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

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Veröffentlicht in:CELL 2020-01, Vol.180 (2), p.403-403
Hauptverfasser: 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
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creator 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
description
doi_str_mv 10.1016/j.cell.2020.01.002
format Article
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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 ; International Multiple Sclerosis Genetics Consortium ; International Multiple Sclerosis Genetics Consortium. 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Electronic address: chris.cotsapas@yale.edu</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>SwePub</collection><collection>SwePub Other</collection><collection>SWEPUB Freely available online</collection><collection>SwePub Other full text</collection><jtitle>CELL</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Patsopoulos, Nikolaos A.</au><au>Beecham, Ashley H.</au><au>Goris, An</au><au>Dubois, Bénédicte</au><au>D’hooghe, Marie B.</au><au>Van Damme, Philip</au><au>Søndergaard, Helle Bach</au><au>Sellebjerg, Finn</au><au>Ullum, Henrik</au><au>Thørner, Lise W.</au><au>Werge, Thomas</au><au>Damotte, Vincent</au><au>Fontaine, Bertrand</au><au>Lathrop, Mark</au><au>Gourraud, Pierre-Antoine</au><au>Pongratz, Viola</au><au>Gasperi, Christiane</au><au>Bayas, Antonios</au><au>Heesen, Christoph</au><au>Linker, Ralf</au><au>Paul, Friedemann</au><au>Stangel, Martin</au><au>Tackenberg, Björn</au><au>Bergh, Florian Then</au><au>Wildemann, Brigitte</au><au>Tumani, Hayrettin</au><au>Gold, Ralf</au><au>Grummel, Verena</au><au>Knier, Benjamin</au><au>Lill, Christina M.</au><au>Dardiotis, Efthimios</au><au>Agliardi, Cristina</au><au>Barizzone, Nadia</au><au>Mascia, Elisabetta</au><au>Bernardinelli, Luisa</au><au>Cusi, Daniele</au><au>Ferrè, Laura</au><au>Comi, Cristoforo</au><au>Galimberti, Daniela</au><au>Leone, Maurizio A.</au><au>Mescheriakova, Julia</au><au>Hintzen, Rogier</au><au>van Duijn, Cornelia</au><au>Teunissen, Charlotte E.</au><au>Bos, Steffan D.</au><au>Myhr, Kjell-Morten</au><au>Celius, Elisabeth G.</au><au>Lie, Benedicte A.</au><au>Comabella, Manuel</au><au>Montalban, Xavier</au><au>Alfredsson, Lars</au><au>Stridh, Pernilla</au><au>Hillert, Jan</au><au>Piehl, Fredrik</au><au>Jelčić, Ilijas</au><au>Martin, Roland</au><au>Sospedra, Mireia</au><au>Hawkins, Clive</au><au>Hysi, Pirro</au><au>Karpe, Fredrik</au><au>Khadake, Jyoti</au><au>Lachance, Genevieve</au><au>Neville, Matthew</au><au>Santaniello, Adam</au><au>Caillier, Stacy J.</au><au>Calabresi, Peter A.</au><au>Cross, Anne</au><au>Davis, Mary F.</au><au>de Bakker, Paul I.W.</au><au>Delgado, Silvia</au><au>Dembele, Marieme</au><au>Edwards, Keith</au><au>Fitzgerald, Kathryn C.</au><au>Hakonarson, Hakon</au><au>Konidari, Ioanna</au><au>Lathi, Ellen</au><au>Manrique, Clara P.</au><au>Pericak-Vance, Margaret A.</au><au>Piccio, Laura</au><au>Schaefer, Cathy</au><au>McCabe, Cristin</au><au>Hadjigeorgiou, Georgios</au><au>Taylor, Bruce</au><au>Tajouri, Lotti</au><au>Charlesworth, Jac</au><au>Booth, David R.</au><au>Harbo, Hanne F.</au><au>Ivinson, Adrian J.</au><au>Hauser, Stephen L.</au><au>Compston, Alastair</au><au>Stewart, Graeme</au><au>Zipp, Frauke</au><au>Barcellos, Lisa F.</au><au>Baranzini, Sergio E.</au><au>Martinelli-Boneschi, Filippo</au><au>Ziegler, Andreas</au><au>McCauley, Jacob L.</au><au>Sawcer, Stephen J.</au><au>De Jager, Philip L.</au><au>Kockum, Ingrid</au><aucorp>International Multiple Sclerosis Genetics Consortium</aucorp><aucorp>International Multiple Sclerosis Genetics Consortium. 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title Low-Frequency and Rare-Coding Variation Contributes to Multiple Sclerosis Risk
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