Treffer 1 - 20 von 77 für Suche 'Amos, Karen E.', Suchdauer: 1,63s Treffer weiter einschränken
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    Ultra-Rare Genetic Variation in the Epilepsies: A Whole-Exome Sequencing Study of 17,606 Individuals von Howrigan, Daniel P., Abbott, Liam E., Tashman, Katherine, Singh, Tarjinder, Watts, Nick, Lal, Dennis, Hakonarson, Hakon, Weckhuysen, Sarah, Petrovski, Slavé, Cossette, Patrick, Cotsapas, Chris, De Jonghe, Peter, Guerrini, Renzo, Marson, Anthony G., Depondt, Chantal, Striano, Pasquale, Freyer, Catharine, Regan, Brigid M., Leu, Costin, Johns, Esther M.C., Macdonald, Alexandra, Bahlo, Melanie, Todaro, Marian, Stamberger, Hannah, Sadoway, Tara R., Kousiappa, Ioanna, Tanteles, George A., Štěrbová, Katalin, Kunz, Wolfram S., Zsurka, Gábor, Elger, Christian E., Rademacher, Michael, van Baalen, Andreas, von Spiczak, Sarah, Afawi, Zaid, Canavati, Christina, Kluger, Gerhard, Blatt, Ilan, Weber, Yvonne G., Wolking, Stefan, Rau, Sarah, Steinhoff, Bernhard J., Schulze-Bonhage, Andreas, Borggräfe, Ingo, Madeleyn, Rene, Kälviäinen, Reetta, Linnankivi, Tarja, Chung, Seo-Kyung, Balestrini, Simona, Braatz, Vera, Johnson, Michael R., Auce, Pauls, Sham, Pak C., Lui, Colin H.T., Doherty, Colin P., Shukralla, Arif, El-Naggar, Hany, Vari, Maria Stella, Salpietro, Vincenzo, Tinuper, Paolo, Gagliardi, Monica, Montomoli, Martino, Doccini, Viola, Inoue, Yushi, Yamakawa, Kazuhiro, Tumiene, Birute, Sadleir, Lynette G., Caglayan, S. Hande, Arslan, Mutluay, Yis, Uluc, Topaloglu, Pınar, Baykan, Betül, Salman, Barış, Haryanyan, Garen, Özkara, Çiğdem, Poduri, Annapurna, Shiedley, Beth R., Shain, Catherine, French, Jacqueline A., Kuzniecky, Ruben I., Hegde, Manu, Helbig, Katherine L., Piras, Federica, Reif, Andreas, McQuillin, Andrew, Johnstone, Mandy, Palotie, Aarno, Carvalho, Celia Barreto, Achtyes, Eric D., Azevedo, Maria Helena, Kotov, Roman, Lehrer, Douglas S., Marder, Stephen R., Medeiros, Helena, Morley, Christopher P., Rapaport, Mark H., Knowles, James A., McCarroll, Steven A., Lowenstein, Daniel H., Goldstein, David B.


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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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    Healthcare Access and Quality Index based on mortality from causes amenable to personal health care in 195 countries and territories, 1990–2015: a novel analysis from the Global Bu... von Abbas, Kaja M, Abdulle, Abdishakur M, Adane, Kelemework, Kiadaliri, Aliasghar Ahmad, Ahmed, Muktar Beshir, Ali, Raghib, Allen, Christine, Al-Raddadi, Rajaa, Amini, Erfan, Amoako, Yaw Ampem, Anderson, Benjamin O, Atre, Sachin R, Banerjee, Amitava, Bayou, Yibeltal Tebekaw, Beyene, Tariku Jibat, Biadgilign, Sibhatu, Bikbov, Boris, Birungi, Charles, Biryukov, Stan, Brauer, Michael, Campos-Nonato, Ismael Ricardo, Chew, Adrienne, Christensen, Hanne, Deribe, Kebede, Ellingsen, Christian Lycke, Ermakov, Sergey Petrovich, Feigl, Andrea B, Fereshtehnejad, Seyed-Mohammad, Fernandes, Jefferson G, Fitzmaurice, Christina, Frostad, Joseph, Geleijnse, Johanna M, Goldberg, Ellen M, Gopalani, Sameer Vali, Greaves, Felix, Havmoeller, Rasmus, Htet, Aung Soe, Iburg, Kim Moesgaard, James, Spencer Lewis, Jayaraman, Sudha P, Juel, Knud, Kamal, Ritul, Kassebaum, Nicholas J, Kastor, Anshul, Kengne, Andre Pascal, Kim, Yun Jin, Kissoon, Niranjan, Kopec, Jacek A, Krohn, Kristopher J, Langan, Sinead M, Larson, Heidi J, Liu, Yang, Logroscino, Giancarlo, Maulik, Pallab K, McAlinden, Colm, Meles, Kidanu Gebremariam, Mirrakhimov, Erkin M, Mock, Charles N, Monasta, Lorenzo, Neupane, Sudan Prasad, Ngunjiri, Josephine Wanjiku, Nolte, Sandra, Opio, John Nelson, PA, Mahesh, Paul, Vinod K, Pearce, Neil, Perez-Padilla, Rogelio, Qorbani, Mostafa, Ram, Usha, Reitsma, Marissa, Renzaho, Andre M N N, Roba, Hirbo Shore, Roth, Gregory A, Safiri, Saeid, Salomon, Joshua A, Satpathy, Maheswar, Seid, Abdulbasit Musa, Seifu, Canaan Negash, Sharma, Rajesh, Shen, Jiabin, Shoman, Haitham, Sigfusdottir, Inga Dora, Silveira, Dayane Gabriele Alves, Steel, Nicholas, Steiner, Caitlyn, Stranges, Saverio, Suliankatchi, Rizwan Abdulkader, Talongwa, Roberto Tchio, Tekelab, Tesfalidet, Uchendu, Uche S, Uthman, Olalekan A, Wang, Yuan-Pang, Weiderpass, Elisabete, Weintraub, Robert G, Werdecker, Andrea, Won, Sungho, Yaghoubi, Mohsen, Yaseri, Mehdi, Yoon, Seok-Jun, Zuhlke, Liesl Joanna

    Veröffentlicht in The Lancet (British edition)

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