Treffer 1 - 20 von 614 für Suche 'Damotte, S.', Suchdauer: 1,38s Treffer weiter einschränken
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    Low-Frequency and Rare-Coding Variation Contributes to Multiple Sclerosis Risk von Patsopoulos, Nikolaos A., Beecham, Ashley H., Goris, An, Dubois, Bénédicte, D’hooghe, Marie B., Van Damme, Philip, Søndergaard, Helle Bach, Sellebjerg, Finn, Ullum, Henrik, Thørner, Lise W., Werge, Thomas, Damotte, Vincent, Fontaine, Bertrand, Lathrop, Mark, Gourraud, Pierre-Antoine, Pongratz, Viola, Gasperi, Christiane, Bayas, Antonios, Heesen, Christoph, Linker, Ralf, Paul, Friedemann, Stangel, Martin, Tackenberg, Björn, Bergh, Florian Then, Wildemann, Brigitte, Tumani, Hayrettin, Gold, Ralf, Grummel, Verena, Knier, Benjamin, Lill, Christina M., Dardiotis, Efthimios, Agliardi, Cristina, Barizzone, Nadia, Mascia, Elisabetta, Bernardinelli, Luisa, Cusi, Daniele, Ferrè, Laura, Comi, Cristoforo, Galimberti, Daniela, Leone, Maurizio A., Mescheriakova, Julia, Hintzen, Rogier, van Duijn, Cornelia, Teunissen, Charlotte E., Bos, Steffan D., Myhr, Kjell-Morten, Celius, Elisabeth G., Lie, Benedicte A., Comabella, Manuel, Montalban, Xavier, Alfredsson, Lars, Stridh, Pernilla, Hillert, Jan, Piehl, Fredrik, Jelčić, Ilijas, Martin, Roland, Sospedra, Mireia, Hawkins, Clive, Hysi, Pirro, Karpe, Fredrik, Khadake, Jyoti, Lachance, Genevieve, Neville, Matthew, Santaniello, Adam, Caillier, Stacy J., Calabresi, Peter A., Cross, Anne, Davis, Mary F., de Bakker, Paul I.W., Delgado, Silvia, Dembele, Marieme, Edwards, Keith, Fitzgerald, Kathryn C., Hakonarson, Hakon, Konidari, Ioanna, Lathi, Ellen, Manrique, Clara P., Pericak-Vance, Margaret A., Piccio, Laura, Schaefer, Cathy, McCabe, Cristin, Hadjigeorgiou, Georgios, Taylor, Bruce, Tajouri, Lotti, Charlesworth, Jac, Booth, David R., Harbo, Hanne F., Ivinson, Adrian J., Hauser, Stephen L., Compston, Alastair, Stewart, Graeme, Zipp, Frauke, Barcellos, Lisa F., Baranzini, Sergio E., Martinelli-Boneschi, Filippo, Ziegler, Andreas, McCauley, Jacob L., Sawcer, Stephen J., De Jager, Philip L., Kockum, Ingrid

    Veröffentlicht in Cell

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    Network-Based Multiple Sclerosis Pathway Analysis with GWAS Data from 15,000 Cases and 30,000 Controls von Baranzini, Sergio E., Khankhanian, Pouya, Patsopoulos, Nikolaos A., Li, Michael, Stankovich, Jim, Cotsapas, Chris, Søndergaard, Helle Bach, Ban, Maria, Barizzone, Nadia, Bergamaschi, Laura, Booth, David, Buck, Dorothea, Cavalla, Paola, Celius, Elisabeth G., Comabella, Manuel, Comi, Giancarlo, Compston, Alastair, Cournu-Rebeix, Isabelle, D’alfonso, Sandra, Damotte, Vincent, Din, Lennox, Dubois, Bénédicte, Elovaara, Irina, Esposito, Federica, Fontaine, Bertrand, Franke, Andre, Goris, An, Gourraud, Pierre-Antoine, Graetz, Christiane, Guerini, Franca R., Guillot-Noel, Léna, Hafler, David, Hakonarson, Hakon, Hall, Per, Hamsten, Anders, Harbo, Hanne F., Hemmer, Bernhard, Hillert, Jan, Kemppinen, Anu, Kockum, Ingrid, Koivisto, Keijo, Larsson, Malin, Lathrop, Mark, Leone, Maurizio, Lill, Christina M., Macciardi, Fabio, Martin, Roland, Martinelli, Vittorio, Martinelli-Boneschi, Filippo, McCauley, Jacob L., Myhr, Kjell-Morten, Naldi, Paola, Olsson, Tomas, Oturai, Annette, Pericak-Vance, Margaret A., Perla, Franco, Reunanen, Mauri, Saarela, Janna, Saker-Delye, Safa, Salvetti, Marco, Sellebjerg, Finn, Sørensen, Per Soelberg, Spurkland, Anne, Stewart, Graeme, Taylor, Bruce, Tienari, Pentti, Winkelmann, Juliane, Zipp, Frauke, Ivinson, Adrian J., Haines, Jonathan L., Sawcer, Stephen, DeJager, Philip, Hauser, Stephen L., Oksenberg, Jorge R.


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    A genome‐wide association meta‐analysis of all‐cause and vascular dementia von Damotte, Vincent, Skrobot, Olivia, Bis, Joshua C., Li, Gloria Hoi‐Yee, Yang, Jingyun, Alessandra, Bizzarro, Chai, Yuek Ling, Knol, M. J., Concas, Maria Pina, Giorgia, Girotto, Riaz, Moeen, Naj, Adam C, Gireud‐Goss, Monica, Wadop, Yannick N., Gudnason, Vilmundur, Battista, Petronilla, Santin, Aurora, Sardone, Rodolfo, Launer, Lenore, Bressler, Jan, Grand, Quentin Le, Caro, Ilana, Roshchupkin, Gennady V., Yang, Chaojie, Bartz, Traci M., Nalls, Mike A., Rich, Stephen S., Setten, Jessica, Vugt, Marion, Grabe, Hans J., Jukema, J Wouter, Wassertheil‐Smoller, Sylvia, Longstreth, W T., Sattar, Naveed, Romero, Jose R, Lioutas, Vasileios, Wang, Ruiqi, Marquié, Marta, Pytel, Vanesa Veronica, Tàrraga, Lluís, Garcia‐Ribas, Guillermo, Pérez‐Tur, Jordi, Real, Luis Miguel, Sáez, María Eugenia, Bullido, María J., Álvarez, Victoria, Küçükali, Fahri, Düzel, Emrah, Wagner, Michael, Grimmer, Timo, Moreno, Fermin, Real, Luis M, Mendonça, Alexandre, Hort, Jakub, Papenberg, Goran, Nordestgaard, Børge G., Kivipelto, Miia, Haapasalo, Annakaisa, Nicolas, Gael, Grünblatt, Edna, Galimberti, Daniela, Mecocci, Patrizia, Tremolizzo, Lucio, Seripa, Davide, Engelborghs, Sebastiaan, Vandenberghe, Rik, Ingelsson, Martin, Lai, Mitchell K. P., Tan, Boon‐Yeow, Cefalù, Angelo Baldassare, Armstrong, Nicola J, Bordet, Anne‐Marie, Brodaty, Henry, D'Onofrio, Grazia, Esiri, Margaret, Gelé, Patrick, Masullo, Carlo, Mather, Karen A, Monastero, Roberto, Panza, Francesco, Sachdev, Perminder S, Thalamuthu, Anbupalam, Tybjærg‐Hansen, Anne, Thomas, Laurent F, Pedersen, Linda M, Bosnes, Ingunn, Duijn, Cornelia, Chen, Christopher, Kamboh, M. Ilyas, Satizabal, Claudia, Adams, Hieab, Hveem, Kristian, Dufouil, Carole, Zwart, John‐Anker, Fornage, Myriam, Winsvold, Bendik, Ruiz, Agustin, Kehoe, Patrick G., Weinstein, Galit, Seshadri, Sudha

    Veröffentlicht in Alzheimer's & dementia

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    Low-Frequency and Rare-Coding Variation Contributes to Multiple Sclerosis Risk von Patsopoulos, Nikolaos A., Beecham, Ashley H., Goris, An, Dubois, Bénédicte, D’hooghe, Marie B., Van Damme, Philip, Søndergaard, Helle Bach, Sellebjerg, Finn, Ullum, Henrik, Thørner, Lise W., Werge, Thomas, Damotte, Vincent, Fontaine, Bertrand, Lathrop, Mark, Gourraud, Pierre-Antoine, Pongratz, Viola, Gasperi, Christiane, Bayas, Antonios, Heesen, Christoph, Linker, Ralf, Paul, Friedemann, Stangel, Martin, Tackenberg, Björn, Bergh, Florian Then, Wildemann, Brigitte, Tumani, Hayrettin, Gold, Ralf, Grummel, Verena, Knier, Benjamin, Lill, Christina M., Dardiotis, Efthimios, Agliardi, Cristina, Barizzone, Nadia, Mascia, Elisabetta, Bernardinelli, Luisa, Cusi, Daniele, Ferrè, Laura, Comi, Cristoforo, Galimberti, Daniela, Leone, Maurizio A., Mescheriakova, Julia, Hintzen, Rogier, van Duijn, Cornelia, Teunissen, Charlotte E., Bos, Steffan D., Myhr, Kjell-Morten, Celius, Elisabeth G., Lie, Benedicte A., Comabella, Manuel, Montalban, Xavier, Alfredsson, Lars, Stridh, Pernilla, Hillert, Jan, Piehl, Fredrik, Jelčić, Ilijas, Martin, Roland, Sospedra, Mireia, Hawkins, Clive, Hysi, Pirro, Karpe, Fredrik, Khadake, Jyoti, Lachance, Genevieve, Neville, Matthew, Santaniello, Adam, Caillier, Stacy J., Calabresi, Peter A., Cross, Anne, Davis, Mary F., de Bakker, Paul I.W., Delgado, Silvia, Dembele, Marieme, Edwards, Keith, Fitzgerald, Kathryn C., Hakonarson, Hakon, Konidari, Ioanna, Lathi, Ellen, Manrique, Clara P., Pericak-Vance, Margaret A., Piccio, Laura, Schaefer, Cathy, McCabe, Cristin, Hadjigeorgiou, Georgios, Taylor, Bruce, Tajouri, Lotti, Charlesworth, Jac, Booth, David R., Harbo, Hanne F., Ivinson, Adrian J., Hauser, Stephen L., Compston, Alastair, Stewart, Graeme, Zipp, Frauke, Barcellos, Lisa F., Baranzini, Sergio E., Martinelli-Boneschi, Filippo, Ziegler, Andreas, McCauley, Jacob L., Sawcer, Stephen J., De Jager, Philip L., Kockum, Ingrid

    Veröffentlicht in Cell

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    Low-Frequency and Rare-Coding Variation Contributes to Multiple Sclerosis Risk von Patsopoulos, Nikolaos A., Beecham, Ashley H., Goris, An, Dubois, Bénédicte, D’hooghe, Marie B., Van Damme, Philip, Søndergaard, Helle Bach, Sellebjerg, Finn, Ullum, Henrik, Thørner, Lise W., Werge, Thomas, Damotte, Vincent, Fontaine, Bertrand, Lathrop, Mark, Gourraud, Pierre-Antoine, Pongratz, Viola, Gasperi, Christiane, Bayas, Antonios, Heesen, Christoph, Linker, Ralf, Paul, Friedemann, Stangel, Martin, Tackenberg, Björn, Bergh, Florian Then, Wildemann, Brigitte, Tumani, Hayrettin, Gold, Ralf, Grummel, Verena, Knier, Benjamin, Lill, Christina M., Dardiotis, Efthimios, Agliardi, Cristina, Barizzone, Nadia, Mascia, Elisabetta, Bernardinelli, Luisa, Cusi, Daniele, Ferrè, Laura, Comi, Cristoforo, Galimberti, Daniela, Leone, Maurizio A., Mescheriakova, Julia, Hintzen, Rogier, van Duijn, Cornelia, Teunissen, Charlotte E., Bos, Steffan D., Myhr, Kjell-Morten, Celius, Elisabeth G., Lie, Benedicte A., Comabella, Manuel, Montalban, Xavier, Alfredsson, Lars, Stridh, Pernilla, Hillert, Jan, Piehl, Fredrik, Jelčić, Ilijas, Martin, Roland, Sospedra, Mireia, Hawkins, Clive, Hysi, Pirro, Karpe, Fredrik, Khadake, Jyoti, Lachance, Genevieve, Neville, Matthew, Santaniello, Adam, Caillier, Stacy J., Calabresi, Peter A., Cross, Anne, Davis, Mary F., de Bakker, Paul I.W., Delgado, Silvia, Dembele, Marieme, Edwards, Keith, Fitzgerald, Kathryn C., Hakonarson, Hakon, Konidari, Ioanna, Lathi, Ellen, Manrique, Clara P., Pericak-Vance, Margaret A., Piccio, Laura, Schaefer, Cathy, McCabe, Cristin, Hadjigeorgiou, Georgios, Taylor, Bruce, Tajouri, Lotti, Charlesworth, Jac, Booth, David R., Harbo, Hanne F., Ivinson, Adrian J., Hauser, Stephen L., Compston, Alastair, Stewart, Graeme, Zipp, Frauke, Barcellos, Lisa F., Baranzini, Sergio E., Martinelli-Boneschi, Filippo, Ziegler, Andreas, McCauley, Jacob L., Sawcer, Stephen J., De Jager, Philip L., Kockum, Ingrid

    Veröffentlicht in CELL

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