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

Theunissen, Charlotte E.; Van Damme, Philip; Ullum, Henrik; Thørner, Lise W.; Werge, Thomas; Vukusik, Sandra; Warnke, Clemens; Wiendl, Heinz; Wildemann, Brigitte; Zettl, Uwe; Ziemann, Ulf; Tumani, Hayrettin; van Duijn, Cornelia; de Bakker, Paul I. W.; Weiner, Howard; Zipp, Frauke; Ziegler, Andreas; Søndergaard, Helle Bach; Sellebjerg, Finn; Sorensen, Per Soelberg; Saarela, Janna; Lathrop, Mark; Mitrovič, Mitja; Pongratz, Viola; Kümpfel, Tania; Linker, Ralf; Paul, Friedemann; Stangel, Martin; Tackenberg, Björn; Patsopoulos, Nikolaos A.; Lill, Christina M.; Knier, Benjamin; Luessi, Felix; Mascia, Elisabetta; Leone, Maurizio A.; Sorosina, Melissa; Mescheriakova, Julia; Teunissen, Charlotte E.; Myhr, Kjell-Morten; Lie, Benedicte A.; Spurkland, Anne; Montalban, Xavier; Stridh, Pernilla; Piehl, Fredrik; Martin, Roland; Sospedra, Mireia; Kalra, Seema; Karpe, Fredrik; Lachance, Genevieve; Khadake, Jyoti; Neville, Matthew; Santaniello, Adam; Konidari, Ioanna; Lathi, Ellen; Manrique, Clara P.; Pericak-Vance, Margaret A.; Piccio, Laura; Schaefer, Cathy; McCabe, Cristin; Olsson, Tomas; Taylor, Bruce; Tajouri, Lotti; Stewart, Graeme; Lemmens, Robin; Martinelli-Boneschi, Filippo; Oturai, Annette; McCauley, Jacob L.; Beecham, Ashley H.; Sawcer, Stephen J.; Oksenberg, Jorge R.; Dankowski, Theresa; Kockum, Ingrid; D’hooghe, Marie B.; Cournu-Rebeix, Isabelle; Consortium, International Multiple Sclerosis Genetics; Damotte, Vincent; Fontaine, Bertrand; Goris, An; Guillot-Noel, Lena; Gourraud, Pierre-Antoine; Gasperi, Christiane; Heesen, Christoph; The Wellcome Trust Case Control Consortium, 2.; Gold, Ralf; Grummel, Verena; Dubois, Bénédicte; Hemmer, Bernhard; Andlauer, Till F. M.; Dardiotis, Efthimios; Buck, Dorothea; Bayas, Antonios; Cusi, Daniele; Esposito, Federica; Ferrè, Laura; Bergh, Florian Then; Galimberti, Daniela; Hintzen, Rogier; Agliardi, Cristina; Barizzone, Nadia; Hillert, Jan; Bernardinelli, Luisa; Jagodic, Maja; Comi, Giancarlo; Comi, Cristoforo; Hawkins, Clive; Hysi, Pirro; Bos, Steffan D.; Celius, Elisabeth G.; Cree, Bruce A. C.; Comabella, Manuel; Cross, Anne; Alfredsson, Lars; Davis, Mary F.; Haines, Jonathan L.; Delgado, Silvia; Dembele, Marieme; Ban, Maria; Edwards, Keith; Dhooghe, M.; Fitzgerald, Kathryn C.; Hakonarson, Hakon; Caillier, Stacy J.; Calabresi, Peter A.; Jelčić, Ilijas; Goldstein, Jacqueline; Hadjigeorgiou, Georgios; Harbo, Hanne F.; Ivinson, Adrian J.; Hauser, Stephen L.; Chris Cotsapas@yale Edu, International Multiple Sclerosis Genetics Consortium Electronic address:; Charlesworth, Jac; Booth, David R.; D’Alfonso, Sandra; Compston, Alastair; Barcellos, Lisa F.; Baranzini, Sergio E.; De Jager, Philip L.; Hafler, David A.; Cotsapas, Chris

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Clemens Warnke
Theunissen et al., 2018

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Elsevier, Cell, 6(175), p. 1679-1687.e7, 2018

DOI: 10.1016/j.cell.2018.09.049

Cell Press, Cell, 2(180), p. 403, 2020

DOI: 10.1016/j.cell.2020.01.002

Cell Press, Cell, 1(178), p. 262

DOI: 10.1016/j.cell.2019.06.016

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@article{Theunissen2018,
  author = {Theunissen, Charlotte E. and Van Damme, Philip and Ullum, Henrik and Thørner, Lise W. and Werge, Thomas and Vukusik, Sandra and Warnke, Clemens and Wiendl, Heinz and Wildemann, Brigitte and Zettl, Uwe and Ziemann, Ulf and Tumani, Hayrettin and van Duijn, Cornelia and de Bakker, Paul I. W. and Weiner, Howard and Zipp, Frauke and Ziegler, Andreas and Søndergaard, Helle Bach and Sellebjerg, Finn and Sorensen, Per Soelberg and Saarela, Janna and Lathrop, Mark and Mitrovič, Mitja and Pongratz, Viola and Kümpfel, Tania and Linker, Ralf and Paul, Friedemann and Stangel, Martin and Tackenberg, Björn and Patsopoulos, Nikolaos A. and Lill, Christina M. and Knier, Benjamin and Luessi, Felix and Mascia, Elisabetta and Leone, Maurizio A. and Sorosina, Melissa and Mescheriakova, Julia and Teunissen, Charlotte E. and Myhr, Kjell-Morten and Lie, Benedicte A. and Spurkland, Anne and Montalban, Xavier and Stridh, Pernilla and Piehl, Fredrik and Martin, Roland and Sospedra, Mireia and Kalra, Seema and Karpe, Fredrik and Lachance, Genevieve and Khadake, Jyoti and Neville, Matthew and Santaniello, Adam and Konidari, Ioanna and Lathi, Ellen and Manrique, Clara P. and Pericak-Vance, Margaret A. and Piccio, Laura and Schaefer, Cathy and McCabe, Cristin and Olsson, Tomas and Taylor, Bruce and Tajouri, Lotti and Stewart, Graeme and Lemmens, Robin and Martinelli-Boneschi, Filippo and Oturai, Annette and McCauley, Jacob L. and Beecham, Ashley H. and Sawcer, Stephen J. and Oksenberg, Jorge R. and Dankowski, Theresa and Kockum, Ingrid and D’hooghe, Marie B. and Cournu-Rebeix, Isabelle and Consortium, International Multiple Sclerosis Genetics and Damotte, Vincent and Fontaine, Bertrand and Goris, An and Guillot-Noel, Lena and Gourraud, Pierre-Antoine and Gasperi, Christiane and Heesen, Christoph and The Wellcome Trust Case Control Consortium, 2. and Gold, Ralf and Grummel, Verena and Dubois, Bénédicte and Hemmer, Bernhard and Andlauer, Till F. M. and Dardiotis, Efthimios and Buck, Dorothea and Bayas, Antonios and Cusi, Daniele and Esposito, Federica and Ferrè, Laura and Bergh, Florian Then and Galimberti, Daniela and Hintzen, Rogier and Agliardi, Cristina and Barizzone, Nadia and Hillert, Jan and Bernardinelli, Luisa and Jagodic, Maja and Comi, Giancarlo and Comi, Cristoforo and Hawkins, Clive and Hysi, Pirro and Bos, Steffan D. and Celius, Elisabeth G. and Cree, Bruce A. C. and Comabella, Manuel and Cross, Anne and Alfredsson, Lars and Davis, Mary F. and Haines, Jonathan L. and Delgado, Silvia and Dembele, Marieme and Ban, Maria and Edwards, Keith and Dhooghe, M. and Fitzgerald, Kathryn C. and Hakonarson, Hakon and Caillier, Stacy J. and Calabresi, Peter A. and Jelčić, Ilijas and Goldstein, Jacqueline and Hadjigeorgiou, Georgios and Harbo, Hanne F. and Ivinson, Adrian J. and Hauser, Stephen L. and Chris Cotsapas@yale Edu, International Multiple Sclerosis Genetics Consortium Electronic address: and Charlesworth, Jac and Booth, David R. and D’Alfonso, Sandra and Compston, Alastair and Barcellos, Lisa F. and Baranzini, Sergio E. and De Jager, Philip L. and Hafler, David A. and Cotsapas, Chris},
  doi = {10.1016/j.cell.2018.09.049},
  journal = {Cell},
  month = {nov},
  pages = {262},
  title = {Low-Frequency and Rare-Coding Variation Contributes to Multiple Sclerosis Risk},
  url = {https://doi.org/10.1016/j.cell.2019.06.016},
  volume = {178},
  year = {2018}
}

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

Journal article published in 2018 by Charlotte E. Theunissen, Philip Van Damme, Henrik Ullum, Lise W. Thørner, Thomas Werge, Sandra Vukusik, Clemens Warnke