Treffer 1 - 20 von 40 für Suche 'Bradfield, Jonathan Paul', Suchdauer: 1,92s Treffer weiter einschränken
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    Genome-wide mega-analysis identifies 16 loci and highlights diverse biological mechanisms in the common epilepsies von Abou-Khalil, Bassel, Auce, Pauls, Avbersek, Andreja, Bahlo, Melanie, Balding, David J., Bast, Thomas, Baum, Larry, Becker, Albert J., Becker, Felicitas, Berghuis, Bianca, Berkovic, Samuel F., Boysen, Katja E., Bradfield, Jonathan P., Brody, Lawrence C., Buono, Russell J., Campbell, Ellen, Cascino, Gregory D., Catarino, Claudia B., Cavalleri, Gianpiero L., Cherny, Stacey S., Chinthapalli, Krishna, Coffey, Alison J., Compston, Alastair, Coppola, Antonietta, Cossette, Patrick, Craig, John J., de Haan, Gerrit-Jan, De Jonghe, Peter, de Kovel, Carolien G. F., Delanty, Norman, Depondt, Chantal, Devinsky, Orrin, Dlugos, Dennis J., Doherty, Colin P., Elger, Christian E., Eriksson, Johan G., Ferraro, Thomas N., Feucht, Martha, Francis, Ben, Franke, Andre, French, Jacqueline A., Freytag, Saskia, Gaus, Verena, Geller, Eric B., Gieger, Christian, Glauser, Tracy, Glynn, Simon, Goldstein, David B., Gui, Hongsheng, Guo, Youling, Haas, Kevin F., Hakonarson, Hakon, Hallmann, Kerstin, Haut, Sheryl, Heinzen, Erin L., Helbig, Ingo, Hengsbach, Christian, Hjalgrim, Helle, Iacomino, Michele, Ingason, Andrés, Jamnadas-Khoda, Jennifer, Johnson, Michael R., Kälviäinen, Reetta, Kantanen, Anne-Mari, Kasperavičiūte, Dalia, Kasteleijn-Nolst Trenite, Dorothee, Kirsch, Heidi E., Knowlton, Robert C., Koeleman, Bobby P. C., Krause, Roland, Krenn, Martin, Kunz, Wolfram S., Kuzniecky, Ruben, Kwan, Patrick, Lal, Dennis, Lau, Yu-Lung, Lehesjoki, Anna-Elina, Lerche, Holger, Leu, Costin, Lieb, Wolfgang, Lindhout, Dick, Lo, Warren D., Lopes-Cendes, Iscia, Lowenstein, Daniel H., Malovini, Alberto, Marson, Anthony G., Mayer, Thomas, McCormack, Mark, Mills, James L., Mirza, Nasir, Moerzinger, Martina, Møller, Rikke S., Molloy, Anne M., Muhle, Hiltrud, Newton, Mark, Ng, Ping-Wing, Nöthen, Markus M., Nürnberg, Peter, O’Brien, Terence J., Oliver, Karen L.

    Veröffentlicht in Nature communications

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    GWAS meta-analysis of over 29,000 people with epilepsy identifies 26 risk loci and subtype-specific genetic architecture von Stevelink, Remi, Campbell, Ciarán, Chen, Siwei, Abou-Khalil, Bassel, Adesoji, Oluyomi M., Afawi, Zaid, Amadori, Elisabetta, Anderson, Alison, Anderson, Joseph, Andrade, Danielle M., Annesi, Grazia, Auce, Pauls, Avbersek, Andreja, Bahlo, Melanie, Baker, Mark D., Balagura, Ganna, Balestrini, Simona, Barba, Carmen, Barboza, Karen, Bartolomei, Fabrice, Bast, Thomas, Baum, Larry, Baumgartner, Tobias, Baykan, Betül, Bebek, Nerses, Becker, Albert J., Becker, Felicitas, Bennett, Caitlin A., Berghuis, Bianca, Berkovic, Samuel F., Beydoun, Ahmad, Bianchini, Claudia, Bisulli, Francesca, Blatt, Ilan, Bobbili, Dheeraj R., Borggraefe, Ingo, Bosselmann, Christian, Braatz, Vera, Bradfield, Jonathan P., Brockmann, Knut, Brody, Lawrence C., Buono, Russell J., Busch, Robyn M., Caglayan, Hande, Campbell, Ellen, Canafoglia, Laura, Canavati, Christina, Cascino, Gregory D., Castellotti, Barbara, Catarino, Claudia B., Cavalleri, Gianpiero L., Cerrato, Felecia, Chassoux, Francine, Cherny, Stacey S., Cheung, Ching-Lung, Chinthapalli, Krishna, Chou, I-Jun, Chung, Seo-Kyung, Churchhouse, Claire, Clark, Peggy O., Cole, Andrew J., Compston, Alastair, Coppola, Antonietta, Cosico, Mahgenn, Cossette, Patrick, Craig, John J., Cusick, Caroline, Daly, Mark J., Davis, Lea K., de Haan, Gerrit-Jan, Delanty, Norman, Depondt, Chantal, Derambure, Philippe, Devinsky, Orrin, Di Vito, Lidia, Dlugos, Dennis J., Doccini, Viola, Doherty, Colin P., El-Naggar, Hany, Elger, Christian E., Ellis, Colin A., Eriksson, Johan G., Faucon, Annika, Feng, Yen-Chen A., Ferguson, Lisa, Ferraro, Thomas N., Ferri, Lorenzo, Feucht, Martha, Fitzgerald, Mark, Fonferko-Shadrach, Beata, Fortunato, Francesco, Franceschetti, Silvana, Franke, Andre, French, Jacqueline A., Freri, Elena, Gagliardi, Monica, Gambardella, Antonio, Geller, Eric B., Giangregorio, Tania, Gjerstad, Leif

    Veröffentlicht in Nature genetics

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    Variants in ADCY5 and near CCNL1 are associated with fetal growth and birth weight von Boomsma, Dorret I, Smith, George Davey, Power, Chris, Jaddoe, Vincent W V, Jarvelin, Marjo-Riitta, Freathy, Rachel M, Mook-Kanamori, Dennis O, Sovio, Ulla, Prokopenko, Inga, Timpson, Nicholas J, Berry, Diane J, Warrington, Nicole M, Widen, Elisabeth, Hottenga, Jouke Jan, Kaakinen, Marika, Lange, Leslie A, Bradfield, Jonathan P, Kerkhof, Marjan, Marsh, Julie A, Mägi, Reedik, Chen, Chih-Mei, Lyon, Helen N, Kirin, Mirna, Adair, Linda S, Aulchenko, Yurii S, Bennett, Amanda J, Borja, Judith B, Bouatia-Naji, Nabila, Charoen, Pimphen, Coin, Lachlan J M, Cousminer, Diana L, de Geus, Eco J C, Deloukas, Panos, Elliott, Paul, Evans, David M, Froguel, Philippe, Glaser, Beate, Groves, Christopher J, Hartikainen, Anna-Liisa, Hassanali, Neelam, Hirschhorn, Joel N, Hofman, Albert, Holly, Jeff M P, Hyppönen, Elina, Kanoni, Stavroula, Knight, Bridget A, Laitinen, Jaana, Lindgren, Cecilia M, McArdle, Wendy L, O'Reilly, Paul F, Pennell, Craig E, Postma, Dirkje S, Pouta, Anneli, Ramasamy, Adaikalavan, Rayner, Nigel W, Ring, Susan M, Rivadeneira, Fernando, Shields, Beverley M, Strachan, David P, Surakka, Ida, Taanila, Anja, Tiesler, Carla, Uitterlinden, Andre G, van Duijn, Cornelia M, Wijga, Alet H, Willemsen, Gonneke, Zhang, Haitao, Zhao, Jianhua, Wilson, James F, Steegers, Eric A P, Hattersley, Andrew T, Eriksson, Johan G, Peltonen, Leena, Mohlke, Karen L, Grant, Struan F A, Hakonarson, Hakon, Koppelman, Gerard H, Dedoussis, George V, Heinrich, Joachim, Gillman, Matthew W, Palmer, Lyle J, Frayling, Timothy M

    Veröffentlicht in Nature genetics

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    Genetic Studies of Leptin Concentrations Implicate Leptin in the Regulation of Early Adiposity von Yaghootkar, Hanieh, Zhang, Yiying, Spracklen, Cassandra N., Karaderi, Tugce, Huang, Lam Opal, Bradfield, Jonathan, Schurmann, Claudia, Fine, Rebecca S., Preuss, Michael H., Kutalik, Zoltan, Wittemans, Laura B. L., Lu, Yingchang, Metz, Sophia, Willems, Sara M., Li-Gao, Ruifang, Grarup, Niels, Wang, Shuai, Molnos, Sophie, Sandoval-Zarate, America A., Nalls, Mike A., Lange, Leslie A., Haesser, Jeffrey, Guo, Xiuqing, Lyytikainen, Leo-Pekka, Feitosa, Mary F., Sitlani, Colleen M., Venturini, Cristina, Mahajan, Anubha, Kacprowski, Tim, Wang, Carol A., Chasman, Daniel I., Amin, Najaf, Broer, Linda, Robertson, Neil, Young, Kristin L., Allison, Matthew, Auer, Paul L., Bluher, Matthias, Borja, Judith B., Bork-Jensen, Jette, Carrasquilla, German D., Christofidou, Paraskevi, Demirkan, Ayse, Doege, Claudia A., Garcia, Melissa E., Graff, Mariaelisa, Guo, Kaiying, Hakonarson, Hakon, Hong, Jaeyoung, Ida Chen, Yii-Der, Jackson, Rebecca, Jakupovic, Hermina, Jousilahti, Pekka, Justice, Anne E., Kahonen, Mika, Kizer, Jorge R., Kriebel, Jennifer, LeDuc, Charles A., Li, Jin, Lind, Lars, Luan, Jian'an, Mackey, David A., Mangino, Massimo, Mannisto, Satu, Martin Carli, Jayne F., Medina-Gomez, Carolina, Mook-Kanamori, Dennis O., Morris, Andrew P., de Mutsert, Renee, Nauck, Matthias, Prokic, Ivana, Pennell, Craig E., Pradhan, Arund D., Psaty, Bruce M., Raitakari, Olli T., Scott, Robert A., Skaaby, Tea, Strauch, Konstantin, Taylor, Kent D., Teumer, Alexander, Uitterlinden, Andre G., Wu, Ying, Yao, Jie, Walker, Mark, North, Kari E., Kovacs, Peter, Ikram, M. Arfan, van Duijn, Cornelia M., Ridker, Paul M., Lye, Stephen, Homuth, Georg, Ingelsson, Erik, Spector, Tim D., McKnight, Barbara, Province, Michael A., Lehtimaki, Terho, Adair, Linda S., Rotter, Jerome I., Reiner, Alexander P., Wilson, James G.

    Veröffentlicht in Diabetes (New York, N.Y.)

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    Common variants at 12q15 and 12q24 are associated with infant head circumference von Taal, H Rob, St Pourcain, Beate, Thiering, Elisabeth, Das, Shikta, Mook-Kanamori, Dennis O, Warrington, Nicole M, Kaakinen, Marika, Kreiner-Møller, Eskil, Bradfield, Jonathan P, Freathy, Rachel M, Geller, Frank, Guxens, Mònica, Cousminer, Diana L, Kerkhof, Marjan, Timpson, Nicholas J, Ikram, M Arfan, Beilin, Lawrence J, Bønnelykke, Klaus, Buxton, Jessica L, Charoen, Pimphen, Chawes, Bo Lund Krogsgaard, Eriksson, Johan, Evans, David M, Hofman, Albert, Kemp, John P, Kim, Cecilia E, Klopp, Norman, Lahti, Jari, Lye, Stephen J, McMahon, George, Mentch, Frank D, Müller-Nurasyid, Martina, O'Reilly, Paul F, Prokopenko, Inga, Rivadeneira, Fernando, Steegers, Eric A P, Sunyer, Jordi, Tiesler, Carla, Yaghootkar, Hanieh, Breteler, Monique M B, Debette, Stéphanie, Fornage, Myriam, Gudnason, Vilmundur, Launer, Lenore J, van der Lugt, Aad, Mosley, Thomas H, Seshadri, Sudha, Smith, Albert V, Vernooij, Meike W, Blakemore, Alexandra I F, Chiavacci, Rosetta M, Feenstra, Bjarke, Fernandez-Banet, Julio, Grant, Struan F A, Hartikainen, Anna-Liisa, van der Heijden, Albert J, Iñiguez, Carmen, Lathrop, Mark, McArdle, Wendy L, Mølgaard, Anne, Newnham, John P, Palmer, Lyle J, Palotie, Aarno, Pouta, Annneli, Ring, Susan M, Sovio, Ulla, Standl, Marie, Uitterlinden, Andre G, Wichmann, H-Erich, Vissing, Nadja Hawwa, DeCarli, Charles, van Duijn, Cornelia M, McCarthy, Mark I, Koppelman, Gerard H, Estivill, Xavier, Hattersley, Andrew T, Melbye, Mads, Bisgaard, Hans, Pennell, Craig E, Widen, Elisabeth, Hakonarson, Hakon, Smith, George Davey, Heinrich, Joachim, Jarvelin, Marjo-Riitta, Jaddoe, Vincent W V

    Veröffentlicht in Nature genetics

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    Shared genetic basis between genetic generalized epilepsy and background electroencephalographic oscillations von Smith, Alexander W., Carpay, Johannes A., Devinsky, Orrin, Braun, Kees P. J., Smit, Dirk J. A., Avbersek, Andreja, Becker, Albert J., Berkovic, Samuel F., Boysen, Katja E., Campbell, Ellen, Cascino, Gregory D., Catarino, Claudia B., Chinthapalli, Krishna, Coffey, Alison J., Coppola, Antonietta, Cossette, Patrick, De Jonghe, Peter, Dlugos, Dennis J., Feucht, Martha, Freytag, Saskia, Geller, Eric B., Guo, Youling, Hakonarson, Hakon, Haut, Sheryl, Heinzen, Erin L., Hengsbach, Christian, Johnson, Michael R., Kälviäinen, Reetta, Kirsch, Heidi E., Lau, Yu‐Lung, Lehesjoki, Anna‐Elina, Lerche, Holger, Lieb, Wolfgang, Malovini, Alberto, McCormack, Mark, Molloy, Anne M., Rau, Sarah, Schachter, Steven C., Vari, Maria S., Weber, Yvonne G., Weisenberg, Judith, Wolff, Markus, Yang, Wanling, Zara, Federico, Howrigan, Daniel P., Cerrato, Felecia, Gabriel, Stacey B., Daly, Mark J., Neale, Benjamin M., Lowenstein, Daniel H., Cossette, Patrick, Cotsapas, Chris, Petrovski, Slavé, Sisodiya, Sanjay M., Freyer, Catharine, McKenna, Kevin, Bennett, Caitlin A., Burgess, Rosemary, O'Brien, Terence J., Stamberger, Hannah, Krestel, Heinz, Gallati, Sabina, Papacostas, Savvas S., Tanteles, George A., Klein, Karl Martin, Rademacher, Michael, Afawi, Zaid, Korczyn, Amos D., Kanaan, Moien, Lemke, Johannes R., Wolking, Stefan, Schulze‐Bonhage, Andreas, Schubert‐Bast, Susanne, Korinthenberg, Rudolf, Dennig, Dieter, Madeleyn, Rene, Kälviäinen, Reetta, Linnankivi, Tarja, Rees, Mark I., Schneider, Natascha, Sills, Graeme J., Shukralla, Arif, McCormack, Mark, Canafoglia, Laura, Franceschetti, Silvana, Iacomino, Michele, Stella Vari, Maria, Salpietro, Vincenzo, Labate, Angelo, Manna, Lorella, Parrini, Elena, Inoue, Yushi, Topaloglu, Pınar, Yücesan, Emrah, Poduri, Annapurna, Buono, Russell J., Sperling, Michael R., Lo, Warren, Hegde, Manu, Helbig, Katherine L.

    Veröffentlicht in Epilepsia (Copenhagen)

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