Treffer 1 - 20 von 16.206 für Suche 'Martin, Roland A', Suchdauer: 1,79s Treffer weiter einschränken
  1. 1
  2. 2
  3. 3

    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

    Volltext
    Artikel
  4. 4
  5. 5
  6. 6
  7. 7

    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.


    Volltext
    Artikel
  8. 8
  9. 9
  10. 10
  11. 11

    NR1H3 p.Arg415Gln Is Not Associated to Multiple Sclerosis Risk von Antel, Jack, Ban, Maria, Baranzini, Sergio, Barcellos, Lisa, Barizzone, Nadia, Beecham, Ashley, Berge, Tone, Bernardinelli, Luisa, Booth, David, Bos, Steffan, Buck, Dorothea, Butkiewicz, Mariusz, Celius, Elisabeth G., Comabella, Manuel, Compston, Alastair, Dedham, Katrina, Cotsapas, Chris, D’ Alfonso, Sandra, De Jager, Phil, Dubois, Benedicte, Duquette, Pierre, Fontaine, Bertrand, Gasperi, Christiane, Gil, Elia, Goris, An, Gourraud, Pierre Antoine, Graetz, Christiane, Gyllenberg, Alexandra, Hadjigeorgiou, Georgios, Hafler, David, Hribko, Deanna, Haines, Jonathan, Harbo, Hanne, Hauser, Stephen, Warto, Shannon, Hawkins, Clive, Hemmer, Bernhard, Henry, Roland, Hintzen, Rogier, Horakova, Dana, Ivinson, Adrian, Howard, Melissa, Jelcic, Ilijas, Kaskow, Belinda, Kira, Jun-Ichi, Kleinova, Pavlina, Kockum, Ingrid, Kucerova, Karolina, Lill, Christina, Luessi, Felix, Malhotra, Sunny, Martin, Roland, Martinelli, Filippo, Matsushita, Takuya, McCabe, Cristin, McCauley, Jacob, Mescheriakkova, Julia, Mitrovic, Mitja, Moen, Stine-Marit, Montalban, Xavier, Muhlau, Mark, Nakmura, Yuri, Oksenberg, Jorge, Olsson, Tomas, Oturai, Annette, Palotie, Aarno, Patsopoulos, Nikolaos, Pavlicova, Jana, Pericak-Vance, Peggy, Piehl, Fredrik, Rebeix, Isabelle, Rioux, John, Saarela, Janna, Sawcer, Stephen, Sellebjerg, Finn, Sondergaard, Helle Bach, Sorensen, Per Soelberg, Sospedra, Mireia, Spurkland, Anne, Stewart, Graeme, Taylor, Bruce, Uitterlinden, Andre, Van Duijn, Cornelia, Zipp, Frauke

    Veröffentlicht in Neuron (Cambridge, Mass.)

    Volltext
    Artikel
  12. 12
  13. 13

    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

    Volltext
    Artikel
  14. 14
  15. 15

    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

    Volltext
    Artikel
  16. 16
  17. 17
  18. 18
  19. 19
  20. 20