, Mark, Qasim, Waseem, Quinn, Ellen, Quinti, Isabella, Samarghitean, Crina, Savic, Sinisa, Seneviratne, Suranjith, Simeoni, Ilenia, Staples, Emily, Steele, Cathal, Thaventhiran, James, Thomas, Moira, Thrasher, Adrian, Worth, Austen, Yong, Patrick, Bradley, John, Hammerton, Tracey, Ouwehand, Willem, Raymond, F Lucy, Veltman, Marijke, Clements-Brod, Naomi, Davis, John, Dewhurst, Eleanor, Erwood, Marie, Frary, Amy, Linger, Rachel, Papadia, Sofia, Rehnstrom, Karola, Astle, William, Attwood, Antony, Bleda, Marta, Carss, Keren, Daugherty, Louise, Deevi, Sri, Graf, Stefan, Greene, Daniel, Halmagyi, Csaba, Matser, Vera, Meacham, Stuart, Megy, Karyn, Shamardina, Olga, Titterton, Catherine, Tuna, Salih, Turro, Ernest, von Ziegenweldt, Julie, Furnell, Abigail, Staines, Simon, Stephens, Jonathan, Whitehorn, Deborah, Watt, Christopher


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    Effects of copy number variations on brain structure and risk for psychiatric illness: Large‐scale studies from the ENIGMA working groups on CNVs von Meer, Dennis, Agartz, Ingrid, Arango, Celso, Ayesa‐Arriola, Rosa, Bakker, Geor, Boomsma, Dorret I., Bülow, Robin, Butcher, Nancy J., Caspers, Svenja, Crespo‐Facorro, Benedicto, Dale, Anders M., Dazzan, Paola, Zubicaray, Greig I., Donohoe, Gary, Espeseth, Thomas, Fisher, Simon E., Ge, Tian, Glahn, David C., Grabe, Hans J., Gur, Raquel E., Håberg, Asta K., Hashimoto, Ryota, Hibar, Derrek P., Holmes, Avram J., Hulshoff Pol, Hilleke E., Kushan, Leila, Liu, Jingyu, Martin‐Brevet, Sandra, Martínez, Kenia, Mather, Karen A., Mathias, Samuel R., Medland, Sarah E., Modenato, Claudia, Mühleisen, Thomas W., Prieto, Carlos, Ragothaman, Anjanibhargavi, Reinbold, Céline S., Reis Marques, Tiago, Repetto, Gabriela M., Reymond, Alexandre, Sachdev, Perminder S., Schmitt, James E., Schofield, Peter R., Silva, Ana I., Stefansson, Hreinn, Stein, Dan J., Tamnes, Christian K., Ulfarsson, Magnus O., Vajdi, Ariana, Ent, Dennis, Bree, Marianne B. M., Vassos, Evangelos, Vázquez‐Bourgon, Javier, Vila‐Rodriguez, Fidel, Walters, G. Bragi, Wen, Wei, Zackai, Elaine H., Thompson, Paul M., Bearden, Carrie E., Blackburn, Nicholas B., Bøen, Rune, Zwarte, Sonja M. C., Forti, Marta Di, Frei, Oleksandr, Fukunaga, Masaki, Hehir‐Kwa, Jayne Y., Hoffmann, Per, Homuth, Georg, Jahanshad, Neda, Koops, Sanne, Kumar, Kuldeep, Kikuchi, Masataka, Le Hellard, Stephanie, Leu, Costin, Murray, Robin M, Nyberg, Lars, Shumskaya, Elena, Sisodiya, Sanjay M., Steen, Vidar M., Teumer, Alexander, Uhlmann, Anne, Wright, Margaret J., Campbell, Linda E., Crossley, Nicolas A., Crowley, T. Blaine, Daly, Eileen, Fiksinski, Ania M., Fremont, Wanda, Goodrich‐Hunsaker, Naomi J., Gudbrandsen, Maria, Jonas, Rachel K., Kates, Wendy R., Lin, Amy, Moss, Hayley, Murphy, Declan G., Murphy, Kieran C., Owen, Michael J., Simon, Tony. J., Amelsvoort, Therese, Vorstman, Jacob A. S.

    Veröffentlicht in Human brain mapping

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    Genetic Differences in the Immediate Transcriptome Response to Stress Predict Risk-Related Brain Function and Psychiatric Disorders von Arloth, Janine, Bogdan, Ryan, Weber, Peter, Frishman, Goar, Menke, Andreas, Wagner, Klaus V., Schmidt, Mathias V., Karbalai, Nazanin, Czamara, Darina, Altmann, Andre, Trümbach, Dietrich, Wurst, Wolfgang, Mehta, Divya, Carey, Caitlin E., Conley, Emily Drabant, Ripke, Stephan, Wray, Naomi R., Lewis, Cathryn M., Hamilton, Steven P., Blackwood, Douglas H.R., Boomsma, Dorret I., Cichon, Sven, Heath, Andrew C., Holsboer, Florian, Muglia, Pierandrea, Noethen, Markus M., Penninx, Brenda P., Pergadia, Michele L., Potash, James B., Lin, Danyu, Müller-Myhsok, Bertram, Shi, Jianxin, Steinberg, Stacy, Grabe, Hans J., Lichtenstein, Paul, Perlis, Roy H., Preisig, Martin, Smoller, Jordan W., Kutalik, Zoltan, Tansey, Katherine E., Teumer, Alexander, Bettecken, Thomas, Binder, Elisabeth B., Breuer, René, Castro, Victor M., Coryell, William H., Craddock, Nick, Czamara, Darina, Degenhardt, Franziska, Fava, Maurizio, Frank, Josef, Gainer, Vivian S., Gallagher, Patience J., Gordon, Scott D., Goryachev, Sergey, Guipponi, Michel, Henders, Anjali K., Hickie, Ian B., Hottenga, Jouke Jan, Jones, Ian, Jones, Lisa, Jung-Ying, Tzeng, Knowles, James A., Kohane, Isaac S., Kohli, Martin A., Korszun, Ania, Landen, Mikael, Lawson, William B., Lewis, Glyn, MacIntyre, Donald, Maier, Wolfgang, Mattheisen, Manuel, McGrath, Patrick J., McIntosh, Andrew, McLean, Alan, Montgomery, Grant M., Murphy, Shawn N., Nauck, Matthias, O’Donovan, Michael, Oskarsson, Högni, Pedersen, Nancy, Schulz, Andrea, Schulze, Thomas G., Shyn, Stanley I., Sigurdsson, Engilbert, Slager, Susan L., Smit, Johannes H., Stefansson, Hreinn, Steffens, Michael, Tozzi, Federica, Treutlein, Jens, Völzke, Henry, Weilburg, Jeffrey B., Willemsen, Gonneke, Neale, Benjamin, Daly, Mark, Levinson, Douglas F., Müller-Myhsok, Bertram, Hariri, Ahmad R., Binder, Elisabeth B.

    Veröffentlicht in Neuron (Cambridge, Mass.)

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