Geometric Predictors of Knotted and Linked Arcs von Sleiman, Joseph L., Burton, Robin H., Caraglio, Michele, Gutierrez Fosado, Yair Augusto, Michieletto, Davide

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Geometric Predictors of Knotted and Linked Arcs von Sleiman, Joseph L, Burton, Robin H, Caraglio, Michele, Fosado, Yair Augusto Gutierrez, Michieletto, Davide

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Geometric Predictors of Knotted and Linked Arcs von Sleiman, Joseph L, Burton, Robin H, Caraglio, Michele, Yair Augusto Gutierrez Fosado, Michieletto, Davide

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Strong synaptic transmission impact by copy number variations in schizophrenia von Glessner, Joseph T., Reilly, Muredach P., Kim, Cecilia E., Takahashi, Nagahide, Albano, Anthony, Hou, Cuiping, Bradfield, Jonathan P., Zhang, Haitao, Sleiman, Patrick M. A., Flory, James H., Imielinski, Marcin, Frackelton, Edward C., Chiavacci, Rosetta, Thomas, Kelly A., Garris, Maria, Otieno, Frederick G., Davidson, Michael, Weiser, Mark, Reichenberg, Abraham, Davis, Kenneth L., Friedman, Joseph I., Cappola, Thomas P., Margulies, Kenneth B., Rader, Daniel J., Grant, Struan F. A., Buxbaum, Joseph D., Gur, Raquel E., Hakonarson, Hakon, Lupski, James R.

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Common genetic variants on 5p14.1 associate with autism spectrum disorders von Wang, Kai, Zhang, Haitao, Ma, Deqiong, Bucan, Maja, Glessner, Joseph T., Abrahams, Brett S., Salyakina, Daria, Imielinski, Marcin, Bradfield, Jonathan P., Sleiman, Patrick M. A., Kim, Cecilia E., Hou, Cuiping, Frackelton, Edward, Chiavacci, Rosetta, Takahashi, Nagahide, Sakurai, Takeshi, Rappaport, Eric, Lajonchere, Clara M., Munson, Jeffrey, Estes, Annette, Korvatska, Olena, Piven, Joseph, Sonnenblick, Lisa I., Alvarez Retuerto, Ana I., Herman, Edward I., Dong, Hongmei, Hutman, Ted, Sigman, Marian, Ozonoff, Sally, Klin, Ami, Owley, Thomas, Sweeney, John A., Brune, Camille W., Cantor, Rita M., Bernier, Raphael, Gilbert, John R., Cuccaro, Michael L., McMahon, William M., Miller, Judith, State, Matthew W., Wassink, Thomas H., Coon, Hilary, Levy, Susan E., Schultz, Robert T., Nurnberger, John I., Haines, Jonathan L., Sutcliffe, James S., Cook, Edwin H., Minshew, Nancy J., Buxbaum, Joseph D., Dawson, Geraldine, Grant, Struan F. A., Geschwind, Daniel H., Pericak-Vance, Margaret A., Schellenberg, Gerard D., Hakonarson, Hakon

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Autism genome-wide copy number variation reveals ubiquitin and neuronal genes von Glessner, Joseph T., Wang, Kai, Cai, Guiqing, Korvatska, Olena, Kim, Cecilia E., Wood, Shawn, Zhang, Haitao, Estes, Annette, Brune, Camille W., Bradfield, Jonathan P., Imielinski, Marcin, Frackelton, Edward C., Reichert, Jennifer, Crawford, Emily L., Munson, Jeffrey, Sleiman, Patrick M. A., Chiavacci, Rosetta, Annaiah, Kiran, Thomas, Kelly, Hou, Cuiping, Glaberson, Wendy, Flory, James, Otieno, Frederick, Garris, Maria, Soorya, Latha, Klei, Lambertus, Piven, Joseph, Meyer, Kacie J., Anagnostou, Evdokia, Sakurai, Takeshi, Game, Rachel M., Rudd, Danielle S., Zurawiecki, Danielle, McDougle, Christopher J., Davis, Lea K., Miller, Judith, Posey, David J., Michaels, Shana, Kolevzon, Alexander, Silverman, Jeremy M., Bernier, Raphael, Levy, Susan E., Schultz, Robert T., Dawson, Geraldine, Owley, Thomas, McMahon, William M., Wassink, Thomas H., Sweeney, John A., Nurnberger, John I., Coon, Hilary, Sutcliffe, James S., Minshew, Nancy J., Grant, Struan F. A., Bucan, Maja, Cook, Edwin H., Buxbaum, Joseph D., Devlin, Bernie, Schellenberg, Gerard D., Hakonarson, Hakon

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Loci on 20q13 and 21q22 are associated with pediatric-onset inflammatory bowel disease von Kugathasan, Subra, Baldassano, Robert N, Bradfield, Jonathan P, Sleiman, Patrick M A, Imielinski, Marcin, Guthery, Stephen L, Cucchiara, Salvatore, Kim, Cecilia E, Frackelton, Edward C, Annaiah, Kiran, Glessner, Joseph T, Santa, Erin, Willson, Tara, Eckert, Andrew W, Bonkowski, Erin, Shaner, Julie L, Smith, Ryan M, Otieno, F George, Peterson, Nicholas, Abrams, Debra J, Chiavacci, Rosetta M, Grundmeier, Robert, Mamula, Petar, Tomer, Gitit, Piccoli, David A, Monos, Dimitri S, Annese, Vito, Denson, Lee A, Grant, Struan F A, Hakonarson, Hakon

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Genome-wide copy number variation study associates metabotropic glutamate receptor gene networks with attention deficit hyperactivity disorder von Elia, Josephine, Glessner, Joseph T, Wang, Kai, Takahashi, Nagahide, Shtir, Corina J, Hadley, Dexter, Sleiman, Patrick M A, Zhang, Haitao, Kim, Cecilia E, Robison, Reid, Lyon, Gholson J, Flory, James H, Bradfield, Jonathan P, Imielinski, Marcin, Hou, Cuiping, Frackelton, Edward C, Chiavacci, Rosetta M, Sakurai, Takeshi, Rabin, Cara, Middleton, Frank A, Thomas, Kelly A, Garris, Maria, Mentch, Frank, Freitag, Christine M, Steinhausen, Hans-Christoph, Todorov, Alexandre A, Reif, Andreas, Rothenberger, Aribert, Franke, Barbara, Mick, Eric O, Roeyers, Herbert, Buitelaar, Jan, Lesch, Klaus-Peter, Banaschewski, Tobias, Ebstein, Richard P, Mulas, Fernando, Oades, Robert D, Sergeant, Joseph, Sonuga-Barke, Edmund, Renner, Tobias J, Romanos, Marcel, Romanos, Jasmin, Warnke, Andreas, Walitza, Susanne, Meyer, Jobst, Pálmason, Haukur, Seitz, Christiane, Loo, Sandra K, Smalley, Susan L, Biederman, Joseph, Kent, Lindsey, Asherson, Philip, Anney, Richard J L, Gaynor, J William, Shaw, Philip, Devoto, Marcella, White, Peter S, Grant, Struan F A, Buxbaum, Joseph D, Rapoport, Judith L, Williams, Nigel M, Nelson, Stanley F, Faraone, Stephen V, Hakonarson, Hakon

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GWAS of blood cell traits identifies novel associated loci and epistatic interactions in Caucasian and African-American children von Li, Jin, Glessner, Joseph T, Zhang, Haitao, Hou, Cuiping, Wei, Zhi, Bradfield, Jonathan P, Mentch, Frank D, Guo, Yiran, Kim, Cecilia, Xia, Qianghua, Chiavacci, Rosetta M, Thomas, Kelly A, Qiu, Haijun, Grant, Struan F A, Furth, Susan L, Hakonarson, Hakon, Sleiman, Patrick M A

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Comparative genetic analysis of inflammatory bowel disease and type 1 diabetes implicates multiple loci with opposite effects von Wang, Kai, Baldassano, Robert, Zhang, Haitao, Qu, Hui-Qi, Imielinski, Marcin, Kugathasan, Subra, Annese, Vito, Dubinsky, Marla, Rotter, Jerome I., Russell, Richard K., Bradfield, Jonathan P., Sleiman, Patrick M.A., Glessner, Joseph T., Walters, Thomas, Hou, Cuiping, Kim, Cecilia, Frackelton, Edward C., Garris, Maria, Doran, James, Romano, Claudio, Catassi, Carlo, Van Limbergen, Johan, Guthery, Stephen L., Denson, Lee, Piccoli, David, Silverberg, Mark S., Stanley, Charles A., Monos, Dimitri, Wilson, David C., Griffiths, Anne, Grant, Struan F.A., Satsangi, Jack, Polychronakos, Constantin, Hakonarson, Hakon

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Diverse Genome-wide Association Studies Associate the IL12/IL23 Pathway with Crohn Disease von Wang, Kai, Zhang, Haitao, Kugathasan, Subra, Annese, Vito, Bradfield, Jonathan P., Russell, Richard K., Sleiman, Patrick M.A., Imielinski, Marcin, Glessner, Joseph, Hou, Cuiping, Wilson, David C., Walters, Thomas, Kim, Cecilia, Frackelton, Edward C., Lionetti, Paolo, Barabino, Arrigo, Van Limbergen, Johan, Guthery, Stephen, Denson, Lee, Piccoli, David, Li, Mingyao, Dubinsky, Marla, Silverberg, Mark, Griffiths, Anne, Grant, Struan F.A., Satsangi, Jack, Baldassano, Robert, Hakonarson, Hakon

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Variants of DENND1B Associated with Asthma in Children von Sleiman, Patrick M.A, Flory, James, Imielinski, Marcin, Bradfield, Jonathan P, Annaiah, Kiran, Willis-Owen, Saffron A.G, Wang, Kai, Rafaels, Nicholas M, Michel, Sven, Bonnelykke, Klaus, Zhang, Haitao, Kim, Cecilia E, Frackelton, Edward C, Glessner, Joseph T, Hou, Cuiping, Otieno, F. George, Santa, Erin, Thomas, Kelly, Smith, Ryan M, Glaberson, Wendy R, Garris, Maria, Chiavacci, Rosetta M, Beaty, Terri H, Ruczinski, Ingo, Orange, Jordan M, Allen, Julian, Spergel, Jonathan M, Grundmeier, Robert, Mathias, Rasika A, Christie, Jason D, von Mutius, Erika, Cookson, William O.C, Kabesch, Michael, Moffatt, Miriam F, Grunstein, Michael M, Barnes, Kathleen C, Devoto, Marcella, Magnusson, Mark, Li, Hongzhe, Grant, Struan F.A, Bisgaard, Hans, Hakonarson, Hakon

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Gene network analysis in a pediatric cohort identifies novel lung function genes von Ong, Bruce A, Li, Jin, McDonough, Joseph M, Wei, Zhi, Kim, Cecilia, Chiavacci, Rosetta, Mentch, Frank, Caboot, Jason B, Spergel, Jonathan, Allen, Julian L, Sleiman, Patrick M A, Hakonarson, Hakon

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Meta-analysis of shared genetic architecture across ten pediatric autoimmune diseases von Li, Yun R, Li, Jin, Zhao, Sihai D, Bradfield, Jonathan P, Mentch, Frank D, Maggadottir, S Melkorka, Hou, Cuiping, Abrams, Debra J, Chang, Diana, Gao, Feng, Guo, Yiran, Wei, Zhi, Connolly, John J, Cardinale, Christopher J, Bakay, Marina, Glessner, Joseph T, Li, Dong, Kao, Charlly, Thomas, Kelly A, Qiu, Haijun, Chiavacci, Rosetta M, Kim, Cecilia E, Wang, Fengxiang, Snyder, James, Richie, Marylyn D, Flatø, Berit, Førre, Øystein, Denson, Lee A, Thompson, Susan D, Becker, Mara L, Guthery, Stephen L, Latiano, Anna, Perez, Elena, Resnick, Elena, Russell, Richard K, Wilson, David C, Silverberg, Mark S, Annese, Vito, Lie, Benedicte A, Punaro, Marilynn, Dubinsky, Marla C, Monos, Dimitri S, Strisciuglio, Caterina, Staiano, Annamaria, Miele, Erasmo, Kugathasan, Subra, Ellis, Justine A, Munro, Jane E, Sullivan, Kathleen E, Wise, Carol A, Chapel, Helen, Cunningham-Rundles, Charlotte, Grant, Struan F A, Orange, Jordan S, Sleiman, Patrick M A, Behrens, Edward M, Griffiths, Anne M, Satsangi, Jack, Finkel, Terri H, Keinan, Alon, Prak, Eline T Luning, Polychronakos, Constantin, Baldassano, Robert N, Li, Hongzhe, Keating, Brendan J, Hakonarson, Hakon

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Efficacy and safety of nerinetide for the treatment of acute ischaemic stroke (ESCAPE-NA1): a multicentre, double-blind, randomised controlled trial von McTaggart, Ryan A, Poppe, Alexandre Y, Swartz, Richard H, Sauvageau, Eric, Ospel, Johanna M, Yu, Amy Y X, Silver, Frank L, Mandzia, Jennifer L, Bharatha, Aditya, McDougall, Cameron G, Sohn, Sung-Il, Almekhlafi, Mohammed, Kashani, Nima, Teleg, Erika, Asuncion, Ria, Wadhwa, Ankur, Wasyliw, Sanchea, Ryckborst, Karla, Newcommon, Nancy, Zimmel, Leslie, Bohn, Shelly, Doram, Craig, Ure, Ashley, Ashforth, Robert, Chow, Michael, Lloret, Mar, Kalashyan, Hayrapet, Jabs, Juline, Pickett, Gwynedd, Wade, Kevin, Weill, Alain, Legault, Catherine, Moore, Angela, Salmon, Kristiana, Khalil, Salma, Selchen, Daniel, Sarma, Dipanka, Bengzon Diestro, Jose Danilo, Sahlas, Demetrios, Deshmukh, Aviraj, Larrazabal, Ramiro, Mattia, Alicia, Taher, Noran, Heran, Manraj, Maclean, Genoveva, Flexman, Alana, Gayton, Yolanda, Boulos, Mark, Khosravani, Houman, Shah, Ruchir, Simpson, Cindy, Kaminsky, Ian, Kupniewski, Sonny, Choe, Hana, Jovin, Tudor, Jankowitz, Brian, Shah, Kavit, Walker, Gregory, Liff, Jeremy, Burgos, Adrian, Cutting, Shawna, Foley, Susan, Fuller, Lindsey, Watkins, Christina, Dellorso, Scott, Schemmel, Derek, Bhatt, Nirav, Bianchi, Nicolas, Al-Bayati, Alhamza, English, Stephen, Bedenk, Ann, Holloway, William, Kaddouh, Firas, Stretz, Hans Christoph, Jasak, Sara, Orgass, Hailey, Umekubo, Mark, Conrad, William, Abbott, Tara, Czerniak, Jennifer, Rai, Vivek, Rha, Joung-Ho, Tsoleridis, Jessica, Laffan, Aoife, Gordon, Patricia, Fearon, Patricia, McFarland, Margaret, Moreira, Tiago, Keselman, Boris, Schlemm, Eckhard, Otto, Dagmar, Haase, Kathrin, Sauer, Angela, Maus, Volker, Müller, Nicole, Potvin, Alphonse, Bermanis, Liat, Cuthbert, Sandra, Kohli, Yatika, Snoke, Kara

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Genetic sharing and heritability of paediatric age of onset autoimmune diseases von Li, Yun R., Zhao, Sihai D., Li, Jin, Bradfield, Jonathan P., Mohebnasab, Maede, Steel, Laura, Kobie, Julie, Abrams, Debra J., Mentch, Frank D., Glessner, Joseph T., Guo, Yiran, Wei, Zhi, Connolly, John J., Cardinale, Christopher J., Bakay, Marina, Li, Dong, Maggadottir, S. Melkorka, Thomas, Kelly A., Qui, Haijun, Chiavacci, Rosetta M., Kim, Cecilia E., Wang, Fengxiang, Snyder, James, Flatø, Berit, Førre, Øystein, Denson, Lee A., Thompson, Susan D., Becker, Mara L., Guthery, Stephen L., Latiano, Anna, Perez, Elena, Resnick, Elena, Strisciuglio, Caterina, Staiano, Annamaria, Miele, Erasmo, Silverberg, Mark S., Lie, Benedicte A., Punaro, Marilynn, Russell, Richard K., Wilson, David C., Dubinsky, Marla C., Monos, Dimitri S., Annese, Vito, Munro, Jane E., Wise, Carol, Chapel, Helen, Cunningham-Rundles, Charlotte, Orange, Jordan S., Behrens, Edward M., Sullivan, Kathleen E., Kugathasan, Subra, Griffiths, Anne M., Satsangi, Jack, Grant, Struan F. A., Sleiman, Patrick M. A., Finkel, Terri H., Polychronakos, Constantin, Baldassano, Robert N., Luning Prak, Eline T., Ellis, Justine A., Li, Hongzhe, Keating, Brendan J., Hakonarson, Hakon

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A Genome-wide Study Reveals Copy Number Variants Exclusive to Childhood Obesity Cases von Glessner, Joseph T., Bradfield, Jonathan P., Wang, Kai, Takahashi, Nagahide, Zhang, Haitao, Sleiman, Patrick M., Mentch, Frank D., Kim, Cecilia E., Hou, Cuiping, Thomas, Kelly A., Garris, Maria L., Deliard, Sandra, Frackelton, Edward C., Otieno, F. George, Zhao, Jianhua, Chiavacci, Rosetta M., Li, Mingyao, Buxbaum, Joseph D., Berkowitz, Robert I., Hakonarson, Hakon, Grant, Struan F.A.

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Tu1787 VEDOLIZUMAB AS A MEDICAL THERAPY FOR SYMPTOMATIC STRICTURING SMALL BOWEL CROHN'S DISEASE - RESULTS FROM AN INTERNATIONAL MULTICENTER COHORT STUDY von Ouali, Sara El, Baker, Mark E., Lu, Cathy, Medellin, Alexandra, Bruining, David H., Fletcher, Joel G., Ottichilo, Ronald K., Schoenoff, Shayla, Bena, James, Qazi, Taha, Sleiman, Joseph, Holubar, Stefan D., Gandhi, Namita S., Cohen, Benjamin L., Goren, Idan, Balci, Numan, Rieder, Florian

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Tu1256 USTEKINUMAB FOR THE TREATMENT OF SYMPTOMATIC SMALL BOWEL STRICTURING CROHN'S DISEASE - RESULTS FROM AN INTERNATIONAL MULTICENTER COHORT STUDY von Ouali, Sara El, Baker, Mark E., Lu, Cathy, Medellin, Alexandra, Bruining, David H., Fletcher, Joel G., Ottichilo, Ronald K., Schoenoff, Shayla, Bena, James, Qazi, Taha, Sleiman, Joseph, Holubar, Stefan D., Gandhi, Namita S., Cohen, Benjamin L., Goren, Idan, Balci, Numan, Rieder, Florian

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Diagnosis of Inflammatory Bowel Disease-Associated Peripheral Arthritis: A Systematic Review von Falloon, Katherine, Dossaji, Zahra, Mude, Pooja, Abushamma, Suha, Ananthakrishnan, Ashwin, Barnes, Edward L, Bhalla, Jaideep, Bhattacharya, Abhik, Cheemalavagu, Shashank, Colombel, Jean-Fred, Cross, Raymond K, Ermann, Joerg, Ha, Christina, Herfarth, Hans, Horst, Sara, Hou, Jason, Husni, M Elaine, Kline, Theresa M, Kuhn, Kristine A, Long, Millie D, Loftus, Jr, Edward V, Lukin, Dana J, Patel, Aditi, Rubin, David T, Scherl, Ellen J, Shah, Samir A, Siaton, Bernadette C, Sleiman, Joseph, Qazi, Taha, Weisman, Michael H, Cohen, Benjamin L, Feagan, Brian G, Rieder, Florian

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