NR1H3 p.Arg415Gln Is Not Associated to Multiple Sclerosis Risk

Autor: 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

Publikováno v: In Neuron 19 October 2016 92(2):333-335

Network-Based Multiple Sclerosis Pathway Analysis with GWAS Data from 15,000 Cases and 30,000 Controls

Autor: 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.

Publikováno v: In The American Journal of Human Genetics 6 June 2013 92(6):854-865

Low-Frequency and Rare-Coding Variation Contributes to Multiple Sclerosis Risk

Autor: Int Multiple Sclerosis Genetics, Mitrovic, Mitja, Patsopoulos, Nikoloas, Beecham, Ashley, Dankowski, Theresa, Goris, An, Dubois, Bénédicte, D'hooghe, Marie B, Lemmens, Robin, Van Damme, Philip, Bach Sondergaard, Helle, Sellebjerg, Finn, Soelberg Sorensen, Per, Ullum, Henrik, Thorner, Lise W, Werge, Thomas, Saarela, Janna, Cournu-Rebeix, Isabelle, Damotte, Vincent, Fontaine, Bertrand, Guillot-Noel, Lena, Lathrop, Mark, Vukusik, Sandra, Gourraud, Pierre-Antoine, Andlauer, Till FM, Pongratz, Viola, Buck, Dorothea, Gasperi, Christiane, Bayas, Antonios, Heesen, Christoph, Kümpfel, Tania, Linker, Ralf, Friedemann, Paul, Stangel, Martin, Tackenberg, Björn, Then Bergh, Florian, Warnke, Clemens, Wiendl, Heinz, Wildemann, Brigitte, Zettl, Uwe, Ziemann, Ulf, Tumani, Hayrettin, Gold, Ralf, Grummel, Verena, Hemmer, Bernhard, Knier, Benjamin, Lill, Christina, Luessi, Felix, Dardiotis, Efthimios, Agliardi, Cristina, Barizzone, Nadia, Mascia, Elisabetta, Bernardinelli, Luisa, Comi, Giancarlo, Cusi, Daniele, Esposito, Federica, Ferrè, Laura, Comi, Cristoforo, Galimberti, Daniela, Leone, Maurizio A, Sorosina, Melissa, Mescheriakova, Julia, Hintzen, Rogier, van Duijn, Cornelia, Theunissen, Charlotte E, Bos, Steffan D, Myhr, Kjell-Morten, Celius, Elisabeth G, Lie, Benedicte A, Spurkland, Anne, Comabella, Manuel, Montalban, Xavier, Alfredsson, Lars, Stridh, Pernilla, Hillert, Jan, Jagodic, Maja, Piehl, Fredrik, Jelcic, Ilijas, Martin, Roland, Sospedra, Mireia, Ban, Maria, Hawkins, Clive, Hysi, Pirro, Kalra, Seema, Karpe, Fredrik, Khadake, Jyoti, Lachance, Genevieve, Neville, Matthew, Santaniello, Adam, Caillier, Stacy J, Calavresi, Peter A, Cree, Bruce AC, Cross, Anne, Davis, Mary F, Haines, Jonathan L, de Bakker, Paul IW, 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, Weiner, Howard, Goldstein, Jacqueline, Olsson, Tomas, Hadjigeorgiou, Georgios, Taylor, Bruce, Tajouri, Lotti, Charlesworth, Jac, Booth, David R, HArbo, Hanne F, Ivinson, Adrian J, Hauser, Stephen L, Compston, Alistair, Stewart, Graeme, Zipp, Frauke, Barcellos, Lisa F, Baranzini, Sergio E, Martinelli-Boneschi, Filippo, D'Alfonso, Sandra, Ziegler, Andreas, Oturai, Annette, McCauley, Jacob L, Sawcer, Stephen J, Oksenberg, Jorge R, De Jager, Philip L, Kockum, Ingrid, Hafler, David A, Cotsapas, Chris

Multiple sclerosis is a complex neurological disease, with ∼20% of risk heritability attributable to common genetic variants, including >230 identified by genome-wide association studies. Multiple strands of evidence suggest that much of the remain

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od______1131::5366a92aac5ee1b785896be136ee22c9
https://lirias.kuleuven.be/handle/123456789/631829

Low-Frequency and Rare-Coding Variation Contributes to Multiple Sclerosis Risk

Autor: Mitrovič, Mitja, Patsopoulos, Nikolaos A., Beecham, Ashley H., Dankowski, Theresa, Goris, An, Dubois, Bénédicte, D’hooghe, Marie B., Lemmens, Robin, Van Damme, Philip, Søndergaard, Helle Bach, Sellebjerg, Finn, Sorensen, Per Soelberg, Ullum, Henrik, Thørner, Lise W., Werge, Thomas, Saarela, Janna, Cournu-Rebeix, Isabelle, Damotte, Vincent, Fontaine, Bertrand, Guillot-Noel, Lena, Lathrop, Mark, Vukusik, Sandra, Gourraud, Pierre-Antoine, Andlauer, Till F.M., Pongratz, Viola, Buck, Dorothea, Gasperi, Christiane, Bayas, Antonios, Heesen, Christoph, Kümpfel, Tania, Linker, Ralf, Paul, Friedemann, Stangel, Martin, Tackenberg, Björn, Bergh, Florian Then, Warnke, Clemens, Wiendl, Heinz, Wildemann, Brigitte, Zettl, Uwe, Ziemann, Ulf, Tumani, Hayrettin, Gold, Ralf, Grummel, Verena, Hemmer, Bernhard, Knier, Benjamin, Lill, Christina M., Luessi, Felix, Dardiotis, Efthimios, Agliardi, Cristina, Barizzone, Nadia, Mascia, Elisabetta, Bernardinelli, Luisa, Comi, Giancarlo, Cusi, Daniele, Esposito, Federica, Ferrè, Laura, Comi, Cristoforo, Galimberti, Daniela, Leone, Maurizio A., Sorosina, Melissa, Mescheriakova, Julia, Hintzen, Rogier, van Duijn, Cornelia, Teunissen, Charlotte E., Bos, Steffan D., Myhr, Kjell-Morten, Celius, Elisabeth G., Lie, Benedicte A., Spurkland, Anne, Comabella, Manuel, Montalban, Xavier, Alfredsson, Lars, Stridh, Pernilla, Hillert, Jan, Jagodic, Maja, Piehl, Fredrik, Jelčić, Ilijas, Martin, Roland, Sospedra, Mireia, Ban, Maria, Hawkins, Clive, Hysi, Pirro, Kalra, Seema, Karpe, Fredrik, Khadake, Jyoti, Lachance, Genevieve, Neville, Matthew, Santaniello, Adam, Caillier, Stacy J., Calabresi, Peter A., Cree, Bruce A.C., Cross, Anne, Davis, Mary F., Haines, Jonathan L., 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, Weiner, Howard, Goldstein, Jacqueline, Olsson, Tomas, 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, D’Alfonso, Sandra, Ziegler, Andreas, Oturai, Annette, McCauley, Jacob L., Sawcer, Stephen J., Oksenberg, Jorge R., De Jager, Philip L., Kockum, Ingrid, Hafler, David A., Cotsapas, Chris

Publikováno v: In Cell 23 January 2020 180(2):403-403

Low-Frequency and Rare-Coding Variation Contributes to Multiple Sclerosis Risk

Autor: Mitrovič, Mitja, Patsopoulos, Nikolaos A., Beecham, Ashley H., Dankowski, Theresa, Goris, An, Dubois, Bénédicte, D’hooghe, Marie B., Lemmens, Robin, Van Damme, Philip, Søndergaard, Helle Bach, Sellebjerg, Finn, Sorensen, Per Soelberg, Ullum, Henrik, Thørner, Lise W., Werge, Thomas, Saarela, Janna, Cournu-Rebeix, Isabelle, Damotte, Vincent, Fontaine, Bertrand, Guillot-Noel, Lena, Lathrop, Mark, Vukusik, Sandra, Gourraud, Pierre-Antoine, Andlauer, Till F.M., Pongratz, Viola, Buck, Dorothea, Gasperi, Christiane, Bayas, Antonios, Heesen, Christoph, Kümpfel, Tania, Linker, Ralf, Paul, Friedemann, Stangel, Martin, Tackenberg, Björn, Bergh, Florian Then, Warnke, Clemens, Wiendl, Heinz, Wildemann, Brigitte, Zettl, Uwe, Ziemann, Ulf, Tumani, Hayrettin, Gold, Ralf, Grummel, Verena, Hemmer, Bernhard, Knier, Benjamin, Lill, Christina M., Luessi, Felix, Dardiotis, Efthimios, Agliardi, Cristina, Barizzone, Nadia, Mascia, Elisabetta, Bernardinelli, Luisa, Comi, Giancarlo, Cusi, Daniele, Esposito, Federica, Ferrè, Laura, Comi, Cristoforo, Galimberti, Daniela, Leone, Maurizio A., Sorosina, Melissa, Mescheriakova, Julia, Hintzen, Rogier, van Duijn, Cornelia, Teunissen, Charlotte E., Bos, Steffan D., Myhr, Kjell-Morten, Celius, Elisabeth G., Lie, Benedicte A., Spurkland, Anne, Comabella, Manuel, Montalban, Xavier, Alfredsson, Lars, Stridh, Pernilla, Hillert, Jan, Jagodic, Maja, Piehl, Fredrik, Jelčić, Ilijas, Martin, Roland, Sospedra, Mireia, Ban, Maria, Hawkins, Clive, Hysi, Pirro, Kalra, Seema, Karpe, Fredrik, Khadake, Jyoti, Lachance, Genevieve, Neville, Matthew, Santaniello, Adam, Caillier, Stacy J., Calabresi, Peter A., Cree, Bruce A.C., Cross, Anne, Davis, Mary F., Haines, Jonathan L., 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, Weiner, Howard, Goldstein, Jacqueline, Olsson, Tomas, 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, D’Alfonso, Sandra, Ziegler, Andreas, Oturai, Annette, McCauley, Jacob L., Sawcer, Stephen J., Oksenberg, Jorge R., De Jager, Philip L., Kockum, Ingrid, Hafler, David A., Cotsapas, Chris

Publikováno v: In Cell 27 June 2019 178(1):262-262